Precise regulation of phosphorus in nitrogen-coordinated porous carbon spheres for tunable CO2 electroreduction to syngas

被引:0
|
作者
Xu, Qi [1 ]
Wang, Wentao [2 ]
Zhang, Yangyang [1 ]
Liu, Huanhuan [1 ]
Wang, Xiaowen [1 ]
Zeng, Suyuan [3 ]
Zhang, Genqiang [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China
[2] Guizhou Educ Univ, Guizhou Prov Key Lab Computat Nanomat Sci, Guiyang 550018, Peoples R China
[3] Liaocheng Univ, Dept Chem & Chem Engn, Liaocheng 252059, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCHEMICAL REDUCTION; EFFICIENT; PERFORMANCE;
D O I
10.1016/j.isci.2024.109470
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
The production of high -demand syngas with tunable ratios by CO 2 electroreduction has attracted considerable research interest. However, it is challenging to balance the evolution performance of H 2 and CO with wide H 2 /CO ratios, while maintaining high efficiency. Herein, nitrogen -coordinated hierarchical porous carbon spheres with varying phosphorus content (P x NC-T) are assembled to regulate syngas production performance. The precise introduction of P modulates the local charge distribution of nitrogen -coordinated carbons, thereby accelerating the protonation process of *CO 2 -to-*COOH and promoting moderate H* adsorption. Specifically, syngas with wide H 2 /CO ratios (0.60-4.98) is obtained over a low potential range ( - 0.46 to - 0.86 V vs. RHE). As a representative, P 1.0 NC-900 presents a remarkable current density ( - 152 mA cm - 2 ) at - 1.0 V vs. RHE in flow cells and delivers a decent peak power density (1.93 mW cm - 2 ) in reversible Zn-CO 2 batteries. Our work provides valuable insights into the rational design of carbon -based catalysts for CO 2 reduction.
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页数:17
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