Bi1-CuCo2O4 Hollow Carbon Nanofibers Boosts NH3 Production from Electrocatalytic Nitrate Reduction

被引:31
作者
Lin, Hexing [1 ,2 ,3 ]
Wei, Jinshan [1 ,2 ,3 ]
Guo, Ying [1 ,2 ,3 ]
Li, Yi [1 ,2 ,3 ]
Lu, Xihui [1 ,2 ,3 ]
Zhou, Chucheng [1 ,2 ,3 ]
Liu, Shaoqing [1 ,2 ,3 ]
Li, Ya-yun [1 ,2 ,3 ]
机构
[1] Shenzhen Univ, Coll Mat Sci & Engn, Guangdong Prov Key Lab New Energy Mat Serv Safety, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen Key Lab Special Funct Mat, Shenzhen 518060, Peoples R China
[3] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen Engn Lab Adv Technol Ceram, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
bismuth doping; CuCo2O4; electrocatalysis; nitrate reduction; single atom catalyst; Zn-NO3-; battery; AMMONIA; ELECTROREDUCTION; NANOPARTICLES; COMPOSITES; EVOLUTION; ENERGY;
D O I
10.1002/adfm.202409696
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ammonia, as a high-energy-density carrier for hydrogen storage, is in great demand worldwide. Electrocatalytic nitrate reduction reaction (NO3RR) provides a green NH3 production process. However, the complex reaction pathways for NO3RR to NH3 and the difficulty in controlling intermediate products limit the reduction process. Herein, by incorporating atomic-level bismuth (Bi) into CuCo2O4 hollow carbon nanofibers, the catalytic activity of the electrocatalyst for NO3RR is enhanced. The maximum Faradaic efficiency of Bi-1-CuCo2O4 is 95.53%, with an NH3 yield of 448.74 mu mol h(-1) cm(-2) at -0.8 V versus RHE. Density Functional Theory calculations show that the presence of Bi lowers the reaction barrier for the hydrogenation step from *NO2 to *NO2H, while promoting mass transfer on the release of *NH3 and the reactivation of surface-active sites. Differential charge density calculations also show that after Bi doping, the charge supplied by the catalyst to NO3- increases from 0.62 to 0.72 e(-), thus reasoned for enhanced NO3RR activity. The established nitrate-Zn battery shows an energy density of 2.81 mW cm(-2), thus implying the potential application.
引用
收藏
页数:10
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