TY - JOUR
T1 - Solar-driven Z-scheme water splitting using tantalum/nitrogen co-doped rutile titania nanorod as an oxygen evolution photocatalyst
AU - Nakada, Akinobu
AU - Nishioka, Shunta
AU - Vequizo, Junie Jhon M.
AU - Muraoka, Kanemichi
AU - Kanazawa, Tomoki
AU - Yamakata, Akira
AU - Nozawa, Shunsuke
AU - Kumagai, Hiromu
AU - Adachi, Shin Ichi
AU - Ishitani, Osamu
AU - Maeda, Kazuhiko
N1 - Publisher Copyright:
© 2017 The Royal Society of Chemistry.
PY - 2017
Y1 - 2017
N2 - A visible-light-driven water-splitting system that involves two-step photoexcitation (Z-scheme) was constructed using rutile TiO2 nanorod doped with Ta and N (TiO2:Ta/N) as an O2 evolution photocatalyst. The Ta-doped TiO2 nanorods, prepared by a solvothermal synthesis, underwent nitridation to possess visible-light absorption under mild conditions, even at 623 K under an ammonia flow. The TiO2:Ta/N powders modified with a RuO2 cocatalyst were active under visible light up to 540 nm for water oxidation for producing O2 in the presence of reversible electron acceptors (IO3- or Fe3+), while TiO2:N exhibited negligible activity. The results of time-resolved infrared absorption spectroscopy indicated that co-doping Ta with N into TiO2 prolonged the lifetime of photogenerated free electrons, leading to high photocatalytic activity. Simultaneous H2 and O2 evolution via water splitting was achieved using a combination of RuO2-modified TiO2:Ta/N, Ru-loaded SrTiO3:Rh and an Fe3+/Fe2+ redox couple under visible-light irradiation (λ > 420 nm) and under AM 1.5G simulated sunlight.
AB - A visible-light-driven water-splitting system that involves two-step photoexcitation (Z-scheme) was constructed using rutile TiO2 nanorod doped with Ta and N (TiO2:Ta/N) as an O2 evolution photocatalyst. The Ta-doped TiO2 nanorods, prepared by a solvothermal synthesis, underwent nitridation to possess visible-light absorption under mild conditions, even at 623 K under an ammonia flow. The TiO2:Ta/N powders modified with a RuO2 cocatalyst were active under visible light up to 540 nm for water oxidation for producing O2 in the presence of reversible electron acceptors (IO3- or Fe3+), while TiO2:N exhibited negligible activity. The results of time-resolved infrared absorption spectroscopy indicated that co-doping Ta with N into TiO2 prolonged the lifetime of photogenerated free electrons, leading to high photocatalytic activity. Simultaneous H2 and O2 evolution via water splitting was achieved using a combination of RuO2-modified TiO2:Ta/N, Ru-loaded SrTiO3:Rh and an Fe3+/Fe2+ redox couple under visible-light irradiation (λ > 420 nm) and under AM 1.5G simulated sunlight.
UR - http://www.scopus.com/inward/record.url?scp=85020880309&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85020880309&partnerID=8YFLogxK
U2 - 10.1039/c6ta10541f
DO - 10.1039/c6ta10541f
M3 - Article
AN - SCOPUS:85020880309
SN - 2050-7488
VL - 5
SP - 11710
EP - 11719
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 23
ER -