Abstract

Developing efficient electrocatalysts consisting of earth-abundant elements for oxygen evolution reaction (OER) is crucial for energy devices and technologies. Herein, we report self-supported highly porous nitrogen-doped graphene foam synthesized through the electrochemical expansion of carbon-fiber paper and subsequent nitrogen plasma treatment. A thorough characterization, such as electron microscopy and synchrotron-based near-edge X-ray absorption fine structure, indicates the well-developed porous structures featuring homogeneously doped nitrogen heteroatoms. These merits ensure enriched active sites, an enlarged active surface area, and improved mass/electron transport within the continuous graphene framework, thus leading to an outstanding capability toward electrocatalyzing OER in alkaline media, even competitive with the state-of-the-art noble-/transition-metal and nonmetal electrocatalysts reported to date, from the perspectives of the sharp onset potential, a small Tafel slope, and remarkable durability. Furthermore, a rechargeable Zn-air battery with this self-supported electrocatalyst directly used as the air cathode renders a low charge/discharge overpotential and considerable life span. The finding herein suggests that a rational methodology to synthesize graphene-based materials can significantly enhance the oxygen electrocatalysis, thereby promoting the overall performance of the energy-related system.

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.