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Engineering and Evaluating the End-Group Assisted Electrodeposition of Conformal Polymer Electrolytes for Ultrathin-Film Batteries

超薄膜电池共形聚合物电解质端基辅助电沉积的工程设计和评估

基本信息

批准号：
2146597
负责人：
Joerg Werner
金额：
$ 55.13万
依托单位：
Trustees of Boston University
依托单位国家：
美国
项目类别：
Standard Grant
财政年份：
2022
资助国家：
美国
起止时间：
2022-07-15 至 2025-06-30
项目状态：
未结题

来源：
https://www.nsf.gov/awardsearch/showAward?AWD_ID=2146597&HistoricalAwards=false
关键词：
Engineering Evaluating End Group Assisted

项目摘要

Lithium-ion batteries are the primary power source for many devices from personal electronics to electric vehicles. While the energy stored in such batteries has steadily increased, a remaining limitation is their inability to safely charge in minutes or sustain a high-power output. The main bottleneck for this sluggishness is the slow movement of the lithium ions across the battery, which is mediated by either a liquid or polymeric electrolyte. Bringing the positive and negative electrodes much closer to each other would dramatically increase the speed at which batteries can operate. However, to avoid short circuits between these electrodes, ultra-thin solid electrolytes are needed that can be fabricated at extremely small scales in a uniform fashion without defects. This research project aims to address this technological need and engineering knowledge gap by developing polymer structures and manufacturing methodologies that enable the uniform fabrication of ultrathin polymer electrolytes capable of fast ion movement while maintaining electronic insulation and safety. Specifically, this research explores electrodeposition as an intrinsically surface-confined process for the uniform coating of complex electrode architectures with polymer electrolytes. To evaluate these ultrathin polymer films on battery-relevant scales, this research program further develops high-throughput multi-scale assays that use light and color to rapidly measure the electronic and ionic properties of the polymeric films. Additionally, this grant will introduce nanomanufacturing research projects in microbatteries to an undergraduate summer research program at BU, combining the traditionally disconnected fields of nanofabrication and energy storage. This research will also include the development of a new lab on ion-diffusion in solid materials for an undergraduate Materials Science course.This project addresses fundamental understanding of new manufacturing processes to enable interdigitated thin-film batteries with both high energy density and high-power density. The project addresses the lack of synthesis and processing methods of ultrathin, conformal, and defect-free polymer electrolytes on three-dimensional (3-D) electrode architectures. To overcome this barrier, this research program seeks to establish a fundamental understanding of the electrodeposition mechanism of polymer electrolytes with electrochemically crosslinkable end-groups. The rationale of this method is to decouple the capability for self-limiting electrodeposition, governed by the electrochemically reactive end-group, from film properties such as ionic conductivity that are determined by the film composition and molecular architecture. First, a systematic study will be conducted on the oxidative electrodeposition of poly(ethylene oxide) with phenolic end-groups on planar and three-dimensional porous electrodes to reveal the impact of the electrochemical conditions, as well as the molecular architecture of the polymer and the phenolic end-group, on the film growth and properties. These tasks will test the hypothesis that successful self-limiting electrodeposition of electronically insulating polymers requires a fast crosslinking rate and concurrent decrease of solubility upon end-group oxidation. Thus, this research will yield multiscale molecular design rules and processing windows that result in the conformal electrodeposition of polymeric electrolytes, creating foundational knowledge needed to overcome an engineering challenge for interdigitated thin-film batteries, as well as other functional polymer coatings. In a second track of the research program, the analytical challenge of the multi-dimensional parameter space posed by the interplay between solution composition, deposition conditions, and resulting film properties will be addressed by developing high-throughput optical screening methods to spatially resolve the key metrics of coverage, electronic resistivity, and ionic conductivity at submicron resolution over battery-relevant areas. These techniques will establish foundational structure-processing-property relationships for self-limiting polymer electrolyte electrodeposition from the molecular to the device level, and their comprehensive evaluation will build the basis of a new suite of multiscale electrochemical analysis tools.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

锂离子电池是从个人电子产品到电动汽车的许多设备的主要电源。虽然存储在这种电池中的能量稳步增加，但仍然存在的限制是它们无法在几分钟内安全充电或维持高功率输出。这种迟缓的主要瓶颈是锂离子在电池中的缓慢移动，这是由液体或聚合物电解质介导的。将正负电极彼此靠近将大大提高电池的运行速度。然而，为了避免这些电极之间的短路，需要超薄固体电解质，其可以以均匀的方式以极小的规模制造而没有缺陷。该研究项目旨在通过开发聚合物结构和制造方法来解决这一技术需求和工程知识缺口，这些聚合物结构和制造方法能够均匀制造能够快速离子移动的可聚合物电解质，同时保持电子绝缘和安全性。具体而言，本研究探讨电沉积作为一个内在的表面限制的过程中，复杂的电极结构与聚合物电解质的均匀涂层。为了在电池相关的尺度上评估这些聚合物薄膜，该研究项目进一步开发了高通量多尺度分析，使用光和颜色快速测量聚合物薄膜的电子和离子特性。此外，这笔赠款将引入微电池的纳米制造研究项目，以BU的本科夏季研究计划，结合传统的纳米制造和储能领域。该研究还将包括为本科材料科学课程开发一个关于固体材料中离子扩散的新实验室。该项目旨在对新制造工艺进行基本理解，以实现高能量密度和高功率密度的叉指薄膜电池。该项目解决了三维（3-D）电极架构上的无缺陷、保形和无缺陷聚合物电解质的合成和加工方法的缺乏。为了克服这一障碍，本研究计划旨在建立一个基本的了解电化学交联端基的聚合物电解质的电沉积机理。该方法的基本原理是将由电化学反应性端基控制的自限性电沉积的能力与由膜组成和分子结构确定的膜性质如离子电导率解耦。首先，将进行一个系统的研究与酚类端基的聚（环氧乙烷）在平面和三维多孔电极上的氧化电沉积，以揭示电化学条件的影响，以及聚合物和酚类端基的分子结构，对膜的生长和性能。这些任务将测试的假设，即成功的自限电沉积的电子绝缘聚合物需要一个快速的交联速率和同时减少的溶解度后，端基氧化。因此，这项研究将产生多尺度分子设计规则和加工窗口，导致聚合物电解质的共形电沉积，创造克服叉指薄膜电池以及其他功能聚合物涂层的工程挑战所需的基础知识。在研究计划的第二个轨道，多维参数空间的分析挑战所造成的溶液组成，沉积条件和由此产生的薄膜性能之间的相互作用将通过开发高通量的光学筛选方法来解决空间解决的关键指标的覆盖范围，电阻率和离子电导率在亚微米分辨率超过电池相关领域。这些技术将为自限性聚合物电解质电沉积从分子到器件水平建立基本的结构-加工-性能关系，其综合评估将为一套新的多尺度电化学分析工具奠定基础。该奖项反映了NSF的法定使命，并被认为值得通过使用基金会的知识价值和更广泛的影响审查标准进行评估来支持。