LiCoPO4(LCP) is a promising high voltage cathode for next-generation high energy Li-ion batteries. However, once electrochemically de-lithiated, it suffers from a spontaneous self-discharge process in open circuit conditions. Here we present our systematic study about the phase composition and structural changes of LCP electrodes upon charging and self-discharging processes by ex situ synchrotron X-ray diffraction and Fast-Fourier Transform Infrared Spectroscopy (FT-IR) analyses. Various initial charging states and different current rates have been studied. Our investigation highlights large structural alterations of the de-lithiated CoPO4phase upon self-discharge. However, after 160 hours with open circuit the pristine LCP structure is recovered. The electrochemically de-lithiated phase reincorporates lithium by a spontaneous reduction reaction releasing gaseous CO2and likely degrading the electrolyte molecules.

Analysis of the self-discharge process in LiCoPO4electrodes: Bulks

Di Lecce, D.;
2015

Abstract

LiCoPO4(LCP) is a promising high voltage cathode for next-generation high energy Li-ion batteries. However, once electrochemically de-lithiated, it suffers from a spontaneous self-discharge process in open circuit conditions. Here we present our systematic study about the phase composition and structural changes of LCP electrodes upon charging and self-discharging processes by ex situ synchrotron X-ray diffraction and Fast-Fourier Transform Infrared Spectroscopy (FT-IR) analyses. Various initial charging states and different current rates have been studied. Our investigation highlights large structural alterations of the de-lithiated CoPO4phase upon self-discharge. However, after 160 hours with open circuit the pristine LCP structure is recovered. The electrochemically de-lithiated phase reincorporates lithium by a spontaneous reduction reaction releasing gaseous CO2and likely degrading the electrolyte molecules.
2015
Manzi, J.; Vitucci, F. M.; Paolone, A.; Trequattrini, F.; Di Lecce, D.; Panero, S.; Brutti, S.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2385937
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