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 inChemical communications (Cambridge, England) Vol. 58; no. 51; pp. 7140 - 7143
Main Authors Zhang, Meijin, Lin, Wenting, Ma, Liang, Pi, Yunhong, Wang, Tiejun
Format Journal Article
LanguageEnglish
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.
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...
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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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