Results 101 to 110 of about 314 (212)
This perspective examines the evolution toward fifth‐generation LiFePO4. Practical volumetric energy density depends on preserving ionic transport, electronic connectivity, mechanical integrity, and active‐material utilization across powder design and manufacturing.
Xia Huang +7 more
wiley +1 more source
Gibbs Free Energy‐Driven Li–MgF2 Composite Anodes for Stable Solid‐State Lithium Batteries
A Li–MgF2 composite anode has been engineered through a Gibbs free energy‐driven reaction of molten Li with MgF2. Benefiting from the synergistic effect of the LiF and LixMg segregated structure, the Li–MgF2|garnet interface achieves a low interfacial resistance of 8.2 Ω cm2, and the Li–MgF2|garnet|Li–MgF2 symmetric cells accomplish ultrastable cycling
Ziduan Li +4 more
wiley +1 more source
Air Stability of Sulfide Solid Electrolytes: From Theoretical Insights to Practical Solutions
This paper reviews research progress on the air stability of SSEs, covering their instability mechanisms and modification strategies, while outlining core challenges and future directions for practical applications. Sulfide solid electrolytes are pivotal for enabling high‐performance all‐solid‐state batteries due to their high ionic conductivity and ...
Hongbing Ding +10 more
wiley +1 more source
Bimetallic Cu and Fe oxide species supported on porous silica with interparticle mesoporosity act as efficient photo‐Fenton‐like catalysts under visible light. Photogenerated electrons drive the Cu2+/Cu1+ redox cycle. Part of Cu1+ is responsible for the regeneration of the Fe3+/Fe2+ cycle at neutral pH. Light irradiation additionally induces structural
Andraž Šuligoj +6 more
wiley +1 more source
The high‐valence Ta5+‐substituted LZC (LZT0.3C) demonstrates high ionic conductivity, excellent compressibility, and impressive moisture stability, contributing to the long‐term cycling durability of ASSLBs. Recently developed halide solid‐state electrolytes (SSEs) have become promising alternatives for the next generation inorganic SSEs, primarily due
Jin Hu +9 more
wiley +1 more source
This work examines formation protocols for stabilizing the cathode–electrolyte interphase (CEI) in sulfide all‐solid‐state batteries, highlighting a special turbo discharging protocol discovery. The methodologies presented here show strong potential for integration into emerging artificial intelligence–driven frameworks. Formation protocols dictate the
Yuanshun Li +8 more
wiley +1 more source
Harnessing Thin‐Film Solid‐State Electrolytes: Enabling Breakthroughs in All‐Solid‐State Batteries
Schematic illustration highlighting the advantages of transitioning from traditional thick solid‐state electrolytes (SSEs) to thin‐film SSEs. Thinning the electrolyte enables higher ionic conductivity, reduced interfacial polarization, improved flexibility, compact electrode contact, and enhanced energy density, offering a promising pathway toward high‐
Yitao He +3 more
wiley +1 more source
This review summarizes the key optimization strategies and challenges for all‐solid‐state lithium–sulfur batteries based on sulfide solid‐state electrolytes, covering electrolyte synthesis, cathode design, interface engineering, and industrialization considerations.
Yongsheng Gao +5 more
wiley +1 more source
The hydrogel exhibits versatile functions, including efficient thermogalvanic conversion under a temperature difference, and acting as a cooling layer/forming a thermally conductive nanoactive composite for thermovoltaic conversion. Additionally, its self‐healing and self‐powered flexibility play a key role in energy storage systems. The growing demand
Eunah Kang
wiley +1 more source
A nanoscale ZrB2/LiCl network encapsulated LiBH4 solid electrolyte was prepared by mechanically reacting LiBH4 with ZrCl4. Such a composite solid electrolyte exhibits fast ionic conduction and high critical current density. More importantly, the resultant solid electrolyte enables unprecedented cyclability of Li|LiNbO3@LiCoO2 and Li|TiS2 full cells at ...
Shuyang Sun +9 more
wiley +1 more source

