Abstract

There is an emerging interest in developing bifunctional oxygen electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), as they are key electrochemical reactions that govern the overall performance of emerging rechargeable metal-air batteries. However, such undertaking has been a huge challenge due to the high cost of noble metals (Pt, Ir, and Ru) and their stability when used as catalysts for both the oxygen reactions. Herein, we report CoMn2O4 embedded on three-dimensional (3D) hierarchical porous carbon (HPC) derived from waste biomass (corn cobs) as an efficient noble metal-free bifunctional electrocatalyst for both ORR and OER. The hybrid catalyst (CoMn2O4/N-3DHPC) is fabricated by solvothermal reaction of as-prepared nitrogen-doped 3D HPC and CoMn2O4. The three-step template-free approach in preparing N-3DHPC ensures ample nitrogen doping using melamine as source to improve electronic conductivity of the carbon and formation of three-dimensional interconnected pore network which is favorable to a well-dispersion of CoMn2O4 crystals. Thus, the N-3DHPC possesses a high specific surface area and good electrical conductivity as a result of N doping. The same hybrid material also presents high catalytic activity towards OER, rendering them high-performing inexpensive dual-function electrocatalyst. Our result opens up new alternative cathode materials based on earth-abundant, scalable, noble metal-free catalysts for future electrochemical energy storage systems. Figure 1

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.