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Enhanced transport and favorable distribution of Li-ion in a poly(ionic liquid) based electrolyte facilitated by Li1.3Al0.3Ti1.7(PO4 )(3) nanoparticles for highly-safe lithium metal batteries
Song, Xianli1,2,4; Zhang, Haitao2; Jiang, Danfeng2; Yang, Lipeng2; Zhang, Jiahe2; Yao, Meng2; Ji, Xiaoyan3; Wang, Gongying1,4; Zhang, Suojiang2
刊名ELECTROCHIMICA ACTA
2021-02-01
卷号368页码:10
关键词Polymerized ionic liquids LATP Organic-inorganic composite electrolyte
ISSN号0013-4686
DOI10.1016/j.electacta.2020.137581
英文摘要Solid-state batteries, which exhibit characteristics including uniform Li deposition, non-flammability and low interfacial resistance, are desirable for novel energy storage devices. Herein, a self-standing, fireproof and electrochemically stable organic-inorganic composite ionogel electrolyte was carefully designed and prepared by using polymerized ionic liquid (PIL), ionic liquid (IL), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and lithium aluminum titanium phosphate (LATP) nanoparticles. The incorporation of LATP nanoparticles into polymer backbone was found to facilitate ionic transport due to the homogenous Li+ distribution, which would further boost the ionic conductivity and mechanical properties. In addition, the introduction of IL favored the reduction of interface resistance. Benefiting from the nonflammability, the thermal shrinkage performance of as-prepared electrolyte could stand over a broad operating temperature range. A Li/Li symmetric cell containing optimized PIL-14 wt% LATP could be cycled steadily for over 2000 h at 50 degrees C. A lithium metal battery containing composite ionogel electrolyte exhibited an outstanding specific capacity of 145 mAh g(-1) and 95% capacity retention at 50 degrees C even after 100 cycles. This study indicates that the co-employment of IL and inorganic nanopartide is an effective strategy for the construction of organic-inorganic hybrid electrolytes for high-safety solid-state lithium metal batteries (LMBs). (C) 2020 Elsevier Ltd. All rights reserved.
资助项目National Key Research and Development Program of China[2016YFB0100303] ; National Natural Science Foundation of China[21878308] ; Major Program of National Natural Science Foundation of China[21890762] ; Interreg Nord and Region Norrbotten in Sweden[304-16169-2019]
WOS关键词COMPOSITE POLYMER ELECTROLYTE ; SOLID ELECTROLYTES ; CONDUCTIVITY ; ANODE ; PERFORMANCE ; SEPARATOR ; MEMBRANE ; DENSITY
WOS研究方向Electrochemistry
语种英语
出版者PERGAMON-ELSEVIER SCIENCE LTD
WOS记录号WOS:000609077900014
资助机构National Key Research and Development Program of China ; National Natural Science Foundation of China ; Major Program of National Natural Science Foundation of China ; Interreg Nord and Region Norrbotten in Sweden
内容类型期刊论文
源URL[http://ir.ipe.ac.cn/handle/122111/43339]  
专题中国科学院过程工程研究所
通讯作者Zhang, Haitao; Wang, Gongying; Zhang, Suojiang
作者单位1.Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
2.Chinese Acad Sci, Inst Proc Engn, Beijing Key Lab Ion Liquids Clean Proc, Beijing, Peoples R China
3.Lulea Univ Technol, Div Energy Sci, Energy Engn, S-97187 Lulea, Sweden
4.Univ Chinese Acad Sci, Natl Engn Lab VOCs Pollut Control Mat & Technol, Beijing 101408, Peoples R China
推荐引用方式
GB/T 7714
Song, Xianli,Zhang, Haitao,Jiang, Danfeng,et al. Enhanced transport and favorable distribution of Li-ion in a poly(ionic liquid) based electrolyte facilitated by Li1.3Al0.3Ti1.7(PO4 )(3) nanoparticles for highly-safe lithium metal batteries[J]. ELECTROCHIMICA ACTA,2021,368:10.
APA Song, Xianli.,Zhang, Haitao.,Jiang, Danfeng.,Yang, Lipeng.,Zhang, Jiahe.,...&Zhang, Suojiang.(2021).Enhanced transport and favorable distribution of Li-ion in a poly(ionic liquid) based electrolyte facilitated by Li1.3Al0.3Ti1.7(PO4 )(3) nanoparticles for highly-safe lithium metal batteries.ELECTROCHIMICA ACTA,368,10.
MLA Song, Xianli,et al."Enhanced transport and favorable distribution of Li-ion in a poly(ionic liquid) based electrolyte facilitated by Li1.3Al0.3Ti1.7(PO4 )(3) nanoparticles for highly-safe lithium metal batteries".ELECTROCHIMICA ACTA 368(2021):10.
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