|Publication number||US3841881 A|
|Publication date||Oct 15, 1974|
|Filing date||Sep 13, 1972|
|Priority date||Sep 13, 1972|
|Publication number||US 3841881 A, US 3841881A, US-A-3841881, US3841881 A, US3841881A|
|Inventors||Feldstein N, Lancsek T|
|Original Assignee||Rca Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (6), Referenced by (16), Classifications (9)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1191 Feldstein et al.
[ METHOD FOR ELECTROLESS DEPOSITION OF METAL USING IMPROVED COLLOIDAL CATALYZING SOLUTION  Inventors: Nathan Feldstein, Kendall Park,
N.J.; Thomas Stephen Lancsek, Morrisville, Pa.
 Assignee: RCA Corporation, New York, NY.  Filed: Sept. 13, 1972 21 Appl. No.: 288,777
 U.S. Cl. 106/1, 117/47 A, 117/130 E, 204/30  Int. Cl. C23c 3/02  Field of Search 106/1; 204/30; 117/47 A, ll7/l30 E  References Cited UNITED STATES PATENTS 3,011,920 12/1961 Shipley mm A .Oct. 15, 1974 DOttavio 106/1 3,616,296 l0/l971 Bernhardt et al.... 204/30 3,650,777 3/1972 Schneble et al. 106/1 3,672,923 6/l972 Zeblisky ct al. 106/1 3,698,919 10/1972 Kuzmik 106/1 Primary Examiner Lorenzo B, Hayes Attorney, Agent, or Firm-G. H. Bruestle; W. S. Hill  ABSTRACT 8 Claims, No Drawings 1. METHOD FOR ELECTROLESS DEPOSITION OF METAL USING IMPROVED COLLOIDAL CATALYZING SOLUTION BACKGROUND OF THE INVENTION Various metals can be deposited on certain substrate surfaces by a process known as autocatalytic electroless plating. Autocatalytic electroless plating baths usually contain a salt of the meta] being deposited, at reducing agent for the metal salt, a complexing or chelating agent and a pH adjustor.
Some metallic surfaces are inherently catalytic for initiating deposition of certain metals from autocatalytic electroless plating baths. However, non-metallic surfaces must be treated to render them catalytic. One common method-of rendering a non-metallic surface catalytic forthe autocatalytic electroless deposition of a number of metals is to treat it, first, with a sensitizing solution of stannous chloride. Then the sensitized surface is treated with an activating solution of palladium chloride which deposits an adherent filmof palladium nuclei. These nuclei serve as catalyst for initiating the reduction of the metal salt and its deposition on the substrate. After an initial layer of the metal is thus deposited, this initial layer catalyzes further deposition.
The above described method of autocatalytic electroless deposition has been widely used. Another method that has been widely used commercially for depositing a catalytic coating on a surface is the so-called colloidal catalyst solution method, as described, for example, in US. Pat. No. 3,011,920. In this method, the initial step of sensitizing the surface with a stannous chloride solution is omitted. Instead the surface is treated with a single solution which comprises an acid soluble salt of a catalytic metal (usually, a noble metal), hydrochloric acid, and a soluble stannous salt which is present in excess of the amount necessary to reduce the catalytic metal salt to colloidal metal. The excess amount of stannous salt reacts to form a protective colloid which inhibits flocculation that would normally occur when stannous ions and noble metal ions are present in the same solution. After treatment of the surface to be plated with the colloidal catalyst solution, the surface is treated with the electroless plating bath in the usual way.
The colloidal catalyst solution method has been found generally satisfactory for deposition of metals such as nickel and copper, on surfaces such as glass and hydrophilic dielectrics, especially where the catalyzed surface is given a treatment with an accelerator such as a solution of sodium hydroxide prior to contact with the electroless plating bath. The accelerator dissolves the protective colloid which is present on the catalyzed surface. j
In the case of hydrophobic surfaces, such as Teflon, for example, neither the colloidal catalyst solution method nor the two-step method first described,'has been satisfactory. On this type of surface, coverage of the deposited metal has usually ranged between zero and very poor.
The present invention is an improvement in the colloidal catalyst solution method which enables it to be used on hydrophobic surfaces and also provides improved reliability on other substrates. The improvement consists in adding to the colloidal catalyst solution, a solution of a stannic compound that has been separately aged. The quantity of stannic ion added is enough to make the solution at least 0.01 molar in this ingredient.
The addition of the aged stannic chloride introduces a hydrolyzed compound containing stannic ions. The improvement appears to be due to this compound.
DESCRIPTION OF PREFERRED EMBODIMENTS Examples l-3 In the examples which follow, the surface being coated was a plate of Teflon plastic. The plating bath was one for autocatalytically electrolessly plating copper and had the composition given below.
Copper Plating Bath Compositions CuSO,.5H O 15 g/l Propylenediamine tetraacetic acid, 60 cc/l sodium salt (40% active solution) NaOH 4.0 g/l H CO (37% solution) 40 cell NaCN 4 mg/l Temperature 40C A plating cycle of 5 minutes was used.
Besides copper (from the above-described bath), nickel, cobalt, gold and alloys of any two or more of these four metals, for example, can be deposited from conventional electroless plating baths using the colloidal catalyst solutions described herein.
The following are colloidal catalyst solutions for catalyzing the surface to be plated. The surface is either dipped in or sprayed with the solution. Treating time can be about 30 seconds or more.
Colloidal Catalyst Solutions Example 1 Example 2 Example 3 H 0 600 cell 600 cell 600 cell HCl (Conc.) 300 cc/l 300 cell 300 cell SnCl g/l 37.5 g/l 375 g/l (Anhydrous) Aged SnCl, 3.2 X 10 1.6 X 10 2.4 X l0 (molar conc.)
Na SnO .3H 0 None None 1.5 g/l PdCl 1 g/l None None HAuCl,.H O None 1 g/l None H PtCl None None 1 g/l The pH of these solutions shouldv be maintained below about I.
The aged SnCl, may be prepared as an aqueous 0.5 molar solution aged for one week at room temperature. In the catalyst solution, its concentration is preferably 0.01 to 0.5 molar. Aging time varies with conditions. At elevated temperatures it can be as little as a few hours. At ordinary room temperature it is preferably at least 4 days to 1 week.
After treating the Teflon surface with the catalyst solution, the surface is rinsed with water and then preferably treated with an accelerator as described in US. Pat. No. 3,011,921. This may be a 5 percent solution of sodium hydroxide, for example, and treating time is a few minutes.
The surface is again rinsed with water after treatment with the accelerator and it is then treated with the plat ing bath.
Platings on Teflon using the above-described materials and procedures have produced about 95 percent plating coverage with all three examples. For comparison purposes, another three Teflon plates were treated with similar colloidal catalyst solutions except that the aged SnCl was omitted. The plating baths and plating cycles were the same. However, in these comparison examples, plating coverage was only about 5 percent on each plate.
An example of a nickel autocatalytic electroless plating bath that can be used in the present process is:
NiSO,.6H O 25 g/l Na P O,.l0H. .0 50 g/l Dimethylamine borane 1.5 g/l NH,OH Leone.) 50 cell Temperature 40C In the present method, the colloidal catalytic metal can be gold or any one of the platinum group of metals. The platinum group of metals consists of platinum, ruthenium, rhodium, palladium, osmium and iridium.
1. A colloidal catalytic solution for catalyzing a substrate prior to electroless metal deposition thereon, said catalyst comprising the solution resulting from the admixture of an acid soluble salt of a catalytic metal selected from the group consisting of gold, and the platinum family of metals, hydrochloric acid, a stannous salt soluble in aqueous solution, said stannous salt being in excess of the amount necessary to reduce said metal lytic metal is palladium.
3; A solution according to claim 1 in which said catalytic metal is gold.
4. A solution according to claim 1 in which said catalytic metal is platinum.
5. The method of making a colloidal catalyst solution for application to a substrate surface prior to electroless metal deposition thereon. comprising admixing an acid soluble salt of a catalytic metal selected from the group consisting of gold, and the platinum family of metals, hydrochloric acid, a stannous salt soluble in aqueous solution, said stannous salt being in excess of the amount necessary to reduce said metal salt to colloidal metal, and a quantity of stannic chloride solution which has been separately aged for a period which is the equivalent of at least 4 days at room temperature and said stannic compound being present in a concentration of about 0.01 to 0.5 molar in said catalyst solution.
6. The method of claim 1 in which said catalytic metal is palladium.
7. The method of claim 5 in which said catalytic metal is gold.
8. The method of claim 5 in which said catalytic metal is platinum.
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|U.S. Classification||106/1.11, 106/1.28, 106/1.26, 106/1.24, 106/1.23|
|International Classification||C23C18/28, C23C18/20|