Platinum nanoparticles supported on single CeO2 and TiO2 metal oxides and Ce0.8Ti0.2O2-delta solid solution were prepared to investigate the effect of Ti4+-doping of ceria on important mechanistic and kinetic aspects of the Water-Gas Shift (WGS) reaction in the 200-300 degrees C range, namely: (i) the concentration and chemical structure of active adsorbed reaction intermediates present in the C-path and H-path of WGS, and (ii) the prevailing mechanistic path among "redox" and "associative" both proposed in the literature. The relationship between the chemical nature of dopant (Zr4+, Ti4+ and La3+) and the concentration of active C-pool and H-pool of reaction intermediates as well as that of specific rate per gram basis (r(CO), mu mol g(-1) s(-1)) for the ceria-doped supported Pt is illustrated for the first time based on relevant results previously reported (Zr4+ and La3+-doped ceria). The 0.5 wt% Pt supported on Ce0.8Ti0.2O2-delta (Ti4+-doped CeO2) exhibits significantly higher WGS activity in terms of CO conversion (%) and specific kinetic rate (mu mol CO g(-1) s(-1) or mu mol CO cm(-1) s(-1)) compared to Pt/CeO2, Pt/TiO2, Pt/Ce0.8La0.2O2-delta and Pt/Ce0.5Zr0.5O2-delta catalysts. This was explained mainly by: (i) the larger concentration of active C-pool of reaction intermediates formed around each Pt nanoparticle, and (ii) the higher reactivity of sites (k, s(-1)) along the Pt-support interface responsible for CO2 and H-2 formation. A very good correlation between the concentration of active C-pool and the specific reaction rate, r(CO) (mu mol g(-1) s(-1)) as a function of the dopant (Zr4+, La3+ and Ti4+) was found. The concentration of labile surface oxygen and its mobility in Ce0.8Ti0.2O2-delta compared to CeO2 (undoped), La3+ or Zr4+-doped ceria are also important factors. It is proposed that on Pt/CeO2-doped catalysts the WGS reaction follows both the "redox" and "associative formate" mechanisms, where the extent of participation of each mechanism depends on the chemical nature of the dopant (Zr4+, La3+ and Ti4+). (C) 2013 Elsevier B.V. All rights reserved.