We report first principles density functional pseudopotential calculations on the molecular and electronic structures of one-dimensional crystals of KI and composites formed upon the intercalation of these ionic crystals within single wall carbon nanotubes (SWNT). For a series of ${\mathrm{K}}_{24}{\mathrm{I}}_{24}@\mathrm{SWNT}$ composites the influence of the diameter and chirality of the SWNT on the structures of the $2\times 2$ KI crystals is discussed. The calculated I-I interplanar spacings along and across the KI crystal in the KI@(10,10) composite ($3.40\mathrm{\AA }$ and $3.66\mathrm{\AA }$, respectively) were in good agreement with the experimental lattice measurements reported by Sloan et al. [$3.46\left(0.03\right)\mathrm{\AA }$ and $3.98\left(0.31\right)\mathrm{\AA }$] for $2\times 2$ KI encapsulated within a SWNT of similar diameter [Chem. Phys. Lett. 329, 61 (2000)]. The energy of intercalating ${\mathrm{K}}_{24}{\mathrm{I}}_{24}$ within a SWNT was calculated and a Mulliken population analysis was performed for each of the four composites considered here. These Mulliken analyses indicate that a small amount of charge transfer occurs from the SWNT to the KI crystal and that the extent of this charge transfer is dependent on the diameter of the confining nanotube. The intercalation energies exhibit a similar dependency on the diameter of the confining nanotube, with insertion of the $2\times 2$ crystal of KI becoming increasingly exothermic upon reduction of the nanotube diameter from $\sim 1.36\mathrm{nm}\text{to}\sim 1.10\mathrm{nm}$.

• Received 1 December 2005

DOI:https://doi.org/10.1103/PhysRevB.73.125441