Issue 2, 2016

Photoinduced charge transfer processes in solar photocatalysis based on modified TiO2

Abstract

High efficiency solar photocatalysis requires an effective separation of photogenerated charge carriers and their rapid transport to the semiconductor interface. The mechanisms and kinetics of charge separation and interfacial/interparticle charge transfers (CT) are significantly influenced by both the bulk and surface properties of the semiconductor. The surface properties are particularly important because the photocatalysis should be driven by the interfacial CT. The most popular and the most investigated semiconductor photocatalyst is based on bare and modified TiO2. This article highlights the interfacial and interparticle CTs under the bandgap excitation of TiO2 particles, visible light-induced photochemical processes via either dye-sensitization or ligand-to-metal CTs at surface modified TiO2 particles, and the applications of the photo-processes to pollutant degradation and simultaneous hydrogen production. While a variety of surface modification techniques using various nanomaterials and chemical reagents have been developed and tested so far, their effects are very diverse depending on the characteristics of the applied photocatalytic systems and even contradictory in some cases. Better understanding of how the modification influences the photoinduced CT events in semiconductors is required, particularly for designing hybrid photocatalysts with controlled CTs, which is sought-after for practical applications of photocatalysis.

Graphical abstract: Photoinduced charge transfer processes in solar photocatalysis based on modified TiO2

Article information

Article type
Perspective
Submitted
20 Aug 2015
Accepted
01 Dec 2015
First published
01 Dec 2015
This article is Open Access
Creative Commons BY-NC license

Energy Environ. Sci., 2016,9, 411-433

Author version available

Photoinduced charge transfer processes in solar photocatalysis based on modified TiO2

H. Park, H. Kim, G. Moon and W. Choi, Energy Environ. Sci., 2016, 9, 411 DOI: 10.1039/C5EE02575C

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