98%
921
2 minutes
20
Lithium metal batteries with gel polymer electrolytes have garnered significant interest due to their high energy-density and enhanced safety. However, the persistent challenges of inactive lithium accumulation and the unstable solid-electrolyte interphase (SEI) remain significant obstacles to their practical application. To mitigate these issues, a tiny amount of iodobenzene is employed as a source of triiodine/iodine ion (I /I) redox couple, exhibiting dual functionality in rejuvenating inactive lithium and simultaneously optimizing the SEI composition. Combined by experimental characterization and theoretical analysis, it is demonstrated that the I /I redox couple can actively participate in lithium regeneration chemistry to compensate for irreversible lithium loss, while promoting the formation of a robust LiI-endorsed and LiF-rich SEI layer. Consequently, symmetrical Li batteries with the engineered electrolyte achieve an improved cycling performance of 4000 h at a current density of 0.2 mA cm. Moreover, the assembled NCM811||Li batteries perform an impressive capacity retention of 70.31% after cycling for 720 cycles at 3C, and even at 4C, an equally remarkable capacity retention rate of 75.94% is maintained after 650 cycles.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/smll.202505952 | DOI Listing |
Due to its sizable direct bandgap and strong light-matter interactions, the preparation of monolayer MoS has attracted significant attention and intensive research efforts. However, multilayer MoS is largely overlooked because of its optically inactive indirect bandgap caused by interlayer coupling. It is highly desirable to modulate and decrease the interlayer coupling so that each layer in multilayer MoS can exhibit a monolayer-like direct-gap behavior.
View Article and Find Full Text PDFJ Mater Chem A Mater
August 2025
Institute for Theoretical Physics, University of Amsterdam Science Park 904 Amsterdam 1098 XH The Netherlands
The quest for high-capacity anode materials is vital in developing future lithium-ion battery technologies. While silicon-based anodes offer high theoretical capacity, their commercial realization is hindered by instability associated with large volume changes. Amorphous silicon nitride (a-SiN) has emerged as a promising alternative, acting as a conversion-type anode where lithium incorporation drives the formation of a structurally robust matrix and active phases.
View Article and Find Full Text PDFNatl Sci Rev
August 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Rapid inactive lithium accumulation and severe lithium dendrite growth critically limit the cycle life of metallic lithium anodes. Herein, cyclic thioether 1,3-dithiane is reported as a novel electrolyte additive for fabricating ultra-stable lithium-metal batteries. Through the preferential decomposition of 1,3-dithiane additive and PF anion ions, robust inorganic-rich electrode interphases could be generated at both the anode and the cathode, which is conducive to enhanced kinetics and structural stability of the electrode interface, endowing alleviated active lithium loss and dendrite-free lithium deposition.
View Article and Find Full Text PDFNano Lett
August 2025
Department of Applied Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.
Coupling chloride solid electrolytes (SEs) with ultrahigh-nickel oxide cathodes (LiNiCoMnO, > 0.9) exhibits higher interfacial stability and better safety than traditional sulfide SE-based cathodes. However, the inevitable ∼30 wt% addition of inactive chloride SEs for sufficient Li percolation sacrifices the electrode-level energy density.
View Article and Find Full Text PDFChemistry
August 2025
Department of Chemistry, Simon Fraser University, 8888 University Drive, Burnaby, B.C, V5A 1S6, Canada.
A series of soluble ring-unsubstituted early-transition metallophthalocyanine (PcM) alkoxides with zirconium(IV) and niobium(V) metal centers was prepared via salt metathesis with PcM chlorides and a range of lithium or sodium alkoxides (NaOMe, NaOEt, LiOPr, and NaOBu); several examples were structurally characterized. Given their large ionic size, the metal centers protrude out of the Pc cavity, engendering cis-axial ligation of the alkoxides and thereby generating substantially improved solubility relative to the starting PcM chlorides. Seven-coordinate PcM(OR)-type coordination spheres were typically observed, with lithium- or sodium-balanced "ate" species PcZr(OPr)Li(THF) and PcZr(OBu)Na(THF) isolated for PcZr(IV), compared to the neutral PcNb(OPr).
View Article and Find Full Text PDF