教授 博士生导师 硕士生导师
性别: 男
毕业院校: 大连理工大学
学位: 博士
所在单位: 材料科学与工程学院
学科: 材料学. 功能材料化学与化工. 化学工程
办公地点: 材料楼330办公室
联系方式: 0411-84706595
电子邮箱: huang@dlut.edu.cn
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论文类型: 期刊论文
发表时间: 2018-01-01
发表刊物: JOURNAL OF THE ELECTROCHEMICAL SOCIETY
收录刊物: SCIE、EI
卷号: 165
期号: 3
页面范围: D152-D159
ISSN号: 0013-4651
摘要: The complexation behavior and co-electrodeposition mechanism of Au-Sn alloy in a highly stable non-cyanide bath were studied by electrochemical analysis and quantum chemical calculation based on density functional theory (DFT). The interactions between metal ions and multiple complexing agents were revealed, and the mechanism on the high stability of the Au-Sn bath was clarified. The complexing agents potassium pyrophosphate (K4P2O7) and ethylene diamine tetraacetic acid (EDTA) have a synergetic complexation to Sn ions, which exist in one valence state of Sn2+ to form three complex ions, i.e., [Sn(P2O7)](2-), [Sn(P2O7)(2)](6-) and Sn-EDTA; while the complexing agents of 5,5-dimethylhydantoin (DMH) and sodium sulfite (Na2SO3) have a complexation to Au ions, which exist in two different valence states (i.e., Au3+ and Au+) to form two complex ions of [Au(DMH)(4)](-) and Au[(SO3)(2)](3-). Moreover, the existence of [Au(DMH)(4)](-) inhibits the decomposition of [Au(SO3)(2)](3-). Meanwhile, EDTA participates in some form of coordination with Au+, inhibites the decomposition of [Au(SO3)(2)](3-) and facilitates the reduction of [Au(SO3)(2)](3-). The co-electrodeposition of Au-Sn alloy is a diffusion-controlled process, and the nucleation of Au-Sn alloy is a progressive nucleation process. The antioxidant catechol significantly increases the overpotential of Au-Sn co-electrodeposition and improves the brightness of electrodeposited films of Au-Sn alloys. (C) The Author(s) 2018. Published by ECS.