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    Electrooxidation of methanol on Ag, AgNi, and AgCo catalysts prepared by combustion synthesis technique

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    Electrooxidation of methanol on Ag, AgNi, and AgCo catalysts prepared by combustion synthesis technique.pdf (2.854Mb)
    Date
    2022-01-01
    Author
    Yuda, Afdhal
    Kumar, Anand
    Abu Reesh, Ibrahim
    Russell, Christopher K.
    Miller, Jeffrey T.
    Ali Saleh Saad, Mohammed
    Al-Marri, Mohammed J.
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    Abstract
    Herein, we report the synthesis of silver-based electrocatalysts (Ag/C, AgCo/C, and AgNi/C) using solution combustion method and their performance towards methanol oxidation reaction. Detailed structural and microscopic analysis confirmed the formation of graphitic carbon, synthesis of crystalline phases with high porosity in all the three electrocatalysts. X-ray photoelectron spectroscopic (XPS) analysis showed a high concentration of Ag2O (or Ag+) on AgNi/C, whereas AgCo/C exhibited a high concentration AgO (or Ag2+) on the surface. XPS analysis on C 1s confirmed the highest concentrations of the sp2 hybridized C-C bond on Ag/C, C-O on AgNi/C, and O-C-O bond on AgCo/C, respectively. The X-ray absorption spectroscopy (XAS) analysis on Ag edge showed a similarity in the bond lengths in AgCo and AgNi samples to that of bulk silver, that has a bond length of 2.89 Å, with only silver-silver scattering and the absence of a different or a nonsilver metal in the nanoparticles. This indicates that there is no Ag-M alloying. Nonetheless, a significant difference in particle sizes was observed, with 2.5 and 6 nm, respectively for AgNi and AgCo. Methanol electrooxidation experiments performed on the electrocatalysts indicated AgNi/C to show better performance in comparison to AgCo/C and Ag/C. Anodic polarization curves obtained from linear sweep voltammetry (LSV) measurements demonstrated a superior performance of AgNi/C with an onset potential of 0.41 V. In addition, 20 h chronoamperometry experiment also confirmed a sustained superior performance of AgNi/C catalyst, which could be due to smaller particle size and stabilization of Ag+ on the surface of the catalyst.
    URI
    https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85141180787&origin=inward
    DOI/handle
    http://dx.doi.org/10.1002/er.8696
    http://hdl.handle.net/10576/37661
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    • Chemical Engineering [‎1198‎ items ]

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