Both layered- and rocksalt-type Li-rich cathode materials are drawing great attention due to their enormous capacity, while the individual phases have their own drawbacks, such as great volume change for the layered phase and low electronic and ionic conductivities for the rocksalt phase. Previously, we have reported the layered/rocksalt intergrown cathodes with nearly zero-strain operation, while the use of precious elements hinders their industrial applications. Herein, low-cost 3d Mn ions are utilized to partially replace the expensive Ru ions, to develop novel ternary Li-rich cathode material Li[RuMnNi]O. The as-designed LiRuMnNiO is revealed to have a layered/rock salt intergrown structure by neutron diffraction and transmission electron microscopy. The as-designed cathode exhibits ultrahigh lithium-ion reversibility, with 0.86 (231.1 mAh g) out of a total Li inventory of 1.15 (309.1 mAh g). The X-ray absorption spectroscopy and resonant inelastic X-ray scattering spectra further demonstrate that the high Li storage of the intergrown cathode is enabled by leveraging cationic and anionic redox activities in charge compensation. Surprisingly, in situ X-ray diffraction shows that the intergrown cathode undergoes extremely low-strain structural evolution during the charge-discharge process. Finally, the Mn content in the intergrown cathodes is found to be tunable, providing new insights into the design of advanced cathode materials for high-energy Li-ion batteries.
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http://dx.doi.org/10.1021/acsami.3c13858 | DOI Listing |
Chem Commun (Camb)
June 2024
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, P. R. China.
Cobalt substitution for manganese sites in NaMnO initiates a dynamic structural evolution process, yielding a composite cathode material comprising intergrown P2 and P3 phases. The novel P2/P3 composite cathode exhibits a reversible phase transition process during Na extraction/insertion, showcasing its attractive battery performance in sodium-ion batteries.
View Article and Find Full Text PDFACS Nano
May 2024
College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Layered sodium transition-metal (TM) oxides generally suffer from severe capacity decay and poor rate performance during cycling, especially at a high state of charge (SoC). Herein, an insight into failure mechanisms within high-voltage layered cathodes is unveiled, while a two-in-one tactic of charge localization and coherent structures is devised to improve structural integrity and Na transport kinetics, elucidated by density functional theory calculations. Elevated Jahn-Teller [MnO] concentration on the particle surface during sodiation, coupled with intense interlayer repulsion and adverse oxygen instability, leads to irreversible damage to the near-surface structure, as demonstrated by X-ray absorption spectroscopy and in situ characterization techniques.
View Article and Find Full Text PDFJ Am Chem Soc
April 2024
Key Laboratory for Renewable Energy, Beijing Key Laboratory for New Energy Materials and Devices, Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China.
ACS Energy Lett
March 2024
Energy Storage and Distributed Resources Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Angew Chem Int Ed Engl
April 2024
College of Engineering and Applied Sciences, National Laboratory of Solid State Microstructures, Nanjing University, 210093, Nanjing, China.
Layered transition metal oxides are extensively considered as appealing cathode candidates for potassium-ion batteries (PIBs) due to their abundant raw materials and low cost, but their further implementations are limited by slow dynamics and impoverished structural stability. Herein, a layered composite having a P2 and P3 symbiotic structure is designed and synthesized to realize PIBs with large energy density and long-term cycling stability. The unique intergrowth of P2 and P3 phases in the obtained layered oxide is plainly characterized by X-ray diffraction refinement, high-angle annular dark field and annular bright field-scanning transmission electron microscopy at atomic resolution, and Fourier transformation images.
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