期刊
CHEMICAL ENGINEERING JOURNAL
卷 415, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128995
关键词
Transitional metal phosphide; Carbonate hydroxide; Core; shell structure; Hybrid supercapacitor
资金
- National Natural Science Foundation of China [51902122]
- Natural Science Foundation of Hubei Province [2019CFB262]
The study presents a novel hybrid supercapacitor cathode material consisting of free-standing FeCoP nanosheets and Ni-CoCH nanoneedles on carbon cloth. Due to the core/shell nanostructure and synergistic effect of two components, the electrode exhibits high specific capacity, outstanding rate capability, and good long-term cyclic stability.
Developing advanced battery-type electrode materials with versatile morphologies and micro-/nanostructures is crucial to realize high-performance hybrid supercapacitors with high energy density and excellent cycle life. Herein, a facile approach is proposed to design free-standing FeCoP nanosheets decorated by Ni substituted Co carbonate hydroxide (Ni-CoCH) nanoneedles on carbon cloth as a novel cathode for hybrid supercapacitor. This smart hetero-network assembled by conductive FeCoP nanosheets as a core and redox active Ni-CoCH nanoneedles as a shell exhibits increased surface area, improved availability of redox active sites, and facilitated ion/ electron transport for faradaic reactions when compared to a single component. Benefiting from its unique core/ shell nanostructure, multifunctionality and synergistic effect of two components, the as-prepared FeCoP@NiCoCH electrode acquires a high specific capacity of 795.5 C g-1 at a current density of 1 A g-1 and outstanding rate capability and good long-term cyclic stability (89.7% of the initial capacitance after 5000 cycles). Furthermore, a hybrid supercapacitor device consisting of FeCoP@Ni-CoCH as cathode and hierarchical porous carbon as anode in 2 M KOH electrolyte delivers a high energy density of 72.7 Wh kg-1 at a power density of 404.9 W kg- 1 and superior cyclic stability.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据