G. Srinivas

Bio: G. Srinivas is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Laves phase & Hydrogen. The author has an hindex of 5, co-authored 14 publications receiving 93 citations.

Thermodynamic and hydrogen-induced structural properties of Ho1−xMmxCo2-hydrides

Abstract: Thermodynamic and hydrogen-induced structural properties of hydrogenated Ho1−xMmxCo2 (x = 0, 0.1, 0.2, 0.3 and 0.4, Mm = mischmetal) alloys have been investigated. The hydrogen absorption pressure-composition isotherms were studied in the temperature range 50–200 °C and pressure range 0.001–1 bar using a Sieverts-type apparatus. The effect of Mm on the equilibrium plateau pressure and hydride stability has been discussed. Structural analyses and hydrogen-induced amorphization of Ho1−xMmxCo2hydrides were performed using powder x-ray diffraction. The structural stability of these alloys upon repeated hydrogenation and dehydrogenation cycles has been investigated. At lower hydriding pressure and temperatures, Ho1−xMmxCo2-hydrides retain their Laves C15 structure; however, the large lattice volume expansion about 24% is observed in the β-phase. The effect of hydrogenation pressure and temperature and Mm concentration on the hydrogen-induced transformation from crystalline Ho1−xMmxCo2-H to amorphous Ho1−xMmxCo2-H and recrystallization into elemental hydrides have been studied and discussed.

Influence of hydrogen absorption?desorption on structural properties of Dy1?xMmxCo2 alloys

Abstract: The effect of hydrogen absorption–desorption on the structural properties of Laves phase Dy1−xMmxCo2 (x = 0.1, 0.3 and 0.5; Mm = mischmetal, a natural mixture of the light rare earth metals containing 50 wt% Ce, 35 wt% La, 8 wt% Pr, 5 wt% Nd and 1.5 wt% of other rare earth elements and 0.5 wt% Fe) alloys has been investigated by means of hydrogen absorption–desorption pressure-composition (PC) isotherms, kinetics of hydrogen absorption and powder x-ray diffraction (XRD). The PC isotherms and kinetics of hydrogen absorption have been studied in the pressure range 0.001–1 bar and temperature range 50–200 °C using Sieverts-type apparatus. The experimental results of the kinetic curves are interpreted using the Johnson–Mehl–Avrami (JMA) model and the reaction order and reaction rate have been determined. The α-, (α+β)- and β-phase regions have been identified from the different slope regions of the PC isotherms and first-order type kinetic plots. The dependence of the reaction rate parameter upon hydriding pressure and temperature in the (α+β)-phase region has been discussed. The effect of hydrogenation pressure, temperature and Mm concentration on the hydrogen-induced transformation from crystalline Dy1−xMmxCo2–H to amorphous Dy1−xMmxCo2–H and decomposition into crystalline (Dy, Mm)H2 and Co have been discussed in detail. Further, the effect of dehydrogenation on the recovery of the crystalline Laves phase structure of Dy1−xMmxCo2 from its decomposed state is presented. This hydrogenation–disproportionation–desorption–recombination (HDDR) process can be conveniently used in powder metallurgy.

Optical switching properties of RCo2-type alloy hydride based solid state device

Abstract: The optical switching properties of a solid state device based on Ho0.6Mm0.4Co2 (HMC) alloy thin film as a switching active layer, water pretreated Nafion membrane as a solid electrolyte, and a transparent conducting indium tin oxide (ITO) as a counterelectrode are investigated. The device is simple and has a reduced layer sequence of HMC/Pd/Nafion/ITO. The reversible optical switching of this device has been studied during electrochemical galvanostatic charging-discharging as well as cyclic voltammetric measurements. Further, the optical switching durability of the device has been tested by repeated electrochemical hydrogenation-dehydrogenation, and the variations in the optical switching properties are discussed. The special characteristic of the device is that it can reversibly switch between a metallic reflecting state and a semiconducting transparent state by a small reversible applied current/voltage indicating the potential substitution for conventional electrochromic devices.

Electromagnetic wave propagation in spatially homogeneous yet smoothly time-varying dielectric media

Abstract: We explore the propagation and transformation of electromagnetic waves through spatially homogeneous yet smoothly time-dependent media within the framework of classical electrodynamics. By modelling the smooth transition, occurring during a finite period τ, as a phenomenologically realistic and sigmoidal change of the dielectric permittivity, an analytically exact solution to Maxwell׳s equations is derived for the electric displacement in terms of hypergeometric functions. Using this solution, we show the possibility of amplification and attenuation of waves and associate this with the decrease and increase of the time-dependent permittivity. We demonstrate, moreover, that such an energy exchange between waves and non-stationary media leads to the transformation (or conversion) of frequencies. Our results may pave the way towards controllable light–matter interaction in time-varying structures.