RESUMO
We employ an exact solution of the thermal bath Lindblad master equation with the Liouvillian superoperator that takes into account both dynamic and environment-induced intermode couplings to study the speed of evolution and quantum speed limit (QSL) times of a open multi-mode bosonic system. The time-dependent QSL times are defined from quantum speed limits, giving upper bounds on the rate of change of two different measures of distinguishability: the fidelity of evolution and the Hilbert-Schmidt distance. For Gaussian states, we derive explicit expressions for the evolution speed and the QSL times. General analytical results are applied to the special case of a two-mode system where the intermode couplings can be characterized by two intermode coupling vectors: the frequency vector and the relaxation rate vector. For the system initially prepared in a two-mode squeezed state, dynamical regimes are generally determined by the intermode coupling vectors, the squeezing parameter and temperature. When the vectors are parallel, different regimes may be associated with the disentanglement time, which is found to be an increasing (a decreasing) function of the length of the relaxation vector when the squeezing parameter is below (above) its temperature-dependent critical value. Alternatively, we study dynamical regimes related to the long-time asymptotic behavior of the QSL times, which is characterized by linear time dependence with the proportionality coefficients defined as the long-time asymptotic ratios. These coefficients are evaluated as a function of the squeezing parameter at varying temperatures and relaxation vector lengths. We also discuss how the magnitude and orientation of the intermode coupling vectors influence the maximum speed of evolution and dynamics of the entropy and the mutual information.
RESUMO
In this paper, we consider the thermal bath Lindblad master equation to describe the quantum nonunitary dynamics of quantum states in a multi-mode bosonic system. For the two-mode bosonic system interacting with an environment, we analyse how both the coupling between the modes and the coupling with the environment characterised by the frequency and the relaxation rate vectors affect dynamics of the entanglement. We discuss how the revivals of entanglement can be induced by the dynamic coupling between the different modes. For the system, initially prepared in a two-mode squeezed state, we find the logarithmic negativity as defined by the magnitude and orientation of the frequency and the relaxation rate vectors. We show that, in the regime of finite-time disentanglement, reorientation of the relaxation rate vector may significantly increase the time of disentanglement.
RESUMO
Heavy metal ions are not subject to biodegradation and could cause the environmental pollution of natural resources and water. Many of the heavy metals are highly toxic and dangerous to human health, even at a minimum amount. This work considered an optical method for detecting heavy metal ions using colloidal luminescent semiconductor quantum dots (QDs). Over the past decade, QDs have been used in the development of sensitive fluorescence sensors for ions of heavy metal. In this work, we combined the fluorescent properties of AgInS2/ZnS ternary QDs and the magnetism of superparamagnetic Fe3O4 nanoparticles embedded in a matrix of porous calcium carbonate microspheres for the detection of toxic ions of heavy metal: Co2+, Ni2+, and Pb2+. We demonstrate a relationship between the level of quenching of the photoluminescence of sensors under exposure to the heavy metal ions and the concentration of these ions, allowing their detection in aqueous solutions at concentrations of Co2+, Ni2+, and Pb2+ as low as ≈0.01 ppm, ≈0.1 ppm, and ≈0.01 ppm, respectively. It also has importance for application of the ability to concentrate and extract the sensor with analytes from the solution using a magnetic field.
RESUMO
Graphene-quantum dot nanocomposites attract significant attention for novel optoelectronic devices, such as ultrafast photodetectors and third-generation solar cells. Combining the remarkable optical properties of quantum dots (QDs) with the exceptional electrical properties of graphene derivatives opens a vast perspective for further growth in solar cell efficiency. Here, we applied (3-mercaptopropyl) trimethoxysilane functionalized reduced graphene oxide (f-rGO) to improve the QDs-based solar cell active layer. The different strategies of f-rGO embedding are explored. When f-rGO interlayers are inserted between PbS QD layers, the solar cells demonstrate a higher current density and a better fill factor. A combined study of the morphological and electrical parameters of the solar cells shows that the improved efficiency is associated with better layer homogeneity, lower trap-state densities, higher charge carrier concentrations, and the blocking of the minor charge carriers.