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本文引用的文献

1
Structural studies of LiMnNiCoO electrode material.LiMnNiCoO 电极材料的结构研究
Mater Charact. 2016 Sep;119:120-128. doi: 10.1016/j.matchar.2016.07.013. Epub 2016 Jul 18.
2
Microscopy Study of Structural Evolution in Epitaxial LiCoO2 Positive Electrode Films during Electrochemical Cycling.电镜研究电化学循环过程中外延 LiCoO2 正极薄膜的结构演变。
ACS Appl Mater Interfaces. 2016 Mar;8(10):6727-35. doi: 10.1021/acsami.5b12025. Epub 2016 Mar 4.
3
Unravelling structural ambiguities in lithium- and manganese-rich transition metal oxides.解析富锂锰过渡金属氧化物中的结构歧义
Nat Commun. 2015 Oct 29;6:8711. doi: 10.1038/ncomms9711.
4
Epitaxial LiCoO2 films as a model system for fundamental electrochemical studies of positive electrodes.外延LiCoO₂薄膜作为正极材料基础电化学研究的模型体系。
ACS Appl Mater Interfaces. 2015 Apr 22;7(15):7901-11. doi: 10.1021/am508512q. Epub 2015 Apr 7.
5
Highly reversible capacity at the surface of a lithium-rich manganese oxide: a model study using an epitaxial film system.富锂锰氧化物表面的高度可逆容量:使用外延薄膜系统的模型研究
Chem Commun (Camb). 2015 Jan 31;51(9):1673-6. doi: 10.1039/c4cc07758j.
6
Dynamic structural changes at LiMn2O4/electrolyte interface during lithium battery reaction.锂电池反应过程中 LiMn2O4/电解质界面的动态结构变化。
J Am Chem Soc. 2010 Nov 3;132(43):15268-76. doi: 10.1021/ja105389t.
7
Structural changes in surface and bulk LiNi0.5Mn0.5O2 during electrochemical reaction on epitaxial thin-film electrodes characterized by in situ X-ray scattering.原位 X 射线散射研究外延薄膜电极中电化学反应过程中表面和体相 LiNi0.5Mn0.5O2 的结构变化。
Phys Chem Chem Phys. 2010 Apr 21;12(15):3815-23. doi: 10.1039/b920271d. Epub 2010 Feb 24.
8
Demonstrating oxygen loss and associated structural reorganization in the lithium battery cathode Li[Ni0.2Li0.2Mn0.6]O2.展示锂电池正极Li[Ni0.2Li0.2Mn0.6]O2中的氧损失及相关结构重组。
J Am Chem Soc. 2006 Jul 5;128(26):8694-8. doi: 10.1021/ja062027+.

富锂锰镍钴氧化物外延薄膜中的畴形成及其对电化学行为解释的意义。

Domain Formation in Lithium-Rich Manganese-Nickel-Cobalt-Oxide Epitaxial Thin Films and Implications for Interpretation of Electrochemical Behavior.

作者信息

Johnston-Peck Aaron C, Takeuchi Saya, Bharathi K Kamala, Herzing Andrew A, Bendersky Leonid A

机构信息

Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, United States.

出版信息

Thin Solid Films. 2018;647. doi: https://doi.org/10.1016/j.tsf.2017.12.006.

PMID:33060869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7552893/
Abstract

Due to the directional dependence of physical properties, it is advantageous to grow and then study materials in specific orientations. Films of battery materials grown in epitaxy offers the possibility to gain new insight into the role of physical structure on electrochemical behaviors. Here we demonstrate the growth, testing, and characterization of monoclinic-phase (space group 2/) Li-Mn-Ni-Co-O epitaxial films. The monoclinic phase is a layered structure and as such lithium diffusion is favored along specific crystallographic directions. Films were grown by pulsed laser deposition onto SrRuO/SrTiO substrates with (001) and (111) orientations. Cyclic voltammetry measured the response of these positive electrode materials, while the film structure was characterized using scanning transmission electron microscopy. A combination of imaging and diffraction identifies the presence of orientational variants. Variants disrupt the orientation anisotropy expected of these layered materials when grown in epitaxy, thereby masking differences in electrochemical behavior as a function of substrate orientation. Learning to control the domain structure now presents itself as a challenge to realize the potential of low symmetry battery materials grown in epitaxy on high symmetry substrates.

摘要

由于物理性质的方向依赖性,在特定取向上生长并随后研究材料是有利的。外延生长的电池材料薄膜为深入了解物理结构对电化学行为的作用提供了可能性。在此,我们展示了单斜相(空间群2/)锂锰镍钴氧化物外延薄膜的生长、测试和表征。单斜相是一种层状结构,因此锂沿特定晶体学方向扩散较为有利。通过脉冲激光沉积在具有(001)和(111)取向的SrRuO/SrTiO衬底上生长薄膜。循环伏安法测量了这些正极材料的响应,同时使用扫描透射电子显微镜对薄膜结构进行了表征。成像和衍射相结合确定了取向变体的存在。当外延生长时,变体破坏了这些层状材料预期的取向各向异性,从而掩盖了作为衬底取向函数的电化学行为差异。学会控制畴结构现在成为实现高对称衬底上外延生长的低对称电池材料潜力的一个挑战。