Non-regular hexagonal 2D carbon, an allotrope of graphene: a first-principles computational study.

In a first principle computational study, using density functional theory, we have identified four types of 2D carbon sheets, similar to graphene, made entirely of non-regular hexagons. In one case, we get a structure where the non-regular hexagons have four sides of length d1 = 1.416 Å and two sides of length d2 = 1.68 Å. Next case, in the non-regular hexagons the side d1 (two times) and d2 (four times) are exchanged. In two other cases, the non-regular hexagons have three pairs (opposite sides) of different lengths (d1 = 1.529 Å, d2 = 1.567 Å, and d3 = 1.612 Å; d1 = 1.387 Å, d2 = 1.348 Å, and d3 = 1.387 Å). By propper choice of the non-regular hexagon sides, one could arrive at a 2D carbon system like graphene, but with a tunable band gap. The structure is more stable when the system has more number of regular C-C bonds than the longer C-C bonds. Due to its non-regular hexagons, special atomic configuration, this system may have, like graphene, unusual properties. It is semiconducting, and there is no need to functionalize it for opening the band gap as is the case with graphene.

Activation of CO and CO2 on homonuclear boron bonds of fullerene-like BN cages: first principles study.

Using density functional theory we investigate the electronic and atomic structure of fullerene-like boron nitride cage structures. The pentagonal ring leads to the formation of homonuclear bonds. The homonuclear bonds are also found in other BN structures having pentagon line defect. The calculated thermodynamics and vibrational spectra indicated that, among various stable configurations of BN-60 cages, the higher number of homonuclear N-N bonds and lower B:N ratio can result in the more stable structure. The homonuclear bonds bestow the system with salient catalytic properties that can be tuned by modifying the B atom bonding environment. We show that homonuclear B-B (B2) bonds can anchor both oxygen and CO molecules making the cage to be potential candidates as catalyst for CO oxidation via Langmuir-Hinshelwood (LH) mechanism. Moreover, the B-B-B (B3) bonds are reactive enough to capture, activate and hydrogenate CO2 molecules to formic acid. The observed trend in reactivity, viz B3 > B2 > B1 is explained in terms of the position of the boron defect state relative to the Fermi level.

Single walled carbon nanotube-metal oxide nanocomposites for reversible and reproducible storage of hydrogen.

Composite material consisting of single walled carbon nanotubes (SWCNTs) and metal oxide nanoparticles has been prepared and their hydrogen storage performance is evaluated. Metal oxides such as tin oxide (SnO2), tungsten trioxide (WO3), and titanium dioxide (TiO2) are chosen as the composite constituents. The composites have been prepared by means of ultrasonication. Then, the composite samples are deposited on alumina substrates and at 100 °C in a Sieverts-like hydrogenation setup. Characterization techniques such as transmission electron microscopy (TEM), Raman spectroscopy, scanning electron microscopy (SEM), powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, energy dispersive spectroscopy (EDS), CHN elemental analysis, and thermogravimetric (TG) measurements are used to analyze the samples at various stages of experiments. Hydrogen storage capacity of the composites namely, SWCNT-SnO2, SWCNT-WO3, and SWCNT-TiO2 are found to be 1.1, 0.9, and 1.3 wt %, respectively. Hydrogenated composite samples are stable at room temperature and desorption of hydrogen is found to be 100% reversible. Desorption temperature ranges and binding energy ranges of hydrogen have been measured from the desorption studies. The hydrogenation, dehydrogenation temperature, and binding energy of hydrogen fall in the recommended range of a suitable hydrogen storage medium applicable for fuel cell applications. Reproducibility and deterioration level of the composite samples have also been examined.

The interaction of nitrogen molecules with (4, 0) single-walled carbon nanotube: electronic and structural effects.

The electronic structure and energetics of (4, 0) single-walled carbon nanotubes (CNTs) interacting with nitrogen have been studied using density-functional calculations. We show that the nanotubes become covered with a stable sheath of N(2) molecules. We have constructed potential energy curves which can be used for the thermodynamic analysis of N(2) adsorption and desorption processes. Our results show that any analysis of the observed properties (for example thermodynamics, stability, and photoluminescence) of air-exposed CNTs needs to consider the N(2) adsorbed on the CNTs.