Kinetic pathways of ionic transport in fast-charging lithium titanate

Author:

Zhang Wei1ORCID,Seo Dong-Hwa2ORCID,Chen Tina23ORCID,Wu Lijun4ORCID,Topsakal Mehmet5ORCID,Zhu Yimei4ORCID,Lu Deyu5ORCID,Ceder Gerbrand23ORCID,Wang Feng1ORCID

Affiliation:

1. Sustainable Energy Technologies Department, Brookhaven National Laboratory, Upton, NY 11973, USA.

2. Department of Materials Science and Engineering, University of California, Berkeley, Berkeley, CA 94720, USA.

3. Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA

4. Department of Condensed Matter Physics and Materials Science, Brookhaven National Laboratory, Upton, NY 11973, USA.

5. Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY 11973, USA.

Abstract

Metastable pathways allow high rates In batteries that allow for fast charging and discharging, lithium usually forms a solid solution with the anode so that the only limiting factor is the ionic diffusion. However, for a lithium titanate (Li 4 Ti 5 O 12 ) anode, the lithium ions interact with two phases and the diffusion is slow in both, but it still shows high-rate capabilities. Zhang et al. used electron energy-loss spectroscopy combined with density functional theory calculations to probe the anomalous behavior. They found that a diffuse interface forms between the starting and ending compositions, Li 4 Ti 5 O 12 and Li 7 Ti 5 O 12 , and this is what allows the lithium ions to travel quickly. Science , this issue p. 1030

Funder

National Science Foundation Graduate Research Fellowship

Laboratory Directed Research and Development program at the Brookhaven National Lab

Vehicle Technologies Office, of the U.S. Department of Energy

U.S. DOE, Office of Basic Energy Science, Division of Materials Science and Engineering

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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