• MARYAM ANAFCHEH

      Articles written in Pramana – Journal of Physics

    • N–N bond cleavage and ring expansion at the surface of exchange and substitutional antisite defective boron nitride nanotubes by boron cluster: A density functional theory study

      MARYAM ANAFCHEH NASRIN SHAHBAZ MANSOUR ZAHEDI

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      Functionalisation of nitrogen–nitrogen bonds of antisite defective boron nitride nanotubes (BNNTs), including exchange antisite defect which is produced by the rotation of BN bond, and substitutional antisite defect which is formed by substitution of an N with B, is investigated through their interaction with a $\rm{B^{−}_{6}}$ cluster. The smaller defect formation energies for the substitutional antisite defects indicate that the substitution of an N atom with B atom is easier than rotation of a BN bond. The formation of antisite defects at the edge or near the edges is more favourable than that in the middle of the tubes. When complexation between double ring $\rm{B^{−}_{6}}$ and nitrogen–nitrogen bonds of antisite defective BNNTs occurs, two-fold coordination, double ring configuration of boron cluster and N–N bond cleavage are seen. In the most stable complex, the $\rm{B^{−}_{6}}$ pulls apart the B–N bond and becomes an integral part of the tube by expanding the hexagonal BN ring, while in the other BNNT-B6 clusters, double ring $\rm{B^{−}_{6}}$ acts as a bridge at the top of the decagon. Functionalisation of N–N bonds at the edge or near the edges is more favourable than that in the middle of tubes.

    • BN-Substituted non-classical fullerenes containing square rings

      MARYAM ANAFCHEH ZAHRA ABOLFATHI MANSOUR ZAHEDI

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      We performed density functional calculations to investigate the electronic and magnetic properties of BN-substituted non-classical fullerenes. The substitutional structures, binding energies, energy gaps between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), ionisation potentials, electron affinities, vibrational frequencies and nucleus-independent chemical shifts (NICS) were systematically investigated. The binding energies of the BN-substituted non-classical fullerenes were found to be slightly smaller than those obtained for pure non-classical fullerenes. While the reverse trend was observed for BN-substituted C$_{46}$ and C$_{32}$ fullerenes, it was found that the BN-substituted C$_{62}$ fullerene has bigger ionisation potentials (IP) and smaller electron affinities (EA) than that of their parents. Because of low concentration of BN impurity, the IR spectra in the BN-substituted fullerenes are very similar to those of their parents, which can be considered as two separate regions: a low-frequency region at 200–1000 cm$^{−1}$ corresponding to the out-of-plane bending and breathing modes and a high-frequency region at 1000–1800 cm$^{−1}$ derived from the stretching of C–B, C–N, B–N and C–C bonds. It was shown that diatropic and paratropic ring currents of hexagons and pentagons together with the harshly antiaromatic character of the four-membered ring combine to produce a relatively small NICS at the centre of the C$_{62}$ and C$_{46}$ fullerene cages. The decrease in the antiaromatic and aromatic character of the B$_{2}$N$_{2}$ ring and the adjacent hexagons affects the aromaticity character of the BN-substituted fullerenes.

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