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Prathmesh Deshmukh

Publications and source records attributed to Prathmesh Deshmukh.

7 recordsLinked to original sources

Cavity-Enhanced Activation of Radiatively Suppressed Light-Hole Exciton Emission in Colloidal Nanoplatelets

Light-hole (LH) excitons provide access to well-defined polarization and spin degrees of freedom that are central to quantum photonics and chiral light-matter interactions. Achieving LH emission is challenging because LH states are energetically unfavoured and typically relax non-radiatively. Existing strategies to access LH excitons rely on modifying the electronic band structure through strain, shape anisotropy, or piezoelectric fields, approaches that are material-specific and offer limited post-synthesis tunability. Here we demonstrate an all-photonic route to activate LH exciton emission in colloidal CdSe-CdS nanoplatelets (NPLs) using a distributed Bragg reflector (DBR) cavity, without altering the underlying band structure. In the absence of a cavity mode, the system exhibits amplified spontaneous emission from heavy-hole (HH) states without detectable LH emission at low excitation powers. By spectrally matching a cavity resonance to the LH exciton, cavity-coupled LH emission emerges at significantly lower excitation powers. Temperature-dependent spectroscopy reveals reversible switching between LH- and HH-coupled emission through exciton-cavity detuning, while polarization-resolved and spectrally resolved time-resolved photoluminescence measurements provide independent evidence distinguishing the cavity-coupled LH and HH emission channels. These findings establish cavity engineering as a general materials-level approach for accessing radiatively suppressed optical states.

physics.optics

Opportunities and Challenges of Solid-State Quantum Nonlinear Optics

Nonlinear interactions between single quantum particles are at the heart of any quantum information system, including analog quantum simulation and fault-tolerant quantum computing. This remains a particularly difficult problem for photonic qubits, as photons do not interact with each other. While engineering light-matter interaction can effectively create photon-photon interaction, the required photon number to observe any nonlinearity is very high, where any quantum mechanical signature disappears. However, with emerging low-dimensional materials, and engineered photonic resonators, the photon number can be potentially reduced to reach the quantum nonlinear optical regime. In this review paper, we discuss different mechanisms exploited in solid-state platforms to attain quantum nonlinear optics. We review emerging materials and optical resonator architecture with different dimensionalities. We also present new research directions and open problems in this field.

physics.optics

Direct writing of room temperature polariton condensate lattice by top-down approach

Realizing lattices of exciton polariton condensates has been of much interest owing to the potential of such systems to realize analog Hamiltonian simulators and physical computing architectures. Prior work on polariton condensate lattices has primarily been on GaAs-based systems, with the recent advent of organic molecules and perovskite systems allowing room-temperature operation. However, in most of these room temperature systems, the lattices are defined using a bottom-up approach by patterning the bottom mirrors, significantly limiting the types of lattices and refractive index contrast that can be realized. Here, we report a direct write approach that uses a Focused Ion Beam (FIB) to etch 2D lattice into a planar microcavity. Such etching of the cavity allows for realizing high refractive index contrast lattices. We realize the polariton condensate lattice using the highly photostable host-guest Frenkel excitons of an organic dye small molecular ionic lattice (SMILES).1,2 The lattice structures are defined on a planar microcavity embedded with SMILES using FIB, allowing the realization of lattices with different geometries, including defect sites on demand. The band structure of the lattice and the emergence of condensation are imaged using momentum-resolved spectroscopy. The present approach allows us to study periodic, quasi-periodic, and disordered polariton condensate lattices at room temperature using a top-down approach without compromising on the quantum yield of the organic excitonic material embedded in the cavity.

cond-mat.mtrl-sci

A plug-and-play molecular approach for room temperature polariton condensation

Exciton-polaritons (EP), half-light half-matter quasiparticles that form in optical cavities, are attractive platforms for creating macroscopic coherent states like BECs. EPs based on organic molecules are of particular interest for realizing such states at room temperature while offering the promise of synthetic tunability. However, the demonstrations of such condensates have been limited to a few specific molecular systems1. Here we report a universal platform for realizing molecular polariton condensates using commercial dyes that solves long standing material challenges. This solution is made possible using a new and programable molecular material called small-molecule, ionic isolation lattices (SMILES) with the potential to incorporate a wide array of molecular fluorophores2. We show EP condensation in rhodamine by incorporating it into SMILES lattice placed in a planar microcavity. The SMILES approach overcomes the major drawbacks of organic molecular photophysical systems such as self-quenching, which sets the foundation for realizing practical polaritonic devices operating at ambient temperatures covering wide spectral range.

physics.optics

Highly nonlinear dipolar exciton-polaritons in bilayer MoS$_2$

Realizing nonlinear optical response in the low photon density limit in solid-state systems has been a long-standing challenge. Semiconductor microcavities in the strong coupling regime hosting exciton-polaritons have emerged as attractive candidates in this context. However, the weak interaction between these quasiparticles has been a hurdle in this quest. Dipolar excitons provide an attractive strategy to overcome this limitation but are often hindered by their weak oscillator strength. The interlayer dipolar excitons in naturally occurring homobilayer MoS$_2$ alleviates this issue owing to their hybridization of interlayer charge transfer exciton and intralayer B exciton. Here we demonstrate the formation of dipolar exciton polaritons in bilayer MoS$_2$ resulting in unprecedented nonlinear interaction strengths. A ten-fold increase in nonlinearity is observed for the interlayer dipolar excitons compared to the conventional A excitons. These highly nonlinear dipolar polaritons will likely be a frontrunner in the quest for solid-state quantum nonlinear devices.

cond-mat.mes-hall

Thermalization of fluorescent protein exciton-polaritons at room temperature

Fluorescent proteins (FPs) have recently emerged as a serious contender for realizing ultralow threshold room temperature exciton-polariton condensation and lasing. Our contribution investigates the thermalization of FP microcavity exciton-polaritons upon optical pumping under ambient conditions. We realize polariton cooling using a new FP molecule, called mScarlet, coupled strongly to the optical modes in a Fabry Perot cavity. Interestingly, at the threshold excitation energy (fluence) of ~ 9 nJ/pulse (15.6 mJ/cm2), we observe an effective temperature, Teff ~ 350 +/- 35 K close to the lattice temperature indicative of strongly thermalized exciton-polaritons at equilibrium. This efficient thermalization results from the interplay of radiative pumping facilitated by the energetics of the lower polariton branch and the cavity Q factor. Direct evidence for dramatic switching from an equilibrium state into a metastable state is observed for the organic cavity polariton device at room temperature via deviation from the Maxwell-Boltzmann statistics at k = 0 above the threshold. Thermalized polariton gases in organic systems at equilibrium hold substantial promise for designing room temperature polaritonic circuits, switches, and lattices for analog simulation.

physics.optics

Single and multiband THz Metamaterial Polarizers

We report single and multiband linear polarizers for terahertz (THz) frequencies using cut-wire metamaterials (MM). The MMs are designed by finite element method, fabricated by electron beam lithography, and characterized by THz time-domain spectroscopy. The MM unit cells consist of single or multiple length cut-wire pads of gold on semi-insulating Gallium Arsenide for single or multiple band polarizers. The dependence of the resonance frequency of the single band polarizer on the length of the cut-wires is explained based a transmission line model.

physics.optics