催化作用
煅烧
烧结
氧化物
限制
材料科学
阳离子聚合
纳米颗粒
化学工程
过渡金属
复合氧化物
混合氧化物
纳米技术
化学
有机化学
高分子化学
冶金
工程类
机械工程
作者
Shuzhen Li,Xuan Luo,Yueshuai Wang,Chaowei Wang,Guizhen Zhang,Huixin Xiang,Yong Yan,Xiaoxing Ke,Lu Yue,Chuanhao Yao,Hongyi Li,Liang Zhang,Ge Chen
标识
DOI:10.1002/ange.202504551
摘要
Abstract Supported metal nanoparticle catalysts often suffer from sintering‐induced size‐dependent deactivation, limiting their high‐temperature applications. Although high‐temperature redispersion offers a potential solution, this strategy remains restricted to reducible support materials, severely limiting the selection of catalyst supports with versatile compositions and tunable functionalities. Here, we engineer cationic vacancies at Al 2 O 3 ‐La 2 O 3 interface via strong oxide‐support interaction (SOSI)—driven interfacial reconstruction during calcination. The vacancy‐mediated confinement effect dynamically intercepts migrating Pt species, enabling the construction of Al 2 O 3 ‐Pt 1 ‐La 2 O 3 structure with precisely defined coordination environments. The resulting catalyst achieves complete CO conversion at 145 °C and maintains stability with minimal decline after a 6‐h treatment at 1100 °C in air with 10% steam. This interfacial engineering strategy proves universal, as demonstrated by ZrO 2 ‐La 2 O 3 counterparts. Our findings break the reducibility dependency in traditional single‐atom catalysts (SACs) stabilization by establishing oxide–oxide interface as universal anchoring platforms, which expands the design space of industrial‐grade SACs beyond conventional reducible oxides.
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