Understanding the diffusion of lithium ions in electrode materials for lithium ion batteries is of great importance for their knowledge-based optimization and development of novel materials and cell designs. The galvanostatic intermittent titration technique (GITT) is widely applied in battery research to study the diffusion of lithium in anode and cathode materials depending on the degree of lithiation. While transport properties of electrode materials at high and ambient temperatures are largely available, low temperature diffusion and rate coefficients are hardly reported in the literature and vary by orders of magnitude for identical active materials. Herein, we demonstrate and discuss several challenges and pitfalls in the application and evaluation of GITT measurements for determining the effective chemical lithium ion diffusion coefficient in lithium insertion electrodes, which become especially important at low temperature. This includes theoretical considerations and an experimental analysis of the promising cathode material LiNi0.5Co0.2Mn0.3O2 (NCM523) in the wide temperature range of −40 °C to 40 °C. We show how the choice of experimental conditions for the GITT measurements and of the subsequent mathematical evaluation significantly influence the derived diffusion coefficient. The results suggest that the large scattering of reported values of the diffusion coefficient could be caused by the use of different evaluation procedures. Simple calculation methods appear to be less suited the lower the temperature is. It is shown that the complementary use of GITT and EIS supplemented by detailed knowledge of the microstructure of the electrode significantly improves the accuracy of determining the diffusion coefficient.

Accurate knowledge of transport properties of Li‐insertion materials in application‐relevant temperature ranges is of crucial importance for the targeted optimization of Li‐ion batteries (LIBs). Galvanostatic intermittent titration technique (GITT) is a widely applied method to determine Li‐ion diffusion coefficients of electrode materials. The well‐known calculation formulas based on Weppner's and Huggins’ approach, imply a square‐root time dependence of the potential during a GITT pulse. Charging the electrochemical double layer capacitance at the beginning of a GITT pulse usually takes less than one second. However, at lower temperatures down to −40 °C, the double layer charging time strongly increases due to an increase of the charge transfer resistance. The charging time can become comparable with the pulse duration, impeding the conventional GITT diffusion analysis. We propose a model to describe the potential change during a galvanostatic current pulse, which includes an initial, relatively long‐lasting double layer charging, and analyze the accuracy of the lithium diffusion coefficient, derived by using the Weppner‐Huggins method within a suitably chosen time interval of the pulse. Effects leading to an inaccurate determination of the diffusion coefficient are discussed and suggestions to improve GITT analyses at low temperature are derived.

In equilibrium the Fe–Pd system on the iron rich side of the phase diagram demixes into Fe and L10-ordered FePd. Here, we examine the suitability of the demixing process for self-organized formation of exchange coupled thin film magnets. In this way the benefit of the high magnetization of Fe is combined with the high magnetocrystalline anisotropy of FePd. By using combinatorial methods the influence of composition and thickness on structure, microstructure, and magnetic properties is analyzed. Experiments show the different thermodynamic and kinetic conditions required for demixing and ordering. In particular, for nanostructures the interface energy during demixing must be considered.