A layered lithium-rich manganese-based oxide cathode, containing 3̅ (LiTMO, TM = Mn, Ni, Co) and 2/ (LiMnO) nanodomains, utilizes both transition metals and oxygen redox to yield substantial energy density. However, the inherent heterogeneous nature and distinct nanodomain redox chemistries of layered lithium-rich oxides will inevitably cause pernicious lattice strain and structural displacement, which can hardly be eliminated by conventional doping or coating strategies and result in accelerated performance decay. Herein, we incorporate a strain-inhibiting perovskite phase coherently grown within the layered structure to effectively restrain the displacement and lattice strain during uneven Li-ion extraction. The enhanced mechanochemical stability of the designed cathode benefits the persistent structure and reversible oxygen redox, thereby achieving high initial Coulombic efficiency and stable cycling and voltage profiles. Our approach of lattice engineering alleviates the strain and displacement caused by inhomogeneous reactivity between heterogeneous nanodomains and promotes the development of advanced cathode materials with long durability.
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http://dx.doi.org/10.1021/jacs.4c11385 | DOI Listing |
J Am Chem Soc
January 2025
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
A layered lithium-rich manganese-based oxide cathode, containing 3̅ (LiTMO, TM = Mn, Ni, Co) and 2/ (LiMnO) nanodomains, utilizes both transition metals and oxygen redox to yield substantial energy density. However, the inherent heterogeneous nature and distinct nanodomain redox chemistries of layered lithium-rich oxides will inevitably cause pernicious lattice strain and structural displacement, which can hardly be eliminated by conventional doping or coating strategies and result in accelerated performance decay. Herein, we incorporate a strain-inhibiting perovskite phase coherently grown within the layered structure to effectively restrain the displacement and lattice strain during uneven Li-ion extraction.
View Article and Find Full Text PDFAdv Mater
December 2024
Tsinghua Center for Green Chemical Engineering Electrification, Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
The use of lithium-rich manganese-based oxides (LRMOs) as the cathode in all-solid-state batteries (ASSBs) holds great potential for realizing high energy density over 600 Wh kg. However, their implementation is significantly hindered by the sluggish kinetics and inferior reversibility of anionic redox reactions of oxygen in ASSBs. In this contribution, boron ions (B) doping and 3D LiBO (LBO) ionic networks construction are synchronously introduced into LRMO materials (LBO-LRMO) by mechanochemical and subsequent thermally driven diffusion method.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institute of Physics, Chinese Academy of Sciences, Beijing, 100190, China.
Lithium-rich manganese-based oxide (LRMO) materials hold great potential for high-energy-density lithium-ion batteries (LIBs) but suffer from severe voltage decay and capacity fading. Herein, we report the construction of LiF-rich solid electrolyte interphase on LRMO through a straightforward ball-milling and electrochemical approach, which exhibits remarkable structural stability and enhanced electrochemical performance.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
Constructing a dense inorganic component-dominated cathode electrolyte interphase (CEI) to meet the long-term cycling requirements of ultrahigh voltage cathodes has been a crucial challenge. Nevertheless, this goal is difficult to achieve in traditional electrolyte compositions due to the inevitable decomposition of organic solvents. Herein, by utilizing the localized mismatch between the strongly coordinating hexafluorophosphate anion (PF) and the weakly coordinating solvent 1,1,1-trifluoro-,-dimethylmethanesulfonamide (TFDMSA), abundant aggregates (AGGs) emerged under a regular Li salt concentration of 1 m lithium bis(fluorosulfonyl)imide (LiFSI) + 0.
View Article and Find Full Text PDFSmall
December 2024
Key Laboratory of Precision and Intelligent Chemistry, CAS Center for Excellence in Nanoscience, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
Lithium-rich manganese-based layered oxides (LRMOs) have received attention from both the academic and the industrial communities in recent years due to their high specific capacity (theoretical capacity ≥250 mAh g), low cost, and excellent processability. However, the large-scale applications of these materials still face unstable surface/interface structures, unsatisfactory cycling/rate performance, severe voltage decay, etc. Recently, solid evidence has shown that lattice oxygen in LRMOs easily moves and escapes from the particle surface, which inspires significant efforts on stabilizing the surface/interfacial structures of LRMOs.
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