光催化
X射线光电子能谱
材料科学
高分辨率透射电子显微镜
可见光谱
光致发光
载流子
异质结
扫描电子显微镜
纳米结构
漫反射红外傅里叶变换
光谱学
制氢
吸收(声学)
透射电子显微镜
光电子学
光化学
纳米技术
氢
化学工程
化学
催化作用
有机化学
物理
量子力学
工程类
复合材料
作者
K. Mallikarjuna,P. Reddy Prasad,Chinna Bathula,Nadavala Siva Kumar,Ahmed S. Al‐Fatesh,Hyun‐Seok Kim,Cheolho Bai,I. Neelakanta Reddy
标识
DOI:10.1016/j.inoche.2023.111619
摘要
The fabrication of efficient photocatalytic organization by the designfor enhanced photocatalytic productivity for produding hydrogen is exceptionally thought-provoking. To address this issue herein we have fabricated the CuS/CdS heterostructures by ultrasonication for photocatalytic H2 production. The structural integrity of the produced heterostructure is confirmed by the analytical tools such as X-ray diffraction studies (XRD), Ultraviolet–Visible Diffuse Reflectance Spectroscopy (UV–vis DRS), scanning electron microscopy (SEM), High-Resolution Transmission Electron Microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). The fabricated CuS/CdS sample exhibited the highest H2 production rate (824 μmol/g) than CuS (67 μmol/g) and CdS (135 μmol/g) under simulated solar illumination. The hydrogen output is noticeably improved due to improved absorption of visible light and competent charge carrier partition. It was confirmed by UV–vis diffuse reflectivity and photoluminescence spectra as charge carrier parting was effective as absorption of visible light was enhanced. A plausible photocatalytic H2 reaction mechanism has been elucidated from increased charge carrier division and visible light absorptivity. This work depicts a new approach for greatly resourceful nano architecture for energy-related applications.
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