Liu Hong, Jin Zhitong, Xu Zhengzheng
Department of Chemical Engineering, School of Environmental and Chemical Engineering, Shanghai University, 99 Shangda Road, Shanghai 200444, P R China.
Dalton Trans. 2015 Aug 28;44(32):14368-75. doi: 10.1039/c5dt01364j.
Novel visible-light-driven Cd0.2Zn0.8S/g-C3N4 inorganic-organic composite photocatalysts were synthesized by a facile hydrothermal method. The prepared Cd0.2Zn0.8S/g-C3N4 composites were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), ultraviolet-visible diffuse reflection spectroscopy (DRS), photoluminescence (PL) spectroscopy and photoelectrochemical (PEC) experiments. Under visible-light irradiation, Cd0.2Zn0.8S/g-C3N4 photocatalysts displayed a higher photocatalytic activity than pure g-C3N4 and Cd0.2Zn0.8S for hydrogen evolution and degradation of pollutants, and the optimal g-C3N4 content was 20 wt%. The optimal composite showed a hydrogen evolution rate of 208.0 μmol h(-1). The enhancement of the photocatalytic activity should be attributed to the well-matched band structure and intimate contact interfaces between Cd0.2Zn0.8S and g-C3N4, which lead to the effective transfer and separation of the photogenerated charge carriers. Furthermore, the Cd0.2Zn0.8S/g-C3N4 photocatalysts showed excellent stability during photocatalytic hydrogen evolution and degradation of pollutants.
通过简便的水热法合成了新型可见光驱动的Cd0.2Zn0.8S/g-C3N4无机-有机复合光催化剂。采用X射线衍射(XRD)、X射线光电子能谱(XPS)、傅里叶变换红外光谱(FT-IR)、透射电子显微镜(TEM)、高分辨率透射电子显微镜(HRTEM)、紫外-可见漫反射光谱(DRS)、光致发光(PL)光谱和光电化学(PEC)实验对制备的Cd0.2Zn0.8S/g-C3N4复合材料进行了表征。在可见光照射下,Cd0.2Zn0.8S/g-C3N4光催化剂在析氢和污染物降解方面表现出比纯g-C3N4和Cd0.2Zn0.8S更高的光催化活性,最佳g-C3N4含量为20 wt%。最佳复合材料的析氢速率为208.0 μmol h(-1)。光催化活性的提高应归因于Cd0.2Zn0.8S和g-C3N4之间匹配良好的能带结构和紧密的接触界面,这导致了光生电荷载流子的有效转移和分离。此外,Cd0.2Zn0.8S/g-C3N4光催化剂在光催化析氢和污染物降解过程中表现出优异的稳定性。