催化作用
选择性
化学
密度泛函理论
甲烷氧化偶联
异构化
甲烷
碳氢化合物
计算化学
多相催化
组合化学
光化学
有机化学
作者
Zhiqiang Wang,Dong Wang,Xue‐Qing Gong
标识
DOI:10.1021/acscatal.9b03066
摘要
Oxidative coupling of methane (OCM) holds the promise to achieve high-value-added products directly from methane, and the strategies to improve the catalytic performance of this process are highly desired. In this work, we performed extensive density functional theory (DFT) calculations to systematically study the activity and selectivity of the OCM reactions on several types of the La2O3 and CeO2 catalysts. We theoretically evidenced that the La2O3 catalyst has high hydrocarbon selectivity but low activity, while the CeO2 shows an opposite performance. These results can be largely rationalized by the calculated reaction energetics in generating the key CH3· intermediates and further protecting them from excessive oxidation on the surface. We then proposed two strategies to improve the OCM activity while maintaining the selectivity of the La2O3 catalyst. Geometrically, by constructing the stepped La2O3(210) surface exposing lattice oxygens with low coordination numbers, both the heterolytic cleavage of the C–H bond in methane and the occurrence of the key CH3· intermediates could be promoted. Electronically, codoping of Sr and Ce into La2O3 could favor the direct formation of CH3· and further avoid its deactivation on the surface, leading to the significantly improved OCM performance. By conducting further analyses on the thermostability of the catalysts and calculating catalytic energetics of the complete reaction cycle, we excluded the practical application of the high-Miller-index La2O3 surfaces, but we theoretically predicted the Sr/Ce–La2O3 catalyst with a proper doping concentration to be highly efficient for catalyzing the OCM reactions.
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