TY - JOUR
T1 - The effect of graphitization temperature on the structure of helical-ribbon carbon nanofibers
AU - Weisenberger, Matthew
AU - Martin-Gullon, Ignacio
AU - Vera-Agullo, José
AU - Varela-Rizo, Helena
AU - Merino, César
AU - Andrews, Rodney
AU - Qian, Dali
AU - Rantell, Terry
PY - 2009/8
Y1 - 2009/8
N2 - Structural rearrangement of helical-ribbon carbon nanofibers (CNFs) was studied as a function of graphitization temperature. The as-produced nanofibers are composed of a helical ribbon of graphene spiralled about and angled to the fiber axis. The discrete layers of graphene ribbon overlap each other forming the helical-ribbon in contrast to the discontinuous cones of the more common stacked-cup CNF morphology. After heat treatment to 2400 °C and above, the CNFs were completely free of residual metal catalyst inclusions, principally nickel used in their synthesis, and other functionalities. The formation of loops at the graphene edges was also observed. Heat treatment through the temperature range 1500-2800 °C resulted in a relatively minor contraction in interlayer spacing d002 from 0.3381 to 0.3363 nm. This was attributed to the highly graphitic character of the as-produced CNFs. However, there were significant increases in the crystallite thickness Lc through this temperature range. In addition, heat treatment above 2400 °C induced a marked change of the nanofiber morphology from circular to faceted polygonal cross-section resulting from the re-ordering of the turbostratic, curved graphene layers to regions of planar graphene layers with 3-dimensional graphitic structure (AB stacking).
AB - Structural rearrangement of helical-ribbon carbon nanofibers (CNFs) was studied as a function of graphitization temperature. The as-produced nanofibers are composed of a helical ribbon of graphene spiralled about and angled to the fiber axis. The discrete layers of graphene ribbon overlap each other forming the helical-ribbon in contrast to the discontinuous cones of the more common stacked-cup CNF morphology. After heat treatment to 2400 °C and above, the CNFs were completely free of residual metal catalyst inclusions, principally nickel used in their synthesis, and other functionalities. The formation of loops at the graphene edges was also observed. Heat treatment through the temperature range 1500-2800 °C resulted in a relatively minor contraction in interlayer spacing d002 from 0.3381 to 0.3363 nm. This was attributed to the highly graphitic character of the as-produced CNFs. However, there were significant increases in the crystallite thickness Lc through this temperature range. In addition, heat treatment above 2400 °C induced a marked change of the nanofiber morphology from circular to faceted polygonal cross-section resulting from the re-ordering of the turbostratic, curved graphene layers to regions of planar graphene layers with 3-dimensional graphitic structure (AB stacking).
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U2 - 10.1016/j.carbon.2009.03.070
DO - 10.1016/j.carbon.2009.03.070
M3 - Article
AN - SCOPUS:67349090168
SN - 0008-6223
VL - 47
SP - 2211
EP - 2218
JO - Carbon
JF - Carbon
IS - 9
ER -