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探索功能化配体在铂基金属有机框架催化剂中的基础作用。

Exploring the Fundamental Roles of Functionalized Ligands in Platinum@Metal-Organic Framework Catalysts.

作者信息

Zhang Wenlei, Ji Wenlan, Li Linjie, Qin Peishan, Khalil Islam E, Gu Zhida, Wang Peng, Li Hongfeng, Fan Yun, Ren Zhen, Shen Yu, Zhang Weina, Fu Yu, Huo Fengwei

机构信息

College of Science, Northeastern University, Shenyang 100819, China.

Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing 211816, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2020 Nov 25;12(47):52660-52667. doi: 10.1021/acsami.0c15340. Epub 2020 Nov 10.

DOI:10.1021/acsami.0c15340
PMID:33169972
Abstract

The metal nodes, functionalized ligands, and uniform channels of metal-organic frameworks (MOFs) are typically utilized to regulate the catalytic properties of metal nanoparticles (MNPs). However, though the ligand functionalization could impact the properties of the metal nodes and channels, which might further regulate the catalytic activity and selectivity of MNPs, related research in the design of MNP/MOF catalysts was usually neglected. Herein, we synthesized a series of Pt@UiO-66 composites (Pt@UiO-66-NH, Pt@UiO-66-SOH, and Pt@UiO-66) with slightly different organic ligands, which enhanced steric hindrance and contributed to multipathway electron transfer in selective hydrogenation of linear citronellal. The selectivity toward citronellol was gradually improved along with the increased size of functional groups (hydrogen, amino groups, and sulfo groups) on organic ligands, which enhanced steric hindrance provided by channels. In addition, the X-ray photoelectron spectroscopy measurements also revealed that the electronic state of Pt NPs was regulated through multipathway electron transfer from Pt NPs to metal nodes, between organic ligands and Pt NPs/metal nodes. Our research proved that the ligand functionalization altered physiochemical properties of the channels and metal nodes, further together managing the catalytic performance of Pt NPs through enhanced steric hindrance and multi-pathway electron transfer.

摘要

金属有机框架材料(MOFs)的金属节点、功能化配体和均匀通道通常用于调节金属纳米颗粒(MNPs)的催化性能。然而,尽管配体功能化会影响金属节点和通道的性质,进而可能调节MNPs的催化活性和选择性,但在MNP/MOF催化剂设计方面的相关研究通常被忽视。在此,我们合成了一系列有机配体略有不同的Pt@UiO-66复合材料(Pt@UiO-66-NH、Pt@UiO-66-SOH和Pt@UiO-66),它们在香茅醛选择性加氢反应中增强了空间位阻并有助于多途径电子转移。随着有机配体上官能团(氢、氨基和磺酸基)尺寸的增加,对香茅醇的选择性逐渐提高,这增强了通道提供的空间位阻。此外,X射线光电子能谱测量还表明,通过从Pt NPs到金属节点、有机配体与Pt NPs/金属节点之间的多途径电子转移,Pt NPs的电子态得到了调节。我们的研究证明,配体功能化改变了通道和金属节点的物理化学性质,进而通过增强空间位阻和多途径电子转移共同调控了Pt NPs的催化性能。

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Photogenerated hole traps in metal-organic-framework photocatalysts for visible-light-driven hydrogen evolution.
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