Abstract

Herein, a novel Poly (melamine) have been successively electrodeposited on glassy carbon electrode and decorated by Pd nanoparticles (Pd NPs) subsequently to fabricate Poly (melamine) – Pd nanocomposite. Structural geometry, morphological view, and elemental composition analysis were ensured by X-ray diffractogram, scanning electron microscope, and X-ray photoelectron spectroscopy. The electrodeposited Poly (melamine) (PME) material depicts an interconnected nano rod (50 nm) morphology leads to a nano exploder (~150 nm) arrangement. Spherical shaped Pd decorated PME morphology was obtained for GC\\PME-Pd NPs composite (150 nm). The electrocatalytic activity of the fabricated anode electrocatalyst was examined by cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry methods. The modified GC\\PME-Pd NPs composite electrode validates superior electrocatalytic behaviour towards methanol and ethanol oxidation in alkaline background. Besides, the electrochemical surface area and electrocatalytic behaviour make it a greater anode catalyst towards methanol and ethanol oxidation. The synergic effects amid the Poly (melamine)-Pd NPs composite enhances the catalytic activity, mechanical stability on the electrocatalysis of methanol and ethanol oxidation reaction superior than modified Poly (melamine) electrode. Hence, the fabricated anode electrocatalyst is proficient to get realistic approach towards the progression in the direct alcohol (methanol and ethanol) oxidation reaction in direct alcohol fuel cells (DAFCs) applications.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.