Abstract Layered transition‐metal dichalcogenides (TMDs) have shown promise to replace carbon‐based compounds as suitable anode materials for Lithium‐ion batteries (LIBs) owing to facile intercalation and de‐intercalation of lithium (Li) during charging and discharging, respectively. While the intercalation mechanism of Li in mono‐ and bi‐layer TMDs has’ been thoroughly examined, mechanistic understanding of Li intercalation‐induced phase transformation in bulk or films of TMDs is still largely unexplored. This study investigates possible scenarios during sequential Li intercalation and aims to gain a mechanistic understanding of the phase transformation in bulk MoS2using density functional theory (DFT) calculations. The manuscript examines the role of concentration and distribution of Li‐ions on the formation of dual‐phase 2H‐1T microstructures that have been observed experimentally. The study demonstrates that lithiation would proceed in a systematic layer‐by‐layer manner wherein Li‐ions diffuse into successive interlayer spacings to render local phase transformation of the adjacent MoS2layers from 2H‐to‐1T phase in the multilayered MoS2. This local phase transition is attributed to partial ionization of Li and charge redistribution around the metal atoms and is followed by subsequent lattice straining. In addition, the stability of single‐phase vs. multiphase intercalated microstructures, and the origins of structural changes accompanying Li‐ion insertion are investigated at atomic scales.
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Disorder Dynamics in Battery Nanoparticles During Phase Transitions Revealed by Operando Single‐Particle Diffraction
Abstract Structural and ion‐ordering phase transitions limit the viability of sodium‐ion intercalation materials in grid scale battery storage by reducing their lifetime. However, the combination of phenomena in nanoparticulate electrodes creates complex behavior that is difficult to investigate, especially on the single‐nanoparticle scale under operating conditions. In this work, operando single‐particle X‐ray diffraction (oSP‐XRD) is used to observe single‐particle rotation, interlayer spacing, and layer misorientation in a functional sodium‐ion battery. oSP‐XRD is applied to Na2/3[Ni1/3Mn2/3]O2, an archetypal P2‐type sodium‐ion‐positive electrode material with the notorious P2‐O2 phase transition induced by sodium (de)intercalation. It is found that during sodium extraction, the misorientation of crystalline layers inside individual particles increases before the layers suddenly align just prior to the P2‐O2 transition. The increase in the long‐range order coincides with an additional voltage plateau signifying a phase transition prior to the P2‐O2 transition. To explain the layer alignment, a model for the phase evolution is proposed that includes a transition from localized to correlated Jahn–Teller distortions. The model is anticipated to guide further characterization and engineering of sodium‐ion intercalation materials with P2‐O2 type transitions. oSP‐XRD, therefore, opens a powerful avenue for revealing complex phase behavior in heterogeneous nanoparticulate systems.
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- Award ID(s):
- 1944907
- PAR ID:
- 10364316
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Energy Materials
- Volume:
- 12
- Issue:
- 12
- ISSN:
- 1614-6832
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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