Physicochemical activation of soap-nut seeds-derived hard carbon as a sustainable anode for lithium-ion batteriesShow others and affiliations
2024 (English)In: New Journal of Chemistry, ISSN 1144-0546, E-ISSN 1369-9261, Vol. 48, no 42, p. 18277-18290Article in journal (Refereed) Published
Abstract [en]
Research studies on biomass-derived hard carbon are gaining notable scientific interest due to its potential application as a sustainable anode for Li-ion batteries (LIBs). The current study presents the development of hard carbon from soap-nut seed biomass, with the optimization of its pyrolysis temperature, followed by chemical activation using KOH- and ZnCl2-activated reagents. The physicochemical behaviour of the developed materials is studied by utilizing XRD, HRTEM, BET, and XPS techniques. CV and galvanostatic charge-discharge curves are examined to assess the potential of the material for the application as a sustainable anode in LIBs. The electrochemical performance of the developed materials obtained at various pyrolysis temperatures (600, 700, 800 and 900 °C) and chemically activated with KOH and ZnCl2 is explained with respect to their interplanar spacing, ID/IG ratio, and specific pore area. Among the different pyrolysis temperatures, the hard carbon pyrolyzed at 700 °C exhibits the maximum reversible specific discharge capacity of 391 mA h g−1 at a current density of 100 mA g−1. The present study also demonstrates that the electrochemical performance of the hard carbon deteriorates after chemical activation with ZnCl2, whereas chemical activation with KOH enhances its performance. The chemically-activated hard carbon using KOH exhibits a reversible specific discharge capacity of 454 mA h g−1 at 100 mA g−1 and delivers a better cycling stability (500 cycles) of 83 mA h g−1 at 300 mA g−1
Place, publisher, year, edition, pages
Royal Society of Chemistry, 2024. Vol. 48, no 42, p. 18277-18290
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:umu:diva-231155DOI: 10.1039/d4nj03372hISI: 001332293800001Scopus ID: 2-s2.0-85206509364OAI: oai:DiVA.org:umu-231155DiVA, id: diva2:1909442
2024-10-302024-10-302025-01-13Bibliographically approved