Characterizing Oxygen Local Environments in Paramagnetic Battery Materials via 17O NMR and DFT Calculations

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• 作者：Ieuan D. Seymour ; Derek S. Middlemiss ; David M. Halat ; Nicole M. Trease ; Andrew J. Pell ; Clare P. Grey
• 刊名：Journal of the American Chemical Society
• 出版年：2016
• 出版时间：August 3, 2016
• 年：2016
• 卷：138
• 期：30
• 页码：9405-9408
• 全文大小：286K
• 年卷期：0
• ISSN：1520-5126

文摘

Experimental techniques that probe the local environment around O in paramagnetic Li-ion cathode materials are essential in order to understand the complex phase transformations and O redox processes that can occur during electrochemical delithiation. While Li NMR is a well-established technique for studying the local environment of Li ions in paramagnetic battery materials, the use of p>17p>O NMR in the same materials has not yet been reported. In this work, we present a combined p>17p>O NMR and hybrid density functional theory study of the local O environments in Li₂MnO₃, a model compound for layered Li-ion batteries. After a simple p>17p>O enrichment procedure, we observed five resonances with large p>17p>O shifts ascribed to the Fermi contact interaction with directly bonded Mnp>4+p> ions. The five peaks were separated into two groups with shifts at 1600 to 1950 ppm and 2100 to 2450 ppm, which, with the aid of first-principles calculations, were assigned to the p>17p>O shifts of environments similar to the 4i and 8j sites in pristine Li₂MnO₃, respectively. The multiple O environments in each region were ascribed to the presence of stacking faults within the Li₂MnO₃ structure. From the ratio of the intensities of the different p>17p>O environments, the percentage of stacking faults was found to be ca. 10%. The methodology for studying p>17p>O shifts in paramagnetic solids described in this work will be useful for studying the local environments of O in a range of technologically interesting transition metal oxides.