Difference between revisions of "Surface Coating Technologies"

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Besides manufacturing contact materials from the solid phase, i.e. by melt or powder metallurgy, the production starting in the liquid or gaseous phase is generally preferred when thin layers within the μm range are required, which cannot be obtained economically by conventional cladding methods (<xr id="tab:Overview_of_Important_Properties_of_Electroplated_Coatings_and_their_Applications"/><!--(Tab. 7.1)-->). Such coatings fulfill different requirements depending on their composition and thickness.
+
Besides manufacturing contact materials from the solid phase, i.e. by melt or
They can serve as corrosion or wear protection or can fulfill the need for thin contact layers for certain technical applications. In addition they serve for decorative purposes as a pleasing and wear resistant surface coating.
+
powder metallurgy, the production starting in the liquid or gaseous phase is
 +
generally preferred when thin layers in the μm range are required which cannot
 +
be obtained economically by conventional cladding methods. Such coatings
 +
fulfill different requirements depending on their composition and thickness.
 +
They can serve as corrosion or wear protection or can fulfill the need for thin
 +
contact layers for certain technical applications. In addition they serve for
 +
decorative purposes as a pleasing and wear resistant surface coating.
  
<figtable id="tab:Overview_of_Important_Properties_of_Electroplated_Coatings_and_their_Applications">
+
Table 7.1: Overview of Important Properties of Electroplated Coatings
<caption>'''<!--Table 7.1:-->Overview of Important Properties of Electroplated Coatings and their Applications'''</caption>
+
and their Applications
  
{| class="twocolortable" style="text-align: left; font-size: 12px"
+
To reduce the mechanical wear of thin surface layers on sliding and connector
|-
+
contacts additional lubricants in liquid form are often used. On silver contacts
!Properties
+
passivation coatings are applied as protection against silver sulfide formation.
!Applications
 
!Examples
 
|-
 
|Color
 
|Pleasing appearance
 
|Brass plated lamps and furniture hardware
 
|-
 
|Luster
 
|Decorative appearance, Light reflection
 
|Chrome plated fixtures, silver coated mirrors
 
|-
 
|Hardness / Wear Resistance
 
|Prolonging of mechanical wear life
 
|Hard chrome plated tools
 
|-
 
|Sliding properties
 
|Improvement of dry sliding wear
 
|Lead-tin-copper alloys for slide bearings
 
|-
 
|Chemical stability
 
|Protection against chemical effects
 
|Lead-Tin coatings as etch resist on PC boards
 
|-
 
|Corrosion resistance
 
|Protection against environmental corrosion
 
|Zinc coatings on steel parts
 
|-
 
|Electrical conductivity
 
|Surface conduction of electrical current
 
|Conductive path on PC boards
 
|-
 
|Thermal conductivity
 
|Improved heat conduction on the surface
 
|Copper plated bottoms for cookware
 
|-
 
|Machining capability
 
|Shaping through machining
 
|Copper coatings on low pressure cylinders
 
|-
 
|Magnetic properties
 
|Increase of coercive force [[#text-reference|<sup>*)</sup>]]
 
|Cobalt-nickel layers on magnetic storage media
 
|-
 
|Brazing and soldering
 
|Brazing without aggressive fluxes
 
|Tin-Lead coatings on PC board paths
 
|-
 
|Adhesion strength
 
|Improvement of adhesion
 
|Brass coating on reinforcement steel wires in tires
 
|-
 
|Lubricating properties
 
|Improvement of formability
 
|Copper plating for wire drawing
 
|}
 
</figtable>
 
<div id="text-reference">*) Coercive force= force to retaim the adopted magnetisation</div>
 
  
To reduce the mechanical wear of thin surface layers on sliding and connector contacts, additional lubricants in liquid form are often used. On silver contacts, passivation coatings are applied as protection against silver sulfide formation.
+
===7.1 Coatings from the Liquid Phase===
 +
For thin coatings starting from the liquid phase two processes are used
 +
differentiated by the metallic deposition being performed either with or without
 +
the use of an external electrical current source. The first one is electroplating
 +
while the second one is a chemical deposition process.
  
==Coatings from the Liquid Phase==
+
===7.1.1 Electroplating (or Galvanic Deposition)===
For thin coatings starting from the liquid phase, two processes are used differentiated by the metallic deposition being performed either with or without the use of an external electrical current source. The first one is electroplating, while the second one is a chemical deposition process.
+
For electroplating of metals, especially precious metals, water based solutions
 +
(electrolytes) are used which contain the metals to be deposited as ions (i.e.
 +
dissolved metal salts). An electric field between the anode and the work pieces
 +
as the cathode forces the positively charged metal ions to move to the cathode
 +
where they give up their charge and deposit themselves as metal on the surface
 +
of the work piece.
 +
Depending on the application, for electric and electronic or decorative end use,
 +
different electrolytic bath solutions (electrolytes) are used. The electroplating
 +
equipment used for precious metal plating and its complexity varies widely
 +
depending on the process technologies employed.
 +
Electroplating processes are encompassing besides the pure metal deposition
 +
also preparative and post treatments of the goods to be coated. An important
 +
parameter for creating strongly adhering deposits is the surface of the goods to
 +
be metallic clean without oily or oxide film residues. This is achieved through
 +
various pre-treatment processes specifically developed for the types of material
 +
and surface conditions of the goods to be plated.
 +
In the following segments electrolytes – both precious and non-precious – as
 +
well as the most widely used electroplating processes are described.
  
=== Electroplating (or Galvanic Deposition)===
+
===7.1.1.1 Electroplating Solutions – Electrolytes===
For electroplating of metals, especially precious metals, water based solutions (electrolytes) are used, which contain the metals to be deposited as ions (i.e. dissolved metal salts). An electric field between the anode and the work pieces as the cathode, forces the positively charged metal ions to move to the cathode where they give up their charge and deposit themselves as metal on the surface of the work piece.
+
The actual metal deposition occurs in the electrolytic solution which contains
Depending on the application, for electric and electronic or decorative end use, different electrolytic bath solutions (electrolytes) are used. The electroplating equipment used for precious metal plating and its complexity varies widely, depending on the process technologies employed.
+
the plating material as metal ions. Besides this basic ingredient, the electrolytes
Electroplating processes are encompassing, besides the pure metal deposition, also preparative and post treatments of the goods to be coated. An important parameter for creating strongly adhering deposits is that the surface of the goods has to be metallic clean without oily or oxide film residues. This is achieved through various pre-treatment processes, specifically developed for the types of material and surface conditions of the goods to be plated.
+
contain additional components depending on the processes used, such as for
In the following segments, electrolytes – both precious and non-precious – as well as the most widely used electroplating processes are described.
+
example conduction salts, brighteners, and organic additives which are codeposited
 +
into the coatings, influencing the final properties of the electroplating
 +
deposit.
  
Main Articel: [[Electroplating (or Galvanic Deposition)| Electroplating (or Galvanic Deposition)]]
+
===7.1.1.1.1 Precious Metal Electrolytes===
 +
All precious metals can be electroplated with silver and gold by far the most
 +
widely used ones ''(Tables 7.1 and 7.2)''.
 +
The following precious metal electrolytes are the most important ones:
  
===<!--7.1.2-->Electroless Plating===
+
*'''Gold electrolytes''' For functional and decorative purposes pure gold, hard gold, low-karat gold, or colored gold coatings are deposited. Depending on the requirements, acidic, neutral, or cyanide electrolytes based on potassium gold cyanide or cyanide free and neutral electrolytes based on gold sulfite complexes are used.
  
Electroless plating is defined as a coating process which is performed without the use of an external current source. It allows a uniform metal coating, independent of the geometrical shape of the parts, to be coated. Because of the very good dispersion capability of the used electrolytes, also cavities and the inside of drilled holes in parts can be coated for example.
+
*'''Palladium and Platinum electrolytes''' Palladium is mostly deposited as a pure metal, for applications in electrical contacts however also as palladium nickel. For higher value jewelry allergy protective palladium intermediate layers are used as a diffusion barrier over copper alloy substrate materials. Platinum is mostly used as a surface layer on jewelry items.
In principal, two different mechanisms are employed for electroless plating: processes in which the carrier material serves as a reduction agent (Immersion processes) and those in which a reduction agent is added to the electrolyte (Electroless processes).
 
  
Main Articel: [[Electroless Plating| Electroless Plating]]
+
*'''Ruthenium electrolytes''' Ruthenium coatings are mostly used for decorative purposes creating a fashionable “grey” ruthenium color on the surface. An additional color variation is created by using “ruthenium-black” deposits which are mainly used in bi-color decorative articles.
  
==<!--7.2-->Coatings from the Gaseous Phase (Vacuum Deposition)==
+
*'''Rhodium electrolytes''' Rhodium deposits are extremely hard (HV 700 – 1000) and wear resistant. They also excel in light reflection. Both properties are of value for technical as well as decorative applications. While technical applications mainly require hard, stress and crack free coatings, the jewelry industry takes advantage of the light whitish deposits with high corrosion resistance.
The term PVD (physical vapor deposition) defines processes of metal, metal alloys and chemical compounds deposition in a vacuum by adding thermal and kinetic energy by particle bombardment. The main processes are the following four coating variations (<xr id="tab:Characteristics of the Most Important PVD Processes"/><!--(Table 7.6-->):
 
  
*Vapor deposition   
+
*'''Silver electrolytes''' Silver electrolytes without additives generate dull soft deposits (HV ~ 80) which are mainly used as contact layers on connectors with limited insertion and withdrawal cycles. Properties required for decorative purposes such as shiny bright surfaces and higher wear resistance are achieved through various additives to the basic Ag electrolyte.
*Sputtering (Cathode atomization)
 
*Arc vaporizing     
 
*Ion implantation
 
  
In all four processes, the coating material is transported in its atomic form to the substrate and deposited on it as a thin layer (a few nm to approx. 10 μm)
+
Table 7.2: Precious Metal Electrolytes for Technical Applications
  
 +
===7.1.1.1.2 Non-Precious Metal Electrolytes===
 +
The most important non-precious metals that are deposited by electroplating
 +
are: Copper, nickel, tin, and zinc and their alloys. The deposition is performed in
 +
the form of pure metals with different electrolytes used ''(Table 7.4).''
  
<figtable id="tab:Characteristics of the Most Important PVD Processes">
+
*'''Copper electrolytes''' Copper electrolytes are used for either depositing an intermediate layer on strips or parts, for building up a printed circuit board structure, or for the final strengthening during the production of printed circuit boards.
<caption>'''<!--Table 7.6:-->Characteristics of the Most Important PVD Processes'''</caption>
 
  
{| class="twocolortable" style="text-align: left; font-size: 12px"
+
*'''Tin electrolytes''' Pure tin and tin alloy deposits are used as dull or also bright surface layers on surfaces required for soldering. In the printed circuit board manufacturing they are also utilized as an etch resist for the conductive pattern design after initial copper electroplating.
|-
 
!Process
 
!Principle
 
!Process Gas Pressure
 
!Particle Energy
 
!Remarks
 
|-
 
|Vapor deposition
 
|Vaporizing in a crucible <br />(electron beam or resistance heating)
 
|10<sup>-3</sup> Pa
 
|< 2eV
 
|Separation of alloy components may occur
 
|-
 
|Arc vaporizing
 
|Vaporizing of the target <br />plate in an electrical arc
 
|10<sup>-1</sup> Pa-1Pa
 
|80eV-300eV
 
|Very good adhesion due to ion bombardement
 
|-
 
|Sputtering
 
|Atomizing of the target plate<br />(cathode) in a gas discharge
 
|10<sup>-1</sup> Pa-1Pa
 
|10eV-100eV
 
|Sputtering of non-conductive materials possible through RF operation
 
|-
 
|Ion implantation
 
|Combination of vapor <br />deposition and sputtering
 
|10<sup>-1</sup> Pa-1Pa
 
|80eV-300eV
 
|Very good adhesion from ion bombardment but also heating of the substrate material
 
|}
 
</figtable>
 
  
 +
Table 7.3: Precious Metal Electrolytes for Decorative Applications
  
The sputtering process has gained the economically most significant usage. Its process principle is illustrated in (<xr id="fig:Principle of sputtering"/><!--(Fig. 7.5)-->).
+
*'''Nickel electrolytes''' Nickel layers are mostly used as diffusion barriers during the gold plating of copper and copper alloys or as an intermediate layer for tinning
  
<figure id="fig:Principle of sputtering">
+
*'''Bronze electrolytes''' Bronze coatings – in white or yellow color tones – are used either as an allergy free nickel replacement or as a surface layer for decorative purposes. For technical applications the bronze layers are utilized for their good corrosion resistance and good brazing and soldering properties.
[[File:Principle of sputtering.jpg|right|thumb|Figure 1: Principle of sputtering Ar = Argon atoms; e = Electrons; M = Metal atoms]]
 
</figure>
 
Initially, a gas discharge is ignited in a low pressure (10<sup>-1</sup> -1 Pa) argon atmosphere. The argon ions generated, are accelerated in an electric field and impact the target of material to be deposited with high energy. Caused by this energy, atoms are released from the target material which condensate on the oppositely arranged anode (the substrate) and form a layer with high adhesion strength. Through an overlapping magnetic field at the target location, the deposition rate can be increased, making the process more economical.
 
  
The advantages of the PVD processes and especially sputtering for electrical contact applications are:
+
Table 7.2: Typical Electrolytes for the Deposition of Non-Precious Metals
  
*High purity of the deposit layers 
+
===7.1.1.2 Electroplating of Parts===
*Low thermal impact on the substrate
+
The complete or all-around electroplating of small mass produced parts like
*Almost unlimited coating materials 
+
contact springs, rivets, or pins is usually done as mass plating in electroplating
*Low coating thickness tolerance   
+
barrels of different shape. During the electroplating process the parts are
*Excellent adhesion (also by using additional intermediate layers)
+
continuously moved and mixed to reach a uniform coating.
  
Coatings produced by PVD processes are used for contact applications, for example on miniature-profiles, in electrical engineering and for electronic components, for solderability in joining processes, for metalizing of nonconductive materials, as well as in semiconductors, opto-electronics, optics and medical technology applications.
+
Larger parts are frequently electroplated on racks either totally or by different
 +
masking techniques also partially. Penetrating the coating into the interior of
 +
drilled holes or tubes can be achieved with the use of special fixtures.
  
There are few limitations regarding the geometrical shape of substrate parts. Only the interior coating of drilled holes and small diameter tubing can be more problematic (ratio of depth to diameter should be < 2:1). Profile wires, strips and foils can be coated from one side or both; formed parts can be coated selectively by using masking fixtures that at the same time serve as holding fixtures  (<xr id="fig:Examples of vacuum coated semi finished materials and parts"/>).
+
===Electroplated Parts===
 +
bild
  
<figure id="fig:Examples of vacuum coated semi finished materials and parts">
+
*'''Materials'''
[[File:Examples of vacuum coated semi finished materials and parts.jpg|left|Figure 2: Examples of vacuum coated semi finished materials and parts]]
 
</figure>
 
  
<br style="clear:both;"/>
+
*'''Coating thickness'''
*'''Materials'''
 
Selection of possible combinations of coating and substrate materials
 
  
<table class="twocolortable">
+
Precious metals: 0.2 – 5 μm (typical layer thicknesses; for Ag also up to 25 μm)
<tr><th rowspan="2"><p class="s8">Substrate Materials</p></th><th colspan="12"><p class="s8">Coating Materials</p></th></tr>
+
Non-precious metals: Up to approx. 20 μm
<tr><th><p><span>Ag</span></p></th><th><p><span>Au</span></p></th><th><p><span>Pt</span></p></th><th><p><span>Pd</span></p></th><th><p><span>Cu</span></p></th><th><p><span>Ni</span></p></th><th><p><span>Ti</span></p></th><th><p><span>Cr</span></p></th><th><p><span>Mo</span></p></th><th><p><span>W</span></p></th><th><p><span>Ai</span></p></th><th><p><span>Si</span></p></th></tr>
+
Tolerances: Strongly varying depending on the geometrical shape of
<tr><td><p class="s8">Precious metal / alloys</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">NF metals / alloys</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Fe alloys / stainless steel</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Special metals (Ti, Mo, W)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Carbide steels (WC-Co)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Ceramics (Al<span class="s16">2</span>O<span class="s16">3</span>, AlN)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Glasses (SiO<span class="s16">2</span>, CaF)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Plastics (PA, PPS)</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr></table>
+
parts (up to 50% at a defined measuring spot).
 +
It is recommended to specify a minimum value for the
 +
coating thickness at a defined measuring spot
  
[[File:K7-gef.png]] can be produced
+
als Bild?
[[File:K7-leer.png]] can be produced with intermediate layer
 
  
*'''Dimensions'''
+
*'''Quality criteria'''  
 +
Besides others the following layer parameters are typically monitored in-process and documented:
  
{| class="twocolortable" style="text-align: left; font-size: 12px;width:40%"
+
*Coating thickness *Solderability
|-
+
*Adhesion strength  *Bonding property
!colspan="2" style="text-align:center"|'''Dimensions'''
+
*Porosity Contact  *resistance
|-
 
|Coating thickness:
 
|10 nm - 15 μm
 
|-
 
|Coating thicknesses for contact applications:
 
|0.1 - 10 μm
 
|}
 
  
For the geometry of semi-finished products to be coated, there are few restrictions. Only the coating of the inside of machined holes and tubing has
+
These quality tests are performed according to industry standards, internal
limitations.
+
standards, and customer specifications resp.
  
*'''Tolerances'''
+
===7.1.1.3 Electroplating of Semi-finished Materials===
 +
The process for overall electroplating of strips, profiles, and wires is mostly
 +
performed on continuously operating reel-to-reel equipment. The processing
 +
steps for the individual operations such as pre-cleaning, electroplating, rinsing
 +
are following the same principles as those employed in parts electroplating.
  
Coating thickness &#177;10 - 30 %, depending on the thickness
+
The overall coating is usually applied for silver plating and tin coating of strips
 +
and wires. Compared to hard gold or palladium these deposits are rather
 +
ductile, ensuring that during following stamping and forming operations no
 +
cracks are generated in the electroplated layers.
  
*'''Quality criteria'''
+
===7.1.1.4 Selective Electroplating===
Depending on the application, the following parameters are tested and recorded (see also: Electroplating of parts):
+
Since precious metals are rather expensive it is necessary to perform the
 +
electroplating most economically and coat only those areas that need the layers
 +
for functional purposes. This leads from overall plating to selective
 +
electroplating of strip material in continuous reel-to-reel processes. Depending
 +
on the final parts design and the end application the processes can be applied
 +
to solid strip material as well as pre-stamped and formed continuous strips or
 +
utilizing wire-formed or machined pins which have been arranged as bandoliers
 +
attached to conductive metal strips.
  
*Coating thickness 
+
The core part of selective precious metal electroplating is the actual
*Solderability
+
electroplating cell. In it the anode is arranged closely to the cathodic polarized
*Adhesion strength 
+
material strip. Cathode screens or masks may be applied between the two to
*Bonding property
+
focus the electrical field onto closely defined spots on the cathode strip.
*Porosity         
 
*Contact resistance
 
  
These quality tests are performed according to industry standards, internal standards and customer specifications resp.
+
Special high performance electrolytes are used in selective electroplating to
 +
reach short plating times and allow a high flow rate of the electrolyte for a fast
 +
electrolyte exchange in the actual coating area.
  
==<!--7.3-->Comparison of Deposition Processes==
+
For a closely targeted electroplating of limited precious metal coating of contact
The individual deposition processes have in part different performance characteristics. For each end application, the optimal process has to be chosen, considering all technical and economical factors. The main selection criteria should be based on the electrical and mechanical requirements for the contact layer and on the design characteristics of the contact component. <xr id="tab:Comparison of different coating processes"/><!--Table 7.7--> gives some indications for a comparative evaluation of the different coating processes.
+
springs so-called brush-electroplating cells are employed ''(Fig. 7.1)''. The “brush”
 +
or “tampon” consists of a roof shaped titanium metal part covered with a special
 +
felt-like material. The metal body has holes in defined spots through which the
 +
electrolyte reaches the felt. In the same spots is also the anode consisting of a
 +
fine platinum net. The pre-stamped and in the contact area pre-formed contact
 +
spring part is guided under a defined pressure over the electrolyte soaked felt
 +
material and gets wetted with the electrolyte. This allows the metal
 +
electroplating in highly selective spots.
  
The electroless metal coating is not covered here because of the low thickness of deposits, which makes them in most cases not suitable for contact
+
Fig. 7.1:
applications.
+
Brush (or “Tampon”) plating cell;
 +
1 Strip; 2 Anode; 3 Electrolyte feed;
 +
4 Felt covered cell
  
 +
For special applications, such as for example electronic component substrates,
 +
a dot shaped precious metal coating is required. This is achieved with two belt
 +
masks running synchronous to the carrier material. One of these two masks has
 +
windows which are open to the spot areas targeted for precious metal plating
 +
coverage.
  
<figtable id="tab:Comparison of different coating processes">
+
===Summary of the processes for selective electroplating===
<caption>'''<!--Table 7.7:-->Comparison of different coating processes'''</caption>
 
  
{| class="twocolortable" style="text-align: left; font-size: 12px"
+
*'''Immersion electroplating'''
|-
+
Overall or selective electroplating of both sides of solid strips or pre-stamped
!Process / Coating Properties
+
parts in strip form
!Mechanical Processes (Cladding)
 
!Electroplating
 
!Vaccum Deposition (Sputtering)
 
|-
 
|Coating material
 
|formabe metal and alloys
 
|metals, alloys only limited
 
|metals and alloys
 
|-
 
|Coating thickness
 
|> 1μm
 
|0.1 - approx. 10 μm <br />(in special cases up to 100 μm)
 
|0.1 approx. 10 μm
 
|-
 
|Coating configuration
 
|selectively, stamping edges not coated
 
|all around and selectively<br />stamping edges coated
 
|mostly selectivity
 
|-
 
|Adhesion
 
|good
 
|good
 
|very good
 
|-
 
|Ductility
 
|good
 
|limited
 
|good
 
|-
 
|Purity
 
|good
 
|inclusions of foreign materials
 
|very good
 
|-
 
|Porosity
 
|good
 
|good for > approx. 1μm
 
|good
 
|-
 
|Temperature stability
 
|goodvery good
 
|good
 
|very good
 
|-
 
|Mechanical wear
 
|little
 
|very little
 
|little
 
|-
 
|Environmental impact
 
|little
 
|significant
 
|none
 
|}
 
</figtable>
 
  
The main differences between the coating processes are found in the coating materials and thickness. While mechanical cladding and sputtering allow the use of almost any alloy material, electroplating processes are limited to metals and selected alloys, such as for example high-carat gold alloys with up to .3 wt% Co or Ni. Electroplated and sputtered surface layers have a technological and economical upper thickness limit of about 10μm. While mechanical cladding has a minimum thickness of approx. 1 μm, electroplating and sputtering can also be easily applied in very thin layers down to the range of 0.1 μm.
+
*'''Stripe electroplating'''
 +
Stripe electroplating on solid strips through wheel cells or using masking
 +
techniques
  
The properties of the coatings are closely related to the coating process. Starting materials for cladding and sputtering targets precious metals and their alloys, which in the case of gold and palladium based materials, are vacuum melted and therefore exhibit a very high purity. During electroplating, depending on the type of electrolytes and the deposition parameters, some electrolyte components such as carbon and organic compounds are incorporated into the precious metal coating. Layers deposited from the gaseous phase however are very pure.
+
*'''Selective electroplating'''
 +
One-sided selective coating of solid, pre-stamped, or metallically belt-linked
 +
strips by brush plating
  
==<!--7.4-->Hot (-Dipped) Tin Coated Strip Materials==
+
*'''Spot electroplating'''
During hot-dip tinning, pre-treated strip materials are coated with pure tin or tin alloys from a liquid solder metal. During overall (or all-around) tinning the strips through a liquid metal melt. For strip tinning, rotating rolls are partially immersed into a liquid tin melt and transport the liquid onto the strip, which is guided above them. Through special wiping and gas blowing procedures, the deposited tin layer can be held within tight tolerances. Hot tinning is performed directly onto the base substrate material without any pre-coating with either copper or nickel. Special cast-on processes or the melting of solder foils onto the carrier strip, also allows the production of thicker solder layers ( > 15 μm).
+
Electroplating in spots of solid strips with guide holes or pre-stamped parts in
 +
strip form
  
The main advantage of hot tinning of copper and copper alloys, compared to tin electroplating, is the formation of an inter-metallic copper-tin phase (Cu<sub>3</sub>Sn, Cu<sub>6</sub>Sn<sub>5</sub>) at the boundary between the carrier material and the tin layer. This thin (0.3 – 0.5 μm) intermediate layer, which is formed during the thermal tinning process, is rather hard and reduces the frictional force and mechanical wear in connectors. Tin coatings produced by hot tinning have a good adhesion to the substrate material and do not tend to tin whisker formation.
+
===Typical examples of electroplated semi-finished materials===
 +
(overall or selectively)
 +
bild
  
A special process of hot tinning is the “Reflow” process. After depositing a tin coating by electroplating, the layer is short-time melted in a continuous process.
+
*'''Materials'''
The properties of these reflow tin coatings are comparable to those created by conventional hot tinning.
 
  
Besides overall tin coating of strip material, the hot tinning can also be applied in the form of single or multiple stripes on both sides of a continuous substrate strip (<xr id="fig:Typical examples of hot tinned strip materials"/>).
+
<table border="1" cellspacing="0" style="border-collapse:collapse"><tr><td><p class="s8">Type of Coatings</p></td><td><p class="s8">Coating Thickness</p></td><td><p class="s8">Remarks</p></td></tr><tr><td><p class="s8">Precious Metals</p></td><td/><td/></tr><tr><td><p class="s8">Pure gold</p><p class="s8">Hard gold (AuCo 0.3)</p></td><td><p class="s8">0.1 - 3 µm</p></td><td><p class="s8">In special cases up to 10 µm</p></td></tr><tr><td><p class="s8">Palladium-nickel (PdNi20)</p></td><td><p class="s8">0.1 - 5 µm</p></td><td><p class="s8">Frequently with additional 0.2 µm AuCo 0.3</p></td></tr><tr><td><p class="s8">Silver</p></td><td><p class="s8">0.5 - 10 µm</p></td><td><p class="s8">In special cases up to 40 µm</p></td></tr><tr><td><p class="s8">Non-precious Metals</p></td><td/><td/></tr><tr><td><p class="s8">Nickel</p></td><td><p class="s8">0.5 - 4 µm</p></td><td><p class="s8">Diffusion barrier especially for gold layers</p></td></tr><tr><td><p class="s8">Copper</p></td><td><p class="s8">1 - 5 µm</p></td><td><p class="s8">Intermediate layer used in tinning of CuZn</p></td></tr><tr><td><p class="s8">Tin, tin alloys</p></td><td><p class="s8">0.8 - 25 µm</p></td><td><p class="s8">materials</p></td></tr></table>
  
<figure id="fig:Typical examples of hot tinned strip materials">
+
*'''Carrier Materials'''
[[File:Typical examples of hot tinned strip materials.jpg|left|Figure 3: Typical examples of hot tinned strip materials]]
+
Copper, copper alloys, nickel, nickel alloys, stainless steel
<br style="clear:both;"/>
 
</figure>
 
<br style="clear:both;"/>
 
*'''Materials'''
 
Coating materials: Pure tin, tin alloys<br>
 
Substrate materials: Cu, CuZn, CuNiZn, CuSn, CuBe and others<br />
 
  
 
*'''Dimensions and Tolerances'''
 
*'''Dimensions and Tolerances'''
{| class="twocolortable" style="text-align: left; font-size: 12px;width:40%"
 
|-
 
|Width of tinning:   
 
|&#8805; 3 &#177; 1 mm
 
|-
 
|Thickness of tinning:   
 
|1 - 15 μm
 
|-
 
|Tolerances (thickness):
 
|&#177; 1 - &#177; 3 μm depending on tin thickness
 
|}
 
  
*'''Quality Criteria'''
+
Bild
Mechanical strength and dimensional tolerances of hot tinned strips are closely related to the standard for Cu and Cu alloy strips according to DIN EN 1652 and DIN EN 1654.
 
Quality criteria for the actual tin coatings are usually agreed upon separately.
 
  
==<!--7.5-->Contact Lubricants==
+
Dimensions
By using suitable lubricants, the mechanical wear and frictional oxidation of sliding and connector contacts can be substantially reduced. In the electrical contact technology, solid as well as high and low viscosity liquid lubricants are used.
+
Carrier thickness d= 0.1 - 1 mm
 +
Carrier width B= 6 - 130 mm
 +
Distance b > 2 mm
 +
Coating width a= 2 - 30mm
 +
Coating thickness s = 0.2 - 5 μm
 +
(typical range)
 +
Distance from edge b > 0.5 mm
 +
depending on the carrier thickness
 +
and the plating process
  
Contact lubricants have to fulfill a multitude of technical requirements:
+
*'''Tolerances'''
 +
Coating thickness approx. 10 %
 +
Coating thickness and position + 0,5 mm
  
*They must wet the contact surface well; after the sliding operation the lubrication film must close itself again, i.e. mechanical interruptions to heal
+
*'''Quality Criteria'''
*They should not transform into resins, not evaporate, and not act as dust collectors
+
Mechanical properties and dimensional tolerances of the carrier materials follow
*The lubricants should not dissolve plastics, they should not be corrosive to non-precious metals or initiate cracking through stress corrosion of plastic components
+
the typical standards, i.e. DIN EN 1652 and 1654 for copper and copper alloys.
*The specific electrical resistance of the lubricants cannot be so low that wetted plastic surfaces lose their isolating properties
+
Depending on the application the following parameters are tested and
*The lubricant layer should not increase the contact resistance; the wear reducing properties of the lubricant film should keep the contact resistance low and consistent over the longest possible operation time
+
recorded (see also: Electroplating of parts):
  
Solid lubricants include for example 0.05 – 0.2 μm thin hard gold layers, which are added as surface layers on top of the actual contact material.
+
*Coating thickness  *Solderability
 +
*Adhesion strength  *Bonding property
 +
*Porosity          *Contact resistance
  
Among the various contact lubricants offered on the market, contact lubrication oils have shown performance advantages. They are mostly synthetic, chemically inert and silicone-free oils which differ in their chemical composition and viscosity.
+
These quality tests are performed according to industry standards, internal
 +
standards, and customer specifications resp.
  
For sliding contact systems with contact forces < 50 cN and higher sliding speeds, oils with a lower viscosity (< 50 mPa·s) are preferential. For applications with higher contact forces and operating at higher temperatures, contact oils with a higher viscosity are advantageous. Contact oils are mainly suited for applications at low current loads. At higher loads and in situations where contact separation occurs during the sliding operation, thermal decomposition may be initiated, which causes the lubricating properties to be lost.
+
===7.1.2 Electroless Plating===
  
 +
===7.1.2.1 Introduction===
 +
Electroless plating is defined as a coating process which is performed without
 +
the use of an external current source. It allows a uniform metal coating
 +
independent of the geometrical shape of the parts to be coated. Because of the
 +
very good dispersion capability of the used electrolytes also cavities and the
 +
inside of drilled holes in parts can be coated for example.
 +
In principal two different mechanisms are employed for electroless plating:
 +
processes in which the carrier material serves as a reduction agent (Immersion
 +
processes) and those in which a reduction agent is added to the electrolyte
 +
(Electroless processes).
  
==<!--7.6-->Passivation of Silver Surfaces==
+
===7.1.2.2 Immersion Processes===
The formation of silver sulfide during the shelf life of components with silver surface in sulfur containing environments, can be significantly eliminated by coating them with an additional protective film layer (Passivation layer). For electrical contact use, such thin layers should be chemically inert and sufficiently conductive, otherwise they are easily broken by the applied contact force.
+
The immersion processes are usually applied in the plating of the metals gold,
<figure id="fig:Typical process flow for the SILVERBRITE W ATPS process">
+
silver, and tin. If the material to be coated is less precious, i.e. exhibits a
[[File:Typical process flow for the SILVERBRITE W ATPS process.jpg|right|thumb|Figure 4: Typical process flow for the SILVERBRITE W ATPS process]]
+
negative standard potential against the metal ions in the surrounding solution, it
</figure>
+
goes into solution releasing electrons while the more precious metal ions are
The passivation process SILVERBRITE W ATPS is a water-based tarnish preventer for silver (<xr id="fig:Typical process flow for the SILVERBRITE W ATPS process"/>). It is free of chromium(VI) compounds and solvents. The passivating layer is applied by immersion, which creates a transparent organic protective film which barely changes the appearance and only slightly
+
reduced by absorbing electrons and being deposited on the electrode. This
increases the good electrical properties such as for example the contact resistance. The good solderability and bond properties of silver are not
+
process can continue until the complete surface of the substrate is covered
negatively affected. Because of its chemical composition, this protective layer has some lubricating properties which reduce the insertion and withdrawal forces of connectors noticeably.
+
with a thin layer of the more precious metal. This limits the maximum achievable
 +
layer thickness to approx. 0.1 μm ''(Table 7.5)''.
  
==References==
+
Table 7.5: Immersion Gold Electrolytes
 +
<table border="1" cellspacing="0" style="border-collapse:collapse"><tr><td><p class="s8">Type of Electrolyte</p></td><td><p class="s8">pH-Range</p></td><td><p class="s8">Coating Properties</p></td><td><p class="s8">Application Ranges</p></td></tr><tr><td><p class="s8">Type of Electrolyte</p></td><td><p class="s8">pH-Range</p></td><td><p class="s8">Hardness</p><p class="s8">HV 0.025</p></td><td><p class="s8">Punity</p></td><td><p class="s8">Application Ranges</p></td></tr><tr><td><p class="s8">Immersion Gold electrolytes</p></td><td/><td/><td/><td/></tr><tr><td><p class="s8">AUROL 4</p><p class="s8">AUROL 16</p><p class="s8">AUROL 20</p></td><td><p class="s8">3.8 - 4.2</p><p class="s8">5.8 - 6.2</p><p class="s8">5.8 - 6.2</p><p class="s8">5.8 - 6.2</p></td><td><p class="s8">60 - 80</p><p class="s8">60 - 80</p><p class="s8">60 - 80</p><p class="s8">60 - 80</p></td><td><p class="s8">99.99% Au</p><p class="s8">99.99% Au</p><p class="s8">99.99% Au</p><p class="s8">99.99% Au</p></td><td><p class="s8">Thin gold layers on Ni, Ni alloys,</p><p class="s8">Fe and Fe alloys for PCB technology and technical applications</p></td></tr></table>
  
Vinaricky, E. (Hrsg.): Elektrische Kontakte, Werkstoffe und Anwendungen.
+
===7.1.2.3 Electroless Processes===
Springer-Verlag, Heidelberg 2002
+
The electroless metal plating with adding reduction agents to the electrolyte is
 +
based on the oxidation of the reducing agent with release of electrons which
 +
then in turn reduce the metal ions. To achieve a controlled deposition from such
 +
solutions the metal deposition has to happen through the catalytic influence of
 +
the substrate surface.
  
Ganz, J.; Heber, J.; Macht, W.; Marka, E.: Galvanisch erzeugte
+
Otherwise a “wild” uncontrollable deposition would occur. In most cases
Edelmetallschichten für elektrische Kontakte. Metall 61 (2007) H.6, 394-398
+
palladium containing solutions are used for the activation which seed the
 +
surfaces with palladium and act as catalysts in the copper and nickel
 +
electrolytes.
  
Song, J.: Edelmetalle in Steckverbindungen - Funktionen und Einsparpotential.
+
The electrolytes contain besides the complex ion compounds of the metals to
VDE - Fachbericht 67 (2011) 13-22
+
be deposited also stabilizers, buffer and accelerator chemicals, and a suitable
 +
reduction agent.
  
Heber, J.: Galvanisch abgeschiedene Rhodiumschichten für den dekorativen
+
These electrolytes are usually operating at elevated temperatures (50° – 90°C).
Bereich. Galvanotechnik, 98 (2007) H.12, 2931-2935
+
The deposits contain besides the metals also process related foreign inclusions
 +
such as for example decomposition products of the reduction agents.
 +
The electroless processes are used mainly for copper, nickel, and gold
 +
deposits.
  
Johler, W.; Pöffel, K.; Weik, G.; Westphal, W.: High Temperature Resistance
+
===7.1.2.4 Electroless Deposition of Nickel/Gold===
th Galvanically Deposited Gold Layers for Switching Contacts. Proc. 15 Holm
 
Conf. on Electrical Contacts, Chicago (2005) 48-54
 
  
Grossmann, H. Schaudt, G.: Untersuchung über die Verwendbarkeit von
+
Electroless deposited nickel coatings with an additional immersion layer of gold
Überzügen der Platinmetallgruppe auf elektrotechnischen Verbindungselementen.
+
are seeing increased importance in the coating of printed circuit boards (PCBs).
Galvanotechnik 67 (1976) 292-297
+
The process sequence is shown in ''(Fig. 7.2)'' using the example of the
 +
DODUCHEM process.
  
Grossmann, H.; Vinaricky, E.: Edelmetalleinsparung in der Elektrotechnik durch
+
Tabelle
selektives Galvanisieren. In: Handbuch der Galvanotechnik. München, Hanser-
 
Verlag, 37 (1981) 132-141
 
  
Grossmann, H.; Schaudt, G.: Hochgeschwindigkeitsabscheidung von Edelmetallen
+
After the pre-cleaning (degreasing and etching) a palladium sulfate activator is
auf Kontaktwerkstoffen. Galvanotechnik 84 (1993) H.5, 1541-1547
+
used which activates the exposed copper surfaces on the printed circuit board
 +
and thus facilitates the nickel deposition. The electroless working chemical
 +
nickel electrolyte contains – besides other ingredients – Sodium-hypophosphite,
 +
which is reduced to phosphorus in a parallel occurring process and
 +
incorporated into the nickel deposit. At the temperature of 87 – 89°C a very
 +
homogeneous nickel-phosphorus alloy layer with approx. 9 wt% P is deposited
 +
with layer thicknesses > 5 μm possible. During a consecutive processing step
 +
a very thin and uniform layer (< 0.1 μm) of gold is added in an immersion
 +
electrolyte. This protects the electroless nickel layer against corrosion achieving
 +
a solderable and well bondable surface for thick or fine aluminum bond wires.
  
Bocking, C.; Cameron, B.: The Use of High Speed Selective Jet
+
It is possible to enhance this layer combination further by adding a immersion
Electrodeposition of Gold for the Plating of Connectors. Trans. IMF. 72 (1994)
+
palladium layer between the electroless nickel and the gold coating
33-40
+
(DODUBOND process). This Pd layer acts as a diffusion barrier and allows the
 +
usage of this surface combination also for gold wire bonding.
  
Endres, B.: Selektive Beschichtungen von Kontaktmaterial im
+
As an alternative, for gold wire bonding applications a thicker gold layer of 0.2 –
Durchzugsverfahren. Metalloberfläche 39 (1985) H.11, 400-404
+
0.5 μm can be applied using an electroless process. Typical electrolytes work at
 +
a temperature of approx. 80°C with deposition rates of 0.3 – 0.4 μm per 30
 +
minutes. There are however limitations with these electroless electrolytes
 +
concerning their stability and the robustness of the process compared to other
 +
electroplating processes which reduces their wider usage ''(Fig. 7.3)''.
  
Kaspar, F.; Marka, E.; Normann, N.: Eigenschaften von chemisch Nickel
+
Fig. 7.3:
Goldschichten für Baugruppen der Elektrotechnik.
+
Coating composition
VDE Fachbericht 47 (1995) 19-27
+
of a printed circuit board with
 +
reductively enhanced gold
  
Schmitt; W.; Kißling, S.; Behrens, V.: Elektrochemisch hergestellte
+
===7.1.2.5 Immersion Deposition of Tin===
Schichtsysteme auf Aluminium für Kontaktanwendungen.
+
A tin coating by ion exchange is usually not possible since copper is the more
VDE - Fachbericht 67 (2011) 136-141
+
precious metal. By adding thio-urea the electro-chemical potential of copper is
 +
reduced to a level (approx. 450 mV, significantly lower than tin) that allows the
 +
exchange reaction. Using a suitable electrolyte composition and enhancer
 +
solutions like with the DODUSTAN process ''(Fig. 7.4)'' tin coatings can be
 +
produced that, even under usually unfavorable conditions of copper
 +
concentrations of 7 g/l in the electrolyte, are well solderable.
  
Freller, H.: Moderne PVD-Technologien zum Aufbringen dünner
+
Fig. 7.4: Process flow for electroless tin deposition using the DODUSTAN process
Kontaktschichten. VDE-Fachbericht 40 (1989) 33-39
 
  
Ganz, J.: PVD-Verfahren als Ergänzung der Galvanik. Metalloberfläche 45 (1991)
+
The immersion tin deposition is suitable for the production of a well solderable
 +
surface on printed circuit boards and electronic components. It is also used as
 +
an etch resist against ammonia based solutions or as corrosion and oxidation
 +
protection of copper surfaces.
  
Schmitt, W.; Franz, S.; Heber, J.; Lutz, O.; Behrens, V.: Formation of Silver
+
===7.2 Coatings from the Gaseous Phase (Vacuum Deposition)===
Sulfide Layers and their Influence on the Electrical Characteristics of Contacts in
+
The term PVD (physical vapor deposition) defines processes of metal, metal
th the Field of Information Technology. Proc. 24 Int. Conf.on Electr. Contacts,
+
alloys, and chemical compounds deposition in a vacuum by adding thermal and
Saint Malo, France (2008) 489-494
+
kinetic energy through particle bombardment. The main processes are the
 +
following four coating variations ''(Table 7.6)'':
  
Buresch, I; Ganz, J.; Kaspar, F.: PVD-Beschichtungen und ihre Anwendungen
+
*Vapor deposition    *Sputtering (Cathode atomization)
für Steckverbinder. VDE-Fachbericht 59 (2003) 73-80
+
*Arc vaporizing      *Ion implantation
  
Gehlert, B.: Edelmetalllegierungen für elektrische Kontakte.
+
In all four processes the coating material is transported in its atomic form to the
Metall 61 (2007) H.6, 374-379
+
substrate and deposited on it as a thin layer (a few nm to approx. 10 μm)
  
Ganz, J.: Einsatz von Sputterverfahren bei komplexen
+
Table 7.6: Characteristics of the Most Important PVD Processes
Beschichtungsaufgaben. JOT 11 (1997)
 
  
Buresch, I.; Bögel, A.; Dürrschnabel, W.: Tin Coating for Electrical Components.
+
tabelle fehlt!
Metall 48 (1994) H.1, 11-14
 
  
Buresch, I.; Horn, J.: Bleifreie Zinnoberflächen.
+
The sputtering process has gained the economically most significant usage. Its
VDE-Fachbericht 61 (2005) 89-94
+
process principle is illustrated in ''(Fig. 7.5)''.
  
Adler, U.; Buresch, I.; Riepe, U.; Tietz, V.: Charakteristische Eigenschaften der
+
Fig. 7.5: Principle of sputtering Ar = Argon atoms; e = Electrons; M = Metal atoms
schmelzflüssigen Verzinnung von Kupferwerkstoffen.
 
VDE-Fachbericht 63 (2007) 175-180
 
  
Huck, M.: Einsatz von Schmiermitteln auf Gleit- und Steckkontakten.
+
Initially a gas discharge is ignited in a low pressure (10 – 1 Pa) argon
Metalloberfläche (1982) 429-435
+
atmosphere. The argon ions generated are accelerated in an electric field and
 +
impact the target of material to be deposited with high energy. Caused by this
 +
energy atoms are released from the target material which condensate on the
 +
oppositely arranged anode (the substrate) and form a layer with high adhesion
 +
strength. Through an overlapping magnetic field at the target location the
 +
deposition rate can be increased, making the process more economical.
  
Abbott, W.,H.: Field and Laboratory Studies of Corrosion Inhibiting Lubricants
+
The advantages of the PVD processes and especially sputtering for electrical
for Gold-Plated Connectors. Proc. HOLM Conf.on Electrical Contacts, Chicago
+
contact applications are:
(1996) 414-428
 
  
Noel, S.; Alarmaguy, D.; Correia, S.; Gendre, P.: Study of Thin Underlayers to
+
*High purity of the deposit layers  *Low thermal impact on the
Hinder Contact resistance Increase Due to Intermetallic Compound Formation.
+
*Almost unlimited coating materials  substrate
th Proc. 55 IEEE Holm Conf. on Electrical Contacts, Vancouver, BC,
+
*Low coating thickness tolerance    *Excellent adhesion (also by using additional intermediate layers)
Canada (2009) 153 – 159
 
  
Weik, G.; Johler, W.; Schrank, C.: Zuverlässigkeit und Eigenschaften von Gold –
+
Coatings produced by PVD processes are used for contact applications, for
Schichten bei hohen Einsatztemperaturen.
+
example on miniature-profiles, in electrical engineering and for electronic
VDE – Fachbericht 65, (2009) 13 – 21
+
components, for solderability in joining processes, for metalizing of nonconductive
 +
materials, as well as in semiconductors, opto-electronics, optics,
 +
and medical technology applications.
  
Buresch, I.; Hack, M.: Eigenschaften von Zinnschichten für elektromechanische
+
There are few limitations regarding the geometrical shape of substrate parts.
Bauelemente – Einflussfaktoren und ihre Auswirkungen. VDE – Fachbericht 65,
+
Only the interior coating of drilled holes and small diameter tubing can be more
(2009) 23 – 30
+
problematic (ratio of depth to diameter should be < 2:1). Profile wires, strips,
 +
and foils can be coated from one side or both; formed parts can be coated
 +
selectively by using masking fixtures that at the same time serve as holding
 +
fixtures.
  
Buresch, I.: Effekte intermetallischer Phasen auf die Eigenschaften von
+
*'''Examples of vacuum coated semi-finished materials and parts'''
Zinnoberflächen auf Kupferlegierungen. VDE – Fachbericht 67 (2011) 38-46
+
bild
  
Schmitt, W.; Heber, J.; Lutz, O.; Behrens, V.: Einfluss des Herstellverfahrens auf
+
*'''Materials'''
das Korrosions- und Kontaktverhalten von Ag – Beschichtungen in
+
Selection of possible combinations of coating and substrate materials
schwefelhaltiger Umgebung. VDE – Fachbericht 65 (2009) 51 – 58
 
  
[[de:Beschichtungsverfahren]]
+
<table border="1" cellspacing="0" style="border-collapse:collapse"><tr><td><p class="s8">Substrate Materials</p></td><td><p class="s8">Coating Materials</p></td></tr><tr><td><p class="s8">Substrate Materials</p></td><td><p><span>Ag</span></p></td><td><p><span>Au</span></p></td><td><p><span>Pt</span></p></td><td><p><span>Pd</span></p></td><td><p><span>Cu</span></p></td><td><p><span>Ni</span></p></td><td><p><span>Ti</span></p></td><td><p><span>Cr</span></p></td><td><p><span>Mo</span></p></td><td><p><span>W</span></p></td><td><p><span>Ai</span></p></td><td><p><span>Si</span></p></td></tr><tr><td><p class="s8">Precious metal / alloys</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">NF metals / alloys</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Fe alloys / stainless steel</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Special metals (Ti, Mo, W)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Carbide steels (WC-Co)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Ceramics (Al<span class="s16">2</span>O<span class="s16">3</span>, AlN)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Glasses (SiO<span class="s16">2</span>, CaF)</p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-leer.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr><tr><td><p class="s8">Plastics (PA, PPS)</p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td><td><p><span>[[File:K7-gef.png]]</span></p></td></tr></table>
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*'''Dimensions'''

Revision as of 15:02, 5 December 2013

Besides manufacturing contact materials from the solid phase, i.e. by melt or powder metallurgy, the production starting in the liquid or gaseous phase is generally preferred when thin layers in the μm range are required which cannot be obtained economically by conventional cladding methods. Such coatings fulfill different requirements depending on their composition and thickness. They can serve as corrosion or wear protection or can fulfill the need for thin contact layers for certain technical applications. In addition they serve for decorative purposes as a pleasing and wear resistant surface coating.

Table 7.1: Overview of Important Properties of Electroplated Coatings and their Applications

To reduce the mechanical wear of thin surface layers on sliding and connector contacts additional lubricants in liquid form are often used. On silver contacts passivation coatings are applied as protection against silver sulfide formation.

7.1 Coatings from the Liquid Phase

For thin coatings starting from the liquid phase two processes are used differentiated by the metallic deposition being performed either with or without the use of an external electrical current source. The first one is electroplating while the second one is a chemical deposition process.

7.1.1 Electroplating (or Galvanic Deposition)

For electroplating of metals, especially precious metals, water based solutions (electrolytes) are used which contain the metals to be deposited as ions (i.e. dissolved metal salts). An electric field between the anode and the work pieces as the cathode forces the positively charged metal ions to move to the cathode where they give up their charge and deposit themselves as metal on the surface of the work piece. Depending on the application, for electric and electronic or decorative end use, different electrolytic bath solutions (electrolytes) are used. The electroplating equipment used for precious metal plating and its complexity varies widely depending on the process technologies employed. Electroplating processes are encompassing besides the pure metal deposition also preparative and post treatments of the goods to be coated. An important parameter for creating strongly adhering deposits is the surface of the goods to be metallic clean without oily or oxide film residues. This is achieved through various pre-treatment processes specifically developed for the types of material and surface conditions of the goods to be plated. In the following segments electrolytes – both precious and non-precious – as well as the most widely used electroplating processes are described.

7.1.1.1 Electroplating Solutions – Electrolytes

The actual metal deposition occurs in the electrolytic solution which contains the plating material as metal ions. Besides this basic ingredient, the electrolytes contain additional components depending on the processes used, such as for example conduction salts, brighteners, and organic additives which are codeposited into the coatings, influencing the final properties of the electroplating deposit.

7.1.1.1.1 Precious Metal Electrolytes

All precious metals can be electroplated with silver and gold by far the most widely used ones (Tables 7.1 and 7.2). The following precious metal electrolytes are the most important ones:

  • Gold electrolytes For functional and decorative purposes pure gold, hard gold, low-karat gold, or colored gold coatings are deposited. Depending on the requirements, acidic, neutral, or cyanide electrolytes based on potassium gold cyanide or cyanide free and neutral electrolytes based on gold sulfite complexes are used.
  • Palladium and Platinum electrolytes Palladium is mostly deposited as a pure metal, for applications in electrical contacts however also as palladium nickel. For higher value jewelry allergy protective palladium intermediate layers are used as a diffusion barrier over copper alloy substrate materials. Platinum is mostly used as a surface layer on jewelry items.
  • Ruthenium electrolytes Ruthenium coatings are mostly used for decorative purposes creating a fashionable “grey” ruthenium color on the surface. An additional color variation is created by using “ruthenium-black” deposits which are mainly used in bi-color decorative articles.
  • Rhodium electrolytes Rhodium deposits are extremely hard (HV 700 – 1000) and wear resistant. They also excel in light reflection. Both properties are of value for technical as well as decorative applications. While technical applications mainly require hard, stress and crack free coatings, the jewelry industry takes advantage of the light whitish deposits with high corrosion resistance.
  • Silver electrolytes Silver electrolytes without additives generate dull soft deposits (HV ~ 80) which are mainly used as contact layers on connectors with limited insertion and withdrawal cycles. Properties required for decorative purposes such as shiny bright surfaces and higher wear resistance are achieved through various additives to the basic Ag electrolyte.

Table 7.2: Precious Metal Electrolytes for Technical Applications

7.1.1.1.2 Non-Precious Metal Electrolytes

The most important non-precious metals that are deposited by electroplating are: Copper, nickel, tin, and zinc and their alloys. The deposition is performed in the form of pure metals with different electrolytes used (Table 7.4).

  • Copper electrolytes Copper electrolytes are used for either depositing an intermediate layer on strips or parts, for building up a printed circuit board structure, or for the final strengthening during the production of printed circuit boards.
  • Tin electrolytes Pure tin and tin alloy deposits are used as dull or also bright surface layers on surfaces required for soldering. In the printed circuit board manufacturing they are also utilized as an etch resist for the conductive pattern design after initial copper electroplating.

Table 7.3: Precious Metal Electrolytes for Decorative Applications

  • Nickel electrolytes Nickel layers are mostly used as diffusion barriers during the gold plating of copper and copper alloys or as an intermediate layer for tinning
  • Bronze electrolytes Bronze coatings – in white or yellow color tones – are used either as an allergy free nickel replacement or as a surface layer for decorative purposes. For technical applications the bronze layers are utilized for their good corrosion resistance and good brazing and soldering properties.

Table 7.2: Typical Electrolytes for the Deposition of Non-Precious Metals

7.1.1.2 Electroplating of Parts

The complete or all-around electroplating of small mass produced parts like contact springs, rivets, or pins is usually done as mass plating in electroplating barrels of different shape. During the electroplating process the parts are continuously moved and mixed to reach a uniform coating.

Larger parts are frequently electroplated on racks either totally or by different masking techniques also partially. Penetrating the coating into the interior of drilled holes or tubes can be achieved with the use of special fixtures.

Electroplated Parts

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  • Materials
  • Coating thickness

Precious metals: 0.2 – 5 μm (typical layer thicknesses; for Ag also up to 25 μm) Non-precious metals: Up to approx. 20 μm Tolerances: Strongly varying depending on the geometrical shape of parts (up to 50% at a defined measuring spot). It is recommended to specify a minimum value for the coating thickness at a defined measuring spot

als Bild?

  • Quality criteria

Besides others the following layer parameters are typically monitored in-process and documented:

  • Coating thickness *Solderability
  • Adhesion strength *Bonding property
  • Porosity Contact *resistance

These quality tests are performed according to industry standards, internal standards, and customer specifications resp.

7.1.1.3 Electroplating of Semi-finished Materials

The process for overall electroplating of strips, profiles, and wires is mostly performed on continuously operating reel-to-reel equipment. The processing steps for the individual operations such as pre-cleaning, electroplating, rinsing are following the same principles as those employed in parts electroplating.

The overall coating is usually applied for silver plating and tin coating of strips and wires. Compared to hard gold or palladium these deposits are rather ductile, ensuring that during following stamping and forming operations no cracks are generated in the electroplated layers.

7.1.1.4 Selective Electroplating

Since precious metals are rather expensive it is necessary to perform the electroplating most economically and coat only those areas that need the layers for functional purposes. This leads from overall plating to selective electroplating of strip material in continuous reel-to-reel processes. Depending on the final parts design and the end application the processes can be applied to solid strip material as well as pre-stamped and formed continuous strips or utilizing wire-formed or machined pins which have been arranged as bandoliers attached to conductive metal strips.

The core part of selective precious metal electroplating is the actual electroplating cell. In it the anode is arranged closely to the cathodic polarized material strip. Cathode screens or masks may be applied between the two to focus the electrical field onto closely defined spots on the cathode strip.

Special high performance electrolytes are used in selective electroplating to reach short plating times and allow a high flow rate of the electrolyte for a fast electrolyte exchange in the actual coating area.

For a closely targeted electroplating of limited precious metal coating of contact springs so-called brush-electroplating cells are employed (Fig. 7.1). The “brush” or “tampon” consists of a roof shaped titanium metal part covered with a special felt-like material. The metal body has holes in defined spots through which the electrolyte reaches the felt. In the same spots is also the anode consisting of a fine platinum net. The pre-stamped and in the contact area pre-formed contact spring part is guided under a defined pressure over the electrolyte soaked felt material and gets wetted with the electrolyte. This allows the metal electroplating in highly selective spots.

Fig. 7.1: Brush (or “Tampon”) plating cell; 1 Strip; 2 Anode; 3 Electrolyte feed; 4 Felt covered cell

For special applications, such as for example electronic component substrates, a dot shaped precious metal coating is required. This is achieved with two belt masks running synchronous to the carrier material. One of these two masks has windows which are open to the spot areas targeted for precious metal plating coverage.

Summary of the processes for selective electroplating

  • Immersion electroplating

Overall or selective electroplating of both sides of solid strips or pre-stamped parts in strip form

  • Stripe electroplating

Stripe electroplating on solid strips through wheel cells or using masking techniques

  • Selective electroplating

One-sided selective coating of solid, pre-stamped, or metallically belt-linked strips by brush plating

  • Spot electroplating

Electroplating in spots of solid strips with guide holes or pre-stamped parts in strip form

Typical examples of electroplated semi-finished materials

(overall or selectively) bild

  • Materials

Type of Coatings

Coating Thickness

Remarks

Precious Metals

Pure gold

Hard gold (AuCo 0.3)

0.1 - 3 µm

In special cases up to 10 µm

Palladium-nickel (PdNi20)

0.1 - 5 µm

Frequently with additional 0.2 µm AuCo 0.3

Silver

0.5 - 10 µm

In special cases up to 40 µm

Non-precious Metals

Nickel

0.5 - 4 µm

Diffusion barrier especially for gold layers

Copper

1 - 5 µm

Intermediate layer used in tinning of CuZn

Tin, tin alloys

0.8 - 25 µm

materials

  • Carrier Materials

Copper, copper alloys, nickel, nickel alloys, stainless steel

  • Dimensions and Tolerances

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Dimensions Carrier thickness d= 0.1 - 1 mm Carrier width B= 6 - 130 mm Distance b > 2 mm Coating width a= 2 - 30mm Coating thickness s = 0.2 - 5 μm (typical range) Distance from edge b > 0.5 mm depending on the carrier thickness and the plating process

  • Tolerances

Coating thickness approx. 10 % Coating thickness and position + 0,5 mm

  • Quality Criteria

Mechanical properties and dimensional tolerances of the carrier materials follow the typical standards, i.e. DIN EN 1652 and 1654 for copper and copper alloys. Depending on the application the following parameters are tested and recorded (see also: Electroplating of parts):

  • Coating thickness *Solderability
  • Adhesion strength *Bonding property
  • Porosity *Contact resistance

These quality tests are performed according to industry standards, internal standards, and customer specifications resp.

7.1.2 Electroless Plating

7.1.2.1 Introduction

Electroless plating is defined as a coating process which is performed without the use of an external current source. It allows a uniform metal coating independent of the geometrical shape of the parts to be coated. Because of the very good dispersion capability of the used electrolytes also cavities and the inside of drilled holes in parts can be coated for example. In principal two different mechanisms are employed for electroless plating: processes in which the carrier material serves as a reduction agent (Immersion processes) and those in which a reduction agent is added to the electrolyte (Electroless processes).

7.1.2.2 Immersion Processes

The immersion processes are usually applied in the plating of the metals gold, silver, and tin. If the material to be coated is less precious, i.e. exhibits a negative standard potential against the metal ions in the surrounding solution, it goes into solution releasing electrons while the more precious metal ions are reduced by absorbing electrons and being deposited on the electrode. This process can continue until the complete surface of the substrate is covered with a thin layer of the more precious metal. This limits the maximum achievable layer thickness to approx. 0.1 μm (Table 7.5).

Table 7.5: Immersion Gold Electrolytes

Type of Electrolyte

pH-Range

Coating Properties

Application Ranges

Type of Electrolyte

pH-Range

Hardness

HV 0.025

Punity

Application Ranges

Immersion Gold electrolytes

AUROL 4

AUROL 16

AUROL 20

3.8 - 4.2

5.8 - 6.2

5.8 - 6.2

5.8 - 6.2

60 - 80

60 - 80

60 - 80

60 - 80

99.99% Au

99.99% Au

99.99% Au

99.99% Au

Thin gold layers on Ni, Ni alloys,

Fe and Fe alloys for PCB technology and technical applications

7.1.2.3 Electroless Processes

The electroless metal plating with adding reduction agents to the electrolyte is based on the oxidation of the reducing agent with release of electrons which then in turn reduce the metal ions. To achieve a controlled deposition from such solutions the metal deposition has to happen through the catalytic influence of the substrate surface.

Otherwise a “wild” uncontrollable deposition would occur. In most cases palladium containing solutions are used for the activation which seed the surfaces with palladium and act as catalysts in the copper and nickel electrolytes.

The electrolytes contain besides the complex ion compounds of the metals to be deposited also stabilizers, buffer and accelerator chemicals, and a suitable reduction agent.

These electrolytes are usually operating at elevated temperatures (50° – 90°C). The deposits contain besides the metals also process related foreign inclusions such as for example decomposition products of the reduction agents. The electroless processes are used mainly for copper, nickel, and gold deposits.

7.1.2.4 Electroless Deposition of Nickel/Gold

Electroless deposited nickel coatings with an additional immersion layer of gold are seeing increased importance in the coating of printed circuit boards (PCBs). The process sequence is shown in (Fig. 7.2) using the example of the DODUCHEM process.

Tabelle

After the pre-cleaning (degreasing and etching) a palladium sulfate activator is used which activates the exposed copper surfaces on the printed circuit board and thus facilitates the nickel deposition. The electroless working chemical nickel electrolyte contains – besides other ingredients – Sodium-hypophosphite, which is reduced to phosphorus in a parallel occurring process and incorporated into the nickel deposit. At the temperature of 87 – 89°C a very homogeneous nickel-phosphorus alloy layer with approx. 9 wt% P is deposited with layer thicknesses > 5 μm possible. During a consecutive processing step a very thin and uniform layer (< 0.1 μm) of gold is added in an immersion electrolyte. This protects the electroless nickel layer against corrosion achieving a solderable and well bondable surface for thick or fine aluminum bond wires.

It is possible to enhance this layer combination further by adding a immersion palladium layer between the electroless nickel and the gold coating (DODUBOND process). This Pd layer acts as a diffusion barrier and allows the usage of this surface combination also for gold wire bonding.

As an alternative, for gold wire bonding applications a thicker gold layer of 0.2 – 0.5 μm can be applied using an electroless process. Typical electrolytes work at a temperature of approx. 80°C with deposition rates of 0.3 – 0.4 μm per 30 minutes. There are however limitations with these electroless electrolytes concerning their stability and the robustness of the process compared to other electroplating processes which reduces their wider usage (Fig. 7.3).

Fig. 7.3: Coating composition of a printed circuit board with reductively enhanced gold

7.1.2.5 Immersion Deposition of Tin

A tin coating by ion exchange is usually not possible since copper is the more precious metal. By adding thio-urea the electro-chemical potential of copper is reduced to a level (approx. 450 mV, significantly lower than tin) that allows the exchange reaction. Using a suitable electrolyte composition and enhancer solutions like with the DODUSTAN process (Fig. 7.4) tin coatings can be produced that, even under usually unfavorable conditions of copper concentrations of 7 g/l in the electrolyte, are well solderable.

Fig. 7.4: Process flow for electroless tin deposition using the DODUSTAN process

The immersion tin deposition is suitable for the production of a well solderable surface on printed circuit boards and electronic components. It is also used as an etch resist against ammonia based solutions or as corrosion and oxidation protection of copper surfaces.

7.2 Coatings from the Gaseous Phase (Vacuum Deposition)

The term PVD (physical vapor deposition) defines processes of metal, metal alloys, and chemical compounds deposition in a vacuum by adding thermal and kinetic energy through particle bombardment. The main processes are the following four coating variations (Table 7.6):

  • Vapor deposition *Sputtering (Cathode atomization)
  • Arc vaporizing *Ion implantation

In all four processes the coating material is transported in its atomic form to the substrate and deposited on it as a thin layer (a few nm to approx. 10 μm)

Table 7.6: Characteristics of the Most Important PVD Processes

tabelle fehlt!

The sputtering process has gained the economically most significant usage. Its process principle is illustrated in (Fig. 7.5).

Fig. 7.5: Principle of sputtering Ar = Argon atoms; e = Electrons; M = Metal atoms

Initially a gas discharge is ignited in a low pressure (10 – 1 Pa) argon atmosphere. The argon ions generated are accelerated in an electric field and impact the target of material to be deposited with high energy. Caused by this energy atoms are released from the target material which condensate on the oppositely arranged anode (the substrate) and form a layer with high adhesion strength. Through an overlapping magnetic field at the target location the deposition rate can be increased, making the process more economical.

The advantages of the PVD processes and especially sputtering for electrical contact applications are:

  • High purity of the deposit layers *Low thermal impact on the
  • Almost unlimited coating materials substrate
  • Low coating thickness tolerance *Excellent adhesion (also by using additional intermediate layers)

Coatings produced by PVD processes are used for contact applications, for example on miniature-profiles, in electrical engineering and for electronic components, for solderability in joining processes, for metalizing of nonconductive materials, as well as in semiconductors, opto-electronics, optics, and medical technology applications.

There are few limitations regarding the geometrical shape of substrate parts. Only the interior coating of drilled holes and small diameter tubing can be more problematic (ratio of depth to diameter should be < 2:1). Profile wires, strips, and foils can be coated from one side or both; formed parts can be coated selectively by using masking fixtures that at the same time serve as holding fixtures.

  • Examples of vacuum coated semi-finished materials and parts

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  • Materials

Selection of possible combinations of coating and substrate materials

Substrate Materials

Coating Materials

Substrate Materials

Ag

Au

Pt

Pd

Cu

Ni

Ti

Cr

Mo

W

Ai

Si

Precious metal / alloys

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NF metals / alloys

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Fe alloys / stainless steel

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Special metals (Ti, Mo, W)

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Carbide steels (WC-Co)

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Ceramics (Al2O3, AlN)

K7-leer.png

K7-leer.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-leer.png

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Glasses (SiO2, CaF)

K7-leer.png

K7-leer.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-gef.png

K7-leer.png

K7-gef.png

Plastics (PA, PPS)

K7-gef.png

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K7-gef.png

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K7-gef.png

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K7-gef.png

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K7-gef.png

  • Dimensions