US3239439A - Electrodeposition of metals - Google Patents

Description

March 8, 1966 G. E. HELMKE 3,239,439

ELEGTRODEPOSITION OF METALS Filed July 9, 1962 A T TOP/V5 5 United States Patent 3,239,439 ELECTRODEPOSITION 0F METALS George E. Helmke, Millington, N.J., assignor to Bell Telephone Laboratories, Incorporated, New York, N.Y., a corporation of New York Filed July 9, 1962, Ser. No. 208,538 6 Claims. (Cl. 20452) This invention relates to the electrodeposition of copper, gold or silver onto molybdenum or tungsten. More particularly, the technique utilizes a sequential combination of alternating current and direct current to initiate an adherent deposit onto the base metal. This expedient in combination with a specific plating solution has been found to give extremely useful and unexpected results.

The electrodeposition of copper, gold or silver directly onto molybdenum or tungsten is useful for the manufacture of many electrical devices, notably electron tubes. Because of difficulty in obtaining a truly clean surface on which to initiate the electrodeposition, a lack of adherence to the base metal often occurs, and in many cases the deposit is blistered. In some procedures this difliculty is overcome by sintering the piecepart in a hydrogen atmosphere furnace at a temperature somewhat below the melting point of the deposited metal.

This invention is directed to a newly developed plating technique by which copper can be electrodeposited onto molybdenum directly with good adherence, and one which eliminates the need for the sintering operation. By formulating the electrolyte with either a gold or a silver salt it is possible to deposit these metals onto molybdenum in the same way as copper. Further, by using the same operating conditions adherent electrodeposits can be made directly on tungsten.

These and other aspects of the invention may be more fully understood from a consideration of the drawing in which:

The figure is a schematic representation of an apparatus useful in conducting the plating operation of this invention.

The figure shows a plating tank 1 containingelectrolyte 2. Suspended within the electrolyte is a workpiece 3 and an anode 4. The anode is preferably an insoluble metal such as platinum. Supporting the workpiece 3 and electrode 4 areconductive holders 5 and 6 which engage electrical bus bars 7 and 8. The circuit for providing the desired current is connected as shown. The circuit consists of a DC. power supply 9 adjustable byvariable resistor 10 and an AC. source 11 varied by autotransformer 12. These current supplies may be alternatively selected by double pole, double throughswitch 13. The D.C. power supply was rated at 0 to 15 v., 0 to amps. The A0. source provided 0 to 24 v. current, 0 to amps.

Specific examplary procedures of this invention are presented in the following detailed description.

A typical plating solution formulation for copper deposition is shown in Example 1. This technique relies in part on the cleaning and striking (or flash plating) of the base metal in a single solution, and the reduction of copper ions at the cathode at an extremely low cathode efficiency and high hydrogen evolution voltage.

Example 1 Sodium hydroxide grams/liter 53 Cuprous cyanide do 1.5 Sodium cyanide do 6.7 Workpiece current density (A.C.)

amperes/square inch 7 Cathode current density (D.C.) do 2.3

The solution (Example 1) contains a relatively high concentration of hydroxide, 5%, and a relatively low con- 3,239,439 Patented Mar. 8, 1966 centration of copper cyanide, 0.15%. The pretreatment phase of the plating operation is carried out through the use of the AC. power supply. A conventional D.C. supply is used for the flash plating phase. The two supplies are connected to the electrodes through the double pole, double throw switch. The power supplied to the bath thus can be readily changed from one power source to another. The pretreating operation owes much of its effectiveness to the scrubbing action of hydrogen evolved when the part is alternately made anodic and cathodic. Copper does not deposit at either electrode during this operation because of the changing polarity. This alternating current treatment is carried out for /5 to 20 seconds, following which the double pole, double throw switch is used to connect the direct current power supply to the plating electrodes.

With direct current applied across the electrolyte, the part to be plated is held steadily at a negative (cathodic) potential. Copper and hydrogen ions reduce at'the cathode but because of the formulation of the electrolyte, this deposition takes places with a high hydrogen deposition potential and a low cathode efliciency for copper. This efficiency has been measured at less than 2%. The low efficiency of this strike contributes to the good adherence which parts plated in this bath exhibit.

The AC pretreatment, D.C. flash plating process is used to deposit amounts of the order of 1 milligram per square inch or less of copper. This deposit can then be effectively built up to the desired thickness by conventional copper plating techniques. Such procedures are well established in the art. For instance, see Modern Electroplating, edited by A. G. Gray, pages 98 to 114 and 194 to 225 (1953).

Example 2 Sodium hydroxide grams/liter 40 Silver cyanide ..do 2 Sodium cyanide do 6 Workpiece current density (A.C.) amperes/inch l0 Cathode current density (D.C.) do 3 Example 3 Sodium hydroxide grams/liter 15 Potassium gold cyanide do 2 Sodium cyanide do 2 Workpiece current density (A.C.) "ampere/inch l Cathode current density (D.C.) do 4 Example 2 has been used to deposit silver directly onto molybdenum or tungsten and Example 3 to deposit gold directly onto molybdenum or tungsten by the same procedure presented in Example 1.

The foregoing embodiments are given by way of example. Limited deviations from the specific current density values and plating conditions can be tolerated while still providing the unexpected results to which this invention is directed. For instance, potassium salts may be substituted for the sodium salts to achieve similar results. Other deviations and permissible operating ranges are set forth below.

Prior art cyanide plating solutions typically use bydroxide-to-metal salt ratios of the order of a fraction to one. As previously indicated, this invention relies in part on a significantly higher hydroxide-to-metal salt ratio. For the purposes of this invention this ratio should lie in the range of 10:1 to approximately :1. This, in term-s of percentage composition of the aqueous electrolyte, is expressed as 3 to 8% hydroxide: 0.05 to 0.3% metal salt. The remaining ingredient, a soluble cyanide salt, such as an alkali metal cyanide, is included to facilitate and maintain the dissolution of the metal salt. This component is used in any amount appropriate for this purpose, generally 1 to 30% The cathode current density useful for the AC. preplating operation generally falls within the range of 1 to 15 amperes/inch The cathode current density for the DC. plating operation is preferably 1 to 5 ampereslinch These .current.densities,.as compared with prior art'procedures, are quite high, which contributes in part 'to the success of .thepresent invention.

Various other modifications and extensions of this in- .vention will become apparent to those skilled in the art. All such variations and deviations which basically rely on the teachings through which this invention. has advanced theiart are properly considered within the spirit and scope of this invention.

Whatiis clairnedis:

1. Arprocess for electro-depositing a metal selected from the group consisting of copper, gold and silver onto a substrate selected from the group consisting of molybdenum and tungsten which comprises the steps of: placing the-substrate in an electrolyte comprising the following aqueous solution:

Percent AOH 3 to 8 MCN 0.05 to 0.3

where A is selected from the group consisting of K and Na and MCN is a solubilized cyanide salt selected from the groupconsisting of copper cyanide, silver cyanide and gold cyanide, passing an alternating current through 3. The process of claim 1 wherein the MCN is AuCN' and the metalelectroplated is .gold.

4. The process of claim 1 wherein the; MCN isJAgCN and the metalelectroplated is silver;

5. The process of :claim l wherein the current density at the substrate during the AC. pretreatment is maintained within th'e range: 1 to. 15 amperes/inch and thecathode current density during the DC. electrodeposit is =maintained within the range lto 5 amperes/inch 6. The process of claim-1 wherein the electrolyte con tainsa soluble cyanide salt in anamount suflicient to facilitate dissolution of the MCN;

References. Cited by the Examiner UNITED STATES PATENTS 2,915,444 12/1959 Meyer 204-341 6/1960 Gulick 204-34 JOHNH. MACK, Primary Examiner. MURRAY TILLMAN, Examiner.

Claims (1)

1. A PROCESS FOR ELECTRO-DEPOSITING A METAL SELECTED FROM THE GROUP CONSISTING OF COPPER, GOLD AND SILVER ONTO A SUBSTRATE SELECTED FROM THE GROUP CONSISTING OF MOLYBDENUM AND TUNGSTEN WHICH COMPRISES THE STEPS OF; PLACING THE SUBSTRATE IN AN ELECTROLYTE COMPRISING THE FOLLOWING AQUEOUS SOLUTION:

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