Phase change materials (PCMs) have shown significant potential in enhancing the thermal regulation of lithium-ion (Li-ion) batteries. However, existing organic solid-liquid PCMs encounter several issues, including leakage, limited energy density, and an inability to fulfill the demands of comprehensive thermal management across various environmental conditions. This study takes inspiration from beavers, which construct dams to regulate the temperature of their habitats in different climates, and introduces a dual-network aerogel-based composite PCM (CPCM) designed for the all-weather thermal control of Li-ion batteries. The developed CPCM incorporates tetradecanol (TD) as the core phase change material, a poly(vinyl alcohol)/carboxylated cellulose nanocrystal (PVA/CNC-C) aerogel as the potting material, borax for cross-linking, and graphene nanoplatelets (GNPs) to facilitate photothermal conversion. This CPCM demonstrates a high energy density of 199.1 J/g and remarkable cyclic durability. Furthermore, it features excellent shape retention, superior mechanical strength, and an impressive photothermal conversion efficiency of 94.5%. In addition, the CPCM effectively regulates the thermal behavior of Li-ion batteries: at elevated temperatures, it ensures that the battery's maximum operating temperature remains below 55 °C, while at lower temperatures, it maintains the battery above 10 °C for 30-40 min. Moreover, it possesses the capability to preheat batteries, enhancing their functionality in cold environments. This research presents an innovative approach to designing materials that address the comprehensive thermal management needs of Li-ion batteries under varying climatic conditions.
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ChemSusChem
March 2025
Vidyasirimedhi Institute of Science and Technology, Chemical and Biomolecular Engineering, 555 Moo 1 Payupnai, Wangchan District, Rayong, THAILAND.
This study investigates the electrochemical performance, stability, and decomposition mechanisms of fluorine-based electrolytes in large-scale cylindrical Ni-rich lithium-ion batteries (LIBs) under high-voltage conditions (up to 4.8 V). We examine fluoroethylene carbonate (FEC) and di-fluoroethylene carbonate (DFEC) in electrolyte formulations and their effects on battery longevity, gas evolution, and solvation dynamics.
View Article and Find Full Text PDFNat Commun
March 2025
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, China.
The discovery of Nb-W-O materials years ago marks the milestone of charging a lithium-ion battery in minutes. Nevertheless, for many applications, charging lithium-ion battery within one minute is urgently demanded, the bottleneck of which largely lies in the lack of fundamental understanding of Li storage mechanisms in these materials. Herein, by visualizing Li intercalated into representative NbWO, we find that the fast-charging nature of such material originates from an interesting rate-dependent lattice relaxation process associated with the Jahn-Teller effect.
View Article and Find Full Text PDFACS Nano
March 2025
College of Materials Science and Engineering, Nanjing Tech University, Nanjing 211816, PR China.
Covalent organic frameworks (COFs) have shown promise as bifunctional catalysts to simultaneously mitigate shuttle effects and Li dendrite issues of lithium-sulfur (Li-S) batteries. However, the inherent low conductivity of the COFs has significantly limited their catalytic activity and stability. Herein, bifunctional catalytic activity and durability of the COF/MXene heterostructure are activated by tuning the surface curvatures of COFs interfaced with MXene.
View Article and Find Full Text PDFAdv Mater
March 2025
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro Yuseong-gu, Daejeon, 34141, Republic of Korea.
The grain sizes of solid electrolyte interphase (SEI) and solvation structure of electrolytes can affect Li ion transport across SEI and control the desolvation kinetics of solvated Li ions during fast-charging of Li-ion batteries (LIBs). However, the impact of the geometric structure of SEI grains on the fast charging capability of LIBs is rarely examined. Here, the correlation between the SEI grain size and fast charging characteristics of cells is explored, and the desolvation kinetics is controlled by replacing the strongly binding ethylene carbonate (EC) solvent with a weakly binding nitrile-based solvent under fast charging conditions.
View Article and Find Full Text PDFNat Mater
March 2025
Chimie du Solide-Energie, UMR 8260, Collège de France, Paris Cedex 05, France.
Anionic redox has reshaped the conventional way of exploring advanced cathode materials for Li-ion batteries. However, how anions participate in the redox process has been the subject of intensive debate, evolving from electron holes to O-O dimerization and currently to a focus on trapped molecular O based on high-resolution resonant X-ray inelastic scattering research. Here we show that the resonant X-ray inelastic scattering signal of molecular O is not exclusive to Li-rich oxide cathodes, but appears consistently in O-redox-inactive oxide materials even with a short beam exposure time as low as 1 min, indicating that molecular O species are not directly related to voltage hysteresis and voltage decay.
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