钌
催化作用
选择性
费托法
一氧化碳
光化学
钴
纳米片
吸附
碳纤维
化学
材料科学
无机化学
化学工程
有机化学
纳米技术
复合数
工程类
复合材料
作者
Jiaqi Zhao,Jinjia Liu,Zhenhua Li,Kaiwen Wang,Run Shi,Pu Wang,Qing Wang,Geoffrey I. N. Waterhouse,Xiaodong Wen,Tierui Zhang
标识
DOI:10.1038/s41467-023-37631-5
摘要
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 C5+ liquid fuels. Herein, we report a ruthenium-cobalt single atom alloy (Ru1Co-SAA) catalyst derived from a layered-double-hydroxide nanosheet precursor. Under UV-Vis irradiation (1.80 W cm-2), Ru1Co-SAA heats to 200 °C and photo-hydrogenates CO to C5+ 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 CHx* intermediates, resulting in a CO photo-hydrogenation turnover frequency of 0.114 s-1 with 75.8% C5+ 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 C5+ liquid fuels. The findings open new vistas towards C5+ liquid fuels under sunlight at mild pressures.
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