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High-Capacity Rechargeable Li/Cl2 Batteries with Graphite Positive Electrodes
Guanzhou Zhu1, Peng Liang1, Cheng-Liang Huang2,3
1Department of Chemistry and Bio-X, Stanford University, Stanford, California94305, United States.
Journal of the American Chemical Society
|November 30, 2022
Summary
This study introduces activated graphite as a high-capacity positive electrode for lithium/chlorine (Li/Cl2) batteries. The activated material demonstrates excellent discharge capacity and cycling stability, utilizing low-cost graphitic materials for advanced energy storage.
Area of Science:
- Electrochemistry
- Materials Science
- Energy Storage
Background:
- Developing high-capacity, high-energy density rechargeable batteries is crucial for consumer electronics, electric vehicles, and grid storage.
- Previous research demonstrated Na/Cl2 and Li/Cl2 batteries using amorphous carbon nanospheres (aCNS) with high reversible capacity.
Purpose of the Study:
- To investigate the potential of initially low surface area graphite (DGr) as a positive electrode material for Li/Cl2 batteries.
- To enhance graphite performance through CO2 activation and understand its electrochemical behavior.
Main Methods:
- Activation of DGr using CO2 at 1000 °C to create DGr_ac.
- Electrochemical testing of Li/Cl2 batteries with DGr_ac as the positive electrode.
- Ex situ Raman spectroscopy and X-ray diffraction (XRD) to analyze electrode evolution.
- Mass spectrometry to probe Cl2 trapping.
Main Results:
- Activated graphite (DGr_ac) achieved a first discharge capacity of ~1910 mAh g-1 and cycling capacity up to 1200 mAh g-1.
- Electrochemical cycling induced graphite exfoliation, creating pores for LiCl/Cl2 redox reactions.
- Mass spectrometry confirmed Cl2 trapping within the graphitic electrode.
Conclusions:
- Low-cost graphitic materials, when activated, are viable for high-capacity alkali metal/Cl2 batteries.
- Graphite activation and in-situ pore generation are key to high performance in Li/Cl2 systems.
- This work provides insights into the operational mechanisms of Li/Cl2 batteries.

