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Solid-state lithium metal batteries (SSLMBs) are promising for realizing higher energy density. However, the poor interfacial Li transport kinetics and Li dendrite growth inhibit SSLMBs, leading to sluggish interfacial ion diffusion and depressive lifespan, which is attributed to high barriers blocked by anions or interface space in solid-state electrolytes. Herein, a flexible solid-state polymer skeleton employed with ionic liquid and metal-organic frameworks (PIM) electrolyte is proposed to strengthen interfacial Li ion exchange by improving the Li sieving effect and interfacial wettability. Thanks to the immobilization effect of TFSI anions affected by positive metal atom centers and pore morphology, the PIM electrolyte exhibits exceptional properties, i.e., a high ionic conductivity up to 3.1 mS cm at 60 °C and an improved Li transference number of 0.65, enabling symmetric cells of Li metal to run steadily for over 1000 h with lower voltage hysteresis (25 mV). Meanwhile, matching with high-voltage electrodes, the solid-state PIM electrolyte exhibits good compatibility and stability toward LiNiCoMnO and LiFePO electrodes, showing the capacity retentions of 85.5% and 96.5% after 120 and 400 cycles, respectively. This work suggests low interfacial diffusion resistances and high compatibility for make it a promising candidate for future solid-state battery.
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http://dx.doi.org/10.1002/cssc.202501351 | DOI Listing |
ChemSusChem
September 2025
i-Lab & CAS Key Laboratory of Nanophotonic Materials and Devices, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, 215123, China.
Solid-state lithium metal batteries (SSLMBs) are promising for realizing higher energy density. However, the poor interfacial Li transport kinetics and Li dendrite growth inhibit SSLMBs, leading to sluggish interfacial ion diffusion and depressive lifespan, which is attributed to high barriers blocked by anions or interface space in solid-state electrolytes. Herein, a flexible solid-state polymer skeleton employed with ionic liquid and metal-organic frameworks (PIM) electrolyte is proposed to strengthen interfacial Li ion exchange by improving the Li sieving effect and interfacial wettability.
View Article and Find Full Text PDFACS Nano
July 2025
College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, PR China.
Porous solid-state polymer electrolytes have emerged as promising candidates for next-generation batteries owing to their superior safety, excellent interfacial compatibility, and efficient ion transport properties. However, systematically tuning the Li solvent microenvironment within the micropores of PIMs (inherent microporous polymers) to significantly enhance Li conduction remains unexplored. Herein, we propose a strategy for performing microenvironmental engineering within microporous channels.
View Article and Find Full Text PDFJ Math Biol
April 2025
Institute of Mathematical Innovation, University of Bath, Bath, UK.
In this work, we present a fundamental mathematical model for proton transport, tailored to capture the key physical processes underpinning Proton Beam Therapy (PBT). The model provides a robust and computationally efficient framework for exploring various aspects of PBT, including dose delivery, linear energy transfer, treatment planning and the evaluation of relative biological effectiveness. Our findings highlight the potential of this model as a complementary tool to more complex and computationally intensive simulation techniques currently used in clinical practice.
View Article and Find Full Text PDFSmall
April 2025
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing, 210009, China.
Aprotic Li-O batteries exhibit ultra-high energy density through the redox reaction of O. However, their open-structure design makes them prone to water infiltration and electrolyte leakage. Traditionally, dense and thick oxygen-permeable membranes (OPMs) are employed to prevent HO intrusion, but this approach limits O permeance and constrains charge current densities.
View Article and Find Full Text PDFJ Thromb Haemost
January 2025
Department of Life Sciences, Faculty of Science and Engineering, Manchester Metropolitan University, Manchester, United Kingdom; Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, Unite
Background: The thromboxane A2 receptor (TPαR) plays an important role in the amplification of platelet responses during thrombosis. Receptor activity is regulated by internalization and receptor desensitization. The mechanism by which constitutive surface expression of the TPαR is regulated is unknown.
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