Abstract
Time-dependent elementary polarizations of FeF3·3H2O/C cathode material were quantitatively investigated in dc polarization in order to determine the key factors that comprise the total polarization. The measurement of electrochemical impedance spectrum at a given state of charge and the subsequent least square fitting of its equivalent circuit allow the calculation of elementary contributions of individual kinetic step to the total polarization. The profiles of the calculations were well consistent with those of experiments based on the same states of charge, and the elementary contributions could be differentiated successfully which reveal that the solid-state diffusion process makes the largest contribution to the total polarization after 2.5 s discharge beginning with open-circuit voltage (OCV) level 3.5 V. The results may be helpful for the design of batteries of better performance with FeF3 cathode.
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Acknowledgments
We gratefully acknowledge the support for this work from 973 Fundamental research program from the Ministry of Science and Technology of China (grant number 2010CB635116), NSFC Project 21173190, Educational Commission of Zhejiang Province (grant number Y201017390), Zhejiang Provincial Natural Science Foundation of China Y13B010020, the New Shoot Talents Program of Zhejiang Province (grant number 2013R405069), and K.C.Wong Magna Fund in Ningbo University.
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Xu, X., Chen, S., Shui, M. et al. The differentiation of elementary polarizations of FeF3·3H2O/C cathode material in LIB. Ionics 21, 1003–1010 (2015). https://doi.org/10.1007/s11581-014-1244-7
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DOI: https://doi.org/10.1007/s11581-014-1244-7