Affiliations 

  • 1 Department of Chemistry, Anna University, Chennai, 600025, India
  • 2 Advanced Materials Laboratory, Central Leather Research Institute, Chennai, 600020, India
  • 3 Nanotechnology & Catalysis Research Centre, University of Malaya, 50603, Kuala Lumpur, Malaysia
  • 4 Department of Mechanical Engineering, Keimyung University, Daegu, 42601, Republic of Korea
  • 5 Department of Chemistry, Anna University, Chennai, 600025, India. Electronic address: [email protected]
Chemosphere, 2024 Jan;348:140650.
PMID: 37951405 DOI: 10.1016/j.chemosphere.2023.140650

Abstract

In recent years, intensive research efforts have focused on translating biomass waste into value-added carbon materials broadcasted for their significant role in energy and environmental applications. For the first time, high-performance carbonaceous materials for energy storage applications were developed from the multi-void structure of the boat-fruited shells of Sterculia Foetida (SF). In that view, synthesized mesoporous graphitic activated carbon (g-AC) via the combination of carbonization at various elevating temperatures of 700, 800, and 900 °C, respectively, and alkali activation by KOH, with a high specific surface area of 1040.5 m2 g-1 and a mesopore volume of 0.295 cm3 g-1. In a three-electrode configuration, the improved electrode (SF-K900) exhibited excellent electrochemical behavior, which was observed in an aqueous electrolyte (1 M H2SO4) with a high specific capacitance of 308.6 F/g at a current density of 1 A/g, owing to the interconnected mesopore structures and high surface area of SF-K900. The symmetric supercapacitor (SSC) delivered the specific capacitance of 138 F/g at 1 A/g with a high energy density (ED) of 13.4 Wh/kg at the power density (PD) of 24.12 kW/kg with remarkable cycle stability and supercapacitive retention of 93% over 5000 cycles. Based on the findings, it is possible to develop low-cost active electrode materials for high-rate performance SSC using mesoporous g-AC derived from SF boat-fruited shells.

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