High-Performance Metal-Free Nanosheets Array Electrocatalyst for Oxygen Evolution Reaction in Acid

被引:95
|
作者
Lei, Chaojun [1 ]
Zheng, Qiang [2 ]
Cheng, Fanpeng [1 ]
Hou, Yang [1 ]
Yang, Bin [1 ]
Li, Zhongjian [1 ]
Wen, Zhenhai [3 ]
Lei, Lecheng [1 ]
Chai, Guoliang [3 ]
Feng, Xinliang [4 ,5 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Minist Educ, Key Lab Biomass Chem Engn, Hangzhou 310027, Peoples R China
[2] Natl Ctr Nanosci & Technol, CAS Key Lab Standardizat & Measurement Nanotechno, CAS Ctr Excellence Nanosci, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, State Key Lab Struct Chem, Fujian Inst Res Struct Matter, Fuzhou 350002, Fujian, Peoples R China
[4] Tech Univ Dresden, Ctr Adv Elect Dresden Cfaed, D-01062 Dresden, Germany
[5] Tech Univ Dresden, Dept Chem & Food Chem, D-01062 Dresden, Germany
基金
中国国家自然科学基金;
关键词
acidic electrolyte; electrocatalysis; metal-free; nanosheets array; water oxidation; N-DOPED CARBON; POROUS CARBON; BIFUNCTIONAL ELECTROCATALYST; HYDROGEN EVOLUTION; ACTIVE-SITES; EFFICIENT; GRAPHENE; CATALYST; NITROGEN; NANOPARTICLES;
D O I
10.1002/adfm.202003000
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of low cost electrocatalysts with outstanding catalytic activity and stability for oxygen evolution reaction (OER) in acid is a major challenge to produce hydrogen energy from water splitting. Herein, a novel metal-free electrocatalyst consisting of a oxygen-functionalized electrochemically exfoliated graphene (OEEG) nanosheets array is reported. Benefitting from a vertically aligned arrays structure and introducing oxygen functional groups, the metal-free OEEG nanosheets array exhibits superior electrocatalytic activity and stability toward OER with a low overpotential of 334 mV at 10 mA cm(-2)in acidic electrolyte. Such a high OER performance is thus far the best among all previously reported metal-free carbon-based materials, and even superior to commercial Ir/C catalysts (420 mV at 10 mA cm(-2)) in acid. Characterization results and electrochemical measurements identify the COOH species in the OEEG acting as active sites for acidic OER, which is further supported by atomic-scale scanning transmission electron microscopy imaging and electron energy-loss spectroscopy. Density functional theory calculations reveal that the reaction pathway of dual sites that is mixed by zigzag and armchair edges (COOH-zig-corner) is better than the pathway of single site.
引用
收藏
页数:9
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