化学选择性
催化作用
异质结
取代基
反应性(心理学)
材料科学
组合化学
化学
电子效应
表面改性
纳米技术
多相催化
电子结构
选择性
电子转移
外延
光化学
化学工程
有机化学
晶体管
作者
Zuxian Cai,Ju Wang,Zhaoxu Wang,Ruirui Yun,Hu Zhou,Baishu Zheng
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-11-13
卷期号:41 (46): 31400-31409
标识
DOI:10.1021/acs.langmuir.5c04445
摘要
Precise modulation of the electronic structure of the catalyst is critical for generating highly active sites in targeted catalytic transformations. We report a strategy to regulate the electronic properties of metal-organic frameworks (MOFs) by constructing functional-group-modified MOF-on-MOF heterojunctions for selective nitroarene hydrogenation. As a representative heterostructure, the ZIF-67-on-NH2-UiO-66 heterostructure is fabricated by epitaxially growing Co-based ZIF-67 on NH2-UiO-66. Combining experimental studies and first-principles calculations demonstrates that the electron-donating substituent (-NH2) group elevates the d-band center of the heterojunction, facilitating electron transfer compared to the unfunctionalized ZIF-67-on-UiO-66 analog. Consequently, ZIF-67-on-NH2-UiO-66 exhibits exceptional reactivity and chemoselectivity for hydrogenating diverse functionalized nitroarenes under mild conditions, surpassing most reported catalysts under comparable settings. This work establishes ZIF-on-MOF functionalization as an effective strategy to engineer electronic structures at catalytic interfaces for advanced selective hydrogenations.
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