Directly Photoexcited Oxides for Photoelectrochemical Water Splitting.

Pan L; Vlachopoulos N; Hagfeldt A

doi:10.1002/cssc.201900849

Back

Journal article

Directly Photoexcited Oxides for Photoelectrochemical Water Splitting.

Pan L Laboratory of Photomolecular Science, Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology in Lausanne (EPFL), 1015, Lausanne, Switzerland.
Vlachopoulos N Laboratory of Photomolecular Science, Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology in Lausanne (EPFL), 1015, Lausanne, Switzerland.
Hagfeldt A Laboratory of Photomolecular Science, Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology in Lausanne (EPFL), 1015, Lausanne, Switzerland.

2019-09-04

Published in:

ChemSusChem. - 2019

English Artificial photosynthesis promises to become a sustainable way to harvest solar energy and store it in chemical fuels by means of photoelectrochemical (PEC) cells. Although it is intriguing to shift the fossil-fuel-based economy to a renewable carbon-neutral one, which will alleviate environmental problems, there is still a long way to go before it rivals traditional energy sources. Existing solar water-splitting devices can be sorted into three categories: photovoltaic-powered electrolysis, PEC water splitting, and photocatalysis (PC). PEC and PC systems hold the potential to further reduce the cost of devices due to their simple structures in which photoabsorbers and catalysts are closely integrated. PC is expected to be the least expensive approach; however, additional costs and concerns are brought about by the subsequent explosive gas separation. At the heart of all devices, semiconductor photoabsorbers should be efficient, robust, and cheap to satisfy the strict requirements on the market. Therefore, this Review intends to give readers an overview on PEC water splitting, with an emphasis on oxide material-based devices, which hold the potential to support global-scale production in the future.

Language