标题:Efficient near-infrared photocatalysts based on NaYF4:Yb3+,Tm3+@ NaYF4:Yb3+, Nd3+@TiO2 core@shell nanoparticles
作者:Huang, Huining; Li, Huiliang; Wang, Zeyan; Wang, Peng; Zheng, Zhaoke; Liu, Yuanyuan; Dai, Ying; Li, Yingjie; Huang, Baibiao
作者机构:[Huang, Huining; Li, Huiliang; Wang, Zeyan; Wang, Peng; Zheng, Zhaoke; Liu, Yuanyuan; Huang, Baibiao] Shandong Univ, State Key Lab Crystal Mat, Jinan 更多
通讯作者:Wang, ZY;Huang, BB
通讯作者地址:[Wang, ZY; Huang, BB]Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Peoples R China.
来源:CHEMICAL ENGINEERING JOURNAL
出版年:2019
卷:361
页码:1089-1097
DOI:10.1016/j.cej.2018.12.174
关键词:Near-infrared irradiation; Photocatalyst; Upcoversion; Core@shell; structure
摘要:In this work, we fabricated NaYF4:Yb3+, Tm3+@NaYF4:Yb3+, Nd3+@TiO2 (Tm@Nd@TiO2) core@shell nanoparticles and investigated their near-infrared (NIR) photocatalytic activities. Comparing to traditional TiO2 based upconversion (UC) photocatalysts (i.e., NaYF4:Yb3+, Tm3+@TiO2, named Tm@TiO2), Tm@Nd@TiO2 exhibits enhanced photocatalytic activity under NIR light irradiation. The photocatalytic activity of Tm@Nd@TiO2 under 980, 808, and 980+ 808 nm laser irradiation is 4.40, 5.84, and 9.83 times as high as that of Tm@TiO2 under only 980 nm irradiation, respectively. The ethylene degradation rate of Tm@Nd@TiO2 under 980 + 808 nm laser irradiation is 6.4 times as that of Tm@TiO2. The photocatalytic activity of Tm@Nd@TiO2 under visible + NIR irradiation is even comparable with (similar to 2/3) that under UV light irradiation during Rhodamine B (RhB) degradation. The enhanced photocatalytic activity of Tm@Nd@TiO2 can be attributed to the stronger light absorption in NIR region ascribed to Nd3+, lower water absorption and the enhanced UC emission of Tm@Nd with unique core@shell nanostructures. This work can provide a possible route to improve the NIR photocatalytic activity and stimulate the applications in many other fields.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85059375382&doi=10.1016%2fj.cej.2018.12.174&partnerID=40&md5=4eabaa45d3555ee4d3556e156cca6cff
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