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Article 2023 · 20 atıf

Design and synthesis of a MnCo-MOF modified flexible 3D graphene sponge electrode for an asymmetric supercapacitor with high power and energy density

Ercarikci, Elif, Topcu, Ezgi, Kiransan, Kader Dagci

Özet

Recently, 3D materials such as graphene sponges with metal-organic frameworks (MOFs) have received a lot of attention as electrodes in energy storage devices. The porous skeleton structure of both graphene sponge and MOFs facilitates the transport of electrolytes and metal ions in the MOF, increasing the active surface area. In this study, an electrode with high capacitive performance was designed by combining a 3D flexible graphene sponge (3DG) with a MnCo-MOF nanostructure. The as-prepared MnCo-MOF/3DG exhibited a capacitive performance of 4086 F g(-1) at 1 A g(-1) and maintained 83% of its initial capacitance value after 10 000 cycles. Additionally, an asymmetric supercapacitor with high energy density was developed successfully using MnCo-MOF/3DG as the positive electrode and 3DG as the negative electrode. This MnCo-MOF/3DG//3DG circuit with stable EDLC behavior showed a high specific capacitance of 2383 F g(-1) at 1 A g(-1) and excellent cycling durability with 92% specific capacitance retained even after 10 000 cycles. The designed flexible asymmetric supercapacitor circuit demonstrated remarkable electrochemical performance with a high energy density of 198.5 W h kg(-1) and a power density of 5823 W kg(-1) as well as excellent mechanical flexibility and cycling stability. The efficient fabrication of MnCo-MOF-modified flexible 3D graphene sponge electrodes with remarkable performance will open a new avenue for potential applications in flexible electronics.

Anahtar Kelimeler
METAL-ORGANIC-FRAMEWORKS HIGH-PERFORMANCE ACTIVATED CARBON OXIDE HYBRID COMPOSITES STORAGE NANOSTRUCTURES NANOSHEETS OXIDATION
WoS Kategorileri
Materials Science, Multidisciplinary Physics, Applied
Künye
Dergi
JOURNAL OF MATERIALS CHEMISTRY C
Yıl
2023
Cilt
11
Sayı
28
Sayfa
9593-9601
ISSN
2050-7526
eISSN
2050-7534
DOI
10.1039/d3tc00970j
WoS UID
WOS:001018500900001
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