Abstract

Although titanium dioxide gathers many of the required properties for its application in photocatalytic processes, its lack of activity in the visible range is a major hurdle yet to be overcome. Among different strategies, the post-synthesis modification of TiO2 powders with organic compounds has already led to commercially available materials, such as KRONOClean 7000. In this work, we apply diffuse reflectance transient absorption spectroscopy on this visible-light active photocatalyst and study the dynamics of the charge carriers alternatively induced by UV or visible light laser irradiation, under inert or reactive atmospheres. Our results can be interpreted by considering the material as TiO2 sensitized by an organic-based layer, in agreement with previous studies on it, and show that the oxidative power of the material is considerably diminished under visible light irradiation. By complementarily performing continuous visible light irradiation photocatalysis experiments in aerated aqueous suspensions, we show that, although the oxidation of methanol proceeds at a very slow rate, the oxidation of chlorpromazine occurs much faster thanks to its better suited redox potential.

Highlights

  • In 1972, Fujishima and Honda reported the photocatalytic splitting of water over titanium dioxide (TiO2 ) photoelectrodes irradiated with UV light [1]

  • We notecation that chlorpromazine oxidation under irradiation of K-7000 experiments has been the subject a recent absorption spectroscopy measurements evince a prompt degradation of chlorpromazine and a study [36] and, we focused here on its visible light degradation

  • We studied the reactivity upon UV and visible light irradiation of the commercially available photocatalyst KRONOClean 7000

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Summary

Introduction

In 1972, Fujishima and Honda reported the photocatalytic splitting of water over titanium dioxide (TiO2 ) photoelectrodes irradiated with UV light [1] Since this discovery, much work has been done to understand the underlying processes in photocatalytic reactions [2] and develop new materials with activity in the visible range [3]. Much work has been done to understand the underlying processes in photocatalytic reactions [2] and develop new materials with activity in the visible range [3] Despite these efforts, TiO2 continues to be the most employed photocatalyst, in particular in its anatase polymorph, due to its higher activity in comparison with the thermodynamically stable form rutile [4,5].

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