Thermal Properties and Ionic Conductivities of Confined LiBF4 Dimethyl Carbonate Solutions

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• 作者：Christopher M. Burba ; Eric D. Butson ; Justin R. Atchley ; Mioto Sato Johnson
• 刊名：Journal of Physical Chemistry C
• 出版年：2014
• 出版时间：January 9, 2014
• 年：2014
• 卷：118
• 期：1
• 页码：366-375
• 全文大小：399K
• ISSN：1932-7455

文摘

Solutions of lithium tetrafluoroborate dissolved in dimethyl carbonate (DMC) are confined within MCM-41, a mesoporous silica matrix. Thermal measurements indicate that the melting points of pure DMC and the DMC solutions are significantly reduced when confined within the pores of MCM-41 compared to unconfined samples; this is an observation that is consistent with the Gibbs鈥揟homson equation. The melting point onsets of confined solutions are slightly lower than that of pure DMC, suggesting the dissolved salts impact the phase-transition temperature of DMC when confined within mesoporous silica. Rotational dynamics of the confined solutions are explored by doping DMC with small quantities of Tempone, an electron paramagnetic resonance (EPR)-active spin probe. Tempone rotational correlation times are an order of magnitude slower for confined liquids compared to unconfined solutions. Temperature-dependent conductivity measurements of the composite materials suggest that the liquid electrolyte solution is distributed among the MCM-41 pores and the intergrain voids between individual MCM-41 particles. Ionic conductivities of confined electrolyte solutions remain above 0.01 mS路cm^鈥? for temperatures greater than 鈭?0 掳C. However, the ionic conductivity of the unconfined solutions (i.e., solution occupying the spaces between the MCM-41 particles) rapidly decreases over subzero temperatures. Limitations associated with directly implementing these materials as low-temperature ion conductors are discussed.