Abstract
Consistent design and cost-effective multifunctional electrocatalyst that comprises of highly abundant earth elements are greatly need for sustainable energy conversion applications. The present study reports a facile single-step strategy for in-situ growth of NiFeCo nanoparticles doped-ultrathin carbon nanosheets (NFC@CNSs) with hierarchical like structure by pyrolysis method. NFC@CNSs catalyst at optimum condition exhibits an outstanding activity with a low overpotential 124 and 256 mV to achieve a current density of 10 mA cm-2 with a small tafel slope 119.22 and 67.83 mV dec-1 for hydrogen and oxygen evolution reactions, respectively, in 1.0 M KOH. Furthermore, NFC@CNSs exhibits the large electrochemical active surface area of 21.30 mF cm-2, highly specific SBET surface area 145.39 m² g-1, low charge transfer resistance 46.87 ohms which forms the superior catalytic performance. The two-electrode system constructed as anode and cathode in an alkaline electrolyzer can achieve a current density of 10 mA cm-2 by a fairly low applied cell-voltage of 1.566 V under the real water splitting condition. The result revealed that, the strong coupling between NiFeCo alloy nanoparticles and carbon nanosheets might have been responsible for formulating such a remarkable electrochemical performances, electronic structure, and robust stability toward overall water splitting. Additionally, ultrathin porous carbon nanosheets structure does not only provides substantial active sites, but also facilitates the charge transfer process during diffusion and saturation of electrolytes which ultimately boost-up catalytic performances. This work provides a facile single-pot approach to construct metal-doped nanostructured materials with earth-abundant elements for sustainable industrial applications.
Published Version
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.