Evidence for enhanced catalytic activity of magnesium arising from anodic dissolution

被引:173
作者
Birbilis, N. [1 ,2 ]
King, A. D. [2 ]
Thomas, S. [1 ]
Frankel, G. S. [3 ]
Scully, J. R. [2 ]
机构
[1] Monash Univ, Dept Mat Engn, Clayton, Vic 3800, Australia
[2] Univ Virginia, Dept Mat Sci & Engn, Charlottesville, VA 22904 USA
[3] Ohio State Univ, Dept Mat Sci & Engn, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
Magnesium; Corrosion; Polarization; Catalytic; Cathodic reaction; VIBRATING ELECTRODE TECHNIQUE; CAST AM50 ALLOY; HIGH-PURITY MG; LOCALIZED CORROSION; PURE MAGNESIUM; CHLORIDE; NACL; ENVIRONMENTS; MG(OH)(2); BEHAVIOR;
D O I
10.1016/j.electacta.2014.03.133
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
The increasing rate of hydrogen evolving from magnesium (Mg) surfaces under anodic polarization is nowadays well documented and often termed the so-called "negative difference effect" (NDE). Recently, this behavior has been explained by a theory involving an increase in the cathodic exchange current density that arises from the anodic dissolution itself rather than a commonly-mentioned theory involving the formation of univalent Mg and its subsequent chemical reaction with water to produce hydrogen gas. In this work, a series of electrochemical tests were performed to provide evidence in support of the enhanced catalytic surface theory explaining the NDE. Potentiostatic, galvanostatic, and potentiodynamic polarization experiments using high purity Mg electrodes indicated substantial increases in the ability to support the rate of the cathodic reaction following discrete periods of anodic dissolution. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:277 / 283
页数:7
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