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Data · dataset · 2026

Multifunctional Fluorine-Rich Ion-Conductive Elastomer for Combustion-Enhanced Energetic Composites

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Achieving a balanced combination of ultra-stretchability, electrostatic safety, self-healing capability, and enhanced combustion performance in polymer-bonded explosives (PBXs) remains a critical challenge.

Description

Herein, we report a series of fluorine-rich ion-conductive elastomers (ICEs) derived from a polymerizable deep eutectic solvent (PDES) composed of 2,2,3,4,4,4-hexafluorobutyl acrylate (HFBA) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI).

The formation mechanism of the PDES(HFBA<sub>2</sub>-LiTFSI) system was elucidated via FT-IR spectroscopy, revealing that the carbonyl groups of HFBA participate in Li<sup>+</sup> solvation, and a homogeneous PDES is formed at an HFBA:LiTFSI molar ratio of 2:1. Three elastomer systems, namely LiF<sub>2</sub>C<sub>No</sub>, LiF<sub>2</sub>C<sub>PEGDA</sub> and LiF<sub>2</sub>C<sub>VFSoil</sub> were systematically investigated.

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By introducing a fluorosiloxane crosslinker (VFSoil), the resulting LiF<sub>2</sub>C<sub>VFSoil</sub> exhibited the most favorable comprehensive performance with toughness of 23.23±0.05 MJ·m<sup>–3</sup>, ionic conductivity of 7.517×10<sup>–5</sup> S/m, thermally activated self-healing capability, and favorable hydrophobicity. When applied as a binder for cyclotetramethylenetetranitramine (HMX, octogen)-based composites, the H<sub>50</sub>(LiF<sub>2</sub>C<sub>VFSoil</sub>)<sub>50</sub> formulation maintained excellent stretchability with an elongation at break of 578.12% and exhibited thermally activated self-healing capability at 80 °C. Furthermore, the H<sub>90</sub>(LiF<sub>2</sub>C<sub>VFSoil</sub>)<sub>10</sub> formulation improved both the mechanical and electrostatic safety relative to pristine HMX.

Moreover, high-speed photography and infrared thermography revealed that the fluorine-rich binder LiF<sub>2</sub>C<sub>VFSoil</sub> effectively disrupted the alumina passivation shell, suppressed aluminum nanoparticles (nano-Al) agglomeration, and delivered superior combustion uniformity and sustained high flame temperatures in aluminized formulations. This work presents a promising molecular design platform for developing next-generation PBXs featuring ultra-stretchability, thermally activated self-healing capability, and enhanced combustion performance.

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