Integration of mesopores and crystal defects in metal-organic frameworks via templated electrosynthesis

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作者
Xinchen Kang
Kai Lyu
Lili Li
Jiangnan Li
Louis Kimberley
Bin Wang
Lifei Liu
Yongqiang Cheng
Mark D. Frogley
Svemir Rudić
Anibal J. Ramirez-Cuesta
Robert A. W. Dryfe
Buxing Han
Sihai Yang
Martin Schröder
机构
[1] University of Manchester,School of Chemistry
[2] Chinese Academy of Science,Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry
[3] Oak Ridge National Laboratory,Diamond Light Source
[4] Harwell Science Campus,ISIS Facility
[5] STFC Rutherford Appleton Laboratory,undefined
来源
Nature Communications | / 10卷
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摘要
Incorporation of mesopores and active sites into metal-organic framework (MOF) materials to uncover new efficient catalysts is a highly desirable but challenging task. We report the first example of a mesoporous MOF obtained by templated electrosynthesis using an ionic liquid as both electrolyte and template. The mesoporous Cu(II)-MOF MFM-100 has been synthesised in 100 seconds at room temperature, and this material incorporates crystal defects with uncoupled Cu(II) centres as evidenced by confocal fluorescence microscopy and electron paramagnetic resonance spectroscopy. MFM-100 prepared in this way shows exceptional catalytic activity for the aerobic oxidation of alcohols to produce aldehydes in near quantitative yield and selectivity under mild conditions, as well as having excellent stability and reusability over repeated cycles. The catalyst-substrate binding interactions have been probed by inelastic neutron scattering. This study offers a simple strategy to create mesopores and active sites simultaneously via electrochemical formation of crystal defects to promote efficient catalysis using MOFs.
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