TY - JOUR
T1 - Template-directed in situ grown bimetallic nanoarchitectures with hydroxide active site enriched multi-charge transfer routes for energy storage
AU - Savariraj, Antonysamy Dennyson
AU - Thondaiman, Pugalenthiyar
AU - Sivakumar, Periyasamy
AU - Manikandan, Ramu
AU - Rodney, John D.
AU - Kim, Byung Chul
AU - Jung, Hyun
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/7/13
Y1 - 2024/7/13
N2 - Cobalt metal-organic frameworks were used as templates to obtain densely stacked two-dimensional ultrathin nanosheets of nickel/cobalt metal-organic frameworks on carbon cloth via in situ deposition at room temperature. The freestanding electrodes made of ultra-thin nanosheets and quasi-one-dimensional pores exhibited a unique electronic structure with Ni(OH)2 anchored to the surface. With distinctive structural superiority, multiple charge transfer routes, and Ni(OH)2 moieties as active sites, the electrode showcased a high areal capacity (Ca) of 2041 mC cm−2 (2 mA cm−2), a specific capacity of (Cs) 671 C g−1, a volumetric capacitance (Cvc) of 1033 F cm−3 (2 A g−1) and a prolonged cycling life of 5000 cycles with an appreciable capacity retention of 91.5% in 6 M KOH. The asymmetric supercapacitor device assembled (CC/CoNi-MOF@Ni(OH)2//CC/O,N,S@AC) delivered a superior specific capacity (Cs) of 284 C g−1, a specific capacitance (Csp) of 189 F g−1, a volumetric capacitance (Cvc) of 128 F cm−3, a maximum specific energy (Es) of 75.0 W h kg−1, and an excellent specific power (Ps) of 17.13 kW kg−1, and withstood 10 000 charge/discharge cycles with a decline of 11.3% in the initial capacity. The proposed method with DFT analysis underpins a strategy to custom-design economically viable freestanding electrodes with a large surface area per volume/mass, a synergy effect at the interface, and multiple charge transfer pathways for potential application in energy storage.
AB - Cobalt metal-organic frameworks were used as templates to obtain densely stacked two-dimensional ultrathin nanosheets of nickel/cobalt metal-organic frameworks on carbon cloth via in situ deposition at room temperature. The freestanding electrodes made of ultra-thin nanosheets and quasi-one-dimensional pores exhibited a unique electronic structure with Ni(OH)2 anchored to the surface. With distinctive structural superiority, multiple charge transfer routes, and Ni(OH)2 moieties as active sites, the electrode showcased a high areal capacity (Ca) of 2041 mC cm−2 (2 mA cm−2), a specific capacity of (Cs) 671 C g−1, a volumetric capacitance (Cvc) of 1033 F cm−3 (2 A g−1) and a prolonged cycling life of 5000 cycles with an appreciable capacity retention of 91.5% in 6 M KOH. The asymmetric supercapacitor device assembled (CC/CoNi-MOF@Ni(OH)2//CC/O,N,S@AC) delivered a superior specific capacity (Cs) of 284 C g−1, a specific capacitance (Csp) of 189 F g−1, a volumetric capacitance (Cvc) of 128 F cm−3, a maximum specific energy (Es) of 75.0 W h kg−1, and an excellent specific power (Ps) of 17.13 kW kg−1, and withstood 10 000 charge/discharge cycles with a decline of 11.3% in the initial capacity. The proposed method with DFT analysis underpins a strategy to custom-design economically viable freestanding electrodes with a large surface area per volume/mass, a synergy effect at the interface, and multiple charge transfer pathways for potential application in energy storage.
UR - http://www.scopus.com/inward/record.url?scp=85199865162&partnerID=8YFLogxK
U2 - 10.1039/d4ta03412k
DO - 10.1039/d4ta03412k
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AN - SCOPUS:85199865162
SN - 2050-7488
VL - 12
SP - 22637
EP - 22654
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 34
ER -