电解质
离子电导率
材料科学
阴极
电化学
阳极
化学工程
电化学窗口
快离子导体
离子液体
锂(药物)
电极
化学
有机化学
物理化学
内分泌学
工程类
催化作用
医学
作者
Hyeju Shin,Seong Jin Choi,Sinho Choi,Bo Yun Jang,Jihong Jeong,Yoon‐Gyo Cho,Sang‐Young Lee,Hyun‐Kon Song,Ji Haeng Yu,Tae‐Hee Kim
标识
DOI:10.1016/j.jpowsour.2022.231926
摘要
Solid electrolytes are regarded as promising candidates replacing organic liquid electrolyte due to much enhanced safety, which is able to use lithium metal as an anode material for high energy system. Among several solid electroytes, garnet-type solid electrolyte has wide electrochemical window as well as high chemical stability and ionic conductivity at room temperature. However, from an assembled full cell's point of view, high interfacial resistance between electrode and solid electrolyte is a huge obstacle which should be overcome. Herein, we synthesize high ionic conductivy of Gallium-doped garnet-type solid electrolyte (Li6.25Ga0.25La3Zr2O12) having 1.2 mS cm-1 at room temperature and then applied gel polymer electrolyte into cathode by in situ gelation method for a full cell system. The interfacial resistance is reduced by about 260 times and rate capability from 0.05C to 1C was 80%, which is superior to a hybrid of liquid electrolyte and LGLZO cell system. Initial capacity retaines 89% even after 800 cycles at 0.5C.
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