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Sn-based alloy compounds have been considered as possible alternatives for carbon in lithium-ion batteries and attract great attentions because of their large electrochemical capacity compared with that of carbon. In this work, a multilayered Sn–Zn/Zn/Cu alloy thin-film electrode has been prepared by electroplating method. The structure and performance of the electrode before and after heat treatment have been investigated. It is found that Cu 6 Sn 5 phase and multilayered structure in electrode are formed after heat treatment. This optimized structure of the heat-treated electrode results in enhanced cycle life. The capacity of the electrode is over 320 mA h g −1 after 100 cycles; though it is 83 mA h g −1 after 20 cycles for as-plated electrode. The Sn–Cu and Zn–Cu alloy formed a network in the electrode is considered to strengthen the electrode and reduce the effect of volume expansion and phase transition during cycling. Experimental results also reveal that lower cut-off potential (0.05 V) for charging and higher one (1.2 V) for discharging result in long cycle life and high discharge capacity, respectively. The reason of capacity decay of the heat-treatment electrode during cycling has also been investigated. All these results show that the electroplated Sn–Zn-based alloy film on Cu foil would be a promising negative material with high capacity and low cost for Li secondary batteries.

スズ-亜鉛共晶合金は, 融点が現行のスズ-鉛共晶合金のそれに近いことから, 鉛フリーはんだの候補として期待されている。ポリオキシエチレン-α-ナフトール (POEN) を添加剤とするスルホコハク酸浴から, カソード電流密度0.5～3A/dm2において, 共晶組成 (亜鉛9mass%) を有する合金皮膜が得られた。POENの添加は, スズ析出の分極を増大し, 低電流密度領域におけるスズの優先析出を抑制することにより, 亜鉛の共析を可能にした。めっき浴は極めて安定であり, 6カ月経過後においてもSn4+化合物の沈殿形成は認められなかった。スズ-亜鉛共晶合金皮膜は, β-スズ相と亜鉛相からなり, その融点は198℃であった。銅素地上のスズ-亜鉛共晶合金皮膜には, 1年間の室温経時後においてもウイスカの発生は認められなかった。

A novel electroless Ni Plating bath using Ti (III) ions as reluctant was proposed. In an industrial application of this plating bath, stability of the plating bath and plating rate are particularly important. Effects of plating bath components on Ni deposition rate onto Urethane foam or copper sheet were investigated, elucidating that Ni (II) ions, nitrilotriacetic acid and ammonium hydroxide concentration were important factors to control Ni deposition rate. Purity of Ni film reduced with Ti (III) ions was very high exceeding 99.9%.

Sn-Cu-Ag合金めっきは, Sn-Pbはんだめっきの代替として有望であり, 優れた耐熱疲労特性を有している。トリスー3ーヒドロキシプロピルホスフイン (T3HPP) , ポリオキシエチレンーαーナフトール (POEN) および2, 2, -ジチオジァニリン (DTDA) を添加剤とするメタンスルホン酸浴から, 電流密度0.5～5A/dm2において, 目的組成Sn-0.7Cu-0.3Ag (組成: mass%) の合金皮膜が得られた。T3HPPの添加は, 浴の安定性を著しく改善した。この合金皮膜は, β-Sn相とCu6Sn5相およびAg3Sn相からなり, その融点はほぼ225℃の値を示した。銅素地上のSn-0.7Cu-0.3Ag合金皮膜には, 6カ月の室温経時後においてもウイスカの発生は認められなかった。

Direct electroless silver plating on copper metal from a succinimide complex bath using imidazole as the reducing agent was examined. Though the electroless silver plating from this bath is essentially an autocatalytic deposition, there is a problem in the properties and adhesion of the plated film because of the substitution deposition of silver due to the dissolution of the base copper metal that occurs during the first stage of plating. By adding glyoxylic acid, which is catalytically reacted on the copper surface to emit electrons, as the second reducing agent, the substitution deposition of silver was suppressed, the surface condition became dense and the adhesion was improved. It has been determined that the mixed potential theory can be applied to this reaction based on the result of the local polarization curve measurement.

A novel electrode composed of activated carbon and DNA together with fluorinated binder has been prepared for an electric double layer capacitor (EDLC) with aqueous electrolytes. The DNA-loaded electrodes improve the rate capability and discharge capacitance of EDLC containing aqueous, neutral salt electrolytes. In contrast, the DNA-composite electrodes have a poor effect on the capacitance enhancement in acidic or basic electrolytes. The enhancement of discharge capacitance is significant especially at high-rate cycling in neutral salt electrolytes, because the presence of DNA reduces the internal resistance of an electrode and hence improves its rate capability.

Tin-zinc alloys of low zinc content are believed to have high corrosion resistance when they are used for protective films on steel surface. This paper describes the following studies: an optimum composition for protective films was selected by electrochemical measurements of the cast alloys; and, zincate-stannate baths and gluconate baths were investigated to obtain such alloy deposits from baths free from cyanides and fluorides. The following results were obtained: (1) The static potential of tinzinc alloys was base enough to act as a sacrificial film for steel, and the potential of an alloy containin more than about 10% of zinc showed almost the same value as that of single zinc. (2) The anodic dissolution in NaCl solution and the formation of white precipitate on the alloy surface in a salt spray test more readily occurred with the increase in zinc content of the alloy. (3) It was difficult to obtain alloy deposits of lower zinc content from zincate-stannate baths under normal plating conditions. (4) A semi-bright zinc alloy deposit of lower zinc content was obtained from the bath containing 0.25mol/l of metal and 0.50mol/l of Na-gluconate with an additive such as 0.25mol/l of triethanolamine, 2.5-5g/l of polyethyleneglycolnonylphenylether (PEGNPE), 0.2-1g/l of peptone, and 0.04-0.06g/l of o-vanillin at pH=5. It was observed that a deposit of fine luster was apt to be obtained at a composition of nearly equi-molecular ratio between tin and zinc. (5) It was further observed that a deposit of highest zinc content was obtained from gluconate baths containing 20 and 35% of zinc at pH=5, and the zinc content of deposit was almost equal to that of the bath when the plating was conducted at a current density of 1-2Amp/dm2.