Space-confined assembly of all-carbon hybrid fibers for capacitive energy storage: realizing a built-to-order concept for micro-supercapacitors

Miniaturized portable and wearable electronics have diverse power requirements, ranging from one microwatt to several milliwatts. Fiber-based micro-supercapacitors are promising energy storage devices that can address these manifold power requirements. Here, we demonstrate a hydrothermal assembly me...

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Veröffentlicht in:Energy & environmental science 2016-01, Vol.9 (2), p.611-622
Hauptverfasser: Jiang, Wenchao, Zhai, Shengli, Qian, Qihui, Yuan, Yang, Karahan, H. Enis, Wei, Li, Goh, Kunli, Ng, Andrew Keong, Wei, Jun, Chen, Yuan
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Sprache:eng
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Zusammenfassung:Miniaturized portable and wearable electronics have diverse power requirements, ranging from one microwatt to several milliwatts. Fiber-based micro-supercapacitors are promising energy storage devices that can address these manifold power requirements. Here, we demonstrate a hydrothermal assembly method using space confinement fillers to control the formation of nitrogen doped reduced graphene oxide and multi-walled carbon nanotube hybrid fibers. Consequently, the all-carbon hybrid fibers have tunable geometries, while maintaining good electrical conductivity, high ion-accessible surface area and mechanical strength; this allows us to address two important issues in micro-supercapacitor research. First, we found a clear correlation between the geometry of the hybrid fibers and their capacitive energy storage properties. Thinner fibers (30 μm in diameter) have higher specific volumetric capacitance (281 F cm −3 ), superior rate capability, and better length dependent performance. In contrast, larger-diameter hybrid fibers (236 μm in diameter) can achieve much higher specific length capacitance (42 mF cm −1 ). Second, we realized the first built-to-order concept for micro-supercapacitors by using all-carbon hybrid fibers with diversified geometry as electrodes. The device energy can cover two orders of magnitude, from
ISSN:1754-5692
1754-5706
DOI:10.1039/c5ee02703a