Imaging Phase Segregation in Nanoscale LixCoO2 Single Particles

被引:6
|
作者
Fuller, Elliot J. [1 ]
Ashby, David S. [1 ]
Polop, Celia [2 ,3 ,4 ]
Salagre, Elena [2 ,3 ]
Bhargava, Bhuvsmita [5 ]
Song, Yueming [5 ]
Vasco, Enrique [6 ]
Sugar, Joshua D. [1 ]
Albertus, Paul [5 ]
Mentes, Tevfik Onur [7 ]
Locatel, Andrea [7 ]
Segovia, Pilar [2 ,3 ,4 ]
Gonzalez-Barrio, Miguel Angel [2 ]
Mascaraque, Arantzazu [2 ,8 ]
Michel, Enrique G. [2 ,3 ,4 ]
Talin, A. Alec [1 ]
机构
[1] Sandia Natl Labs, Livermore, CA 94550 USA
[2] Univ Autonoma Madrid, Dept Fis Mat Condensada, Madrid 28049, Spain
[3] Univ Autonoma Madrid, Inst Univ Ciencia Mat Nicolas Cabrera INC, Madrid 28049, Spain
[4] Univ Autnoma Madrid, IFIMAC, Condensed Phys Ctr, Madrid 28049, Spain
[5] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20740 USA
[6] CSIC, Inst Ciencia Mat Madrid, Madrid 28049, Spain
[7] Sincrotrone Trieste S C p A, I-34149 Basovizza, Trieste, Italy
[8] Univ Complutense Madrid, Dept Fis Mat, Madrid 28040, Spain
基金
欧盟地平线“2020”;
关键词
intercalation oxides; conductive atomic force microscopy; photoemission electron microscopy; phase separation; battery; ELECTRON-MICROSCOPY; LICOO2; TRANSITION; INTERCALATION; LIFEPO4;
D O I
10.1021/acsnano.2c05594
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
LixCoO2 (LCO) is a common battery cathode material that has recently emerged as a promising material for other applications including electrocatalysis and as electro-chemical random access memory (ECRAM). During charge- discharge cycling LCO exhibits phase transformations that are significant l y complicated by electron correlation. While the bulk phase diagram for an ensemble of battery particles has been studied extensively, it remains unclea r how these phases scale to nanometer dimensions and the effects of strain and diffusional anisotropy at the single-particle scale. Under-stand i n g these effects is critical to modeling battery performance and for predicting the scalability and performance of electrocatalysts and ECRAM. Here we investigate isolated, epitaxial LiCoO2 islands grown by pulsed laser deposition. After electrochemical cycling of the islands, conduc t i v e atomic force microscopy (c-AFM) is used to image the spatial distribution of conductive and insulating phases. Above 20 nm island thicknesses, we observe a kinetically arrested state in which the phase boundary is perpendicular to the Li-planes; we propose a model and present image analysis results that show smaller LCO islands have a higher conduc t i v e fraction than larger area islands, and the overal l conductive fraction is consistent with the lithiation state. Thinner islands (14 nm), with a larger surface to volume ratio, are found to exhibit a striping pattern, which suggests surface energy can dominate below a critical dimension. When increasing force is applied through the AFM tip to strain the LCO islands, significant shifts in current flow are observed, and underlying mechanisms for this behavior are discussed. The c-AFM images are compared with photoemission electron microscopy images, which are used to acquire statistics across hundreds of particles. The results indicate that strain and morphology become more critical to electrochemical performance as particles approach nanometer dimensions.
引用
收藏
页码:16363 / 16371
页数:9
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