TY - JOUR
T1 - 3D Printing Manufacturing of Thick Electrodes With Hierarchical Porous Structures for High-Power Lithium Metal Batteries
AU - Lv, Junhong
AU - Zhao, Pengcheng
AU - Shen, Fang
AU - Lv, Bohao
AU - Wang, Xudong
AU - Sun, Cheng
AU - Zhang, Lan
AU - Zhang, Songtong
AU - Hua, Weibo
AU - Liao, Bin
AU - Liao, Xiangbiao
AU - Zhang, Dongcai
AU - Huang, Yanping
AU - Qiu, Jingyi
AU - Chen, Xibang
N1 - Publisher Copyright:
© 2026 Wiley-VCH GmbH.
PY - 2026/4/22
Y1 - 2026/4/22
N2 - Thick electrodes of Lithium Metal battery face significant challenges in balancing ionic transport kinetics with structural stability, particularly under high-rate conditions. This study develops a synergistic fabrication strategy integrating direct ink writing 3D printing with ice-templating and phase separation to construct LiFePO4 thick electrodes with hierarchical porous architectures. Systematic rheological optimization identifies the P-30% ink with ideal shear-thinning behavior and shape retention capability (yield stress: 538.9 Pa, storage modulus: 21 480 Pa). The resulting electrode features macro-printed channels and interconnected phase-separated micropores, achieving high porosity (79.57%) and low tortuosity. This unique architecture delivers exceptional electrochemical performance: a specific capacity of 109.3 mAh g−1 at 5C rate, 90.8% capacity retention after 2000 cycles, reduced charge transfer resistance (69.8 Ω), and enhanced Li-ion diffusion coefficient (1.65 × 10−10 cm2 s−1). COMSOL simulations confirm improved ion transport efficiency and mitigated concentration polarization. The assembled pouch cell maintains stable performance over 10 000 bending cycles, demonstrating superior mechanical flexibility and practical application potential for high-power energy storage systems.
AB - Thick electrodes of Lithium Metal battery face significant challenges in balancing ionic transport kinetics with structural stability, particularly under high-rate conditions. This study develops a synergistic fabrication strategy integrating direct ink writing 3D printing with ice-templating and phase separation to construct LiFePO4 thick electrodes with hierarchical porous architectures. Systematic rheological optimization identifies the P-30% ink with ideal shear-thinning behavior and shape retention capability (yield stress: 538.9 Pa, storage modulus: 21 480 Pa). The resulting electrode features macro-printed channels and interconnected phase-separated micropores, achieving high porosity (79.57%) and low tortuosity. This unique architecture delivers exceptional electrochemical performance: a specific capacity of 109.3 mAh g−1 at 5C rate, 90.8% capacity retention after 2000 cycles, reduced charge transfer resistance (69.8 Ω), and enhanced Li-ion diffusion coefficient (1.65 × 10−10 cm2 s−1). COMSOL simulations confirm improved ion transport efficiency and mitigated concentration polarization. The assembled pouch cell maintains stable performance over 10 000 bending cycles, demonstrating superior mechanical flexibility and practical application potential for high-power energy storage systems.
KW - 3D printing
KW - hierarchical porous structure
KW - ionic kinetics
KW - lithium metal batteries
KW - rheological properties
UR - https://www.scopus.com/pages/publications/105030880480
U2 - 10.1002/aenm.202506389
DO - 10.1002/aenm.202506389
M3 - 文章
AN - SCOPUS:105030880480
SN - 1614-6832
VL - 16
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 16
M1 - e06389
ER -