Preparation of a highly active MoS2/TiO2 composite for photocatalytic oxidation of nitrite under solar irradiation

被引:9
|
作者
Cao, Huazhen [1 ]
Jia, Chenxi [1 ]
Zhang, Huibin [1 ]
Hou, Guangya [1 ]
Tang, Yiping [1 ]
Zheng, Guoqu [1 ]
机构
[1] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Peoples R China
关键词
TIO2; MOS2; REDUCTION; CO2; DEGRADATION; PERFORMANCE; REMOVAL; FILMS;
D O I
10.1039/d1nj00707f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MoS2/TiO2 composite photocatalysts with visible-light activity were in situ fabricated on titanium substrates via a simple two-step hydrothermal synthesis method, using titanium foil as the Ti source. The structure, morphology, composition and optical properties of the as-prepared photocatalysts were characterized by XRD, SEM, TEM, XPS, UV-vis and PL analyses, respectively. TiO2 exists in the form of nanofibers (NFs), with their length ranging from about 40 nm to 150 nm and a diameter of about 10 nm. MoS2 microspheres are homogeneously dispersed on the surface of TiO2 NFs, forming a MoS2/TiO2 composite. The photocatalytic oxidation rate of NO2- under simulated solar irradiation can reach 62% by the MoS2/TiO2 composite synthesized in a hydrothermal system with a C2H5NS/Na2MoO4 molar ratio of 1 : 0.6 under 200 degrees C for 24 h, which is much higher than that by pristine TiO2 NFs, P25 and pure MoS2. The photocatalytic oxidation process of NO2- obeys the Langmuir-Hinshelwood kinetic model (pseudo-first order reaction), and the reaction rate constant (k) of the as-prepared composite is about 0.19194 h(-1). The presence of MoS2 significantly enhances the visible light absorption of the catalyst, which is conducive to the generation of electrons and holes, thus guaranteeing good photoactivity of the catalyst. The band gap of the composite is about 2.2 eV, indicating the enhanced absorption of visible light. By this simple and low-consumption method, the composite is firmly combined with the titanium substrate, which is convenient for recycling and environmentally friendly implementation.
引用
收藏
页码:10608 / 10617
页数:10
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