• 文献标题:   Ultrafine Ni(OH)(2) nanoplatelets grown on 3D graphene hydrogel fabricated by electrochemical exfoliation for high-performance battery-type asymmetric supercapacitor applications
  • 文献类型:   Article
  • 作  者:   HUANG Y, BUFFA A, DENG HQ, SARKAR S, OUYANG Y, JIAO XY, HAO QL, MANDLER D
  • 作者关键词:   exfoliated graphite, doublephase electrochemical deposition, 3d electrode, asymmetric supercapacitor, graphene hydrogel
  • 出版物名称:   JOURNAL OF POWER SOURCES
  • ISSN:   0378-7753 EI 1873-2755
  • 通讯作者地址:   Xiao Ling Wei 200
  • 被引频次:   3
  • DOI:   10.1016/j.jpowsour.2019.227046
  • 出版年:   2019

▎ 摘  要

Rechargeable energy storage systems with merits of durable, powerful, and inexpensive are urgently desired along with the rapid development in portable electronics and electric vehicles. Herein, a facile electrochemical method is employed to prepare a free-standing exfoliated graphite (EG) electrode with significantly enhanced surface area and pore volume. Then a binder-free composite electrode is fabricated by a double-phase (DP) electrochemical deposition of vertical arrays of Ni(OH)(2) throughout the EG hydrogel electrode in an organic electrolyte. The obtained composite, Ni(OH)(2)@EG-DP, exhibits battery-type capacitive behavior and much higher capacity than its counterparts fabricated either by single-phase electrochemical deposition or with non-exfoliated graphite foil. Ni(OH)(2)@EG-DP also exhibits remarkable rate capability and cycling stability, due to the well-dispersed ultrathin Ni(OH)(2) nanoplatelets and the graphene-like expanded gallery of EG, enabling the efficient transportation of both electrons and ions. When coupling with an active carbon anode, the assembled asymmetric supercapacitor shows 84.5% capacity retention after 20000 cycles at 8 A g(-1), and a high energy density of 34.7 Wh kg(-1) at the power density of 15 kW kg(-1). This work opens an avenue towards the efficient construction of free-standing three-dimensional (3D) conductive substrates and high-performance 3D hybrid electrodes using electrochemistry.