Issue 15, 2026, Issue in Progress

Maximal electrocatalytic activity of Sr-doped Nd1−xSrxMnO3 perovskite oxides (x = 0.1, 0.2, 0.3) towards ORR: for next-generation power systems

Abstract

By using the sol–gel method, a series of Nd1−xSrxMnO3 perovskite oxides (x = 0.1, 0.2, 0.3), designated as NSM-0.9, NSM-0.8, and NSM-0.7, were prepared and characterized using analytical techniques including XRD, FESEM, TEM, EDS, and XPS. Our investigation revealed that NSM-0.7 (Nd0.7Sr0.3MnO3) is the most effective electrocatalyst for the oxygen reduction reaction (ORR). Its superior electrocatalytic performance in a 0.1 M KOH solution, evaluated with RDE and RRDE techniques, was quantified by an onset potential (Eon) of 0.82 V vs. RHE, a half-wave potential (E1/2) of 0.58 V vs. RHE, a limiting current density (JL) of −5 mA cm−2, which is the same as the current density of Pt/C, and a kinetic current density (Jk) of 0.41 mA cm−2 at 1600 rpm. This material also favoured a highly efficient 4e pathway with the formation of a minimal amount of H2O2. NSM-0.7's superior catalytic performance is attributed to optimal Sr-doping at the perovskite's A-site, a process that significantly enhances its Mn valence and oxygen adsorption capacity. Furthermore, chronoamperometry confirmed that NSM-0.7 exhibits superior stability compared to the benchmark Pt/C catalyst, demonstrating that strategic A-site doping is a promising approach for improving conventional perovskite oxides for electrocatalytic applications.

Graphical abstract: Maximal electrocatalytic activity of Sr-doped Nd1−xSrxMnO3 perovskite oxides (x = 0.1, 0.2, 0.3) towards ORR: for next-generation power systems

Supplementary files

Article information

Article type
Paper
Submitted
13 Jan 2026
Accepted
06 Feb 2026
First published
10 Mar 2026
This article is Open Access
Creative Commons BY license

RSC Adv., 2026,16, 13408-13419

Maximal electrocatalytic activity of Sr-doped Nd1−xSrxMnO3 perovskite oxides (x = 0.1, 0.2, 0.3) towards ORR: for next-generation power systems

B. B. Nayak, R. R. Das, P. Parida and P. Parhi, RSC Adv., 2026, 16, 13408 DOI: 10.1039/D6RA00332J

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