Single atomically anchored iron on graphene quantum dots for a highly efficient oxygen evolution reaction

被引:27
作者
Chang, C. -Y. [1 ]
Kashale, A. A. [1 ]
Lee, C. -M. [1 ]
Chu, S. -L. [1 ]
Lin, Y. -F. [2 ]
Chen, I-W. P. [1 ]
机构
[1] Natl Taitung Univ, Dept Appl Sci, 369,Sec 2,Univ Rd, Taitung 95092, Taiwan
[2] Natl Taiwan Univ, Dept Chem, 1,Sec 4,Roosevelt Rd, Taipei 10617, Taiwan
关键词
Graphene quantum dots; Dinitrosyl iron complex; Oxygen evolution reaction; NITROGEN-DOPED GRAPHENE; RATIONAL DESIGN; ELECTROCATALYSIS; NANOPARTICLES; REDUCTION; COMPLEXES; OXIDES;
D O I
10.1016/j.mtener.2021.100693
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
Single-atom catalysts (SACs) supported on carbon-based materials are very promising for maximizing their electrocatalytic activity. However, carbon-based SACs are primarily bonded with carbons, resulting in an inferior performance in the oxygen evolution reaction (OER). Herein, we develop a novel coordination adsorption strategy for the synthesis of a monodispersed Fe(NO)(2) moiety anchored on the nitrogen sites of the nitrogen-doped graphene quantum dots (N-GQDs) to form a Fe(NO)(2)-N-GQDs complex as an efficient OER catalyst. The resultant Fe(NO)(2)-N-GQDs complex exhibits a highly stable overpotential of 270 mV at a current density of 10 mA cm(-2) and a Tafel slope of 48 mV dec(-1) together with long-term durability, which greatly outperforms the state-of-the-art RuO2. Our finding emphasizes the role of electron-transfer resistance changes during a simple synthesis method to enhance electrocatalytic efficiency. Therefore, this work will envision numerous opportunities for creating novel-type carbon-based SACs via nitrogen-metal coordination as highly robust OER catalysts. (C) 2021 Elsevier Ltd. All rights reserved.
引用
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页数:9
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