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Alok Sharan

Publications and source records attributed to Alok Sharan.

12 recordsLinked to original sources

Unified Framework for Bidirectional and Cyclic Teleportation under Noise

Quantum teleportation has evolved from single-qubit, unidirectional communication to multi-qubit and multidirectional protocols. However, most existing schemes rely on protocol-specific entangled resources, motivating the development of universal quantum channels capable of supporting multiple communication tasks simultaneously. In this work, we demonstrate that a single twelve-qubit entangled channel exhibits such versatility by enabling the bidirectional teleportation of arbitrary three-qubit states and the cyclic teleportation of arbitrary two-qubit states through local Bell-state measurements and single-qubit operations. Both protocols are further generalized to multi-qubit and multi-party configurations, establishing the scalability of the proposed framework. To assess its practical applicability, the protocols are analyzed under amplitude-damping, phase-damping, bit-flip, phase-flip, and depolarizing noise channels by plotting the teleportation fidelity as a function of both the input-state parameters and noise strength. The analysis reveals distinct noise sensitivities, with the bidirectional protocol remaining perfectly faithful under bit-flip noise for all input states and noise strengths, while the cyclic protocol is consistently more vulnerable to environmental disturbances. The proposed schemes achieve an intrinsic efficiency of $25\%$, which is compared with several existing protocols. The framework therefore provides a scalable and resource-efficient approach to unified quantum communication in realistic noisy quantum networks.

quant-ph

Enhanced Two-Way Teleportation of Entangled States with Six-Qubit Cluster State

This work presents a two-way teleportation protocol for the transfer of an unknown two-qubit quantum state between two parties Alice and Bob, utilizing a six-qubit cluster state. This bidirectional exchange is achieved by performing Bell measurements on the qubit pairs of Alice and Bob, ensuring the successful teleportation of the quantum state for both parties. We demonstrate the proposed protocol by designing a teleportation circuit that incorporates the necessary quantum gates. The fidelity of the teleportation process is evaluated through simulations, confirming the accuracy and reliability of the proposed scheme. The protocol restores teleported states without requiring CNOT operations or auxiliary qubits, offering a significant advantage in resource efficiency(utilization). A comparative analysis of the intrinsic efficiency with previous approaches establishes that the proposed protocol brings forth an efficient approach for achieving two-way quantum teleportation.

quant-ph

Configurable controlled teleportation using multipartite GHZ states

We propose a controlled quantum teleportation protocol for securely transferring an unknown $n$-qubit state from a sender to a receiver, under the supervision of $m$ controller participants. The protocol uses $n$ copies of an $m$-qubit Greenberger-Horne-Zeilinger state as the quantum resource. Message qubits can be distributed among participants to enhance security against targeted external attacks. Each intermediate party may hold at most one resource qubit, reducing the total number of resource qubits required. The sender selects the end receiver during protocol execution, ensuring anonymity and minimizing the risk of interception by an external eavesdropper. We assess the protocol's performance by calculating teleportation fidelities for various $m$ and $n$ values and visualize the quantum states through Hinton diagrams. The results confirm the protocol's effectiveness for secure quantum communication in multi-party settings.

quant-ph

Ab initio insights on the ultrafast strong-field dynamics of anatase TiO$_2$

Electron dynamics of anatase TiO$_2$ under the influence of ultrashort and intense laser field is studied using the real-time time-dependent density functional theory (TDDFT). Our findings demonstrate the effectiveness of TDDFT calculations in modeling the electron dynamics of solids during ultrashort laser excitation, providing valuable insights for designing and optimizing nonlinear photonic devices. We analyze the perturbative and non-perturbative responses of TiO$_2$ to 30 fs laser pulses at 400 and 800 nm wavelengths, elucidating the underlying mechanisms. At 400 nm, ionization via single photon absorption dominates, even at very low intensities. At 800 nm, we observe ionization through two-photon absorption within the intensity range of $1\times10^{10}$ to $9\times10^{12}$ W/cm$^2$, with a transition from multiphoton to tunneling ionization occurring at $9\times10^{12}$ W/cm$^2$. We observe a sudden increase in energy and the number of excited electrons beyond $1\times10^{13}$ W/cm$^2$, leading to their saturation and subsequent laser-induced damage. We estimate the damage threshold of TiO$_2$ for 800 nm to be 0.1 J/cm$^2$. In the perturbative regime, induced currents exhibit a phase shift proportional to the peak intensity of the laser pulse. This phase shift is attributed to the intensity-dependent changes in the number of free carriers, indicative of the optical Kerr effect. Leveraging the linear dependence of phase shift on peak intensities, we estimate the nonlinear refractive index ($n_2$) of TiO$_2$ to be $3.54\times10^{-11}$ cm$^2$/W.

physics.optics

Quasiparticle electronic structure and optical response ($G_0W_0$+BSE) of anatase TiO$_2$ starting from modified HSE06 functionals

The quasiparticle electronic structure and optical excitation of anatase TiO$_2$ is determined within the framework of many-body perturbation theory (MBPT) by combining the $G_0W_0$ method and the Bethe-Salpeter Equation (BSE). A modified version of the HSE06 screened hybrid functional, that includes 20\% exact Fock exchange (HSE06(20)) as opposed to 25\% in the standard HSE06 functional, is used to set up the starting Hamiltonian for $G_0W_0$+BSE calculations. The HSE06(20) functional accurately predicts the ground state electronic band structure. BSE calculations based on data from $G_0W_0$+HSE06(20) yield direct optical excitation energies and oscillator strengths in excellent agreement with existing experiments and theoretical calculations characterizing direct excitation. In particular, an exciton binding energy of 229 $\pm$ 10 meV is obtained, in close agreement with experiments. The projections of excitonic states onto the quasiparticle band structure in a fatband representation shows that the lowest optical transition of anatase TiO$_2$ consists of excitons originating from the mixing of direct transitions within band pairs running parallel to the $\Gamma -Z $ direction in the tetragonal Brillouin zone. This implies a strong spatial localization of excitons in the $xy$ plane of the lattice. This investigation highlights the importance of a suitable non-interacting Hamiltonian for the MBPT based quasiparticle $G_0W_0$ and subsequent BSE calculations and suggests HSE06(20) as an optimal choice in the case of anatase TiO$_2$.

cond-mat.mtrl-sci

Study of a bi-axial (KTP) crystal using Double Stokes Mueller Polarimetry

We report the significance of the double Stokes Mueller polarimetry (DSMP) technique, to characterize a large size (3 X 3 X 5mm) KTP (Potassium titanyl phosphate) crystal. The crystal undergoes second harmonic generation with type II phase matching. The study of standard KTP crystal using the DSMP technique helps to validate the efficiency of this technique. We were able to extract the crystal's double Mueller matrix, the relative contribution of the susceptibility tensor components, the phase difference between the susceptibility tensor components, etc. We could determine the crystal axes orientation using this optical technique, which was not possible through a single crystal X-Ray diffraction technique for such a large size crystal for which both optic axes and crystallographic axes are the same. Axes direction determined from polarization microscope measurements and Laue diffraction measurements on KTP crystal is compared with those obtained from DSMP measurements.

physics.optics

Detection of excited state absorption cross-section of porphyrin through cw and femto-second laser pump-probe technique

We report on direct detection of excited states absorption cross-section using dual wavelength pump-probe technique. Also, we experimentally demonstrate using porphyrin composite molecules (porphyrin derivatives such as 5,10,15,20-meso-tetrakis phenyl porphyrin (H2TPP), 5,10,15,20 - meso-tetrakis(4-hydroxyphenyl) porphyrin (H2TPP(OH)4)). The cw laser at 761 nm wavelength is used as a pump to maintain excited state population. Changes in the population of excited states lead to the change in transmission are monitored using femto-second probe pulses of 130 fs width and repeated at a 1kHz rate with central wavelength around 800 nm. Transmittance changes due to excited state population are modeled using rate equation approach. The effect of the absorption on the transmitted pulse shape has been discussed as a function of fluence. Obtained excited state absorption cross-sections of H2TPP and H2TPP(OH)4 doped boric acid glass (BAG) films are 4.9X10-18 cm2 and 1.2X10-17 cm2 respectively.

physics.optics

A Method to Determine the Ultrafast Laser Beams Spot Size

From the standard TEM00 Gaussian beam profile equations, we have derived the equations for beam waist at lens focus as a function of variable spot size. In this process, we obtained two equations for beam waist and the validity of these equations is studied with respect to Rayleigh length. The physical validity of the equations has been theoretically checked and also experimentally verified with He-Ne laser at 632 nm. The derived equations are useful for the estimation of the spot size of high peak power lasers (those spot sizes less than few mm). In complicated experimental setup by inserting a beam splitter, we can walk out the some of the beam and the spot size of this beam at the particular position can be measured by normal methods (pinhole and knife-edge techniques). By using our derived equations we can know the spot size of the beam at any position in the experimental setup form the measured spot size.

physics.gen-ph

Third order nonlinear study of ZnO nano particles under femto-second laser illumination

ZnO nano particles are synthesized at different percentages of Ag dopant by facile precipitation method. Two photon absorption (2PA) cross-section and nonlinear refractive index of ZnO nano particles are studied with 130 femto-second laser pulses at a repletion rate of 1 kHz with central wavelength of 532 nm by z-scan technique. The 2PA cross-section of ZnO nano particles are obtained by theoretical calculations, using rate equation approach. Both absorption cross-section and nonlinear refractive index increased with increasing the Ag dopant percentage. We have observed an increase of order of 104 in the nonlinear refractive index in the presence of femto-second laser excitation with reference to nano-second laser excitation.

physics.optics

Nonlinear Spectroscopic Study of Porphyrin Under cw and Femto-second Laser Pulse Excitation

Single Beam Transmittance (SBT) was used as nonlinear spectroscopic tool to investigate the absorption cross-sections and lifetimes of Tetra Phenyl porphyrin (H2TPP) and its OH- group derivative (H2TPP(OH)4) doped in boric acid glass (BAG). We have used 671 nm wavelength as exciting wavelength for both CW (incident intensity up to 1010 W/cm2) and femto-second laser pulse (up to fluence of 102 mJ/cm2). Under cw laser excitation, H2TPP doped BAG demonstrates Double Saturable Absorber (DSA) behavior whereas H2TPP(OH)4 doped BAG act as Revere Saturable Absorber (RSA). Rate equation model espouses to extract the spectroscopic parameters from the experimental data. Excited state life times and absorption cross-sections were obtained as parameters for theoretical fit on SBT data. Porphyrin molecules act as four level systems under cw laser excitation, whereas in the presence of femto-second laser excitation they act as a two level system. We have derived the equations for transmitted energy through the material in the presence of femto-second laser illumination. Both systems viz., H2TPP and H2TPP(OH)4 doped BAG behaves as saturable absorbers when excited by femto-second laser pulses.

physics.optics

Spatial self-phase modulation in the H2TPP(OH)4 doped in Boric Acid Glass

Self-diffraction rings or spatial self-phase modulation (SSPM) was observed in tetra-phenyl porphyrin derivative 5,10,15,20 - meso-tetrakis (4-hydroxyphenyl) porphyrin (H2TPP(OH)4) doped in boric acid glass (BAG) at 671 nm excitation wave-length lying within the absorption band of sample with TEM00 mode profile. Intensity modulated Z-scan was performed on these systems to study the thermal diffusion and to estimate the thermo-optic coefficients. The results obtained from self-diffraction rings experiment and modulated Z-scan are compared and analyzed for different concentration.

physics.optics

Generalized Stokes vector for three photon process

Stokes Muller formalism is important to understand the optical properties of materials by measuring the change in the polarization state of light upon scattering. The formalism can be extended to nonlinear scattering processes involving two and three photon processes. In this work, we derive a triple Stokes vector analytically using operator approach used in quantum theory of light. A three photon polarization state can be described by Stokes vector that has sixteen components involving cubes of intensities. The response of a material for the scattering of light in a three photon process is described by 4 x 16 Muller matrix. Polarization in Polarization out (PIPO) experiments can be carried out to determine the elements of Muller matrix. For that we identify 16 independent points in Poincare sphere and construct triple Stokes vector for each point. Four measurements to find the linear Stokes vector of the scattered light for incident light in each of the sixteen three photon states determine the Muller matrix of the sample.

physics.optics