催化作用
Atom(片上系统)
金属
化学
氧原子
组合化学
等离子体
氧气
纳米技术
氧还原反应
化学工程
材料科学
物理化学
计算机科学
物理
有机化学
分子
工程类
嵌入式系统
量子力学
电化学
电极
作者
Peng Rao,Daoxiong Wu,Junming Luo,Jing Li,Peilin Deng,Yijun Shen,Xinlong Tian
标识
DOI:10.1016/j.xcrp.2022.100880
摘要
Single-atom catalysts (SACs) have attracted tremendous attention owing to their unique intrinsic properties, while the facile synthesis, especially the direct transformation of metal salts into single-metal atoms, is still a huge challenge. Here we report a practical approach to access the large-scale synthesis of SACs, in which the metal salts are excited and stripped as mobile single-metal atoms flow under the "plasma bombing" treatment. Simultaneously, they are trapped and anchored by the defective and nitrogenous sites of the supports. More importantly, the synthesis approach is quite general, and it can be extended to the fabrication of various SACs. As an illustration, the prepared SAC-Fe/NC delivers a remarkable oxygen reduction reaction (ORR) performance. In combination with the theoretical analysis, an adsorbent-induced spin-crossover ORR mechanism is proposed, and the Fe species coordination with four pyridinic-type N atoms is demonstrated as the main contributor to the high performance of the prepared SAC-Fe/NC.
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