Abstract
Two-dimensional (2D) hydroxide nanosheets can exhibit exceptional electrochemical performance owing to their shortened ion diffusion distances, abundant active sites, and various valence states. Herein, we report ZnCo1.5(OH)4.5Cl0.5·0.45H2O nanosheets (thickness ∼30 nm) which crystallize in a layered structure and exhibit a high specific capacitance of 3946.5 F g-1 at 3 A g-1 for an electrochemical pseudocapacitor. ZnCo1.5(OH)4.5Cl0.5·0.45H2O was synthesized by a homogeneous precipitation method and spontaneously crystallized into 2D nanosheets in well-defined hexagonal morphology with crystal structure revealed by synchrotron X-ray powder diffraction data analysis. In situ growth of ZnCo1.5(OH)4.5Cl0.5·0.45H2O nanosheet arrays on conductive Ni foam substrate was successfully realized. Asymmetric supercapacitors based on ZnCo1.5(OH)4.5Cl0.5·0.45H2O nanosheets @Ni foam// PVA, KOH//reduced graphene oxide exhibits a high energy density of 114.8 Wh kg-1 at an average power density of 643.8 W kg-1, which surpasses most of the reported all-solid-state supercapacitors based on carbonaceous materials, transition metal oxides/hydroxides, and MXenes. Furthermore, a supercapacitor constructed from ZnCo1.5(OH)4.5Cl0.5·0.45H2O nanosheets@PET substrate shows excellent flexibility and mechanical stability. This study provides layered bimetallic hydroxide nanosheets as promising electroactive materials for flexible, solid-state energy storage devices, presenting the best reported performance to date.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.