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采用连续离子层吸附反应法制备的用于染料降解的BiVO4-TiO2复合光催化剂。

BiVO4 -TiO2 Composite Photocatalysts for Dye Degradation Formed Using the SILAR Method.

作者信息

Odling Gylen, Robertson Neil

机构信息

School of Chemistry, University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh, EH9 3FJ, Scotland.

出版信息

Chemphyschem. 2016 Sep 19;17(18):2872-80. doi: 10.1002/cphc.201600443. Epub 2016 Jul 29.

DOI:10.1002/cphc.201600443
PMID:27257947
Abstract

Composite photocatalyst films have been fabricated by depositing BiVO4 upon TiO2 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 BiVO4 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 BiVO4 conduction band and valence band lying cathodically shifted from those of TiO2 . 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 ZrO2 film, where the mismatch of conduction and valence band energies disallows charge separation. The photocatalytic activity of the BiVO4 -ZrO2 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.

摘要

通过连续离子层吸附反应(SILAR)法在TiO₂上沉积BiVO₄制备了复合光催化剂薄膜。通过X射线衍射(XRD)、透射电子显微镜(TEM)、紫外/可见漫反射、电感耦合等离子体发射光谱(ICP-OES)、X射线光电子能谱(XPS)、光致发光和莫特-肖特基分析对光催化材料进行了研究。发现SILAR工艺可将单斜白钨矿型BiVO₄纳米颗粒沉积在表面,从而使薄膜的可见光捕获能力不断提高。电化学和价带XPS研究表明,所制备的异质结具有II型能带结构,BiVO₄的导带和价带相对于TiO₂的导带和价带发生了阴极位移。通过使用波长大于400 nm的可见光使罗丹明6G染料脱色来测量薄膜的光催化活性。发现五个SILAR循环是最佳的,其假一级反应速率常数为0.004 min⁻¹。作为参考材料,对无活性的宽带隙ZrO₂薄膜进行了相同的SILAR改性,其中导带和价带能量不匹配,不允许电荷分离。发现BiVO₄-ZrO₂体系的光催化活性显著降低,突出了界面电荷分离的重要性。还研究了光催化剂的作用机制,特别是模型有机染料的自敏化作用以及染料将电子注入光催化剂导带的能力。

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