Volume 44, Issue 11 pp. 8591-8605
RESEARCH ARTICLE

Pinecone biomass-derived activated carbon: the potential electrode material for the development of symmetric and asymmetric supercapacitors

Murugesan Rajesh

Murugesan Rajesh

Laboratoire de Réactivité et Chimies des Solides (LRCS), UMR CNRS 7314, Université de Picardie Jules Verne, Hub de l'énergie, 15 rue Baudelocque, 80000, Amiens, France

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Ramu Manikandan

Ramu Manikandan

Department of Printed Electronics Engineering, Sunchon National University, 255, Jungang-ro, Suncheon-si, Jellanamdo, 57922 Republic of Korea

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Seungil Park

Seungil Park

Department of Chemistry, Dongguk University, Jung-gu, Seoul, 04620 Republic of Korea

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Byung Chul Kim

Byung Chul Kim

Department of Printed Electronics Engineering, Sunchon National University, 255, Jungang-ro, Suncheon-si, Jellanamdo, 57922 Republic of Korea

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Won-Je Cho

Won-Je Cho

Accelerator Application Research Division, Korea Atomic Energy Research Institute, Gyeongju, Gyeongbuk, 38180 Republic of Korea

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Kook Hyun Yu

Kook Hyun Yu

Department of Chemistry, Dongguk University, Jung-gu, Seoul, 04620 Republic of Korea

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C. Justin Raj

Corresponding Author

C. Justin Raj

Department of Chemistry, Dongguk University, Jung-gu, Seoul, 04620 Republic of Korea

Correspondence

C. Justin Raj, Department of Chemistry, Dongguk University, Jung-gu, Seoul-04620, Seoul, Republic of Korea.

Email: [email protected]

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First published: 21 May 2020
Citations: 118

Funding information: Ministry of Education, Grant/Award Number: NRF-2014R1A6A1030419; Ministry of Science, ICT and Future, Grant/Award Number: NRF-2015M3D1A1069710

Summary

Activated carbon, from biomass (pinecone), was synthesized by conventional pyrolysis/chemical activation process and utilized for the fabrication of supercapacitor electrodes. The pinecone-activated carbon synthesized with 1:4 ratio of KOH (PAC4) showed an increase in surface area and pore density with a considerable amount of oxygen functionalities on the surface. Moreover, PAC4, as supercapacitor electrode, exhibited excellent electrochemical performances with specific capacitance value ∼185 Fg−1 in 1 M H2SO4, which is higher than that of nonactivated pinecone carbon and 1:2 ratio KOH-based activated carbon (PAC2) (∼144 Fg−1). The systematic studies were performed to design various forms of devices (symmetric and asymmetric) to investigate the effect of device architecture and operating voltage on the performance and stability of the supercapacitors. The symmetric supercapacitor, designed utilizing PAC4 in H2SO4 electrolyte, exhibited a maximum device-specific capacitance of 43 Fg−1 with comparable specific energy/power and excellent stability (∼96% after 10 000 cycles). Moreover, a symmetric supercapacitor was specially designed using PAC4, as a positive electrode, and PAC2, as a negative electrode, under their electrolytic ion affinity, and which operates in aqueous Na2SO4 electrolyte for a wide cell voltage (1.8 V) and showed excellent supercapacitance performances. Also, a device was assembled with poly(3,4-ethylene dioxythiophene) (PEDOT) nanostructure, as positive electrode, and PAC4, as a negative electrode, to evaluate the feasibility of designing a hybrid supercapacitor, using polymeric nanostructure, as an electrode material along with biomass-activated carbon electrode.

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