Cobalt-free cation-disordered rocksalt (DRX) cathodes are a promising class of materials for next-generation Li-ion batteries. Although they have high theoretical specific capacities (>300 mA h/g) and moderate operating voltages (∼3.5 V vs Li/Li), DRX cathodes typically require a high carbon content (up to 30 wt %) to fully utilize the active material which has a detrimental impact on cell-level energy density. To assess pathways to reduce the electrode's carbon content, the present study investigates how the carbon's microstructure and loading (10-20 wt %) influence the performance of DRX cathodes with the nominal composition LiMnTiOF. While electrodes prepared with conventional disordered carbon additives (C65 and ketjenblack) exhibit rapid capacity fade due to an unstable cathode/electrolyte interface, DRX cathodes containing 10 wt % graphite show superior cycling performance (e.g., reversible capacities ∼260 mA h/g with 85% capacity retention after 50 cycles) and rate capability (∼135 mA h/g at 1000 mA/g). A suite of characterization tools was employed to evaluate the performance differences among these composite electrodes. Overall, these results indicate that the superior performance of the graphite-based cathodes is largely attributed to the: (i) formation of a uniform graphitic coating on DRX particles which protects the surface from parasitic reactions at high states of charge and (ii) homogeneous dispersion of the active material and carbon throughout the composite cathode which provides a robust electronically conductive network that can withstand repeated charge-discharge cycles. Overall, this study provides key scientific insights on how the carbon microstructure and electrode processing influence the performance of DRX cathodes. Based on these results, exploration of alternative routes to apply graphitic coatings is recommended to further optimize the material performance.
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http://dx.doi.org/10.1021/acsami.3c05619 | DOI Listing |
Adv Mater
December 2024
Department of Material Science and Engineering, University of California, Berkeley, CA, 94706, USA.
Mn-rich disordered rocksalt materials with Li-excess (DRX) materials have emerged as a promising class of earth-abundant and energy-dense next-generation cathode materials for lithium-ion batteries. Recently, an electrochemical transformation to a spinel-like "δ" phase has been reported in Mn-rich DRX materials, with improved capacity, rate capability, and cycling stability compared with previous DRX compositions. However, this transformation unfolds slowly over the course of cycling, complicating the development and understanding of these materials.
View Article and Find Full Text PDFACS Nano
November 2024
School of Materials Science and Engineering, Peking University, Beijing 100871, China.
The practical application of Na-ion cathode materials is currently restricted by their low energy density and sluggish dynamics, while the cation-disordered rocksalt (DRX) structures offer a possible solution to the challenge. In this study, among the 24 candidates containing elements, we use mixing temperature as a descriptor to screen the synthesizable Na-excess DRX, and we have identified NaMnMoO as the most promising candidate that exhibits a Na percolating fraction of 53%, which is higher than that of LiMnTiO (35%) proposed in the previous study due to the larger lattice constant in Na-excess DRX cathodes. More importantly, NaMnMoO is predicted to have a capacity of 228 mAh/g with an energy density of 552 Wh/kg derived from percolation theory and cluster-expansion Monte Carlo simulations, which is higher than that of NaNbMnO and NaMnTiO synthesized recently.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
State Key Laboratory of Mesoscience and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
Mn-based cation disordered rock-salt (DRX) cathode materials exhibit promising application prospects due to their cost-effectiveness and high specific capacity. However, the synthesis methods commonly employed for these materials rely on the solid-state reaction method and mechanochemistry method, primarily attributed to the influence of low-valence states of Mn. Currently, sol-gel approaches for preparing Mn-based DRX cathode materials are limited to systems involving Mn.
View Article and Find Full Text PDFNat Commun
August 2024
Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei, Anhui, China.
The positive electrode|electrolyte interface plays an important role in all-solid-state Li batteries (ASSLBs) based on garnet-type solid-state electrolytes (SSEs) like LiLaZrTaO (LLZTO). However, the trade-off between solid-solid contact and chemical stability leads to a poor positive electrode|electrolyte interface and cycle performance. In this study, we achieve thermodynamic compatibility and adequate physical contact between high-entropy cationic disordered rock salt positive electrodes (HE-DRXs) and LLZTO through ultrafast high-temperature sintering (UHS).
View Article and Find Full Text PDFJ Am Chem Soc
September 2024
Materials Department, University of California Santa Barbara, Santa Barbara 93106, California, United States.
Li-excess Mn-based disordered rock salt oxides (DRX) are promising Li-ion cathode materials owing to their cost-effectiveness and high theoretical capacities. It has recently been shown that Mn-rich DRX LiMnMO ( ≥ 0.5, M are hypervalent ions such as Ti and Nb) exhibit a gradual capacity increase during the first few charge-discharge cycles, which coincides with the emergence of spinel-like domains within the long-range DRX structure coined as "δ phase".
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