Back to Search
Start Over
Electrocatalytic activities of electrochemically reduced tubular titania arrays loaded with cobalt ions in flow-through processes.
- Source :
-
Chemical Engineering Journal . Jan2021, Vol. 404, pN.PAG-N.PAG. 1p. - Publication Year :
- 2021
-
Abstract
- • Titania nanotube arrays grown onto perforate Ti foils are electrochemically reduced and loaded with Co2+. • The electrochemical reduction enhances Co2+ adsorption by 7 times. • The surface modification facilitates the charge transfer kinetics. • The modified TNTs exhibit remarkably high electrocatalytic activities. • The production of OOH radicals is significantly enhanced with the modified TNTs. This study examines the electrocatalytic activity of disordered titania nanotube arrays modified with Co2+ for the oxidation of (in)organic substrates and inactivation of E. coli in a flow-through electrochemical device. As-anodized TiO 2 nanotubes (TNTs) on perforated Ti foils are electrochemically reduced to create Ti3+ states and oxygen vacancies. The electrochemically reduced TNTs (r-TNTs) are capable of adsorbing Co2+ in ~7 times larger amounts than the bare TNTs. Among the bare and modified TNT samples (TNTs, r-TNTs, Co-TNTs, and Co-r-TNTs), Co-r-TNTs exhibit the lowest interfacial charge-transfer resistance and fastest internal charge-transfer kinetics. The electron spin resonance analysis further reveals an enhanced production of OOH radicals in Co-r-TNTs. The combined effect of the excellent charge-transfer behavior and the radical production of Co-r-TNTs leads to faster decomposition of N,N -dimethyl-p-nitrosoaniline, higher current efficiency in the oxidation of iodide to triiodide, and greater inactivation of E. coli as compared to r-TNTs. Details on the surface characterization of the bare and modified TNTs samples are presented and the role of the adsorbed Co2+ is discussed. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 13858947
- Volume :
- 404
- Database :
- Academic Search Index
- Journal :
- Chemical Engineering Journal
- Publication Type :
- Academic Journal
- Accession number :
- 146712569
- Full Text :
- https://doi.org/10.1016/j.cej.2020.126410