4.8 Article

Interfacial barrier free organic-inorganic hybrid electrolytes for solid state batteries

期刊

ENERGY STORAGE MATERIALS
卷 37, 期 -, 页码 306-314

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ELSEVIER
DOI: 10.1016/j.ensm.2021.02.013

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资金

  1. Technology Development Program to Solve Climate Changes of the National Research Foundation (NRF) - Ministry of Science ICT [2017M1A2A2044492]
  2. Electronics and Telecommunications Research Institute (ETRI) - Korea government [21ZB1200]
  3. National Creative Research Initiative (CRI) Center for Multi-Dimensional Directed Nanoscale Assembly, National Research Foundation of Korea (NRF) - Ministry of Science [2015R1A3A2033061]
  4. National Research Foundation of Korea [2017M1A2A2044492] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Organic-inorganic hybrid solid electrolytes (HSEs) are proposed as a solution for the limitations of traditional inorganic electrolytes in solid state batteries. By incorporating highly conducive polyvinylidene fluoride (PVDF)-based HSEs with etched LLZO fillers, researchers achieved improved ionic conductivity and low interfacial resistance, demonstrating the potential for high capacity solid state batteries.
Organic-inorganic hybrid solid electrolytes (HSEs) are expected to overcome the inherent limitations of rigid fragile inorganic electrolytes for solid state batteries. Li-ion conducive filler such as garnet Li7La3Zr2O12 (LLZO) is proposed for the high performance of HSEs, unfortunately, which suffers from native surface layer resistance to Li-ion transport. Here we present highly conducive polyvinylidene fluoride (PVDF)-based HSEs incorporating LLZO fillers, whose resistive barriers are eliminated by dry etching. Our optimal composition of etched LJZO fillers (30 wt%) leads to ionic conductivity of 4.05 x 10(-4) S cm(-1), about two-fold improvement from non-etched counterpart. Li symmetric cells with etched fillers exhibit low interfacial resistance of 110 Omega cm(2) and minimal overpotential of 90 mV. Moreover, high capacity of 79 mA h g(-1) is highlighted at 4C, comparable or superior to liquid electrolyte or sulfide-based electrolyte devices. Interfacial environment in HSEs ideally modified for Li-ion transport is identified by Li-7 NMR measurements.

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