氢甲酰化
形态学(生物学)
磷化氢
催化作用
多相催化
化学
化学工程
材料科学
铑
有机化学
工程类
生物
遗传学
作者
Boyang Liu,Yifan Sun,Muhan Li,Z.P. Fan,Xiao Chen,Xiaocheng Lan,Qin Zhong,Tiefeng Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-10-12
卷期号:14 (21): 15956-15964
被引量:1
标识
DOI:10.1021/acscatal.4c04921
摘要
Heterogeneous hydroformylation enhances the separation process, avoiding the use of phosphine ligands and reducing the loss of precious metals. However, enhancing catalytic activity and elucidating reaction mechanisms remain challenging. In this work, we develop single-atom catalysts (SACs) of Rh1/CeO2 with different morphologies and study their structure–performance relationships at the molecular level. The turnover frequency (TOF) of the Rh1/CeO2-Rod catalysts reaches 9386 h–1 with a relatively high Rh loading (1.08 wt %), outperforming most reported SACs. The presence of oxygen atoms with dangling bonds and the local stress surrounding the embedded Rh atoms are identified as the key factors behind the morphology effects. Our work deepens the molecular understanding of the morphology effects underlying the enhancement of hydroformylation activity and paves the way for the future design of highly active heterogeneous hydroformylation SACs with both high TOF and optimal Rh loading.
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