Resonant spin-flavor precession (RSFP) scenario with twisting solar magnetic fields has been confronted with the solar neutrino data from various ongoing experiments. The anticorrelation apparent in the Homestake solar neutrino data has been taken seriously to constrain (Δm²,φ′) parameter space and the twisting profiles of the magnetic field in the convective zone of the Sun. The twisting profiles, thus derived, have been used to calculate the variation of the neutrino detection rates with the solar magnetic activity for the Homestake, Super-Kamiokande and the gallium experiments. It is found that the presence of twisting reduces the degree of anticorrelation in all the solar neutrino experiments. However, the anticorrelation in the Homestake experiment is expected to be more pronounced in this scenario. Moreover, the anticorrelation of the solar neutrino flux emerging from the southern solar hemisphere is expected to be stronger than that for the neutrinos emerging from the northern solar hemispheres.

We present first-principle calculations of 2D nanostructures of graphene functionalized with hydrogen and fluorine, respectively, in chair conformation. The partial density of states, band structure, binding energy and transverse displacement of C atoms due to functionalization (buckling) have been calculated within the framework of density functional theory as implemented in the SIESTA code. The variation in band gap and binding energy per add atom have been plotted against the number of add atoms, as the number of add atoms are incremented one by one. In all, 37 nanostructures with 18C atoms, $3 \times 3 \times 1$ (i.e., the unit cell is repeated three times along 𝑥-axis and three times along 𝑦-axis) supercell, have been studied. The variation in C–C, C–H and C–F bond lengths and transverse displacement of C atoms (due to increase in add atoms) have been tabulated. A large amount of buckling is observed in the carbon lattice, 0.0053–0.7487 Å, due to hydrogenation and 0.0002–0.5379 Å, due to fluorination. As the number of add atoms (hydrogen or fluorine) is increased, a variation in the band gap is observed around the Fermi energy, resulting in change in behaviour of nanostructure from conductor to semiconductor/insulator. The binding energy per add atom increases with the increase in the number of add atoms. The nanostructures with 18C+18H and 18C+18F have maximum band gap of 4.98 eV and 3.64 eV, respectively, and binding energy per add atom –3.7562 eV and –3.3507 eV, respectively. Thus, these nanostructures are stable and are wide band-gap semiconductors, whereas the nanostructures with 18C+2H, 18C+4H, 18C+4F, 18C+8F, 18C+10F and 18C+10H atoms are small band-gap semiconductors with the band gap lying between 0.14 eV and 1.72 eV. Fluorine being more electronegative than hydrogen, the impact of electronegativity on band gap, binding energy and bond length is visible. It is also clear that it is possible to tune the electronic properties of functionalized graphene, which makes it a suitable material in microelectronics.