Li Xia, Wang Bo, Shu Xia, Wang Dongmei, Xu Guangqing, Zhang Xinyi, Lv Jun, Wu Yucheng
School of Material Sciences and Engineering, Hefei University of Technology Hefei 230009 China
Guangxi Key Laboratory for Electrochemical Energy Materials, Guangxi University Nanning 530004 China.
RSC Adv. 2019 May 21;9(28):15900-15909. doi: 10.1039/c8ra09806a. eCollection 2019 May 20.
In this work, an MoS /g-CN composite photocatalyst was successfully fabricated by a sonochemical approach, where amorphous MoS was synthesized using a hydrothermal method with NaMoO·HO, HSiO(WO) and CHCSNH as precursors, and g-CN nanosheets were produced using a two-step thermal polycondensation method. The hydrogen-evolution performance of the MoS /g-CN composite was tested under visible light. The results show that the H-evolution rate of the MoS /g-CN (7 wt%) photocatalyst reaches a maximum value of 1586 μmol g h, which is about 70 times that of pure g-CN nanosheets. The main reason is that amorphous MoS forms intimate heterojunctions with g-CN nanosheets, and the introduction of MoS into g-CN nanosheets not only enhances the ability to convert H into H, but also promotes the separation of photoinduced electron-hole pairs for the photocatalyst. BET analysis shows that the specific surface area and pore volume of g-CN are decreased in the presence of MoS . XPS analysis manifests that MoS provides a number of active sites. Mott-Schottky plots show that the conduction band of MoS (-0.18 V , pH = 7) is more negative than that of g-CN nanosheets.
在本工作中,通过超声化学方法成功制备了一种MoS₂/g-C₃N₄复合光催化剂,其中采用水热法以Na₂MoO₄·2H₂O、H₂SiO₃(WO₃)和CH₃CSNH为前驱体合成非晶态MoS₂,并用两步热缩聚法制备g-C₃N₄纳米片。在可见光下测试了MoS₂/g-C₃N₄复合材料的析氢性能。结果表明,MoS₂/g-C₃N₄(7 wt%)光催化剂的析氢速率达到最大值1586 μmol g⁻¹ h⁻¹,约为纯g-C₃N₄纳米片的70倍。主要原因是无定形MoS₂与g-C₃N₄纳米片形成紧密的异质结,并且将MoS₂引入g-C₃N₄纳米片中不仅增强了将H⁺转化为H₂的能力,还促进了光催化剂光生电子-空穴对的分离。BET分析表明,在存在MoS₂的情况下,g-C₃N₄的比表面积和孔体积减小。XPS分析表明,MoS₂提供了许多活性位点。莫特-肖特基曲线表明,MoS₂(-0.18 V vs. NHE,pH = 7)的导带比g-C₃N₄纳米片的导带更负。