Phosphorus-Doped Graphene Aerogel as Self-Supported Electrocatalyst for CO2-to-Ethanol Conversion

被引:51
|
作者
Yang, Fangqi [1 ,2 ,3 ]
Liang, Caihong [4 ]
Yu, Haoming [2 ]
Zeng, Zheling [2 ]
Lam, Yeng Ming [4 ,5 ]
Deng, Shuguang [6 ]
Wang, Jun [2 ]
机构
[1] Nanchang Univ, Sch Resource & Environm, 999 Xuefu Ave, Nanchang 330031, Jiangxi, Peoples R China
[2] Nanchang Univ, Chem & Chem Engn Sch, 999 Xuefu Ave, Nanchang 330031, Jiangxi, Peoples R China
[3] Natl Univ Singapore, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore
[4] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[5] Nanyang Technol Univ, Facil Anal Characterizat Testing & Simulat FACTS, Singapore 639798, Singapore
[6] Arizona State Univ, Sch Engn Matter Transport & Energy, 551 E Tyler Mall, Tempe, AZ 85287 USA
基金
中国国家自然科学基金;
关键词
CO2; reduction; electrocatalysis; ethanol; graphene aerogel; phosphorus; SELECTIVE ELECTROCHEMICAL REDUCTION; POROUS CARBON; CO2; REDUCTION; CATALYSTS; COPPER; ETHYLENE;
D O I
10.1002/advs.202202006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical reduction of carbon dioxide (CO2) to ethanol is a promising strategy for global warming mitigation and resource utilization. However, due to the intricacy of CC coupling and multiple proton-electron transfers, CO2-to-ethanol conversion remains a great challenge with low activity and selectivity. Herein, it is reported a P-doped graphene aerogel as a self-supporting electrocatalyst for CO2 reduction to ethanol. High ethanol Faradaic efficiency (FE) of 48.7% and long stability of 70 h are achieved at -0.8 V-RHE. Meanwhile, an outstanding ethanol yield of 14.62 mu mol h(-1) cm(-2) can be obtained, outperforming most reported electrocatalysts. In situ Raman spectra indicate the important role of adsorbed *CO intermediates in CO2-to-ethanol conversion. Furthermore, the possible active sites and optimal pathway for ethanol formation are revealed by density functional theory calculations. The graphene zigzag edges with P doping enhance the adsorption of *CO intermediate and increase the coverage of *CO on the catalyst surface, which facilitates the *CO dimerization and boosts the EtOH formation. In addition, the hierarchical pore structure of P-doped graphene aerogels exposes abundant active sites and facilitates mass/charge transfer. This work provides inventive insight into designing metal-free catalysts for liquid products from CO2 electroreduction.
引用
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页数:8
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