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      Localized concentration reversal of lithium during intercalation into nanoparticles

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          Abstract

          Inhomogeneous Li intercalation and localized concentration reversal in nanoparticles are investigated on a nanometer scale.

          Abstract

          Nanoparticulate electrodes, such as Li x FePO 4, have unique advantages over their microparticulate counterparts for the applications in Li-ion batteries because of the shortened diffusion path and access to nonequilibrium routes for fast Li incorporation, thus radically boosting power density of the electrodes. However, how Li intercalation occurs locally in a single nanoparticle of such materials remains unresolved because real-time observation at such a fine scale is still lacking. We report visualization of local Li intercalation via solid-solution transformation in individual Li x FePO 4 nanoparticles, enabled by probing sub-angstrom changes in the lattice spacing in situ. The real-time observation reveals inhomogeneous intercalation, accompanied with an unexpected reversal of Li concentration at the nanometer scale. The origin of the reversal phenomenon is elucidated through phase-field simulations, and it is attributed to the presence of structurally different regions that have distinct chemical potential functions. The findings from this study provide a new perspective on the local intercalation dynamics in battery electrodes.

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          Electrochemical and In Situ X-Ray Diffraction Studies of Lithium Intercalation in Li[sub x]CoO[sub 2]

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            Ultimate limits to intercalation reactions for lithium batteries.

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              Batteries. Capturing metastable structures during high-rate cycling of LiFePO₄ nanoparticle electrodes.

              The absence of a phase transformation involving substantial structural rearrangements and large volume changes is generally considered to be a key characteristic underpinning the high-rate capability of any battery electrode material. In apparent contradiction, nanoparticulate LiFePO4, a commercially important cathode material, displays exceptionally high rates, whereas its lithium-composition phase diagram indicates that it should react via a kinetically limited, two-phase nucleation and growth process. Knowledge concerning the equilibrium phases is therefore insufficient, and direct investigation of the dynamic process is required. Using time-resolved in situ x-ray powder diffraction, we reveal the existence of a continuous metastable solid solution phase during rapid lithium extraction and insertion. This nonequilibrium facile phase transformation route provides a mechanism for realizing high-rate capability of electrode materials that operate via two-phase reactions.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                January 2018
                12 January 2018
                : 4
                : 1
                : eaao2608
                Affiliations
                [1 ]Sustainable Energy Technologies Department, Brookhaven National Laboratory, Upton, NY 11973, USA.
                [2 ]Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
                [3 ]Condensed Matter Physics and Materials Science, Brookhaven National Laboratory, Upton, NY 11973, USA.
                [4 ]Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK.
                [5 ]Department of Materials Science and Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
                [6 ]Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201, P. R. China.
                [7 ]National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, NY 11973, USA.
                [8 ]Department of Materials Science and Engineering, University of California, Berkeley, Berkeley, CA 94720, USA.
                Author notes
                [*]

                These authors contributed equally to this work.

                [†]

                Present address: Department of Computational Mathematics, Science and Engineering and Department of Chemical Engineering and Materials Science, Michigan State University, East Lansing, MI 48824, USA.

                [‡]

                Present address: X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, USA.

                [§ ]Corresponding author. Email: kthorn@ 123456umich.edu (K.T.); fwang@ 123456bnl.gov (F.W.)
                Author information
                http://orcid.org/0000-0001-7031-162X
                http://orcid.org/0000-0002-4351-3581
                http://orcid.org/0000-0002-8443-250X
                http://orcid.org/0000-0003-0345-6647
                http://orcid.org/0000-0001-8046-4996
                http://orcid.org/0000-0002-7505-6135
                http://orcid.org/0000-0002-0575-2987
                http://orcid.org/0000-0002-3153-6954
                http://orcid.org/0000-0002-1638-7217
                http://orcid.org/0000-0002-1227-5293
                http://orcid.org/0000-0001-5572-192X
                http://orcid.org/0000-0003-4068-9212
                Article
                aao2608
                10.1126/sciadv.aao2608
                5766330
                c6a94298-eaa9-42f8-929a-fc63a844a080
                Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 30 June 2017
                : 04 December 2017
                Funding
                Funded by: doi http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: award356909
                Award ID: ACI-1053575
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354589
                Award ID: DE-SC0001294
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354590
                Award ID: DE-SC0012583
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354596
                Award ID: DE-SC0001294
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354602
                Award ID: DE-SC0001294
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award363988
                Award ID: DE-AC02-05CH11231
                Funded by: Extreme Science and Engineering Discovery Environment;
                Award ID: award356907
                Award ID: TG-DMR110007
                Funded by: CAS-DOE;
                Award ID: award364559
                Award ID: CAS-DOE, Grant No. 174433KYSB20150047
                Funded by: National Key Research and Development Program of China;
                Award ID: award354609
                Award ID: 2016YFB0100100
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354608
                Award ID: DE-SC0012704
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354603
                Award ID: DE-SC-0012583
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354604
                Award ID: DE-SC0001294
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354605
                Award ID: DE-SC-0012583
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354606
                Award ID: DE-SC0012704
                Funded by: doi http://dx.doi.org/10.13039/100000015, U.S. Department of Energy;
                Award ID: award354607
                Award ID: DE-SC0012673
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