Triazine-based COP/Mn2O3 composite for supercapacitors: unraveling the electrolyte-dependent charge storage mechanism

Nakul Desai, Y. N. Sudhakar*, Selvakumar M

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

A covalent organic polymer (COP) composite incorporated with Mn2O3 (COP/Mn2O3) was synthesized and systematically explored for supercapacitor applications. FTIR confirmed successful polymerization and Mn incorporation, whereas XRD revealed π–π stacking and bixbyite Mn2O3 phases. FE-SEM revealed morphological densification, and EDS/XPS analyses confirmed that uniform Mn dispersion and mixed Mn2 + /Mn3+ states enhanced redox activity. BET analysis revealed a mesoporous structure with an average pore diameter of 14.81 nm. A key novelty of this study lies in the multielectrolyte electrochemical evaluation conducted in aqueous (1 M H2SO4 and 1 M Na2SO4) and organic (1 M NaPF6 in propylene carbonate) media, providing deeper insight into electrolyte-dependent charge storage mechanisms. In 1 M H2SO4, the COP/Mn2O3 composite achieved a high specific capacitance of 660 F g−1 at 5 mV s−1 and 232.8 F g−1 at 1 A g−1, with an excellent energy density of 21 Wh kg−1 and a superior power density of 10,000 W kg−1. The fabricated symmetric supercapacitor device delivered an energy density of 5.8 Wh kg−1, a power density of 2500 W kg−1, and excellent cycling stability with 93.3 % capacitance retention after 10,000 cycles in a 1 M H2SO4 electrolyte. These results highlight COP/Mn2O3 as a promising electrode material for next-generation supercapacitors.

Original languageEnglish
Article number181728
JournalJournal of Alloys and Compounds
Volume1036
DOIs
Publication statusPublished - 20-07-2025

All Science Journal Classification (ASJC) codes

  • Mechanics of Materials
  • Mechanical Engineering
  • Metals and Alloys
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Triazine-based COP/Mn2O3 composite for supercapacitors: unraveling the electrolyte-dependent charge storage mechanism'. Together they form a unique fingerprint.

Cite this