BACKGROUND AND SUMMARY OF THE INVENTION
[0001] The invention relates to an electrical contact surface (such as an electrical switch
contact) having low contact resistance, relatively low cost, acceptable solderability,
and high corrosion resistance. The electrical contact surface, and method of formation
thereof, according to the present invention are particularly designed to replace conventional
electrical contact surfaces wherein a gold layer of at least about 30 microinches
thickness is applied over a crystalline substrate..
[0002] In the electrical connector industry where low voltage and/or current signals must
be conducted reliably, and in some situations where intermediate voltage and/or current
signals must be conducted, gold is currently used to insure low contact resistance,
and thus effective conduction. Usually the gold is applied over a crystalline base
metal such as copper, brass, or silver, with or without an intermediate strike of
nickel, and the thickness of the gold layer is normally at least about 30 microinches
(e.g. 50-100 microinches). At a thickness of 50 microinches the cost of the gold layer
is on the order of 5 cents/cm
2. It is the characteristic of gold -- with such a thickness -- that it is porous and
thus through time the underlying material, or its corrosinn;products, may migrate
to the surface of the gold and unacceptably raise the contact resistance. Additionally,
certain organic materials or sulfur compounds can polymerize on a gold surface and
cause high contact resistance. Additionally, gold has less than ideal solderability
since it dissolves in and embrittles some solder alloys.
[0003] According to the present invention an electrical contact surface is provided which
overcomes the drawbacks associated with the conventional electrical contact surfaces
described above, so that in low and intermediate voltage and/or current signal situations
effective conduction can be obtained at less cost and over longer periods of time.
According to the present invention, an electrical contact surface is provided comprising
an electrically conductive substrate (preferably a metal such as copper, bronze, brass,
aluminum, or silver) with an amorphous (as opposed to crystalline) transition metal
alloy electrolytically deposited thereon.
[0004] An "amorphous" alloy is one that has a geometric or topological configuration of
the atoms forming the alloy that is different from crystalline (i.e. non-crystalline).
Typically, metal alloys are crystalline. When X-ray diffraction tests are done on
crystalline materials, it can be seen that the materials exhibit sharp peaks for the
d-spacings between planes in the ordered crystal structure, the narrowness or width
of these peaks relative to thick height gives an indication of the size of the crystals.
For amorphous materials, there are no particularly sharp peaks, the amorphous material
being characterized by lack of order in the atomic structure. The exact nature of
the amorphous structures is not known, however there are a number of theories which
attempt to describe the configurations of the atoms in amorphous materials. In this
regard attention is directed to an article entitled "Metallic Glasses" by Chaudhari
et al, appearing in Scientific American, Volume 242, No. 4, 1980, pages 98-117.
[0005] The amorphous transition metal alloy according to the invention preferably is a nickel-phosphorus
alloy, such as one having about 15-25 atomic percent phosphorus (preferably about
20 percent), with cobalt, or some other transition metals, utilizable in addition
to, or in place of, the nickel. Various materials may be added to the plating bath
to enhance the corrosion protection of the electrical contact surface being formed,
particularly advantageous materials being hexafluosilicate (SiF
6--), hexafluotitanate (TiF
6--), or hexafluozir- conate (ZrF
6--) ions.
[0006] After the amorphous nickel alloy has been electrolytically deposited on the substrate,
the amorphous nickel alloy is preferably coated with a layer of gold. When the amorphous
nickel alloy is coated with a layer of gold of a given thickness, the contactor that
results exhibits superior properties compared to conventional contactors wherein the
same thickness of gold is coated on a crystalline metal alloy. For instance, a gold
thickness of less than 30 microinches over the amorphous nickel alloy produces an
electrical contact structure according to the invention that is equal to, or superior
to, conventional contactors wherein a coating of 50-100 microinches of gold is provided.
In fact, it is possible to obtain entirely acceptable contactors even when the gold
coating is one microinch thick (at this thickness the cost of the gold is only about
0.1 cents/cm
2), although a range of 5-15 microinches is preferred. The electrical contact surface
resulting has stable contact resistance both initially and after exposure to a series
of common atmospheric corrodants, and initially (soon after production) when tested
pursuant to ASTM B667-80 has a contact resistance less than 4 milliohms.
[0007] According to another aspect of the present invention, a method of producing an electrical
contact surface is provided. The method comprises the steps of providing a plating
bath for electrolytically depositing an amorphous transition metal alloy on a conductive
substrate, immersing the substrate in the bath, and then subsequently coating the
amorphous electrolytically deposited alloy with a flash of gold. Nickel chloride,
cobalt carbonate, and phosphorous acid are preferred bath constituents. A number of
bath additives can be provided to influence contact resistance and corrosion protection
in a positive way. Typical bath additives include boric acid, hydroxyacetic acid,
acetic acid,
B-alanine, succinic acid, surfactants of the alkoxylated linear alcoholic class, SiF
6-- ions, TiF
6-- ions and ZrF
6-- ions. The bath temperature conditions, and the current density at the cathode,
are maintained so that effective electrolytic deposition takes place.
[0008] It is the primary object of the present invention to provide for the production of
electrical contact surfaces that have low, stable contact resistance over extended
periods of time even when subjected to corrosive conditions, and at a relatively low
cost. This and other objects of the invention will become clear from an inspection
of the detailed description of the invention and from the appended claims.
DETAILED DESCRIPTION
[0009] A deposition of an amorphous transition metal alloy can be provided on a substrate
by immersing the substrate (or a portion thereof) in a plating bath. Amorphous transition
metal alloys have been found to have better corrosion resistance than crystalline
materials, and a thinner coating of gold over an amorphous transition metal alloy
produces a contactor having the same, or better, properties than a contactor formed
by a thicker coating of gold over a crystalline material. Further, acceptable contacts
can be obtained, according to the invention, with only a very thin coating of gold.
[0010] Typical transition metal alloys that are useful in forming electrical contact surfaces
(such as electrical switch contacts) according to the invention are nickel and cobalt.
Nickel is the preferred transition metal since it has the least cost for the most
corrosion resistance, of suitable transition metals. However, generally comparable,
and sometimes superior, results can be achieved substituting cobalt, for all or part
of the nickel, in the plating bath.
[0011] An amorphous deposition of the nickel on the conductive substrate (which preferably
comprises a metal such as copper, bronze, brass, aluminum, or silver, or alloys thereof)
is formed when phosphorous acid is included in the plating bath, and a relatively
high percentage of phosphorus is provided in the alloy that is formed. A phosphorus
concentration of at least about 12%, and preferably of about 15-25 atomic percent
is desired in order to achieve good corrosion resistance and low contact resistance.
Most preferably the amorphous deposited alloy has about 20 atomic percent phosphorus.
[0012] The bath temperature conditions, and the current density at the cathode, are controlled
in order to maximize the corrosion resistance and minimize the contact resistance.
Typically current density is about 50 amp./ft.
2 - 2500 amp./ft.
2, with a range of about 100-900 amp./ft.
2 preferred. Typical temperatures are 70-85°C with 75-80°C preferred. Temperature is
not critical, but lower temperature will have a tendency to increase the preference
of cobalt for nickel in the plating where both are present in the bath.
[0013] Various additives may be provided in the bath in order to positively affect the contact
resistance and corrosion resistance. When the bath contains hexafluosilicate ions
at a concentration of about 0.1 molar to the solubility limit (with the addition of
small amounts of HF to maintain solubility if necessary) the overall corrosion resistance
of the amorphous nickel alloy may be enhanced. A generally comparable enhancement
of corrosion resistance may also be obtained by substituting TiF
6-- or ZrF
6-- ions for part or all of the SiF
6-- ions.
[0014] In a plating bath containing nickel or cobalt ions and phosphorous acid any suitable
anode and cathode materials may be utilized. For instance the anode can either be
inert (platinized titanium, platinum, or graphite), or can be of nickel (or like transition
metal to be deposited). If TiF
6--, SiF
6-- or ZrF
6-- ions are included in the bath a nickel or cobalt anode must be used. With an inert
anode additions of nickel or cobalt must be made from time to time (preferably in
the form of NiC0
3 or C
OC0
3) to maintain the nickel content. With the nickel anode the content of nickel ion
in the bath tends to rise since each two electrons at the anode cause the dissolution
of about one nickel ion, while at the cathode both nickel and phosphorus are being
reduced. A nickel and an inert anode can be used together such that each carries only
a portion of the current, and thus maintain a balanced bath with regard to nickel.
Phosphorous, in the form of phosphorous or hypophosphorous acid, and preferably in
the form of phosphorous acid, must be added from time to time -- irrespective of the
anode construction -- to maintain the proper bath balance, although the proportion
of phosphorous acid is not critical and the bath balance can be maintained rather
easily..
[0015] After deposition of the nickel phosphorous alloy, or the like, on a substrate, a
coating of gold is applied over the amorphous alloy. Preferably this is accomplished
by providing an electrodeposit that is applied for a controlled time at a controlled
current density. The thickness of the gold coating is determined by the desired end
properties of the contactor produced. Within wide ranges, whatever the thickness of
the gold coating on the amorphous alloy, the contactor that results can be expected
to have enhanced properties compared to contactors formed by the same thickness of
gold coating over a crystalline material. In fact, acceptable electric contacts can
be produced even when the thickness of the gold coating is about 1 microinch. Preferably
the gold coating is in the range of 5-30 microinches, and more preferably 5-15 microinches.
[0016] The gold used for the coating preferably is hard gold, although soft gold is also
practical although usually with somewhat less desirable results. The thickness of
the amorphous transition metal alloy on the substrate is not particularly critical.
It merely need be thick enough to achieve the desired results according to the invention.
A preferred thickness is in the range of about 50 microinches - 150 microinches. Ranges
of 25 microinches - 1000 microinches are practical.
[0017] In the typical manufacture of an electrical contact according to the invention (which
may be of a wide variety of forms, such as edge card connectors, contact leaf springs,
rigid electrical switch contact structures, etc.), desirably, the electrically conductive
substrate is formed into the desired final contact shape. It is then immersed in a
cleaner, and then deionized water, and then a dilute hydrochloric acid solution. Then
it is placed in the Ni-Co-P plating bath and after plating it is rinsed is deionized
water. Then the gold plating is provided thereon in any conventional way, such as
in a gold plating bath maintained at about 30-35°C with a current density of about
10 amp./ft.
2. After the gold plating is applied it is again immersed in deionized water.
[0018] Alternatively, for many electrical contact shapes (such as edge card connectors),
it is possible to plate blanks or coupons first, and only after they have been plated
and a gold strike applied are they formed into the desired shape.
[0019] The following are examples of the practice of the invention:
Example 1
[0020] A plating bath was formed with the following composition:
.75 M/1 NiCl2 . 6H20
.25 M/l NiC03
1.25 M/l H3PO3
[0021] An electrically conductive substrate was immersed in the bath, which was maintained
at a temperature of about 80°C, and with a current density at the cathode of about
150 ma/cm
2. When removed from the bath, the substrate had an amorphous nickel-phosphorus alloy
thereon. A one (1) microinch strike of gold was provided on the amorphous alloy. The
electrical contact surface that resulted had a contact resistance that was substantially
as low as a similar substrate with a 50 microinch or greater coating of gold, the
contact resistance was stable over time, and as stable in corrosive environments (such
as when subjected to the S0
2 test -- 100 percent relative humidity and 1 percent concentration of sulfur dioxide,
room temperature, over forty hours --, and the mixed gas test -- the same conditions
as the S0
2 test only adding 1 percent nitrogen dioxide and 1 percent chlorine). The electrical
contact surface formed was much less expensive than the conventional one, and had
better solderability characteristics.
Example 2
[0022] In this example, the bath composition, temperature, and current density characteristics
were substantially the same as in example 1. After the substrate with an amorphous
nickel-phosphorus alloy was removed from the bath, an approximately 10 microinch strike
of gold was provided on the amorphous alloy. The electrical contact surface that resulted
had contact resistance, and other properties, equal, or superior to, an electrical
contact surface formed utilizing similar materials in crystalline form, and with a
50 microinch coating of gold.
Example 3
[0023] The bath composition in this example was as follows:
.2 M/1 NiCl2 .6 (H20)
.8 M/1 NiS04 .6 (H20)
.5 M/l H3PO3
-.5 M/1 H3PO4
[0024] The bath temperature conditions, current density, and like parameters, were substantially
the same as for example 1, and after deposition of the amorphous nickel-phosphorus
alloy on the substrate a 1 microinch flash of gold was applied. By testing, the electrical
contact surface formed was found to have acceptable contact resistance (i.e. less
than 4 milliohms when tested according to ASTM B667-80) and corrosion resistance,
although it was not as good as the electrical contact surface produced in example
1.
Example 4
[0025] The bath composition for this example was as follows:
.88 M/l NiCl2 . 6H20
.25 M/l NiC03
1.25 M/l H3P03
.4 M/1 H3B03
.2 M/1 Acetic acid
.1 M/l COC03
[0026] The bath temperature was maintained at about 75°C, with a current density at the
cathode of about 200 ma/cm
2. An anal sis of the plating resulting from immersion of the substrate in this bath
showed bulk values (in atomic percent) of 6.8 ±4%.cobalt, 0.6 oxygen, 73.3 percent
nickel, and 19.3 percent phosphorus. A 1 microinch strike of gold was provided on
the amorphous alloy. The electrical contact surface formed had low contact resistance
and high corrosion resistance, and was an excellent substitute for conventional electrical
contact surfaces of gold about 50 microinches thick (or thicker) applied over a crystalline
base metal.
Example 5
[0027] A member of platings were produced on electrically conductive substrates to produce
platings having about 20% phosphorous, X% cobalt, and 80-X% nickel, utilizing the
constituents indicated in the following table:

[0028] Plating was accomplished at 75-78°C using a hard anode (e.g. platinum or platinized
titanium) and a current density of about 100 amp./ft.
2.
[0029] The sum of the nickel plus cobalt is one mole/liter in each formulation, and CoCO
3 is the source of all the cobalt in each of the formulations. Therefore, the Co
+2/Ni
+2 ratio in the bath is M/1 CoCO
3/(1-M/1 CoC0
3). The Co/Ni ratio in the plating is %Co(80-%Co). The relationship between Co
+2/Ni
+2 in the bath and Co/Ni in the plate is:

[0030] It is evident that the cobalt is being plated preferentially to the nickel and that
at low cobalt levels this preference is slightly greater. Operating at lower temperature
will make the preference (Co/Ni in plating) greater, as will operating at higher current
density. Further, these formulations produce lower than nominal amounts of cobalt
when they are new, i.e. for the first 100 amp-minutes/liter the baths will produce
only ca. 1/2 to 2/3 the desired cobalt content in the plating.
[0031] The plating, formed as actual electrical connectors, having 10% Co were coated with
5, 10, or 15 microinches of hard gold, or 5 microinches soft gold, and subjected to
durability cycling utilizing conventional techniques, and exposure in a BCL Class
III environment, and utilizing the same material on both the PC boards and the connector
openings. The following results were achieved, wherein
Rc= the contact resistance and
a= a measure of the deviations of the individual contact values from their average


[0032] These results indicate improved performance of the electrical connectors according
to the invention compared to a 50 microinch plating of hard gold over conventional
sulfamate nickel.
[0033] While the invention has been herein shown and described in what is presently conceived
to be the most practical and preferred embodiment thereof, it will be apparent to
those of ordinary skill in the art that many modifications may be made thereof within
the scope of the invention, which scope is to be accorded the broadest interpretation*of
the appended claims so as to encompass all equivalent structures and methods.
1. An electrical contact having a contact resistance soon after production of less
than 4 milliohms, and comprising an electrically conductive substrate; and characterized
by: an amorphous transition metal alloy deposited on said substrate; and an uncovered
coating of gold over said amorphous transition metal alloy, sa=d gold coating being
between about 1-30 microinches thick.
2. An electrical contact as recited in claim 1 further characterized in that said
transition metal alloy is a nickel-phosphorus alloy.
3. An electrical contact as recited in claim 2 further characterized in that said
nickel-phosphorus alloy includes about 15-25 atomic percent phosphorus; and includes
about 5-15 atomic percent cobalt.
4. An electrical contact as recited in claim 3 further characterized in that said
uncovered coating of gold is hard gold between about 5-15 microinches thick.
5. A method of forming a structure comprising the steps of: (a) immersing a substrate
in a plating bath including transition metal alloying elements; and (b) controlling
the bath temperature conditions and current density at the cathode to effect electrolytic
deposition of the transition metal alloying elements, in amorphous form, on the substrate;
and characterized in that the substrate is an electrically conductive substrate, and
characterized by the further step of (c) applying a coating of gold having a thickness
of between 1-30 microinches to the electrolytically deposited amorphous transition
metal alloy, to produce an electrical contact structure having an uncovered gold surface.
6. A method as recited in claim 5 further characterized in that step (a) is practiced
utilizing a plating bath containing phosphorus acid and nickel alone, or nickel and
cobalt.
7. A method as recited in claim 5 further characterized in that step (b) is practiced
so that the temperature of the bath is between about 70-85°C, and so that the current
density at the cathode is between about 100-900 amp./ft.2 and to effect an electrolytic deposition of the amorphous material so that it has
a thickness of about 25-1000 microinches; and further characterized in that step (a)
is practiced by including in the plating bath between 0.1 molar to the solubility
limit of ions selected from the group consisting of TiF6--, SiF6--and ZrF6-- ions.
8. A method as recited in claim 7 further characterized in that steps (a) and (b)
are practiced so that the amorphous alloy deposited on the substrate is a nickel cobalt
phosphorus alloy, including about 15-25 atomic percent phosphorus, and at least 5
atomic percent cobalt.
9. A method as recited in claim 5 further characterized in that step (c) is practiced
so as to apply a coating of hard gold having a thickness of between 5-15 microinches.