介孔材料
材料科学
催化作用
结晶
选择性
金属
化学工程
聚乙烯吡咯烷酮
氧化物
多孔性
多相催化
催化氧化
无机化学
多孔介质
介孔有机硅
金属有机骨架
部分氧化
纳米技术
氧气
氧化还原
纳米晶
复合氧化物
格子(音乐)
作者
Yangbo Dong,Tao Wang,Wei Li,Yan Song,Shuzhen Dou,Yan Yang,Ling Zhang,Zhen‐An Qiao
摘要
ABSTRACT Mesoporous single‐crystal metal oxides are highly attractive for heterogeneous catalysis because they combine high surface accessibility with long‐range lattice coherence; however, their synthesis remains fundamentally challenging due to the thermodynamic incompatibility between crystallization and pore formation. Here we report a template‐free, energy‐driven facet‐oriented crystallization strategy that enables the formation of mesoporous single‐crystal metal oxides with tunable pore architectures and exposed high‐energy facets. Polyvinylpyrrolidone functions simultaneously as a pore maintainer and surface‐energy regulator, preserving mesoporosity while selectively stabilizing high‐energy facets to direct single‐crystal growth. The method is applicable to multiple oxides, including Co 3 O 4 , MgO, NiO, and mixed‐metal systems. As a representative example, mesoporous single‐crystal Co 3 O 4 with preferentially exposed (111) facets exhibits outstanding performance in the selective oxidation of aromatic alkanes, achieving up to 99% conversion and selectivity under mild conditions. Experimental and theoretical analyses suggest that the synergy between mesoporosity and active‐facet exposure enhances reactant adsorption, oxygen activation, and reaction kinetics, providing a general design principle for crystallographically defined porous catalysts.
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