Ammonia electrosynthesis on carbon-supported metal single-atom catalysts

被引:0
|
作者
Li, Mu-Lin [1 ]
Xie, Yi-Meng [1 ]
Song, Jingting [1 ]
Yang, Ji [1 ]
Dong, Jin-Chao [1 ]
Li, Jian-Feng [1 ,2 ]
机构
[1] Xiamen Univ, Coll Energy, Coll Chem & Chem Engn, Coll Phys Sci & Technol,State Key Lab Phys Chem So, Xiamen 361005, Fujian, Peoples R China
[2] Innovat Lab Sci & Technol Energy Mat Fujian Prov I, Xiamen 361005, Fujian, Peoples R China
来源
基金
中国博士后科学基金;
关键词
Ammonia synthesis; Nitrogen -transforming reaction; Electrochemical reduction; Single -atom catalyst; Dinitrogen; Nitrogen oxides; NITRATE REDUCTION; ELECTROCATALYTIC REDUCTION; ELECTROCHEMICAL NITRATE; NITROGEN REDUCTION; IDENTIFICATION; SITE;
D O I
10.1016/S1872-2067(24)60032-X
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ammonia, a feedstock platform for fertilizer and pharmaceutical production, is regarded as a zero-carbon energy carrier. The electrochemical synthesis of ammonia, powered by clean and renewable electricity, has garnered increased attention as an alternative to the Haber-Bosch process. Very recently, single-atom catalysts (SACs) have become highly effective electrocatalysts for such electrochemical transformation, where the isolated metal sites ensure the high atomic utilization efficiency as well as the prevention of nitrogen-nitrogen coupling. In this review, we focus on the recent progress of single-atom catalysts in electrochemical ammonia synthesis and briefly introduce nitrogen cycles in both natural and artificial ecosystems, followed by a discussion of catalyst design by theoretical and experimental methods. Synthesis routes from different nitrogen sources, including dinitrogen (N2) and nitrogen oxides (NOx), are also highlighted. Besides, the catalysis dynamics as an indispensable section is presented and discussed in-depth. Finally, we tackle challenges and offer perspectives, aspiring to provide insightful guidance for researchers in this community striving for advanced ammonia electrosynthesis. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 67
页数:26
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