光催化
X射线光电子能谱
制氢
材料科学
漫反射红外傅里叶变换
锐钛矿
介电谱
高分辨率透射电子显微镜
光谱学
透射电子显微镜
化学工程
纳米复合材料
可见光谱
催化作用
漫反射
光化学
电化学
纳米技术
化学
光电子学
光学
电极
物理化学
生物化学
物理
量子力学
工程类
作者
N. Lakshmana Reddy,Saim Emin,Matjaž Valant,M.V. Shankar
标识
DOI:10.1016/j.ijhydene.2016.12.154
摘要
Abstract Here we report on Bi2O3 clusters immobilized on anatase TiO2 nanostructures for an enhanced rate of photocatalytic H2 evolution. Structural, morphological, and optical properties of the Bi2O3@TiO2 nanocomposite (BT) were characterized by a series of techniques including X-ray diffraction, high resolution transmission electron microscopy, X-ray photoelectron spectroscopy, diffuse reflectance spectroscopy and electrochemical impedance spectroscopy. The catalytic H2 evolution experiments were carried out under different light sources: natural solar light, LED UV (365 ± 5 nm) and LED visible (420 ± 5 nm) light source. Under the solar light a pristine anatase TiO2 nanostructured (TNS) catalyst generated 4.20 mmol h−1 g−1, whereas in the presence of Bi2O3@TNS showed much higher H2 production 26.02 mmol h−1 g−1. The photocatalytic activity of the BT and its reproducible performance for five recycles is ascribed to an efficient separation of photogenerated charge carriers. A plausible reaction mechanism for the H2 generation is proposed.
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