A Facile Route to Synthesize a TiNT-RuO2 Electrocatalyst for Electro-Generated Active Chlorine Production. Issue 15 (1st January 2019)

• Record Type: Journal Article
• Authors: Elizarragaz, D.; Carrera-Crespo, J. E.; Vazquez-Arenas, J.; Romero-Ibarra, I.; Ruiz-Ruiz, E. J.; Chairez, I.
• Is Part Of: Journal of the Electrochemical Society. Volume 166:Issue 15(2019)
• Page Start: H783
• Page End: H790
• Publication Date: 2019-01-01
• Subjects: Electrocatalysis -- active chlorine -- dimensionally stable anodes -- TiNT-RuO2; Electrochemistry -- Periodicals; 541.3705
• DOI: 10.1149/2.0071915jes
• Languages: English
• ISSNs: 0013-4651

Abstract

Abstract : This study aimed to fabricate a novel TiNT-RuO2 electrocatalyst to produce active chlorine with the capacity to oxidize recalcitrant organic matter. Titanium oxide nanotubes (TiNTs) were first grown via Ti foil anodization in potentiostatic mode in an ethylene glycol solution containing H2 O and NH4 F and then annealed at 450°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.