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用于选择性光催化将CO转化为CHOH的BiS量子点中S空位的定向向内迁移

Directed Inward Migration of S-Vacancy in BiS QDs for Selective Photocatalytic CO to CHOH.

作者信息

Wang Jing, Wang Wenlei, Deng Yao, Zhang Zhen, Wang Hui, Wu Yiqiang

机构信息

College of Materials Science and Engineering, National and Local Joint Engineering Research Center for Green Processing, Technology of Agricultural and Forestry Biomass, Central South University of Forestry and Technology, Changsha, 410004, China.

College of Chemistry and Chemical Engineering, National Forestry and Grassland Administration Bioethanol Research Center, College of Chemistry and Chemical Engineering, Central South University of Forestry and Technology, Changsha, 410004, China.

出版信息

Adv Sci (Weinh). 2025 Feb;12(8):e2406925. doi: 10.1002/advs.202406925. Epub 2025 Jan 9.

Abstract

The directional migration of S-vacancy is beneficial to the separation of photogenerated carriers and the transition of electrons in semiconductors. In this study, Bi/BiS@carboxylic-cellulose (CC) photocatalyst with bionic chloroplast structure is obtained by electron beam irradiation to induce S-vacancy in BiS@CC. The results of CO photoreduction experiments demonstrate that the reduction rate of CO to CHOH by Bi/BiS@CC-450 samples is 10.74 µmol·g·h, and the selectivity is 92.82%. The results show that the inward migration behavior of the borderline S-vacancy (b-S) induces the redistribution of electrons in Bi/BiS@CC. The Bi° clusters in Bi/BiS@CC is conducive to adsorb CO, and the internal S-vacancy (i-S) is conducive to adsorb CHOH, which accelerate the transfer of gas-phase products to realize the controllable conversion of CO and photoreduction products at the gas-liquid-solid three-phase interface. This study provides a new idea for the development and utilization of green photocatalysts in clean energy.

摘要

S空位的定向迁移有利于半导体中光生载流子的分离和电子的跃迁。在本研究中,通过电子束辐照在BiS@CC中诱导S空位,得到具有仿生叶绿体结构的Bi/BiS@羧基纤维素(CC)光催化剂。CO光还原实验结果表明,Bi/BiS@CC-450样品将CO还原为CHOH的速率为10.74 μmol·g·h,选择性为92.82%。结果表明,边界S空位(b-S)的向内迁移行为诱导了Bi/BiS@CC中电子的重新分布。Bi/BiS@CC中的Bi°团簇有利于吸附CO,内部S空位(i-S)有利于吸附CHOH,加速了气相产物的转移,实现了气-液-固三相界面处CO和光还原产物的可控转化。该研究为清洁能源中绿色光催化剂的开发利用提供了新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0929/11848541/c60359192f99/ADVS-12-2406925-g003.jpg

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