Relating the 3D electrode morphology to Li-ion battery performance; a case for LiFePO4

Journal Article (2016)
Author(s)

Zhao Liu (Northwestern University)

Tomas Verhallen (TU Delft - RST/Fundamental Aspects of Materials and Energy)

DP Singh (TU Delft - RST/Fundamental Aspects of Materials and Energy)

Hongqian Wang (Northwestern University)

M. Wagemaker (Northwestern University)

Scott Barnett (Northwestern University)

Research Group
RST/Fundamental Aspects of Materials and Energy
Copyright
© 2016 Zhao Liu, T.W. Verhallen, D.P. Singh, Hongqian Wang, M. Wagemaker, Scott Barnett
DOI related publication
https://doi.org/10.1016/j.jpowsour.2016.05.097
More Info
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Publication Year
2016
Language
English
Copyright
© 2016 Zhao Liu, T.W. Verhallen, D.P. Singh, Hongqian Wang, M. Wagemaker, Scott Barnett
Research Group
RST/Fundamental Aspects of Materials and Energy
Volume number
324
Pages (from-to)
358-367
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Abstract

One of the main goals in lithium ion battery electrode design is to increase the power density. This requires insight in the relation between the complex heterogeneous microstructure existing of active material, conductive additive and electrolyte providing the required electronic and Li-ion transport. FIB-SEM is used to determine the three phase 3D morphology, and Li-ion concentration profiles obtained with Neutron Depth Profiling (NDP) are compared for two cases, conventional LiFePO4 electrodes and better performing carbonate templated LiFePO4 electrodes. This provides detailed understanding of the impact of key parameters such as the tortuosity for electron and Li-ion transport though the electrodes. The created hierarchical pore network of the templated electrodes, containing micron sized pores, appears to be effective only at high rate charge where electrolyte depletion is hindering fast discharge. Surprisingly the carbonate templating method results in a better electronic conductive CB network, enhancing the activity of LiFePO4 near the electrolyte-electrode interface as directly observed with NDP, which in a large part is responsible for the improved rate performance both during charge and discharge. The results demonstrate that standard electrodes have a far from optimal charge transport network and that significantly improved electrode performance should be possible by engineering the microstructure.

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