TY - JOUR
T1 - Design Lithium Exchanged Zeolite Based Multifunctional Electrode Additive for Ultra-High Loading Electrode Toward High Energy Density Lithium Metal Battery
AU - Gao, Yunnan
AU - Yang, Yi
AU - Yang, Tingzhou
AU - Zhang, Zhen
AU - Tang, Liang
AU - Mao, Zhiyu
AU - Zhang, Yongguang
AU - Luo, Dan
AU - Chen, Zhongwei
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/2/4
Y1 - 2025/2/4
N2 - The practicalization of a high energy density battery requires the electrode to achieve decent performance under ultra-high active material loading. However, as the electrode thickness increases, there is a notable restriction in ionic transport in the electrodes, limiting the diffusion kinetics of Li+ and the utilization rate of active substances. In this study, lithium-ion-exchanged zeolite X (Li-X zeolite) is synthesized via Li+ exchange strategy to enhance Li+ diffusion kinetics. When incorporated Li–X zeolite into the ultra-high loading cathodes, it possesses i) high electron conductivity with a uniform network by reducing tortuosity, ii) decent ion conductivity attributes to modulated Li+ diffusivity of Li-X and iii) high elasticity to prevent particle-level cracking and electrode-level disintegration. Moreover, Li–X zeolite at the solid/liquid interface facilitates the formation of a stable cathode electrolyte interface, which effectively suppresses side reactions and mitigates the dissolution of transition cations. Therefore, an ultra-high loading (66 mg cm−2) cathode is fabricated via dry electrode technology, demonstrating a remarkable areal capacity of 12.7 mAh cm−2 and a high energy density of 464 Wh kg−1 in a lithium metal battery. The well-designed electrode structure with multifunctional Li–X zeolite as an additive in thick cathodes holds promise to enhance the battery's rate capability, cycling stability, and overall energy density.
AB - The practicalization of a high energy density battery requires the electrode to achieve decent performance under ultra-high active material loading. However, as the electrode thickness increases, there is a notable restriction in ionic transport in the electrodes, limiting the diffusion kinetics of Li+ and the utilization rate of active substances. In this study, lithium-ion-exchanged zeolite X (Li-X zeolite) is synthesized via Li+ exchange strategy to enhance Li+ diffusion kinetics. When incorporated Li–X zeolite into the ultra-high loading cathodes, it possesses i) high electron conductivity with a uniform network by reducing tortuosity, ii) decent ion conductivity attributes to modulated Li+ diffusivity of Li-X and iii) high elasticity to prevent particle-level cracking and electrode-level disintegration. Moreover, Li–X zeolite at the solid/liquid interface facilitates the formation of a stable cathode electrolyte interface, which effectively suppresses side reactions and mitigates the dissolution of transition cations. Therefore, an ultra-high loading (66 mg cm−2) cathode is fabricated via dry electrode technology, demonstrating a remarkable areal capacity of 12.7 mAh cm−2 and a high energy density of 464 Wh kg−1 in a lithium metal battery. The well-designed electrode structure with multifunctional Li–X zeolite as an additive in thick cathodes holds promise to enhance the battery's rate capability, cycling stability, and overall energy density.
KW - dry electrode technology
KW - high energy density
KW - lithium exchanged zeolite
KW - lithium–metal battery
UR - http://www.scopus.com/inward/record.url?scp=85207373687&partnerID=8YFLogxK
U2 - 10.1002/aenm.202403063
DO - 10.1002/aenm.202403063
M3 - 文章
AN - SCOPUS:85207373687
SN - 1614-6832
VL - 15
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 5
M1 - 2403063
ER -