Patent Application
20150008131
The present disclosure generally relates to the field of tin electroplating. More specifically, the present disclosure relates to methods for mitigating tin whisker formation on tin-plated films and tin-plated surfaces by doping the tin with gold.
The worldwide transition to lead-free electronics is forcing most major suppliers of electronic components to convert their product lines from tin/lead-containing finishes to lead-free finishes. As a result, most electronics suppliers have moved to pure electroplated tin finishes. However, there is a tendency of electroplated pure tin finishes to form tin whiskers that extend a distance from the surface. Such tin whiskers have been found to form on a wide variety of tin-plated components, and under a wide range of environmental conditions. Since these tin whiskers are comprised of nearly pure tin and are therefore electrically conductive, they can cause problems, such as, for example, shorting of electronic components. Therefore the growth of tin whiskers from tin-plated surfaces continues to cause reliability issues and other problems for electronic systems that use tin-plated components. Undesirable effects attributable to tin whisker formation on tin-plated surfaces have caused significant customer dissatisfaction resulting in significant financial impact on electronics manufacturers. To date, the only way to ensure that tin whiskers do not grow within an electronic system is to eliminate pure tin from such a system. However, the increasing reliance on the use of tin and tin-plated components in the electronic industry makes this tin elimination strategy unworkable. For example, a tin coating on components helps to protect the components from corrosion. Tin coatings also help to provide a suitable surface for soldering.
One tin whisker mitigation strategy has been to immerse all tin-plated component leads into molten tin/lead, from the tip of the lead up to the component body. However, this process can undesirably affect the component and is expensive to implement into the manufacturing process. Other systems have tried immersion plating or otherwise providing a metallic or non-metallic overcoat to tin surfaces. However, no known methods have provided predictable long-term economical, reproducible and scalable solutions to the eventual and undesirable whisker formation on tin-plated surfaces.
According to one variation, the present disclosure relates to a method for mitigating tin whisker growth on a substrate surface comprising the steps of providing a substrate surface; providing a solution comprising an amount of a gold-containing compound and a tin-containing compound and at least one appropriate complexing agent, and a buffer; and immersing electrodes into the solution with the electrodes connected to an electrical power source capable of providing an electrical current to the electrodes, resulting in co-depositing a controlled amount of gold and tin onto the substrate surface. The systems, methods and apparatuses of the present disclosure could also be used and incorporated into systems and methods using a three electrode system with the third electrode being a reference electrode.
The gold-containing compound provided to the first solution is preferably a water soluble gold salt, such as, for example, sodium tetrachloroaurate. An amount of sodium sulfite is preferably provided as a complexing agent to complex the gold in the first solution. In addition, an amount of a complexing agent to complex the tin is added, such as, for example 1-ascorbic acid. An amount of buffer, such as, for example, triammonium citrate is dissolved in water to form the second solution to which the tin-containing compound is added. The tin-containing compound provided to the second solution is preferably a water-soluble tin-containing salt, such as, for example, tin (II) chloride. An amount of non-ionic surfactant/leveling agent (e.g. Triton X-100, etc.) is preferably then added to the first or second solution. Once the first and second solutions are combined to form the third electrolyte solution, containing gold and tin ions, an amount of surfactant/leveling agent, preferably a phenolphthalein solution, is added to the third solution. The third solution is preferably maintained at a pH of about 5.4.
According to a further variation, the cathodic substrate surface comprises copper, a commonly used material for electronic components such as, for example, leads. Preferably, controlled amounts of gold and tin are co-deposited onto the substrate surface to a thickness of from about 1 to about 10 microns, with a gold concentration of from about 0.5 to about 5 weight percent, and more preferably from about 1 to about 2 weight percent.
The present disclosure also relates to a method for making an electroplating bath comprising, in a first solution, dissolving an amount of gold-containing compound (preferably sodium tetrachloroaurate) in water (preferably deionized water) and adding an amount of a first and second complexing agent (preferably sodium sulfite and 1-ascorbic acid). In a second solution, an amount of a triammonium citrate buffer is dissolved in water (preferably deionized water) to which is added an amount of water-soluble tin-containing compound (preferably tin (II) chloride), and optionally an amount of a non-ionic surfactant/leveling agent. The first and second solutions are combined to make a third solution, to which is added an amount of surfactant/leveling agent (preferably phenolphthalein). In addition, the present disclosure contemplates an electroplating bath made according to the above method.
The present disclosure further relates to an electroplating bath comprising water, an amount of a water-soluble gold-containing compound (preferably sodium tetrachloroaurate), first and second complexing agents (preferably sodium sulfite and 1-ascorbic acid), an amount of water-soluble tin-containing compound (preferably tin (II) chloride), an amount of buffer (preferably triammonium citrate), and preferably amounts of surfactant/leveling agents (preferably non-ionic Triton X-100 and phenolphthalein).
Still further, the present disclosure relates to a coating for mitigating tin whisker growth on a substrate surface comprising an amount of gold and tin co-deposited onto the substrate surface. According to a preferred variation, the gold and tin are electro-deposited onto the substrate surface, preferably to a thickness of from about 1 micron to about 10 microns. Preferably, the substrate surface comprises copper, and the gold is preferably co-deposited with the tin onto the substrate at a concentration of from about 0.5 to about 5 weight percent gold.
The present disclosure contemplates the described coatings as usefully coating any object, including, but in no way limited to, electronic components where it is desirable to mitigate the formation of tin whiskers by replacing a substantially pure tin-plated surface with a gold and tin plating. The present disclosure also contemplates the coatings and methods presented herein as useful in the manufacture of any object comprising electronic components that comprise the disclosed gold and tin platings.
Having thus described variations of the disclosure in general terms, reference will now be made to the accompanying drawings, which are not necessarily drawn to scale, and wherein:
a and 1b are flowcharts for preferred processes of plating a coating comprising gold and tin onto a substrate surface;
The present disclosure relates to the development of electroplated tin films that are doped with controlled amounts of from about 0.5 to about 5 weight percent gold to suppress the growth of tin whiskers from the plated substrate surface, as otherwise commonly occurs with pure tin-plated substrates. The addition of controlled amounts of gold to tin-plated films has now been shown to significantly suppress and effectively eliminate undesired tin whisker growth for extended periods of time.
a shows a flow chart for a preferred variation of the present disclosure. According to the variation, a first electrolyte solution 10a and a second electrolyte solution 11a are prepared. To make solution 10a, in a first step 12a, an amount of a water-soluble gold-containing compound is dissolved in water. An amount of a first complexing agent for gold is added 14a, followed by adding an amount of a second complexing agent 16a as a complexing agent for tin. In the second solution 11a, an amount of buffer is dissolved in water 13a, followed by adding an amount of a water-soluble tin-containing compound 15a, and an amount of surfactant/leveling agent, 17a. The two solutions 10a and 11a are then combined with additional water 18a. An amount of phenolphthalein 19a is added to the solution. The resulting solution is then used as an electroplating solution to co-deposit tin and gold (from about 0.5 to about 5 weight percent, and more preferably from about 1 to about 2 weight percent gold) onto a substrate surface 20a.
b shows a flow chart for one preferred variation. According to the variation, a first electrolyte solution 10b and a second electrolyte solution 11b are prepared. To make solution 10b, in a first step 12b, an amount of a sodium tetrachloroaurate salt (NaAuCl4-2H2O) is dissolved in deionized water. An amount of sodium sulfite (Na2SO3) is added 14b, followed by adding an amount of 1-ascorbic acid 16b as a complexing agent for tin. In the second solution 11b, an amount of triammonium citrate buffer is dissolved in deionized water 13b, followed by adding an amount of tin (II) chloride (Sn(II)Cl2-2H2O) 15b, and an amount of Triton X-100, 17b. The two solutions 10b and 11b are then combined with the addition of deionized water 18b. An amount of phenolphthalein 19b is added to the solution. The resulting solution is then used as an electroplating solution to co-deposit tin and gold (from about 0.5 to about 5 weight percent, and more preferably from about 1 to about 2 weight percent gold) onto a substrate surface 20b.
As shown in
NaAuCl4-2H2O (99%, Aldrich) in an amount of 0.111 grams was dissolved in 100 mls of deionized water in a beaker. An amount of 0.385 g of Na2SO3 (>98%, Aldrich) was dissolved into the NaAuCl4 solution with stirring. An amount of 4.494 g of 1-ascorbic acid (>99%, Aldrich) was added to the above electrolyte solution with stirring to obtain a clear, very pale amber solution. In a separate beaker, 30.00 g of triammonium citrate (>97%, Aldrich) was dissolved in 150 mls of deionized water with stirring. An amount of 1.459 g of Sn(II)Cl2-2H2O (Reagent grade, Alfa Aesar) was dissolved in the triammonium citrate solution with stirring. An amount of 0.250 g of Triton X-100 (Dow Chemical) was added to the tin-containing electrolyte solution and dissolved with stirring. The tin-containing electrolyte solution was then combined with the gold-containing electrolyte solution, with the total volume being brought up to 300 mls with deionized water. An amount of 0.304 g of a 0.5% phenolphthalein solution (Aldrich) was added drop-wise to the combined tin- and gold-containing solution with stirring. The pH of the solution was measured and found to be 5.4 (microfine pH paper).
Plating was conducted using 30 mls of the combined tin- and gold-containing electrolyte at 69° C. in a 50 ml glass beaker with stirring. The anode was constructed from tin sheet (99.998%, Aldrich). One coupon was plated at a time and fresh electrolyte was used for each sample (coupon) plated. Plating was conducted at 0.500 volts and 2.2 milliamps for 25 minutes to yield a light gray, satin matte plated film. The cathode was gently wiped every 5 minutes during the plating with a swab to remove fine particulates and gas bubbles. The tin electrode was cleaned using 500 grit SiC paper before each sample was plated. Fresh electrolyte was used for plating each sample. The first and seventh runs for the gold-doped tin films were analyzed by inductively coupled plasma (ICP) spectroscopy. The ICP spectroscopy results are shown in Table 1 below. Typically, the plated films were completely dissolved off the coupons using 8 mls of 1:1 nitric acid plus 4 mls of concentrated hydrochloric acid in a small beaker. This solution was then transferred to a 100 ml volumetric flask, diluted with deionized water, and analyzed for elements of interest using an ICP spectrometer.
Pure tin-coated coupons were prepared for use as comparative control samples. This was achieved using the method developed by Yun Zhang (described in U.S. Pat. No. 5,750,017). Triton X-100 (Dow Chemical) in an amount of 0.1259 g was dissolved in 80 ml of deionized water. Methanesulfonic acid (70%, Aldrich) in an amount of 20 ml was added. Phenolphthalein solution (0.5%) (Aldrich) in an amount of 2.00 g was added dropwise while stirring. Tin methane sulfonate solution (50%, Aldrich) in an amount of 10 ml was added to the solution while stirring. Plating was conducted using 30 ml of the above electrolyte solution held at 50° C. in a 50 ml glass beaker while stirring. The anode was constructed from 99.998% tin sheet (Aldrich). Plating was performed at 0.045 V and 10.9 milliamps for 8 minutes to yield a gray satin plating.
Immediately after plating, the test specimens were put into a 50° C./50% relative humidity chamber in an effort to accelerate tin whisker formation and growth. Specimens plated with pure tin were also put into the test chamber for use as a control. At approximately 6 months, 12 months and 18 months, the test specimens were examined using a scanning electron microscope (SEM). The pure tin-plated films had numerous nodules and whiskers growing from the surface. See
As shown in the Example above, various surfactants can be added to the electrolyte solution containing the gold and tin. Preferred surfactants are non-ionic surfactants that act as leveling agents to help obtain a substantially uniform coating when plating onto a substrate. Preferred surfactants include Triton X-100, Igepal CA-630, Nonidet P-40, Conco NI, Dowfax 9N, Igepal CO, Makon, Neutronyx 600 series, Nonipol NO, Plytergent B, Renex 600 series, Solar NO, Sterox, Serfonic N, T-DET-N, Tergitol NP, Triton N, etc., with Triton X-100 being particularly preferred.
Without being bound to a particular theory, it is believed that the sodium sulfite serves to complex the gold ions as well as the tin ions in solution. The 1-ascorbic acid complexes the tin in solution to prevent it from reacting with the water. In theory, two metals with different electromotive potentials cannot be practically plated at the same time. This limitation is usually overcome by chemically complexing one or both metals, which effectively brings their electromotive potentials closer together and allows them both to be plated/deposited at the same time. Other complexing agents that may work for the Sn/Au system include without limitation, citric acid, succinic acid, aspartic acid, EDTA, mannitol, or any organic compound with carboxylic acid groups, or other groups capable of complexing metal ions in solution, etc.
The gold-doped tin coatings made according to the preferred processes set forth in this disclosure are understood to be deposited onto a substrate of choice to a preferred thickness of from about 1 to about 50 microns, and more preferably to a thickness of from about 1 to about 10 microns, with a preferred gold concentration of from about 0.5 to about 5 weight percent, and more preferably from about 1 to about 2 weight percent. It is understood that the gold may be present in concentrations in excess of 5 weight percent, however, the tin whisker mitigation observed during 18 months of observation was achieved with gold concentrations of only about 1 weight percent. It is believed that excessive gold concentrations could impact the economic feasibility of the disclosed methods and coatings, without offering enhanced performance. In addition, the gold concentration must not interfere with the physical and chemical performance of the tin relative to, for example, soldering of the coated component, etc.
The examples presented herein contemplate use of the Sn/Au platings on objects including electronic components such as, for example, quad flat packs, plastic dual in-line packages (PDIPs), small-outline integrated circuits (SOICs), relays, etc., or as a plating for traces on printed circuit boards, etc. It is further contemplated that such electronic parts plated with the Sn/Au coatings of the present disclosure will find utility in any electronics systems used, for example, in any object such as aircraft, spacecraft, terrestrial or non-terrestrial vehicles, as well as stationary structures and other objects. A non-exhaustive list of contemplated vehicles include manned and unmanned aircraft, spacecraft, satellites, terrestrial, non-terrestrial and surface and sub-surface water-borne vehicles, etc.
While the preferred variations and alternatives of the present disclosure have been illustrated and described, it will be appreciated that various changes and substitutions can be made therein without departing from the spirit and scope of the disclosure. Accordingly, the scope of the disclosure should only be limited by the accompanying claims and equivalents thereof.
This invention was made with Government support under Contract Number W912HQ-10-C-0022 awarded by the U.S. Department of Defense. The U.S. Government has certain rights in this invention.
