Back to Search Start Over

Hydrothermal synthesis of Nb5+-doped SrTiO3 mesoporous nanospheres with greater photocatalytic efficiency for Cr(VI) reduction.

Authors :
Zhu, Jing
Zhang, Yongcai
Shen, Li
Li, Jing
Li, Liangliang
Zhang, Fen
Zhang, Ya
Source :
Powder Technology. Sep2022, Vol. 410, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

The Nb5+-doping strategy was adopted to enhance the photocatalytic efficiency of SrTiO 3 to overcome the limitation for its practical photocatalytic applications. Different amounts of Nb5+ doped SrTiO 3 (Nb-SrTiO 3) mesoporous nanospheres were synthesized via a convenient hydrothermal approach. The photocatalytic reduction of aqueous Cr(VI) using the Nb-SrTiO 3 products under xenon lamp irradiation was investigated. Results indicated that 3% Nb-SrTiO 3 was the optimum product, which exhibited a photocatalytic efficiency 3 times as much as that of SrTiO 3 and a fair reuse stability. Moreover, 3% Nb-SrTiO 3 also demonstrated higher photocatalytic efficiency than many other metal cations doped SrTiO 3 synthesized via the same process and a number of previously reported photocatalysts. The best photocatalytic activity of 3% Nb-SrTiO 3 was found to be predominantly due to its most efficient separation and transfer of photogenerated holes and electrons. This study suggests that Nb-SrTiO 3 is a potential efficient photocatalyst for the remediation of Cr(VI)-contaminated water. [Display omitted] • Nb5+-doped SrTiO 3 mesoporous nanospheres were synthesized by a hydrothermal method. • 3% Nb-SrTiO 3 has far higher photocatalytic activity than SrTiO 3 in Cr(VI) reduction. • It outperforms many other metal ions doped SrTiO 3 and many reported photocatalysts. • It has good photocatalytic stability. • Its higher activity mainly results from enhanced separation and transfer of e − and h + . [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00325910
Volume :
410
Database :
Academic Search Index
Journal :
Powder Technology
Publication Type :
Academic Journal
Accession number :
159170467
Full Text :
https://doi.org/10.1016/j.powtec.2022.117886