Effect of Se in Co-based selenides towards oxygen reduction electrocatalytic activity

被引:33
作者
Zhao, Dongjiang [1 ,2 ]
Zhang, Sheng [1 ]
Yin, Geping [1 ]
Du, Chunyu [1 ]
Wang, Zhenobo [1 ]
Wei, Jie [1 ]
机构
[1] Harbin Inst Technol, Sch Chem Engn & Technol, State Key Lab Urban Water Resource & Environm, Harbin 150001, Peoples R China
[2] Suihua Univ, Dept Chem & Med Engn, Suihua 152061, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen reduction; Non-noble metal catalyst; Cobalt selenide; Polymer electrolyte membrane fuel cells; SUPPORTED COSE2 NANOPARTICLES; POLYMER ELECTROLYTE MEMBRANE; THIN-FILMS; FUEL-CELL; MODEL CATALYSTS; CARBON; ACID; CHALCOGENIDE; O-2; ELECTROREDUCTION;
D O I
10.1016/j.jpowsour.2012.01.018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, Co-based selenides with various selenium contents have been synthesized by heating dodecacarbonyltetracobalt [Co-4(CO)(12)] and elemental selenium in 1,6-hexanediol solvent under refluxing conditions. The synthesized catalyst powders are characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The samples exhibit cauliflower-like surface morphologies and reveal the crystalline characteristics of orthorhombic CoSe2 compound. Electrocatalytic performances of the Co-Se compounds for the oxygen reduction reaction in 0.5 M H2SO4 electrolyte are evaluated by rotating disk electrode (ROE). Co-Se catalysts are electrochemical stable in the potential range of 0.05-0.80 V (vs. NHE). The catalytic activity changes with increasing selenium content, and the highest activity is obtained at 67.1 mol% Se in the catalyst, which can be attributed to the modification of selenium element on the electronic structure of cobalt. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 107
页数:5
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