Journal of Power Sources, Journal Year: 2024, Volume and Issue: 629, P. 235932 - 235932
Published: Dec. 5, 2024
Language: Английский
Journal of Power Sources, Journal Year: 2024, Volume and Issue: 629, P. 235932 - 235932
Published: Dec. 5, 2024
Language: Английский
Energy Materials, Journal Year: 2025, Volume and Issue: 5(8)
Published: March 3, 2025
Compositing inorganic ceramics and polymer materials to form all-solid-state electrolytes has been recognized as a feasible approach for the development of batteries. However, polymer-based such polyethylene oxide can electrochemically decompose above 3.9 V (vs . Li+/Li), which results in undesirable battery performance. Moreover, dendrite growth occur on anode side further lead short-circuit. This work designs successfully fabricates stable electrode/electrolyte interfaces both composite cathode sides after employing alucone coating layers made through atomic layer deposition. Due protection capability layers, electrochemical degradation between solid-state Li7La3Zr2O12/polyethylene oxide/lithium bis(trifluoromethane-sulfonyl) imide film nickel-rich high voltage (LiNi0.8Mn0.1Co0.1O2) obviously suppressed significantly improved anti-oxidation electrolyte. Simultaneously, function protective barrier lithium metal anode, remarkably suppressing dendrites. As result, obtained batteries with dual show capacity retention long cycle life, whereas contrasting without shows fast decay micro-shorting behavior. presents an effective strategy constructing more polymers-based batteries, also provides design rationale structure field energy storage conversion.
Language: Английский
Citations
1Journal of Energy Storage, Journal Year: 2024, Volume and Issue: 100, P. 113683 - 113683
Published: Sept. 13, 2024
Language: Английский
Citations
4International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 140309 - 140309
Published: Jan. 1, 2025
Language: Английский
Citations
0Published: Jan. 1, 2025
Citations
0Nano Energy, Journal Year: 2025, Volume and Issue: unknown, P. 110979 - 110979
Published: April 1, 2025
Language: Английский
Citations
0Materials Today Energy, Journal Year: 2025, Volume and Issue: 51, P. 101891 - 101891
Published: April 22, 2025
Language: Английский
Citations
0Journal of Power Sources, Journal Year: 2025, Volume and Issue: 644, P. 237080 - 237080
Published: April 26, 2025
Language: Английский
Citations
0Batteries & Supercaps, Journal Year: 2024, Volume and Issue: unknown
Published: July 30, 2024
Abstract Cellulose‐based separator exhibits excellent electrolyte affinity, thermal stability, and mechanical strength, which acts as a promising alternative to commercial polyolefin separators in lithium metal batteries (LMBs). Fiber size cellulose‐based plays crucial role determining their physicochemical structure well the electrochemical performance of corresponding LMBs. Herein, fiber was first time regulated optimize stability related battery performance. The influences on chemical structure, properties, surface morphology, behavior were investigated detail, underlying mechanism between elucidated. As result, optimized by regulation exhibited under 180 °C, good tensile strengths 6.0 MPa Young's moduli 315.9 MPa, superior room temperature ionic conductivity 1.87 mS cm −1 , significantly improved batteries. It can be concluded that optimization for through is an effective indispensable approach towards high safety
Language: Английский
Citations
2Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 17, 2024
Abstract The key issue in utilizing solid polymer electrolytes for high‐energy‐density lithium metal batteries is to balance the conflicting demands of superior processability, adequate ionic conductivity, and mechanical stability. Inspired by molecular structure design, a metal‐organic framework‐derived polyether poly(urethane urea) electrolyte (denoted as ePU@H SPE) has been synthesized via facile polycondensation method involving covalent crosslinking. reduced crystallinity numerous polar groups SPEs enhance Li salt dissociation create efficient + ion diffusion channels, yielding remarkable conductivity (1.48 × 10 −4 S cm −1 ). backbones, incorporating bonds dynamic hydrogen bonds, provide superb strength (5.12 GPa), high toughness (1240%), excellent resilience, which suppress dendrite growth buffer electrode volume fluctuations during cycling. Leveraging these attributes, well‐designed SPE enables ultra‐high durability plating/stripping over 2300 h. Moreover, integrated LFP|ePU@H|Li batteries, generating delicate electrode/electrolyte interfacial contact, deliver an exceptionally long lifespan (86% retention 500 cycles at 1 C). pouch cell operates reliably even under severe deformation external damage. Impressively, stable cycling performance full high‐voltage LCO high‐capacity cathodes further verifies significant potential advanced practical applications.
Language: Английский
Citations
2Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 28, 2024
Abstract Electrochemical aging of electrode materials usually leads to capacity decay and voltage drop in conventional rocking‐chair batteries. Here we report an anomalous electrochemical strengthening behavior Ti 3 C 2 T x MXene a dual‐ion battery, whose capacity/power grows under cycling eventually reaches optimal state once the co‐storage PF 6 − anion Li + cation is activated by wide window. Experimental theoretical results reveal that there anion‐cation synergy between during process electrodes, where small intercalation expands interlayer spacing at low discharge voltages, residual charging can act as anchor center promote storage large high voltages; meanwhile, turn provides additional active sites coordinate with , raising capacity. Thereafter, offers 310 mAh/g, robust stability over 800 cycles, rate performance up 1000 mA/g, which among best reported co‐storage. This counter‐intuitive discovery, resembling aging‐strengthening phenomenon metallurgy, deepens our understanding unconventional battery chemistry new avenue for design high‐performance materials.
Language: Английский
Citations
0