An in situ derived MOF@In2S3 heterojunction stabilizes Co(ii)-salicylaldimine for efficient photocatalytic formic acid dehydrogenation
We report here the hierarchical construction of a molecular Co(ii)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3 heterojunction through sequentially controllable in situ etching and post-synthetic modification for photocatalytic hydrogen production from formic ac...
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Published in | Chemical communications (Cambridge, England) Vol. 58; no. 51; pp. 7140 - 7143 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
23.06.2022
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Abstract | We report here the hierarchical construction of a molecular Co(ii)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3 heterojunction through sequentially controllable in situ etching and post-synthetic modification for photocatalytic hydrogen production from formic acid. The enhanced catalyst stability and facilitated charge carrier mobility between the In2S3 photosensitizers and Co catalyst realize a superior H2 production rate of 18 746 μmol g−1 h−1 (selectivity > 99.9%) with a turnover number (TON) of up to 6146 in 24 h (apparent quantum efficiency of 3.8% at 420 nm), indicating a 165-fold enhancement over that of the pristine MOF. This work highlights a powerful strategy for synergistic Earth-abundant metal-based MOF photocatalysis in promoting H2 production from FA. |
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AbstractList | We report here the hierarchical construction of a molecular Co(ii)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3 heterojunction through sequentially controllable in situ etching and post-synthetic modification for photocatalytic hydrogen production from formic acid. The enhanced catalyst stability and facilitated charge carrier mobility between the In2S3 photosensitizers and Co catalyst realize a superior H2 production rate of 18 746 μmol g−1 h−1 (selectivity > 99.9%) with a turnover number (TON) of up to 6146 in 24 h (apparent quantum efficiency of 3.8% at 420 nm), indicating a 165-fold enhancement over that of the pristine MOF. This work highlights a powerful strategy for synergistic Earth-abundant metal-based MOF photocatalysis in promoting H2 production from FA. We report here the hierarchical construction of a molecular Co(ii)-salicylaldimine catalyst and an in situ derived In₂S₃ semiconductor in a MOF@In₂S₃ heterojunction through sequentially controllable in situ etching and post-synthetic modification for photocatalytic hydrogen production from formic acid. The enhanced catalyst stability and facilitated charge carrier mobility between the In₂S₃ photosensitizers and Co catalyst realize a superior H₂ production rate of 18 746 μmol g⁻¹ h⁻¹ (selectivity > 99.9%) with a turnover number (TON) of up to 6146 in 24 h (apparent quantum efficiency of 3.8% at 420 nm), indicating a 165-fold enhancement over that of the pristine MOF. This work highlights a powerful strategy for synergistic Earth-abundant metal-based MOF photocatalysis in promoting H₂ production from FA. We report here the hierarchical construction of a molecular Co(II)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3 heterojunction through sequentially controllable in situ etching and post-synthetic modification for photocatalytic hydrogen production from formic acid. The enhanced catalyst stability and facilitated charge carrier mobility between the In2S3 photosensitizers and Co catalyst realize a superior H2 production rate of 18 746 μmol g-1 h-1 (selectivity > 99.9%) with a turnover number (TON) of up to 6146 in 24 h (apparent quantum efficiency of 3.8% at 420 nm), indicating a 165-fold enhancement over that of the pristine MOF. This work highlights a powerful strategy for synergistic Earth-abundant metal-based MOF photocatalysis in promoting H2 production from FA.We report here the hierarchical construction of a molecular Co(II)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3 heterojunction through sequentially controllable in situ etching and post-synthetic modification for photocatalytic hydrogen production from formic acid. The enhanced catalyst stability and facilitated charge carrier mobility between the In2S3 photosensitizers and Co catalyst realize a superior H2 production rate of 18 746 μmol g-1 h-1 (selectivity > 99.9%) with a turnover number (TON) of up to 6146 in 24 h (apparent quantum efficiency of 3.8% at 420 nm), indicating a 165-fold enhancement over that of the pristine MOF. This work highlights a powerful strategy for synergistic Earth-abundant metal-based MOF photocatalysis in promoting H2 production from FA. |
Author | Ma, Liang Lin, Wenting Zhang, Meijin Pi, Yunhong Wang, Tiejun |
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Snippet | We report here the hierarchical construction of a molecular Co(ii)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3... We report here the hierarchical construction of a molecular Co(II)-salicylaldimine catalyst and an in situ derived In2S3 semiconductor in a MOF@In2S3... We report here the hierarchical construction of a molecular Co(ii)-salicylaldimine catalyst and an in situ derived In₂S₃ semiconductor in a MOF@In₂S₃... |
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SubjectTerms | Carrier mobility Catalysts Current carriers Dehydrogenation Formic acid Heterojunctions Hydrogen production Metal-organic frameworks Photocatalysis Quantum efficiency Selectivity semiconductors |
Title | An in situ derived MOF@In2S3 heterojunction stabilizes Co(ii)-salicylaldimine for efficient photocatalytic formic acid dehydrogenation |
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