TY - JOUR
T1 - Homogeneous 3D Porous Conductive Electrodes for High-Energy Battery Fast Charging
AU - Ai, Huayue
AU - Cai, Angela
AU - Holoubek, John
AU - Zhang, Wenbo
AU - Greenburg, Louisa C.
AU - Lee, Junyoung
AU - Holmes, Sarah
AU - Suzuki, Yoshiaki
AU - Kuwajima, Hideaki
AU - Matsumoto, Ryuhei
AU - Ye, Yusheng
AU - Nakayama, Yuri
AU - Cui, Yi
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025
Y1 - 2025
N2 - Fast charging in high-energy-density lithium-ion batteries (LIBs) is hindered by increased impedance and sluggish kinetics associated with thicker electrode coatings. In conventional batteries, the topmost active layer of the electrodes often experiences the highest electrical resistance due to its distance from the current collector. This, along with variations in planar electrical conductivity, creates localized charge flux imbalances that promote electrode reaction heterogeneity and, ultimately, lithium plating. Thicker electrodes also extend ionic pathways, further limiting the rate performance. Here, we develop three-dimensional porous electrodes─integrating current collectors and active materials─with homogeneous electrical conductivity and double the ionic transfer efficiency of traditional electrodes. These electrodes demonstrate thickness-independent electrical conductivity in both in-plane and out-of-plane directions. At an areal capacity of 3 mAh/cm2, pouch cells with the designed electrodes exhibit excellent performance and stability, achieving 79.2%, 72.5%, and 62.3% state-of-charge (SOC) at 5C, 7C, and 10C, respectively. The straightforward fabrication process expands a potential route toward large-scale manufacturing.
AB - Fast charging in high-energy-density lithium-ion batteries (LIBs) is hindered by increased impedance and sluggish kinetics associated with thicker electrode coatings. In conventional batteries, the topmost active layer of the electrodes often experiences the highest electrical resistance due to its distance from the current collector. This, along with variations in planar electrical conductivity, creates localized charge flux imbalances that promote electrode reaction heterogeneity and, ultimately, lithium plating. Thicker electrodes also extend ionic pathways, further limiting the rate performance. Here, we develop three-dimensional porous electrodes─integrating current collectors and active materials─with homogeneous electrical conductivity and double the ionic transfer efficiency of traditional electrodes. These electrodes demonstrate thickness-independent electrical conductivity in both in-plane and out-of-plane directions. At an areal capacity of 3 mAh/cm2, pouch cells with the designed electrodes exhibit excellent performance and stability, achieving 79.2%, 72.5%, and 62.3% state-of-charge (SOC) at 5C, 7C, and 10C, respectively. The straightforward fabrication process expands a potential route toward large-scale manufacturing.
UR - https://www.scopus.com/pages/publications/105013569621
U2 - 10.1021/acsenergylett.5c01406
DO - 10.1021/acsenergylett.5c01406
M3 - Article
AN - SCOPUS:105013569621
SN - 2380-8195
VL - 10
SP - 4203
EP - 4211
JO - ACS Energy Letters
JF - ACS Energy Letters
ER -