光催化
X射线光电子能谱
电子顺磁共振
材料科学
光降解
钛
漫反射红外傅里叶变换
光谱学
光化学
煅烧
光致发光
氧化剂
氧化钛
核化学
化学
催化作用
化学工程
核磁共振
有机化学
工程类
物理
量子力学
光电子学
冶金
作者
Zuzanna Bielan,Szymon Dudziak,Agnieszka Sulowska,Daniel Pelczarski,Jacek Ryl,Anna Zielińska‐Jurek
出处
期刊:Materials
[Multidisciplinary Digital Publishing Institute]
日期:2020-06-18
卷期号:13 (12): 2763-2763
被引量:22
摘要
Among various methods of improving visible light activity of titanium(IV) oxide, the formation of defects and vacancies (both oxygen and titanium) in the crystal structure of TiO2 is an easy and relatively cheap alternative to improve the photocatalytic activity. In the presented work, visible light active defective TiO2 was obtained by the hydrothermal reaction in the presence of three different oxidizing agents: HIO3, H2O2, and HNO3. Further study on the effect of used oxidant and calcination temperature on the physicochemical and photocatalytic properties of defective TiO2 was performed. Obtained nanostructures were characterized by X-ray diffractometry (XRD), specific surface area (BET) measurements, UV-Vis diffuse reflectance spectroscopy (DR-UV/Vis), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR) spectroscopy. Degradation of phenol as a model pollutant was measured in the range of UV-Vis and Vis irradiation, demonstrating a significant increase of photocatalytic activity of defective TiO2 samples above 420 nm, comparing to non-defected TiO2. Correlation of EPR, UV-Vis, PL, and photodegradation results revealed that the optimum concentration of HIO3 to achieve high photocatalytic activity was in the range of 20–50 mol%. Above that dosage, titanium vacancies amount is too high, and the obtained materials’ photoactivity was significantly decreased. Studies on the photocatalytic mechanism using defective TiO2 have also shown that •O2− radical is mainly responsible for pollutant degradation.
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