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Highly effective photoreduction of CO2 to CO promoted by integration of CdS with molecular redox catalysts through metal–organic frameworks

机译:通过金属有机框架将CdS与分子氧化还原催化剂结合在一起可将CO2高效光还原为CO

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摘要

We propose a strategy to synthesize ternary CdS/UiO-bpy/Co composites by integration of CdS and molecular redox catalysts through metal–organic framework (MOF) UiO-bpy. The CdS/UiO-bpy/Co composites were very effective for photocatalytic conversion of CO2 to CO under visible light irradiation. The evolution rate of CO could reach 235 μmol g–1 h–1, which was a 10.2-fold improvement compared to that for the parent CdS, and selectivity for CO was 85%. The outstanding performance of the CdS/UiO-bpy/Co composites resulted from promoting the separation and migration of photo-induced charge carriers, enhancing the adsorption of CO2 molecules, and offering abundant active sites for CO2 reduction. As far as we know, this is the first study to integrate inorganic semiconductors and molecular redox catalysts through MOFs.
机译:我们提出了一种通过金属有机骨架(MOF)UiO-bpy整合CdS和分子氧化还原催化剂来合成三元CdS / UiO-bpy / Co复合材料的策略。 CdS / UiO-bpy / Co复合材料在可见光照射下非常有效地将CO2光催化转化为CO。一氧化碳的释放速率可以达到235μmolg –1 h –1 ,与母体CdS相比提高了10.2倍,对CO的选择性为85%。 CdS / UiO-bpy / Co复合材料的出色性能归因于促进光诱导电荷载流子的分离和迁移,增强了CO2分子的吸附并提供了丰富的CO2还原活性位。据我们所知,这是首次通过MOF集成无机半导体和分子氧化还原催化剂的研究。

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