TY - JOUR
T1 - Pinecone biomass-derived activated carbon
T2 - the potential electrode material for the development of symmetric and asymmetric supercapacitors
AU - Rajesh, Murugesan
AU - Manikandan, Ramu
AU - Park, Seungil
AU - Kim, Byung Chul
AU - Cho, Won Je
AU - Yu, Kook Hyun
AU - Raj, C. Justin
N1 - Publisher Copyright:
© 2020 John Wiley & Sons Ltd
PY - 2020/9/1
Y1 - 2020/9/1
N2 - 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.
AB - 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.
KW - asymmetric supercapacitor
KW - biomass activated carbon
KW - impedance spectroscopy
KW - PEDOT
KW - specific energy
UR - http://www.scopus.com/inward/record.url?scp=85085026018&partnerID=8YFLogxK
U2 - 10.1002/er.5548
DO - 10.1002/er.5548
M3 - Article
AN - SCOPUS:85085026018
SN - 0363-907X
VL - 44
SP - 8591
EP - 8605
JO - International Journal of Energy Research
JF - International Journal of Energy Research
IS - 11
ER -