Perovskite oxides have emerged as promising alternatives to platinum group metal based state-of-the-art electrocatalysts for alkaline oxygen evolution reaction, such as RuO2 and IrO2. Specifically, LaNiO3 is a highly efficient OER electrocatalyst in alkaline environment, nevertheless, its performance is strongly dependent on the preparation conditions. In this work, a one-pot solution combustion synthesis (SCS) is presented as a straightforward method to enhance LaNiO3 OER descriptors. The process involves a clever combination of low-cost, easily available fuels: glycine (Gly) and citric acid monohydrate (CAM). The SCS Gly +CAM LaNiO3 is compared to other LaNiO3 samples obtained via sustainable wet-chemistry techniques like coprecipitations and other SCS methods. Although all samples show comparable XRD patterns, the SCS Gly +CAM route ensures superior textural properties and optimal Ni3+/Ni2+ratio, resulting in higher intrinsic OER activity. SCS Gly +CAM displays the lowest overpotential, 377 ±7 mV, further decreasing to 350 ±5 mV after 25 cycles, due to surface reconstruction. Over 25 cycles, SCS Gly +CAM LaNiO3 outperformes the state-of-the-art RuO2. To the best of our knowledge, the Gly +CAM combination has not been explored for LaNiO3 and presents a cost-effective alternative for scaled-up production of high-performance OER electrocatalysts.

Pagano, G., Panunzi, A.p., Del Gobbo, S., Lisi, N., Guglielmotti, V., Di Bartolomeo, E., et al. (2026). Boosting oxygen evolution reaction activity descriptors in LaNiO3 perovskite oxide via one-pot synthesis for alkaline electrolysis. JOURNAL OF POWER SOURCES, 663 [10.1016/j.jpowsour.2025.238820].

Boosting oxygen evolution reaction activity descriptors in LaNiO3 perovskite oxide via one-pot synthesis for alkaline electrolysis

Pagano, Giorgio;Panunzi, Anna Paola;Del Gobbo, Silvano;Guglielmotti, Valeria;Di Bartolomeo, Elisabetta;Duranti, Leonardo
2026-01-30

Abstract

Perovskite oxides have emerged as promising alternatives to platinum group metal based state-of-the-art electrocatalysts for alkaline oxygen evolution reaction, such as RuO2 and IrO2. Specifically, LaNiO3 is a highly efficient OER electrocatalyst in alkaline environment, nevertheless, its performance is strongly dependent on the preparation conditions. In this work, a one-pot solution combustion synthesis (SCS) is presented as a straightforward method to enhance LaNiO3 OER descriptors. The process involves a clever combination of low-cost, easily available fuels: glycine (Gly) and citric acid monohydrate (CAM). The SCS Gly +CAM LaNiO3 is compared to other LaNiO3 samples obtained via sustainable wet-chemistry techniques like coprecipitations and other SCS methods. Although all samples show comparable XRD patterns, the SCS Gly +CAM route ensures superior textural properties and optimal Ni3+/Ni2+ratio, resulting in higher intrinsic OER activity. SCS Gly +CAM displays the lowest overpotential, 377 ±7 mV, further decreasing to 350 ±5 mV after 25 cycles, due to surface reconstruction. Over 25 cycles, SCS Gly +CAM LaNiO3 outperformes the state-of-the-art RuO2. To the best of our knowledge, the Gly +CAM combination has not been explored for LaNiO3 and presents a cost-effective alternative for scaled-up production of high-performance OER electrocatalysts.
30-gen-2026
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore ING-IND/22
Settore IMAT-01/A - Scienza e tecnologia dei materiali
English
Con Impact Factor ISI
Oxygen evolution reaction; OER; Perovskite oxide; LaNiO3; Solution combustion synthesis; Alkaline electrolysis
https://www.sciencedirect.com/science/article/pii/S0378775325026564
Pagano, G., Panunzi, A.p., Del Gobbo, S., Lisi, N., Guglielmotti, V., Di Bartolomeo, E., et al. (2026). Boosting oxygen evolution reaction activity descriptors in LaNiO3 perovskite oxide via one-pot synthesis for alkaline electrolysis. JOURNAL OF POWER SOURCES, 663 [10.1016/j.jpowsour.2025.238820].
Pagano, G; Panunzi, Ap; Del Gobbo, S; Lisi, N; Guglielmotti, V; Di Bartolomeo, E; Duranti, L
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/439644
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