Issue 10, 2017, Issue in Progress

Nitrogen, sulfur and phosphorus-codoped carbon with a tunable nanostructure as an efficient electrocatalyst for the oxygen reduction reaction

Abstract

Novel types of N,S,P-codoped carbons with varied nanostructures are developed as efficient and stable electrocatalysts for the oxygen reduction reaction (ORR). The carbon catalysts were facilely prepared using poly(cyclotriphosphazene-co-4,4′-sulfonyldiphenol) (PZS) nanospheres as single precursors through a pyrolysis procedure in the presence or absence of melamine. The as-prepared microporous carbon nanospheres NSP-PC-1 with a high surface area (967 m2 g−1) exhibit a significantly enhanced ORR catalytic activity compared to their solely N-doped counterpart (N-PC-1), suggesting the remarkable contribution of additional S,P-doping on the ORR performance. More importantly, the as-prepared mesoporous carbon nanosheets NSP-PC-2 with a moderately high surface area (613 m2 g−1) and comparable overall NSP content show greatly improved ORR catalytic activity relative to that of NSP-PC-1, which is even slightly superior to that of commercial Pt/C catalysts. The excellent performance of NSP-PC-2 is mainly attributed to its proper N,S,P-codoping as well as advanced structural features.

Graphical abstract: Nitrogen, sulfur and phosphorus-codoped carbon with a tunable nanostructure as an efficient electrocatalyst for the oxygen reduction reaction

Supplementary files

Article information

Article type
Paper
Submitted
28 Aug 2016
Accepted
16 Dec 2016
First published
04 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 5782-5789

Nitrogen, sulfur and phosphorus-codoped carbon with a tunable nanostructure as an efficient electrocatalyst for the oxygen reduction reaction

K. Chen, Y. Hao, M. Zhang, D. Zhou, Y. Cao, Y. Wang and L. Feng, RSC Adv., 2017, 7, 5782 DOI: 10.1039/C6RA21540H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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