Porous nitrogen-doped carbon derived from biomass for electrocatalytic reduction of CO2 to CO

被引:76
|
作者
Li, Fengwang [1 ,2 ]
Xue, Mianqi [3 ,4 ]
Knowles, Gregory P. [1 ]
Chen, Lu [1 ]
MacFarlane, Douglas R. [1 ,2 ]
Zhang, Jie [1 ,2 ]
机构
[1] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[2] Monash Univ, ARC Ctr Excellence Electromat Sci, Sch Chem, Clayton, Vic 3800, Australia
[3] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[4] Chinese Acad Sci, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China
基金
澳大利亚研究理事会;
关键词
Heteroatom doping; Carbon materials; Biomass-derived materials; CO2; reduction; Electrocatalysis; HIGH-PERFORMANCE SUPERCAPACITORS; OXYGEN REDUCTION; ELECTROCHEMICAL REDUCTION; HIGHLY EFFICIENT; KOH ACTIVATION; SUPERIOR PERFORMANCE; EVOLUTION REACTIONS; DIOXIDE REDUCTION; NANOTUBE ARRAYS; HUMAN HAIR;
D O I
10.1016/j.electacta.2017.05.174
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical reduction of CO2 using electricity from renewable sources is emerging as a promising approach for reducing global CO2 emissions and converting CO2 into useful chemicals. Here, a nitrogen-doped porous carbon material is proposed to electrocatalytically reduce CO (2) to CO with high activity, selectivity and superior durability. The material is synthesized by a facile one-step pyrolysis approach using biomass, namely wheat flour, and KOH as starting materials. The resulting materials show high surface area with hierarchical porous structures, and the nitrogen content and functional species can be controlled to some extent via the pyrolysis temperature. The catalyst exhibits a maximum faradaic efficiency of 83.7% and a partial current density of CO of 6.6 mA cm(-2) at an overpotential of 0.71 V in aqueous bicarbonate medium. Moreover, it also demonstrates superior long-term durability with trivial loss of activity and selectivity. Mechanistic study indicates that the pyridinic nitrogen is responsible for the high catalytic activity. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:561 / 568
页数:8
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