材料科学
阴极
法拉第效率
锂(药物)
离子电导率
电化学
微尺度化学
复合数
化学工程
电导率
阳极
渗透(认知心理学)
离子键合
离子
粒子(生态学)
纳米颗粒
吸收(声学)
磷酸铁锂
纳米技术
锂离子电池
纳米尺度
工作(物理)
粒径
氧化还原
作者
Jaturon Kumchompoo,Bo-Huei Yang,Jintara Padchasri,Pinit Kidkhunthod,Jyh‐Tsung Lee,Chia-Chen Li
标识
DOI:10.1021/acsami.5c25967
摘要
High Resolution Image Download MS PowerPoint Slide Solid-state lithium batteries (SSLBs) offer improved safety and stability over conventional liquid-electrolyte systems but often suffer from sluggish ion transport and poor interfacial contact within the cathode. To address these limitations, we investigate the incorporation of nanosized Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 (nano-LLZTO) particles into a LiFePO 4 cathode to enhance ionic conductivity and electrochemical performance. Finite element method simulations and experiments reveal that downsizing LLZTO from the microscale to the nanoscale substantially enhances Li + flux uniformity and ionic conductivity (6.48 × 10 –5 S cm –1 vs 1.03 × 10 –5 S cm –1 ), forming more continuous ion-transport networks. The LiFePO 4 /nano-LLZTO cathode exhibits reduced polarization, higher Coulombic efficiency (99.6%), and superior high-rate capability compared with the microsized LLZTO counterpart, achieving 144 mAh g –1 at 1C. Cross-sectional analyses confirm that nano-LLZTO forms homogeneous interfacial coatings, improving ionic percolation and mitigating transport bottlenecks. In situ X-ray absorption near edge structure and extended X-ray absorption fine structure analyses further confirm enhanced redox reversibility and structural stability of Fe sites. Consequently, the LiFePO 4 /nano-LLZTO composite cathode retains 95% of its initial capacity (154 mAh g –1 ) after 200 cycles at 0.2C and 25 °C. This work demonstrates that reducing LLZTO particle size effectively enhances the cathode ion-transport network and ionic conductivity, thereby improving the rate capability and cycling stability of LiFePO 4 -based SSLBs.
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