Electrostatically charged rutile TiO2 surfaces with enhanced photocatalytic activity for bacteria inactivation

光催化 吸附 金红石 甲基橙 开尔文探针力显微镜 氧化钛 亚甲蓝 化学工程 材料科学 表面电荷 接触角 粘附 化学 纳米技术 光化学 催化作用 原子力显微镜 有机化学 物理化学 复合材料 工程类
作者
Alejandra Romero-Morán,Anai Zavala-Franco,Jose Luis Sanchez-Salas,Miguel Ángel Méndez-Rojas,Joel Molina-Reyes
出处
期刊:Catalysis Today [Elsevier BV]
卷期号:392-393: 154-166 被引量:2
标识
DOI:10.1016/j.cattod.2022.01.002
摘要

In this work, the fabrication of a series of rutile-TiO 2 films with different submicron thicknesses supported on thermally grown SiO 2 is proposed. The aim is to determine the correlation between the generation of a positively charged TiO 2 surface, caused by the presence of dipoles formed at the TiO 2 /SiO 2 interface, with E. coli attraction. This electrostatic interaction leads to an improvement in the photocatalytic antibacterial activity. The positively charged TiO 2 surface formation was confirmed by Kelvin Probe Force Microscopy, E. coli adhesion tests, molecular docking, methylene blue, and methyl orange adsorption experiments. This effect on the photocatalytic surface of R-TiO 2 could favor the adsorption and degradation of negatively charged substances, as well as most of the pathogenic bacteria and viruses. • The fabrication of a series of rutile-TiO 2 films with different thicknesses on thermally grown SiO 2 was performed. • The generation of a positively charged TiO 2 surface caused by the presence of dipoles formed at the TiO 2 /SiO 2 was studied. • A correlation between the generation of a positively charged TiO 2 surface with E. coli attraction was determined. • KPFM, molecular docking E. coli and dyes adsorption experiments confirmed the formation of positively charged TiO 2 surface.

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