Fabrication and Performance Study of 3D-Printed Ceramic-in-Gel Polymer Electrolytes

材料科学 电解质 离子电导率 锂(药物) 陶瓷 化学工程 制作 电化学 准固态 聚合物 纳米技术 储能 快离子导体 复合材料 电极 色素敏化染料 化学 替代医学 医学 工程类 病理 内分泌学 物理化学 功率(物理) 量子力学 物理
作者
Xueli Yao,Wang Qin,Qiankun Hun,Naiyao Mao,Jinping Li,Xinghua Liang,Ying Long,Yifeng Guo
出处
期刊:Gels [Multidisciplinary Digital Publishing Institute]
卷期号:11 (7): 534-534
标识
DOI:10.3390/gels11070534
摘要

Solid-state electrolytes (SSEs) have emerged as a promising solution for next-generation lithium-ion batteries due to their excellent safety and high energy density. However, their practical application is still hindered by critical challenges such as their low ionic conductivity and high interfacial resistance at room temperature. The innovative application of 3D printing in the field of electrochemistry, particularly in solid-state electrolytes, endows energy storage devices with attractive characteristics. In this study, ceramic-in-gel polymer electrolytes (GPEs) based on PVDF-HFP/PAN@LLZTO were fabricated using a direct ink writing (DIW) 3D printing technique. Under the optimal printing conditions (printing speed of 40 mm/s and fill density of 70%), the printed electrolyte exhibited a uniform and dense sponge-like porous structure, achieving a high ionic conductivity of 5.77 × 10-4 S·cm-1, which effectively facilitated lithium-ion transport. A structural analysis indicated that the LLZTO fillers were uniformly dispersed within the polymer matrix, significantly enhancing the electrochemical stability of the electrolyte. When applied in a LiFePO4|GPEs|Li cell configuration, the electrolyte delivered excellent electrochemical performance, with high initial discharge capacities of 168 mAh·g-1 at 0.1 C and 166 mAh·g-1 at 0.2 C, and retained 92.8% of its capacity after 100 cycles at 0.2 C. This work demonstrates the great potential of 3D printing technology in fabricating high-performance GPEs. It provides a novel strategy for the structural design and industrial scalability of lithium-ion batteries.
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