Journal of Power Sources, Journal Year: 2024, Volume and Issue: 629, P. 236074 - 236074
Published: Dec. 17, 2024
Language: Английский
Journal of Power Sources, Journal Year: 2024, Volume and Issue: 629, P. 236074 - 236074
Published: Dec. 17, 2024
Language: Английский
Chemical Reviews, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 11, 2025
Solid electrolytes, as the core of all-solid-state batteries (ASSBs), play a crucial role in determining kinetics ion transport and interface compatibility with cathodes anodes, which can be subdivided into catholytes, bulk anolytes based on their functional characteristics. Among various inorganic solid ductile distinguished from rigid oxide exhibit excellent properties even under cold pressing, thus holding greater promise for industrialization. However, challenge lies finding electrolyte that simultaneously serve catholyte, electrolyte, anolyte. Fortunately, due to immobility combining multiple types electrolytes allows leveraging respective advantages. In this review, we discuss five sulfides, halides, nitrides, antiperovskite-type, complex hydrides, challenges superiorities these are also addressed. The impact pressure ASSBs has been systematically discussed. Furthermore, suitability anolyte is discussed characteristics physicochemical properties. This discussion aims deepen our understanding enabling us harness advantages develop practical, high-performance ASSBs.
Language: Английский
Citations
1Advanced Materials, Journal Year: 2025, Volume and Issue: unknown
Published: March 6, 2025
Ultra-high nickel layered oxides are recognized as promising cathode candidates for high-energy-density lithium-ion batteries due to their enhanced overall capacity and elevated operating voltage. However, the interlayer sliding of transition metal-oxygen octahedra (TMO6) instability lattice oxygen at high voltages ultra-high oxide cathodes pose significant challenges development. Herein, origin framework stability is investigated by incorporating high-covalent element Mo in both bulk surface using a one-step integrated method material LiNi0.92Co0.08O2. It revealed that apart from isolation protection effect Mo-enriched layer, suppression Li/Ni antisite defects Mo6+ with strong covalency plays critical role reducing configurations activated anionic redox reaction stabilizing structure. Benefiting this, reversibility significantly enhanced, enabling more oxidized exist form dimer ions O2n-$O_2^{n - }$ rather than being lost gaseous O2. Consequently, modified demonstrates improved diffusion kinetics optimized electrochemical performance
Language: Английский
Citations
1ACS Energy Letters, Journal Year: 2025, Volume and Issue: unknown, P. 1577 - 1584
Published: March 10, 2025
Language: Английский
Citations
0Journal of Energy Storage, Journal Year: 2025, Volume and Issue: 119, P. 116433 - 116433
Published: March 30, 2025
Language: Английский
Citations
0ACS Applied Materials & Interfaces, Journal Year: 2025, Volume and Issue: unknown
Published: April 4, 2025
The practical application of nickel-rich layered transition metal oxide is hampered by its fast capacity decay, deriving from the side reactions with electrolyte, crack formation caused volume variation, and phase change near surface during charging/discharging processes. Here, we experimentally realize mechano-chemo-electrochemical coupling effect nanolayer on to greatly improve electrochemical performance. According detailed atomic structure analysis, this facilitates consuming residual lithium left oxide, suppressing reducing due variation long-term cycles. This design plays an in mechanical, chemical, aspects simultaneously which beneficial for their development.
Language: Английский
Citations
0Energy storage materials, Journal Year: 2025, Volume and Issue: unknown, P. 104251 - 104251
Published: April 1, 2025
Language: Английский
Citations
0Molecules, Journal Year: 2025, Volume and Issue: 30(8), P. 1746 - 1746
Published: April 14, 2025
LaOCl-mediated ethane chlorination into 1,2-dichloroethane offers a promising pathway for low-temperature, large-scale upgrading. However, under Cl2-rich conditions, LaOCl undergoes detrimental lanthanum chloride (LaCl3), accompanied by extensive surface hydroxylation. Such severe structural evolution limits the practical application of La-based catalysts industrially relevant conditions. In this study, an alumina-stabilized La catalyst was prepared via coprecipitation method. We demonstrated that strong La-O-Al interactions effectively resist degradation species reaction enabling modified to maintain exceptional stability high Cl2 concentrations. At C2H6/Cl2 ratio 4:9, optimized achieves conversion 61%, with selectivity sustained above 74% 12 h without noticeable deactivation. contrast, bulk counterpart suffers from rapid over-chlorination, shifting product dominance trichloroethane within 10 h. Advanced spectroscopy characterization reveals loss in originates phase collapse LaCl3, whereas Al2O3 stabilization preserves metastable LaOClx highly dispersed state, ensuring selective C–Cl bond formation. These results highlight critical role stabilizing oxychloride phases through robust metal oxide interactions, establishing design framework rare-earth high-concentration chlorine environments.
Language: Английский
Citations
0ACS Sustainable Chemistry & Engineering, Journal Year: 2025, Volume and Issue: unknown
Published: April 18, 2025
Language: Английский
Citations
0Chemical Science, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
This work reported a novel method to enhance the solid-state calcination homogeneity of LiNi 0.9 Co 0.05 Mn O 2 by depositing WO 3 layer on precursor surface via atomic deposition, obtaining high-performance nickel-rich layered cathode.
Language: Английский
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 27, 2025
Abstract Fabricating P2/O3 intergrowth structure in layered cathode materials is a viable strategy to improve the electrochemical property of sodium‐ion batteries. Unfortunately, such biphasic have bear obscure thermodynamic formation process and complicated structure‐property associations between multiple phase transitions Na + diffusion kinetics at high state charge. Here this issue addressed by tailoring crystalline domains P2 O3 while reducing residual alkali content target P2/O3‐Na 0.8 Mg 0.06 Ni 0.34 Mn 0.54 Ti O 2 material, which consists 24.26% 75.74% phase. The distribution atomic resolution dynamic evolution identification are parsed out experimental scanning transmission electron microscopy FAULTS simulations. Moreover, dislocations boundary serve prevent O‐type stacking therefore allow most P‐type dominate deep Na‐depleted state, thereby facilitating ensure high‐rate capability. Consequently, material exhibits energy density 534 Wh kg −1 reversible capacity 110 mAh g 10 C. This work highlights importance modulation improving transport obtain high‐energy materials.
Language: Английский
Citations
0