Regulating the surface of anion-doped TiO2 nanorods by hydrogen annealing for superior photoelectrochemical water oxidation

Dedications to achieve the highly efficient metal oxide semiconductor for the photoelectrochemical water splitting system have been persisted to utilize the TiO 2 as the promising photoanode material. Herein, we report notable progress for nanostructured TiO 2 photoanodes using facile sequential one...

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Veröffentlicht in:Nano convergence 2022-07, Vol.9 (1), p.33-14, Article 33
Hauptverfasser: Park, Jongseong, Lee, Seonyong, Lee, Tae Hyung, Kim, Changyeon, Jun, Sang Eon, Baek, Ji Hyun, Kim, Jae Young, Lee‬, Mi Gyoung, Ahn, Sang Hyun, Jang, Ho Won
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Sprache:eng
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Zusammenfassung:Dedications to achieve the highly efficient metal oxide semiconductor for the photoelectrochemical water splitting system have been persisted to utilize the TiO 2 as the promising photoanode material. Herein, we report notable progress for nanostructured TiO 2 photoanodes using facile sequential one-pot hydrothermal synthesis and annealing in hydrogen. A photocurrent density of 3.04 mA·cm −2 at 1.23 V vs. reversible hydrogen electrode was achieved in TiO 2 nanorod arrays annealed in hydrogen ambient, which is approximately 4.25 times higher than that of pristine TiO 2 annealed in ambient air. 79.2% of incident photon-to-current efficiency at 380 nm wavelength demonstrates the prominence of the material at the near-UV spectral range region and 100 h chronoamperometric test exhibits the stability of the photoanode. Detailed studies regarding crystallinity, bandgap, and elemental analysis provide the importance of the optimized annealing condition for the TiO 2 -based photoanodes. Water contact angle measurement displays the effect of hydrogen annealing on the hydrophilicity of the material. This study clearly demonstrates the marked improvement using the optimized hydrogen annealing, providing the promising methodologies for eco-friendly mass production of water splitting photoelectrodes. Graphical Abstract
ISSN:2196-5404
2196-5404
DOI:10.1186/s40580-022-00323-9