Intrinsic-structural-modulated carbon cloth as efficient electrocatalyst for water oxidation

被引:47
作者
Fan, Xi-Zheng [1 ]
Pang, Qing-Qing [1 ]
Yi, Sha-Sha [2 ]
Du, Xin [1 ]
Zhang, Shuo [3 ]
Liu, Zhong-Yi [1 ]
Yue, Xin-Zheng [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
[3] Lanzhou Univ, Sch Nucl Sci & Technol, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Self-supporting electrode; Electronic structure regulation; Density functional theory; Oxygen evolution reaction; DOPED CARBON; OXYGEN ELECTROCATALYST; DEFECT-RICH; NANOSHEETS; GRAPHENE; NANOPARTICLES; FRAMEWORKS; CATALYSTS; VACANCIES;
D O I
10.1016/j.apcatb.2021.120152
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
Efficient metal-free catalysts for oxygen evolution reaction (OER) are challenged for enhancing the efficiency of water electrolysis. Here, an extremely simple one-step calcination route is put forward to synthesize free-standing N-doped C electrocatalyst for the OER. The incorporation of N into carbon cloth (CC) can tune the electronic structure around the C sites for enhancing the reaction active sites and electrical conductivity, and optimizing adsorption energies for intermediates. As expected, the as-prepared CC-9NH(3)-3h electrode demonstrates remarkable OER performance in alkaline medium, affording an extremely low overpotential of 298 mV (@10 mA cm(-2)) and Tafel slope of 62 mV dec(-1), which is comparable to that of a commercial RuO2 and other promising metal-based OER catalysts. Our findings provide opportunities to explore CC as a new class of self-supporting OER electrocatalyst, and to improve its performance by modulating their intrinsic structure.
引用
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页数:8
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