Manganese acting as a high-performance heterogeneous electrocatalyst in carbon dioxide reduction

被引:296
作者
Zhang, Bingxing [1 ,2 ]
Zhang, Jianling [1 ,2 ]
Shi, Jinbiao [1 ,2 ]
Tan, Dongxing [1 ,2 ]
Liu, Lifei [1 ,2 ]
Zhang, Fanyu [1 ,2 ]
Lu, Cheng [1 ,2 ]
Su, Zhuizhui [1 ,2 ]
Tan, Xiuniang [1 ,2 ]
Cheng, Xiuyan [1 ,2 ]
Han, Buxing [1 ,2 ]
Zheng, Lirong [3 ]
Zhang, Jing [3 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Colloid Interface & Chem Thermodynam, CAS Res Educ Ctr Excellence Mol Sci,BNLMS, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, BSRF, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; REDUCTION; EFFICIENT ELECTROREDUCTION; SELECTIVE CONVERSION; ORGANIC FRAMEWORKS; CATALYSTS; COORDINATION; IDENTIFICATION; COMPLEX; SITES; METAL;
D O I
10.1038/s41467-019-10854-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Developing highly efficient electrocatalysts based on cheap and earth-abundant metals for CO(2 )reduction is of great importance. Here we demonstrate that the electrocatalytic activity of manganese-based heterogeneous catalyst can be significantly improved through halogen and nitrogen dual-coordination to modulate the electronic structure of manganese atom. Such an electrocatalyst for CO2 reduction exhibits a maximum CO faradaic efficiency of 97% and high current density of similar to 10 mA cm(-2) at a low overpotential of 0.49 V. Moreover, the turnover frequency can reach 38347 h(-1) at overpotential of 0.49 V, which is the highest among the reported heterogeneous electrocatalysts for CO2 reduction. In situ X-ray absorption experiment and density-functional theory calculation reveal the modified electronic structure of the active manganese site, on which the free energy barrier for intermediate formation is greatly reduced, thus resulting in a great improvement of CO2 reduction performance.
引用
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页数:8
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