ACS Applied Materials & Interfaces, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 18, 2024
High-voltage LiCoO
Language: Английский
ACS Applied Materials & Interfaces, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 18, 2024
High-voltage LiCoO
Language: Английский
Chemical Science, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Silicon (Si) is considered a promising anode material for next-generation lithium-ion batteries due to its high theoretical specific capacity and earth-abundancy. However, challenges such as significant volume expansion, unstable solid electrolyte interphase (SEI) formation in incompatible electrolytes, slow transport lead poor cycling rate performance. In this work, it demonstrated that superior cyclability capability of Si anodes can be achieved using ethyl fluoroacetate (EFA) fluoroethylene carbonate (FEC) solvents with low binding energy Li+ but sufficiently relative dielectric constants. By weakening the interaction between solvent, barrier desolvation process lowered, while ensuring conductivity diffusion Li+. As result, silicon-carbon optimized exhibits excellent performance, work reversibly 1709.1 mAh g-1 proceeds over 250 cycles retains 85.2% at 0.2C. Furthermore, Si/C‖LiFePO4 (LFP) full cell shows an extended service life more than 500 cycles. This offers valuable insights into design weakly solvating electrolytes high-performance Si-based batteries.
Language: Английский
Citations
1Angewandte Chemie International Edition, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 7, 2025
LiCoO2 batteries for 3 C electronics demand high charging voltage and wide operating temperature range, which are virtually impossible existing electrolytes due to aggravated interfacial parasitic reactions sluggish kinetics. Herein, we report an electrolyte design strategy based on a partially fluorinated ester solvent (i.e., DFEA) that achieves balance between weak Li+-solvent interactions, sufficient salt dissociation, stability, superior thermal stability address the aforementioned challenges. The resulting high-voltage wide-temperature (HWE) not only possesses low desolvation energy, fast Li+ transport, oxidation excellent thermal-abuse tolerance non-flammability, but also enables formation of both inorganic-rich cathode interphase (CEI) solid (SEI). Owing above merits, this HWE endows highly stable operation cathodes under ultra-high 4.7 V Graphite || in ultra-wide range -30 70 °C. Meanwhile, 1.7 Ah-level 4.6 pouch cell with energy density 240 Wh kg-1 delivers cycling representing significant advancement towards batteries.
Language: Английский
Citations
1Advanced Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 21, 2025
Abstract Low‐concentration electrolytes (LCEs) present significant potential for actual applications because of their cost‐effectiveness, low viscosity, reduced side reactions, and wide‐temperature electrochemical stability. However, current electrolyte research predominantly focuses on regulation strategies conventional 1 m electrolytes, high‐concentration localized leaving design principles, optimization methods, prospects LCEs inadequately summarized. face unique challenges that cannot be addressed by the existing theories approaches applicable to three common mentioned above; thus, tailored provide development guidance are urgently needed. Herein, a systematic overview recent progress in is provided subsequent directions suggested. This review proposes core challenge high solvent ratio LCEs, which triggers unstable organic‐enriched electrolyte/electrode interface formation anion depletion near anode. On basis these issues, modification including passivation construction solvent‒anion interaction optimization, used various rechargeable battery systems. Finally, role advanced simulations cutting‐edge characterization techniques revealing LCE failure mechanisms further highlighted, offering new perspectives future practical application next‐generation batteries.
Language: Английский
Citations
0Journal of the American Chemical Society, Journal Year: 2025, Volume and Issue: unknown
Published: May 1, 2025
Great electrochemical stability and intrinsic safety are of critical significance in realizing large-scale applications Na-ion batteries (NIBs). Unfortunately, the notorious decomposition electrolyte undesirable side reactions on cathode-electrolyte interphase (CEI) pose major obstacles to practical implementation NIBs. Besides, flammability traditional carbonate-based electrolytes raises increasing concerns about batteries. Herein, a flame-retardant all-fluorinated is proposed achieve an anion-aggregated inner solvation shell by modulating cation-anion interactions through low-coordination number cosolvent. The more electrochemically antioxidant fluorinated solvents anion-dominated interfacial chemistry contribute construction both mechanically chemically stable F-rich CEI. Such thin, homogeneous effectively inhibits parasitic reaction, strengthens stability, enables fast Na+ diffusion kinetics interface. When employing this electrolyte, Na0.95Ni0.4Fe0.15Mn0.3Ti0.15O2 (NFMT) cathode delivers remarkable discharge capacity up 169.7 mAh g-1, with cycling at 1C for 500 cycles. Impressively, NFMT//hard carbon pouch cells such also steady operation 100 cycles 0.5C 86.8% remaining. This study offers reference developing high-performance electrolytes.
Language: Английский
Citations
0Nano Letters, Journal Year: 2025, Volume and Issue: unknown
Published: April 30, 2025
Developing high-energy-density lithium metal batteries (LMBs) necessitates robust solid electrolyte interphases (SEIs) capable of enduring prolonged cycling. While fluoride (LiF) is recognized as crucial for anode (LMA) protection, the effects different LiF sources in SEIs remain insufficiently understood. In this study, we systematically introduce single fluorine sources─anion LiF, solvent and native LiF─into a fluoride-free system to elucidate impact originating from on SEI composition properties. Results reveal that performance depends not only content but also coexisting organic components. During deep cycling, solvent-derived LiF-rich SEIs, containing elevated organics, offer superior LMA protection ability. These maintain structural integrity during significant volume changes, effectively suppressing dead Li formation achieving enhanced Coulombic efficiency. This work reexamines LiF's protective mechanisms while advancing chemistry understanding, providing critical insights developing high-performance LMBs.
Language: Английский
Citations
0Chinese Chemical Letters, Journal Year: 2025, Volume and Issue: unknown, P. 110972 - 110972
Published: Feb. 1, 2025
Language: Английский
Citations
0Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 162078 - 162078
Published: April 1, 2025
Language: Английский
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 26, 2025
Abstract The cathode‐electrolyte interphase (CEI) is vital for the stability of LiCoO 2 (LCO) beyond 4.55 V (vs Li/Li + ). Herein, full coverage boron‐based CEI achieved on LCO surface via utilizing self‐wetting synthesis boric acid (i.e., B‐LCO), accompanying with subsequent electrochemical self‐assembly process upon cycles. Initially, B‐LCO coated borate deposits (size 10–20 nm), then it melts and fully covers sintering, leading to artificial CEI, which directly reduces side reactions induced by highly oxidative Co 4+ /O n− (0 < n 2). Significantly, during cycling, in situ interfacial between species LiF promote formation crystalline LiB 6 O 9 F components, showing mechanically robust Li conductive characteristics. Due synergism structurally tough rocksalt (RS) phase, not only more reversible phase transition uniform (de)lithiation are achieved, but also particle cracks deterioration issues effectively inhibited. As a result, B‐LCO||Li cells show excellent cycle stability, high retention 84.0% 500 cycles 3–4.65 V.
Language: Английский
Citations
0Materials Today, Journal Year: 2025, Volume and Issue: unknown
Published: April 1, 2025
Language: Английский
Citations
0Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 163516 - 163516
Published: May 1, 2025
Language: Английский
Citations
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