MOF-Mediated Synthesis of Supported Fe-Doped Pd Nanoparticles under Mild Conditions for Magnetically Recoverable Catalysis

被引:12
作者
Darawsheh, Mohanad D. [1 ]
Mazario, Jaime [2 ]
Lopes, Christian W. [3 ]
Gimenez-Marques, Monica [1 ]
Domine, Marcelo E. [2 ]
Meira, Debora M. [4 ,5 ]
Martinez, Jordan [2 ]
Minguez Espallargas, Guillermo [1 ]
Ona-Burgos, Pascual [2 ,6 ]
机构
[1] Univ Valencia, Inst Ciencia Mol ICMol, C Catedrat Jose Beltran 2, Paterna 46980, Spain
[2] Univ Politecn Valencia, CSIC, UPV, Inst Tecnol Quim, Avda Naranjos S-N, Valencia 46022, Spain
[3] Univ Fed Rio Grande do Sul, Inst Chem, Lab React & Catalysis, BR-91501970 Porto Alegre, Brazil
[4] Argonne Natl Lab, Adv Photon Source, CLS APS Sect 20, 9700 S Cass Ave, Lemont, IL 60439 USA
[5] Canadian Light Source Inc, 44 Innovat Blvd, Saskatoon, SK S7N 2V3, Canada
[6] Univ Almeria, Res Ctr CIAIMBITAL, Dept Chem & Phys, Ctra Sacramento S-N, Almeria 04120, Spain
关键词
catalysis; iron; metal-organic frameworks; nanoparticles; palladium; METAL-ORGANIC FRAMEWORKS; CARBON; ELECTROCATALYSTS; HYDROGENATION; CORE; GRAPHENE; NITROBENZENE; PERFORMANCE; PLATINUM; CLUSTERS;
D O I
10.1002/chem.202001895
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic framework (MOF)-driven synthesis is considered as a promising alternative for the development of new catalytic materials with well-designed active sites. This synthetic approach is used here to gradually transform a new bimetallic MOF, with Pd and Fe as the metal components, by the in situ generation of aniline under mild conditions. This methodology results in a compositionally homogeneous nanocomposite formed by Fe-doped Pd nanoparticles that, in turn, are supported on iron oxide-doped carbon. The nanocomposite has been fully characterized by several techniques such as IR and Raman spectroscopy, TEM, XPS, and XAS. The performance of this nanocomposite as an heterogeneous catalyst for hydrogenation of nitroarenes and nitrobenzene coupling with benzaldehyde has been evaluated, proving it to be an efficient and reusable catalyst.
引用
收藏
页码:13659 / 13667
页数:9
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