Three‐Dimensional MoS2@CNT/RGO Network Composites for High‐Performance Flexible Supercapacitors

Two‐dimensional atomically thick materials, reduced graphene oxide (RGO), and layered molybdenum disulfide (MoS2) have been investigated as potential novel energy storage materials because of their distinct physicochemical properties. These materials suffer, however, from rapid capacity decay and lo...

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Veröffentlicht in:Chemistry : a European journal 2017-03, Vol.23 (14), p.3438-3446
Hauptverfasser: Wang, Shouzhi, Zhu, Jiayan, Shao, Yongliang, Li, Weiran, Wu, Yongzhong, Zhang, Lei, Hao, Xiaopeng
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Sprache:eng
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Zusammenfassung:Two‐dimensional atomically thick materials, reduced graphene oxide (RGO), and layered molybdenum disulfide (MoS2) have been investigated as potential novel energy storage materials because of their distinct physicochemical properties. These materials suffer, however, from rapid capacity decay and low rate capability. This study describes a facile, binder‐free approach to fabricate large‐scale, 3D network structured MoS2@carbon nanotube (CNT)/RGO composites for application in flexible supercapacitor devices. The as‐obtained composites possess a hierarchical porosity, and an interconnected framework. The electrochemical supercapacitive measurements of the MoS2@CNT/RGO electrode show a high specific capacitance of 129 mF cm−2 at 0.1 mA cm−2. The symmetric supercapacitor devices based on the as‐obtained composites exhibit a long lifetime (94.7 % capacitance retention after 10 000 cycles), and a high electrochemical performance (29.7 mF cm−2). The present experimental findings will lead to scalable, binder‐free synthesis of MoS2@CNT/RGO hybrid electrodes, with enhanced, flexible, supercapacitive performance, in portable and wearable energy storage devices. Will it bend? A novel 3D porous network MoS2@CNT/RGO membrane was designed, fabricated, and assembled into a symmetric flexible supercapacitor. The supercapacitor exhibits a high rate capability, stable cycling life at high rates, and high power density. The study may provide opportunities for expanding the potential of self‐supporting electrode materials in portable/wearable electronics.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201605465