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Selective Photocatalytic Dehydrogenation of Formic Acid by an in Situ-Restructured Copper-Postmetalated Metal-Organic Framework under Visible Light

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dc.contributor.author Issa Hamoud, Houeida
dc.contributor.author Damacet, Patrick
dc.contributor.author Fan, Dong
dc.contributor.author Assaad, Nisrine
dc.contributor.author Lebedev, Oleg I.
dc.contributor.author Krystianiak, Anna
dc.contributor.author Gouda, Abdelaziz M.
dc.contributor.author Heintz, Olivier
dc.contributor.author Daturi, Marco
dc.contributor.author Maurin, Guillaume T.
dc.contributor.author Hmadeh, Mohamad
dc.contributor.author El-Roz, Mohamad
dc.date.accessioned 2025-01-24T11:22:25Z
dc.date.available 2025-01-24T11:22:25Z
dc.date.issued 2022
dc.identifier.uri http://hdl.handle.net/10938/25505
dc.description.abstract Formic acid is considered as one of the most promising liquid organic hydrogen carriers. Its catalytic dehydrogenation process generally suffers from low activity, low reaction selectivity, low stability of the catalysts, and/or the use of noble-metal-based catalysts. Herein we report a highly selective, efficient, and noble-metal-free photocatalyst for the dehydrogenation of formic acid. This catalyst, UiO-66(COOH)2-Cu, is built by postmetalation of a carboxylic-functionalized Zr-MOF with copper. The visible-light-driven photocatalytic dehydrogenation process through the release of hydrogen and carbon dioxide has been monitored in real-time via operando Fourier transform infrared spectroscopy, which revealed almost 100% selectivity with high stability (over 3 days) and a conversion yield exceeding 60% (around 5 mmol·gcat-1·h-1) under ambient conditions. These performance indicators make UiO-66(COOH)2-Cu among the top photocatalysts for formic acid dehydrogenation. Interestingly, the as-prepared UiO-66(COOH)2-Cu hetero-nanostructure was found to be moderately active under solar irradiation during an induction phase, whereupon it undergoes an in-situ restructuring process through intraframework cross-linking with the formation of the anhydride analogue structure UiO-66(COO)2-Cu and nanoclustering of highly active and stable copper sites, as evidenced by the operando studies coupled with steady-state isotopic transient kinetic experiments, transmission electron microscopy and X-ray photoelectron spectroscopy analyses, and Density Functional Theory calculations. Beyond revealing outstanding catalytic performance for UiO-66(COO)2-Cu, this work delivers an in-depth understanding of the photocatalytic reaction mechanism, which involves evolutive behavior of the postmetalated copper as well as the MOF framework over the reaction. These key findings pave the way toward the engineering of new and efficient catalysts for photocatalytic dehydrogenation of formic acid. © 2022 American Chemical Society. All rights reserved.
dc.language.iso en
dc.publisher American Chemical Society
dc.relation.ispartof Journal of the American Chemical Society
dc.source Scopus
dc.subject Carbon dioxide
dc.subject Catalyst selectivity
dc.subject Cobalt compounds
dc.subject Copper
dc.subject Density functional theory
dc.subject Formic acid
dc.subject Fourier transform infrared spectroscopy
dc.subject High resolution transmission electron microscopy
dc.subject Light
dc.subject Metal-organic frameworks
dc.subject Photocatalytic activity
dc.subject Precious metals
dc.subject X ray photoelectron spectroscopy
dc.subject Catalytic dehydrogenation
dc.subject Hydrogen carriers
dc.subject Metal-based catalysts
dc.subject Metalorganic frameworks (mofs)
dc.subject Operando
dc.subject Organics
dc.subject Photo-catalytic
dc.subject Reaction selectivity
dc.subject Visible light
dc.subject ]+ catalyst
dc.subject Acidity
dc.subject Adsorption
dc.subject Article
dc.subject Atomic absorption spectrometry
dc.subject Catalyst
dc.subject Chemical reaction
dc.subject Chemical structure
dc.subject Conductance
dc.subject Dehydrogenation
dc.subject Electron
dc.subject Energy dispersive x ray spectroscopy
dc.subject Impedance spectroscopy
dc.subject Metallation
dc.subject Porosity
dc.subject Reaction analysis
dc.subject Scanning electron microscopy
dc.subject Steady state
dc.subject Surface property
dc.subject Thermodynamics
dc.subject Transmission electron microscopy
dc.subject X ray photoemission spectroscopy
dc.title Selective Photocatalytic Dehydrogenation of Formic Acid by an in Situ-Restructured Copper-Postmetalated Metal-Organic Framework under Visible Light
dc.type Article
dc.contributor.department Department of Chemistry
dc.contributor.faculty Faculty of Arts and Sciences (FAS)
dc.contributor.institution American University of Beirut
dc.identifier.doi https://doi.org/10.1021/jacs.2c04905
dc.identifier.pmid 36047929
dc.identifier.eid 2-s2.0-85137730284


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