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Encapsulated CdSe/CdS nanorods in double-shelled porous nanocomposites for efficient photocatalytic CO2 reduction

Hui LiKey Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, P. R. ChinaCaikun ChengKey Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, P. R. ChinaZhijie YangKey Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, P. R. ChinaJingjing WeiKey Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, P. R. China. [email protected]
2022en
ABI

Аннотация

Abstract Colloidal quantum dots have been emerging as promising photocatalysts to convert CO 2 into fuels by using solar energy. However, the above photocatalysts usually suffer from low CO 2 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 −1 h −1 ) toward CO 2 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 2 adsorption and conversion by integrating the inorganic and organic semiconductors.

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