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Harshavardhan R. Kalluru

Publications and source records attributed to Harshavardhan R. Kalluru.

4 recordsLinked to original sources

Evaluating the transition dipole moment of quantum dots with absorption and angle resolved photo-luminescence spectroscopy

In this manuscript, the evaluation procedure of transition dipole moment (TDM) is discussed. Semiconducting Cd_{x}Zn_{1-x}Se_{y}S_{1-y} alloyed quantum dots (AQDs) are used as the two level emitting system. The AQDs are then self-assembled into monolayers by the Langmuir-Schaefer method. The TDM magnitude and orientation of AQDs are extracted from the absorption spectrum and the angle resolved Photo-luminescence emission spectrum measurements respectively. The TDM of AQDs in vacuum is evaluated as 9.07 D and the anisotropy coefficient shows that the AQD emission is isotropic.

physics.optics↗

Inhibited spontaneous emission of quantum dots weakly coupled to off resonant silver nanoplatelets and silver nanowires

Spontaneous emission (SE) rate of any light emitters directly scales with the locally available modes for photons. The emission rate can be modified, by changing the dielectric environment of light emitters. Generally cavities with modes in resonance to light emission frequency, are used to amplify the light emission rate. The Fermi golden rule predicts that if the cavity modes are offresonant to the emission frequency, then the SE rate is suppressed. In this study, we demonstrate that the SE of colloidal alloyed quantum dots is inhibited by coupling them to chemically synthesized Silver nanowires and Silver nanoplatelet systems. The silver nanoplatelet and silver nanowire plasmonic resonance modes are in ultraviolet and infrared regions of the electromagnetic spectrum. The quantum dots emit in visible region of light. This off-resonant weak coupling of emitters and cavities results in emission rate suppression and is quantified by time resolved photoluminescence (TRPL) measurements. TRPL decay profiles show that the emission rate can be suppressed by coupling self assembled quantum dot monolayers to a single silver nanoplatelet and a single silver nanowire respectively.

physics.optics↗

Selectively strong coupling MoS$_2$ excitons to a metamaterial at room temperature

Light emitters in vicinity of a hyperbolic metamaterial (HMM) show a range of quantum optical phenomena from spontaneous decay rate enhancement to strong coupling. In this study, we integrate monolayer Molybdenum disulfide (MoS$_2$) emitter in near field region of HMM. The MoS$_2$ monolayer has A and B excitons, which emit in the red region of visible spectrum. We find that the B excitons couple to HMM differently compared to A excitons. The fabricated HMM transforms to a hyperbolic dispersive medium at 2.13 eV, from an elliptical dispersive medium. The selective coupling of B Excitons to the HMM modes is attributed to the inbuilt field gradient of the transition. The B exciton energy lies close to the transition point of the HMM, relative to A Exciton. So, the HMM modes couple more to the B excitons and the metamaterial functions as selective coupler. The coupling strength calculations show that coupling is 2.5 times stronger for B excitons relative to A excitons. High near field of HMM, large magnitude and the in-plane transition dipole moment of MoS$_2$ Excitons, result in strong coupling of B excitons and formation of hybrid light-matter states. The measured differential Reflection and Photoluminescence spectra indicate the presence of hybrid light-matter states i.e. Exciton-Polaritons. Rabi splitting of at least 129 meV at room temperature is observed. The low temperature Photoluminescence measurement shows mode anticrossing, which is characteristic feature of hybrid states. Our results show that the HMM works as a energy selective coupler for multi-excitonic systems as MoS$_2$.

physics.optics↗

Spontaneous emission dynamics of $Eu^{ 3+}$ ions coupled to hyperbolic metamaterials

Sub-wavelength nanostructured systems with tunable electromagnetic properties, such as hyperbolic metamaterials (HMMs), provide a useful platform to tailor spontaneous emission processes. Here, we investigate a system comprising $Eu^{ 3+}(NO_{3})_{3}6H_{2}O$ nanocrystals on an HMM structure featuring a hexagonal array of Ag-nanowires in a porous $Al_{2}O_{3}$ matrix. The HMM-coupled $Eu^{ 3+}$ ions exhibit up to a 2.4-fold increase of their decay rate, accompanied by an enhancement of the emission rate of the $^{ 5}D_{0}\rightarrow$ $^{ 7}F_{2}$ transition. Using finite-difference time-domain modeling, we corroborate these observations with the increase in the photonic density of states seen by the $Eu^{ 3+}$ ions in the proximity of the HMM. Our results indicate HMMs can serve as a valuable tool to control the emission from weak transitions, and hence hint at a route towards more practical applications of rare-earth ions in nanoscale optoelectronics and quantum devices.

physics.optics↗