光催化
X射线光电子能谱
材料科学
异质结
罗丹明B
吸附
带隙
可见光谱
分析化学(期刊)
化学工程
纳米技术
光化学
光电子学
化学
物理化学
有机化学
工程类
催化作用
作者
Gylen Odling,Neil Robertson
出处
期刊:ChemPhysChem
[Wiley]
日期:2016-07-29
卷期号:17 (18): 2872-2880
被引量:40
标识
DOI:10.1002/cphc.201600443
摘要
Abstract Composite photocatalyst films have been fabricated by depositing BiVO 4 upon TiO 2 via a sequential ionic layer adsorption reaction (SILAR) method. The photocatalytic materials were investigated by XRD, TEM, UV/Vis diffuse reflectance, inductively coupled plasma optical emission spectrometry (ICP‐OES), XPS, photoluminescence and Mott–Schottky analyses. SILAR processing was found to deposit monoclinic‐scheelite BiVO 4 nanoparticles onto the surface, giving successive improvements in the films′ visible light harvesting. Electrochemical and valence band XPS studies revealed that the prepared heterojunctions have a type II band structure, with the BiVO 4 conduction band and valence band lying cathodically shifted from those of TiO 2 . The photocatalytic activity of the films was measured by the decolourisation of the dye rhodamine 6G using λ >400 nm visible light. It was found that five SILAR cycles was optimal, with a pseudo‐first‐order rate constant of 0.004 min −1 . As a reference material, the same SILAR modification has been made to an inactive wide‐band‐gap ZrO 2 film, where the mismatch of conduction and valence band energies disallows charge separation. The photocatalytic activity of the BiVO 4 –ZrO 2 system was found to be significantly reduced, highlighting the importance of charge separation across the interface. The mechanism of action of the photocatalysts has also been investigated, in particular the effect of self‐sensitisation by the model organic dye and the ability of the dye to inject electrons into the photocatalyst′s conduction band.
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