The Effect of Water Contamination on the Aging of a Dual-Carbon Lithium-Ion Capacitor Employing LiFSI-Based Electrolyte
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arXiv
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| Autores principales: | , , , , , |
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| Formato: | Preprint |
| Publicado: |
2025
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| _version_ | 1866915160499683328 |
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| author | Schweigart, Philipp Hamonnet, Johan Eleri, Obinna Egwu King, Laura Lai, Samson Yuxiu Svensson, Ann Mari |
| author_facet | Schweigart, Philipp Hamonnet, Johan Eleri, Obinna Egwu King, Laura Lai, Samson Yuxiu Svensson, Ann Mari |
| contents | Fabricating electrochemical energy storage devices demands significant energy for drying cell components to ensure optimal performance. The development of new, water-tolerant materials would represent a tremendous advance in cost savings and sustainability. Although it is generally established that water deteriorates cell performance, there are few systematic studies on the maximum amount of tolerable water contamination, and most of the studies employed the electrolyte salt $\mathrm{LiPF_6}$, which inevitably decomposes upon exposure to humidity. In this work, the potential of using the non-hydrolyzing salt LiFSI is explored with respect to its performance in Li-ion capacitor cells based on activated carbon (AC) and pre-lithiated graphite (Gr). Water is deliberately added in various amounts (950, 2300, and 6000 ppm), and its effect on the electrochemical performance and aging of AC and Gr electrodes is systematically studied. While the addition of 950 ppm water has no evident impact on capacity retention (96% after 2000 cycles), the addition of 2300 ppm water or 6000 ppm water shows a distinct capacity fade, attributed to a significant loss of lithium inventory and increased resistivity due to irreversible reactions of the water with lithiated Gr. Post-mortem analysis reveals that water promotes the oxidative and reductive decomposition of LiFSI on AC and lithiated Gr, respectively. A significant thickening of the SEI on Gr is observed as the water concentration is increased. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2502_13323 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | The Effect of Water Contamination on the Aging of a Dual-Carbon Lithium-Ion Capacitor Employing LiFSI-Based Electrolyte Schweigart, Philipp Hamonnet, Johan Eleri, Obinna Egwu King, Laura Lai, Samson Yuxiu Svensson, Ann Mari Materials Science Applied Physics Chemical Physics Fabricating electrochemical energy storage devices demands significant energy for drying cell components to ensure optimal performance. The development of new, water-tolerant materials would represent a tremendous advance in cost savings and sustainability. Although it is generally established that water deteriorates cell performance, there are few systematic studies on the maximum amount of tolerable water contamination, and most of the studies employed the electrolyte salt $\mathrm{LiPF_6}$, which inevitably decomposes upon exposure to humidity. In this work, the potential of using the non-hydrolyzing salt LiFSI is explored with respect to its performance in Li-ion capacitor cells based on activated carbon (AC) and pre-lithiated graphite (Gr). Water is deliberately added in various amounts (950, 2300, and 6000 ppm), and its effect on the electrochemical performance and aging of AC and Gr electrodes is systematically studied. While the addition of 950 ppm water has no evident impact on capacity retention (96% after 2000 cycles), the addition of 2300 ppm water or 6000 ppm water shows a distinct capacity fade, attributed to a significant loss of lithium inventory and increased resistivity due to irreversible reactions of the water with lithiated Gr. Post-mortem analysis reveals that water promotes the oxidative and reductive decomposition of LiFSI on AC and lithiated Gr, respectively. A significant thickening of the SEI on Gr is observed as the water concentration is increased. |
| title | The Effect of Water Contamination on the Aging of a Dual-Carbon Lithium-Ion Capacitor Employing LiFSI-Based Electrolyte |
| topic | Materials Science Applied Physics Chemical Physics |
| url | https://arxiv.org/abs/2502.13323 |