Isolated Nano-Island Catalysts Enable Efficient Double-Bond Migration over Pd Nanoparticles

作者：Bing Lü, Shipan Liang, Yanling Liu, Wencong Liu, Ting Liu, Liwei Zhang, Zhengyang Chen, Sibin Ying, Jianguo Zhu, Chengwei Liu, Shanjun Mao, Yong Wang · 发表于：ACS Nano · 年份：2025 · DOI：10.1021/acsnano.5c15574 · 被引用次数：7 · 研究领域：Catalysis for Biomass Conversion、Catalytic Processes in Materials Science、Asymmetric Hydrogenation and Catalysis

Nanoparticles (NPs) play a key role in heterogeneous catalysis due to their unique nanoscale effects, but their thermodynamic instability makes stabilizing small metal species challenging. Herein, we develop a series of Pd/xCeO 2 /SiO 2 catalysts with a nanoisland architecture that enables precise control over Pd particle size and electronic properties via a confinement effect. CeO 2 nanoparticles were first dispersed on a SiO 2 support, followed by selective Pd deposition on the CeO 2 surface through strong metal–support interactions and electron transfer between Pd and reducible CeO 2 . The resulting in situ-formed nanoisland structure enhances catalytic performance through optimized Pd–CeO 2 synergy. In the double-bond migration (DBM) of 2-pentylidene cyclopentanone, a key step in fragrance synthesis, the Pd/7%CeO 2 /SiO 2 catalyst achieved 90% isomerization selectivity at full conversion and a TOF of 26,000 h –1, 3–8 times higher than single-support catalysts. This catalyst has been successfully scaled up for the kiloton-scale annual production of methyl dihydrojasmonate, demonstrating the industrial relevance of this nanostructuring strategy.