Experimental and theoretical studies of DMH as a complexing agent for a cyanide-free gold electroplating electrolyte

被引:56
|
作者
Ren, Xuefeng [1 ]
Song, Ying [1 ]
Liu, Anmin [1 ]
Zhang, Jie [1 ]
Yang, Peixia [1 ]
Zhang, Jinqiu [1 ]
An, Maozhong [1 ]
机构
[1] Harbin Inst Technol, Sch Chem Engn & Technol, State Key Lab Urban Water Resource & Environm, Harbin 150001, Peoples R China
来源
RSC ADVANCES | 2015年 / 5卷 / 80期
关键词
DENSITY-FUNCTIONAL THEORY; MOLECULAR-DYNAMICS SIMULATIONS; CORROSION-INHIBITORS; TOXIC CYANIDE; COPPER; ADSORPTION; SURFACE; CHEMISTRY; ELECTRODEPOSITION; CU(111);
D O I
10.1039/c5ra13140e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a cyanide-free gold electroplating electrolyte using 5,5-dimethylhydantoin (DMH) as a complexing agent was introduced. A golden bright gold electrodeposit with smooth and compact surface was obtained from the introduced cyanide-free gold electroplating electrolyte. The results of scanning electron microscopy (SEM) measurements confirmed that the golden bright gold electrodeposit possesses an excellent leveling capability as well as smooth and compact morphology. The crystalline structure of the gold electrodeposits was characterized by X-ray diffraction (XRD) analysis. Computational chemistry was employed to provide an insight view of the reason for selecting DMH among the various hydantoin derivatives as the complexing agent for the introduced cyanide-free gold electroplating electrolyte. Quantum chemical calculations were employed to study the electronic properties and orbital information of the investigated complexing agents. The adsorption interactions between these complexing agents and the metal surfaces were investigated by molecular dynamic (MD) simulations. Consequently, the results of these theoretical studies revealed that DMH was selected among the various hydantoin derivatives as the complexing agent for the introduced cyanide-free gold electroplating electrolyte due to its strong electron donating abilities and high adsorption energies on the metal surfaces.
引用
收藏
页码:64997 / 65004
页数:8
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