Two series of self-assembled TiO 2 nanotube (NT) arrays were grown by electrochemical anodization on a metallic titanium substrate with different anodization times and applied potentials in HF-containing ethylene glycol electrolyte solutions and postcalcined at 450 °C. The obtained thin films were characterized by FESEM, XRD, and UV-vis- NIR DRS analyses and tested as photoanodes in incident photon to current efficiency (IPCE) measurements and in a two-compartment photoelectrochemical cell (PEC) for separate H 2 and O 2 production. The photocatalytic perform- ance of the NT arrays significantly increased with an increase in the potential applied during anodization (i.e., with increasing the NT inner diameter) and the incident angle of the light. IPCE measurements revealed that such unexpected behavior is due to a red shift of the activity threshold that allows harvesting and converting a larger portion of the solar spectrum. This phenomenon is ascribed to the parallel shift of the photonic band gap position originated by the intrinsic photonic crystal properties and demonstrates the important role played by ordered hierarchical structures in improving the photocatalytic performance of NT arrays by confining and manipulating light.

Exploiting the Photonic Crystal Properties of TiO2 Nanotube Arrays to Enhance Photocatalytic Hydrogen Production

2016

Abstract

Two series of self-assembled TiO 2 nanotube (NT) arrays were grown by electrochemical anodization on a metallic titanium substrate with different anodization times and applied potentials in HF-containing ethylene glycol electrolyte solutions and postcalcined at 450 °C. The obtained thin films were characterized by FESEM, XRD, and UV-vis- NIR DRS analyses and tested as photoanodes in incident photon to current efficiency (IPCE) measurements and in a two-compartment photoelectrochemical cell (PEC) for separate H 2 and O 2 production. The photocatalytic perform- ance of the NT arrays significantly increased with an increase in the potential applied during anodization (i.e., with increasing the NT inner diameter) and the incident angle of the light. IPCE measurements revealed that such unexpected behavior is due to a red shift of the activity threshold that allows harvesting and converting a larger portion of the solar spectrum. This phenomenon is ascribed to the parallel shift of the photonic band gap position originated by the intrinsic photonic crystal properties and demonstrates the important role played by ordered hierarchical structures in improving the photocatalytic performance of NT arrays by confining and manipulating light.
2016
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
electrochemical anodization
photocatalytic water splitting
photoelectrochemical cell
photonic bandgap
photonic crystals
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/308153
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