Kinetics of Topological Stone-Wales Defect Formation in Single Walled Carbon

Topological Stone-Wales defect in carbon nanotubes plays a central role in plastic deformation, chemical functionalization, and superstructure formation. Here, we systematically investigate the formation kinetics of such defects within density functional approach coupled with the transition state theory. We find that both the formation and activation energies depend critically on the nanotube chairality, diameter, and defect orientation. The microscopic origin of the observed dependence is explained with curvature induced rehybridization in nanotube. Surprisingly, the kinetic barrier follows an empirical Br{\o}nsted-Evans-Polanyi type correlation with the corresponding formation energy, and can be understood in terms of overlap between energy-coordinate parabolas representing the structures with and without the defect. Further, we propose a possible route to substantially decrease the kinetic activation barrier. Such accelerated rates of defect formation are desirable in many novel electronic, mechanical and chemical applications, and also facilitate the formation of three-dimensional nanotube superstructures.Comment: 10 pages, Supporting information, The Journal of Physical Chemistry C (2015

Structure, electronic properties and magnetic transition in manganese clusters

We systematically investigate the structural, electronic and magnetic properties of Mn$_n$ clusters ($n =$ 2$-$20) within the {\it ab-initio} pseudopotential plane wave method using generalized gradient approximation for the exchange-correlation energy. A new kind of icosahedral structural growth has been predicted in the intermediate size range. Calculated magnetic moments show an excellent agreement with the Stern-Gerlach experiment. A transition from ferromagnetic to ferrimagnetic Mn$-$Mn coupling takes place at $n=$ 5 and the ferrimagnetic states continue to be the ground states for the entire size range. Possible presence of multiple isomers in the experimental beam has been argued. No signature of non-metal to metal transition is observed in this size range and the coordination dependence of $d-$electron localization is discussed.Comment: 11 Pages and 9 Figures. Physical Review B (in press

Structure, reactivity and electronic properties of V-doped Co clusters

Structures, physical and chemical properties of V doped Co$_{13}$ clusters have been studied in detail using density functional theory based first-principles method. We have found anomalous variation in stability of the doped clusters with increasing V concentration, which has been nicely demonstrated in terms of energetics and electronic properties of the clusters. Our study explains the nonmonotonic variation in reactivity of Co$_{13-m}$V$_m$ clusters towards H$_2$ molecules as reported experimentally [J. Phys. Chem. {\bf 94}, 2744 (1990)]. Moreover, it provides useful insight into the cluster geometry and chemically active sites on the cluster surface, which can help to design better catalytic processes.Comment: 10 pages, 9 figures, 4 table

Engineering the magnetic properties of the Mn13_{13} cluster by doping

With a goal to produce giant magnetic moment in Mn$_{13}$ cluster which will be useful for practical applications, we have considered the structure and magnetic properties of pure Mn$_{13}$ cluster and substitutionally doped it with X = Ti, V, Cr, Fe, Co, Ni atom to produce Mn$_{12}$X clusters. We find that Ti and V substitutions in Mn$_{13}$ cluster are the most promising in terms of gaining substantial binding energy as well as achieving higher magnetic moment through ferromagnetic alignment of atom-centered magnetic moments. This has been demonstrated in terms of energetics and electronic properties of the clusters. For comparison, we have also studied the effect of N-capping of Mn$_{13}$ cluster, predicted in the earlier work [Phys. Rev. Lett. {\bf 89}, 185504 (2002)] as a means to produce stable giant magnetic moment in Mn clusters upto cluster size of 5 Mn atoms.Comment: 8 pages, 9 figures, 2 table