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Academic research in the battery field frequently remains limited to small coin or pouch cells, especially for new materials that are still rather far from commercialization, which renders a meaningful evaluation at an early stage of development challenging. Here, the realization of large lab‐scale pouch cells comprising Sn0.9Mn0.1O2 (SMO), prepared via an easily scalable hydrothermal synthesis method, as an alternative active material for the negative electrode and LiNi0.6Mn0.2Co0.2O2 (NMC622) as a commercially available active material for the positive electrode is reported. Nine double‐layer pouch cells are connected in series and parallel, suitable for powering a remote‐controlled vehicle. Subsequently, these SMO‖NMC622 cells are critically evaluated by means of an early‐stage life cycle assessment and compared to graphite‖NMC622 cells, in order to get first insights into the potential advantages and challenges of such lithium‐ion chemistry. [ABSTRACT FROM AUTHOR]

The incorporation of transition metals (TMs) such as Co, Fe, and Mn into SnO2 substantially improves the reversibility of the conversion and the alloying reaction when used as a negative electrode active material in lithium-ion batteries. Moreover, it was shown that the specific benefits of different TM dopants can be combined when introducing more than one dopant into the SnO2 lattice. Herein, a careful characterization of Co and Mn co-doped SnO2 via transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy and X-ray diffraction including Rietveld refinement is reported. Based on this in-depth investigation of the crystal structure and the distribution of the two TM dopants within the lattice, an ex situ X-ray photoelectron spectroscopy and ex situ X-ray absorption spectroscopy were performed to better understand the de-/lithiation mechanism and the synergistic impact of the Co and Mn co-doping. The results specifically suggest that the antithetical redox behaviour of the two dopants might play a decisive role for the enhanced reversibility of the de-/lithiation reaction. [ABSTRACT FROM AUTHOR]

Experimental evidence for the presence of two computationally theorised diffusion pathways, namely the oxygen dumbbell hop (ODH) and tetrahedral site hop (TSH), has been given for the first time by muon spin relaxation (µSR) on sub-stoichiometric LixNi0.77Co0.14Al0.09O2. µSR has proven to be a powerful tool that is able to discriminate between diffusion pathways that occur on different timescales on a local level, where bulk electrochemical techniques cannot. Whereas the estimated values of DLi at lithium concentrations of 0.87 and 0.71 were found to be on the order of 10−11 by electrochemical impedance spectroscopy, contributions to diffusion from ODH and TSH were determined to be on the order of 10−11 and 10−10 cm2 s−1, and a factor of four decrease in Ea for both samples, in excellent agreement with theoretical calculations on related compounds. Rietveld refinement of both X-ray and neutron diffraction data was also used to interrogate the local structure of the materials where no contribution from Li+/Ni2+ cation mixing was observed. [ABSTRACT FROM AUTHOR]

It has been shown that the introduction of several transition metal (TM) dopants into SnO2 lithium‐ion battery anodes can overcome the issues associated with the irreversible capacity loss from the conversion reaction of SnO2 and the aggregation of the metallic Sn particles formed upon lithiation. As the choice of the single dopant, however, plays a decisive role for the achievable energy density – precisely its redox potential – we investigate herein TM co‐doped SnO2, prepared by using a readily scalable continuous hydrothermal flow synthesis (CHFS) process, to tailor the dis‐/charge profile and by this the energy density. It is shown that the judicious choice of different elemental doping combinations in samples made via CHFS simultaneously improves the cycling performance and the full‐cell energy density. To support these findings, we realized a lithium‐ion full‐cell incorporating the best performing co‐doped SnO2 as negative electrode and high‐voltage LiNi0.5Mn1.5O4 (LNMO) as positive electrode–to the best of our knowledge, the first full‐cell based on such anode material in combination with LNMO as cathode active material. [ABSTRACT FROM AUTHOR]

Nanosized metal germanates (M2GeO4; M = Co, Mn, Zn) are synthesized using a continuous hydrothermal flow synthesis process for the first time. The electrochemical properties of all samples as active materials for negative electrodes in Li‐ion half cells are explored. The galvanostatic and potentiodynamic testing is conducted in the potential range of 3.00–0.05 V versus Li/Li+. The results suggest that both alloying and conversion reactions associated with Ge contribute to the stored charge capacity; Zn2GeO4 shows a high specific capacity of 600 mAh g−1 (ten cycles at 0.1 A g−1) due to alloying and conversion reactions for both Ge and Zn. Mn2GeO4 is studied for the first time as a potential negative electrode material in a Li‐ion half cell; an excellent specific charge capacity of 510 mAh g−1 (10 cycles per 0.1 A g−1) is obtained with a significant contribution to charge arising from the conversion reaction of Mn to MnO upon delithiation. In contrast, Co2GeO4 only shows a specific capacity of 240 mAh g−1, after ten cycles at the same current rate, which suggests that cobalt has little or no benefit for enhancing stored charge in germanate. [ABSTRACT FROM AUTHOR]

A library of 66 perovskite Ba x Sr y Ca z TiO 3 ( x + y + z = 1) samples (ca. three grams per sample) was made in ca. 14 h using a high-throughput continuous hydrothermal flow synthesis system. The as-synthesized samples were collected from the outlet of the process and then cleaned and freeze-dried before being evaluated individually as oxygen reduction catalysts using a rotating disk electrode testing technique. To establish any correlations between physical and electrochemical characterization data, the as-synthesized samples were investigated using analytical methods including BET surface area, powder X-ray diffraction (PXRD) and in selected cases, transmission electron microscopy (TEM). The aforementioned approach was validated as being able to quickly identify oxygen reduction catalysts from new libraries of electrocatalysts.