High-pressure behaviors of carbon nanotubesIn this paper, we have reviewed the experimental and theoretical studies on pressure-induced polygonization, ovalization, racetrack-shape deformation, and polymerization of carbon nanotubes (CNTs). The corresponding electronic, optical, and mechanical changes accompanying these behaviors have been discussed. The transformations of armchair (n, n) CNT bundles (n = 2, 3, 4, 6, and 8)
Keywords: pressure-induced carbon nanotubes, polymerization, novel metastable carbons, electronic and mechanical characteristics.
INTRODUCTIONCarbon adopts a wide range of allotropes with unique physical and chemical properties, e.g., graphite, diamond, fullerenes, nanotubes, chaoite, graphene, and amorphous carbon due to its ability to form sp-, sp 2 -, and sp 3 -hybridized bonds. Graphite, the most stable form of carbon at ambient pressure, has a layered and planar structure with the stacked graphene layers coupled by delocalized weak π bonds resulting in conductive and soft nature. Graphene, a recently rising star material, is one-atom-thick planar sheet with a honeycomb crystal lattice like that of graphite. Graphene has the amazing conductivity and strongest tensile strength along the planar layer directions but flexile in the other directions because of the conductive, strong, and flexile sp 2 bonds. Fullerenes and carbon nanotubes (CNTs) represent another two classes of fully sp 2 bonding carbons and are the focus of modern nanoscience and nanotechnology. Structurally, fullerenes are hollow graphitic cage structures composed of nonplanar 5-and 6-membered carbon rings. The smallest fullerene is C 20 [1] . Larger fullerene with increased diameter can also be formed [2,3]. Among them, purified C 60 and C 70 are now commercially available. CNTs can be considered as seamless cylinders formed by rolling single-or multilayer graphene. Different rolling manners yield distinct diametral and chiral CNTs. Given these unique configurations, CNTs possess a wide range of chemical and physical properties, e.g., low density, versatile electronic properties (insulating, semiconducting, Pressure is an effective means to induce the sp 2 -to-sp 3 bond change in carbon, and the produced metastable carbon phases strongly depend on the crystal structure and hybridization scheme of raw carbons, as well as on applied hydrostatic/nonhydrostatic pressure. For example, the compression of graphite can experimentally yield cubic and hexagonal diamonds, as well as a superhard coldcompressed post-graphite phase [5][6][7][8][9][10]. The glass carbon under pressure can transform into a superhard amorphous diamond [11], whereas the compression of C 60 and C 70 fullerenes can produce interesting 1D, 2D, and 3D C 60 and C 70 polymers, as well as other elusive new carbon phases [12][13][14][15][16][17][18][19][20][21][22][23][24][25]. Because a variety of CNT configurations can now be synthesized with a high yield, more interesting pressure-induced structural, electronic, and mechanical changes in CNTs are expected an...