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Composite of a perovskite oxide (LaCoO3) with polyaniline: a novel electrode material for OER

Lamia Abu El Maati, Muneerah Alomar, Al-Juri T. Al-Dows, Eman Alzahrani, Rizwan Ul Hassan, and Aqsa Batool

Department of Physics, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia

 

E-mail: rizwanhassan72@gachon.ac.kr

Received: 15 March 2026  Accepted: 7 May 2026

Abstract:

The fabrication and development of extremely effective catalyst for OER is crucial for advancement of water oxidation technologies. Perovskite oxides, especially LaCoO₃, have garnered substantial interest attributed to their advantageous electronic structure and catalytic properties; yet, their practical application is constrained by elevated overpotential and slow charge-transfer kinetics. This study successfully combined polyaniline (PANI) with LaCoO3 using a straightforward hydrothermal method to improve its electrocatalytic activity. Various physical approaches were applied to assess surface area, morphology and crystalline framework of fabricated composite. The physical characterization results indicate an enhanced surface area (SA = 98.57 m2/g) for the composite. The synthesized LaCoO3-PANI composite demonstrated boosted OER performance, attaining a less overpotential (η) of 270 mV at current density (j) of 10 mA/cm2 and low Tafel value of 38 mV/dec, signifying accelerated reaction kinetics. Furthermore, LaCoO3-PANI showed a greater electrochemical surface area (ECSA) of 250 cm2, remarkable stability of 30 h and negligible solution resistance (Rs = 0.99 Ω). The enhanced efficacy is due to the conductive PANI network, which boosts surface exposure and enables swift electron movement. These findings emphasize LaCoO3-PANI as a potential and effective electrocatalyst in sustainable water-splitting applications.

Keywords: LaCoO3-PANI; Porous substrate; Conductive polymer; OER; Electrocatalyst

Full paper is available at www.springerlink.com.

DOI: 10.1007/s11696-026-05028-5

 

Chemical Papers 80 (9) 10601–10611 (2026)

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