Dissociation-Assembly-Carbonization: A Strategy for Constructing Indium Sulfide Photocatalysts with Increased Reactive Sites and Spatial Charge Separation
Dissociation-Assembly-Carbonization: A Strategy for Constructing Indium Sulfide Photocatalysts with Increased Reactive Sites and Spatial Charge Separation
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DOI:
10.1021/acscatal.3c03494
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发表时间:
2023-10
期刊:
影响因子:
12.9
通讯作者:
Haobo Zhang;Shuo Zhou;Dong Li;Wenwen Zhan;Huade Liu;Liming Sun;Mengge Li;Lei Yang;Jianwei Zhao;Xiaoxiao He;Jianhua Xu;Xiguang Han
中科院分区:
文献类型:
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作者:
Haobo Zhang;Shuo Zhou;Dong Li;Wenwen Zhan;Huade Liu;Liming Sun;Mengge Li;Lei Yang;Jianwei Zhao;Xiaoxiao He;Jianhua Xu;Xiguang Han
Sufficient surface reaction sites and a high separation of photogenerated carriers are two important guarantees for photocatalytic reactions. In this work, using a layered coordination compound In(pydc)2as a precursor, through the dissociation-assembly-carbonization process, a three-dimensional (3D) complex hierarchical structure assembled by uniform N,O-codoped carbon-encapsulated In2S3ultrathin nanosheets (N,O–C/In2S3DP) has been obtained. The unique 3D hierarchical structure can expose the surface-active sites of ultrathin nanosheets to the greatest extent, which provides enough surface sites for photocatalytic reactions. The coated N,O-codoped carbon layer can not only realize the spatial separation of photogenerated electrons and holes but also promote the activation for organic reactants. In addition, the multielectron codoping of N and O in a carbon layer is conducive to the generation of superoxide radicals (O2·–), which is an important active group in a photocatalytic organic selective oxidation reaction. Thus, N,O–C/In2S3DP exhibits good catalytic activity for the selective oxidation of sulfides to sulfoxides under the irradiation of various light sources (blue light, green light, and yellow light). This study provides a design and synthesis strategy (dissociation-assembly-carbonization) for constructing a suitable structure with a specific composition as excellent photocatalysts in the future.