氯苯
氧化还原
催化作用
氧气
氧化物
化学
退火(玻璃)
无机化学
光化学
再分配(选举)
材料科学
化学工程
萤石
曲面重建
原位
光谱学
多相催化
电子转移
析氧
氧还原
作者
Yong Yin,Yide Jiang,Zichen Xu,Min Liu,Emiliano Cortés,Yifei Sun
摘要
ABSTRACT Low‐temperature redox catalysis over mixed oxides is typically optimized by tuning bulk composition, yet the decisive chemistry occurs at the surface and subsurface interface. Here, we show that this interface can be deliberately reconstructed to enhance Mn–Ce oxide catalysis. Sequential vacuum annealing followed by reduced‐pressure O 2 treatment induces near‐surface Mn enrichment in an as‐prepared Mn–Ce oxide while largely preserving the fluorite CeO 2 framework. This reconstruction increases the near‐surface abundance of Mn‐containing species, modifies the Mn–Ce–O interfacial electronic and redox environment, and facilitates oxygen activation and redox cycling. Under coupled conditions, R‐MnCe achieved 95.5% NO x conversion at 100°C and complete chlorobenzene conversion at 200°C. In situ spectroscopy and DFT calculations reveal that interfacial electron redistribution lowers the oxygen activation barrier and sustains activated oxygen species that connect NH 3 ‐SCR and chlorobenzene oxidation through a shared oxygen‐mediated pathway. These results highlight near‐surface reconstruction as a promising postsynthetic strategy for improving noble‐metal‐free mixed‐oxide catalysts.
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