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Boosting the electrocatalytic activities of SnO2 electrodes for remediation of aqueous pollutants by doping with various metals

兴奋剂 水溶液 电化学 电催化剂 掺杂剂 电极 苯酚 材料科学 基质(水族馆) 化学 无机化学 核化学 光电子学 有机化学 地质学 物理化学 海洋学
作者
So Young Yang,Yeon Sik Choo,Soonhyun Kim,Sang Kyoo Lim,Jaesang Lee,Hyunwoong Park
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:111-112: 317-325 被引量:134
标识
DOI:10.1016/j.apcatb.2011.10.014
摘要

The purpose of this study is to search for effective dopants and their optimal combinations to improve the electrocatalytic activity of the SnO2 electrode for the remediation of aqueous pollutants. For this purpose, Sb was selected as the primary dopant for SnO2 and six elements (Fe(III), Ni(II), Co(II), Ru(III), Ce(III), and Pd(II)) were also introduced into the optimized Sb–SnO2 electrodes. The electrodes were checked for their electrochemical properties at different doping levels and tested for their electrocatalytic activities for the degradation of phenol and Eosin Y. In addition, RNO (N,N-dimethyl-p-nitrosoaniline) was used as a probe molecule for OH radicals to examine the reaction mechanism occurring at the electrodes. Sb with a 5–10 at.% was most effective in making SnO2 an electrocatalyst and Ni (∼1%) enhanced the degradation rate and TOC removal rate of phenol at the Sb–SnO2 anode by a factor of 14 and 8, respectively. Fe also increased the activity moderately. Enhanced Ni–Sb–SnO2 activity was also found for Eosin Y. The other co-dopants exhibited various degrees of positive or negative effects depending on the substrate. The lack of a correlation in the kinetics between substrate degradation and the RNO changes indicated that the primary electrocatalytic reactions may proceed via direct electron transfer and/or organic peroxy radical-mediation, not OH radical-mediation. Detailed analyses of the electrode surfaces (SEM, TEM, XRD, and XPS) and quantification of intermediates were carried out to obtain insight into the heterogeneous electrocatalytic reaction.
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