TY - JOUR
T1 - Fabrication of cobalt oxide@cellulose/nitrogen doped carbon nanotubes decorated metal organic frameworks composite for symmetric supercapacitor applications
AU - Ramesh, Sivalingam
AU - Rabani, Iqra
AU - Indumathi, T.
AU - Yadav, H. M.
AU - Selvaraj, Manickam
AU - Pai Sunajadevi, Kalathiparambil Rajendra
AU - Seo, Young Soo
AU - Kim, Joo Hyung
AU - Kim, Heung Soo
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - The two main issues facing the world's population now are energy storage needs and environmental protection. A lot of work has gone into creating electrochemical energy storage using chemical processes and a variety of possible electrode active materials. Supercapacitors, which are energy storage devices with a unique structure and morphology of cellulose materials for green energy resource. In this regard, solid state hydrothermal process is used to fabricate Co3O4@Cellulose (CE), Co3O4@CE/N-MWCNT, and Co3O4@CE/N-MWCNT/ZIF-67 composite materials. XRD, XPS, BET, and HR-TEM analyses verified the structural, surface, and morphological analysis. The electrochemical studies by a three- and two-electrode fabrication in presence of 1M KOH electrolyte for supercapacitor applications. When 1M KOH electrolyte is present, the fabricated Co3O4@CE/N-MWCNT/ZIF-67composite electrode displayed exceptional cyclic stability and a specific capacitance of ∼835 F g−1 at 1 A/g. The constructed composite electrodes of Co3O4, Co3O4@CE, and Co3O4@CE/N-MWCNT have specific capacitances of 263, 406, and 576 F g−1 at 1 A/g, respectively, which improves electrochemical properties using a three-electrode design. The Co3O4@CE-N-MWCNT/ZIF-67//1MKOH/SSC composite is produced using two electrode configurations. The final material showed a capacitance of 258 F g−1 at 1 A/g, a capacitance retention of 84.95 % across 8000 cycles, and an energy density of 30.99 W h kg−1 at a power density of 5409 W kg−1. Hence, the composite electrodes that have been produced have the potential to be used in electrochemical systems.
AB - The two main issues facing the world's population now are energy storage needs and environmental protection. A lot of work has gone into creating electrochemical energy storage using chemical processes and a variety of possible electrode active materials. Supercapacitors, which are energy storage devices with a unique structure and morphology of cellulose materials for green energy resource. In this regard, solid state hydrothermal process is used to fabricate Co3O4@Cellulose (CE), Co3O4@CE/N-MWCNT, and Co3O4@CE/N-MWCNT/ZIF-67 composite materials. XRD, XPS, BET, and HR-TEM analyses verified the structural, surface, and morphological analysis. The electrochemical studies by a three- and two-electrode fabrication in presence of 1M KOH electrolyte for supercapacitor applications. When 1M KOH electrolyte is present, the fabricated Co3O4@CE/N-MWCNT/ZIF-67composite electrode displayed exceptional cyclic stability and a specific capacitance of ∼835 F g−1 at 1 A/g. The constructed composite electrodes of Co3O4, Co3O4@CE, and Co3O4@CE/N-MWCNT have specific capacitances of 263, 406, and 576 F g−1 at 1 A/g, respectively, which improves electrochemical properties using a three-electrode design. The Co3O4@CE-N-MWCNT/ZIF-67//1MKOH/SSC composite is produced using two electrode configurations. The final material showed a capacitance of 258 F g−1 at 1 A/g, a capacitance retention of 84.95 % across 8000 cycles, and an energy density of 30.99 W h kg−1 at a power density of 5409 W kg−1. Hence, the composite electrodes that have been produced have the potential to be used in electrochemical systems.
KW - Cellulose (CE)
KW - Cobalt oxides
KW - Composite
KW - Hydrothermal process
KW - Nitrogen doped MWCNT
KW - Symmetric supercapacitor (SSC)
KW - Zeolite imidazole frame work (ZIF-67)
UR - http://www.scopus.com/inward/record.url?scp=85215841391&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2025.236288
DO - 10.1016/j.jpowsour.2025.236288
M3 - Article
AN - SCOPUS:85215841391
SN - 0378-7753
VL - 631
JO - Journal of Power Sources
JF - Journal of Power Sources
M1 - 236288
ER -