富氧空位ZnO对亚甲基蓝的敏化作用

A. Ranjbari, Ju Ho Kim, Jiyun Kim, Ji-Hui Yu, P. Heynderickx
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引用次数: 0

摘要

金属氧化物光催化剂作为一种绿色环境修复技术受到了广泛的关注。氧化锌具有良好的电子性能、低成本、低毒性以及能完全矿化有机污染物等优点,是一种广受欢迎的半导体光催化剂。然而,ZnO的缺点,如高的电子-空穴复合率和宽的带隙来收集可见光,限制了ZnO的应用[1]。克服金属氧化物限制的一种可能方法是在纳米颗粒表面提供氧空位(OV)。OVs可以捕获光产生的电子,它们可以作为吸附位点,在那里被激发的电子可以转移到被吸附的化合物上。因此,OVs的存在将通过减少电子-空穴复合来增强光催化降解[2]。在本研究中,通过程序升温还原(TPR)方法获得了富集的OVs ZnO。为此,在10% h2 /Ar的流量下,以10°C/min的斜坡速率加热到500°C。通过TPR、TPO、PCO、XPS、XRD、PL、EPR、FE-SEM、TEM、BET和tac图等表征分析研究了OVs的形成。商用氧化锌(C-ZnO)的吸附性能及光催化活性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methylene Blue Sensitization by Enriched Oxygen Vacancy ZnO
Metal oxide photocatalysts have gained special attention as a green technology for environmental remediation. Zinc oxide is a popular semiconductor photocatalyst due to its electronic properties, low cost and toxicity, and the ability to mineralize organic pollutants completely. However, disadvantages such as a high rate of electron-hole recombination, and a wide bandgap for harvesting visible light, limit the application of ZnO [1]. One of the possible methods to overcome the metal oxide limitations is providing oxygen vacancies (OV) at the surface of the nanoparticles. OVs can trap the photo-generated electrons and they can act as an adsorption site, where the excited electron can transfer to the adsorbed compound. Hence, the presence of OVs will enhance photocatalytic degradation by reducing the electron-hole recombination [2]. In this study, the enriched OVs ZnO were provided by a temperature-programmed reduction (TPR) method. To this aim, commercial ZnO was heated by a ramp rate of 10°C/min to 500°C in a flow of 10% H 2 /Ar. The formation of OVs was investigated by several characterization analyses such as TPR, TPO, PCO, XPS, XRD, PL, EPR, FE-SEM, TEM, BET, and Tauc plot. The adsorption capacity and photocatalytic activity of commercial ZnO (C-ZnO
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