材料科学
电化学
离子液体
化学工程
锂(药物)
三甘醇
电解质
硫化物
无机化学
电极
离子键合
高分子化学
离子
有机化学
物理化学
化学
冶金
催化作用
内分泌学
工程类
医学
作者
Dae Yang Oh,Young Jin Nam,Kern Ho Park,Sung Hoo Jung,Kyu Tae Kim,Adams Ha,Yoon Seok Jung
标识
DOI:10.1002/aenm.201802927
摘要
Abstract For mass production of all‐solid‐state lithium‐ion batteries (ASLBs) employing highly Li + conductive and mechanically sinterable sulfide solid electrolytes (SEs), the wet‐slurry process is imperative. Unfortunately, the poor chemical stability of sulfide SEs severely restrict available candidates for solvents and in turn polymeric binders. Moreover, the binders interrupt Li + ‐ionic contacts at interfaces, resulting in the below par electrochemical performance. In this work, a new scalable slurry fabrication protocol for sheet‐type ASLB electrodes made of Li + ‐conductive polymeric binders is reported. The use of intermediate‐polarity solvent (e.g., dibromomethane) for the slurry allows for accommodating Li 6 PS 5 Cl and solvate‐ionic‐liquid‐based polymeric binders (NBR‐Li(G3)TFSI, NBR: nitrile−butadiene rubber, G3: triethylene glycol dimethyl ether, LiTFSI: lithium bis(trifluoromethanesulfonyl)imide) together without suffering from undesirable side reactions or phase separation. The LiNi 0.6 Co 0.2 Mn 0.2 O 2 and Li 4 Ti 5 O 12 electrodes employing NBR‐Li(G3)TFSI show high capacities of 174 and 160 mA h g −1 at 30 °C, respectively, which are far superior to those using conventional NBR (144 and 76 mA h g −1 ). Moreover, high areal capacity of 7.4 mA h cm −2 is highlighted for the LiNi 0.7 Co 0.15 Mn 0.15 O 2 electrodes with ultrahigh mass loading of 45 mg cm −2 . The facilitated Li + ‐ionic contacts at interfaces paved by NBR‐Li(G3)TFSI are evidenced by the complementary analysis from electrochemical and 7 Li nuclear magnetic resonance measurements.
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