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Cd0.2Zn0.8S与g-C3N4纳米片的杂化:一种用于光催化水制氢及有机污染物降解的可见光驱动光催化剂。

Hybridization of Cd0.2Zn0.8S with g-C3N4 nanosheets: a visible-light-driven photocatalyst for H2 evolution from water and degradation of organic pollutants.

作者信息

Liu Hong, Jin Zhitong, Xu Zhengzheng

机构信息

Department of Chemical Engineering, School of Environmental and Chemical Engineering, Shanghai University, 99 Shangda Road, Shanghai 200444, P R China.

出版信息

Dalton Trans. 2015 Aug 28;44(32):14368-75. doi: 10.1039/c5dt01364j.

Abstract

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.

摘要

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。

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