Exfoliated 2D Layered and Nonlayered Metal Phosphorous Trichalcogenides Nanosheets as Promising Electrocatalysts for CO2 Reduction

被引:6
作者
Wang, Honglei [1 ,2 ]
Jiao, Yunfei [3 ]
Wu, Bing [4 ]
Wang, Dong [1 ,2 ]
Hu, Yueqi [1 ,2 ]
Liang, Fei [5 ]
Shen, Chen [5 ]
Knauer, Andrea [6 ]
Ren, Dan [3 ,7 ]
Wang, Hongguang [8 ]
van Aken, Peter A. [8 ]
Zhang, Hongbin [5 ]
Sofer, Zdenek [4 ]
Graetzel, Michael [3 ]
Schaaf, Peter [1 ,2 ]
机构
[1] TU Ilmenau, Inst Mat Sci & Engn, Chair Mat Elect Engn & Elect, Gustav Kirchhoff Str 5, D-98693 Ilmenau, Germany
[2] TU Ilmenau, Inst Micro & Nanotechnol MacroNano, Gustav Kirchhoff Str 5, D-98693 Ilmenau, Germany
[3] Ecole Polytech Fed Lausanne, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[4] Univ Chem & Technol Prague, Dept Inorgan Chem, Techn 5, Prague 16628 6, Czech Republic
[5] Tech Univ Darmstadt, Inst Mat Wissensch, D-64289 Darmstadt, Germany
[6] TU Ilmenau, Inst Micro & Nanotechnol MacroNano, Gustav Kirchhoff Str 7, D-98693 Ilmenau, Germany
[7] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Xian 710049, Peoples R China
[8] Max Planck Inst Solid State Res, Heisenbergstr 1, D-70569 Stuttgart, Germany
关键词
2D Materials; CO2; ECR; Exfoliation; MPCh(3) Nanosheets; Nonlayered; CATALYSTS; INSIGHTS; NITROGEN;
D O I
10.1002/anie.202217253
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two-dimensional (2D) materials catalysts provide an atomic-scale view on a fascinating arena for understanding the mechanism of electrocatalytic carbon dioxide reduction (CO2 ECR). Here, we successfully exfoliated both layered and nonlayered ultra-thin metal phosphorous trichalcogenides (MPCh(3)) nanosheets via wet grinding exfoliation (WGE), and systematically investigated the mechanism of MPCh(3) as catalysts for CO2 ECR. Unlike the layered CoPS3 and NiPS3 nanosheets, the active Sn atoms tend to be exposed on the surfaces of nonlayered SnPS3 nanosheets. Correspondingly, the nonlayered SnPS3 nanosheets exhibit clearly improved catalytic activity, showing formic acid selectivity up to 31.6 % with -7.51 mA cm(-2) at -0.65 V vs. RHE. The enhanced catalytic performance can be attributed to the formation of HCOO* via the first proton-electron pair addition on the SnPS3 surface. These results provide a new avenue to understand the novel CO2 ECR mechanism of Sn-based and MPCh(3)-based catalysts.
引用
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页数:8
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