超级电容器
材料科学
硫化
聚吡咯
电化学
阴极
化学工程
电容
硫化钴
双金属片
氢氧化物
硫化物
法拉第效率
储能
阳极
电极
纳米技术
冶金
化学
金属
硫黄
功率(物理)
物理
物理化学
量子力学
工程类
作者
Xueyan Zhao,Qingxiang Ma,Kai Tao,Lei Han
标识
DOI:10.1021/acsaem.1c00516
摘要
Bimetallic transition metal sulfide is considered to be an excellent cathode material for asymmetric supercapacitors (ASCs) because of its outstanding electrochemical activity and rich valences for the faradaic reactions. However, it usually shows a small specific surface area and sluggish reaction kinetics leading to poor energy storage capacity and unsatisfactory rate performance. Herein, a zeolitic imidazolate framework-67 (ZIF-67) dodecahedron is uniformly stringed on intercrosslinked polypyrrole (PPy) via an in situ synthesis, and the ZIF-67 is converted into NiCo layered double hydroxide (LDH) through an etching and coprecipitation process with Ni(NO3)2. The final porous nickel cobalt sulfide@PPy (NiCoS@PPy) is obtained after a solution sulfidation. The NiCoS@PPy electrode achieves an ultrahigh specific capacitance of 2316.6 and 1409.5 F g–1 at 1 and 10 A g–1, largely outperforming control NiCoS or NiCo-LDH@PPy. Furthermore, the fabricated ASC utilizing NiCoS @PPy as the cathode displays outstanding energy storage capability (34.4 Wh kg–1 at 799 W kg–1) and splendid cyclic life (retaining ∼84% initial capacitance after 8500 cycles). The excellent electrochemical performance makes the NiCoS@PPy electrode have prospective applications in electrochemical energy storage.
科研通智能强力驱动
Strongly Powered by AbleSci AI