• Lin, Yung-Chang
• Siao, Ming-Deng
• Matsumoto, Rika
• Liu, Qiunan

Abstract

<jats:title>Abstract</jats:title><jats:p>Alkali metal (AM) intercalation between graphene layers holds promise for electronic manipulation and energy storage, yet the underlying mechanism remains challenging to fully comprehend despite extensive research. In this study, we employ low-voltage scanning transmission electron microscopy (LV-STEM) to visualize the atomic structure of intercalated AMs (potassium, rubidium, and cesium) in bilayer graphene (BLG). Our findings reveal that the intercalated AMs adopt bilayer structures with <jats:italic>hcp</jats:italic> stacking, and specifically a C<jats:sub>6</jats:sub>M<jats:sub>2</jats:sub>C<jats:sub>6</jats:sub> composition. These structures closely resemble the bilayer form of <jats:italic>fcc</jats:italic> (111) structure observed in AMs under high-pressure conditions. A negative charge transferred from bilayer AMs to graphene layers of approximately 1~1.5×10<jats:sup>14</jats:sup> e<jats:sup>−</jats:sup>/cm<jats:sup>−2</jats:sup> was determined by electron energy loss spectroscopy (EELS), Raman, and electrical transport. The bilayer AM is stable in BLG and graphite superficial layers but absent in the graphite interior, primarily dominated by single-layer AM intercalation. This hints at enhancing AM intercalation capacity by thinning the graphite material.</jats:p>

Topics

• impedance spectroscopy
• Potassium
• transmission electron microscopy
• additive manufacturing
• electron energy loss spectroscopy
• Rubidium
• Accelerator mass spectrometry