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On the chemistry and electrochemistry of LiPON breakdown
Battery safety and cycle life remain of concern to current Li-ion batteries that use a liquid organic electrolyte. Both issues can be resolved by employing a solid electrolyte. Numerous Li-ion conducting solids are known today, however the stability of most of these is too low to engender widespread...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (11), p.4848-4859 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Battery safety and cycle life remain of concern to current Li-ion batteries that use a liquid organic electrolyte. Both issues can be resolved by employing a solid electrolyte. Numerous Li-ion conducting solids are known today, however the stability of most of these is too low to engender widespread usage. Here, we report on the decomposition chemistry and electrochemistry of LiPON, at present the most commonly used solid electrolyte. The decomposition potential was calculated from basic thermodynamic quantities and was linked to current-voltage (
I
-
V
) measurements with great consistency. The decomposition of LiPON was shown to occur at a potential of 4.3 V and proceeds in a diffusion limited way. The LiPON layer decomposes into Li-ions, O
2
or N
2
gas and a phosphate rich compound. Ultimately hard breakdown could occur through the formation of metallic lithium filaments that short circuit the LiPON layer as shown by TOF-SIMS imaging experiments. As such the work provided here also provides insight in the breakdown mechanism of RRAM devices.
Electrolyte stability remains one of the key hurdles for the increasing the battery output potential. In the present work, we determine the electrochemical stability of LiPON both experimentally and based on thermodynamic considerations. Different breakdown modes are suggested depending on bias polarity. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c7ta07928a |