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Role of lattice oxygen content and Ni geometry in the oxygen evolution activity of the Ba-Ni-O system

DOI: 10.1016/j.jpowsour.2018.09.098 DOI Help

Authors: María Retuerto (CSIC) , Federico Calle-vallejo (Universitat de Barcelona) , Laura Pascual (CSIC) , Pilar Ferrer (Diamond Light Source) , Álvaro García (CSIC) , Jorge Torrero (CSIC) , Diego Gianolio (Diamond Light Source) , José Luis G. Fierro (CSIC) , Miguel A. Peña (CSIC) , José Antonio Alonso (CSIC) , Sergio Rojas (CSIC)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Journal Of Power Sources , VOL 404 , PAGES 56 - 63

State: Published (Approved)
Published: November 2018
Diamond Proposal Number(s): 18119

Abstract: The activity of oxides towards the oxygen evolution reaction (OER) is usually tuned by changing the transition metal components and/or the surface facets. An important yet less studied feature is the repercussion of the lattice oxygen content of the oxide in the active site's coordination and catalytic performance. This is illustrated here for the Ba-Ni-O system. We synthesized two oxides with Ni in different coordination and oxidation states, namely BaNiO2 with Ni2+ in square-planar positions, and BaNiO2.78(2) with Ni3+ and Ni4+ in octahedral positions. We show that the square-planar configuration of Ni endows BaNiO2 with high intrinsic OER activity, comparable to the best catalysts in the literature. DFT indicates that progressively lowering the lattice oxygen content from BaNiO3 to BaNiO2 increases the Ni sites' affinity for the reaction intermediates, thereby lowering the OER overpotential. Thus, oxygen content is an important parameter in oxide catalysts, as it modulates the coordination, orbital splitting, oxidation number, and catalytic activity of the active sites.

Journal Keywords: Oxygen Evolution Reaction; Perovskite; Ni; Electrolysis; Electrochemical Step Symmetry Index

Subject Areas: Chemistry, Materials


Instruments: B18-Core EXAFS

Documents:
1-s2.0-S0378775318310772-main.pdf