固溶体
光催化
催化作用
带隙
硫化镉
材料科学
纳米颗粒
晶体结构
化学工程
硫化锌
Crystal(编程语言)
纳米技术
锌
结晶学
化学
冶金
光电子学
生物化学
程序设计语言
计算机科学
工程类
作者
Luis Fernando Morelos Medina,R. Nava,María de los Ángeles Cuán Hernández,Omar Said Yáñez Soria,B. Pawelec,R.M. Navarro,Carlos Gutierrez
出处
期刊:Energies
[Multidisciplinary Digital Publishing Institute]
日期:2020-10-26
卷期号:13 (21): 5603-5603
被引量:8
摘要
A simple ultrasonic radiation method was employed for the preparation of zinc and cadmium sulfide solid solution (ZnxCd1−xS; x = 0–0.25 wt.%) with the aim to investigate its efficiency for H2 production via a visible light-driven water-splitting reaction. The catalyst characterization by X-ray diffraction confirmed the formation of solid solution (ZnxCd1−xS) between CdS and ZnS phases. All catalysts exhibited hierarchical morphology (from SEM and TEM) formed by aggregated nanoparticles of ZnxCd1−xS solid solution with crystals showing mainly (111) planes of cubic CdS phase. The crystal size linearly decreased with an increase in Zn incorporation in the crystal lattice (from 4.37 nm to 3.72 nm). The ZnxCd1−xS photocatalysts showed a gradual increase in the H2 evolution, with an increase in the Zn concentration up to 0.2 wt.% making the most effective Zn0.2Cd0.8S catalyst toward H2 production. From the catalyst activity–structure correlation, it has been concluded that the twin-like CdS structure, the (111) plane and specific morphology are the main factors influencing the catalyst effectivity toward H2 production. All those factors compensated for the negative effect of an increase in band gap energy (Ebg) after ZnS incorporation into solid solution (from 2.21 eV to 2.34 eV). The effect of the catalyst morphology is discussed by comparing H2 evolution over unsupported and supported Zn0.2Cd0.8S solid solutions.
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