Electroreduction of CO2 to CO on a Mesoporous Carbon Catalyst with Progressively Removed Nitrogen Moieties

被引:140
|
作者
Daiyan, Rahman [1 ]
Tan, Xin [2 ]
Chen, Rui [1 ]
Saputera, Wibawa Hendra [1 ]
Tahini, Hassan A. [2 ]
Lovell, Emma [1 ]
Ng, Yun Hau [1 ]
Smith, Sean C. [2 ]
Dai, Liming [1 ,3 ]
Lu, Xunyu [1 ]
Amal, Rose [1 ]
机构
[1] Univ New South Wales, Sch Chem Engn, Sydney, NSW 2052, Australia
[2] Australian Natl Univ, Res Sch Phys & Engn, Integrated Mat Design Lab, Canberra, ACT 2601, Australia
[3] Case Western Reserve Univ, Ctr Adv Sci & Engn Carbon Case4carbon, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
来源
ACS ENERGY LETTERS | 2018年 / 3卷 / 09期
基金
澳大利亚研究理事会;
关键词
ELECTROCHEMICAL REDUCTION; ELECTROCATALYTIC REDUCTION; OXYGEN REDUCTION; GRAPHENE; DEFECTS; EFFICIENT; NANOPARTICLES; IMPURITIES; EVOLUTION;
D O I
10.1021/acsenergylett.8b01409
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
In this study, we prepared nitrogen-removed mesoporous carbon (NRMC) catalysts by applying various heat treatments to nitrogen-doped mesoporous carbon (NMC), which were applied as novel electrocatalysts for CO2 reduction reaction (CO2RR). With the nitrogen moieties being progressively removed, the NRMC catalysts exhibited enhanced CO generation from CO2RR, whereas the competing hydrogen evolution reaction (HER) has been suppressed. Through suitable annealing treatment, the defect-rich NRMC catalyst is able to convert CO2 to CO with a Faradaic efficiency (FE co ) of similar to 80% and a partial current density for CO (j(CO)) of -2.9 mA cm(-2) at an applied overpotential of 490 mV. Density functional theory (DFT) calculations further revealed the active sites within NRMC catalysts were the defects generated by N removal, which lowered the energy barriers for CO2RR and will not be passivated by hydrogen. These findings provide design guidelines to develop efficient carbon-based catalysts that can display metal-like, and even better, performances for potential scalable CO2RR to fuels and chemicals.
引用
收藏
页码:2292 / 2298
页数:13
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