Unlocking solid-state conversion batteries reinforced by hierarchical microsphere stacked polymer electrolyte

材料科学 电解质 阴极 阳极 化学工程 聚合物 电池(电) 锂(药物) 准固态 电极 纳米技术 复合材料 化学 色素敏化染料 工程类 内分泌学 物理化学 功率(物理) 物理 医学 量子力学
作者
Jiulin Hu,Keyi Chen,Zhenguo Yao,Chilin Li
出处
期刊:Science Bulletin [Elsevier]
卷期号:66 (7): 694-707 被引量:93
标识
DOI:10.1016/j.scib.2020.11.017
摘要

Pursuing all-solid-state lithium metal batteries with dual upgrading of safety and energy density is of great significance. However, searching compatible solid electrolyte and reversible conversion cathode is still a big challenge. The phase transformation at cathode and Li deformation at anode would usually deactivate the electrode-electrolyte interfaces. Herein, we propose an all-solid-state Li-FeF3 conversion battery reinforced by hierarchical microsphere stacked polymer electrolyte for the first time. This g-C3N4 stuffed polyethylene oxide (PEO)-based electrolyte is lightweight due to the absence of metal element doping, and it enables the spatial confinement and dissolution suppression of conversion products at soft cathode-polymer interface, as well as Li dendrite inhibition at filler-reinforced anode-polymer interface. Two-dimensional (2D)-nanosheet-built porous g-C3N4 as three-dimensional (3D) textured filler can strongly cross-link with PEO matrix and LiTFSI (TFSI: bistrifluoromethanesulfonimide) anion, leading to a more conductive and salt-dissociated interface and therefore improved conductivity (2.5 × 10-4 S/cm at 60 °C) and Li+ transference number (0.69). The compact stacking of highly regular robust microspheres in polymer electrolyte enables a successful stabilization and smoothening of Li metal with ultra-long plating/striping cycling for at least 10,000 h. The corresponding Li/LiFePO4 solid cells can endure an extremely high rate of 12 C. All-solid-state Li/FeF3 cells show highly stabilized capacity as high as 300 mAh/g even after 200 cycles and of ~200 mAh/g at extremely high rate of 5 C, as well as ultra-long cycling for at least 1200 cycles at 1 C. High pseudocapacitance contribution (>55%) and diffusion coefficient (as high as 10-12 cm2/s) are responsible for this high-rate fluoride conversion. This result provides a promising solution to conversion-type Li metal batteries of high energy and safety beyond Li-S batteries, which are difficult to realize true "all-solid-state" due to the indispensable step of polysulfide solid-liquid conversion.
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