Collaborative Research: Fundamental understanding of interface dynamics in solid electrolyte batteries with liquid metal anode

合作研究：对液态金属阳极固体电解质电池界面动力学的基本了解

• 批准号: 2323475
• 负责人: Lei Chen
• 金额: $ 26.16万
• 依托单位: Regents of the University of Michigan - Dearborn
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2023
• 资助国家: 美国
• 起止时间: 2023-08-01 至 2026-07-31
• 项目状态: 未结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=2323475&HistoricalAwards=false
• 关键词: Collaborative; Research; Fundamental; understanding; interface

Solid-state lithium-ion batteries (LIBs) present a safer alternative to their commercially available counterparts that utilize liquid electrolytes, due to the substantial safety risks associated with solvent leakage and flammability. Such batteries could even support smaller and more powerful battery packs by diminishing the necessity for extra safety features. However, despite the benefits of these highly ionic conductive solid electrolytes, achieving comparable specific capacity, rate capability, and cycle life to that of liquid electrolyte LIBs remains challenging. Research indicates a major obstacle being inadequate interfacing between solid electrolytes and solid electrodes. Contrarily, the liquid-solid interface in liquid electrolytes permits full electrode infiltration, fostering comprehensive lithium-ion transport across the surface of active material particles. To leverage the benefits of the liquid-solid interface in solid-state batteries, the research team proposes a transition from the solid-solid interface to a liquid-solid interface. This could be achieved by replacing the solid electrode with a liquid metal electrode within solid-state LIBs. During the processes of lithium-ion insertion and removal, both the electrode-electrolyte interface and the interior of the liquid metal particle experience continuous alterations due to the shift between liquid and solid states. It is essential to understand these dynamic changes to fully investigate the potential of liquid metal solid electrolyte LIBs. The objective of this project is to gain a fundamental understanding of the interface dynamics between the liquid metal anode and the solid electrolyte during lithium-ion insertion and removal processes. The project will cultivate a diverse and inclusive team, encompassing graduate students, undergraduate students, precollege students, and K-12 teachers, with special emphasis on encouraging the participation of underrepresented populations. The project aims to provide interdisciplinary training to students, bridging the gap between theoretical understanding and experimentation. In this project, the team proposes an innovative approach to study a novel solid electrolyte LIB, the first to utilize a liquid metal electrode and a solid electrolyte, forming a liquid-solid interface at room temperature. Their objective is to understand how the transition between this liquid-solid interface and the solid-solid interface occurs during lithium-ion insertion and removal processes. Insight gained from this investigation will foster the development of new techniques that incorporate liquid metal electrodes in solid electrolyte batteries. The team will utilize in situ and operando focused ion beam-scanning electron microscopy (FIB-SEM) to analyze dynamic changes in morphology and monitor the advancement of the liquid-solid reaction front in liquid metal particles during cycling processes. Furthermore, the researchers aim to investigate the influence of dopants by studying dynamic phase changes obtained through operando X-ray diffraction (XRD). To understand the development of stress and strain, along with its effect on phases and morphologies within a liquid metal particle during lithium-ion insertion and removal, numerical simulations based on a phase field model, incorporating fluid-structure interaction, electrochemical reaction, species diffusion, and interfacial effects, will be conducted.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.

固态锂离子电池(LIB)提供了一种比商业上使用液体电解液的电池更安全的选择，因为与溶剂泄漏和易燃性相关的重大安全风险。这种电池甚至可以支持更小、更强大的电池组，因为它减少了对额外安全功能的需求。然而，尽管这些高离子导电性固体电解质具有诸多优点，但要获得与液体电解质LiBS相当的比容量、倍率能力和循环寿命仍然具有挑战性。研究表明，一个主要的障碍是固体电解质和固体电极之间的接口不充分。相反，液体电解质中的液-固界面允许充分的电极渗透，促进锂离子在活性物质颗粒表面的全面传输。为了利用固态电池中液-固界面的优势，研究小组建议从固-固界面过渡到液-固界面。这可以通过在固态LIBS中用液态金属电极取代固体电极来实现。在锂离子的插入和去除过程中，由于液态和固态之间的转换，电极-电解液界面和液态金属颗粒内部都经历了不断的变化。了解这些动态变化对于充分研究液态金属固体电解质LiBS的电势是至关重要的。本项目的目的是对锂离子插入和去除过程中液态金属阳极和固体电解液之间的界面动力学有一个基本的了解。该项目将培养一支多元化和包容性的团队，包括研究生、本科生、大学预科学生和K-12教师，特别强调鼓励代表性不足的人群参与。该项目旨在为学生提供跨学科培训，弥合理论理解和实验之间的差距。在这个项目中，该团队提出了一种创新的方法来研究一种新型的固体电解质LiB，它首次利用液态金属电极和固体电解质，在室温下形成液-固界面。他们的目标是了解在锂离子插入和移除过程中，液-固界面和固-固界面之间的转变是如何发生的。从这项研究中获得的见解将促进在固体电解质电池中加入液体金属电极的新技术的开发。该团队将利用原位和操作聚焦离子束扫描电子显微镜(FIB-SEM)来分析循环过程中液态金属颗粒中液-固反应前沿的动态变化。此外，研究人员的目标是通过研究操纵面X射线衍射(XRD)获得的动态相变来研究掺杂剂的影响。为了了解在锂离子插入和移除过程中应力和应变的发展及其对液态金属颗粒内物相和形貌的影响，将进行基于相场模型的数值模拟，其中包括流体-结构相互作用、电化学反应、物种扩散和界面效应。该奖项反映了NSF的法定使命，并通过使用基金会的智力优势和更广泛的影响审查标准进行评估，被认为值得支持。