Boron-Doped Nickel-Nitrogen-Carbon Single-Atom Catalyst for Boosting Electrochemical CO2 Reduction

被引:7
|
作者
Song, Jian [1 ,2 ]
Lei, Xue [3 ]
Mu, Jiali [1 ]
Li, Jingwei [1 ]
Song, Xiangen [1 ]
Yan, Li [1 ]
Ding, Yunjie [1 ,3 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, 457 Zhongshan Rd, Dalian 116023, Peoples R China
关键词
CO2; reduction; coordination environment; heteroatom doping; nickel single atoms; LARGE-SCALE; ELECTROREDUCTION; DIOXIDE; CONVERSION; SITES;
D O I
10.1002/smll.202305666
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tuning the coordination environment of the metal center in metal-nitrogen-carbon (M-N-C) single-atom catalysts via heteroatom-doping (oxygen, phosphorus, sulfur, etc.) is effective for promoting electrocatalytic CO2 reduction reaction (CO2RR). However, few studies are investigated establishing efficient CO2 reduction by introducing boron (B) atoms to regulate the M-N-C structure. Herein, a B-C3N4 self-sacrifice strategy is developed to synthesize B, N co-coordinated Ni single atom catalyst (Ni-BNC). X-ray absorption spectroscopy and high-angle annular dark field scanning transmission electron microscopy confirm the structure (Ni-N3B/C). The Ni-BNC catalyst presents a maximum CO Faradaic efficiency (FECO) of 98.8% and a large CO current density (j(CO)) of -62.9 mA cm(-2) at -0.75 and -1.05 V versus reversible hydrogen electrode, respectively. Furthermore, FECO could be maintained above 95% in a wide range of potential windows from -0.65 to -1.05 V. In situ experiments and density functional theory calculations demonstrate the Ni-BNC catalyst with B atoms coordinated to the central Ni atoms could significantly reduce the energy barrier for the conversion of *CO2 to *COOH, leading to excellent CO2RR performance.
引用
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页数:9
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