Zinc Indium Sulfide‐Based Photocatalysts for Selective Organic Transformations
The burgeoning field of semiconductor‐mediated organic conversion is of paramount significance, with zinc indium sulfide (ZnIn2S4) emerging as a standout candidate owing to its benign nature, optimal bandgap, extensive light absorption spectrum, remarkable physicochemical properties, and straightfor...
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Veröffentlicht in: | ChemCatChem 2024-07, Vol.16 (13), p.n/a |
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Sprache: | eng |
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Zusammenfassung: | The burgeoning field of semiconductor‐mediated organic conversion is of paramount significance, with zinc indium sulfide (ZnIn2S4) emerging as a standout candidate owing to its benign nature, optimal bandgap, extensive light absorption spectrum, remarkable physicochemical properties, and straightforward synthesis. This review examines the latest breakthroughs and the trajectory of ZnIn2S4‐based photocatalysts in the realm of selective organic transformation. We start with a distinct overview of the intrinsic physical attributes of ZnIn2S4 and the underlying mechanisms driving its efficacy in photocatalytic organic transformations. Subsequently, the preparation methods of ZnIn2S4 are summarized. The main focus is the state‐of‐the‐art photocatalytic application of various ZnIn2S4‐based photocatalysts, such as redox reactions, the construction of C−C, C−S and S−S bonds, and the cleavage of C−O, C−C, and C=C bonds. In the conclusion part, we provide our perspectives on the prospective advancements and the remaining challenges that lie ahead in the optimization of ZnIn2S4‐based photocatalysts, with the ultimate goal of enhancing their efficacy for a diverse array of photosynthetic applications. It is anticipated to inspire the strategic engineering of ZnIn2S4 and other semiconductor‐based photocatalysts for various artificial photosynthesis reactions.
This review article presents a summary of the recent advancements in the application of ZnIn2S4‐based photocatalysts for various chemical transformations, including selective redox processes, construction of C−C, C−S, and S−S bonds, cleavage of C−O, C−C, and C=C bonds. The potential directions for future research and the imminent challenges in this research field are further discussed. |
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ISSN: | 1867-3880 1867-3899 |
DOI: | 10.1002/cctc.202301553 |