化学
脱氢
再分配(选举)
催化作用
激进的
氧气
氧化物
烷烃
密度泛函理论
光化学
化学物理
电子
计算化学
无机化学
有机化学
政治学
物理
法学
政治
量子力学
作者
Yuanyuan Zhu,Peter V. Sushko,Daniel Melzer,Eric Jensen,Libor Kovařík,Colin Ophus,Maricruz Sanchez‐Sanchez,Johannes A. Lercher,Nigel D. Browning
摘要
A novel pathway of increasing the surface density of catalytically active oxygen radical sites on a MoVTeNb oxide (M1 phase) catalyst during alkane oxidative dehydrogenation is reported. The novel sites form when a fraction of Te 4+ is reduced and emitted from the M1 crystals under catalytic operating conditions, without compromising structural integrity of the catalyst framework. Density functional theory calculations show this Te reduction induces multiple inter-related electron transfers, and the associated cooperative effects lead to the formation of O – radicals. The in situ observations identify complex dynamic changes in the catalyst on an atomistic level, highlighting a new way to tailor structure and dynamics for highly active catalysts.
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