In-situ surface activation of polycrystalline LaNiO3 electrocatalyst for the oxygen evolution reaction

被引:1
作者
De Amicis, Giuditta [1 ]
Testolin, Anna [2 ]
Cazzaniga, Cristina [2 ]
D'Acapito, Francesco [3 ]
Minguzzi, Alessandro [4 ,5 ,6 ]
Ghigna, Paolo [1 ,4 ]
Vertova, Alberto [4 ,5 ]
机构
[1] Univ Pavia, Dipartimento Chim, Viale Taramelli 16, I-27100 Pavia, Italy
[2] Ind Nora SpA, Via Leonardo Bistolfi 35, I-20134 Milan, Italy
[3] CNR, IOM, OGG, LISA CRG,ESRF, 71 Ave Martyrs, F-38000 Grenoble, France
[4] Ist Nazl Sci & Tecnol Mat, Via Giusti 9, Florence, Italy
[5] Univ Milan, Dipartimento Chim, Via Golgi 19, I-20133 Milan, Italy
[6] Politecn Milan, Dipartimento Energia, Via Lambruschini 4A, I-20156 Milan, Italy
关键词
Alkaline water electrolysis; Oxygen evolution reaction; Surface disorder; Polycrystalline LaNiO 3; Operando X-ray absorption; RAY-ABSORPTION SPECTROSCOPY; WATER OXIDATION; OPERANDO; IRIDIUM; STABILITY; PHOTOANODES; REDUCTION; CATALYST; OXIDES;
D O I
10.1016/j.ijhydene.2024.09.038
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The efficiency of hydrogen production from water electrolysis is limited by the sluggish kinetics of the Oxygen Evolution Reaction (OER), necessitating catalytic material to avoid the high overpotentials. This study investigates LaNiO3 as a promising electrocatalyst for the OER in Alkaline Water Electrolysis selected for its cost-effectiveness and easy scale-up. LaNiO3, prepared by a co-precipitation method, shows good OER activity and electrochemical stability. Operando X-Ray Absorption Spectroscopy (XAS), reveals a crucial role of the Ni(II)/Ni(III) redox couple. Notably, a layer of a Ni(II) compound formed at the catalyst surface is oxidized under anodic potentials and possibly becomes the active sites for the adsorption of OH- and for the OER reaction. High resolution transmission electron microscopy confirms the formation of a defective outer layer during operation, indicating the presence of disordered structure on the surface of the electrocatalyst, which increases the number of active sites for the OER.
引用
收藏
页码:890 / 901
页数:12
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