Issue 35, 2020

Highly ordered macroporous dual-element-doped carbon from metal–organic frameworks for catalyzing oxygen reduction

Abstract

Multiple heteroatom-doped carbons with 3D ordered macro/meso-microporous structures have not been realized by simple carbonization of metal–organic frameworks (MOFs). Herein, ordered macroporous phosphorus- and nitrogen-doped carbon (M-PNC) is prepared successfully by carbonization of double-solvent-induced MOF/polystyrene sphere (PS) precursors accompanied with spontaneous removal of the PS template, followed by post-doping. M-PNC shows a high specific surface area of 837 m2 g−1, nitrogen doping of 3.17 at%, and phosphorus doping of 1.12 at%. Thanks to the hierarchical structure, high specific surface area, and multiple heteroatom-doping, M-PNC exhibits unusual catalytic activity as an electrocatalyst for the oxygen reduction reaction. Computational calculation reveals that the P[double bond, length as m-dash]O group helps stabilize the adsorption of intermediates, and the position of P[double bond, length as m-dash]O relative to graphitic N significantly improves the activity of the adjacent carbons for electrocatalysis.

Graphical abstract: Highly ordered macroporous dual-element-doped carbon from metal–organic frameworks for catalyzing oxygen reduction

Supplementary files

Article information

Article type
Edge Article
Submitted
03 May 2020
Accepted
04 Aug 2020
First published
11 Aug 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2020,11, 9584-9592

Highly ordered macroporous dual-element-doped carbon from metal–organic frameworks for catalyzing oxygen reduction

W. Xia, M. A. Hunter, J. Wang, G. Zhu, S. J. Warren, Y. Zhao, Y. Bando, D. J. Searles, Y. Yamauchi and J. Tang, Chem. Sci., 2020, 11, 9584 DOI: 10.1039/D0SC02518F

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.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements