This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues.Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. The electrochemical stability of Pt deposited on TiO 2 based nanofibers was compared with commercially available carbon supported Pt. Prior to the Pt deposition the TiO 2 material, which was either undoped or Nb doped, was air calcined. In one case the undoped TiO 2 was also reduced in a hydrogen atmosphere. XRD analysis revealed that the unreduced TiO 2 was present in the anatase phase, irrespective of whether the Nb dopant was present, whereas the rutile phase was formed due to reduction with H 2 . The diameter of the TiO 2 fibers varied from 50 to 100 nm, and the average Pt particle diameter was approximately 5 nm. Pt supported on TiO 2 was more stable than Pt supported on C when subjected to 1000 voltammetric cycles in the range of 0.05-1.3 V vs. RHE. Nb doped TiO 2 showed the highest stability, retaining 60% of the electrochemically active surface area after 1000 cycles compared to the state after 100 cycles, whereas the carbon supported catalyst retained 20% of the active surface area. The commercial catalyst had the highest oxygen reduction activity due to its larger specific area (17.1 m 2 g −1 vs. 5.0 m 2 g −1 for Pt/TiO 2 -Nb, measured after 100 cycles) and the higher support conductivity. The Pt supported on Nb doped or on H 2 reduced TiO 2 was more active than Pt supported on air calcined and otherwise unmodified TiO 2 .Crown