Ward Ashleigh L, Doris Sean E, Li Longjun, Hughes Mark A, Qu Xiaohui, Persson Kristin A, Helms Brett A
The Joint Center for Energy Storage Research, Computational Research Division, and The Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, United States.
Department of Chemistry, Department of Chemical and Biomolecular Engineering, and Department of Materials Science and Engineering, University of California, Berkeley, California 94720, United States.
ACS Cent Sci. 2017 May 24;3(5):399-406. doi: 10.1021/acscentsci.7b00012. Epub 2017 Apr 27.
Selective ion transport across membranes is critical to the performance of many electrochemical energy storage devices. While design strategies enabling ion-selective transport are well-established, enhancements in membrane selectivity are made at the expense of ionic conductivity. To design membranes with both high selectivity and high ionic conductivity, there are cues to follow from biological systems, where regulated transport of ions across membranes is achieved by transmembrane proteins. The transport functions of these proteins are sensitive to their environment: physical or chemical perturbations to that environment are met with an adaptive response. Here we advance an analogous strategy for achieving adaptive ion transport in microporous polymer membranes. Along the polymer backbone are placed redox-active switches that are activated in situ, at a prescribed electrochemical potential, by the device's active materials when they enter the membrane's pore. This transformation has little influence on the membrane's ionic conductivity; however, the active-material blocking ability of the membrane is enhanced. We show that when used in lithium-sulfur batteries, these membranes offer markedly improved capacity, efficiency, and cycle-life by sequestering polysulfides in the cathode. The origins and implications of this behavior are explored in detail and point to new opportunities for responsive membranes in battery technology development.
跨膜的选择性离子传输对于许多电化学储能装置的性能至关重要。虽然实现离子选择性传输的设计策略已经成熟,但膜选择性的提高是以离子电导率为代价的。为了设计出具有高选择性和高离子电导率的膜,可以从生物系统中寻找线索,在生物系统中,离子跨膜的调节运输是由跨膜蛋白实现的。这些蛋白质的运输功能对其环境敏感:对该环境的物理或化学扰动会引发适应性反应。在此,我们提出了一种在微孔聚合物膜中实现适应性离子传输的类似策略。沿着聚合物主链放置氧化还原活性开关,当装置的活性材料进入膜孔时,这些开关在规定的电化学电位下原位激活。这种转变对膜的离子电导率影响很小;然而,膜对活性材料的阻挡能力增强了。我们表明,当用于锂硫电池时,这些膜通过在阴极中隔离多硫化物,显著提高了电池的容量、效率和循环寿命。详细探讨了这种行为的起源和影响,并指出了响应性膜在电池技术发展中的新机遇。