Issue 36, 2016, Issue in Progress

Influence of over-discharge on the lifetime and performance of LiFePO4/graphite batteries

Abstract

In this study, the degradation of a LiFePO4/graphite battery under an over-discharge process and its effect on further cycling stability are investigated. Batteries are over-discharged to 1.5, 1.0, 0.5 or 0.0 V and then cycled 110 times under over-discharge conditions. The batteries over-discharged to 0.5 and 0.0 V experience serious irreversible capacity losses of 12.56% and 24.88%, respectively. The same batteries lost 7.79 and 24.46% more capacity after they were further subjected to 110 cycles between 3.65 and 2.0 V at 1C/1C, respectively. This shows that a serious loss of active lithium and loss of anode material occur at 0.0 V during both over-discharging and the normal cycling stage. Dissolution and breakdown of solid electrolyte interphase (SEI) films are suggested to be the main reason for degradation under over-discharge at low voltage and further lead to a poor cycling performance. Gas generation can be found on the cycled batteries below 1 V and the gas mainly contains H2, CH4 and C2H6. The structures of LiFePO4 and graphite materials have almost no change according to the results of XRD tests. Half-cell study suggests that almost no irreversible capacity loss occurs at the LiFePO4 cathode, whereas a decline in the capacity is observed at the graphite anode, especially for the batteries over-discharging bellow 1.0 V. Evidence for fierce side reactions at 0.5 and 0.0 V is provided as well, as demonstrated by the developed rich surface chemistry and an significant impedance increase for the aged electrodes.

Graphical abstract: Influence of over-discharge on the lifetime and performance of LiFePO4/graphite batteries

Supplementary files

Article information

Article type
Paper
Submitted
20 Jan 2016
Accepted
01 Mar 2016
First published
02 Mar 2016

RSC Adv., 2016,6, 30474-30483

Influence of over-discharge on the lifetime and performance of LiFePO4/graphite batteries

Y. Zheng, K. Qian, D. Luo, Y. Li, Q. Lu, B. Li, Y. He, X. Wang, J. Li and F. Kang, RSC Adv., 2016, 6, 30474 DOI: 10.1039/C6RA01677D

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