Photoassisted enhancement of the electrocatalytic oxidation of formic acid on platinized TiO₂ nanotubes

ACS Appl Mater Interfaces. 2014 Apr 23;6(8):5585-94. doi: 10.1021/am406040v. Epub 2014 Apr 4.

Abstract

A solvothermal method is used to deposit Pt nanoparticles on anodized TiO2 nanotubes (T_NT). Surface characterization using SEM, EDX, and XRD indicates the formation of polycrystalline TiO2 nanotubes of 110 ± 10 nm diameter with Pt nanoparticle islands. The application of the T_NT/Pt photoanode has been examined toward simultaneous electrooxidation and photo(electro)oxidation of formic acid (HCOOH). Upon UV-vis photoillumination, the T_NT/Pt photoelectrode generates a current density of 72 mA/cm(2), which is significantly higher (∼39-fold) than that of the T_NT electrode (1.85 mA/cm(2)). This boosting in the overall current is attributable to the enhanced oxidation of formic acid at the T_NT/Pt-electrolyte interface. Further, a series of cyclic voltammetric (CV) responses, of which each anodic scan is switched to photoillumination at a certain applied bias (i.e., 0.2 V, 0.4 V, etc.), is used to identify the role of T_NT/Pt as a promoter for the photoelectrooxidation of formic acid and understand a carbon monoxide (CO)-free pathway. Chronoamperometric (j/t) measurements demonstrate the evidence of an external bias dependent variation in the time lag during the current stabilization. An analysis of the CV plots and j/t profiles suggests the existence of both the charge-transfer controlled process and the diffusion-controlled process during formic acid photoelectrooxidation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.