Abstract

The energy storing devices such as batteries as well as super-capacitors are limited due to poor electrochemical performance and less cycling stability of electrode materials. To achieve significantly high performance and stability which are critical criteria for examining an electrode material for supercapacitor applications, the production of nanostructured materials for improving specific surface area and electrical conductivity is very crucial. In present work, simple and economical coprecipitation route is used to synthesize ZrO2/CdS nanohybrid. Structure, chemical composition, oxidation state and morphology of the synthesized materials i.e. ZrO2, CdS and ZrO2/CdS nanohybrid were seasoned via X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), transmission electron microscopy (TEM), respectively. Energy dispersive x-ray spectroscopy (EDX) was used to confirm the elemental composition of all prepared materials. The incorporation of CdS nanowires in ZrO2 sheets improves the morphology of the nanohybrid. Due to improved morphology, the nanohybrid (ZrO2/CdS) showed a remarkable stability (2000 cycles), specific capacitance (1391F/g) and specific energy (48.27 Wh/Kg) at a current density of 2.5A/g measured via three electrode galvanostatic charge discharge (GCD) system. Additionally, extraordinary electrochemical performances of ZrO2/CdS nanohybrid have remarkable technological applications in future.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.