arXiv subjects

Atanu Jana

Publications and source records attributed to Atanu Jana.

4 recordsLinked to original sources

arXiv2024

Surface plasmon-mediated photoluminescence boost in graphene-covered CsPbBr$_3$ quantum dots

The optical properties of graphene (Gr)-covered CsPbBr$_3$ quantum dots (QDs) were investigated using micro-photoluminescence spectroscopy, revealing a remarkable three-orders-of-magnitude enhancement in photoluminescence (PL) intensity compared to bare CsPbBr$_3$ QDs. To elucidate the underlying mechanisms, we combined experimental techniques with density functional theory (DFT) calculations. DFT simulations showed that the graphene layer generates interfacial electrostatic potential barriers when in contact with the CsPbBr$_3$ surface, impeding carrier leakage from perovskite to graphene and enhancing radiative recombination. Additionally, graphene passivates CsPbBr$_3$ surface defect states, suppressing nonradiative recombination of photo-generated carriers. Our study also revealed that graphene becomes n-doped upon contact with CsPbBr$_3$ QDs, activating its plasmon mode. This mode resonantly couples with photo-generated excitons in the perovskite. The momentum mismatch between graphene plasmons and free-space photons is resolved through plasmon scattering at Gr/CsPbBr$_3$ interface corrugations, facilitating the observed super-bright emission. These findings highlight the critical role of graphene as a top contact in dramatically enhancing CsPbBr$_3$ QDs' PL. Our work advances the understanding of graphene-perovskite interfaces and opens new avenues for designing high-efficiency optoelectronic devices. The multifaceted enhancement mechanisms uncovered provide valuable insights for future research in nanophotonics and materials science, potentially leading to breakthroughs in light-emitting technologies.

cond-mat.mtrl-sci↗

arXiv2022

Universal properties of single particle excitations across the many-body localization transition

Understanding the nature of the transition from the delocalized to the many-body localized (MBL) phase is an important unresolved issue. To probe the nature of the MBL transition, we investigate the universal properties of single-particle excitations produced in highly excited many-body eigenstates of a disordered interacting quantum many-body system. In a class of one-dimensional spinless fermionic models with random disorder, we study the finite size scaling of the ratio of typical to average values of the single-particle local density of states and the scattering rates across the MBL transition. Our results indicate that the MBL transition in this class of one-dimensional models of spinless fermions is continuous in nature. For various ranges of interactions in the system, the critical exponent $\nu$ with which the correlation length $\xi$ diverges at the transition point $W_c$, $\xi \sim |W-W_c|^{-\nu}$, satisfies the Chayes-Chayes-Fisher-Spencer(CCFS) bound $\nu \ge 2/d$ where $d$ is the physical dimension of the system. We also discuss why the critical exponent obtained from finite-size scaling of the conventional diagnostic of many-body localization, the level-spacing ratio, strongly violates the CCFS bound while the single-particle density of states and scattering rates are consistent with the CCFS criterion.

cond-mat.dis-nn↗

arXiv2021

Local density of states and scattering rates across the many-body localization transition

Characterizing the many-body localization (MBL) transition in strongly disordered and interacting quantum systems is an important issue in the field of condensed matter physics. We study the single particle Green's functions for a disordered interacting system in one dimension using exact diagnonalization in the infinite temperature limit and provide strong evidence that single particle excitations carry signatures of delocalization to MBL transition. In the delocalized phase, the typical values of the local density of states and the scattering rate are finite while in the MBL phase, the typical values for both the quantities become vanishingly small. The probability distribution functions of the local density of states and the scattering rate are broad log-normal distributions in the delocalized phase while the distributions become very narrow and sharply peaked close to zero in the MBL phase. We also study the eigenstate Green's function for all the many-body eigenstates and demonstrate that both, the energy resolved typical scattering rate and the typical local density of states, can track the many-body mobility edges.

cond-mat.dis-nn↗

arXiv2021

Resonantly pumped bright-triplet exciton lasing in caesium lead bromide perovskites

The surprising recent observation of highly emissive triplet-states in lead halide perovskites accounts for their orders-of-magnitude brighter optical signals and high quantum efficiencies compared to other semiconductors. This makes them attractive for future optoelectronic applications, especially in bright low-threshold nano-lasers. Whilst non-resonantly pumped lasing from all-inorganic lead-halide perovskites is now well-established as an attractive pathway to scalable low-power laser sources for nano-optoelectronics, here we showcase a resonant optical pumping scheme on a fast triplet-state in CsPbBr3 nanocrystals. The scheme allows us to realize a polarized triplet-laser source that dramatically enhances the coherent signal by one order of magnitude whilst suppressing non-coherent contributions. The result is a source with highly attractive technological characteristics including a bright and polarized signal, and a high stimulated-to-spontaneous emission signal contrast that can be filtered to enhance spectral purity. The emission is generated by pumping selectively on a weakly-confined excitonic state with a Bohr radius ~10 nm in the nanocrystals. The exciton fine-structure is revealed by the energy-splitting resulting from confinement in nanocrystals with tetragonal symmetry. We use a linear polarizer to resolve two-fold non-degenerate sub-levels in the triplet exciton and use photoluminescence excitation spectroscopy to determine the energy of the state before pumping it resonantly.

physics.optics↗