Classification of Heat Evolution Terms in Li-Ion Batteries Regarding the OCV Hysteresis in a Li- and Mn-Rich NCM Cathode Material in Comparison to NCA

We investigate the heat release of Li- and Mn-rich NCM (LMR-NCM) and NCA half-cells during cycling at different C-rates and quantify the individual contributions to the overall heat flow using a combination of isothermal micro-calorimetry and electrochemical methods. The paper focuses in particular on the open-circuit voltage (OCV) hysteresis of the LMR-NCM material, which results in a significant reduction in energy round-trip efficiency (≈90% for LMR-NCM/Li cells vs ≈99% for NCA/Li cells at C/10) and therefore in an additional source of heat that has to be considered for the thermal management of the cell. The total heat release of the LMR-NCM/Li cells is found to be nine times higher than that of the corresponding NCA/Li cells (at C/10). In the case of the LMR-NCM cathode, the heat due to OCV hysteresis is responsible for up to 55% of the total energy loss. Using the applied approach, the OCV hysteresis heat is separated into its share during charge and discharge and is furthermore presented as a function of SOC. Additional sources of heat, such as reversible entropic heat, parasitic effects, and measurement limitations, are discussed in terms of their contribution to the overall energy balance of the two cell chemistries

The LiNiO2_2 Cathode Active Material: A Comprehensive Study of Calcination Conditions and their Correlation with Physicochemical Properties. Part I. Structural Chemistry

Following the demand for increased energy density of lithium-ion batteries, the Ni content of the Nickel-Cobalt-Manganese oxide (NCM) cathode materials has been increased into the direction of LiNiO$_2$ (LNO), which regained the attention of both industry and academia. To understand the correlations between physicochemical parameters and electrochemical performance of LNO, a calcination study was performed with variation of precursor secondary particle size, maximum calcination temperature and Li stoichiometry. The structural properties of the materials were analyzed by means of powder X-ray diffraction, magnetization measurements and half-cell voltage profiles. All three techniques yield good agreement concerning the quantification of Ni excess in the Li layer (1.6%–3.7%). This study reveals that the number of Li equivalents per Ni is the determining factor concerning the final stoichiometry rather than the calcination temperature within the used calcination parameter space. Contrary to widespread belief, the Ni excess shows no correlation to the 1$^{st}$ cycle capacity loss, which indicates that a formerly overlooked physical property of LNO, namely primary particle morphology, has to be considered

The LiNiO2_{2} Cathode Active Material: A Comprehensive Study of Calcination Conditions and their Correlation with Physicochemical Properties Part II. Morphology

A better understanding of the cathode active material (CAM) plays a crucial role in the improvement of lithium-ion batteries. We have previously reported the structural properties of the model cathode material LiNiO$_{2}$ (LNO) in dependence of its calcination conditions and found that the deviation from the ideal stoichiometry in LiNiO2 (Ni excess) shows no correlation to the 1st cycle capacity loss. Rather, the morphology of LNO appears to be decisive. As CAM secondary agglomerates fracture during battery operation, the surface area in contact with the electrolyte changes during cycle life. Thus, particle morphology and especially the primary particle size become critical and are analyzed in detail in this report for LNO, using an automated SEM image segmentation method. It is shown that the accessible surface area of the pristine CAM powder measured by physisorption is close to the secondary particle geometric surface area. The interface area between CAM and electrolyte is measured by an in situ capacitance method and approaches a value proportional to the estimated primary particle surface area determined by SEM image analysis after just a few cycles. This interface area is identified to be the governing factor determining the 1st cycle capacity loss and long-term cycling behavior

Editors\u27 Choice—Understanding Chemical Stability Issues between Different Solid Electrolytes in All-Solid-State Batteries

Sulfide-based solid electrolytes (SE) are quite attractive for application in all-solid-state batteries (ASSB) due to their high ionic conductivities and low grain boundary resistance. However, limited chemical and electrochemical stability demands for protection on both cathode and anode side. One promising concept to prevent unwanted reactions and simultaneously improve interfacial contacting at the anode side consists in applying a thin polymer film as interlayer between Li metal and the SE. In the present study, we investigated the combination of polyethylene oxide (PEO) based polymer films with the sulfide-based SE Li10SnP2S12 (LSPS). We analyzed their compatibility using both electrochemical and chemical techniques. A steady increase in the cell resistance during calendar aging indicated decomposition reactions at the interfaces. By means of X-ray photoelectron spectroscopy and further analytical methods, the formation of polysulfides, P–[S]n–P like bridged PS43− units and sulfite, SO32−, was demonstrated. We critically discuss potential reasons and propose a plausible mechanism for the degradation of LSPS with PEO. The main objective of this paper is to highlight the importance of understanding interfaces in ASSBs not only from an electrochemical perspective, but also from a chemical point of view

Synthesis optimization of carbon-supported ZrO2 nanoparticles from different organometallic precursors

Abstract We report here the synthesis of carbon-supported ZrO2 nanoparticles from zirconium oxyphthalocyanine (ZrOPc) and acetylacetonate [Zr(acac)4]. Using thermogravimetric analysis (TGA) coupled with mass spectrometry (MS), we could investigate the thermal decomposition behavior of the chosen precursors. According to those results, we chose the heat treatment temperatures (T HT) using partial oxidizing (PO) and reducing (RED) atmosphere. By X-ray diffraction we detected structure and size of the nanoparticles; the size was further confirmed by transmission electron microscopy. ZrO2 formation happens at lower temperature with Zr(acac)4 than with ZrOPc, due to the lower thermal stability and a higher oxygen amount in Zr(acac)4. Using ZrOPc at T HT ≥900 °C, PO conditions facilitate the crystallite growth and formation of distinct tetragonal ZrO2, while with Zr(acac)4 a distinct tetragonal ZrO2 phase is observed already at T HT ≥750 °C in both RED and PO conditions. Tuning of ZrO2 nanocrystallite size from 5 to 9 nm by varying the precursor loading is also demonstrated. The chemical state of zirconium was analyzed by X-ray photoelectron spectroscopy, which confirms ZrO2 formation from different synthesis routes

Slurry-Based Processing of Solid Electrolytes: A Comparative Binder Study

Limited energy density of today\u27s Li-ion battery technologies demands for novel cell technologies, such as the all-solid-state battery (ASSB). In order to achieve high energy densities and enable large-scale processing, thin and flexible solid electrolyte (SE) layers have to be implemented. This study focuses on slurry-based processing of the sulfidic solid electrolyte Li$_{10}$SnP$_{2}$S$_{12}$ (LSPS). Various polymers were investigated concerning their suitability as binders for thin and freestanding SE sheets. We conducted a parameter study in order to optimize e.g. LSPS-to-binder ratio, solids content and porosity. Significant differences were found with regard to the minimum amount of binder required for mechanically stable sheets as well as the homogeneity, density and flexibility of the resulting SE layers. The impacts of binder type and weight fraction on ionic conductivity were examined through lithium diffusion measurements. Impedance analysis was conducted in comparison, proving sufficiently high ionic conductivity for potential application of the SE sheets in ASSB. This work highlights the important role of the polymeric binder in slurry-based processing of SEs and gives an impression how important a well-considered selection of parameters is to achieve good processing properties as well as desirable features for the final SE sheet

Modification of the Electrochemical Surface Oxide Formation and the Hydrogen Oxidation Activity of Ruthenium by Strong Metal Support Interactions

A major hurdle for the wide spread commercialization of proton exchange membrane based fuel cells (PEMFCs) and water electrolyzers are the durability and high cost of noble metal catalysts. Here, alternative support materials might offer advantages, as they can alter the properties of a catalyst by means of a strong metal support interaction (SMSI) that has been shown to prevent platinum oxidation and suppress the oxygen reduction reaction on titanium oxide supported platinum nanoparticles deposited on a carbon support (Pt/TiOx/C). Herein, we report a novel Ru/TiOx/C catalyst that according to tomographic transmission electron microscopy analysis consists of partially encapsulated Ru particles in a Ru/TiOx-composite matrix supported on a carbon support. It is shown by cyclic voltammetry and X-ray photoelectron spectroscopy that ruthenium oxidation is mitigated by an SMSI between Ru and TiOx after reductive heat-treatment (Ru/TiOx/C400°C,H2). As a result, the catalyst is capable of oxidizing hydrogen up to the onset of oxygen evolution reaction, in stark contrast to a Ru/C reference catalyst. PEMFC-based hydrogen pump measurements confirmed the stabilization of the hydrogen oxidation reaction (HOR) activity on Ru/TiOx/C400°C,H2 and showed a ≈3-fold higher HOR activity compared to Ru/C, albeit roughly two orders of magnitude less active than Pt/C.DFG, 390776260, EXC 2089: e-conversionBMWi, 03ET6096A, Verbundprojekt: innoKA - Materialinnovationen für die PEM-Brennstoffzelle - Platinfreie Kathode, anodenseitige Materialstabilisierung durch neue Katalysatorkonzept; Teilvorhaben: Synthese neuer (Ko-)Katalysatoren für die Anode und deren Integration sowie die von platinfreien Kathodenkatalysatoren in MEAs

Fast Ionic Conductivity in the Most Lithium-Rich Phosphidosilicate Li14SiP6.

Solid electrolytes with superionic conductivity are required as a main component for all-solid-state batteries. Here we present a novel solid electrolyte with three-dimensional conducting pathways based on "lithium-rich" phosphidosilicates with ionic conductivity of σ > 10-3 S cm-1 at room temperature and activation energy of 30-32 kJ mol-1 expanding the recently introduced family of lithium phosphidotetrelates. Aiming toward higher lithium ion conductivities, systematic investigations of lithium phosphidosilicates gave access to the so far lithium-richest compound within this class of materials. The crystalline material (space group Fm3m), which shows reversible thermal phase transitions, can be readily obtained by ball mill synthesis from the elements followed by moderate thermal treatment of the mixture. Lithium diffusion pathways via both tetrahedral and octahedral voids are analyzed by temperature-dependent powder neutron diffraction measurements in combination with maximum entropy method and DFT calculations. Moreover, the lithium ion mobility structurally indicated by a disordered Li/Si occupancy in the tetrahedral voids plus partially filled octahedral voids is studied by temperature-dependent impedance and 7Li NMR spectroscopy