共 45 条
Hydrogen-intercalation PdZn bimetallene for urea electro-synthesis from nitrate and carbon dioxide
被引:0
|作者:
Wang, Ziqiang
[1
]
Wang, Yanan
[1
]
Xu, Shan
[1
]
Deng, Kai
[1
]
Yu, Hongjie
[1
]
Xu, You
[1
]
Wang, Hongjing
[1
]
Wang, Liang
[1
]
机构:
[1] Zhejiang Univ Technol, Coll Chem Engn, State Key Lab Breeding Base Green Chem Synth Techn, Hangzhou 310014, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CO2;
NANOSHEETS;
REDUCTION;
FORMATE;
D O I:
10.1039/d4ta04802d
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Electrochemical co-reduction of carbon dioxide and nitrate is a green technology to replace traditional energy-intensive methods for urea synthesis, and the development of high-performance catalysts is still a great challenge. Here, we propose the incorporation of nonmetallic hydrogen and oxophilic zinc into palladium metallene for the preparation of hydrogen-intercalation PdZn (H-PdZn) bimetallene, serving as an active electrocatalyst for co-reduction of carbon dioxide and nitrate to synthesize urea via the C-N coupling reaction. The H-PdZn bimetallene affords a high urea yield of 314.17 mu g h-1 mg-1 and a Faraday efficiency of 24.39%, better than those of PdZn bimetallene (144.25 mu g h-1 mg-1 and 16.03%). The strong electronic interaction between the Pd, Zn and H atoms can induce the downshift of the Pd d-band center of H-PdZn bimetallene, which can promote the formation of the key intermediates of *NH2 and *CO, and lower the energy barrier for their C-N coupling to synthesize urea. This work offers a hydrogenation strategy for the construction of advanced PdH-based metallenes towards electrochemical C-N coupling to synthesize urea.
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页码:305 / 311
页数:7
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