Abstract

Exploring high-activity electrocatalysts for an oxygen reduction reaction (ORR) is of great significance for a variety of renewable energy conversion and storage technologies. Here, ultrafine Mo2C nanoparticles assembled in N and P-co-doped carbon (Mo2C@NPC) was developed from ZIF-8 encapsulated molybdenum-based polyoxometalates (PMo12) as a highly efficient ORR electrocatalyst and shows excellent performance for zinc-air batteries. The well distribution of the PMo12 in ZIF-8 results in the formation of ultrafine Mo2C nanocrystallites encapsulated in a porous carbon matrix after pyrolysis. Significantly, from experimental and theoretical investigations, the highly porous structure, highly dispersed ultrafine Mo2C and the N and P co-doping in the Mo2C@NPC lead to the remarkable ORR activity with an onset potential of ∼1.01 V, a half-wave potential of ∼0.90 V and a Tafel slope of 51.7 mV dec-1 at 1600 rpm in 0.1 M KOH. In addition, the Mo2C@NPC as an ORR catalyst in zinc-air batteries achieved a high power density of 266 mW cm-2 and a high specific capacity of 780.9 mA h g-1, exceeding that driven by commercial Pt/C. Our results revealed that the porous architecture and ultrafine Mo2C nanocrystallites of the electrocatalysts could facilitate mass transport and increase the accessibility of active sites, thus optimizing their performances in an ORR. The present study provides some guidelines for the design and synthesis of efficient nanostructured electrocatalysts.

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.