催化作用
胶束
化学
煅烧
合理设计
介孔材料
纳米技术
两亲性
结晶
共聚物
纳米颗粒
接口(物质)
化学工程
介孔二氧化硅
金属
纳米晶
多相催化
化学稳定性
自组装
氧原子
作者
Xun Kan,Shouchao Zhong,Xiaoyuan Qin,Lusi Zhao,Fujian Liu,Xi Wang,Yong Zheng,Runmin Gao,Jian Zhang,Guanqing Zhang,Guangtao Yu,Wei Chen,Liang Wang,Lilong Jiang,Feng-Shou Xiao
摘要
Metal-support interfaces serve as the key active sites for catalytic reactions. The design of catalysts that simultaneously possess high interfacial density, superior activity, and robust stability represents a central challenge in enhancing the overall performance. Herein, we report an innovative synchronic assembly of multilevel micelles, where small metal-acetylacetonate micelles spontaneously assemble at the amphiphilic interfaces of larger triblock copolymer micelles. Subsequent crystallization and calcination semi-fix diverse metal nanoparticles (MNPs) within the walls of the resulting ordered mesoporous crystals, thereby achieving maximized interfacial density and structural robustness. The constructed representative interfaces, such as Cu(I)-O-Ti and Pd@Cu-O-Ti, demonstrated an enhanced oxygen activation capacity, which drove their exceptional catalytic oxidation performance and surpassed nearly all existing benchmarks. Synchronic assembly of multilevel micelles offers a bottom-up strategy to simultaneously control MNP properties, mesostructural ordering, and interface formation, enabling the precise design of high-performance catalysts and providing new insights for rational cross-scale and cross-dimensional interface engineering.
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