Multiscale carbon foam confining single iron atoms for efficient electrocatalytic CO2 reduction to CO

被引:92
作者
Zhang, Zheng [1 ,2 ]
Ma, Chao [3 ]
Tu, Yunchuan [1 ,2 ]
Si, Rui [4 ]
Wei, Jie [1 ]
Zhang, Shuhong [1 ]
Wang, Zhen [5 ]
Li, Jian-Feng [1 ]
Wang, Ye [1 ]
Deng, Dehui [1 ,2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Collaborat Innovat Ctr Chem Energy Mat IChEM, Coll Chem & Chem Engn, Xiamen 361005, Fujian, Peoples R China
[2] Chinese Acad Sci, State Key Lab Catalysis, IChEM, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[3] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
[5] Int Bioisl, Thermo Fisher Sci, Mat & Struct Anal Div, Guangzhou 510320, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; reduction; electrocatalysis; multiscale structure; carbon foam; single iron atoms; OXYGEN REDUCTION; SELECTIVE CONVERSION; ACTIVE-SITES; CATALYSTS; FE; ELECTROREDUCTION; IDENTIFICATION; DESIGN;
D O I
10.1007/s12274-019-2316-9
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
Electrocatalytic CO2 reduction to CO is a sustainable process for energy conversion. However, this process is still hindered by the diffusion-limited mass transfer, low electrical conductivity and catalytic activity. Therefore, new strategies for catalyst design should be adopted to solve these problems and improve the electrocatalytic performance for CO production. Herein, we report a multiscale carbon foam confining single iron atoms prepared with the assistant of SiO2 template. The pore-enriched environment at the macro-scale facilitates the diffusion of reactants and products. The graphene nanosheets at the nano-scale promote the charge transfer during the reaction. The single iron atoms confined in carbon matrix at the atomic-scale provide the active sites for electrocatalytic CO2 reduction to CO. The optimized catalyst achieves a CO Faradaic efficiency of 94.9% at a moderate potential of -0.5 V vs. RHE. Furthermore, the performance can be maintained over 60 hours due to the stable single iron atoms coordinated with four nitrogen atoms in the carbon matrix. This work provides a promising strategy to improve both the activity and stability of single atom catalysts for electrocatalytic CO2 reduction to CO.
引用
收藏
页码:2313 / 2317
页数:5
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