Electrodeposition of Metastable Au-Ni Alloys

被引:20
作者
Rouya, E. [1 ]
Stafford, G. R. [2 ]
Bertocci, U. [2 ]
Mallett, J. J. [1 ]
Schad, R. [3 ]
Begley, M. R. [1 ]
Kelly, R. G. [1 ]
Reed, M. L. [1 ]
Zangari, G. [1 ]
机构
[1] Univ Virginia, Charlottesville, VA 22904 USA
[2] NIST, Gaithersburg, MD 20899 USA
[3] Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USA
基金
美国国家科学基金会;
关键词
annealing; crystal morphology; electrochemical electrodes; electrodeposition; free energy; gold alloys; grain boundaries; grain size; metallic thin films; nickel alloys; phase separation; surface diffusion; SELF-DIFFUSION; FREE-ENERGY; GOLD; SACCHARIN; NICKEL; SULFUR; MICROSTRUCTURE; THERMODYNAMICS; SULFITE;
D O I
10.1149/1.3421749
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrodeposition of Au-Ni alloys from near-neutral, sulfite-based electrolytes derived from a commercial bath for soft gold plating is investigated. Alloy compositions ranging from 0 to 90 atom % Ni were obtained by varying the deposition potential, with Ni content increasing with overpotential. Cathodic efficiency was lower than 50% due to concurrent parasitic reactions, including the reduction of products from the decomposition of sulfites and the hydrogen evolution reaction. As-deposited films form a continuous series of metastable solid solutions and exhibit a nanocrystalline morphology, with grain size decreasing with increasing Ni content and a possible Ni enrichment at the grain boundaries. Thermal annealing at 200 degrees C was sufficient to start the relaxation of the metastable solid solution toward the thermodynamically stable biphasic configuration of pure Au and Ni phases; however, 400 degrees C was necessary to complete the phase separation process within similar to 1 h. The formation of a metastable structure is interpreted in terms of the limited surface diffusivities of adatoms at the growing interface and atomic volume differences. The excess free energy of the as-deposited alloys with respect to the stable, phase separated configuration is estimated between 6 and 18 kJ/mol, consistent with what can be expected in electrochemical processing. (C) 2010 The Electrochemical Society. [DOI: 10.1149/1.3421749] All rights reserved.
引用
收藏
页码:D396 / D405
页数:10
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