14
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Quantifying Bulk Electrode Strain and Material Displacement within Lithium Batteries via High‐Speed Operando Tomography and Digital Volume Correlation

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Tracking the dynamic morphology of active materials during operation of lithium batteries is essential for identifying causes of performance loss. Digital volume correlation (DVC) is applied to high‐speed operando synchrotron X‐ray computed tomography of a commercial Li/MnO 2 primary battery during discharge. Real‐time electrode material displacement is captured in 3D allowing degradation mechanisms such as delamination of the electrode from the current collector and electrode crack formation to be identified. Continuum DVC of consecutive images during discharge is used to quantify local displacements and strains in 3D throughout discharge, facilitating tracking of the progression of swelling due to lithiation within the electrode material in a commercial, spiral‐wound battery during normal operation. Displacement of the rigid current collector and cell materials contribute to severe electrode detachment and crack formation during discharge, which is monitored by a separate DVC approach. Use of time‐lapse X‐ray computed tomography coupled with DVC is thus demonstrated as an effective diagnostic technique to identify causes of performance loss within commercial lithium batteries; this novel approach is expected to guide the development of more effective commercial cell designs.

          Related collections

          Most cited references12

          • Record: found
          • Abstract: found
          • Article: not found

          Size-dependent fracture of silicon nanoparticles during lithiation.

          Lithiation of individual silicon nanoparticles was studied in real time with in situ transmission electron microscopy. A strong size dependence of fracture was discovered; that is, there exists a critical particle diameter of ∼150 nm, below which the particles neither cracked nor fractured upon first lithiation, and above which the particles initially formed surface cracks and then fractured due to lithiation-induced swelling. The unexpected surface cracking arose owing to the buildup of large tensile hoop stress, which reversed the initial compression, in the surface layer. The stress reversal was attributed to the unique mechanism of lithiation in crystalline Si, taking place by movement of a two-phase boundary between the inner core of pristine Si and the outer shell of amorphous Li-Si alloy. While the resulting hoop tension tended to initiate surface cracks, the small-sized nanoparticles nevertheless averted fracture. This is because the stored strain energy from electrochemical reactions was insufficient to drive crack propagation, as dictated by the interplay between the two length scales, that is, particle diameter and crack size, that control the fracture. These results are diametrically opposite to those obtained previously from single-phase modeling, which predicted only compressive hoop stress in the surface layer and thus crack initiation from the center in lithiated Si particles and wires. Our work provides direct evidence of the mechanical robustness of small Si nanoparticles for applications in lithium ion batteries.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            In-operando high-speed tomography of lithium-ion batteries during thermal runaway

            Prevention and mitigation of thermal runaway presents one of the greatest challenges for the safe operation of lithium-ion batteries. Here, we demonstrate for the first time the application of high-speed synchrotron X-ray computed tomography and radiography, in conjunction with thermal imaging, to track the evolution of internal structural damage and thermal behaviour during initiation and propagation of thermal runaway in lithium-ion batteries. This diagnostic approach is applied to commercial lithium-ion batteries (LG 18650 NMC cells), yielding insights into key degradation modes including gas-induced delamination, electrode layer collapse and propagation of structural degradation. It is envisaged that the use of these techniques will lead to major improvements in the design of Li-ion batteries and their safety features.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              MnO2 prepared by hydrothermal method and electrochemical performance as anode for lithium-ion battery

              Two α-MnO2 crystals with caddice-clew-like and urchin-like morphologies are prepared by the hydrothermal method, and their structure and electrochemical performance are characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), galvanostatic cell cycling, cyclic voltammetry, and electrochemical impedance spectroscopy (EIS). The morphology of the MnO2 prepared under acidic condition is urchin-like, while the one prepared under neutral condition is caddice-clew-like. The identical crystalline phase of MnO2 crystals is essential to evaluate the relationship between electrochemical performances and morphologies for lithium-ion battery application. In this study, urchin-like α-MnO2 crystals with compact structure have better electrochemical performance due to the higher specific capacity and lower impedance. We find that the relationship between electrochemical performance and morphology is different when MnO2 material used as electrochemical supercapacitor or as anode of lithium-ion battery. For lithium-ion battery application, urchin-like MnO2 material has better electrochemical performance.
                Bookmark

                Author and article information

                Journal
                Adv Sci (Weinh)
                Adv Sci (Weinh)
                10.1002/(ISSN)2198-3844
                ADVS
                Advanced Science
                John Wiley and Sons Inc. (Hoboken )
                2198-3844
                18 December 2015
                March 2016
                : 3
                : 3 ( doiID: 10.1002/advs.v3.3 )
                : 1500332
                Affiliations
                [ 1 ] Electrochemical Innovation Lab Department of Chemical EngineeringUniversity College London Torrington Place London WC1E 7JEUK
                [ 2 ] Division of Solid MechanicsLund University 221 00 LundSweden
                [ 3 ] ESRFThe European Synchrotron 71 Rue des Martyrs 38000 GrenobleFrance
                [ 4 ]Synchrotron Soleil, L'Orme des Merisiers Saint‐Aubin 91192 Gif‐sur‐YvetteFrance
                [ 5 ] Manchester X‐ray Imaging Facility School of MaterialsUniversity of Manchester Oxford Road Manchester M13 9PLUK
                [ 6 ]Research Complex at Harwell Harwell Oxford, Didcot Oxfordshire OX11 0FAUK
                [ 7 ] School of Mechanical Industrial and Manufacturing EngineeringOregon State University Corvallis OR 97331‐6001USA
                [ 8 ]National Physical Laboratory Hampton Road Teddington Middlesex TW11 0LWUK
                Author notes
                Article
                ADVS97
                10.1002/advs.201500332
                4991305
                77385391-2b74-4944-b63b-837d12312813
                © 2015 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 October 2015
                : 12 November 2015
                Page count
                Pages: 11
                Funding
                Funded by: Engineering and Physical Sciences Research Council
                Funded by: Royal Academy of Engineering
                Funded by: National Physical Laboratory
                Funded by: Science and Technology Facilities Council
                Categories
                Full Paper
                Full Papers
                Custom metadata
                2.0
                advs97
                March 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:19.08.2016

                degradation,digital volume correlation,lithium batteries,operando imaging,x‐ray computed tomography

                Comments

                Comment on this article