Distinct influence for carbon nano-morphology on the activity and optimum metal loading of Ni/C composite used for ethanol oxidation

Basically, the alcohols electrooxidation process is considered to be a combination of adsorption and electrochemical reaction on the catalyst surface. Accordingly, due to the adsorption capacity, different carbonaceous nanomaterials are invoked as supports for different electrocatalysts. The influence of carbon support nanomorphology on the electrocatalytic performance of nickel toward ethanol oxidation is investigated. Typically, Ni/C nanoparticles, Ni-incorporated carbon nanofibers and Ni-decorated graphene are synthesized as 0D, 1D and 2D nanostructures, respectively. The synthesized Ni/C nanocomposites are prepared with different Ni contents to investigate the optimum corresponding active metal loading. Compared to pristine Ni NPs, the three formulations exhibit higher performance in both of the current density and the optimum ethanol concentration. For instance, at 10 wt% nickel content and 2 M ethanol concentration, the observed maximum current density in case of exploiting graphene, carbon nanofibers and carbon nanoparticles was 45, 67 and 9.5 mA/cm(2), respectively. However, the maximum obtained current densities were 37.5, 46, 67 and 103.5 mA/cm(2) for pristine Ni NPs, Ni/C NPs (6 wt% Ni), Ni-incorporated CNFs (10 wt% Ni) and Ni-decorated graphene (60 wt% Ni) with a corresponding ethanol concentration of 0.5, 1, 3 and 4 M, respectively. For the nanofibrous and nanoparticulate morphologies, the performance is enhanced with increasing the Ni content up to specific thresholds after that it decreases dramatically. However, in case of the graphene support, the performance is linearly improved with increasing the nickel content due to intercalating the metal nanoparticles inter alia the graphene sheets. Overall, the experimental results conclude that active material loading should be optimized in case of the nanofibrous and nanoparticulate morphologies. (C) 2015 Elsevier Ltd. All rights reserved.