沸石
催化作用
选择性
化学
密度泛函理论
水煤气变换反应
分子筛
分子
光化学
无机化学
计算化学
有机化学
作者
Jeong-Cheol Seo,Gyungah Park,Malik Waqar Arshad,Chundong Zhang,Sungtak Kim,Seok Ki Kim
标识
DOI:10.1016/j.jcou.2022.102291
摘要
The introduction of the frustrated Lewis pair (FLP) concept in heterogeneous catalysis, particularly zeolites, is effective in activating stable molecules, such as CO2. However, regulating the FLP density structure to control the activity and selectivity remains challenging. This study examined the effects of the FLP density and zeolite structure on the reverse water-gas shift reaction using Pt/zeolite catalysts. The reaction results obtained using catalysts with various zeolites showed that the presence of FLP in the zeolite promoted CO2 conversion and CO selectivity, but a high FLP density was not necessarily beneficial. A high density of FLP could delay the intracrystalline diffusion of intermediates and could lower the CO selectivity. Operando infrared spectroscopy and density functional theory calculations suggested that FLP could effectively stabilize the intermediate responsible for CO production through selective hydrogenation of the oxygen atom of CO2 at the initial stage of the reaction.
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