Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 7, Issue 33, Pages 18429-18434Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b04521
Keywords
spontaneous hydrogen evolution; water splitting; tandem cell; TiO2 nanotube
Funding
- NRF of Korea Grant - Ministry of Science, ICT & Future Planning [NRF-2013R1A2A1A09014038, 2011-0030254]
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Vertically aligned one-dimensional (1D) titanium dioxide (TiO2) arrays on transparent conducting oxide (TCO) substrates, which can act as host electron transport materials for low bandgap materials, were synthesized via a hydrothermal reaction combined with a controlled chemical etching process. By controlling the chemical etching conditions, we can maximize the light transmission properties of the 1D TiO2 arrays, which is beneficial for the front electrode in photoelectrochemical (PEG) tandem configurations. As a result, dual sensitization to form 1D TiO2@ CdS@CdSe (CdS and CdSe coated 1D TiO2) results in excellent photocurrent density, as well as transparency, and the resulting material is able to pass unabsorbed photons through the front electrode into the rear bias solar cell. Owing to the improved light transmission in combination with the increased specific surface area of the obtained 1D TiO2 arrays from the controlled etching process, a high-efficiency PEG tandem device with similar to 2.1% was successfully fabricated for unassisted hydrogen evolution. Efficient PEG tandem device was fabricated for unassisted solar hydrogen generation using highly transparent composite electrode composed of dual sensitization to form 1D TiO2@CdS@CdSe.
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