Construction of (001)-TiO2/g-C3N4 heterojunction for enhanced photocatalytic degradation of methylene blue

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Ran Gao, Wensong Lin, Huanxia Lin, Yong He, Xin Mai, Yeheng Zhang
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Abstract

The (001)-TiO2 (001 crystal plane-oriented titanium oxide) nanoparticles was precipitated on the surface of as-prepared graphitic carbon nitride (g-C3N4) and the composites with heterogeneous structures were manufactured. Methylene blue (MB) as the target pollutant was used to evaluate the performance of the composite photocatalysts. The decrease of the band gap, suppression of electron–hole recombination and the increased specific surface area of the composites enhance the the photocatalytic degradation performance. The mass ratio of (001)-TiO2 and g-C3N4 in the composites with the best degradation performance for MB was found to be 1:5, which was denoted as TCN2. The rate for MB to be degraded after exposure to light for 60 min was 95% by TCN2. The degradation rate constant k of TCN2 is 0.0442 min−1, which is 7 times that of (001)-TiO2 and 4 times that of g-C3N4. After four rounds of photocatalytic experiments, the photocatalytic efficiency of TCN2 remains at a high level. The composition and microstructure of the materials were characterized by XRD, XPS, FTIR, SEM, TEM, and BET. The optical properties and degradation mechanism of the material were investigated by PL, DRS, PEC, EIS, and active substance capture experiments. The mechanism of MB photocatalytic degradation was proposed.

Abstract Image

(001)-TiO2/g-C3N4异质结的构建增强光催化降解亚甲基蓝
将(001)-TiO2(001晶面取向氧化钛)纳米颗粒沉淀在制备好的石墨氮化碳(g-C3N4)表面,制备出具有非均相结构的复合材料。以亚甲基蓝(MB)为目标污染物,对复合光催化剂的性能进行了评价。带隙的减小、电子-空穴复合的抑制以及复合材料比表面积的增加都提高了光催化降解性能。发现复合材料中(001)-TiO2与g-C3N4的质量比为1:5,表征为TCN2,降解MB性能最佳。TCN2在光照60 min后对MB的降解率为95%。TCN2的降解速率常数k为0.0442 min−1,是(001)-TiO2的7倍,g-C3N4的4倍。经过四轮光催化实验,TCN2的光催化效率保持在较高水平。采用XRD、XPS、FTIR、SEM、TEM、BET等表征了材料的组成和微观结构。通过PL、DRS、PEC、EIS和活性物质捕获实验研究了材料的光学性质和降解机理。提出了MB光催化降解的机理。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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