Broken holey graphene oxide for electrocatalytic N2-to-NH3 fixation at ambient condition

被引:21
|
作者
Wang, Fei [1 ]
Wang, Haoyu [2 ]
Mao, Jian [1 ]
机构
[1] Sichuan Univ, Coll Mat Sci & Engn, 24 South Sect 1,Yihuan Rd, Chengdu 610065, Peoples R China
[2] Univ New South Wales, Sch Mat Sci & Engn, Sydney, NSW 2052, Australia
关键词
Metal-free catalyst; Broken holey graphene oxide; Electrocatalysis; Nitrogen reduction reaction; Density functional theory; AMMONIA-SYNTHESIS; NITROGEN REDUCTION; DOPED GRAPHENE; N-2; EFFICIENT; PERFORMANCE; CARBON; CATALYSTS; NH3;
D O I
10.1016/j.colsurfa.2020.125345
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
Electrocatalysts is critical for nitrogen reduction reaction (NRR) under ambient conditions. Defect engineering is generally employed to prepared high-performance electrocatalysts. Herein, we report a broken holey graphene oxide (BHGO) prepared by a facile high-temperature etching method. Compared with the holey graphene oxide (HGO) and graphene oxide (GO), the BHGO exhibits higher electron transfer capability and richer active sites (coordination of one-dimensional edges and zero-dimensional oxygen-doping defects). The BHGO catalyst reaches excellent NRR performance (NH3 yield of 22.27 mu g h(-1) mg(-1) and Faraday efficiency (FE) of 11.01 % in 0.1 M Na2SO4 solution at the ambient condition. Illustrated by the density functional theory (DFT) calculations, the introduction of coordinated mull-dimensional defects redistributes the charge, enhancing adsorption of nitrogen (N-2) and reducing energy barrier at rate-determining step (N*-> NH*). Moreover, catalytic performance can be well preserved in an aqueous solution. The proposed mull-dimensional defect engineering strategy and established DFT simulations may pave an exciting avenue toward the design and development of high-performance catalysts.
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页数:8
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