Asymmetry of mass and charge division in spontaneous fission

The order-disorder model has been used to explain asymmetry of mass and charge division and related phenomena in fission. According to this model the fission process involves two steps consisting of charge polarisation into two ‘impending fragment clusters’ with beta stable neutron numbers and subsequent distribution of the balance neutrons between the two. Mode of elemental division of the fissioning nuclei is attributed to the charge polarisation in the first step. Theory of reaction rate has been applied to the system. The frequency term is obtained by applying the conditional stochastic process under charge polarisation constraint and the energy-dependent term is given by the condition of minimum in free energy of the system. Using this, the relative probability of polarisation into given charge pair is arrived at. The model uses stable neutron numbers for the charges as the only input. No explicit assumption or quantification on the preference of formation of shell closure species in fission is necessary. The statistics developed on the principle of equala priori probability of all charge polarisation is used. The shell effects come into play only in deciding a stable neutron number for the charges. The total isotopic yield distribution for a number of fission reactions shows asymmetry in the actinide region which reduces with increasing mass/charge of the fissioning nuclide and bunching of the higherz peaks. Although the mass yields obtained therefrom for a number of fission reactions agree with experimental results, the peaks of the distributions are slightly shifted away from the symmetric point and the distributions are somewhat narrower. Charge distribution parameters obtained from these results are also presented.     

Oxidation of alcohols to carbonyl compounds with chromium(V) reagents

Two pentavalent chromium complexes have been used effectively for the oxidation of alcohols to carbonyl compounds.     

Curie temperature of a spin-one bethe lattice

The exact expression for the Curie temperature of a spin-1 Bethe lattice with dipolar and quadrupolar interactions is derived and the nature of variation of the Curie temperature with quadrupolar interaction constant is studied.     

Impact of Halo Doping on the Subthreshold Performance of Deep-Submicrometer CMOS Devices and Circuits for Ultralow Power Analog/Mixed-Signal Applications

In addition to its attractiveness for ultralow power applications, analog CMOS circuits based on the subthreshold operation of the devices are known to have significantly higher gain as compared to their superthreshold counterpart. The effects of halo [both double-halo (DH) and single-halo or lateral asymmetric channel (LAC)] doping on the subthreshold analog performance of 100-nm CMOS devices are systematically investigated for the first time with extensive process and device simulations. In the subthreshold region, although the halo doping is found to improve the device performance parameters for analog applications (such as g_m/I_d, output resistance and intrinsic gain) in general, the improvement is significant in the LAC devices. Low angle of tilt of the halo implant is found to give the best improvement in both the LAC and DH devices. Our results show that the CMOS amplifiers made with the halo implanted devices have higher voltage gain over their conventional counterpart, and a more than 100% improvement in the voltage gain is observed when LAC doping is made on both the p- and n-channel devices of the amplifier     

Remotely controlled electro-responsive on-demand nanotherapy based on amine-modified graphene oxide for synergistic dual drug delivery

This study focuses on the development of a new electric field responsive graphene oxide (GO) nanoparticle system for on-demand drug delivery. Today, GO is an attractive option adopted in various biological applications for its exclusive features such as flexibility, conductiveness, cost-effectiveness, and external stimuli-responsive nature. It is usual to utilize multiple drugs in cancer treatment. This kind of therapy has lesser side-effects, drug resistance, and is more effective than utilizing only one drug. This study aims to determine low-voltage-controlled dual drug (aspirin and doxorubicin) release from GO surface. Here, we have demonstrated how to control the drug release rate remotely with a handy mobile phone, with zero passive release at idle time. In addition, the study focused to estimate the synergism of aspirin with doxorubicin in the release mechanism from GO in the presence of external voltage, using the spectroscopic method. Moreover, we observed aspirin- and doxorubicin-induced synergistic antitumor activity in MDA-MB 231 (breast cancer cell) in vitro. Thus, our study presents a noble combination of aspirin and doxorubicin that could be utilized for remotely controlled on-demand drug delivery for triple negative breast cancer treatment, using GO as a carrier.     

Order parameter modeling of fluid dynamics in narrow confinements subjected to hydrophobic interactions

A novel phase-field approach is developed for quantitative modeling of the complex thermophysics over reduced length scales in narrow fluidic confinements, as induced by the surface roughness-hydrophobicity coupling and the consequent hydrodynamic interactions. The method is tested for flows on micro- and nano- corrugated surfaces in narrow confinements, and the agreement with molecular dynamics and lattice Boltzmann simulations is found to be quantitative.     

Entropy and temperature of a static granular assembly: an ab initio approach

We construct a statistical framework for static assemblies of deformable grains which parallels that of equilibrium statistical mechanics but with a conservation principle based on the mechanical stress tensor. We define a state function that has all the attributes of entropy. In particular, maximizing this function leads to a well-defined granular temperature and the equivalent of the Boltzman distribution for ensembles of grain packings. Predictions of the ensemble are verified against simulated packings of frictionless, deformable disks.     

Giant enhancement in low energy photoemission of ar confined in C60

Considering an Ar atom endohedrally sequestered in C60, a phenomenal increase in the photoionization cross section of the confined atom through the dominant outer 3p channel is predicted. The effect occurs owing to a powerful dynamical coherent interchannel coupling between the atomic and the cage ionization channels which redirects the bulk of oscillator strength from the giant surface plasmon to the atomic ionization.     

Zero kinetic energy spectroscopy of hydroquinone-water (1:1) complex: a probe for conformer assignment

Zero kinetic energy (ZEKE) photoelectron spectroscopy of the hydroquinone-water (HQW) complex was carried out to characterize its S(1)-S(0) resonantly enhanced multiphoton ionization (REMPI) spectrum in terms of the cis and trans conformers. The ZEKE spectra of the hydroquinone isomers show differences in the Franck-Condon (FC) activity of a few ring modes, viz., modes 15, 9b, and 6b, due to the different symmetries of the two isomers. These modes were used as a "diagnostic tool" to carry out the categorical assignment of the REMPI spectrum of the HQW complex. It was found that the FC activity of these diagnostic modes in the cationic ground state (D(0)) of the water complex is similar as that of the monomer. The two lowest energy transitions in the REMPI spectrum of the water complex, 33,175 and 33,209 cm(-1), were reassigned as the band origins of the cis and trans hydroquinone-water complexes, which is opposite of the previous assignment. The intermolecular stretching mode (sigma) of the complex shows a long progression, up to v(')=4, in the cationic ground state and is strongly coupled to other observed ring modes. The Franck-Condon factors for different members in the progression were calculated using the potential energy surfaces computed ab initio. These agree well with the observed intensity patterns in the progression. The ionization potential of the trans and cis complexes was determined to be 60,071+/-4 and 60,024+/-4 cm(-1), respectively.