journal article·2024-08-09Open access

Oxygen Dimerization as a Defect-Driven Process in Bulk LiNiO 2

Alexander G. Squires, Lavan Ganeshkumar, Christopher N. Savory, Seán R. Kavanagh, David O. Scanlon

ACS Energy Letters· Volume 9· Issue 8

Abstract

High Resolution Image Download MS PowerPoint Slide To explore the possibility of oxygen dimerization─particularly, the formation of molecular oxygen-like species─in the bulk of LiNiO 2 lithium ion cathode materials at high states of charge, we conduct a redox-product structure search inspired by recent methodological developments for point-defect structure prediction. We find that (1) delithiated Li 1– x NiO 2 ( x = 1) has good kinetic stability toward decomposition into molecular oxygen and reduced transition-metal oxides but (2) defects can act as nucleation sites for oxygen dimerization. These results help reconcile conflicting reports on the formation of bulk molecular oxygen in LiNiO 2 and other nickel-rich cathode materials, highlighting the role of defect chemistry in driving the bulk degradation of these compounds.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Semiconductor materials and devices

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Affiliations

School of Chemistry, The University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom

The Faraday Institution, Quad One, Becquerel Avenue, Harwell Campus, Didcot OX11 0RA, United Kingdom

Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom

John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02134, United States

Funding

Engineering and Physical Sciences Research Council · Faraday Institution · University College London

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