Issue 36, 2024

Evolution of high spin state single-atom catalyst active centers in Na–O2 batteries

Abstract

Due to the abundance and economic viability of Na resources, Na–O2 batteries are regarded as promising energy storage devices in achieving the carbon neutrality goals, featuring an ultra-high theoretical energy density. Nevertheless, the slow ion diffusion kinetics hinders the applications of batteries. Spin-induced single-atom catalysts (SACs) offer a promising avenue to ameliorate the activation process of the battery reaction. Herein, we study the adsorption–activation mechanism of O2 on six spin-induced SACs (i.e., MnN3, MnN4, CoN3, CoN4, NiN3, and NiN4) in Na–O2 batteries. We find that oxygen in mono-vacancy catalysts with high spin states favors the side-on adsorption mode. This mode enhances the coupling between the 3dxy orbital of metal and O2, and alters the active center structures which further reduces the reaction overpotential by cutting down the OER potential. Moreover, we establish the scaling relationship between the oxygen adsorption energy and battery overpotential with a correlation coefficient of 0.98. Our study elucidates the evolution of the SAC active center induced by a shift of spin states and its impact on the oxygen adsorption–activation process which strongly determines the battery performance. The established structure–activity relationship of spin induced SACs may shed light on the catalyst modification involving the oxygen adsorption and activation to achieve a better performance.

Graphical abstract: Evolution of high spin state single-atom catalyst active centers in Na–O2 batteries

Supplementary files

Article information

Article type
Paper
Submitted
04 4 2024
Accepted
08 8 2024
First published
09 8 2024

J. Mater. Chem. A, 2024,12, 24285-24295

Evolution of high spin state single-atom catalyst active centers in Na–O2 batteries

J. Li, A. Mao, J. Li, H. Liu and C. Lian, J. Mater. Chem. A, 2024, 12, 24285 DOI: 10.1039/D4TA02309A

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