Sulfur Incorporated CoFe2O4/Multiwalled Carbon Nanotubes toward Enhanced Oxygen Evolution Reaction

被引:36
作者
Sun, Xu [1 ]
Gao, Lingfeng [1 ]
Guo, Chengying [1 ]
Zhang, Yong [1 ]
Kuang, Xuan [1 ]
Yan, Tao [1 ]
Ji, Lei [1 ]
Wei, Qin [1 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Key Lab Interfacial React & Sensing Anal Univ Sha, Jinan 250022, Shandong, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Electrocatalyst; Oxygen evolution reaction; Water oxidation; Anion doping; Active sites modulation; HYDROGEN EVOLUTION; WATER OXIDATION; BIFUNCTIONAL ELECTROCATALYST; COFE2O4; NANOPARTICLES; ULTRATHIN NANOSHEETS; NITRIDE NANOSHEETS; EFFICIENT; REDUCTION; CATALYST; OXIDE;
D O I
10.1016/j.electacta.2017.07.091
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Developing efficient and non-noble metal electrocatalysts for oxygen evolution reaction (OER) at lower overpotential has been considered as a clean and effective strategy for replacing fossil feedstocks. Transitional metal oxides (TMO) electrocatalysts have been actively pursued because of their low-cost and strong stability in alkaline. However, the efficiency for most of developed TMO has been refrained by poor intrinsic electrical conductivity and exposed active sites. Herein, we demonstrate a sulfur incorporation strategy to accomplish greatly optimized OER performance in CoFe2O4/MWCNT (S-CFO/MWCNT) nanocomposite. Sulfur incorporation into CoFe2O4 not only brings about more active sites in CFO frameworks, but also retains the pristine stable inverse spinel crystal structure which renders the high durability of the S-CFO/MWCNT catalyst. Specifically, the electrocatalysts exhibited greatly optimized OER catalytic activity with overpotential of about 0.36 V achieving current density of about 10 mA cm (2) and Tafel slope of about 43 mV dec (1), together with stronger stability. Our work demonstrates an effective way to pursue highly efficient OER electrocatalysts. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:843 / 850
页数:8
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