光催化
罗丹明B
材料科学
可见光谱
甲基橙
X射线光电子能谱
贵金属
光电流
漫反射红外傅里叶变换
扫描电子显微镜
光化学
异质结
透射电子显微镜
金属
纳米技术
光电子学
化学
化学工程
催化作用
冶金
生物化学
复合材料
工程类
作者
Tingjiang Yan,Hongwen Zhang,Yuping Liu,Wenfei Guan,Jinlin Long,Wenjuan Li,Jinmao You
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2014-08-04
卷期号:4 (70): 37220-37220
被引量:67
摘要
M/Ag3PO4 (M = Pt, Pd, Au) Schottky-type heterostructures were successfully fabricated by a chemical deposition route using NaBH4 as a reduction agent. The structure and optical properties of the as-synthesized samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectroscopy, and electrochemical techniques. The photocatalytic activity was evaluated by the decomposition of dyes (methyl orange, methylene blue, and rhodamine B) under visible light irradiation (λ > 420 nm). These noble metals as nanoparticles were highly dispersed on the surface of Ag3PO4 polyhedrons. The light absorption of Ag3PO4 in both the UV and visible regions was extensively increased upon noble metal deposition. The photocurrent response over M/Ag3PO4 electrodes was much higher than that of pure Ag3PO4 and followed the decreased order of Pt > Pd > Au. The metallic nanoparticles deposited on Ag3PO4 could promote the transfer of photo-generated electrons, which not only inhibited the recombination of electrons and holes effectively, but also suppressed the photocorrosion of Ag3PO4, leading to a significant increase in photocatalytic activity and stability. On the basis of radical-trapping experiments and the PL technique, h+ and ˙O2− were well-established to correspond to the quick photo-degradation of dyes and a possible mechanism was proposed.
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