Title Composite electrolytes of pyrrolidone-derivatives-PEO enable to enhance performance of all solid state lithium-ion batteries
Authors Li, Xin
Wang, Zijian
Lin, Hai
Liu, Yidong
Min, Yong
Pan, Feng
Affiliation Peking Univ, Shenzhen Grad Sch, Sch Adv Mat, Shenzhen 518055, Peoples R China
Guangdong Univ Technol, Sch Mat & Energy, Guangzhou 510006, Guangdong, Peoples R China
Keywords Li ion battery
Solid state
Composite electrolytes
Pyrrolidone derivatives
High ambient conductivity
Issue Date 2019
Publisher ELECTROCHIMICA ACTA
Abstract All-solid-state batteries with LiFePO4 cathodes and polyethylene oxide (PEO) based electrolytes are optimized with organic polymer synthesized from allyl amine and tartaric acid which show better properties including ionic conductivity, electrochemical window, charge-discharge capacity and rate performance. The rate of PEO ((MW) over bar = 4,000,000) and lithium salt (Lithium bis(trifluoromethanesulphonyl) imide, LiTFSI) is 75: 20 (w/w) and polymers of different molecular weight are tested at a wide temperature range from 27 degrees C (ambient temperature) to 120 degrees C. Electrolytes with larger amount (weighting more than half of PEO) of low-molecular-weight polymer show conductivity of above 10(-4) S cm(-1), which is similar to typical gel-polymer-electrolyte. Electrolytes made of high-molecular-weight dopant, PEO and LiTFSI through ball milling show better conductivity (5.4 x 10(-6) S cm(-1)) as well as better strength than electrolytes without dopant (1.3 x 10(-6) S cm(-1)) at room temperature. And a sensitive dependence on temperature increasing is also observed constructing to the sample without dopant. Stability below 120 degrees C also indicates promising use of this composite electrolyte in solid state lithium ion batteries. (c) 2018 Elsevier Ltd. All rights reserved.
URI http://hdl.handle.net/20.500.11897/551515
ISSN 0013-4686
DOI 10.1016/j.electacta.2018.10.023
Indexed SCI(E)
EI
Appears in Collections: 深圳研究生院待认领

Files in This Work
There are no files associated with this item.

Web of Science®


0

Checked on Last Week

Scopus®



Checked on Current Time

百度学术™


0

Checked on Current Time

Google Scholar™





License: See PKU IR operational policies.