Photoelectrocatalytic degradation of 2,4-dichlorophenol in a TiO2 nanotube-coated disc flow reactor.

Photoelectrocatalytic (PEC) water treatment is a promising technology for organic pollution abatement. Much of the prior research focused on material discovery and optimization. However, challenges exist in scaling-up PEC processes and are associated with designing reactors with effective light irradiation on electrode surfaces and, simultaneously, efficient electrode configurations. We design and demonstrate key reactor design principles, which influence reaction mechanisms, for a reactor using a TiO2 nanotube-coated disc flow reactor. Degradation of organochlorinated 2,4-dichlorophenol was studied as representative carcinogenic micropollutant. The synergistic photoelectrocatalytic process showed 5-fold faster degradation kinetics than solely electrocatalytic treatment or a greater than 2-fold enhancement over photocatalysis alone. Applicability of photoelectrocatalytic treatment was demonstrated over a wide range of micropollutant concentrations with almost complete abatement even at concentrations up to 25 mg L-1 of 2,4-dichlorophenol. Mechanistically, the increase in applied current density efficiency for degradation of 2,4-dichlorophenol was due to stabilization of charge carriers and higher oxidants production rates in the PEC system. Carboxylic acids were identified as the main by-products formed from cleavage of the phenolic ring moieties in 2,4-dichlorophenol. However, very importantly we achieved dehalogenation photoelectrocatalysis with evidence of chlorine heteroatoms released as innocuous chloride anions. Overall, this research demonstrates the importance of PEC reactor design and how properly orientated TiO2 nanotube-coated disc flow reactors leverage both novel material designs and reactor architectures to achieve pollutant degradation.

Portable point-of-use photoelectrocatalytic device provides rapid water disinfection.

Portable water purification devices are needed to provide safe drinking water in rural communities, developing communities with low quality centralized water distribution, and military or recreational applications. Filtration, ultraviolet light, or chemical additives provide a spectrum of alternatives to remove pathogens from water. For the first time, we design, fabricate and demonstrate the performance of a small portable photoelectric point-of-use device, and document its performance on pathogen inactivation. The device utilizes a commercial teacup from which TiO2 nanotube photoanodes were produced in-situ and, with a small rechargeable battery powered 365 nm light emitting diode, was able to achieve 5-log inactivation of Escherichia coli in 10 s and 2.6-log of Legionella in 60 s of treatment in model water samples. Treatment of natural water achieved a 1-log bacteria inactivation after 30 s due to matrix effects. The electro-photocatalytic disinfection reactor in a kup (e-DRINK) can provide a feasible and affordable solution to ensure access to clean water. More broadly, this work demonstrates the potential for illumination to improve the efficiency of electrocatalytic surfaces.