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具有暴露的{001}和{101}晶面的碳量子点/单晶TiO纳米片的构建及其可见光驱动催化活性。

Construction of carbon quantum dots/single crystal TiO nanosheets with exposed {001} and {101} facets and their visible light driven catalytic activity.

作者信息

Huang Hongqin, Ouyang Hao, Han Tiehu, Wang Huigang, Zheng Xuming

机构信息

Department of Chemistry, Key Laboratory of Advanced Textiles Materials, Manufacture Technology of the Ministry of Education, Engineering Research Center for Eco-Dyeing, Finishing of Textiles of the Ministry of Education, Zhejiang Sci-Tech University Davis Hangzhou 310018 P. R. China

出版信息

RSC Adv. 2019 Jan 25;9(7):3532-3541. doi: 10.1039/c8ra10311a.

Abstract

Carbon quantum dots were successfully doped into anatase TiO single crystal nanosheets (TNS) with exposed {001} and {101} reactive facets by a facile solvothermal process. SEM and TEM confirmed the as-prepared TiO nanosheet structure and that the dominant exposed face is the {001} facet, and the loaded N-CDs are nearly spherical with an average size of about 3 nm. XPS results confirmed that the deposited N-CDs were chemically integrated into the TiO nanosheets. UV-vis DRS spectroscopy shows that with the dotting of N-CDs, the absorption edge of N-CDs/TNS has been extended into the visible light region. The ability of the N-CDs/TNS to degrade Rhodamine B (RhB) in aqueous solution under visible light irradiation ( ≥ 400 nm) was investigated. The results show that the photocatalytic performance of N-CDs/TNS was substantially improved relative to pure TNS. The photodegradation efficiency reached its maximum value with 6 mL of N-CDs/TNS, showing a 9.3-fold improvement in photocatalytic activity over TNS. Fluorescence spectroscopy (PL) and electron paramagnetic resonance (EPR) studies were conducted to characterize the active species during the degradation period, based on which the possible photodegradation mechanism of N-CDs/TNS by visible light irradiation was given.

摘要

通过简便的溶剂热法,成功地将碳量子点掺杂到具有暴露的{001}和{101}反应面的锐钛矿TiO单晶纳米片(TNS)中。扫描电子显微镜(SEM)和透射电子显微镜(TEM)证实了所制备的TiO纳米片结构,且主要暴露面为{001}面,负载的N-CDs近乎球形,平均尺寸约为3 nm。X射线光电子能谱(XPS)结果证实,沉积的N-CDs化学整合到TiO纳米片中。紫外可见漫反射光谱(UV-vis DRS)表明,随着N-CDs的点缀,N-CDs/TNS的吸收边缘已扩展到可见光区域。研究了N-CDs/TNS在可见光照射(≥400 nm)下对水溶液中罗丹明B(RhB)的降解能力。结果表明,相对于纯TNS,N-CDs/TNS的光催化性能有显著提高。当使用6 mL N-CDs/TNS时,光降解效率达到最大值,其光催化活性比TNS提高了9.3倍。进行了荧光光谱(PL)和电子顺磁共振(EPR)研究以表征降解过程中的活性物种,并据此给出了可见光照射下N-CDs/TNS可能的光降解机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f2e/9060303/7ed8e8bce29f/c8ra10311a-s1.jpg

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