Selective deposition of metal oxide nanoflakes on graphene electrodes to obtain high-performance asymmetric micro-supercapacitors

To meet the charging market demands of portable microelectronics, there has been a growing interest in high performance and low-cost microscale energy storage devices with excellent flexibility and cycling durability. Herein, interdigitated all-solid-state flexible asymmetric micro-supercapacitors (...

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Veröffentlicht in:Nanoscale 2021-02, Vol.13 (5), p.3285-3294
Hauptverfasser: Xia, Zhenyuan, Mishukova, Viktoriia, Sollami Delekta, Szymon, Sun, Jinhua, Sanchez, Jaime S, Li, Jiantong, Palermo, Vincenzo
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Sprache:eng
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Zusammenfassung:To meet the charging market demands of portable microelectronics, there has been a growing interest in high performance and low-cost microscale energy storage devices with excellent flexibility and cycling durability. Herein, interdigitated all-solid-state flexible asymmetric micro-supercapacitors (A-MSCs) were fabricated by a facile pulse current deposition (PCD) approach. Mesoporous Fe 2 O 3 and MnO 2 nanoflakes were functionally coated by electrodeposition on inkjet-printed graphene patterns as negative and positive electrodes, respectively. Our PCD approach shows significantly improved adhesion of nanostructured metal oxide with crack-free and homogeneous features, as compared with other reported electrodeposition approaches. The as-fabricated Fe 2 O 3 /MnO 2 A-MSCs deliver a high volumetric capacitance of 110.6 F cm −3 at 5 μA cm −2 with a broad operation potential range of 1.6 V in neutral LiCl/PVA solid electrolyte. Furthermore, our A-MSC devices show a long cycle life with a high capacitance retention of 95.7% after 10 000 cycles at 100 μA cm −2 . Considering its low cost and potential scalability to industrial levels, our PCD technique could be an efficient approach for the fabrication of high-performance MSC devices in the future. Interdigitated asymmetric micro-supercapacitors based on Fe 2 O 3 and MnO 2 were selectively fabricated by a facile pulse current deposition (PCD) approach.
ISSN:2040-3364
2040-3372
2040-3372
DOI:10.1039/d0nr07076a