Journal
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 166, Issue 15, Pages H783-H790Publisher
ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.0071915jes
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Funding
- CONACYT
- SECITI-CDMXMEXICO [CM 8995c19 SECITI/2019]
- CONACyT, Investigacion Cientifica Basica 2017-2018 grant [A1-S-21608]
- PAICYT program of the Universidad Autonoma de Nuevo Leon
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This study aimed to fabricate a novel TiNT-RuO2 electrocatalyst to produce active chlorine with the capacity to oxidize recalcitrant organicmatter. Titanium oxide nanotubes (TiNTs) were first grown via Ti foil anodization in potentiostatic mode in an ethylene glycol solution containing H2O and NH4F and then annealed at 450 degrees C in air. RuO2 nanoparticles were deposited on the TiNTs using a hybrid strategy that included pulsed electrodeposition of the Ru nanoparticles, followed by thermal treatment. X-ray diffraction (XRD) only revealed peaks related to metallic Ti and anatase (TiO2) for the TiNTs, whereas additional peaks associated with the tetragonal RuO2 structure were shown for TiNT-RuO2. Scanning electron microscopy showed a well-organized structure for the TiNTs with an average inner diameter of approximately 185 nm for the NTs, while RuO2 nanoparticles (size<10 nm) were homogenously deposited on the walls and around the openings of the TiNTs. TiNT-RuO2 preferred the active chlorine formation over oxygen evolution owing to the presence of the RuO2 nanoparticles. Rapid degradation testing revealed complete elimination of picloram (PCL) in 2 h when 10 mA cm(-2) was imposed on the TiNT-RuO2, whereas 48% of the 2,4-dichlorophenoxyacetic acid (2,4-D) was removed under the same conditions using the electro-generated active chlorine on the TiNTs. (C) 2019 The Electrochemical Society.
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