Abstract
Polyyne and cumulene of infinite length as the typical covalent onedimensional (1D) monatomic linear chains of carbon have been demonstrated to be metallic and semiconductor (Eg = 1.859 eV), respectively, by firstprinciples calculations. Comparing with singlewalled carbon nanotubes, the densities are evidently low and the thermodynamic properties are similar below room temperature but much different at the high temperature range. Polyyne possesses a Young's modulus as high as 1.304 TPa, which means it is even much stiffer than carbon nanotubes and to be the superlative strong 1D material along the axial direction. The Young's modulus of cumulene is estimated to be 760.78 GPa. In addition, polyyne is predicted to be as a onedimensional electronic material with very high mobility.
Keywords:
carbon atomic chains; Young's modulus; heat capacity; singlewalled carbon nanotubesIntroduction
Carbon nanomaterials possess different mechanical and electronic properties when the hybridization of carbon atoms changes from sp, sp^{2 }to sp^{3}. As quasi onedimensional carbon nanostructures, carbon nanotubes [1], composed of sp^{2}/sp^{3}hybridized carbon atoms, possess outstanding mechanical, optical, and electronic properties, offering carbon nanotubes many promising applications as composite materials and sensors, as well as technology areas such as nanoelectronics. Graphene [2], a oneatomthick twodimensional sheet of sp^{2}hybridized carbon atoms, has also attracted increasing attentions due to its excellent thermal conductivity, mechanical stiffness, and extraordinary electronic transport properties, rendering graphene potentially valuable for applications in nanoelectronics, solar cell window layers, and composite materials [3]. Among all carbon nanostructures, carbon atomic chain, comprised of monatomic linear chains of carbon atoms, is a truly onedimensional nanomaterial and has been predicted to have extremely outstanding properties for various applications [46]. Recently, Zhao et al reported the experimental fabrication of monatomic carbon linear chain which was shown to be inside doublewalled carbon nanotubes of 0.7 nm in diameter [4]. Three characteristic Raman shift peaks were observed in the range of 1,790 to 1,860 cm^{1}. Mikhailovskij et al. reported fabrication of freestanding short monatomic carbon linear chains using a developed experimental highfield technique [7]. However, desirable quantity of freestanding polyyne and cumulene samples for experimental characterization has not gotten until now.
Among various possible covalent onedimensional (1D) monatomic linear chains of carbon, cumulene of infinite length (···C ≡ C  C···) constructed with alternate sp conjugated band and sp^{3 }conjugated bond chain and polyyne of infinite length (···C = C = C···) with sp^{2 }conjugated bond chain are typical rigid covalent period conjugated bond chains. Polyynes are found in interstellar molecular clouds where hydrogen is scarce. The longest reported (synthetic) polyyne to date contains 22 acetylenic units and is endcapped with triisopropylsilyl groups [8]. The polyyne of infinite length is the elusive compound called carbyne; linear acetylenic carbon is one of the carbon allotropes [9]. To date, the difference of physical properties in these two types of carbon atomic chains has not been reported. However, there is no effective method reported in the literature to synthesize and characterize freestanding carbon atomic chains. In this investigation, theoretical study of carbon atomic chains properties has been conducted. Two kinds of carbon atomic chains have been investigated by firstprinciples calculations. Periodic carbon atomic chain structure has been created and geometry optimized in order to build a stable structure. Thermodynamic, mechanical, and electronic properties of carbon atomic chains have been calculated, and the results of physical properties are discussed.
Calculations
Firstprinciples calculations have been performed to investigate the physical properties of carbon atomic chains by the pseudopotential plane wave method [10] with the generalized gradient approximation [11] of PerdewBurkeErnzerhof for the exchangecorrelation potential [12].
For all structures, the MonkhorstPack scheme is used in the Brillouin zone with 2 × 2 × 10 for all the geometry optimization and total energy calculations [13]. For all relaxation calculations, the volume of cell is fixed and the structure considered are fully relaxed to accuracy where the selfconsistent field was done with a convergence criterion of 2 × 10^{5 }eV/atom.
Since experiment data on physical properties of singlewalled carbon nanotubes (SWNTs) have been extensively reported [14], the model of a (5,5) SWNT is chosen as a reference for firstprinciples calculation: the physical data are compared in order to confirm the accuracy of calculation method and the feasibility of carbon atomic chain.
With the reference of the distance between two neighbor layers in graphite is 3.42 Å, and linear monatomic carbon linear chain was shown to be inside doublewalled carbon nanotubes of 0.7 nm in diameter, therefore, the smallest distance can be chosen as 3.42 Å between two free carbon atomic chains. The geometrical structure model of (5,5) SWNT, cumulene, and polyyne are shown in Figure 1.
Figure 1. Geometrical structure model. (a) (5,5) SWNTs, (b) cumulene, and (c) polyyne.
The calculated geometrical model of (5,5) SWNT contains 80 carbon atoms, as shown in Figure 1a, with periodic border condition. Structural optimization has been established using a bond length of 1.42 Å, which is slight shorter than that in graphene inducing from the surface curving of the SWNT. The model of cumulene as shown in Figure 1b is built with 12 carbon atoms with alternate sp conjugated band and sp^{3 }bonds and periodic border condition. The length of sp conjugated bond is 0.1264 nm and that of sp^{3 }bond is 0.1476 nm. Polyyne is in the same set as cumulene, as shown in Figure 1c with 12 carbon atoms, and there are only sp^{2 }conjugated bond of length up to 0.1404 nm with periodic border condition.
Results and discussion
The calculated data of (5,5) SWNT, cumulene, and polyyne are listed in Table 1 in which diamond and graphene are included for comparing. At first, the structure stability of cumulene and polyyne is demonstrated to be lower than SWNT because their Gibbs free energy is more minus than that of (5,5) SWNT. Secondly, SWNT has been known as a super light onedimensional material. However, cumulene and polyyne have even much lower density for potential applications as typical onedimensional carbon materials.
Table 1. Calculated data of (5,5) SWNT, cumulene, and polyyne
It has been reported that the experimental Young's modulus of (5,5) SWNT is about 0.3 to 0.6 TPa with zero bandgap [15,16]. The calculated Young's modulus of SWNTs in this investigation is 805.12 GPa, which is quite close to the experiment data, demonstrating the successful application of the firstprinciples theory to calculate the mechanical properties of carbon nanoscale structures. The mechanical properties and bandgap energy of (5,5) SWNTs and carbon atomic chains are listed in Table 1.
The calculated Young's modulus of polyyne is as high as 1,304.19 GPa, which is much larger than that of (5,5) SWNTs, cumulene (760.78 GPa), or any known materials. The high Young's modulus of polyyne can be attributed to the high strength of sp^{2 }conjugated bonds. We note, however, that in the SWNT structure, the carbon bonds may be considered as a hybrid sp^{x }(2 < x < 3) bond, which is much weaker than sp^{2 }conjugated bond. In the cumulene structure, there exists the single sp^{3 }bond, which is even weaker than the sp^{x }(2 < x < 3) bond in SWNT structure. Therefore, we conclude that polyyne possesses the highest strength along its axial compared to any other materials.
The calculation results show that cumulene is a semiconductor (Eg = 1.859 eV), but polyyne is metallic. As we know, the electronic conductivity of carbon structures comes from enlarged moving range of electrons through sp^{2 }conjugated bonds, which decrease the system energy level and result in the effect of the electron mobility increasing significantly [1720]. Because of a single sp^{3 }carbon bond in the cumulene structure, the electronic conductivity is much lower than that of polyyne, and the bandgap energy of cumulene widens and renders cumulene to be a semiconductor.
The specific heat capacity chart of cumulene in Figure 2 shows that heat capacity increases with increasing temperature. According to the thermal equation:
Figure 2. Specific heat capacity sketch of cumulene, polyyne and (5,5) SWNT.
where K is the coefficient of heat conductivity, c is specific heat capacity, m is mass, and X replaces other parameters. Specific heat capacity is proportional to heat capacity; therefore, the coefficient of heat conductivity is proportional to heat capacity [21]. It can be noticed that the heat conductivity coefficient of cumulene increases with rising temperature.
SWNT is a onedimensional super lowdensity material, with very high Young's modulus. In this investigation, the heat capacity chart is calculated and shows a trend rises with increasing temperature gradually, as shown in Figure 2. Comparing at 300 K, the specific heat capacities of cumulene, polyyne, and (5,5) SWNT are about 1.307, 1.162, and 0.174 J g^{1 }K^{1}, respectively. The specific heat capacity of (5,5) SWNT is about an order smaller than that of the cumulene and polyyne. Meanwhile, the increasing rate of the specific heat capacity of (5,5) SWNT is slower grading as the temperature increases from 300 K. These results indicate that the thermodynamic properties of cumulene and polyyne are different obviously from that of SWNTs. SWNT has been known as a super onedimensional material with very high Young's modulus and low density for application in many fields. However, cumulene and polyyne have even much lower density and extremely high Young's modulus for some potential applications.
On the other hand, lowdimensional carbon materials, such as carbon nanotubes and graphene, have been reported to have very high mobility values of 100,000 cm^{2}/V·s [22] and 200,000 cm^{2}/V·s [23] at room temperature, respectively. The reason for such high mobility is related to the carbon structure of sp^{x }conjugation. For example, graphite with similar carbon structure is a good conductor of electricity. The mobility of charges in graphite is as high as 20,000 cm^{2}/V·s at room temperature. Graphite is also strong, lightweight, and an excellent conductor of heat. The mobilities in nanotubes and graphenes turn out to be even higher than in graphite because lowdimensional carbon structures of sp^{x }conjugation behave as highmobility electron gases. Another reason may lie in the quantum confinement nature of the lowdimensional carbon structure, which is harder to scatter electrons in lowdimensional confined structure. According to the typical structure of polyyne, it has the most favorable quantum confined carbon structure of sp^{x }conjugation for possessing a possible super high electron mobility and super conductivity as well. However, cumulene may have a relatively lower electron mobility due to its sp conjugated band and sp^{3 }bond alternate chain structure. Electrons can only go forward or backward but not sideways. Metallic carbon atomic chains can behave as onedimensional electron gases, having outstanding properties in bandgap energy as well as Young's modulus. Indeed, the results of this investigation suggest that monatomic carbon linear chains, cumulene and polyyne, have promising potential application in many fields.
Conclusions
Firstprinciples calculations have been performed to investigate the properties of covalent onedimensional (1D) monatomic linear chains of carbon. Polyyne and cumulene of infinite length, as the two typical chains, have been studied with SWNT, graphene, and diamond to reveal the fundamental and technologically interesting features. The Young's modulus of polyyne has been demonstrated to be high as 1.304 TPa, which is even much higher than that of (5,5) SWNT (0.805 TPa) and diamond (1.050 TPa). This means that polyyne is an extremely strong 1D material along the axial direction. Specific heat capacity analysis shows that the thermodynamic properties of cumulene and polyyne are different obviously from those of SWNTs and that cumulene and polyyne have much larger specific heat capacity. According to the typical electronic structure of polyyne, a super high electron mobility is predicted to exist in the most favorable quantum confined electron gas structure in 1D. Cumulenes as a semiconductor (Eg ≈ 1.859 eV) and polyynes as a metallic monatomic chains are distinguished from other organic chains by their rigidity, which makes them promising for applications in nanotechnology.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
YZ carried out the study and drafted the manuscript. YS participated in the sequence alignment. LW participated in the design of the study and sequence alignment. ESK participated in the sequence alignment. XC participated in the sequence alignment. YZ participated in the design of the study and sequence alignment.
Acknowledgements
We acknowledge the financial supports from National Natural Science Foundation of China (no. 50730008, 61006002), Shanghai Science and Technology Grant (no. 1052nm02000), and the support from the UM/SJTU Collaborative Research Program in Renewable Energy Science and Technology.
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