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空心金属有机框架微环境中钯银纳米笼上的光诱导选择性氢化反应

Light-Induced Selective Hydrogenation over PdAg Nanocages in Hollow MOF Microenvironment.

作者信息

Li Luyan, Li Yanxiao, Jiao Long, Liu Xiaoshuo, Ma Zhentao, Zeng Yu-Jia, Zheng Xusheng, Jiang Hai-Long

机构信息

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, P. R. China.

Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.

出版信息

J Am Chem Soc. 2022 Sep 21;144(37):17075-17085. doi: 10.1021/jacs.2c06720. Epub 2022 Sep 7.

Abstract

Selective hydrogenation with high efficiency under ambient conditions remains a long-standing challenge. Here, a yolk-shell nanostructured catalyst, PdAg@ZIF-8, featuring plasmonic PdAg nanocages encompassed by a metal-organic framework (MOF, namely, ZIF-8) shell, has been rationally fabricated. PdAg@ZIF-8 achieves selective (97.5%) hydrogenation of nitrostyrene to vinylaniline with complete conversion at ambient temperature under visible light irradiation. The photothermal effect of Ag, together with the substrate enrichment effect of the catalyst, improves the Pd activity. The near-field enhancement effect from plasmonic Ag and optimized Pd electronic state by Ag alloying promote selective adsorption of the -NO group and therefore catalytic selectivity. Remarkably, the unique yolk-shell nanostructure not only facilitates access to PdAg cores and protects them from aggregation but also benefits substrate enrichment and preferential -NO adsorption under light irradiation, the latter two of which surpass the core-shell counterpart, giving rise to enhanced activity, selectivity, and recyclability.

摘要

在环境条件下实现高效选择性氢化仍然是一个长期存在的挑战。在此,一种具有核壳纳米结构的催化剂PdAg@ZIF-8已被合理制备,其特征是由金属有机框架(MOF,即ZIF-8)壳包围的具有等离子体效应的PdAg纳米笼。PdAg@ZIF-8在可见光照射下的环境温度下实现了硝基苯乙烯到乙烯基苯胺的选择性(97.5%)氢化,转化率达到100%。Ag的光热效应与催化剂的底物富集效应共同提高了Pd的活性。等离子体Ag的近场增强效应以及通过Ag合金化优化的Pd电子态促进了-NO基团的选择性吸附,从而提高了催化选择性。值得注意的是,独特的核壳纳米结构不仅便于接触PdAg核并防止它们聚集,而且有利于底物富集和光照下优先吸附-NO,后两者超过了核壳结构的对应物,从而提高了活性、选择性和可回收性。

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