TY - JOUR A1 - Leonhardt, Robert A1 - Böttcher, Nils A1 - Dayani, Shahabeddin A1 - Rieck, Arielle A1 - Markötter, Henning A1 - Schmidt, Anita A1 - Kowal, Julia A1 - Tichter, Tim A1 - Krug von Nidda, Jonas T1 - Exploring the electrochemical and physical stability of lithium-ion cells exposed to liquid nitrogen N2 - The transport and storage of lithium-ion (Li-ion) batteries — damaged or in an undefined state — is a major safety concern for regulatory institutions, transportation companies, and manufacturers. Since (electro)chemical reactivity is exponentially temperature-dependent, cooling such batteries is an obvious measure for increasing their safety. The present study explores the effect of cryogenic freezing on the electrochemical and physical stability of Li-ion cells. For this purpose, three different types of cells were repeatedly exposed to liquid nitrogen (LN2). Before and after each cooling cycle, electrical and electrochemical measurements were conducted to assess the impact of the individual freezing steps. While the electrochemical behavior of the cells did not change significantly upon exposure to LN2 , it became apparent that a non-negligible number of cells suffered from physical changes (swelling) and functional failures. The latter defect was found to be caused by the current interrupt device of the cylindrical cells. This safety mechanism is triggered by the overpressure of expanding nitrogen which enters the cells at cryogenic temperatures. This study underlines that the widely accepted reversibility of LN2 -cooling on a material scale does not allow for a direct extrapolation toward the physical integrity of full cells. Since nitrogen enters the cell at cryogenic temperatures and expands upon rethermalization, it can cause an internal overpressure. This can, in turn, lead to mechanical damage to the cell. Consequently, a more appropriate temperature condition — less extreme than direct LN2 exposure — needs to be found KW - Lithium-ion battery KW - LN2 cooling KW - Battery characterization PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-599248 DO - https://doi.org/10.1016/j.est.2024.111650 VL - 89 SP - 1 EP - 7 PB - Elsevier B.V. AN - OPUS4-59924 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scharpmann, Philippa A1 - Leonhardt, Robert A1 - Schmidt, Anita A1 - Kowal, Julia A1 - Tichter, Tim A1 - Krug von Nidda, Jonas T1 - Exploring restrictive overdischarge cycling as a method to accelerate characteristic ageing in lithium-ion cells N2 - This study presents a test protocol that greatly accelerates the ageing process of lithium-ion battery cells comprising a positive electrode of nickel manganese cobalt oxide while preserving their characteristic degradation upon cyclic ageing. Applying a repetitive restricted overdischarge, resulting in a depth of discharge larger than 100%, a capacity loss of 20% is achieved over five times faster compared to conventional cycling. The well-known overdischarge degradation phenomenon of copper current collector dissolution is deliberately prevented by setting a discharge cutoff voltage above the theoretical threshold of copper oxidation. Hence, the accelerated degradation can be primarily connected to solid electrolyte interphase growth. A comparative assessment of the ageing dynamics using electrochemical impedance spectroscopy and differential voltage analysis hints towards similar, characteristic degradation processes during accelerated and conventional ageing. A post-ageing examination of the electrical behaviour (i.e., coulombic and energy efficiency, capacity fade) under reference conditions reveals very little to no lasting damages caused by overdischarging. Additionally, post-mortem analysis discloses no increased copper dissolution when comparing cells subjected to accelerated and conventional ageing. Generally, the developed ageing method appears suitable for providing cells with a defined state of health at a reasonable timescale without altering the main degradation mechanisms significantly. KW - Lithium-ion cell KW - Accelerated ageing KW - Overdischarge KW - Degradation processes KW - Differential voltage analysis KW - Electrochemical impedance spectroscopy PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-650917 DO - https://doi.org/10.1016/j.jpowsour.2025.239072 SN - 0378-7753 VL - 665 SP - 1 EP - 9 PB - Elsevier B.V. AN - OPUS4-65091 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Leonhardt, Robert A1 - Krug von Nidda, Jonas A1 - Andrae, Dirk A1 - Schmidt, Anita A1 - Kowal, Julia A1 - Tichter, Tim T1 - Reconstructing the distribution of relaxation times with analytical basis functions N2 - The present work proposes the implementation of non-singular basis functions into the algorithm for reconstructing the distribution of relaxation times (DRT) function of impedance data. These functions reflect the dispersed and asymmetrical nature of non-ideal capacitive–resistive processes. Inclusion is achieved by combining the singular Debye distribution basis with distributed relaxation functions, such as those derived from the analytical models of Cole–Cole and Havriliak–Negami. The shapes of the introduced basis functions are described by constant parameters, for which an empirical optimization approach is provided alongside. Using synthetic impedance data of non-ideal capacitive–resistive processes subjected to white noise, it is shown that the demand for regularization can be reduced significantly by using distributed bases. To underline the practical relevance of non-singular basis functions in DRT reconstruction, an experimental study comprising 100 sodium-ion and 80 lithium-ion ommercial cells is presented. In this context, it is shown that auxiliary information from the non-ideal nature of real-world electrochemical processes is outsourced into the basis and, hence, easily filtered out of the resulting DRT. This facilitates the separation of single processes without post-DRT curve fitting and thus improves the interpretation and classification of impedance data significantly. KW - Electrochemical Impedance Spectroscopy; KW - Distribution of relaxation times KW - Basis function KW - Cole-Cole KW - Cole-Davidson KW - Havriliak-Negami PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-635486 DO - https://doi.org/10.1016/j.jpowsour.2025.237403 SN - 0378-7753 VL - 652 SP - 1 EP - 11 PB - Elsevier B.V. AN - OPUS4-63548 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -