Abstract

A nitrogen-doped carbon quantum dot/graphene (N-CQD/G) hybrid nanocomposite was synthesized in-situ using a sacrificial template-assisted pyrolysis method with an oligomeric phenolic resin as the carbon source and dicyandiamide as the sacrificial template precursor/nitrogen source. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction, atomic force microscopy, nitrogen adsorption–desorption, Raman and X-ray photoelectron spectroscopy were employed to characterize N-CQD/G samples. The Pt nanoparticles were then deposited onto N-CQD/G hybrids (Pt/N-CQD/G) using a polyol reduction method. Structural and morphological investigations for the Pt/N-GQD/G revealed that ultrafine Pt particles with an average size of 2.1 nm, together with CQDs, are uniformly dispersed on the surfaces of graphene nanosheets. Compared with commercial Pt/C catalysts, Pt/N-CQD/G with highly electrochemical active surface area (ca. 123.4 m2 g−1Pt) show remarkably enhanced electrocatalytic activity and durability toward oxygen reduction reaction (ORR). The superior ORR catalytic performance of Pt/N-CQD/G can be attributed to highly distributed Pt nanoparticles with small size, nitrogen-doping, and strong interaction between metal and support, as well as the unique structure of N-CQD/G hybrids which combines the advantages of both carbon quantum dot and graphene, such as abundant edges and doping sites, high surface area, large pore size and high electrical conductivity.

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.