Since the first discovery of single-walled carbon Nanotubes (SWCNTs) by Iijima and Bethune in 1993 (Bethune et al., 1993), many applications as molecular components for nanotechnology including conductivity and high-strength composites; energy storage and energy conversion devices; sensors; field emission displays and radiation sources; hydrogen storage media; and nanometer-sized semiconductor devices, probes, and interconnects are known (Ajayan et al., 1994; Saito et al., 1997; de Heer et al., 1995; Collins et al., 1997; Nardelli et al., 1998; Huang et al., 2006). SWCNTs have been considered as the leading candidate for Nan device applications because of their one-dimensional electronic bond structure, molecular size, biocompatibility, controllable property of conducting electrical current and reversible response to biological reagents. Hence SWCNTs make possible bonding to polymers and biological systems such as DNA and carbohydrates. Most SWCNTs have a diameter of close to 1 nanometer, with a tube length that can be many millions of times longer. The average diameter of a SWNT is 1.2 nm (Spires & Brown, 1996). However, Nanotubes can vary in size, and they aren't always perfectly cylindrical. As in Fig. 1, the average bond length and carbon separation values for the hexagonal lattice were shown. The carbon bond length of 1.42 Å was measured by Spires and Brown in 1996 (Spires & Brown, 1996) and later confirmed by Wilder et al. in 1998 (Wilder et al., 1998).
The structure of a SWNT can be formed by the rolling of a single layer of sp2 carbon, called a graphene layer, into a seamless hollow cylindrical tube with Nan scale dimensions of 1-1.5 nm. The length is usually in the order of microns to centimeters. Besides their unique physical properties (elasticity, tensile strength, stiffness, and deformation), Nano tubes exhibit varying electrical properties (depending on the direction that the graphite structure spirals around the tube (quantified by the “Chiral vector”), and other factors, such as doping), and can be superconductor, conductor (metallic), semiconductor or, insulator. The band structure can even be further manipulated, by introducing defects into a tube. Single-walled nanotubes exhibit electric properties that are not shared by the multi-walled carbon nanotube (MWNT) variants. In particular, their band gap can vary from zero to about 2 eV and their electrical conductivity can show metallic or semiconducting behavior, whereas MWNTs are zero-gap metals. The C-C tight bonding overlap energy is in the order of 2.5 eV. Wilder
Recently, theoretical and experimental work have predicted that the infinity length SWCNTs are Pi-bonded aromatic molecules that the electrical properties depending upon the tubular diameter and helical angle (Zhou et al., 2004; Baron et al., 2005). SWCNTs can be chiral or nonchiral, again depending on the way of the rolling up vector. As a graphene sheet was rolled in many ways in horizontal, vertical, and diagonal direction represent as arrow vectors,, as in Fig. 1, the different types of carbon nanotubes were produced. The three main types are armchair, zig-zag, and chiral nanotube. The geometrical and electronic structure of SWCNT can be described by a chiral vector, the angle between the axis of its hexagonal pattern and the axis of the tube which is presented by a pair of indices (
Although, scientific efforts focused on the electrostatics properties and commercial applications of these materials (Ouyango et al., 2002; Kane & Mele, 1997; Hartschuh et al. 2005), there have been no experimental structural data sufficiently accurate for the identification of the chirality indices of SWCNTs, especially for the kind of smaller diameter nanotubes. In all experimental methods for the identification commonly utilized so far is Raman spectroscopy and phonon dispersion. Phonon dispersion relations in one dimension of this system have been studied by using zonefolding along one direction of Brillouin zone considering the tube symmetry (Eklund et al., 1995). The tight binding electronic band structure and the reverse of the diameter (1/d) dependence of the frequency of the radial breathing mode (RBM) were employed (Jorio et al., 2001; Bachilo et al, 2002; Pfeiffer et al. 2003; Kurti et al., 2004; Maultizsch et al., 2005). The size and chirality of the carbon nanotubes were typical determined from the SWCNT Raman energy spectra of a peak around 150–300 cm-1, due to the radial breathing mode (Maultizsch et al., 2005; Jorio et al., 2005). Further Raman studies of SWCNT modified by various reactions e.g. oxidation reactions, ozonolysis, fluorination, residues modification (Srano et al., 2003; Umek et al., 2003; Peng et al., 2003; Bahr et al., 2001; Holzinger et al., 2003; Mickelson et al., 1998; Cai et al., 2002; Banerjee & Wong, 2002; Herrera & Resasco, 2003; Martinez et al., 2003) have revealed that covalent functionalization mainly affects the intensity of the Raman bands. Characterization of nanotube in adsorption gas has been studied by Monte Carlo and Langevin Dynamic Simulation (Monajjemi et al., 2008b). It is also important to investigate the effects of diameter on a SWCNT structure how the diameter depends on geometrical parameters such as the C-C bond lengths and some of the dihedral angles of SWCNTs.
For a better understanding of the physical and electronic properties of SWCNT, a challenging task in theoretical calculation is needed to specify the material properties because of the large size of the SWCNTs and their complicated (and size-dependent) electronic structure. Quantum calculation in prediction the properties of single-walled carbon nanotubes (SWCNTs) will be discussed.
2. Vibrational mode of SWCNT
Normal mode analysis has become one of the standard techniques in the study of the dynamics of nanotubes. It is primarily used for identifying and characterizing the slowest motions in a poly system, which are inaccessible by other methods. This text explains what normal mode analysis is and what one can do with it without going beyond its limit of validity. By definition, normal mode analysis is the study of harmonic potential wells by analytic means. The first section of this study will therefore deal with potential wells and harmonic approximations. This study is about normal mode approaches to different physical situations, and it discusses how useful information can be extracted from normal modes. Normalmode coordinates are obtained by a linear combination of Cartesian coordinates. Thus, there are no couplings in the kinetic part; that is, they diagonalize the kinetic energy as well the quadratic part of the potential energy operator. They include simultaneous motion of all atoms during the vibration, which leads to a natural description of molecular vibrations. Therefore, they are good candidates for representation of the molecular Hamiltonian. Since a transformation between different sets of coordinates is possible, the anharmonic terms can be calculated in one representation, and then transformed into another one.
2.1. Symmetry of SWCNT
Because a single carbon nanotube may be thought of as a graphene sheet rolled up to form a tube, carbon nanotubes should be expected to have many properties derived from the energy bands and lattice dynamics of graphite. For the very smallest tubule diameters, however, one might anticipate new effects stemming from the curvature of the tube wall and the closing of the graphene sheet into a cylinder. A method for identifying the Raman modes of single-wall carbon nanotubes (SWNT) based on the symmetry of the vibration modes has been widely used. The Raman intensity of each vibration mode varies with polarization direction, and the relationship can be expressed as analytical functions. Each Raman-active mode of SWNT can be distinguished from the group theory principle. The symmetry properties of periodic lattices of carbon nanotubes and the symmetry operations of chiral and achiral nanotubes (Damnjanović et al., 1999; Damnjanović et al., 2001; Alon, 2001, 2003) are usually described in terms of the group of the wavevector (Dresselhaus et al., 2006). However, since nanotubes can be viewed as quasi-1D systems, the line groups approach by Damnjanović et al. is suited to describe nanotube properties (Damnjanović et al., 1999).
As described earlier, the properties of nanotubes are determined by their diameter and chiral angle, both of which depend on n1 and n2. Typically, SWCNT is presented by a pair of integers (n1, n2). Its geometrical structure as shown in diagram can be represented in term of a chiral vector on a two-dimensional sp2-carbon sheet where with integer n1 and n2. Here, and represent the unit vectors of the hexagonal graphene lattice. This sheet is then rolled up to a cylinder so that becomes the circumference of the tube. The direction of the nanotube axis is naturally perpendicular to. The diameter, d, is simply the length of the chiral vector divided by ¼, and, where ac-c is the distance between neighbouring carbon atoms in the flat sheet. In turn, the chiral angle () is given by.
The translational period, a, is the shortest possible lattice vector along z direction. The translatory unit cell of a nanotube is a cylinder with a length in tube axis direction equal to the magnitude of the translation vector as shown in Fig. 1 which can be calculated as following equation:
where n is the greatest common divisor of n1 and n2,
if (n1 -n2)/3n ≠ integer, then R = 1
if (n1 -n2)/3n = integer, then R = 3andand form an angle of 60 o and their length is | a1| = | a2| = a0 = 2.461 Å
Since the translational period, a, depends inversely on n and R the translation periodicity and thus the number of carbon atoms varies strongly for tubes with similar diameter. The number of graphene cells in the nanotube unit cell (nc) obtained from:
The groups of infinite line L are products L = ZP, where P is a point group and Z is the group of translations (screw axis, pure translations, and glide planes). Applying the above symmetry formulation to armchair (n1 = n2) and zigzag (n2 = 0) nanotubes, such nanotubes with no caps have a isogonal point groups given by q (the number of graphene cells in the unit cell of the nanotubes) namely, Dnd when n is odd, Dnh when n is even, or Dqh = D2nh for achiral and Dq for chiral tubes. Whether the symmetry groups for armchair and zigzag tubules are taken to be Dnd or Dnh, the calculated vibrational frequencies will be the same; the symmetry assignments for these modes, however, will be different. It is, thus, expected that modes that are Raman or IR-active under Dnd (or Dnh ) but are optically under D2nh will only show a weak activity resulting from the fact that the existence of caps lowers the symmetry that would exist for a nanotube of infinite length.
2.2. Active modes of Raman and IR
The phonon symmetries are found by decomposing the dynamical representation into its irreducible representations using symmetries of carbon and other nanotubes studied for line groups (Damnjanović et al., 1999). One direct set up of the dynamical representation from the atomic and vector representation is to use factor group analysis. A representation can be decomposed into the sum of its irreducible representations by the following formula
where f αis the appearance frequency of the irreducible representation α, g is the order of the symmetry group; the sum is over all symmetry operations G.
The Raman ΓR and infrared active ΓIR vibrations transform according to the representation of the second rank tensor and the vector representation, respectively (Damnjanović et al., 1983)
ΓR= [ΓvecΓvec]=A1gE1gE2g (A2g)
According to the symmetries of Raman-active modes (Pelletier, 1999) for the armchair carbon nanotube with the chair vector (n1, n2), the point group for this kind nanotube belongs to Dnh when n is even and its Raman-active modes are denoted by A1g + E1g + E2g. Three flavors of modes are longitudinal, transversal radial (orthogonal to tube surface) and transversal axial (parallel to tube surface). Satio et al. (Satio et al., 1998) pointed out that the low frequency A1g mode is a radial breathing mode and two high frequency is belong to Eg modes, E1g and E2g. E mode has the same displacement pattern with additional standing wave on the circumference.
2.3. Projection operators
The zigzag single-walled carbon nanotubes (SWCNTs) with (3,0), (4,0), and (5,0) structure were built using the tool in HyperChem7.0. The symmetries of the nanotube are D3d, D4d, and D5d respectively. Four different systems were studied in this work as follow: (1) gas-phase SWCNT, (2) SWCNT with 23 water molecules in the a x b x c box, (3) SWCNT with 23 methanol molecules in the a x b x c box, and (4) SWCNT with mixed solvent of water and methanol molecules in the a x b x c box. Energy minima of systems (2) – (4) were carried out by Metropolis Monte carlo (MC) calculation which generate random configurations in regions of space that make the important contributions to the calculation of thermodynamic averages. Then the ab initio and semiemperical with AM1 were used to optimize the structure of the nanotubes. All the normal mode frequencies and IR intensity were calculated using the optimized structures.
To find a function or the displacement pattern of eigenvectors transforming as a particular irreducible representation, the projection operators in group theory have been applied. Consider an arbitrary function F. This function can, in general, be expanded into several irreducible represent ations where α labels the irreducible representations, are the coefficients of the expansion, and the are functions transforming according to the representation α. A projection operator defined by applied to F picks out the symmetry adapted function. In equation is the degeneracy of the irreducible representation β, g the order of the symmetry group, G are the symmetry operations, and ln is the lnth element of the representation matrix. From a given function, and its irreducible presentation, functions can be generating if that function has a “component” or a “non-zero projection” along the irreducible presentation of interest. This explains the name of “projector”. As an example, if there is an orthonormal set Li of the function i1, i2,…,iLi which is used to form the ith irreducible representation of a group by order h, for each operator, R, in the group, by definition we can have:
By producting (1) in [Γ(R)ist ]* and summing all over the symmetrical functions in the group we will have:
Considering is are functions independent from R, the right side of (2) can be written as:
Σsis ΣRΓ(R)ist [Γ(R) ist]* So we have a series of Li terms and each of them are equal to a production of is and a coefficient. These coefficients are following the orthogonality rule:
Now, by introducing
The Eq. 4 gives the following form:
The Pjst is call projection operator. The application of this operator on each it is non-zero only when this function or some of its terms is a function of is. One of the most important application of this operator is projecting function it from any function it. In other words
By use of the projection operator on the base of Lj diagonal elements of a matrix, we can have some it functions, which are the bases for the jth irreducible presentation (Wilson, et al., 1955)
2.4. The relation between projection and transfer operators
Assume that Γk (p) ij is the ijth element of the matrix which shows the pth operator (Op) in k the kth irreducible presentation. By this assumption the operator O k, ij is defined as follows
Where h is group order and Lk is the presentation dimension. If i = j these operators called
Projection operators, Pk,ii, in other words:
The non- diagonalized operators are called Transfer operators or shift operators,
In one-dimensional presentations Pk,ij and Ok,ii are the same and we have no Tk,ij. With use of the above definitions, making the irreducible basis becomes possible in the following way:
At first the point group of the molecule is determined.Then the character of the system (Γangles or Γbonding) is calculated. By use of the standard reduce formulation these characters can be reduced to give the irreducible presentations:
Where h is the order of the group, ng is the number of the symmetry operation in the class of g, χR is the character of reducible presentation and χΓ is the character of irreducible presentation for the symmetric operations of class g. In this part there is a note about the reducing the Cv and Dh point groups. The method of reduce is a different from the normal method of reduce. For more information see from the references (Cotton, 1971; Schafer & Cyvrin, 1971; Strommen & Lippincott, 1972; Alvarino, 1978; Flurry, 1979; Strommen, 1979).
At the next step, the interested function is written by use of the projection operator. A set of the results gives the internal coordinate system for a given point group. There are several examples to illustrate this procedure in Table 1. The geometry and electrical properties of nanotube are very sensitive to dielectric constants. The normal modes also will be changed in the high dielectric constants. With the calculation of the normal modes using the U Matrix it is possible to get the F Matrix from the multiplication of frequency to the U Matrix. Solving the determination of F Matrix versus dielectric can be useful for understanding of the electrical behavior of nanotubes in the quantitative structure activity relationship (QSAR) studies. With use of the resulting coordinate system, the U Matrix (UMAT) can be written easily. These are matrices which perform the linear transformations on the internal coordinates sets (Alvarino & Chammoro, 1980).
2.5. Linear combination of primitive’s harmonic vibrations and UMAT
The molecules and their internal coordinates of D4d have been given in Fig. 2. By following the above steps a complete set of the linear combinations and their normalization coefficients are achieved. The irreducible representations of the symmetry group are given by A and B. These data are given in Table 1. We use the application of projection operator method in finding the coordinate system, and by using it the U matrix is written and finally the frequencies and distributions of peak position are achieved. The (3, 0), (4, 0), (5, 0) zig-zag nanotubes were investigated. They have 66, 138, and 174 normal modes, respectively.
The character of the system assigned by Γ was calculated from the character tables and the UMAT are written from the application of projection operator. Vibrational Calculation was carried out by the MOLVIB algorithms and by Hyper Chem. Calculation and a few sets of calculation were performed. Molecular motions can be assigned by the potential energy distribution (PED) analysis among internal coordinates by the method of the projection operator. There are good agreements between the most cases.
2.6. Normal mode dependence on dielectric
As can be inferred from Table 1 and the Fig. 3, 4, and 5, there are good agreements between the semi and Monte Carlo and even ab initio calculation. In Table 1 the various of intensity and frequency and potential energy from different methods are shown versus the inverse dielectric for some normal modes. From Fig. 3 we have two maximum for both of energy and frequency in the dielectric between 77.40 up to 70.42 and also the third maximum is located in the 61.76. This region range is considered to be the unstable geometry of nanotubes which are very sensitive to dielectric. After these range the frequency, intensity and energy goes toward a stable geometry which are not sensitive to dielectric. The same results are obtained in the insets Fig. B and C of Fig. 3 for D3d of normal mode 61 and 66 respectively. In the Fig 4, similar to normal mode 1 and 131 and 138 are shown with A, B, and C respectively for nano tube (4 0) in D4d point group, a common general behavior is observed in this nanotube as same as (3 0) nanotube, only with a shift in data, this shift is due to the difference between the geometrical structures of two nanotubes.
2.7. Potential energy dependence on the dielectrics of zigzag nanotubes
In Fig. 3 three line of potential energy for three nanotubes are shown by the Monte Carlo calculation versus dielectric constants. For D3d symmetric nanotube, the logarithm of potential energy increases as the dielectric constant reduces from 78.39 up to 76.10 while the D4d and D5d symmetries show an unchanged potential energy in this region. Beyond this point, the potential energy of D4d and D5d nanotubes drop and rise again to be in a new equilibrium, whereas the potential energy of the D3d mostly constant as the dielectric constant decreases. There are some changing in the energy in variable with the dielectrics above 60, and by decreasing the dielectrics the energy of three nanotubes goes toward constant variables. Similar trends between three figures and there are very good agreement with ab initio calculation in the Table 1.
3. Stability of SWCNTs: Solvents and temperature effects by molecular dynamics simulation and quantum mechanics calculations
Structural properties of solvents such as water, methanol, and ethanol surrounding single-walled carbon nanotube (SWCNT) and mixtures of them as well have an effects on the relative energies and dipole moment values. Because some of the physicochemical parameters are elated to structural properties of SWCNT, the different force fields can be examined to determine energy and other types of geometrical parameters, on the particular SWCNT. Because of the differences among force fields, the energy of a molecule calculated using two different force fields will not be the same. The structure of SWCNT as well as its dipole moments and relative energies has been studied by molecular dynamics simulation and quantum mechanics calculations (Monajjemi et al., 2010). The term “Ab Initio" is given to computations which are derived directly from theoretical principles, with no inclusion of experimental data. The most common type of ab initio calculation is called a Hartree-Fock (HF) calculation, in which the primary approximation is called the central field approximation. A method, which avoids making the HF mistakes in the first place, is called Quantum Monte Carlo (QMC). There are several favors of QMC variational, diffusion, and Green's functions. These methods work with an explicitly correlated wave function and evaluate integrals numerically using a Monte Carlo integration. These calculations can be very time consuming, but they are probably the most accurate methods known today. In general, ab initio calculations give very good qualitative results and can give increasingly accurate quantitative results as the molecules in question become smaller (Monajjemi et al., 2008a). In general, there are three steps in carrying out any quantum mechanical calculation. First, prepare a molecule with an appropriate starting geometry. Second, choose a calculation method and its associated options. Third, choose the type of calculation with the relevant options and finally, analyze the results. We will give a short detail of computational method in the following section.
3.1. Molecular mechanics (Monte Carlo simulation)
The Metropolis implementation of the Monte Carlo algorithm has been developed by studying the equilibrium thermodynamics of many-body systems. Choosing small trial moves, the trajectories obtained applying this algorithmagree with those obtained by Langevin's dynamics (Tiana et al., 2007). This is understandable because the Monte Carlo simulations always detect the so-called “important phase space" regions which are of low energy (Liu & Monson, 2005). Because of imperfections of the force field, this lowest energy basin usually does not correspond to the native state in most cases, so the rank of native structure in those decoys produced by the force field itself is poor. In density function theory the exact exchange (HF) for a single determination is replaced by a more general expression of the exchange correlation functional, which can include terms accounting for both exchange energy and the electron correlation, which is omitted from HartreeFock theory:
where E() is the exchange function and EC() is the correlation functional. The correlation function of Lee et al. includes both local and nonlocal terms (Lee et al., 1988).
3.2. Langevin dynamics (LD) simulation
The Langevin equation is a stochastic differential equation in which two force terms have been added to Newton's second law to approximate the effects of neglected degrees of freedom (Wang & Skeel, 2003). These simulations can be much faster than molecular dynamics. The molecular dynamics method is useful for calculating the time-dependent properties of an isolated molecule. However, more often, one is interested in the properties of a molecule that is interacting with other molecules.
3.3. Effect of differenct solvents of temperatures of SWCNTusing molecular dynamics simulation and quantum mechanics calculations
Difference in force field is illustrated by comparing the energy calculated by using force fields, MM+, Amber, and Bio+. The quantum mechanics (QM) calculations were carried out with the GAUSSIAN98 program based on HF/3-21G level. In the Gaussian program a simple approximation is used in which the volume of the solute is used to compute the radius of a cavity which forms the hypothetical surface of the molecule (Witanowski et al., 2002; Mora-Diez et al., 2006). The structures in gas phase and different solvent media such as water, methanol, ethanol, and mixtures of them have been compared. The structure of SWCNT as well as its dipole moments and relative energies has been studied by molecular dynamics simulation and quantum mechanics calculations within the Onsager self-consistent reaction field (SCRF) model using a Hartree-Fock method (HF) at the HF/3-21G level and the structural stability of considered nanotube in different solvent media and temperature (between 309K and 327K) have been compared and analyzed.
Since the influence between a molecule in solution and its medium can describe most simply by using Onsager model, in this model we have assumed that the solute is placed in a spherical cavity inside the solvent. The latter is described as a homogeneous, polarizable medium of dielectric constant. We started our studies with HF/3-21G gas phase geometry and water, methanol and ethanol surrounding SWCNT and mixtures of them as well. The results obtained from Onsager model calculations are illustrated using the energy difference between these conformers which are quite sensitive to the polarity of the surrounding solvent. The solvent effect has been calculated using SCRF model. According to this method, the total energy of solute and solvent, which depends on the dielectric constant has been listed in Table 2.
These energies have been compared with the gas phase total energy CNT at the HF/3-21G level of theory and different solvents, and the graph of energy values versus dielectric constant of different solvents has been displayed at considered temperatures in Fig. 6.
Since the solute dipole moment induces a dipole moment in opposite direction in the surrounding medium, polarization of the medium in turn polarizes the charge distribution in the solvent. The dipole moment value of SWCNT in different solvent media and at different temperatures has been reported in Table 3.
One much more practical approach consists of calculating the molecular volume as defined through the contour of constant electron density, equating this (nonspherical) molecular volume to the radius of an ideally spherical cavity, and adding a constant increment for the closest possible approach of solvent molecules. This latter approach was used in Gaussian when the volume keyword was being used. In this work, we studied the structural properties of water, methanol, and ethanol surrounding SWCNT and mixtures of them as well as using molecular dynamics simulations. We used different force fields for determination of energy and other types of geometrical parameters, on the particular SWCNT. Because of the differences among force fields, the energy of a molecule calculated using two different force fields will not be the same. So, it is not reasonable to compare the energy of one molecule calculated with a particular force field with the energy of another molecule calculated using a different force field. In this study difference in force field illustrated by comparing the energy calculated by using force fields, MM+, AMBER, and BIO+. Theoretical energy values using difference force fields which are the combination of attraction van der Waals forces due to dipole-dipole interactions and empirical repulsive forces due to Pauli repulsion have been demonstrated in Table 4 and Fig. 8.
The result of the calculated dipole moment, quadrupole moment, octapole moment, and hexadecapole moment values of SWCNT has been reported in Table 5, and optimized structures of nanotube in different media are shown in Fig. 9.
4. NMR and IR theoretical study on the interaction of doping metal with carbon nanotube (CNT)
Numerous electrical measurements on SWCNT ensembles have revealed that chemical doping by donors (Li, K, Cs, or Rb) or acceptors (Br2, I2, or acids) decreases the room temperature electrical resistance by up to two orders of magnitude at saturation doping (Kaaoui et al., 1999; Coluci et al. 2006). The important problem is metals passing through cells membrane. Because, there are barriers for them passing through protein canals in cells membrane. Additionally, upon interaction, changes in activity, stability, and solubility ions compatibility may occur in cells. A lot of studies are for replacing protein canals into cells membrane for passing proteins, drug and ions of metal. Therefore the presence of the SWCNT and its consequences to the biological activity of ions metal are of high impact in the development of biosensors, immunoassays and drug delivery systems (Zhang et al., 2005; Ganjali et al., 2006). This work, we used armchair carbon nanotube (5, 5) and (6, 6). Indeed, vibrational frequencies of ﬁnite-length carbon nanotubes were recently examined (Tagmatarchris & Prato, 2004) and another result of 319.9 cm–1 is consistent with oscillations along the radial directions (radial modes), although it cannot be assessed accurately due to the sensitivity to the number of rings (Yumura et al., 2005). We suggest that SWCNT intercalate into cells membrane replacing protein canals and are studying passing metal ions (Na, Mg, Al, and Si) in length of SWCNT by Quantum Mechanics (QM).
4.1. Computational details
The geometry optimizations were performed using an all-electron linear combination of atomic orbitals Hatree–Fock (HF) and density functional theory (DFT) calculations using the Gaussian A7 package. SWCNTs (100–120) from kind of armchair carbon nanotubes (5, 5) and (6, 6) show in Fig. 10. We are interested in the structural features of single-walled carbon nanotube (SWCNT) in the ground state an atomic and amino acids (His and Ser). In HF theory the energy has from:
where ν is the nuclear repulsion energy, ρ is the density matrix, 〈hp〉 is the one electron (kinetic plus potential energy). 1/2 〈Pj(ρ)〉 is the classical coulomb repulsion of the electrons and –1/2 〈Pk(ρ)〉 is the exchange energy resulting from the quantum (fermions) nature of electrons.
In density function theory the exact exchange (HF) for a single determinant is replaced by a more general expression the exchange correlation functional, which can include terms accounting for both exchange energy and the electron correlation, which is omitted from Hartree–Fock theory:
where, E() is the exchange function and EC() is the correlation functional. The correlation function of Lee, Yang, and Parr is includes both local and non-local term (Kar et al., 2006). The optimizations of solids are carried out including exchange and correlation contributions using Becks three parameters hybrid and Lee–Yang–Parr (LYP) correlation [B3LYP]; including both local and non-local terms with the program Gaussian A7 package (Lee et al., 1988; Becke, 1993; Becke, 1997).
Compared to Raman spectroscopy, much less information about the vibration properties of carbon nanotubes can be gained from IR spectra. This limitation mainly results from the strong absorption of SWCNTs in the IR range. Accurate predictions of molecular response properties to external ﬁelds are of general signiﬁcance in various areas of chemical physics. This especially refers to the second-order magnetic response properties (NMR), since the magnetic resonance based techniques have gained substantial importance in chemistry and biochemistry that NMR data shown with two parameters isotropic (σiso) and an isotropic (σaniso) shielding.
4.2. Interaction of Na, Mg, Al, Si with Carbon Nanotube (CNT): NMR and IR Study
The B3LYP and HF by 6–31G and 6–31G* calculaion for the molecular SWCNT models with Na, Mg, Al, and Si considered were validated by the calculated 13C and 1H NMR shifts and thermodynamic properties of an open-ended SWCNT (5, 5) and (6, 6) molecular systems (Monajjemi et al., 2009). The total energy (Etotal) of this interaction is listed in Table 6, which the Etotal increase to converge with an increasing carbon number.
In this study the metals on the center of a hexagon (HC) and muse are related to competitive interactions between ions metal and SWCNTs. The structural electronic and magnetic properties have been investigated. The most stable conﬁguration for Si adsorbed on SWCNTs is also at the (HC) site at competitive another atoms of SWCNT because the electro negativity is the most great. The calculated amounts of Dipole, Quadrupole, Octapole, and Hexa-decapole moments at the HF and B3LYP levels in various basis set are given in Table 7. Hybridizing Coefﬁcient is different in various methods and basis set.
Calculations of the NMR shifts with the magnetic ﬁeld perturbation method of GIAO (gauge in dependent atomic orbital) incorporated with the program Gaussian A7 package. The results of the calculations for the carbon nearest neighbors' atoms in SWCNTs are presented in Table 7. The calculated magnetic shielding in Figs. 11, 12 was converted into σiso, σaniso chemical shifts by 13C absolute shielding in SWCNT (5, 5). They are worth noting that the last approach leads to a substantial improvement in the calculated magnetic properties. Regarding the method for achievement of gauge invariance for the present case, at the B3LYP and HF levels on the other hand at the hybrid B3LYP level, GIAO is found to be slightly superior. The calculated infrared is for C100 at HF/6–31G with Na, Mg, Al, and Si. They showed in Table 2. The properties thermodynamic are decrease with increase electro negativity atoms.
Carbon Nanotubes have been intensively studied due to their importance as building block in nanotechnology. The special geometry and unique properties of carbon Nanotube offer great potential applications, including Nanoelectronic devices, energy storage, gas sensing, chemical probe, electron transport, and biosensors, field emission display, etc. Such devices operate typically on the changes of electrical response characteristics of the Nanowire active component with the application of an externally applied mechanical stress or the adsorption of chemical or bio-molecule. For a better understanding of the physical and electronic properties of single-walled carbon Nanotubes (SWCNTs) at the Nano scale, a challenging task in theoretical calculation is needed in order to design the specific material properties because of the large size of the SWCNTs and their complicated and size dependent electronic structure. Modeling of functionalized Nanotubes and nanostructures for such technologies of SWCNTs can be greatly benefit from the first principles methods based on the density functional theory (DFT). The equilibrium position, adsorption energy, binding energy, charge transfer, and electronic band structures can be computed for different kinds of SWNTs. Effects of surrounding medium and intrinsic structural defects can also be taken into account. In this work we review some recent DFT investigation on the gas-sensing properties and the dielectric properties. Charge transfer and gas-induced charge fluctuation might significantly affect the transport properties of SWNTs. The size and chirality’s of the carbon Nanotubes were typical determined from the SWCNT Raman energy spectra of a peak around 150–300 cm–1, due to the radial breathing mode. Besides, the geometry and electrical properties of Nanotube are very sensitive to dielectric constants which we can observe from the normal mode analysis. A calculation method for identifying the Raman modes of SWCNTs based on the symmetry of the vibration modes has been discussed. The Raman intensity of each vibration mode varies with polarization direction, and the relationship can be expressed as analytical functions. Each Raman active mode of SWCNT can be distinguished from the group theory principle.
In section 2, with the calculation of the normal modes using the U Matrix it is possible to get the F Matrix from the multiplication of frequency to the U Matrix. Solving the determination of F Matrix versus dielectric can be useful for understanding of the electrical behavior of nanotubes in the quantitative structure activity relationship studies. The geometry and electrical properties of nanotube are very sensitive to dielectric constants. The normal modes also will be changed in the high dielectric constants.
In section 3, Ab initio calculations were carried out with GAUSSIAN 98 program at the HF/3-21G level of theory to investigate the effects of polar solvents and different temperatures on the stability of SWCNT in various solvents. The results obtained from Onsager model calculations are illustrated using the energy difference between these conformers which are quite sensitive to the polarity of the surrounding solvent, that the water and methanol solvents can be suggested as the most compatible solvent for studying the structural properties of SWCNT. Also orientation of the water molecules at the CNT-water interface can be affected by the orientation of the water dipole moment. Moreover, among the energy values obtained from different MM+, AMBER, and BIO+ force fields, the AMBER force field is the most proper force field for studying SWCNT.
In section 4, A Quantum Mechanics (QM) is used for investigated the nature of metals transport and interaction with single-walled carbon nanotubes (SWCNTs) inter membranes. Metal species can be transported actively by a combination of SWCNT-membranes conducting channels that have been used for bio-molecular and detection. Ab initio calculations using DFT/B3LYP and HF levels with 6–31G and 6–31G* basis set of theory have allowed the determination of structure electronic, properties thermodynamic, magnetic properties for SWCNTs with Na, Mg, Al, and Si. NMR chemical shielding tensors in the methods framework makes it possible to study the chemical shift of speciﬁc group in carbon nanotubes in absence and presence metals. A comprehensive on effects of atoms on SWCNTs were revealed that it is on its electronic structure: 1) transfer of charge from the atom to the SWCNTs; 2) electrostatic interactions between the delocalized e electrons of the SWCNTs and atoms. The basis set used 6–31G and 6–31G* that increasing electronegativity metals increased the total energy. The proportion SWCNTs were changed by them. The results are presented for T = 310 K, the temperature of human’s body. In fact, it was determined that SWCNT blocked potassium channels in a dose-dependent manner. Fullerenes were discovered to be less effective channel Blockers than CNT. The mechanism was solely dependent on the size and shape of the nano-particles. They also concluded that electrochemical interactions are between CNT and the ion channels.
The work has been supported by Thailand Research Fund (TRF), Thailand Center of Excellence in Physics (ThEP), Center for Innovation in Chemistry (PERCH-CIC), and the National Research University Project under Thailand's Office of the Higher Education Commission, Thailand for financial support.