2021
DOI: 10.1016/j.memsci.2020.118702
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Hybridizing polymer electrolyte with poly(ethylene glycol) grafted polymer-like quantum dots for all-solid-state lithium batteries

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Cited by 32 publications
(9 citation statements)
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“…Small-sized nanofillers are uniformly dispersed in the PEO electrolyte, which will produce abundant filler–polymer interfaces, effectively destroying the orderly arrangement of PEO and increasing the amorphous phase of SPE. In addition, nanofillers can form Lewis acid–base effects with lithium salts to release more free lithium ions, thereby increasing the ionic conductivity of SPE . According to the indefinite integral formula of the Arrhenius formula ln­( k ) = − E a /( RT ) + B , the activation energy ( E a ) of different electrolytes is calculated as shown in Figure f.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Small-sized nanofillers are uniformly dispersed in the PEO electrolyte, which will produce abundant filler–polymer interfaces, effectively destroying the orderly arrangement of PEO and increasing the amorphous phase of SPE. In addition, nanofillers can form Lewis acid–base effects with lithium salts to release more free lithium ions, thereby increasing the ionic conductivity of SPE . According to the indefinite integral formula of the Arrhenius formula ln­( k ) = − E a /( RT ) + B , the activation energy ( E a ) of different electrolytes is calculated as shown in Figure f.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, nanofillers can form Lewis acid−base effects with lithium salts to release more free lithium ions, thereby increasing the ionic conductivity of SPE. 62 According to the indefinite integral formula of the Arrhenius formula ln(k) = −E a /(RT) + B, the activation energy (E a ) of different electrolytes is calculated as shown in Figure 2f. After AM is added, the activation energy of P-P-A SPE (9.37 kJ mol −1 ) decreases compared with that of P-P SPE (12.8 kJ mol −1 ), indicating that it accelerates the transmission of lithium ions, which may be due to the formation of an additional lithium environment between AM and LiTFSI.…”
Section: Resultsmentioning
confidence: 99%
“…[47] In addition, the melting point (T m ) of PEO CPE was 51.9 °C corresponding to high melting enthalpy, which also indicated high crystallinity of PEO inhibited the ion transport in the polymer chains. [48,49] Besides, TGA was used to determine the safe operating temperature range of the CPEs. Figure 2 (d) shows distinct mass loss corresponding to the decomposition of the polymer matrices of the 30 H-Z-CPE at 400 °C and the PEO CPE at 300 °C, indicating that hollow ZIF-8/IL filler effectively increases the thermal stability of the CPEs.…”
Section: Li-conductivity Of the Cpesmentioning
confidence: 99%
“…The study of polymer systems can be traced back to the 1970s when Wright and co-workers demonstrated poly­(ethylene oxide) (PEO)-based polymer electrolytes . Up to now, most of the all-solid-state polymer electrolytes are still based on modified PEO that are produced through various strategies such as grafting, copolymerization, and blending. In spite of great efforts in improving the performance of PEO-based electrolytes, investigation of high ionic conductivity at ambient temperature is quite challenging due to cation–dipole interactions . In 2012, Tominaga and co-workers demonstrated a poly­(ethylene carbonate)-based polymer electrolyte with an ionic conductivity of 1.6 × 10 –5 S/cm at 30 °C, which laid the groundwork for future development. , In 2015, Zhang explored a poly­(propylene carbonate)-based electrolyte for solid-state lithium batteries .…”
Section: Introductionmentioning
confidence: 99%