This study concentrates on the development of catalytic materials capable of enhancing oxidation of ethanol particularly at low potentials, i.e. at conditions resembling operation of anodes in low temperature fuel cells. Indeed, the ethanol oxidation currents measured under voltammetric and chronoamperometric conditions have been significantly increased following dispersing bimetallic PtRu nanoparticle (∼4 nm) catalysts over TiO 2 (80% anatase, 20% rutile) nanostructures (∼20-30 nm) supported onto multi-walled carbon nanotubes. The improvement in activity is attributed not only to better dispersion of PtRu centers (some increase of active surface area) or improved (carbon-nanotube-assisted) propagation of electrons at the catalytic interface but also to the presence of hydroxyl groups and high mobility of protons at neighboring (to PtRu) TiO 2 . Further, specific interactions between TiO 2 and Pt or Ru metallic components are feasible. Importance of addition of TiO 2 is also evident from kinetic analysis based on measurements of steady-state currents at different concentrations. Ethanol is a renewable low-cost biofuel acting not only during simple combustion but also under electrochemical oxidation (catalytic) conditions thus becoming a reactant of potential importance to the technology of low-temperature direct-alcohol fuel cells. In principle, ethanol has high energy density, 29.7 kJ g −1 (23.3 kJ cm −3 ), moderate toxicity, and it exists as liquid at room temperature what allows its easier handling, transportation and storage. Although ethanol (C 2 H 5 OH) is a model di-carbonic (ethyl) alcohol, its electrooxidation is much more complex when compared to the oxidation mechanism of mono-carbonic (methyl) alcohol. Indeed, methanol (CH 3 OH) can be readily oxidized to the final product, CO 2 , through the transfer of six electrons.1 Due to high toxicity of methanol and its capability to undergo crossover through proton-conducting membranes to the cathodic compartments of fuel cells, intense research involving other small organic molecules including ethanol 2-10 has been recently pursued.If electrooxidation of ethanol proceeded ideally to carbon dioxide, the reaction would involve twelve electrons; under such conditions, the fuel cell (with an oxygen cathode) would theoretically produce the open circuit potential of 1.14 V. But complete oxidation of ethanol under electrochemical conditions is a complex reaction because the process would require cleavage of the strong C-C bond in the C 2 H 5 OH molecule.11-13 Consequently, the reaction rate is rather slow at ambient conditions, and typically acetaldehyde (two-electron oxidation) or acetic acid (four-electron oxidation) are formed during electrooxidations at common Pt-based (e.g. PtRu or PtSn) catalytic systems.Despite the unique ability of metallic platinum catalysts to break C-C bond in the ethanol molecule, Pt alloys with Ru or Sn tend to produce higher electrocatalytic currents than platinum itself. 14,15 Practical utility of bare Pt is largely limited by blocki...