RS Fellow - EPSRC grant (2014): Lattice-matched electrode-electrolyte interfaces for high-performance Li-batteries

RS 院士 - EPSRC 资助（2014 年）：用于高性能锂电池的晶格匹配电极-电解质界面

• 批准号: EP/N004302/1
• 负责人: Benjamin Morgan
• 金额: $ 30.79万
• 依托单位: University of Bath
• 依托单位国家: 英国
• 项目类别: Fellowship
• 财政年份: 2015
• 资助国家: 英国
• 起止时间: 2015 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=EP%2FN004302%2F1
• 关键词: RS; Fellow; EPSRC; grant; 2014

Lithium-ion batteries are all around us. They are used for energy storage in portable electronics, hybrid-electric vehicles, even the Curiosity Mars rover. As we reduce our dependence on fossil fuels, the use of lithium-ion batteries will only increase. Today's commercial lithium-ion batteries, however, face problems of short lifespans - the degrading charge-time of a laptop or phone battery - and safety issues - illustrated recently by the fires reported on aircraft and in electric cars. If lithium-ion batteries are to be used more widely they must have both longer lifetimes and improved s!afety characteristics.One technology that may potentially address is an "all-solid-state" lithium-ion battery. Conventional batteries have liquid electrolytes that transport lithium ions between the cathode and anode as the battery is charged or discharged. These electrolytes are chemically unstable, and degrade with time - leading to reduced capacity - or can react explosively in the case of a short-circuit or intense heating. In an all-solid-state battery, these are replaced by ceramic solids that are chemically inert and robust, yet still allow lithium ions to move between the electrodes. The challenge is to develop solid electrolytes that meet these specifications of chemical stability and good lithium-ion conductivity, while also being electronically insulating.One of the limiting factors for battery performance is the rate at which lithium can move through the device: this dictates the speed with which it charges and the total power density of the battery. a specific issue for all-solid-state batteries is that even in the case of solid electrolytes that allow rapid lithium transport, transferring lithium between the electrolyte and an electrode (or vice-versa) can be slow, ultimately limiting the overall lithium transport rate. This ability of the boundary between electrode and electrolyte to impede the conduction of lithium ions is the "interfacial resistance", which should be low for high-power applications.In 1985 a patent was filed that proposed a strategy for designing solid-state batteries with low interfacial resistance: if the electrodes and electrolyte all have structures based on the same underlying crystal lattice, then it should be possible to find combinations of materials that are "lattice-matched", with similar crystal lattice dimensions for the electrodes and electrolyte. It was proposed that this would allow the lithium- conduction pathways to line up across the electrode-electrolyte interfaces, forming continuous channels with low interfacial resistance, and enabling fast ionic transport through the battery.The application of this idea has until recently been limited by an absence of promising solid electrolytes with crystal structures that permit lattice-matching with known solid electrodes. In 2013, however, a new family of solid-electrolytes was reported with the same underlying "spinel-structure" as a number of widely studied solid electrodes, breathing new life into this concept.This research project seeks to use computer simulations to understand how the chemical composition of spinel-structured lithium-electrolytes affects their suitability for lattice-matched solid-state batteries. We will construct new models that are able to describe numerically the motions and interactions of atoms that make up these materials. These models will then be used in large-scale computer simulations to study how differences in chemistry control the details of crystal structure and rates of lithium ion conduction in these materials. By extending these models to also describe electrode-electrolyte interfaces, we will directly calculate interfacial resistances, and explore the potential for "lattice-matching" as a strategy for the design of high-performance solid-state lithium-ion batteries.

锂离子电池无处不在。它们被用于便携式电子产品、混合动力汽车，甚至是好奇号火星漫游车的能量储存。随着我们减少对化石燃料的依赖，锂离子电池的使用只会增加。然而，今天的商用锂离子电池面临着寿命短的问题--笔记本电脑或手机电池充电时间的下降--以及安全问题--最近飞机和电动汽车上发生的火灾就证明了这一点。如果锂离子电池要得到更广泛的应用，它们必须既要有更长的寿命，又要有更好的S！安全特性。其中一项可能解决的技术是“全固态”锂离子电池。传统电池有液体电解液，当电池充电或放电时，液体电解液会在正负极之间传输锂离子。这些电解液在化学上不稳定，会随着时间的推移而降解--导致容量降低--或者在短路或强烈加热的情况下会发生爆炸反应。在全固态电池中，它们被化学惰性和坚固的陶瓷固体所取代，但仍然允许锂离子在电极之间移动。所面临的挑战是开发出既满足化学稳定性和良好的锂离子导电性，同时又具有电子绝缘性的固体电解液。电池性能的限制因素之一是锂在设备中的移动速度：这决定了充电的速度和电池的总功率密度。全固态电池的一个具体问题是，即使在允许快速锂传输的固体电解液的情况下，锂在电解液和电极之间的传输(反之亦然)可能会很慢，最终限制了整体锂传输速率。电极和电解液之间的边界阻碍锂离子传导的这种能力是“界面电阻”，对于高功率应用来说，它应该是低的。1985年，一项专利申请提出了一种设计低界面电阻的固态电池的策略：如果电极和电解液都具有基于相同晶格的结构，那么应该有可能找到“晶格匹配”的材料组合，电极和电解液具有相似的晶格尺寸。有人提出，这将允许锂传导路径在电极-电解液界面上排列，形成具有低界面电阻的连续通道，并使离子能够快速通过电池。直到最近，由于缺乏具有与已知固体电极晶格匹配的晶体结构的有前途的固体电解质，这一想法的应用一直受到限制。然而，在2013年，一种新的固体电解液家族被报道，它与一些被广泛研究的固体电极具有相同的基本“尖晶石结构”，为这一概念注入了新的活力。本研究项目试图通过计算机模拟来了解尖晶石结构的锂电解液的化学组成如何影响其对晶格匹配固态电池的适用性。我们将构建新的模型，能够以数字方式描述组成这些材料的原子的运动和相互作用。然后，这些模型将被用于大规模的计算机模拟，以研究化学差异如何控制这些材料中晶体结构和锂离子传导速度的细节。通过将这些模型扩展到描述电极-电解液界面，我们将直接计算界面电阻，并探索“晶格匹配”作为高性能固态锂离子电池设计策略的潜力。

项目成果

Variation in surface energy and reduction drive of a metal oxide lithium-ion anode with stoichiometry: a DFT study of lithium titanate spinel surfaces

• DOI: 10.1039/c6ta05980e
• 发表时间: 2016-11
• 期刊: Journal of Materials Chemistry
• 作者: B. Morgan;J. Carrasco;G. Teobaldi

crystal-torture: A crystal tortuosity module

crystal-torture：水晶曲折模块

• DOI: 10.21105/joss.01306
• 发表时间: 2019
• 期刊: Journal of Open Source Software
• 作者: O'Rourke C

Interfacial strain effects on lithium diffusion pathways in the spinel solid electrolyte Li-doped MgAl 2 O 4

• DOI: 10.1103/physrevmaterials.2.045403
• 发表时间: 2017-12
• 期刊: Physical Review Materials
• 影响因子: 3.4
• 作者: C. O’Rourke;B. Morgan

bsym: A basic symmetry module

bsym：基本对称模块

• DOI: 10.21105/joss.00370
• 发表时间: 2017
• 期刊: The Journal of Open Source Software
• 作者: J. Morgan B