ABSTRACT
The presented study is concerned with a new multi-step method to synthesize PtCo/C materials based on composite CoxOy/C that combines the advantages of different liquid-phase synthesis methods. Based on the results of studying the materials at each stage of synthesis with the TG, XRD, TEM, SEI, TXRF, CV and LSV methods, a detailed overview of the sequential changes in catalyst composition and structure at each stage of the synthesis is presented. The PtCo/C catalyst synthesized with the multi-step method is characterized by a uniform distribution of bimetallic nanoparticles of about 3 nm in size over the surface of the support, which result in its high ESA and ORR activity. The activity study for the synthesized PtCo/C catalyst in an MEA showed better current-voltage characteristics and a higher maximum specific power compared with an MEA based on a commercial Pt/C catalyst. Therefore, the results of the presented study demonstrate high prospects for the developed approach to the multi-step synthesis of PtM/C catalysts, which may enhance the characteristics of proton-exchange membrane fuel cells (PEMFCs).
ABSTRACT
A carbon supported PtCux/C catalyst, which demonstrates high activity in the oxygen electroreduction and methanol electrooxidation reactions in acidic media, has been obtained using a method of chemical reduction of Pt (IV) and Cu (2+) in the liquid phase. It has been found that the potential range of the preliminary voltammetric activation of the PtCux/C catalyst has a significant effect on the de-alloyed material activity in the oxygen electroreduction reaction (ORR). High-resolution transmission electron microscopy (HRTEM) demonstrates that there are differences in the structures of the as-prepared material and the materials activated in different potential ranges. In this case, there is practically no difference in the composition of the PtCux-y/C materials obtained after activation in different conditions. The main reason for the established effect, apparently, is the reorganized features of the bimetallic nanoparticles' surface structure, which depend on the value of the limiting anodic potential in the activation process. The effect of the activation conditions on the catalyst's activity in the methanol electrooxidation reaction is less pronounced.
ABSTRACT
Platinum-carbon catalysts are widely used in the manufacturing of proton-exchange membrane fuel cells. Increasing Pt/C activity and stability is an urgent task and the optimization of their structure seems to be one of the possible solutions. In the present paper, Pt/C electrocatalysts containing small (2-2.6 nm) nanoparticles (NPs) of a similar size, uniformly distributed over the surface of a carbon support, were obtained by the original method of liquid-phase synthesis. A comparative study of the structural characteristics, catalytic activity in the oxygen electroreduction reaction (ORR), and durability of the synthesized catalysts, as well as their commercial analogs, was carried out. It was shown that the uniformity of the structural and morphological characteristics of Pt/C catalysts makes it possible to reduce the negative effect of the small size of NPs on their stability. As a result, the obtained catalysts were significantly superior to their commercial analogs regarding ORR activity, but not inferior to them in terms of stability.
