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Monolayer Amorphous Carbon: Unlocking Disorder-Induced Lithiophilicity
Lu Shi1, Hanning Zhang2, Artem K Grebenko3
1Department of Materials Science and Engineering, National University of Singapore, Singapore, 117575, Singapore.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|November 25, 2025
Summary
A monolayer amorphous carbon film uniformly enhances lithium binding on current collectors, enabling homogeneous lithium deposition for advanced anode-less batteries. This approach overcomes challenges posed by dendritic lithium growth.
Area of Science:
- Materials Science
- Electrochemistry
- Surface Science
Background:
- Dendritic lithium growth on current collectors hinders anode-less battery development due to uneven lithium nucleation and surface lithiophilicity.
- Current methods using interlayers often fail due to mechanical issues or inconsistent lithium affinity.
Purpose of the Study:
- To investigate the effect of a monolayer amorphous carbon (MAC) film on lithium nucleation and deposition.
- To establish intrinsic structural disorder as a strategy for designing uniformly lithiophilic current collectors.
Main Methods:
- Growth of a monolayer amorphous carbon (MAC) film on copper current collectors.
- Contact angle measurements to assess surface lithiophilicity.
- Electrochemical tests to evaluate nucleation overpotential.
- Density functional theory (DFT) and scanning tunneling microscopy (STM) for theoretical analysis.
Main Results:
- MAC film exhibits significantly enhanced lithiophilicity with a low lithium contact angle (31 ± 5°).
- Homogeneous lithium wetting and deposition observed on the MAC surface.
- Reduced nucleation overpotential (28.9 mV at 0.5 mA cm⁻²) demonstrated.
- DFT and STM confirm disorder-induced electron localization enhances lithium binding.
Conclusions:
- Topological disorder in MAC films uniformly strengthens lithium binding through electron-rich sites.
- Intrinsic structural disorder is an effective strategy for creating uniformly lithiophilic surfaces.
- This approach offers a promising route for next-generation anode-less batteries.
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