Abstract
Carbon is a remarkable element showing a variety of stable forms ranging from 3D semiconducting diamond to 2D semi-metallic graphite to 1D conducting and semiconducting carbon nanotubes to 0D fullerenes [1]. One distinction between these forms of carbon relates to the many possible configurations of the electronic states of a carbon atom, which is known as the hybridization of atomic orbitals and relates to the bonding of a carbon atom to its nearest neighbors. Carbon is the sixth element of the periodic table and has the lowest atomic number of any element in column IV of the periodic table. Each carbon atom has six electrons which occupy 1s2 , 2s2, and 2p2 atomic orbitals. The 1s2 orbital contains two strongly bound core electrons. Four more weakly bound electrons occupy the 2s22p6 valence orbitals. In the crystalline phase, the valence electrons give rise to 2s, 2px, 2py, and 2pz orbitals which are important in forming covalent bonds in carbon materials. Since the energy difference between the upper 2p energy levels and the lower 2s level in carbon is small compared with the binding energy of the chemical bonds, the electronic wave functions for these four electrons can readily mix with each other, thereby changing the occupation of the 2s and three 2p atomic orbitals so as to enhance the binding energy of the C atom with its neighboring atoms. The general mixing of 2s and 2p atomic orbitals is called hybridization, whereas the mixing of a single 2s electron with one, two, or three 2p electrons is called spn hybridization with n= 1,2,3. Thus three possible hybridizations occur in carbon: sp, sp2 and sp3, while other group IV elements such as Si and Ge exhibit primarily sp3 hybridization. Carbon differs from Si and Ge insofar as carbon does not have inner atomic orbitals, except for the spherical Is orbitals, and the absence of nearby inner orbitals facilitates hybridizations involving only valence s and p orbitals for carbon. The various bonding states are connected with certain structural arrangements, so that sp bonding gives rise to chain structures, sp2 bonding to planar structures and sp3 bonding to tetrahedral structures (Fig. 1).
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Rao, A.M., Dresselhaus, M.S. (2001). Nanostructured Forms of Carbon : An Overview. In: Benedek, G., Milani, P., Ralchenko, V.G. (eds) Nanostructured Carbon for Advanced Applications. NATO Science Series, vol 24. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0858-7_1
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DOI: https://doi.org/10.1007/978-94-010-0858-7_1
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