Abstract

P-doped, O-rich graphitic carbon (POGC) was synthesized via an environmentally friendly, cost effective microwave (MW)-assisted treatment using a phytic acid precursor. The treatment facilitated the formation of coral-like clusters and barrel-like graphitic structures; the P-doped graphitic structures and P–C bonds increased with the increasing irradiation time. The irradiation process increased the graphitization degree of the P-doped structure, resulting in high catalytic activity toward vanadium ion redox reactions (VIRRs), as well as improved electrical conductivity. The optimal treatment time (60 s) for POGC (POGC-60) was determined by evaluating the cyclic voltammetry curves of VIRR using POGC. POGC-60 exhibited the highest peak current densities in the anolyte and catholyte, approximately three times higher than that of the control electrode. Additionally, POGC-60 significantly reduced the charge-transfer resistance, indicating a decrease in the overpotential of VIRR. Similar improvements (increased peak current densities, reduced potential differences, and reduced charge-transfer resistance) were observed when POGC was combined with commercial graphite felt (GF) electrodes, GF/POGC. The vanadium redox flow batteries (VRFBs) utilizing the GF/POGC electrodes demonstrated enhanced efficiencies and discharge capacities (even at high current densities), as well as exceptional long-cycle stability. These findings highlight MW irradiation as a commercially feasible option for achieving the facile manufacture of cost effective, outstanding, environmentally friendly catalysts for VRFBs.

Full Text
Paper version not known

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.