2019
DOI: 10.1002/ange.201905667
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The First Study on the Reactivity of Water Vapor in Metal–Organic Frameworks with Platinum Nanocrystals

Abstract: We first studied the reactivity of H 2 Ovapor in metalorganic frameworks (MOFs) with Pt nanocrystals (NCs) through the water-gas shift (WGS) reaction. Aw ater-stable MOF,UiO-66, serves as ahighly effective support material for the WGS reaction compared with ZrO 2 .The origin of the high catalytic performance was investigated using in situ IR spectroscopy. In addition, from ac omparison of the catalytic activities of Pt on UiO-66, where Pt NCs are located on the surface of UiO-66 and Pt@UiO-66, where Pt NCs are… Show more

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Cited by 4 publications
(2 citation statements)
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“…In terms of the synergetic effect, Fe­(III) in PMOF­(Fe) acts as a promoting center for the generation of a ferryl species (Fe­(IV) = O), as a porphyrin radical cation and as an electron donor to Pt NPs. The high interface between Pt NPs and PMOF­(Fe) in Pt@PMOF­(Fe) and the H 2 O 2 adsorbed on the PMOF­(Fe) could promote H 2 O 2 activation on the most acidic Fe 3+ Lewis sites in proximity to Pt sites, which could decrease the Pt 4f binding energies and Pt–OH bond strength, so electrochemical activity toward H 2 O 2 could be promoted . The catalytic process of Pt@PMOF­(Fe) immobilized on the electrode surface could be expressed as follows First, H 2 O 2 was formed adsorbing OH species and adsorbed on the surface of Pt.…”
Section: Resultsmentioning
confidence: 99%
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“…In terms of the synergetic effect, Fe­(III) in PMOF­(Fe) acts as a promoting center for the generation of a ferryl species (Fe­(IV) = O), as a porphyrin radical cation and as an electron donor to Pt NPs. The high interface between Pt NPs and PMOF­(Fe) in Pt@PMOF­(Fe) and the H 2 O 2 adsorbed on the PMOF­(Fe) could promote H 2 O 2 activation on the most acidic Fe 3+ Lewis sites in proximity to Pt sites, which could decrease the Pt 4f binding energies and Pt–OH bond strength, so electrochemical activity toward H 2 O 2 could be promoted . The catalytic process of Pt@PMOF­(Fe) immobilized on the electrode surface could be expressed as follows First, H 2 O 2 was formed adsorbing OH species and adsorbed on the surface of Pt.…”
Section: Resultsmentioning
confidence: 99%
“…The high interface between Pt NPs and PMOF(Fe) in Pt@PMOF(Fe) and the H 2 O 2 adsorbed on the PMOF(Fe) could promote H 2 O 2 activation on the most acidic Fe 3+ Lewis sites in proximity to Pt sites, which could decrease the Pt 4f binding energies and Pt−OH bond strength, so electrochemical activity toward H 2 O 2 could be promoted. 53 The catalytic process of Pt@PMOF(Fe) immobilized on the electrode surface could be expressed as follows 54−56 2Pt H O 2Pt(OH)…”
Section: •+mentioning
confidence: 99%