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Ruthenium-cobalt single atom alloy for CO photo-hydrogenation to liquid fuels at ambient pressures

Photothermal Fischer-Tropsch synthesis represents a promising strategy for converting carbon monoxide into value-added chemicals. High pressures (2-5 MPa) are typically required for efficient C-C coupling reactions and the production of C(5+) liquid fuels. Herein, we report a ruthenium-cobalt single...

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Detalles Bibliográficos
Autores principales: Zhao, Jiaqi, Liu, Jinjia, Li, Zhenhua, Wang, Kaiwen, Shi, Run, Wang, Pu, Wang, Qing, Waterhouse, Geoffrey I. N., Wen, Xiaodong, Zhang, Tierui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076290/
https://www.ncbi.nlm.nih.gov/pubmed/37019942
http://dx.doi.org/10.1038/s41467-023-37631-5
Descripción
Sumario:Photothermal Fischer-Tropsch synthesis represents a promising strategy for converting carbon monoxide into value-added chemicals. High pressures (2-5 MPa) are typically required for efficient C-C coupling reactions and the production of C(5+) liquid fuels. Herein, we report a ruthenium-cobalt single atom alloy (Ru(1)Co-SAA) catalyst derived from a layered-double-hydroxide nanosheet precursor. Under UV-Vis irradiation (1.80 W cm(−2)), Ru(1)Co-SAA heats to 200 °C and photo-hydrogenates CO to C(5+) liquid fuels at ambient pressures (0.1-0.5 MPa). Single atom Ru sites dramatically enhance the dissociative adsorption of CO, whilst promoting C-C coupling reactions and suppressing over-hydrogenation of CH(x)* intermediates, resulting in a CO photo-hydrogenation turnover frequency of 0.114 s(−1) with 75.8% C(5+) selectivity. Owing to the local Ru-Co coordination, highly unsaturated intermediates are generated during C-C coupling reactions, thereby improving the probability of carbon chain growth into C(5+) liquid fuels. The findings open new vistas towards C(5+) liquid fuels under sunlight at mild pressures.