催化作用
纳米技术
固氮酶
星团(航天器)
Atom(片上系统)
氧化还原
纳米颗粒
材料科学
产量(工程)
氨生产
化学
组合化学
氮气
固氮
计算机科学
无机化学
有机化学
冶金
嵌入式系统
程序设计语言
作者
Haihong Meng,Yinghe Zhao,Fengyu Li,Zhongfang Chen
出处
期刊:Journal of materials informatics
[OAE Publishing Inc.]
日期:2025-01-13
卷期号:5 (1)
被引量:11
摘要
The traditional Haber-Bosch process for ammonia synthesis is both energy-intensive and capital-demanding. Electrocatalytic nitrogen reduction reaction (NRR) has emerged as a promising, sustainable alternative, with recent advantages highlighting its potential. Single-atom catalysts (SACs) and single-cluster catalysts (SCCs) are promising catalysts for NRR due to their atomically dispersed active sites, maximized atom utilization, and distinctive coordination and electronic structures, all of which facilitate mechanism insights at the atomic level. Benefiting from efficient atom utilization, for example, the ammonia yield rate on Au1/C3N4 is roughly 22.5 times as high as that of supported Au nanoparticles, fully demonstrating the significant advantages of SACs over nanoparticles. In this review, we focus on the theoretical progress in SACs and SCCs for electrocatalyzing NRR, including nitrogenase-like bio-inspired catalysts and other metal-based catalysts. We further examine key adsorption energy and electronic descriptors that enhance our understanding of catalytic performance. Finally, we discuss the remaining challenges and future directions for advancing SACs and SCCs in electrocatalytic NRR applications.
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