By delivering defect‑free, tunable graphene at scale, the technique can accelerate the rollout of fast‑charging lithium‑ion batteries and other graphene‑based technologies, reducing reliance on hazardous chemical processes.
The demand for high‑quality graphene has outpaced conventional production methods, which often rely on harsh chemical oxidation to unzip carbon nanotubes (CNTs). Such routes introduce oxygen functional groups and structural defects that compromise electrical conductivity and mechanical strength. The newly reported electrochemical unzipping process sidesteps these drawbacks by operating in an oxygen‑free molten salt environment, preserving the pristine carbon lattice while converting CNTs directly into graphene sheets. This breakthrough aligns with industry goals for cleaner, more controllable graphene synthesis.
Temperature emerges as the primary lever for tailoring the graphene architecture. Experiments conducted below 850 °C yield few‑layer turbostratic stacks, characterized by random rotational alignment and minimal interlayer coupling, whereas temperatures exceeding 900 °C promote Bernal‑type graphite with ordered AB stacking. Both regimes exhibit ultralow defect densities, confirmed by Raman spectroscopy and electron microscopy, because the electrochemical reaction proceeds without oxidative side‑reactions. The molten CaCl₂‑NaCl mixture provides high ionic conductivity and a stable medium, enabling uniform current distribution and scalable batch processing.
The structural control directly translates into electrochemical performance. Graphene stacks derived at sub‑850 °C function as lithium‑ion battery anodes that accommodate rapid ion intercalation, delivering fast‑charging capabilities with minimal capacity fade. Bernal‑type graphite produced at higher temperatures offers higher volumetric energy density, suitable for compact cell designs. Beyond batteries, the defect‑free, tunable graphene is poised for catalysis, supercapacitors, and thermal management applications, where conductivity and layer ordering are critical. By eliminating hazardous oxidants and offering a temperature‑driven pathway, the process positions itself as a commercially viable route for next‑generation graphene materials.
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