光催化
光子上转换
纳米颗粒
锐钛矿
催化作用
材料科学
辐照
化学工程
纳米技术
亚甲蓝
纳米复合材料
光化学
发光
化学
物理
有机化学
光电子学
工程类
核物理学
作者
Yanna Tang,Weihua Di,Xuesong Zhai,Renyuan Yang,Weiping Qin
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2013-01-29
卷期号:3 (3): 405-412
被引量:367
摘要
Core–shell structured nanoparticles for near-infrared (NIR) photocatalysis were synthesized by a two-step wet-chemical route. The core is composed of upconversion luminescence NaYF4:Yb,Tm prepared by a solvothermal process, and the shell is anatase TiO2 nanocrystals around NaYF4 particles formed via a method similar to a Stöber process. Methylene blue compound as a model pollutant was used to investigate the photocatalytic activity of NaYF4:Yb,Tm@TiO2 composites under NIR irradiation. To understand the nature of NIR-responsive photocatalysis of NaYF4:Yb,Tm@TiO2, we investigated the energy transfer process between NaYF4:Yb,Tm and TiO2 and the origin of the degradation of organic pollutants under NIR radiation. Results indicate that the energy transfer route between NaYF4:Yb,Tm and TiO2 is an important factor that influences the photocatalytic activity significantly and that the degradation of organic pollutants under NIR irradiation is caused mostly by the oxidation of reactive oxygen species generated in the photocatalytic reaction, rather than by the thermal energy generated by NIR irradiation. The understanding of NIR-responsive photocatalytic mechanism helps to improve the structural design and functionality of this new type of catalytic material.
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