催化作用
铜
热解
化学
选择性
金属
无机化学
二氧化碳
水煤气变换反应
有机化学
作者
Chonghao Chen,Guiyao Song,Zihao Wang,Jianhua Song,Qisheng Jiang,Yangzhou Zhai,Dianhua Liu
标识
DOI:10.1016/j.apcatb.2023.123330
摘要
One-step hydrogenation of carbon dioxide (CO2) to aromatics is a promising strategy for relieving the stress of fossil fuels. Here, a copper and sodium co-modified Fe-based catalyst (3-NFC-5) was synthesized through the pyrolysis of Cu-doped MIL-101(Fe) and Na impregnation. After combining with HZSM-5, 42.11% CO2 conversion and 50.68% total aromatics selectivity was achieved. Through multiple characterization and DFT calculations, the synergistic promotion of Na and Cu on light olefins intermediate production was revealed. Na was crucial for COOH* formation as the intermediate for reverse water gas shift reaction (RWGS), whose concentration could be further enhanced after Cu modification. Controlled C-C coupling towards C2-C4 hydrocarbons was realized by the enhanced CO non-dissociative activation and the increased content of χ-Fe5C2 after Cu doping, which was responsible for the inhibited surface CHx* concentration and selective production of light olefins, respectively.
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