催化作用
水煤气变换反应
化学
甲烷化
氧化还原
选择性
格式化
吸附
钾
离解(化学)
无机化学
联想代换
物理化学
有机化学
作者
Jingjing Xu,Xingxing Gong,Rongrong Hu,Zhong‐Wen Liu,Zhao‐Tie Liu
标识
DOI:10.1016/j.mcat.2021.111954
摘要
• 100% CO selectivity was achieved by RWGS over the Cu/Mo 2 C-1 K catalyst at low temperatures. • The structural and electronic effects induced by K species facilitate the adsorption and activation of CO 2 . • The redox and association mechanism coexists in the RWGS reaction on the K-promoted Cu/Mo 2 C catalysts. The K-promoted Cu/β-Mo 2 C catalysts with different K loadings were prepared for the reverse water gas shift (RWGS) reaction. The results showed that the incorporation of potassium into the Cu/β-Mo 2 C catalyst significantly increased CO 2 conversion and CO selectivity at an optimal K loading. The remarkable catalytic performance of the 1K-Cu/Mo 2 C catalyst was due to the presence of highly dispersed Cu nanoparticles and the improved CO 2 activation and dissociation caused by the structural and electronic effect of potassium. The presence of K also suppresses H 2 adsorption and inhibits the methanation of CO 2 . The gas switching experiments and in-situ DRIFTS analyses suggest that both the redox and associative mechanism coexists in the RWGS reaction and that the formate species act as the intermediates in converting CO 2 to CO for the K-promoted Cu/β-Mo 2 C catalysts.
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