阳极
材料科学
结构精修
粒径
阴极
电解质
电极
氧化物
电化学
硫代磷酸盐
纳米技术
粒子(生态学)
化学工程
化学
冶金
晶体结构
结晶学
工程类
物理化学
海洋学
地质学
有机化学
作者
Florian Strauss,Timo Bartsch,Lea de Biasi,A‐Young Kim,Jürgen Janek,Pascal Hartmann,Torsten Brezesinski
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-03-21
卷期号:3 (4): 992-996
被引量:233
标识
DOI:10.1021/acsenergylett.8b00275
摘要
The implementation of all-solid-state batteries (ASSBs) is regarded as an important step toward next-generation energy storage systems, in particular for electric vehicles and portable electronics. This may be achieved through application of layered Ni-rich oxide cathode materials such as Li1+x(Ni1–y–zCoyMnz)1–xO2 (NCM) with high specific capacity and thiophosphate-based solid electrolytes. Here, the profound effect that the secondary particle size of the cathode active material has on the capacity of ASSB cells comprising NCM622 (60% Ni), β-Li3PS4, and In anode is demonstrated. We show the benefits of using small particles (d ≪ 10 μm), allowing virtually full charge capacity. This finding is rationalized through galvanostatic charge–discharge tests and complementary ex situ and operando X-ray diffraction experiments combined with Rietveld refinement analysis. Our results indicate the importance of considering and avoiding electrochemically inactive electrode material in bulk-type ASSBs, which we show using charge transport measurements is due to poor electronic contact (in carbon-free cathode composites).
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