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Boosting oxygen evolution reaction on graphene through engineering electronic structure.

Authors :
Wang, Changlai
Tong, Huigang
Lu, Jian
Liu, Bin
Zheng, Fangcai
Tao, Weiwei
Zhang, Wenjun
Chen, Qianwang
Source :
Carbon. Dec2020, Vol. 170, p414-420. 7p.
Publication Year :
2020

Abstract

Graphene is electrochemically inert toward the oxygen evolution reaction (OER) owing to the zero-band property, nevertheless doping it with heteroatoms could modulate its electronic structure and increase its chemical reactivity. Notwithstanding the achieved progress, the overpotential of heteroatom doped graphene is still very large. Herein, we coat FeNiIr nanoalloys by nitrogen-doped graphene with core-shell structure (FeNiIr@NG) to further boost the OER activity on graphene surface. Because of the unique core-shell structure, FeNiIr@NG delivers high electrocatalytic OER activity and durability, even exceeding that of commercial IrO 2 electrocatalyst. Density functional theory calculations demonstrate that the nanoalloys core could transfer electron to outer graphene shells, which optimizes the electronic structure of graphene and balances the adsorption strength of OER intermediates, thereby triggering OER activity on the graphene surface. The OER activity on graphene surface is triggered through coating FeNiIr nanoalloys to modulate the electronic structure of graphene. Image 1 • The OER activity on graphene surface is triggered by coating FeNiIr with graphene. • This unique FeNiIr@NG core-shell catalyst exhibits better OER activity than IrO 2. • The adsorption strength of ∗ O, ∗OH and ∗OOH is depended on electronic structure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00086223
Volume :
170
Database :
Academic Search Index
Journal :
Carbon
Publication Type :
Academic Journal
Accession number :
146481419
Full Text :
https://doi.org/10.1016/j.carbon.2020.08.041