水煤气变换反应
碳化钒
钒
化学计量学
催化作用
密度泛函理论
碳化物
离解(化学)
吸附
材料科学
结合能
选择性
过渡金属
化学工程
物理化学
无机化学
化学
计算化学
冶金
有机化学
核物理学
工程类
物理
作者
Arturo Pajares,Hèctor Prats,Alexandre Romero,Francesc Viñes,Pilar Ramı́rez de la Piscina,R. Sayós,Narcı́s Homs,Francesc Illas
标识
DOI:10.1016/j.apcatb.2020.118719
摘要
Experimental and theoretical evidences show that carbon vacancies determine the catalytic behavior of vanadium carbides in the CO2 conversion to CO via the Reverse Water Gas Shift (RWGS) reaction. Two VCx samples, one mostly containing stoichiometric VC and the other being C deficient, mainly V8C7, were synthesized, characterized, and studied. The samples show different CO2 adsorption heats, which correlate with those calculated using Density Functional Theory (DFT) on suitable models. The sample containing more V8C7 shows a higher CO2 conversion and CO selectivity and a lower apparent activation energy, being a stable catalyst over long-time tests. DFT calculations confirm that C vacancies in V8C7 are responsible for the observed catalytic behavior, allowing reactants to adsorb more strongly and lowering the energy barrier for both H2 and CO2 dissociation steps. The present work highlights the importance of such native point defects in the transition metal carbides surface chemistry and catalytic properties.
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