TY - JOUR
T1 - Photo-reduction assisted synthesis of W-doped TiO2 coupled with Au nanoparticles for highly efficient photocatalytic hydrogen evolution
AU - Liu, Bing
AU - Su, Shuangyue
AU - Zhou, Wenhui
AU - Wang, Yin
AU - Wei, Ding
AU - Yao, Lihua
AU - Ni, Yuanman
AU - Cao, Minhua
AU - Hu, Changwen
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2017
Y1 - 2017
N2 - The practical applications of TiO2 have been greatly suppressed by its low quantum yield, which arises from the rapid recombination of photo-induced electrons and holes, and poor solar efficiency, which is determined by its band gap. Herein, W-doped TiO2 coupled with Au nanoparticles (W-TiO2/Au) was designed and synthesized by a facile multi-step process. The W-doping in the TiO2 lattice, on the one hand, can hinder the phase transition of TiO2 from anatase to rutile structure, and the pure anatase structure is well preserved. On the other hand, W-doping can narrow the band gap of TiO2 and result in oxygen vacancies, which may act as trapping sites to retard charge recombination. Furthermore, Au loading on the surface of TiO2 can effectively suppress the recombination of photo-induced electrons and holes, leading to improvement in the quantum yields of TiO2. Benefiting from the unique dual-hybrid strategy, the W-TiO2/Au catalyst possesses a strong solar adsorption narrowed band gap, abundant active sites, strong synergetic coupling, enhanced electron transfer, and high efficiencies in H2 generation. Its maximum H2 generation rate can reach as high as 24 mmol g−1 h−1 under simulated solar light. A synergetic effect was proposed to explain the enhancement of the photocatalytic activity of TiO2.
AB - The practical applications of TiO2 have been greatly suppressed by its low quantum yield, which arises from the rapid recombination of photo-induced electrons and holes, and poor solar efficiency, which is determined by its band gap. Herein, W-doped TiO2 coupled with Au nanoparticles (W-TiO2/Au) was designed and synthesized by a facile multi-step process. The W-doping in the TiO2 lattice, on the one hand, can hinder the phase transition of TiO2 from anatase to rutile structure, and the pure anatase structure is well preserved. On the other hand, W-doping can narrow the band gap of TiO2 and result in oxygen vacancies, which may act as trapping sites to retard charge recombination. Furthermore, Au loading on the surface of TiO2 can effectively suppress the recombination of photo-induced electrons and holes, leading to improvement in the quantum yields of TiO2. Benefiting from the unique dual-hybrid strategy, the W-TiO2/Au catalyst possesses a strong solar adsorption narrowed band gap, abundant active sites, strong synergetic coupling, enhanced electron transfer, and high efficiencies in H2 generation. Its maximum H2 generation rate can reach as high as 24 mmol g−1 h−1 under simulated solar light. A synergetic effect was proposed to explain the enhancement of the photocatalytic activity of TiO2.
UR - http://www.scopus.com/inward/record.url?scp=85010028176&partnerID=8YFLogxK
U2 - 10.1039/c6ce02417c
DO - 10.1039/c6ce02417c
M3 - Article
AN - SCOPUS:85010028176
SN - 1466-8033
VL - 19
SP - 675
EP - 683
JO - CrystEngComm
JF - CrystEngComm
IS - 4
ER -