双金属片
双金属
选择性
催化作用
人工光合作用
金属
镝
Atom(片上系统)
材料科学
吸附
铜
物理化学
化学
无机化学
光催化
有机化学
冶金
计算机科学
嵌入式系统
作者
Han Wu,Yurui Xue,Feng He,Siao Chen,Yang Gao,Siyi Chen,Yuliang Li
出处
期刊:Small
[Wiley]
日期:2025-04-14
卷期号:21 (21): e2501867-e2501867
被引量:2
标识
DOI:10.1002/smll.202501867
摘要
Abstract The birth of metal atom catalysts marked a new historical stage in the field of catalysis, allowing scientists to better understand the science of catalysis at the atomic level. On the basis of anchoring independent metal atoms, bimetal dysprosium‐copper atoms are successfully anchored on graphdiyne (DyCu/GDY). Dy and Cu metal atoms are selectively anchored in triangular holes of GDY and stabilized by non‐integer charge transfer and the confined space effect between the metals and GDY. The dynamic charge‐transfer equilibrium caused by the inherent non‐integer charge transfer between GDY and metal atoms produces sustained high activity, inducing a redistribution of surface charge. This result shows that the non‐integer charge transfer strongly promotes the adsorption activation of CO 2 and the desorption of the reaction intermediates, realizing the unpredictable selectivity and activity of CO 2 conversion in the process of artificial photosynthesis, where the selectivity and yield of CO are 98% and 279 µmol g cat. −1 h −1 , respectively.
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