尖晶石
氧气
钙钛矿(结构)
化学
格子(音乐)
材料科学
原子单位
矿物学
结晶学
物理
冶金
声学
量子力学
有机化学
作者
Xiyang Wang,Ziye Pan,Xuefeng Chu,Keke Huang,Yingge Cong,Rui Cao,Ritimukta Sarangi,Liping Li,Guangshe Li,Shouhua Feng
标识
DOI:10.1002/anie.201905543
摘要
Abstract Surface lattice oxygen in transition‐metal oxides plays a vital role in catalytic processes. Mastering activation of surface lattice oxygen and identifying the activation mechanism are crucial for the development and design of advanced catalysts. A strategy is now developed to create a spinel Co 3 O 4 /perovskite La 0.3 Sr 0.7 CoO 3 interface by in situ reconstruction of the surface Sr enrichment region in perovskite LSC to activate surface lattice oxygen. XAS and XPS confirm that the regulated chemical interface optimizes the hybridized orbital between Co 3d and O 2p and triggers more electrons in oxygen site of LSC transferred into lattice of Co 3 O 4 , leading to more inactive O 2− transformed into active O 2− x . Furthermore, the activated Co 3 O 4 /LSC exhibits the best catalytic activities for CO oxidation, oxygen evolution, and oxygen reduction. This work would provide a fundamental understanding to explain the activation mechanism of surface oxygen sites.
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