材料科学
超级电容器
层状双氢氧化物
剥脱关节
黑磷
镍
电化学
钴
纳米结构
石墨烯
化学工程
纳米技术
冶金
电极
光电子学
氢氧化物
化学
物理化学
工程类
作者
Yun Zheng,Yang Zhang,Zengming Man,Wenxing Chen,Wangyang Lü,Guan Wu
标识
DOI:10.1002/adfm.202401738
摘要
Abstract Advanced innovation of flexible electrode with adequate redox activity and stably mechanical endurance that promotes charges kinetic migration and faradaic storage is pivotal for textile‐based supercapacitors (T‐SCs). Herein, this study reports a high‐performance T‐SCs electrode based on nickel–cobalt layered double hydroxides@black phosphorus (NiCo‐LDHs@BP) on a conductive silk (c‐silk) textile (NiCo‐LDHs@BP/c‐silk). Under negative voltage‐induced electrochemical exfoliation, the Ni 2+ and Co 2+ are embedded into bulk BP framework to form exfoliated BP nanosheets, and the NiCo‐LDHs are in situ grown within the BP networks, generating 3D NiCo‐LDHs@BP hetero‐nanostructure. Significantly, the NiCo‐LDHs@BP exhibits a large space‐charge area, enhanced adsorption energy for OH − and accelerated charges transfer/storage as confirmed using density functional theory calculations. Additionally, the T‐SCs electrode is fabricated by loading the blended NiCo‐LDHs@BP, sericin, and carbon nanotubes on fibroin textile via a silk reconstruction strategy, producing large area production, superior mechanical flexibility, and impressive electrochemical performance. The resultant NiCo‐LDHs@BP/c‐silk electrode exhibits large specific capacitance of 1291.3 F g −1 and considerable rate capacity in 1 M KOH electrolyte. Furthermore, the flexible solid‐state asymmetric T‐SCs deliver high specific areal energy density of 279.6 µWh cm −2 and robust folding capability (85.6% capacitance retention after 5000 folding cycles), which successfully power wearable watch and heart rate meter devices.
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