4.6 Review

Recent Advances in TiO2-based Photoanodes for Photoelectrochemical Water Splitting

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 17, Issue 20, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.202200668

Keywords

charge transport; photoanode; photoelectrocatalysi; TiO(2)s; water splitting

Funding

  1. National Natural Science Foundation of China (NSFC) [51972318]
  2. Natural Science Foundation of Shanghai [19ZR1479300]

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This review focuses on the application of TiO2-based photoanodes in PEC water splitting. TiO2 exhibits high PEC water splitting performance, but its performance is hindered by certain disadvantages. The review highlights the mechanisms and key factors for achieving high solar-to-hydrogen conversion efficiency, as well as controllable synthesis and modification strategies. The future trends for TiO2-based photoanodes in PEC water splitting are also discussed.
Photoelectrochemical (PEC) water splitting has attracted great attention in the past several decades as it holds great promise to address global energy and environmental issues by converting solar energy into hydrogen. However, its low solar-to-hydrogen (STH) conversion efficiency remains a bottleneck for practical application. Developing efficient photoelectrocatalysts with high stability and high STH conversion efficiency is one of the key challenges. As a typical n-type semiconductor, titanium dioxide (TiO2) exhibits high PEC water splitting performance, especially high chemical and photo stability. But, TiO2 has also disadvantages such as wide band gap and fast electron-hole recombination rate, which seriously hinder its PEC performance. This review focuses on recent development in TiO2-based photoanodes as well as some key fundamentals. The corresponding mechanisms and key factors for high STH, and controllable synthesis and modification strategies are highlighted in this review. We conclude finally with an outlook providing a critical perspective on future trends on TiO2-based photoanodes for PEC water splitting.

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