Direct pyrolysis of a carbon molecular crystal (coronene) yields low-surface-area nanocrystalline graphitic carbon rich in pseudocapacitive lithium binding sites that retain capacity at ultrafast charge rates up to about 40C.
The global shift toward renewable energy, electrified transportation, and AI infrastructure is creating urgent demand for lithium-ion batteries that charge rapidly while maintaining energy density, cost efficiency, cycle life, and safety. The DOE targets 5-15 minute charging to 80% state of charge, costs under $100/kWh, and 300-mile range per charge. Graphite, the dominant anode material since the 1990s, cannot meet these combined requirements.
Pseudocapacitive materials are considered the most promising for extreme fast charging, but state-of-the-art options are metal oxides with high costs, high lithiation potential, or reliance on rare, heavy elements.
MSU researchers developed a new class of carbon-based anode materials using crystalline polycyclic aromatic hydrocarbon (PAH) molecular solids. The lead material, hexa-peri-hexabenzocoronene (HBC), features a crystal structure enabling rapid edge-site lithiation plus interlayer lithiation. "True pseudocapacitance has not previously been achieved" by carbon-based anodes. The herringbone structure supports ultrafast charging rates graphite cannot sustain—reaching 6-minute charges without exceeding 20% capacity loss or compromising cycling stability.
The technology is available for licensing and commercialization. Research collaboration with MSU includes expanding the PAH platform and optimizing cell-level performance. The technology applies to electric vehicles, energy storage, consumer electronics, defense applications, and grid storage (data centers). A comprehensive characterization is under peer-review publication.
Provisional patent filed: Application number 64/037,824.
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