TY - JOUR
T1 - Purely-natural stem based self-standing carbon current collector
T2 - Guiding internal preferred Li deposition via gradient conductivity
AU - Yang, Feiyang
AU - Xu, Qike
AU - Gan, Siqi
AU - Gou, Zhaolin
AU - Chen, Ziyi
AU - Zhang, Cunzhong
AU - Su, Yuefeng
AU - Yao, Ying
N1 - Publisher Copyright:
Copyright © 2026. Published by Elsevier B.V.
PY - 2026/5
Y1 - 2026/5
N2 - Lithium dendrite growth and unstable solid electrolyte interphase remain critical challenges for practical lithium metal anodes (LMA). Directly converted from plant stems, the monolithic and self-standing carbon current collector (ADC) inherits vertically aligned channels and abundant carbon defects from its natural precursor. By engineering a longitudinal electrical conductivity gradient, we construct an electrode denoted P-ADC-G (indicating the polymer coated and gradient-conductive anode) that enables co-regulate ion and electron fluxes, guiding sustained internal-preferred lithium deposition. Remarkably, this optimized kinetics unlocks high-rate electrodeposition, enabling rapid anode fabrication (10 mAh cm-2 in just 2 h). The resulting Li@P-ADC-G composite anode exhibits exceptional stability, cycling over 2000 h at 4 mA cm-2 with an average Coulombic efficiency of 97.56%, and enables LiFePO4 full cells to retain above 70% capacity after 400 cycles at 1C. Moreover, the same ADC serves as an efficient metal-free cathode catalyst in Li–O2 cells, achieving stable operation for over 800 h when paired with Li@P-ADC-G. This work demonstrates a scalable, bioinspired strategy for co-regulating ionic and electronic pathways to achieve highly reversible LMA across diverse battery chemistries.
AB - Lithium dendrite growth and unstable solid electrolyte interphase remain critical challenges for practical lithium metal anodes (LMA). Directly converted from plant stems, the monolithic and self-standing carbon current collector (ADC) inherits vertically aligned channels and abundant carbon defects from its natural precursor. By engineering a longitudinal electrical conductivity gradient, we construct an electrode denoted P-ADC-G (indicating the polymer coated and gradient-conductive anode) that enables co-regulate ion and electron fluxes, guiding sustained internal-preferred lithium deposition. Remarkably, this optimized kinetics unlocks high-rate electrodeposition, enabling rapid anode fabrication (10 mAh cm-2 in just 2 h). The resulting Li@P-ADC-G composite anode exhibits exceptional stability, cycling over 2000 h at 4 mA cm-2 with an average Coulombic efficiency of 97.56%, and enables LiFePO4 full cells to retain above 70% capacity after 400 cycles at 1C. Moreover, the same ADC serves as an efficient metal-free cathode catalyst in Li–O2 cells, achieving stable operation for over 800 h when paired with Li@P-ADC-G. This work demonstrates a scalable, bioinspired strategy for co-regulating ionic and electronic pathways to achieve highly reversible LMA across diverse battery chemistries.
KW - Gradient conductivity
KW - Internal preferred deposition
KW - Lithium metal anode
KW - Natural plant microstructure
KW - Self-standing electrode
UR - https://www.scopus.com/pages/publications/105037455142
U2 - 10.1016/j.ensm.2026.105152
DO - 10.1016/j.ensm.2026.105152
M3 - Article
AN - SCOPUS:105037455142
SN - 2405-8297
VL - 88
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 105152
ER -