氧合物
铑
催化作用
铈
纳米线
甲烷
选择性
材料科学
Atom(片上系统)
氧化铈
化学工程
化学
纳米技术
无机化学
有机化学
嵌入式系统
工程类
计算机科学
作者
Shuxing Bai,Fangfang Liu,Bolong Huang,Fan Li,Haiping Lin,Tong Wu,Mingzi Sun,Jianbo Wu,Qi Shao,Yong Xu,Xiaoqing Huang
标识
DOI:10.1038/s41467-020-14742-x
摘要
Abstract Direct methane conversion (DMC) to high value-added products is of significant importance for the effective utilization of CH 4 to combat the energy crisis. However, there are ongoing challenges in DMC associated with the selective C−H activation of CH 4 . The quest for high-efficiency catalysts for this process is limited by the current drawbacks including poor activity and low selectivity. Here we show a cerium dioxide (CeO 2 ) nanowires supported rhodium (Rh) single-atom (SAs Rh-CeO 2 NWs) that can serve as a high-efficiency catalyst for DMC to oxygenates (i.e., CH 3 OH and CH 3 OOH) under mild conditions. Compared to Rh/CeO 2 nanowires (Rh clusters) prepared by a conventional wet-impregnation method, CeO 2 nanowires supported Rh single-atom exhibits 6.5 times higher of the oxygenates yield (1231.7 vs. 189.4 mmol g Rh −1 h −1 ), which largely outperforms that of the reported catalysts in the same class. This work demonstrates a highly efficient DMC process and promotes the research on Rh single-atom catalysts in heterogeneous catalysis.
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