Issue 18, 2021

Metal free-covalent triazine frameworks as oxygen reduction reaction catalysts – structure–electrochemical activity relationship

Abstract

Nitrogen-rich porous carbon polymers are highly promising oxygen reduction reaction (ORR) catalysts and possess great potential to replace Pt-based precious metals used in energy storage and conversion systems. In this study, covalent triazine frameworks (CTFs) were synthesized via an ionothermal route based on different monomers and synthesis temperatures (400–750 °C) and tested in alkaline media with a rotating disk electrode (RDE). The effect of the applied monomer and temperature on the surface functionalities of the frameworks and thus correlation to their ORR activities are deeply discussed. Micro/mesoporous, hierarchically ordered and highly conductive N-rich materials with up to 2407 m2 g−1 specific surface areas and 2.49 cm3 g−1 pore volumes were achievable. Owing to the high surface area (1742 m2 g−1), pore volume (1.56 cm3 g−1), highest conductivity, electrochemically active surface area and hierarchical mesoporous structure, CTF DCBP-750 facilitated 0.9 V onset potential (only 0.06 V larger than that of the benchmark 10 wt% Pt/C) with 5.1 mA cm−2 limiting current density. In addition to the structural properties, graphitic nitrogen species, active sites responsible for binding and activating O2, rather than pyridinic nitrogen appear to be more important for the overall ORR performance. Thus, the trade-off point is crucial to obtain optimal ORR activity with metal-free CTFs.

Graphical abstract: Metal free-covalent triazine frameworks as oxygen reduction reaction catalysts – structure–electrochemical activity relationship

Supplementary files

Article information

Article type
Paper
Submitted
07 Marts 2021
Accepted
11 Jūn. 2021
First published
06 Aug. 2021

Catal. Sci. Technol., 2021,11, 6191-6204

Metal free-covalent triazine frameworks as oxygen reduction reaction catalysts – structure–electrochemical activity relationship

T. Sönmez, K. S. Belthle, A. Iemhoff, J. Uecker, J. Artz, T. Bisswanger, C. Stampfer, H. H. Hamzah, S. A. Nicolae, M. Titirici and R. Palkovits, Catal. Sci. Technol., 2021, 11, 6191 DOI: 10.1039/D1CY00405K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements