Abstract

The design and synthesis of nitrogen-doped (N-doped) carbon nanosheets network offer a tremendous electro-catalytic activity due to their high surface area and tunable porous structures for the development of direct alcohol fuel cells (DAFCs). In this work, nickel (Ni) nanoparticles entrapped onto the N-doped mesoporous carbon nanosheets network such as Ni–C-1, Ni–C-2, and Ni–C-3 are fabricated and characterized using SEM, TEM, XRD, XPS, and electrochemical methods. The physicochemical characterization of synthesized nanocomposite material confirmed that sodium chloride (NaCl) plays a major role in the formation of porous nanostructure during carbonization process. Under optimized conditions, all the above carbon samples are tested as potential electro-catalyst towards the electro-oxidation of glycerol for DAFCs application. Among them, the Ni–C-2 catalyst displays enhanced catalytic current density (~2.6 mA) and low onset oxidation potential (0.11 V) for electro-oxidation of glycerol than the Ni–C-1, and Ni–C-3 catalysts in alkaline electrolyte. In addition, the mesoporous carbon network structure containing Ni nanoparticles delivers substantial longer durability/robustness when compared to the conventional Pt/C-catalyst towards stable- and efficient electro-oxidation of glycerol for the first time. Thus, the obtained electro-catalytic performance revealed that Ni–C-2 is considered as a promising earth abundant non-noble low-cost catalyst material for DAFCs application.

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.