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A Coacervate-Based Mixed-Conducting Binder for High-Power, High-Energy Batteries AITranslate

University of California; University of California; University of California; University of California
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Publisher: ACS
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Abstract AITranslate

Polymer binders add crucial structural integrity to lithium ion battery composite cathodes, but industry standard binders, such as polyvinylidene fluoride (PVDF), are insulating to ions and electrons, detrimentally adding resistance to the overall system. In this work, we use electrostatics to stabilize a blend of a charged conjugated polymer with an oppositely charged polyelectrolyte, providing a processable, stable binder with high ionic and electronic conduction. Using LiFePO4 cathodes as a model system, we show significant improvement in rate capability and stability, with the conducting binder enabling a 39% utilization at 6C compared to 1.6% when PVDF is the binder. Additionally, the conducting binder affords a 63% capacity retention over 400 C/2 cycles, compared to only a 6% retention over 400 cycles when PVDF is the binder. These results show that electrostatically stabilized complexation is a promising strategy to integrate both electronic and ionic conductivity into a binder, while simultaneously maintaining stability and processability.

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DOI:https://doi.org/10.1021/acsenergylett.3c00829

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Citation Information:

Polymer binders add crucial structural integrity to lithium ion battery composite cathodes, but industry standard binders, such as polyvinylidene fluoride (PVDF), are insulating to ions and electrons, detrimentally adding resistance to the overall system. In this work, we use electrostatics to stabilize a blend of a charged conjugated polymer with an oppositely charged polyelectrolyte, providing a processable, stable binder with high ionic and electronic conduction. Using LiFePO4 cathodes as a model system, we show significant improvement in rate capability and stability, with the conducting binder enabling a 39% utilization at 6C compared to 1.6% when PVDF is the binder. Additionally, the conducting binder affords a 63% capacity retention over 400 C/2 cycles, compared to only a 6% retention over 400 cycles when PVDF is the binder. These results show that electrostatically stabilized complexation is a promising strategy to integrate both electronic and ionic conductivity into a binder, while simultaneously maintaining stability and processability.

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GB/T 7714-2015 [1] Gordon T. Pace, My Linh Le, Raphaële J. Clément, et al. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.3c00829.
MLA [1] Gordon T. Pace, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.3c00829.
APA [1] Gordon T. Pace, My Linh Le, Raphaële J. Clément, & Rachel A. Segalman. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.3c00829
IEEE [1] Gordon T. Pace, My Linh Le, Raphaële J. Clément, and Rachel A. Segalman, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.3c00829.