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      Versatile electrochemical cell for Li/Na-ion batteries and high-throughput setup for combinedoperandoX-ray diffraction and absorption spectroscopy

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          Abstract

          A fundamental understanding of de/intercalation processes (single phaseversusmulti-phase), structural stability and voltage–composition profiles is pivotal for optimization of electrode materials for rechargeable non-aqueous batteries. A fully operational setup (electrochemical cells, sample changer and interfacing software) that enables combined quasi-simultaneousoperandoX-ray diffraction (XRD) and absorption (XANES and EXAFS) measurements coupled with electrochemical characterization is presented. Combined XRD, XANES and EXAFS analysis provides a deep insight into the working mechanisms of electrode materials, as shown for the high-voltage Li insertion cathode material LiMn1.5Ni0.5O4and the high-capacity sodium conversion anode material Bi2S3. It is also demonstrated that the cell design can be used for in-house XRD characterization. Long-term cycling experiments on both Li and Na electrode materials prove the hermeticity and chemical stability of the design as a versatileoperandoelectrochemical cell.

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          Sodium-Ion Batteries

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            Na-ion batteries, recent advances and present challenges to become low cost energy storage systems

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              Origin of additional capacities in metal oxide lithium-ion battery electrodes.

              Metal fluorides/oxides (MF(x)/M(x)O(y)) are promising electrodes for lithium-ion batteries that operate through conversion reactions. These reactions are associated with much higher energy densities than intercalation reactions. The fluorides/oxides also exhibit additional reversible capacity beyond their theoretical capacity through mechanisms that are still poorly understood, in part owing to the difficulty in characterizing structure at the nanoscale, particularly at buried interfaces. This study employs high-resolution multinuclear/multidimensional solid-state NMR techniques, with in situ synchrotron-based techniques, to study the prototype conversion material RuO2. The experiments, together with theoretical calculations, show that a major contribution to the extra capacity in this system is due to the generation of LiOH and its subsequent reversible reaction with Li to form Li2O and LiH. The research demonstrates a protocol for studying the structure and spatial proximities of nanostructures formed in this system, including the amorphous solid electrolyte interphase that grows on battery electrodes.
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                Author and article information

                Journal
                JACGAR
                Journal of Applied Crystallography
                J Appl Crystallogr
                International Union of Crystallography (IUCr)
                1600-5767
                December 2016
                October 2016
                : 49
                : 6
                : 1972-1981
                Article
                10.1107/S160057671601428X
                d194d5a7-f686-47af-871f-34695db80f38
                © 2016
                History

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