Abstract

Heteroatom is doped in hollow carbon materials could be an excellent approach for enhancing sluggish cathodic oxygen reduction reaction (ORR) in fuel cells. Herein, we proposed a facile one step synthesis of N and P dual heteroatom doped hollow mesoporous carbon sphere (NPHS) derived from dopamine hydrochloride (DA) and phytic acid (PA) precursors is inspected for the same. By altering PA addition time interval and its loading concentration we achieved NPHS with high surface area and excellent sphere morphology. We established that the addition of 0.4 g PA at an interval of 30 h into DA mixture found to be optimum condition for the formation of NPHS-0.4. Such conditions favored formation of high surface area (1120 m2 g−1), better shell thickness (31 nm), enriched pyridinic N, P–C and P–N sites thereby resulted to an exceptional ORR activity. Moreover, electrochemical studies proved that NPHS-0.4 material possess a moderate carrier concentration (2.3 × 1015 cm−3) and flat band potential (0.56 V vs RHE) leads to a positive onset potential (0.97 V), limiting current density (4.7 mA cm−2) by adopting a close to four electron ORR pathway. In addition, it shows a remarkable electrochemical stability and excellent methanol oxidation tolerance than the Pt/C catalyst. Thus, this interesting outcome absolutely provides a platform to develop a new type of active dual doped mesoporous carbon materials for various energy storage/conversion applications.

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.