4.8 Article

Effect of crystallite geometries on electrochemical performance of porous intercalation electrodes by multiscale operando investigation

Journal

NATURE MATERIALS
Volume 21, Issue 2, Pages 217-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41563-021-01151-8

Keywords

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Funding

  1. National Science Foundation (NSF) [DMR 1809866]
  2. Welch Foundation [A-1978-20190330]
  3. German Science Foundation (DFG) [398072825]
  4. NSF [DMR 1944674]
  5. X-Grants Initiative at Texas AM University
  6. Argonne National Laboratory
  7. National Science Foundation [1805656]
  8. Advanced Photon Source of Argonne National Laboratory [DE-AC02-06CH11357]
  9. Div Of Chem, Bioeng, Env, & Transp Sys
  10. Directorate For Engineering [1805656] Funding Source: National Science Foundation

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This study used operando techniques to investigate the impact of electrode particle geometry on the phase transformations induced by lithiation in lithium-ion batteries. It found that the particle geometry affects the modulation of metastable phase regimes and electrode tortuosity, providing key design principles for intercalation cathodes.
Lithium-ion batteries are yet to realize their full promise because of challenges in the design and construction of electrode architectures that allow for their entire interior volumes to be reversibly accessible for ion storage. Electrodes constructed from the same material and with the same specifications, which differ only in terms of dimensions and geometries of the constituent particles, can show surprising differences in polarization, stress accumulation and capacity fade. Here, using operando synchrotron X-ray diffraction and energy dispersive X-ray diffraction (EDXRD), we probe the mechanistic origins of the remarkable particle geometry-dependent modification of lithiation-induced phase transformations in V2O5 as a model phase-transforming cathode. A pronounced modulation of phase coexistence regimes is observed as a function of particle geometry. Specifically, a metastable phase is stabilized for nanometre-sized spherical V2O5 particles, to circumvent the formation of large misfit strains. Spatially resolved EDXRD measurements demonstrate that particle geometries strongly modify the tortuosity of the porous cathode architecture. Greater ion-transport limitations in electrode architectures comprising micrometre-sized platelets result in considerable lithiation heterogeneities across the thickness of the electrode. These insights establish particle geometry-dependent modification of metastable phase regimes and electrode tortuosity as key design principles for realizing the promise of intercalation cathodes. Designing electrode architectures for Li-ion batteries that can be reversibly accessible for ion storage can be challenging. Using operando techniques the mechanistic origin of lithiation-induced phase transformations in a V2O5 model cathode is now clarified.

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