材料科学
碳纤维
石墨氮化碳
聚合物
固态
电解质
氮化物
兴奋剂
填料(材料)
快离子导体
化学工程
纳米技术
复合材料
复合数
电极
有机化学
图层(电子)
催化作用
化学
光电子学
工程物理
光催化
物理化学
工程类
作者
Yu Kang,Ju Ye Kim,Yu Jin Hong,Da Eun Han,Hyo Won Bae,Dong Wook Kim,Kyu Hyoung Lee,Andrew A. Peterson,Mihye Wu
标识
DOI:10.1021/acsami.4c18540
摘要
In the quest to enhance the safety of lithium-ion batteries, substantial research is underway to develop all-solid-state batteries, facing challenges in achieving high ion conductivity in solid electrolytes. This study aims to enhance the ion conductivity by incorporating carbon-doped graphitic carbon nitride (C-doped g-C3N4) microspheres as an inorganic filler into the poly(ethylene oxide)-based solid polymer electrolyte (SPE). Leveraging the advantageous properties of g-C3N4 as an effective inorganic filler by enhancing its Lewis acid-base interactions with lithium, we modified g-C3N4 through carbon doping to improve the ionic conductivity of the SPE. Our experimental analysis supports the increased lithium transference number after hybridizing electrolytes with C-doped g-C3N4, signifying heightened ion mobility resulting from carbon substitution on g-C3N4. Subsequent density functional theory (DFT) calculations reveal increased lithium binding energy due to the carbon doping of g-C3N4, thereby ultimately enhancing the ion conductivity by promoting salt dissociation. Optimizing carbon doping levels and hybrid electrolyte composition yields improved ion conductivity and electrochemical performance, with optimal outcomes observed at 7% C-doped g-C3N4 with SPE. Evaluation in a pouch cell with the NCM811 cathode underscores the applicability of the hybrid electrolyte on a large scale, showcasing promising advancements in battery technology. Our carbon-doped g-C3N4 filler demonstrates promising potential in advancing ion conductivity through enhanced salt dissociations.
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