Efficient Electroreduction of Nitrate to Ammonia with CuPd Nanoalloy Catalysts

被引:13
|
作者
Song, Zhimin [1 ,2 ]
Qin, Lang [2 ]
Liu, Yan [2 ]
Zhong, Yongzhi [2 ]
Guo, Qing [1 ]
Geng, Zhigang [2 ]
Zeng, Jie [2 ]
机构
[1] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Guangdong, Peoples R China
[2] Chinese Acad Sci, Univ Sci & Technol China, Key Lab Strongly Coupled Quantum Matter Phys, Hefei Natl Res Ctr Phys Sci Microscale,Energy Cata, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysis; ammonia synthesis; nitrate electroreduction; CuPd nanoalloys; renewable resources; REDUCTION;
D O I
10.1002/cssc.202300202
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electroreduction of nitrate (NO3-) to valuable ammonia (NH3) is a green and appealing alternative to the Haber-Bosch process. Nevertheless, this process suffers from low performance for NH3 due to the sluggish multi-electron/proton-involved steps. In this work, a CuPd nanoalloy catalyst was developed toward NO3- electroreduction at ambient conditions. By modulating the atomic ratio of Cu to Pd, the hydrogenation steps of NH3 synthesis during NO3- electroreduction can be effectively controlled. At -0.7 V versus reversible hydrogen electrode (vs. RHE), the optimized CuPd electrocatalysts achieved a Faradaic efficiency for NH3 of 95.5 %, which was 1.3 and 1.8 times higher than that of Cu and Pd, respectively. Notably, at -0.9 V vs. RHE, the CuPd electrocatalysts showed a high yield rate of 36.2 mg h(-1) cm(-2) for NH3 with a corresponding partial current density of -430.6 mA cm(-2). Mechanism investigation revealed the enhanced performance originated from the synergistic catalytic cooperation between Cu and Pd sites. The H-atoms adsorbed on the Pd sites prefer to transfer to adjacent nitrogen intermediates adsorbed on the Cu sites, thereby promoting the hydrogenation of intermediates and the formation of NH3.
引用
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页数:6
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