Correlated X-Ray 3D Ptychography and Diffraction Microscopy Visualize Links between Morphology and Crystal Structure of Lithium-Rich Cathode Materials

被引:30
作者
Tsai, Esther H. R. [1 ,3 ]
Billaud, Juliette [2 ]
Sanchez, Dario F. [1 ]
Ihli, Johannes [1 ,4 ]
Odstrcil, Michal [1 ]
Holler, Mirko [1 ]
Grolimund, Daniel [1 ]
Villevieille, Claire [2 ]
Guizar-Sicairos, Manuel [1 ]
机构
[1] PSI, Swiss Light Source, CH-5232 Villigen, Switzerland
[2] PSI, Electrochem Lab, CH-5232 Villigen, Switzerland
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[4] Univ Oxford, Dept Mat, Oxford OX2 6HT, England
基金
瑞士国家科学基金会;
关键词
TRANSITION-METAL DISSOLUTION; ION BATTERIES; HIGH-VOLTAGE; ELECTROCHEMICAL PERFORMANCE; ELECTRODE MATERIALS; POSITIVE ELECTRODE; CAPACITY FADE; MN-RICH; NI-RICH; LI;
D O I
10.1016/j.isci.2018.12.028
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The search for higher performance, improved safety, and lifetime of lithium-ion batteries relies on the understanding of degradation mechanisms. Complementary to methods and studies on primary par tides or crystalline structure on bulk materials, here we use spatially correlated ptychographic X-ray computed nanotomography with a 35 nm resolution and scanning X-ray diffraction microscopy with 1 pm resolution to visualize in 3D the hidden morphological and structural degradation processes in individual secondary particles of lithium-rich nickel, cobalt, and manganese oxides. From comparative examination of pristine and cycled particles, we suggest that morphological degradation could have radial dependency and secondary particle size dependency. The same particles were examined to correlate the degradation to crystallinity, which shows surprising core-shell structures. This study reveals the inner 3D structure of the secondary particles while opening up questions on the unexpected crystalline structural distributions, which could offer clues for future studies on this promising cathode material for lithium-ion batteries.
引用
收藏
页码:356 / +
页数:20
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