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High-efficiency direct methane conversion to oxygenates on a cerium dioxide nanowires supported rhodium single-atom catalyst

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 fo...

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Detalles Bibliográficos
Autores principales: Bai, Shuxing, Liu, Fangfang, Huang, Bolong, Li, Fan, Lin, Haiping, Wu, Tong, Sun, Mingzi, Wu, Jianbo, Shao, Qi, Xu, Yong, Huang, Xiaoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031227/
https://www.ncbi.nlm.nih.gov/pubmed/32075982
http://dx.doi.org/10.1038/s41467-020-14742-x
Descripción
Sumario: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.