In-situ photo-polymerized elastomeric composite electrolytes containing Li6.4La3Zr1.4Ta0.6O12 particles for stable operation in lithium metal batteries

IF 10.7 Q1 CHEMISTRY, PHYSICAL
EcoMat Pub Date : 2024-11-13 DOI:10.1002/eom2.12503
Seung Ho Kwon, Seongmin Kim, Jinseok Park, Michael J. Lee, Youyoung Byun, Hyun Jung Kim, Young Min Baek, Jaegyeom Kim, Eunji Lee, Seung Woo Lee, Bumjoon J. Kim
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Abstract

Composite polymer electrolytes (CPEs), produced by incorporating inorganic nanoparticles (NPs) into polymer matrices, have gained significant attention as promising candidates for solid-state lithium metal batteries (LMBs). However, the aggregation of dense inorganic fillers results in nonuniform CPEs, thereby impeding LMB performance. Here, we fabricated in-situ photo-polymerized CPEs by incorporating different weight ratios (0–20 wt%) of Li6.4La3Zr1.4Ta0.6O12 (LLZTO) into a polymer electrolyte system composed of poly(butyl acrylate)-based elastomer and succinonitrile-based plastic crystal phases. The rapid photo-polymerization process (~5 min) enabled homogeneous dispersion of LLZTO within the CPE matrix at 10 wt% LLZTO (L10), resulting in the high ionic conductivity (1.02 mS cm−1 at 25°C) and mechanical elasticity (elongation at break ≈ 1250%) compared to those of CPE without LLZTO (L0). As a result, the L10-based LMB with a LiNi0.8Co0.1Mn0.1O2 cathode exhibited a high capacity of 166.7 mAh g−1 after 200 cycles at 0.5C, significantly higher than those of L0 (74.0 mAh g−1) and L20 (104.8 mAh g−1). In comparison, in-situ thermal polymerized CPE with 10 wt% LLZTO NPs showed aggregation of NPs due to slow polymerization kinetics (~2 h), resulting in inferior LMB cycling performance compared to the L10. This work highlights the importance of in-situ photo-polymerized CPEs with homogenous dispersion of inorganic NPs to achieve high ionic conductivity and mechanical robustness suitable for the stable operation of LMBs.

Abstract Image

含 Li6.4La3Zr1.4Ta0.6O12 颗粒的原位光聚合弹性复合电解质,用于锂金属电池的稳定运行
复合聚合物电解质(cpe)是一种将无机纳米颗粒(NPs)掺入聚合物基质中制备的聚合物电解质,作为固态锂金属电池(lmb)的有前途的候选材料而受到广泛关注。然而,致密无机填料的聚集导致cpe不均匀,从而阻碍了LMB的性能。在这里,我们将不同重量比(0-20 wt%)的Li6.4La3Zr1.4Ta0.6O12 (LLZTO)加入到由聚丙烯酸丁酯基弹性体和琥珀腈基塑料晶体相组成的聚合物电解质体系中,制备了原位光聚合cpe。快速光聚合过程(~5 min)使LLZTO以10 wt%的LLZTO (L10)均匀分散在CPE基体内,与不含LLZTO (L0)的CPE相比,具有较高的离子电导率(25°C时1.02 mS cm−1)和机械弹性(断裂伸长率≈1250%)。结果表明,以LiNi0.8Co0.1Mn0.1O2为阴极的l10基LMB在0.5C下循环200次后,其电池容量达到166.7 mAh g−1,显著高于L0 (74.0 mAh g−1)和L20 (104.8 mAh g−1)。相比之下,含有10 wt% LLZTO NPs的原位热聚合CPE由于聚合动力学缓慢(~2 h)而出现NPs聚集,导致LMB循环性能不如L10。这项工作强调了原位光聚合cpe与无机NPs均匀分散的重要性,以实现适合lmb稳定运行的高离子电导率和机械鲁棒性。
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来源期刊
CiteScore
17.30
自引率
0.00%
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审稿时长
4 weeks
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