• 文献标题:   Cobalt oxide nanoparticle-decorated reduced graphene oxide (Co3O4-rGO): active and sustainable nanoelectrodes for water oxidation reaction
  • 文献类型:   Article
  • 作  者:   MUNDE AV, MULIK BB, DIGHOLE RP, SATHE BR
  • 作者关键词:  
  • 出版物名称:   NEW JOURNAL OF CHEMISTRY
  • ISSN:   1144-0546 EI 1369-9261
  • 通讯作者地址:   Dr Babasaheb Ambedkar Marathwada Univ
  • 被引频次:   0
  • DOI:   10.1039/d0nj02598d
  • 出版年:   2020

▎ 摘  要

Herein, cobalt oxide (Co3O4)-decorated reduced graphene oxide (rGO)-based nanoelectrodes were fabricated by the chemical reduction method using hydrazine hydrate. It showed enhanced electrocatalytic activity for oxygen evolution (water oxidation) reactions (OER) in an alkaline medium. These as-synthesized materials were characterized by X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) spectroscopy, energy dispersive analysis of X-ray (EDAX), Raman spectroscopy and transmission electron microscopy (TEM). The XRD studies confirmed that Co(3)O(4)had a cubic spinal structure and morphological studies based on TEM analysis showed that Co(3)O(4)existed with similar to 5 nm-thick chain-like nanostructures that decorated rGO. This Co3O4-modified reduced graphene oxide (Co3O4-rGO) electrocatalyst was found to be extraordinarily active towards oxygen evolution reactions (OER) and is one of the complex reactions of water splitting technique. This was further confirmed by an ultra-low onset potential of 1.38 Vvs.RHE with a high current density of 10 mA mg(-1)of Co(3)O(4)loading (calculated from TGA) at the constant potential of 1.50 Vvs.RHE. The enhancement factor of Co3O4-rGO = 2000 was almost 3.25 times higher compared with that of Co3O4= 600 under similar electrolytic conditions probably due to the synergetic co-operative interactions at modified interfaces. Chronoamperometric (i-t) and electrochemical impedance spectroscopic (EIS) measurements demonstrated higher current/potential stability and lower charge transfer resistance, respectively, for Co3O4-rGO compared with those of rGO and Co(3)O(4)towards the water oxidation reaction.