Remarkable Enhancement of Photocatalytic Activity of High-Energy TiO2 Nanocrystals for NO Oxidation through Surface Defluorination

材料科学 光催化 纳米晶 单线态氧 氢氟酸 吸附 煅烧 激进的 光化学 纳米技术 试剂 傅里叶变换红外光谱 氧气 漫反射红外傅里叶变换 化学工程 无机化学 催化作用 有机化学 化学 冶金 工程类
作者
Xiaofeng Wu,Jie Zhou,Qiuyan Tan,Kaining Li,Qin Li,Sónia A. C. Carabineiro,Kangle Lv
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (9): 11479-11488 被引量:6
标识
DOI:10.1021/acsami.3c16994
摘要

The superior photocatalytic activity of TiO2 nanocrystals with exposed high-energy (001) facets, achieved through the use of hydrofluoric acid as a shape-directing reagent, is widely reported. However, in this study, we report for the first time the detrimental effect of surface fluorination on the photoreactivity of high-energy faceted TiO2 nanocrystals towards NO oxidation (resulting in a NO removal rate of only 5.9%). This study aims to overcome this limitation by exploring surface defluorination as an effective strategy to enhance the photocatalytic oxidation of NO on TiO2 nanocrystals enclosed with (001) facets. We found that surface defluorination, achieved through either NaOH washing (resulting in an improved NO removal rate of 23.2%) or calcination (yielding an enhanced NO removal rate of 52%), leads to a large increase in the photocatalytic oxidation of NO on TiO2 nanocrystals with enclosed (001) facets. Defluorination processes stimulate charge separation, effectively retarding recombination and significantly promoting the production of reactive oxygen species, including superoxide radicals (·O2–), singlet oxygen (1O2), and hydroxyl radicals (·OH). Both in situ diffuse reflectance infrared Fourier-transform spectroscopy and density functional theory calculations confirm the higher adsorption of NO after defluorination, thus facilitating the oxidation of NO on TiO2 nanocrystals.
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