The electrochemical stability of Pt deposited on mesoporous carbon, which was either applied in its unmodified state or coated with 20 wt% TiO 2 , was investigated by cyclic voltammetry in N 2 purged 0.5 M sulfuric acid. XRD analysis revealed that TiO 2 was present in the anatase phase. The mean Pt particle diameter was ∼6 and ∼4 nm for mesoporous carbon with and without TiO 2 , respectively. Pt supported on TiO 2 modified substrates was more stable than Pt supported on conventional mesoporous carbon when subjected to 1000 cycles in the potential range from 0.05 to 1.25 V vs. RHE. This was evident from the observation that the support with TiO 2 retained ∼53% of the electrochemically active surface area relative to the state observed after 100 cycles, whereas ∼33% of the active area remained in the case without TiO 2 . The oxygen reduction mass activity was identical for both fresh samples (i.e., 18 A g
−1 Pt). After 1000 cycles the mass activity decreased to 10 A g −1 Pt for the case without TiO 2 , whereas with TiO 2 the deactivation was minor; i.e., the mass activity after 1000 cycles was 17 A g .