TY - JOUR
T1 - Synergistic Nanoarchitectonics of SrNiO3 Reinforced with rGO Matrix for Improved Catalytic Performance in Oxygen Evolution Reaction
AU - Abou Taleb, Manal F.
AU - Albalwi, Hanan A.
AU - Ibrahim, Mohamed M.
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2025.
PY - 2025
Y1 - 2025
N2 - The ongoing demand for sustainable and efficient electrode material for efficient oxygen evolution reaction (OER) has simulated considerable research in the development of novel electroactive catalysts. This study shows substantial advancement in the utilization of an optimized framework of metal oxides like perovskite-type oxides, combined with reduced graphene oxide (rGO) as an electroactive material for a slower OER process. In this way, we designed a rGO/SrNiO3 composite as viable and economical electrocatalysts using a sonication technique for enhanced OER activity. The composite electrochemical activity in the context of OER was assessed in a 1.0 M KOH electrolytic solution. Electrochemical outcomes of composite rGO/SrNiO3 displayed remarkable potential for the OER process by demanding an overpotential (η) of 259 mV at current density (10 mA/cm2). Moreover, the produced nanocomposite demonstrated a minimal Tafel slope (34 mV dec) and lower impedance, illustrating the efficient charge transfer resulting in improved catalytic OER performance. Further, investigation demonstrated that the nanocomposite showed an increased electrochemically active surface area (261.25 cm2) and significant stability for 50 h. The above-stated results indicate that the composite exhibits a high active site density showcasing enhanced charge transfer, improved reaction kinetics and prolonged stability resulting from a synergistic combination of rGO and SrNiO3.This study investigates how the rGO/SrNiO3 composite surpasses conventional electrocatalysts, presenting a new approach for efficient and economical catalysts for OER.
AB - The ongoing demand for sustainable and efficient electrode material for efficient oxygen evolution reaction (OER) has simulated considerable research in the development of novel electroactive catalysts. This study shows substantial advancement in the utilization of an optimized framework of metal oxides like perovskite-type oxides, combined with reduced graphene oxide (rGO) as an electroactive material for a slower OER process. In this way, we designed a rGO/SrNiO3 composite as viable and economical electrocatalysts using a sonication technique for enhanced OER activity. The composite electrochemical activity in the context of OER was assessed in a 1.0 M KOH electrolytic solution. Electrochemical outcomes of composite rGO/SrNiO3 displayed remarkable potential for the OER process by demanding an overpotential (η) of 259 mV at current density (10 mA/cm2). Moreover, the produced nanocomposite demonstrated a minimal Tafel slope (34 mV dec) and lower impedance, illustrating the efficient charge transfer resulting in improved catalytic OER performance. Further, investigation demonstrated that the nanocomposite showed an increased electrochemically active surface area (261.25 cm2) and significant stability for 50 h. The above-stated results indicate that the composite exhibits a high active site density showcasing enhanced charge transfer, improved reaction kinetics and prolonged stability resulting from a synergistic combination of rGO and SrNiO3.This study investigates how the rGO/SrNiO3 composite surpasses conventional electrocatalysts, presenting a new approach for efficient and economical catalysts for OER.
KW - Electrocatalysts
KW - OER
KW - Perovskite type oxide
KW - rGO/SrNiO Composite
KW - Sonication technique
UR - http://www.scopus.com/inward/record.url?scp=105006703368&partnerID=8YFLogxK
U2 - 10.1007/s10904-025-03842-0
DO - 10.1007/s10904-025-03842-0
M3 - Article
AN - SCOPUS:105006703368
SN - 1574-1443
JO - Journal of Inorganic and Organometallic Polymers and Materials
JF - Journal of Inorganic and Organometallic Polymers and Materials
ER -