TY - JOUR
T1 - Role of hydroxyl radicals and mechanism of escherichia coli inactivation on Ag/AgBr/TiO2 nanotube array electrode under visible light irradiation
AU - Hou, Yang
AU - Li, Xinyong
AU - Zhao, Qidong
AU - Chen, Guohua
AU - Raston, Colin L.
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2012/4/3
Y1 - 2012/4/3
N2 - A ternary Ag/AgBr/TiO2 nanotube array electrode with enhanced visible-light activity was synthesized by a two-step approach including electrochemical process of anodization and an in situ photoassisted deposition strategy. The dramatically enhanced photoelectrocatalytic activity of the composite electrode was evaluated via the inactivation of Escherichia coli under visible light irradiation (>420 nm), whose performance of complete sterilization was much superior to other reference photocatalysts. PL, ESR, and radicals trapping studies revealed hydroxyl radicals were involved as the main active oxygen species in the photoelectrocatalytic reaction. The process of the damage of the cell wall and the cell membrane was directly observed by ESEM, TEM, and FTIR, as well as further confirmed by determination of potassium ion leakage from the killed bacteria. The present results pointed to oxidative attack from the exterior to the interior of the Escherichia coli by OH •, O2•-, holes and Br0, causing the cell to die as the primary mechanism of photoelectrocatalytic inactivation. © 2012 American Chemical Society.
AB - A ternary Ag/AgBr/TiO2 nanotube array electrode with enhanced visible-light activity was synthesized by a two-step approach including electrochemical process of anodization and an in situ photoassisted deposition strategy. The dramatically enhanced photoelectrocatalytic activity of the composite electrode was evaluated via the inactivation of Escherichia coli under visible light irradiation (>420 nm), whose performance of complete sterilization was much superior to other reference photocatalysts. PL, ESR, and radicals trapping studies revealed hydroxyl radicals were involved as the main active oxygen species in the photoelectrocatalytic reaction. The process of the damage of the cell wall and the cell membrane was directly observed by ESEM, TEM, and FTIR, as well as further confirmed by determination of potassium ion leakage from the killed bacteria. The present results pointed to oxidative attack from the exterior to the interior of the Escherichia coli by OH •, O2•-, holes and Br0, causing the cell to die as the primary mechanism of photoelectrocatalytic inactivation. © 2012 American Chemical Society.
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U2 - 10.1021/es204079d
DO - 10.1021/es204079d
M3 - RGC 21 - Publication in refereed journal
C2 - 22385264
SN - 0013-936X
VL - 46
SP - 4042
EP - 4050
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 7
ER -