Abstract
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.
| Original language | English |
|---|---|
| Article number | 105152 |
| Journal | Energy Storage Materials |
| Volume | 88 |
| DOIs | |
| Publication status | Published - May 2026 |
Keywords
- Gradient conductivity
- Internal preferred deposition
- Lithium metal anode
- Natural plant microstructure
- Self-standing electrode
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