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Room-Temperature CO(2) Hydrogenation to Methanol over Air-Stable hcp-PdMo Intermetallic Catalyst

[Image: see text] CO(2) hydrogenation to methanol is one of the most promising routes to CO(2) utilization. However, difficulty in CO(2) activation at low temperature, catalyst stability, catalyst preparation, and product separation are obstacles to the realization of a practical hydrogenation proce...

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Detalles Bibliográficos
Autores principales: Sugiyama, Hironobu, Miyazaki, Masayoshi, Sasase, Masato, Kitano, Masaaki, Hosono, Hideo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161205/
https://www.ncbi.nlm.nih.gov/pubmed/36995761
http://dx.doi.org/10.1021/jacs.2c13801
Descripción
Sumario:[Image: see text] CO(2) hydrogenation to methanol is one of the most promising routes to CO(2) utilization. However, difficulty in CO(2) activation at low temperature, catalyst stability, catalyst preparation, and product separation are obstacles to the realization of a practical hydrogenation process under mild conditions. Here, we report a PdMo intermetallic catalyst for low-temperature CO(2) hydrogenation. This catalyst can be synthesized by the facile ammonolysis of an oxide precursor and exhibits excellent stability in air and the reaction atmosphere and significantly enhances the catalytic activity for CO(2) hydrogenation to methanol and CO compared with a Pd catalyst. A turnover frequency of 0.15 h(–1) was achieved for methanol synthesis at 0.9 MPa and 25 °C, which is comparable to or higher than that of the state-of-the-art heterogeneous catalysts under higher-pressure conditions (4–5 MPa).