电解质
碳酸乙烯酯
聚碳酸酯
循环伏安法
玻璃化转变
镁
高分子化学
差示扫描量热法
材料科学
介电谱
聚合物
离子电导率
无机化学
化学
电化学
有机化学
物理化学
物理
热力学
电极
作者
David A. Sundermann,Bumjun Park,Valerian Hirschberg,Jennifer L. Schaefer,Patrick Théato
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-06-20
卷期号:8 (26): 23510-23520
被引量:6
标识
DOI:10.1021/acsomega.3c00761
摘要
Magnesium electrolytes based on a polycarbonate with either magnesium tetrakis(hexafluoroisopropyloxy) borate (Mg(B(HFIP)4)2) or magnesium bis(trifluoromethanesulfonyl)imide (Mg(TFSI)2) for magnesium batteries were prepared and characterized. The side-chain-containing polycarbonate, poly(2-butyl-2-ethyltrimethylene carbonate) (P(BEC)), was synthesized by ring opening polymerization (ROP) of 5-ethyl-5-butylpropane oxirane ether carbonate (BEC) and mixed with Mg(B(HFIP)4)2 or Mg(TFSI)2 to form low- and high-salt-concentration polymer electrolytes (PEs). The PEs were characterized by impedance spectroscopy, differential scanning calorimetry (DSC), rheology, linear sweep voltammetry, cyclic voltammetry, and Raman spectroscopy. A transition from classical salt-in-polymer electrolytes to polymer-in-salt electrolytes was indicated by a significant change in glass transition temperature as well as storage and loss moduli. Ionic conductivity measurements indicated the formation of polymer-in-salt electrolytes for the PEs with 40 mol % Mg(B(HFIP)4)2 (HFIP40). In contrast, the 40 mol % Mg(TFSI)2 PEs showed mainly the classical behavior. HFIP40 was further found to have an oxidative stability window greater than 6 V vs Mg/Mg2+, but showed no reversible stripping-plating behavior in an Mg||SS cell.
科研通智能强力驱动
Strongly Powered by AbleSci AI