Abstract
The increasing global demand for energy conversion and storage technologies including water electrolysis, fuel cells, batteries & supercapacitors depend critically on the performance of their electrode components. Metal Organic Frameworks (MOFs), particularly Nickel Zeolite Imidazole Frameworks (Ni-ZIF) have drawn significant attention due to their greater electrocatalytic performance. Still, their restricted active sites & stability hinder their broader implementation in alkaline/saline water electrolysis & supercapacitor applications. Here, we are reporting the intercalation of heterostructure consisting of silver sulfide (Ag2S)/graphitic carbon nitride (g-C3N4) on Boronized Ni-ZIF (B:NZ) for empowered alkaline/saline water splitting and supercapacitor applications. These heterostructure addition over Boronized Ni-ZIF demonstrated minimal overpotentials for the oxygen evolution reaction (OER) (324 mV at 10.0 mA cm-2) and the hydrogen evolution reaction (HER) (78 mV at 10.0 mA cm-2) in alkaline medium (1 M KOH). The observed improvement in activity is ascribed to the decreased charge transfer resistance (Rct) & the augmented electrochemical active surface area (ECSA). Furthermore, Ag2S/g-C3N4/Boronized Ni-ZIF exhibited high specific capacitances of 1076.6 F/g and areal capacitance of 2584 F/cm2 at 0.50 A g-1 in supercapacitor applications. The incorporation of the g-C3N4 layer has enhanced the surface area and roughness facilitating stronger adhesion between hybrid layers which in turn resulted in prolonged stability exceeding 20 h in water splitting and 86 % retention in supercapacitor application.
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.