Journal
SMALL
Volume 17, Issue 42, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202102039
Keywords
ion pair; ion transference number; ionic conductivity; oxygen vacancies
Categories
Funding
- National Key R&D Program of China [2016YFB0700600]
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The introduction of oxygen vacancies carried by nanosized Al2O3 fillers promotes Li+-conduction in poly(ethylene oxide) by weakening the Coulombic attraction within ion pairs and preferentially constraining the movement of anions, leading to significant and selective improvement in Li-ion conductivity. Solid state batteries built on such PEO-based electrolytes exhibit superior performance at high current density, offering a universal approach to tailor superior polymer-based electrolytes for next generation solid-state batteries.
Despite their promised safety and mechanical flexibility, solvent-free polymer electrolytes suffer from low Li-ion conductivities due to poor dissociation of conducting salts and low Li+-transference numbers due to Li+-trapping by ether-linkages. In this work, the authors found that oxygen vacancies carried by nanosized Al2O3 fillers preferentially promotes Li+-conduction in poly(ethylene oxide) (PEO). These vacancies and free electrons therein, whose concentration can be tuned, effectively break up the ion pairs by weakening the Coulombic attraction within them, while simultaneously interacting with the anions, thus preferentially constraining the movement of anions. This synergistic dissociation-and-trapping effect leads to the significant and selective improvement in Li-ion conductivity. Solid state batteries built on such PEO-based electrolytes exhibits superior performance at high current density. This discovery reveals a molecular-level rationale for the long-observed phenomenon that certain inorganic nano-fillers improve ion conduction in PEO, and provides a universal approach to tailor superior polymer-based electrolytes for the next generation solid-state batteries.
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