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Enhanced Oxygen Evolution via Electrochemical Water Oxidation using Conducting Polymer and Nanoparticle Composites
Author(s) -
Mahfoz Wael,
Abdul Aziz Md.,
Shaheen Shah Syed,
AlBetar AbdulRahman
Publication year - 2020
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.202001163
Subject(s) - polypyrrole , dielectric spectroscopy , materials science , x ray photoelectron spectroscopy , chemical engineering , electrochemistry , conductive polymer , composite number , tin oxide , nanoparticle , electrocatalyst , oxide , electrode , composite material , polymer , nanotechnology , chemistry , polymerization , engineering , metallurgy
Nano‐Co 3 O 4 was used for electrocatalytic water oxidation due to its promising features of better performance and low cost. An enhanced electrochemical water oxidation performance of the nanoparticles can be achieved by mixing them with other types of highly conductive nano/micro‐structured materials. Conductive polymers would be one of the candidates to achieve this goal. Here, we report our recently developed nano‐Co 3 O 4 and polypyrrole composites for enhanced electrochemical water oxidation. We chose polypyrrole as a support of nano‐Co 3 O 4 to obtain highly active sites of nano‐Co 3 O 4 with high conductivity. Morphological and chemical characterization of the prepared materials were performed using scanning electron microscopy (SEM), energy‐dispersive spectroscopy (EDS), and X‐ray photoelectron spectroscopy (XPS). After immobilizing them individually on fluorine doped tin oxide (FTO) substrate, their electrocatalytic properties toward water oxidation were investigated. The optimum composite materials showed significantly higher electrocatalytic properties compared to that of pure nano‐Co 3 O 4 and polypyrrole. Electrochemical impedance studies indicated that the composite materials possess significantly less electron transfer resistance toward water oxidation reaction compared to that of only polypyrrole or nano‐Co 3 O 4 , while the higher double‐layer capacitance and polarization resistance values obtained from fitting of the impedance data represent the faster electrode kinetics in the composite electrocatalyst. Due to the synergetic effect, the optimum nano‐Co 3 O 4 and polypyrrole composites could be represent a novel and promising material for water oxidation.