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In situ polymerized polyether electrolytes are promising for solid-state Li metal batteries due to their high ionic conductivity and excellent interfacial contact. However, their practical application is hindered by Li dendrite formation, interfacial degradation, and limited oxidative stability. Herein, we propose an in situ polymerized polyfluorinated crosslinked polyether electrolyte (PDOL-OFHDBO), synthesized by copolymerizing 1,3-dioxolane (DOL) with 2,2'-(2,2,3,3,4,4,5,5-octafluorohexane-1,6-diyl)bis(oxirane) (OFHDBO) as a polyfluorinated crosslinker. The electron-withdrawing polyfluorinated groups endow PDOL-OFHDBO with enhanced oxidative stability and interfacial compatibility, while reducing the solvation power of the polymer matrix to promote an anion-derived inorganic-rich solid electrolyte interphase for uniform Li deposition. Consequently, PDOL-OFHDBO exhibits a wide electrochemical stability window (>5.6 V) and enables long-term stable Li plating/stripping for over 1100 h. Furthermore, Li||LiNiCoMnO (NCM811) full cells utilizing PDOL-OFHDBO demonstrate outstanding cycling stability with high-loading cathodes (≈3.8 mAh cm) and thin Li anodes (50 µm), achieving capacity retention of 95.5% and 89.1% over 100 cycles at cut-off voltages of 4.3 and 4.5 V, respectively. Remarkably, Ah-level Li||NCM811 pouch cells deliver an impressive specific energy of 401.8 Wh kg, highlighting their potential for practical solid-state Li metal batteries.
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http://dx.doi.org/10.1002/adma.202504333 | DOI Listing |
PNAS Nexus
September 2025
Department of Materials Science and Engineering, Westlake University, Hangzhou 310030, PR China.
Uniform dispersion of carbon nanotubes in a polymer matrix is a prerequisite for high-performance nanotube-based composites. Here, we report an in situ polymerization route to synthesize a range of phenolic composites with high loading of single-wall carbon nanotubes (SWCNTs, >40 wt%) and continuously tunable viscoelasticity. SWCNTs can be directly and uniformly dispersed in cresols through noncovalent charge-transfer interactions without the need for surfactants, and further concentrated before in situ polymerization of the solvent molecules, yielding phenolic composites in the forms of conductive pastes, highly stretchy doughs, and hardened solids with high nanotube loading and much enhanced electrical conductivity (up to 2.
View Article and Find Full Text PDFChemSusChem
September 2025
Leibniz Institute for Catalysis e.V., Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
The palladium-catalyzed Suzuki-Miyaura cross coupling reaction to forge carbon-carbon bonds fundamentally changes the practice of organic synthesis. Herein an isolated palladium catalyst supported on polymeric carbon nitride (Pd/PCN) for efficient cross coupling of bromobenzene and phenylboronic acid at room temperature is reported. It is demonstrated that the Pd/PCN catalyst with a 2 wt% Pd loading achieves the highest mole-specific activity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology of Materials, Beijing University of Chemical Technology, Beijing, 10029, P.R. China.
Lithium metal batteries (LMBs) have emerged as the most promising candidate for next-generation high-energy-density energy storage systems. However, their practical implementation is hindered by the inability of conventional carbonate electrolytes to simultaneously stabilize the lithium metal anode and LiNiCoMnO (NCM811) cathode interfaces, particularly under extreme operating conditions. Herein, we present a transformative molecular design using 3,5-difluorophenylboronic acid neopentyl glycol ester (DNE), which uniquely integrates dual interfacial stabilization mechanisms in a single molecule.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
MOE Key Laboratory of Pollution Processes and Environmental Criteria/Tianjin Engineering Center of Environmental Diagnosis and Contamination Remediation, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.
Sulfidized zero-valent iron (S-ZVI) holds promise in the remediation of chlorinated hydrocarbons. However, S-ZVI is susceptible to corrosion in aquifers with elevated dissolved oxygen (DO) levels. This study demonstrates, for the first time, that a trade-off between the passivation and oxidative corrosion of aged S-ZVI can be achieved in the presence of silicate to promote its dechlorination performance on trichloroethylene.
View Article and Find Full Text PDFDalton Trans
September 2025
Sun Yat-Sen University, MOE Laboratory of Polymeric Composite and Functional Materials, School of Materials Science and Engineering, Guangzhou 510275, China.
The main bottleneck faced by traditional hydrogen production technology through water electrolysis lies in the high energy consumption of the anodic oxygen evolution reaction (OER). Combining the thermodynamically favorable ethanol oxidation reaction (EOR) with the hydrogen evolution reaction provides a promising route to reduce the energy consumption of hydrogen production and generate high value-added products. In this study, a facile method was developed for nickel oxyhydroxide (NiOOH) fabrication.
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