| Literature DB >> 26680196 |
Eric McCalla1, Artem M Abakumov2, Matthieu Saubanère3, Dominique Foix4, Erik J Berg5, Gwenaelle Rousse6, Marie-Liesse Doublet3, Danielle Gonbeau4, Petr Novák5, Gustaaf Van Tendeloo7, Robert Dominko8, Jean-Marie Tarascon9.
Abstract
Lithium-ion (Li-ion) batteries that rely on cationic redox reactions are the primary energy source for portable electronics. One pathway toward greater energy density is through the use of Li-rich layered oxides. The capacity of this class of materials (>270 milliampere hours per gram) has been shown to be nested in anionic redox reactions, which are thought to form peroxo-like species. However, the oxygen-oxygen (O-O) bonding pattern has not been observed in previous studies, nor has there been a satisfactory explanation for the irreversible changes that occur during first delithiation. By using Li2IrO3 as a model compound, we visualize the O-O dimers via transmission electron microscopy and neutron diffraction. Our findings establish the fundamental relation between the anionic redox process and the evolution of the O-O bonding in layered oxides.Entities:
Year: 2015 PMID: 26680196 DOI: 10.1126/science.aac8260
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728