TY - JOUR A1 - Wöhrl, Katharina A1 - Kotak, Yash A1 - Geisbauer, Christian A1 - Barra, Sönke A1 - Wilhelm, Gudrun A1 - Schneider, Gerhard A1 - Schweiger, Hans-Georg T1 - Analysis of Deactivation of 18,650 Lithium-Ion Cells in CaCl2, Tap Water and Demineralized Water for Different Insertion Times JF - Sensors N2 - The deployment of battery-powered electric vehicles in the market has created a naturally increasing need for the safe deactivation and recycling of batteries. Various deactivating methods for lithium-ion cells include electrical discharging or deactivation with liquids. Such methods are also useful for cases where the cell tabs are not accessible. In the literature analyses, different deactivation media are used, but none include the use of calcium chloride (CaCl2) salt. As compared to other media, the major advantage of this salt is that it can capture the highly reactive and hazardous molecules of Hydrofluoric acid. To analyse the actual performance of this salt in terms of practicability and safety, this experimental research aims to compare it against regular Tap Water and Demineralized Water. This will be accomplished by performing nail penetration tests on deactivated cells and comparing their residual energy against each other. Moreover, these three different media and respective cells are analysed after deactivation, i.e., based on conductivity measurements, cell mass, flame photometry, fluoride content, computer tomography and pH value. It was found that the cells deactivated in the CaCl2 solution did not show any signs of Fluoride ions, whereas cells deactivated in TW showed the emergence of Fluoride ions in the 10th week of the insertion. However, with the addition of CaCl2 in TW, the deactivation process > 48 h for TW declines to 0.5–2 h, which could be an optimal solution for real-world situations where deactivating cells at a high pace is essential. UR - https://doi.org/10.3390/s23083901 KW - lithium-ion cells KW - cell deactivation KW - 18,650 lithium-ion cells KW - cell deactivation in tap water KW - cell deactivation in demineralized water KW - cell deactivation in CaCl2 solution Y1 - 2023 UR - https://doi.org/10.3390/s23083901 UR - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:573-35154 SN - 1424-8220 VL - 23 IS - 8 PB - MDPI CY - Basel ER - TY - INPR A1 - Rufino Júnior, Carlos Antônio A1 - Riva Sanseverino, Eleonora A1 - Gallo, Pierluigi A1 - Amaral, Murilo Machado A1 - Koch, Daniel A1 - Kotak, Yash A1 - Diel, Sergej A1 - Walter, Gero A1 - Schweiger, Hans-Georg A1 - Zanin, Hudson T1 - A Comprehensive Review of EV Lithium-Ion Battery Degradation N2 - Lithium-ion batteries with improved energy densities have made understanding the Solid Electrolyte Interphase (SEI) generation mechanisms that cause mechanical, thermal, and chemical failures more complicated. SEI processes reduce battery capacity and power. Thus, a review of this area's understanding is important. It is essential to know how batteries degrade in EVs to estimate battery lifespan as it goes, predict, and minimize losses, and determine the ideal time for a replacement. Lithium-ion batteries used in EVs mainly suffer two types of degradation: calendar degradation and cycling degradation. Despite the existence of several existing works in the literature, several aspects of battery degradation remain unclear or have not been analyzed in detail. This work presents a systematic review of existing works in the literature. The results of the present investigation provide insight into the complex relationships among various factors affecting battery degradation mechanisms. Specifically, this systematic review examined the effects of time, side reactions, temperature fluctuations, high charge/discharge rates, depth of discharge, mechanical stress, thermal stress, and the voltage relationship on battery performance and longevity. The results revealed that these factors interact in complex ways to influence the degradation mechanisms of batteries. For example, high charge currents and deep discharges were found to accelerate degradation, while low temperatures and moderate discharge depths were shown to be beneficial for battery longevity. Additionally, the results showed that the relationship between cell voltage and State-of-Charge (SOC) plays a critical role in determining the rate of degradation. Overall, these findings have important implications for the design and operation of battery systems, as they highlight the need to carefully manage a range of factors to maximize battery performance and longevity. The result is an analysis of the main articles published in this field in recent years. This work aims to present new knowledge about fault detection, diagnosis, and management of lithium-ion batteries based on battery degradation concepts. The new knowledge is presented and discussed in a structured and comprehensive way. UR - https://doi.org/10.20944/preprints202306.0228.v2 Y1 - 2023 UR - https://doi.org/10.20944/preprints202306.0228.v2 UR - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:573-58428 PB - Preprints CY - Basel ER - TY - JOUR A1 - Rufino Júnior, Carlos Antônio A1 - Riva Sanseverino, Eleonora A1 - Gallo, Pierluigi A1 - Koch, Daniel A1 - Kotak, Yash A1 - Schweiger, Hans-Georg A1 - Zanin, Hudson T1 - Towards a business model for second-life batteries – barriers, opportunities, uncertainties, and technologies JF - Journal of Energy Chemistry UR - https://doi.org/10.1016/j.jechem.2022.12.019 KW - Business models KW - Batteries KW - Sustainability KW - Electric vehicles KW - Challenges KW - Opportunities KW - Lithium-ion batteries KW - Reuse Y1 - 2023 UR - https://doi.org/10.1016/j.jechem.2022.12.019 SN - 2096-885X SN - 2095-4956 N1 - Corrigendum verfügbar unter https://doi.org/10.1016/j.jechem.2023.11.010 VL - 2023 IS - 78 SP - 507 EP - 525 PB - Elsevier CY - Amsterdam ER -