Investigation of electrochemical reduction of GeO2 to Ge in molten CaCl2- NaCl

被引:28
作者
Rong, Liangbin [1 ]
He, Rui [1 ]
Wang, Zhiyong [1 ]
Peng, Junjun [1 ]
Jin, Xianbo [1 ]
Chen, George Z. [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Univ Nottingham, Fac Engn, Dept Chem & Environm Engn, Nottingham NG7 2RD, England
[3] Univ Nottingham, Fac Engn, Energy & Sustainabil Res Div, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
Solid state reduction; Calcium germanates; GeO2; Ge; Molten salt; DIRECT ELECTROLYTIC REDUCTION; CALCIUM-CHLORIDE; GERMANIUM NANOWIRES; TITANIUM-DIOXIDE; 3-PHASE INTERLINES; SOLID OXIDES; SIO2; PELLETS; DEOXIDATION; SILICON; SALTS;
D O I
10.1016/j.electacta.2014.09.107
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical reduction of solid GeO2 has been investigated in the mixed CaCl2-NaCl melt at 1023 K for developing a more efficient process for preparation of Ge. Cyclic voltammetry and potentiostatic electrolysis were applied to study the GeO2-loaded metallic cavity electrode. In addition, porous GeO2 pellets were reduced by potentiostatic and constant cell voltage electrolysis with a graphite anode, and the electrolysis products were analyzed by powder X-ray diffraction, scanning electron microscopy and energy-dispersive X-ray spectrometry, focusing on understanding the reduction mechanism and the impact of electrode potential on the product purity. It was found that the reduction of GeO2 to Ge occurred at a potential of about -0.50 V (vs. Ag/Ag+), but generating various calcium germanates simultaneously, whose reduction was a little more difficult and needed a potential more negative than -1.00 V. However, if the cathode potential exceeded -1.60 V, Ca (or Na) -Ge intermetallic compounds might form. These results gave an appropriate potential range between -1.10 and -1.40 V for the production of pure germanium. Rapid electrolysis of GeO2 to pure Ge has been realized at a cell voltage of 2.5 V with a current efficiency of about 92%. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:352 / 359
页数:8
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