Monolithic Photoelectrochemical Device for Direct Water Splitting with 19% Efficiency
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Authors
Cheng, WH
Richter, MH
May, MM
Ohlmann, J
Lackner, D
Dimroth, F
Hannappel, T
Lewerenz, HJ
Publication Date
2018Journal Title
ACS Energy Letters
ISSN
2380-8195
Publisher
American Chemical Society (ACS)
Volume
3
Issue
8
Pages
1795-1800
Type
Article
Metadata
Show full item recordCitation
Cheng, W., Richter, M., May, M., Ohlmann, J., Lackner, D., Dimroth, F., Hannappel, T., et al. (2018). Monolithic Photoelectrochemical Device for Direct Water Splitting with 19% Efficiency. ACS Energy Letters, 3 (8), 1795-1800. https://doi.org/10.1021/acsenergylett.8b00920
Abstract
Recent rapid progress in efficiencies for solar water splitting by
photoelectrochemical devices has enhanced its prospects to enable storable
renewable energy. Efficient solar fuel generators all use tandem photoelectrode
structures, and advanced integrated devices incorporate corrosion protection
layers as well as heterogeneous catalysts. Realization of near thermodynamic
limiting performance requires tailoring the energy band structure of the
photoelectrode and also the optical and electronic properties of the surface
layers exposed to the electrolyte. Here, we report a monolithic device
architecture that exhibits reduced surface reflectivity in conjunction with
metallic Rh nanoparticle catalyst layers that minimize parasitic light
absorption. Additionally, the anatase TiO2 protection layer on the photocathode
creates a favorable internal band alignment for hydrogen evolution. An initial
solar-to-hydrogen efficiency of 19.3 % is obtained in acidic electrolyte and an
efficiency of 18.5 % is achieved at neutral pH condition (under simulated
sunlight).
Keywords
cond-mat.mtrl-sci, cond-mat.mtrl-sci
Identifiers
External DOI: https://doi.org/10.1021/acsenergylett.8b00920
This record's URL: https://www.repository.cam.ac.uk/handle/1810/285122
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