Operando X-ray photoelectron spectroscopy of solid electrolyte interphase formation and evolution in Li2S-P2S5 solid-state electrolytes

被引:238
作者
Wood, Kevin N. [1 ]
Steirer, K. Xerxes [2 ]
Hafner, Simon E. [3 ]
Ban, Chunmei [1 ]
Santhanagopalan, Shriram [1 ]
Lee, Se-Hee [3 ]
Teeter, Glenn [1 ]
机构
[1] Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA
[2] Colorado Sch Mines, 1500 Illinois St, Golden, CO 80401 USA
[3] Univ Colorado, 596 UCB,Boulder, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
LITHIUM METAL ANODES; ION BATTERIES; STABILITY; BEHAVIOR; LI; MICROSCOPY; LIPON; XPS;
D O I
10.1038/s41467-018-04762-z
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
Solid-state electrolytes such as Li2S-P2S5 compounds are promising materials that could enable Li metal anodes. However, many solid-state electrolytes are unstable against metallic lithium, and little is known about the chemical evolution of these interfaces during cycling, hindering the rational design of these materials. In this work, operando X-ray photoelectron spectroscopy and real-time in situ Auger electron spectroscopy mapping are developed to probe the formation and evolution of the Li/Li2S-P2S5 solid-electrolyte interphase during electrochemical cycling, and to measure individual overpotentials associated with specific interphase constituents. Results for the Li/Li2S-P2S5 system reveal that electrochemically driving Li+ to the surface leads to phase decomposition into Li2S and Li3P. Additionally, oxygen contamination within the Li2S-P2S5 leads initially to Li3PO4 phase segregation, and subsequently to Li2O formation. The spatially non-uniform distribution of these phases, coupled with differences in their ionic conductivities, have important implications for the overall properties and performance of the solid-electrolyte interphase.
引用
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页数:10
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