Abstract

The multiple-step synthesis, harmful organic solvents, and hazardous binders are the major obstacles for supercapacitor (SC) designers. A conventional synthesis of nanocomposite is normally involves complex steps and time-consuming. To reduce these multiple steps and process time, we report carbon nitride-doped gadolinium sulfide (CN/Gd2S3) nanocomposite obtained via a one-step in situ thermal reduction method. In our study, we introduce poly(3,4-ethylenedioxythiophenes): polystyrene sulfonate (PEDOT–PSS) to act as a dual role of binder and conducting additive, and we use DI water as the solvent for the SC electrode. Despite the reduced fabrication steps, our electrode exhibits an extraordinary specific capacity valueof 1831 F g−1 at 1 A g−1 in an aqueous 2 M KOH electrolyte, as well as 98.5 % retention after 5000 cycles. Moreover, a solid-state asymmetric SC (ASC) was further made up with activated carbon (AC) as a negative electrode and CN/Gd2S3 as a positive electrode, providing a high energy density of 70.95 W h kg−1 at a specific power density of 250 W kg−1 at 1 A g−1. The remarkable specific capacitance retention of the ASC could maintain 86.8 % after 5000 cycles, indicating the potential application of CN/Gd2S3 electrode material for energy storage devices. This device (CN/Gd2S3//AC) showcased its practical application by powering twenty-six light-emitting diodes (LEDs) (each of 2.7 V) and appeared as an attractive energy storage unit for portable devices.

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.