Affiliations 

  • 1 Battery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC; Department of Chemical Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC
  • 2 Battery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC
  • 3 Graduate Institute of Science and Technology, National Taiwan University of Science and Technology, 43, Sec. 4, Keelung Road, Taipei 106, Taiwan, ROC
  • 4 Department of Materials Science and Engineering, National Yang Ming Chiao Tung University, 1001 University Road, Hsinchu 30010, Taiwan, ROC
  • 5 Battery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC; Faculty of Industrial Sciences and Technology, University Malaysia Pahang Al-Sultan Abdullah, 26300 Kuantan, Malaysia. Electronic address: rjose@ump.edu.my
  • 6 Battery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC; Department of Chemical Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC; Department of Chemical and Materials Engineering & Center for Sustainability and Energy Technologies, Chang Gung University, Taoyuan City 333, Taiwan. Electronic address: ccyang@mail.mcut.edu.tw
J Colloid Interface Sci, 2025 Feb 15;680(Pt A):845-858.
PMID: 39546905 DOI: 10.1016/j.jcis.2024.11.066

Abstract

Rechargeable lithium-oxygen (Li-O2) batteries are being considered as the next-generation energy storage systems due to their higher theoretical energy density. However, the practical application of Li-O2 batteries is hindered by slow kinetics and the formation of side products during the oxygen reduction and evolution reactions on the cathode. These reactions lead to high overpotentials during charging and discharging. To address these challenges, we propose a simple ultrasonic method for synthesizing cobalt nanoclusters embedded in nitrogen-doped graphene nanosheets (GrZnCo) derived from metal-organic frameworks (MOFs). The resulting material, due to the retention of metallic cobalt structure, exhibits better electronic conductivity. Additionally, the GrZnCo catalyst shows vigorous catalytic activity, which can improve reaction kinetics and suppress side reactions, thus lowering the charging overpotential. We have investigated the impact of different catalyst compositions (GrZnCox; x  = 1, 3, 5) by varying the amounts of cobalt and zinc. The optimum catalyst, GrZnCo3, contains high cobalt-N active components, graphitic-N, pyridinic-N, pyrrolic-N, and abundant defect structures, which enhance the electrochemical performance. The defect-rich GrZnCo3 catalyst enables Li-O2 batteries to achieve a high discharge capacity of 13500 mAh·g-1 at 50 mA·g-1 and a remarkable long-term cycling performance of over 400 cycles at 100 mA·g-1 with a limited capacity of 500 mAh·g-1. This work demonstrates an effective approach to fabricate cost-effective electrocatalysts for various energy storage systems.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.