2D α-MoO3-x truncated microplates and microdisks as electroactive materials for highly efficient asymmetric supercapacitors

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Two-dimensional truncated microplates and microdisks of molybdenum oxide are synthesized, and their capabilities for superior performance in the charge storage devices are demonstrated. The chemistry of protonated urea with the heptamolybdate [Mo7O24]6− and octamolybdate [Mo8O26]4− ions is innovatively utilized to transform the MoO3-x nanoparticles into truncated microplates and microdisks, without the need of any expensive templates or hydro/solvothermal treatment. The 2D-MoO3-x truncated microplates and microdisks exhibit excellent supercapacitor performance with a high specific capacitance of 410 and 226 F g−1 at a remarkable current density of 20 A g−1. The microstructures also exhibit substantial capacitance retention of > 90% and Coulombic efficiency > 98% for over 12000 continuous charge-discharge cycles, respectively. An asymmetric supercapacitor device of 2D MoO3-x microstructures has been assembled. The device exhibited remarkable energy and power densities of nearly 41 W h kg−1 and 2108 W kg−1 for MoO3-x truncated microplates, and 30 W h kg−1 and 2107 W kg−1 for MoO3-x truncated microdisks, respectively. Our method thus provides a route for facile fabrication of 2D MoO3-x microstructures which can function as excellent charge storage materials even at very high current densities while maintaining their electrochemical stabilities.

Original languageBritish English
Article number103958
JournalJournal of Energy Storage
Volume48
DOIs
StatePublished - Apr 2022

Keywords

  • Asymmetric supercapacitor
  • Electrochemical studies
  • Microdisks
  • Microplates
  • MoO
  • Oxygen vacancies

Fingerprint

Dive into the research topics of '2D α-MoO3-x truncated microplates and microdisks as electroactive materials for highly efficient asymmetric supercapacitors'. Together they form a unique fingerprint.

Cite this