氮气
磷
催化作用
化学
还原(数学)
氮原子
Atom(片上系统)
电催化剂
无机化学
材料科学
计算机科学
电极
物理化学
有机化学
电化学
数学
群(周期表)
几何学
嵌入式系统
作者
Zhiyong Zhu,Shuai Lv,Xinyi Sun,Cong Liu,X. R. Qi,Xiao Liu,Li Wang,Jinglai Zhang
标识
DOI:10.1016/j.apcata.2024.119824
摘要
Electrochemical carbon dioxide reduction (CO2RR) is a promising approach to accomplish the CO2 net emission. Ni-based single-atom catalysts (Ni-SACs) with the Ni-N-C structure have been the hotspot in this field. However, its catalytic activity is still unsatisfied. Regulation of the coordination environment of the active site via heteroatom doping is an efficient strategy to improve its catalytic characteristics and activity. Herein, the heteroatom phosphorus is introduced into the N-doped carbon supporter to form Ni-SA/CN-P catalyst achieving the CO Faraday efficiency of 91.8% at a potential of -1.1 V along with the CO current density 91.2 mA cm-2 in the flow cell, which is superior to the sample Ni-SA/CN without P dopant. It is attributed that the more defects are built in the Ni-SA/CN-P catalyst due to the different atomic radiuses of P and N atoms. Moreover, the gap between d-band center and Femi energy level is narrowed due to the doped P atoms, which reduces the rate-limiting barrier height leading to the promoted catalytic performance. The cooperation of various items finally results in the overall performance. This work provides a simple method for establishing single-atom catalysts with P doping to improve catalytic performance for CO2RR.
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