Issue 23, 2022

Highly efficient OER catalyst enabled by in situ generated manganese spinel on polyaniline with strong coordination

Abstract

The oxygen evolution reaction (OER), as the rate-determining step of electrochemical water splitting, is extremely crucial, and thus it is a requisite to engineer feasible and effective electrocatalysts to shrink the reaction energy barrier and accelerate the reaction. Herein, monodisperse Mn3O4 nanoparticles on a PANI substrate were synthesized by polymerization and in situ oxidation. Combining Mn3O4 nanoparticles and PANI fibers can not only maximize the strong coupling effect and synergistic effect but also construct a well-defined three-dimensional structure with extensive exposed active sites, where the permeation and adherence of the electrolyte are made exceedingly feasible, thus displaying excellent OER activity. Benefiting from the outstanding structural stability, the resulting Mn3O4/PANI/NF is able to deliver a low overpotential of 262 mV at a current density of 10 mA cm−2, which outperforms the commercial RuO2 catalyst (275 mV) as well as presently reported representative Mn-based and PANI-based electrocatalysts and state-of-the-art OER electrocatalysts. The synthetic method for Mn3O4/PANI not only provides a brand-new avenue for the rational design of inorganic material/conductive polymer composites but also broadens the understanding of the mechanism of Mn-based catalysts for highly enhanced OER.

Graphical abstract: Highly efficient OER catalyst enabled by in situ generated manganese spinel on polyaniline with strong coordination

Supplementary files

Article information

Article type
Paper
Submitted
20 Apr 2022
Accepted
18 May 2022
First published
03 Jun 2022

Dalton Trans., 2022,51, 9116-9126

Highly efficient OER catalyst enabled by in situ generated manganese spinel on polyaniline with strong coordination

Y. Duan, Z. Huang, J. Ren, X. Dong, Q. Wu, R. Jia, X. Xu, S. Shi and S. Han, Dalton Trans., 2022, 51, 9116 DOI: 10.1039/D2DT01236G

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