Xiaoyan Zhou, Xiaogang Li, Zhuo Li, Huixin Xie, Jialong Fu, Lu Wei, Hui Yang and Xin Guo
{"title":"Hybrid electrolytes with an ultrahigh Li-ion transference number for lithium-metal batteries with fast and stable charge/discharge capability†","authors":"Xiaoyan Zhou, Xiaogang Li, Zhuo Li, Huixin Xie, Jialong Fu, Lu Wei, Hui Yang and Xin Guo","doi":"10.1039/D1TA04631D","DOIUrl":null,"url":null,"abstract":"<p >Electrolytes with a high ionic transference number hold great promise for reducing battery polarization and achieving safe energy storage. Herein, single-ion electrolytes containing α-LiAlO<small><sub>2</sub></small>@γ-Al<small><sub>2</sub></small>O<small><sub>3</sub></small> nanosheets as fillers in PVDF-HFP are prepared. The α-LiAlO<small><sub>2</sub></small>@γ-Al<small><sub>2</sub></small>O<small><sub>3</sub></small> nanosheets show excellent anion-anchoring ability due to the high adsorption energy to anions on the surfaces, leading to a remarkable lithium-ion (Li<small><sup>+</sup></small>) transference number of 0.92 and a great ionic conductivity of 0.85 mS cm<small><sup>?1</sup></small> at room temperature. Such a high Li<small><sup>+</sup></small> transference number effectively alleviates the concentration gradient polarization, improves the homogeneous Li<small><sup>+</sup></small> deposition, and suppresses the Li dendrite growth. As a result, the symmetric Li‖Li cell realizes superior interfacial stability and dendrite suppression capability for 1000 h at a current density of 0.5 mA cm<small><sup>?2</sup></small>. Moreover, the LiNi<small><sub>0.85</sub></small>Co<small><sub>0.05</sub></small>Al<small><sub>0.1</sub></small>O<small><sub>2</sub></small>‖Li and LiFePO<small><sub>4</sub></small>‖Li batteries with the electrolyte demonstrate significantly improved specific capacities and excellent cycling durabilities at high rates. Especially, the LiFePO<small><sub>4</sub></small>‖Li battery exhibits a capacity retention of 88% over 2000 charge/discharge cycles at a rate of 2C. This work offers a strategy for designing single-ion electrolytes toward high-performance energy storage.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 34","pages":" 18239-18246"},"PeriodicalIF":9.5000,"publicationDate":"2021-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2021/ta/d1ta04631d","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 11
Abstract
Electrolytes with a high ionic transference number hold great promise for reducing battery polarization and achieving safe energy storage. Herein, single-ion electrolytes containing α-LiAlO2@γ-Al2O3 nanosheets as fillers in PVDF-HFP are prepared. The α-LiAlO2@γ-Al2O3 nanosheets show excellent anion-anchoring ability due to the high adsorption energy to anions on the surfaces, leading to a remarkable lithium-ion (Li+) transference number of 0.92 and a great ionic conductivity of 0.85 mS cm?1 at room temperature. Such a high Li+ transference number effectively alleviates the concentration gradient polarization, improves the homogeneous Li+ deposition, and suppresses the Li dendrite growth. As a result, the symmetric Li‖Li cell realizes superior interfacial stability and dendrite suppression capability for 1000 h at a current density of 0.5 mA cm?2. Moreover, the LiNi0.85Co0.05Al0.1O2‖Li and LiFePO4‖Li batteries with the electrolyte demonstrate significantly improved specific capacities and excellent cycling durabilities at high rates. Especially, the LiFePO4‖Li battery exhibits a capacity retention of 88% over 2000 charge/discharge cycles at a rate of 2C. This work offers a strategy for designing single-ion electrolytes toward high-performance energy storage.
具有高离子转移数的电解质在减少电池极化和实现安全储能方面具有很大的前景。本文制备了以α-LiAlO2@γ-Al2O3纳米片为填料的PVDF-HFP单离子电解质。α-LiAlO2@γ-Al2O3纳米片由于对表面阴离子具有较高的吸附能,表现出优异的阴离子锚定能力,导致锂离子(Li+)转移数达到0.92,离子电导率达到0.85 mS cm?1在室温下。如此高的Li+转移数有效地缓解了浓度梯度极化,改善了Li+的均匀沉积,抑制了Li枝晶的生长。因此,对称Li‖锂电池在0.5 mA cm?2的电流密度下实现了优越的界面稳定性和1000小时的枝晶抑制能力。此外,使用该电解质的LiNi0.85Co0.05Al0.1O2‖锂电池和LiFePO4‖锂电池在高倍率下表现出显着提高的比容量和出色的循环耐久性。特别是,LiFePO4‖锂电池在2000次充电/放电循环中以2C的速率显示出88%的容量保持率。这项工作为设计高性能能量存储的单离子电解质提供了一种策略。
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.