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具有镍电荷和钠空位有序排列的动态稳定阴极相NaNiO的结构解析。

Structural Elucidation of NaNiO, a Dynamically Stabilized Cathode Phase with Nickel Charge and Sodium Vacancy Ordering.

作者信息

Steele James M A, Genreith-Schriever Annalena R, Bocarsly Joshua D, Nagle-Cocco Liam A V, Sayed Farheen N, Juramy Marie, O'Keefe Christopher A, Orlandi Fabio, Manuel Pascal, Dutton Siân E, Grey Clare P

机构信息

Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, U.K.

Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge CB3 0HE, U.K.

出版信息

Chem Mater. 2025 Mar 24;37(7):2581-2591. doi: 10.1021/acs.chemmater.5c00084. eCollection 2025 Apr 8.

Abstract

NaNiO (NNO) has been investigated as a promising sodium-ion battery cathode material, but it is limited by degradation-induced capacity fade. On desodiation, NNO forms multiple phases with large superstructures due in part to Na-ion vacancy ordering; however, their structures are unknown. Here, we report a structural solution to the NaNiO (P3) desodiated phase using combined Rietveld refinement of high-resolution synchrotron X-ray (SXRD) and neutron powder diffraction (NPD) data, magnetic susceptibility, and Na solid-state nuclear magnetic resonance (ssNMR) spectroscopy. Our experimental results are compared to molecular dynamics (AIMD) simulations, which indicate multiple low-energy structures that are dynamically populated. We observe a combination of competing effects that contribute to the resultant dynamic nature of the structure, including honeycomb ordering of mixed-valence Ni, orbital ordering of Jahn-Teller (JT) distorted Ni, and zigzag Na/vacancy ordering. Our work provides evidence of multiple contributions to the structures of desodiated NaNiO, along with a framework for investigating the other unsolved desodiated structures. This work may also inform our understanding of the Jahn-Teller evolution in other nickel-rich lithium- and sodium-ion cathodes, such as LiNiO.

摘要

氧化镍钠(NNO)已被作为一种有前景的钠离子电池正极材料进行研究,但它受到降解导致的容量衰减的限制。在脱钠过程中,NNO会形成具有大超结构的多个相,部分原因是钠离子空位有序化;然而,它们的结构尚不清楚。在此,我们通过结合高分辨率同步加速器X射线(SXRD)和中子粉末衍射(NPD)数据的Rietveld精修、磁化率以及钠固态核磁共振(ssNMR)光谱,报告了氧化镍钠(P3)脱钠相的结构解析。我们将实验结果与分子动力学(AIMD)模拟进行了比较,模拟结果表明存在多个动态填充的低能量结构。我们观察到多种相互竞争的效应共同导致了结构的动态特性,包括混合价态镍的蜂窝状有序排列、 Jahn - Teller(JT)畸变镍的轨道有序排列以及锯齿状钠/空位有序排列。我们的工作为脱钠氧化镍钠的结构提供了多种贡献的证据,同时也为研究其他未解决的脱钠结构提供了一个框架。这项工作还可能有助于我们理解其他富镍锂和钠离子正极中的 Jahn - Teller 演化,例如LiNiO。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9283/11983708/0872d64bb49a/cm5c00084_0001.jpg

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