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用于高效光催化 CO 还原的双壳层多孔纳米复合材料中的封装 CdSe/CdS 纳米棒

Encapsulated CdSe/CdS nanorods in double-shelled porous nanocomposites for efficient photocatalytic CO reduction.

作者信息

Li Hui, Cheng Caikun, Yang Zhijie, Wei Jingjing

机构信息

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, P. R. China.

出版信息

Nat Commun. 2022 Oct 29;13(1):6466. doi: 10.1038/s41467-022-34263-z.

Abstract

Colloidal quantum dots have been emerging as promising photocatalysts to convert CO into fuels by using solar energy. However, the above photocatalysts usually suffer from low CO adsorption capacity because of their nonporous structures, which principally reduces their catalytic efficiency. Here, we show that synchronizing imine polycondensation reaction to self-assembly of colloidal CdSe/CdS nanorods can produce micro-meso hierarchically porous nanocomposites with double-shelled nanocomposites. Owing to their hierarchical pores and the ability to separate photoexcited electrons, the self-assembled porous nanocomposites exhibit remarkably higher activity (≈ 64.6 μmol g h) toward CO to CO in solid-gas regime than that of nonporous solids from self-assembled CdSe/CdS nanorods under identical conditions. Importantly, the length of the nanorods is demonstrated to be crucial to correlate their ability to long-distance separation of photogenerated electrons and holes along their axial direction. Overall, this approach provides a rational strategy to optimize the CO adsorption and conversion by integrating the inorganic and organic semiconductors.

摘要

胶体量子点已成为一种很有前景的光催化剂,可利用太阳能将一氧化碳转化为燃料。然而,上述光催化剂由于其无孔结构,通常具有较低的一氧化碳吸附能力,这在很大程度上降低了它们的催化效率。在此,我们表明,将亚胺缩聚反应与胶体CdSe/CdS纳米棒的自组装同步进行,能够制备出具有双壳结构的微米-介观分级多孔纳米复合材料。由于其分级孔隙结构以及分离光激发电子的能力,在相同条件下,自组装的多孔纳米复合材料在固-气体系中对一氧化碳转化为二氧化碳表现出比自组装CdSe/CdS纳米棒形成的无孔固体显著更高的活性(约64.6 μmol g⁻¹ h⁻¹)。重要的是,已证明纳米棒的长度对于关联其沿轴向长距离分离光生电子和空穴的能力至关重要。总体而言,该方法通过整合无机和有机半导体,提供了一种优化一氧化碳吸附和转化的合理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a15c/9617972/2c0549161959/41467_2022_34263_Fig1_HTML.jpg

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