Enhancing Charge Carrier Lifetime in Metal Oxide Photoelectrodes through Mild Hydrogen Treatment

Ji-Wook Jang, Dennis Friedrich, Sönke Müller, Marlene Lamers, Hannes Hempel, Sheikha F. Lardhi, Zhen Cao, Moussab Harb, Luigi Cavallo, René Heller, Rainer Eichberger, Roel van de Krol, Fatwa F. Abdi

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110 Scopus citations


Widespread application of solar water splitting for energy conversion is largely dependent on the progress in developing not only efficient but also cheap and scalable photoelectrodes. Metal oxides, which can be deposited with scalable techniques and are relatively cheap, are particularly interesting, but high efficiency is still hindered by the poor carrier transport properties (i.e., carrier mobility and lifetime). Here, a mild hydrogen treatment is introduced to bismuth vanadate (BiVO4), which is one of the most promising metal oxide photoelectrodes, as a method to overcome the carrier transport limitations. Time-resolved microwave and terahertz conductivity measurements reveal more than twofold enhancement of the carrier lifetime for the hydrogen-treated BiVO4, without significantly affecting the carrier mobility. This is in contrast to the case of tungsten-doped BiVO4, although hydrogen is also a donor type dopant in BiVO4. The enhancement in carrier lifetime is found to be caused by significant reduction of trap-assisted recombination, either via passivation or reduction of deep trap states related to vanadium antisite on bismuth or vanadium interstitials according to density functional theory calculations. Overall, these findings provide further insights on the interplay between defect modulation and carrier transport in metal oxides, which benefit the development of low-cost, highly-efficient solar energy conversion devices.
Original languageEnglish (US)
Pages (from-to)1701536
JournalAdvanced Energy Materials
Issue number22
StatePublished - Aug 25 2017

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: This research was supported by the PECDEMO project (cofunded by Europe's Fuel Cell and Hydrogen Joint Undertaking under Grant Agreement no. 621252) and the German Bundesministerium für Bildung und Forschung (BMBF), project “MeOx4H2” (03SF0478A). Parts of this research were carried out at IBC at Helmholtz-Zentrum Dresden-Rossendorf e.V., a member of the Helmholtz Association. The authors thank Dr. Klaus Ellmer and Karsten Harbauer for the assistance in the electrical conductivity measurements.


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