光降解
光催化
材料科学
X射线光电子能谱
扫描电子显微镜
带隙
拉曼光谱
石墨烯
纳米复合材料
光化学
漫反射红外傅里叶变换
分析化学(期刊)
核化学
催化作用
化学工程
化学
纳米技术
有机化学
复合材料
工程类
物理
光电子学
光学
作者
Jie Zhang,Xiao Xu,Huan Yang,Ho Youkang,Zhong Zhiyao
标识
DOI:10.1080/09593330.2019.1625955
摘要
A series of TiO2-rGO-Ag nanocomposites were prepared in this work via a facile one-pot hydrothermal method utilized for formaldehyde (HCHO) photodegradation; using TiO2, graphene oxide(GO) as well as AgNO3 as the raw materials, and sodium citrate as a reducing agent. Characterization by X-ray diffraction (XRD), Raman spectra, Transmission electron microscopy (TEM) and Field emission scanning electron microscopy (FESEM) demonstrated that GO and Ag+ were reduced during the formation of TiO2-rGO-Ag nanocomposites. X-ray photoelectron spectroscopy(XPS), UV–vis diffuse reflectance spectroscopy (DRS), photoluminescence spectra(PL) and Photocurrent spectrum measurement were applied to quantitatively characterize the bonding between TiO2 and rGO, the band gap energy of catalysts as well as electron–hole pairs recombination rate. The results revealed that the introduction of rGO sheets and Ag nanoparticles reduced the band gap energy of catalysts; it also suppressed the recombination of electron–hole pairs. However, C–O–Ti bond, which played a key role in photocatalysis, was reduced to some extent by the existence of Ag. Photodegradation results showed that, when the Ag loading was 9 mol% of TiO2, the reaction rate constant of formaldehyde (HCHO) removal improved distinctly, by about 22.3 times that of TiO2. The radical scavenger tests and electron paramagnetic resonance(EPR) analysis revealed that superoxide radical (·O2−), hole (h+), and hydroxylradical (·OH) were reactive species of formaldehyde photodegradation.
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