This suggests that the high possibility is to grow αselleck compound -graphdiyne epitaxially on Si(111) substrate. After the epitaxial structure is cooled down, one can remove the substrate by chemical etching. In this way, the isolation of monolayer α-graphdiyne might be obtained in experiments. Figure 1 Crystal structure of α -graphdiyne. (a) A unit cell and (b) a 4×4 supercell. (c) A simplified model to mimic the hopping matrix elements along two carbon triple bonds in α-graphdiyne. Carbon atoms 1 and 6 are at vertices of a hexagon
in α-graphdiyne. The black balls and blue line represent carbon atoms and the crystalline cell, respectively. The band structure and density of Ralimetinib states (DOS) of α-graphdiyne are shown in Figure 2a,b, respectively. The most
important observations from Figure 2a are the linear dispersion near the K point and the zero DOS at the Fermi energy level. However, the corresponding slope of the Dirac cone is obviously smaller ATM Kinase Inhibitor than that of graphene and α-graphyne. This has a big effect on the Fermi velocity, as discussed below. The bonding and antibonding orbitals at the Fermi energy level touch each other and develop two slight flat bands as K approaches M, which correspond to the two peaks near the Fermi level in the DOS plot. Similar to the case of graphene and α-graphyne, the Dirac points are located at the K and K ′, which means that there are even (six) Dirac points in the Brillouin zone, which is in a striking difference from the odd Dirac points observed in topological insulator Bi2Te3[20]. Figure 2 Electronic properties of α -graphdiyne. (a) Band structure
and (b) DOS. (c) First Brillouin zone with the letters designating high-symmetry points. (d) 2D Dirac cone representing the valence and conduction bands in the vicinity of the K and K ′ points. E F is the Fermi energy. Due to the breaking symmetry associated with spin-orbit interaction (SOI) in 2D layered materials, a small band gap will be induced at the Dirac points, which can in principle be used to study the quantum spin Hall effect. The energy bands with SOI (not shown for brevity) open a band gap of 22 ×10-3 meV Tau-protein kinase in α-graphdiyne, and the magnitude is close to the value of graphene [21]. To understand the nature of the Dirac cone in α-graphdiyne, we employ the tight-binding method proposed in [22], where an effective hopping parameter is introduced. It is notable that there are six carbon atoms along the effective hopping direction in α-graphdiyne, as shown in Figure 1, while only four in α-graphyne. This makes it more complex to exploit α-graphdiyne than α-graphyne. To simplify the model, two triple bonds with the hopping parameters t 1 and t 2 for the single and triple carbon bonds are taken. The simplified Hamiltonian equations at the carbon triple bond, i.e., sites 2, 3, 4, and 5, are (1) where E and V are the electron and on-site energies, respectively.