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

被引:1
|
作者
Xia, Zhenyuan [1 ,2 ]
Mishukova, Viktoriia [3 ]
Sollami Delekta, Szymon [3 ]
Sun, Jinhua [1 ]
Sanchez, Jaime S. [1 ]
Li, Jiantong [3 ]
Palermo, Vincenzo [1 ,2 ]
机构
[1] Chalmers Univ Technol, Dept Ind & Mat Sci, Horsalsvagen 7B, S-41258 Gothenburg, Sweden
[2] CNR, Ist Sintesi Organ & Fotoreattivita, Via Gobetti 101, I-40129 Bologna, Italy
[3] KTH Royal Inst Technol, Sch Elect Engn & Comp Sci, Electrum 229, S-16440 Kista, Sweden
基金
瑞典研究理事会; 欧盟地平线“2020”;
关键词
PULSE CURRENT DEPOSITION; MANGANESE OXIDE; ENERGY-STORAGE; MICROSUPERCAPACITORS; FABRICATION; CHARGE; NANOSHEETS; NANOWIRES; MECHANISM; HEMATITE;
D O I
10.1039/d0nr07076a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 Fe2O3 and MnO2 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 Fe2O3/MnO2 A-MSCs deliver a high volumetric capacitance of 110.6 F cm(-3) at 5 mu A 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 mu A 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.
引用
收藏
页码:3285 / 3294
页数:10
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