催化作用
甲酸
纳米棒
Atom(片上系统)
碳纤维
扫描透射电子显微镜
选择性
材料科学
透射电子显微镜
纳米技术
碳原子
化学
结晶学
有机化学
复合材料
烷基
嵌入式系统
复合数
计算机科学
作者
Yezhou Hu,Changsheng Chen,Tao Shen,Xuyun Guo,Chen Yang,Deli Wang,Ye Zhu
出处
期刊:Advanced Science
[Wiley]
日期:2022-11-11
卷期号:9 (36): e2205299-e2205299
被引量:33
标识
DOI:10.1002/advs.202205299
摘要
Nearly theoretical 100% atomic utilization (supposing each atom could serve as independent sites to play a role in catalyz) of single-atom catalysts (SACs) makes it highly promising for various applications. However, for most SACs, single-atom sites are trapped in a solid carbon matrix, which makes the inner parts hardly available for reaction. Herein, a hollow N-doped carbon confined single-atom Rh (Rh-SACs/HNCR) is developed via a coordination-template method. Both aberration-corrected scanning transmission electron microscopy and energy dispersive X-ray spectroscopy mapping confirm the uniform distribution of Rh single atoms. Owning to the unique hollow structure and effective carbon confinement, excessive conversion from pyridinic/pyrrolic N to graphic N is hindered. As a proof of concept, Rh-SACs/HNCR exhibits superior activity, stability, selectivity, and anti-poisoning capability in formic acid oxidation reaction compared with the counterpart Rh/C, Pd/C, and Pt/C catalysts. This work provides a powerful strategy for synthesizing hollow carbon confined single-atom catalysts apply in various energy-related systems.
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