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The field of quantum technology has been rapidly expanding in the past decades, yielding numerous applications, such as quantum information, quantum communication, and quantum cybersecurity. At the core of these applications lies the quantum emitter (QE), a precisely controllable generator of either single photons or photon pairs. Semiconductor QEs, such as perovskite nanocrystals and semiconductor quantum dots, have shown much promise as emitters of pure single photons, with the potential for generating photon pairs when hybridized with plasmonic nanocavities. In this study, we have developed a system in which individual quantum emitters and their ensembles can be traced before, during, and after the interaction with an external plasmonic metasurface in a controllable way. Upon coupling the external plasmonic metasurface to the QE array, the individual QEs switch from the single-photon emission mode to the multiphoton emission mode. Remarkably, this method preserves the chemical structure and composition of the QEs, allowing them to revert to their initial state after decoupling from the plasmonic metasurface. This significantly expands the potential applications of semiconductor QEs in quantum technologies.

Plexcitonic systems based on metal nanostructures and molecular J-aggregates offer an excellent opportunity to explore the intriguing interplay between plasmonic excitations and excitons, offering unique insights into light–matter interactions at the nanoscale. Their potential applications in photocatalysis have prompted a growing interest in both their synthesis and the analysis of their properties. However, in order to construct a high-performing system, it is essential to ensure chemical and spectral compatibility between both components. We present the results of a study into a hybrid system, achieved through the coupling of gold nanobipyramids with organic molecules, and demonstrate the strengthened photochemical properties of such a system in comparison with purely J-aggregates. Our analysis includes the absorbance and photoluminescence characterization of the system, revealing the remarkable plexcitonic interaction and pronounced coupling effect. The absorbance spectroscopy of the hybrid systems enabled the investigation of the coupling strength (g). Additionally, the photoluminescence response of the J-aggregates and coupled systems reveals the impact of the coupling regime. Utilizing fluorescence lifetime imaging microscopy, we established how the photoluminescence lifetime components of the J-aggregates are affected within the plexcitonic system. Finally, to assess the photodegradation of J-aggregates and plexcitonic systems, we conducted a comparative analysis. Our findings reveal that plasmon-enhanced interactions lead to improved photostability in hybrid systems.

Analysis of the pH influence in the JC1 J-aggregates formation using absorbance and photoluminescence spectra and estimation of the mean lifetime of monomer and J-aggregates, results of the pH influence in the exciton coherence length applying the four explained methods to different experiments, and summary of reported J-aggregates’ exciton coherence length.

The coherence length of the Frenkel excitons (Ncoh) is one of the most critical parameters governing many key features of supramolecular J-aggregates. Determining experimentally the value of Ncoh is a nontrivial task since it is sensitive to the technique/method applied, causing discrepancies in the literature data even for the same chemical compound and aggregation conditions. By using a combination of different experimental techniques including UV–vis–NIR, fluorescence emission, time-resolved photoluminescence, and transient absorption spectroscopies, we determined Ncoh values for J-aggregates of a cyanine dye. We found that the absorption spectroscopy alone - a widely used technique- fails in determining right value for Ncoh. The correct approach is based on the modification of photoluminescence lifetime and nonlinear response upon aggregation and careful analysis of the Stokes shift and electron–phonon coupling strength. This approach revealed that Ncoh of JC-1 J-aggregates ranges from 3 to 6.

Discerning the kinetics of photoluminescence (PL) decay of packed quantum dots (QDs) and QD-based hybrid materials is of crucial importance for achieving their promising potential. However, the interpretation of the decay kinetics of QD-based systems, which usually are not single-exponential, remains challenging. Here, we present a method for analyzing photoluminescence (PL) decay curves of fluorophores by studying their statistical moments. A certain combination of such moments, named as the n-th order moments’ ratio, Rn, is studied for several theoretical decay curves and experimental PL kinetics of CdSe quantum dots (QDs) acquired by time-correlated single photon counting (TCSPC). For the latter, three different case studies using the Rn ratio analysis are presented, namely, (i) the effect of the inorganic shell composition and thickness of the core–shell QDs, (ii) QD systems with Förster resonance energy transfer (FRET) decay channels, and (iii) system of QDs near a layer of plasmonic nanoparticles. The proposed method is shown to be efficient for the detection of slight changes in the PL kinetics, being time-efficient and requiring low computing power for performing the analysis. It can also be a powerful tool to identify the most appropriate physically meaningful theoretical decay function, which best describes the systems under study.

Strong exciton–plasmon interaction enables effective control of the photonic properties of hybrid organic–inorganic nanostructures encompassing light absorption, scattering and luminescence. Whereas the manifestations of light-matter interactions in the absorption and scattering are reasonably well understood their relation to the luminescence as well as luminescence properties themselves in strongly coupled plexcitonic hybrids is still largely underexplored especially for a system with a complex mechanism of hybridisation of states. Here we report on investigation of the interaction between localized and hybridized plasmons in gold nanostars and excitons in J-aggregates under ambient conditions. Our findings demonstrate the quality performance of the formed plexciton system with multiple hybridization channels in terms of the parameters of strong coupling, such as Rabi splitting (230 meV), coupling-strength-to-transition energy ratio (0.07), and cooperativity (2.03). The results of time-resolved experiments elucidate the observed enhanced spontaneous emission rate with regard to the Purcell effect, whose value was estimated from the extinction spectra of the strongly coupled plexciton system.

Plasmonic catalysis in the colloidal phase requires robust surface ligands that prevent particles from aggregation in adverse chemical environments and allow carrier flow from reagents to nanoparticles. This work describes the use of a water-soluble conjugated polymer comprising a thiophene moiety as a surface ligand for gold nanoparticles to create a hybrid system that, under the action of visible light, drives the conversion of the biorelevant NAD+ to its highly energetic reduced form NADH. A combination of advanced microscopy techniques and numerical simulations revealed that the robust metal–polymer heterojunction, rich in sulfonate functional groups, directs the interaction of electron-donor molecules with the plasmonic photocatalyst. The tight binding of polymer to the gold surface precludes the need for conventional transition-metal surface cocatalysts, which were previously shown to be essential for photocatalytic NAD+ reduction but are known to hinder the optical properties of plasmonic nanocrystals. Moreover, computational studies indicated that the coating polymer fosters a closer interaction between the sacrificial electron-donor triethanolamine and the nanoparticles, thus enhancing the reactivity.

The interaction of several components in the strong coupling regime yielding multiple Rabi splittings opens up remarkable possibilities for studies of multimode hybridization and energy transfer, which is of considerable interest in both fundamental and applied science. Here we demonstrate that three different components, such as core−shell Au@Ag nanorods and J-aggregates of two different dyes, can be integrated into a single hybrid structure, which leads to strong collective exciton− plasmon coupling and double-mode Rabi splitting totaling 338 meV. We demonstrate strong coupling in these multicomponent plexitonic nanostructures by means of magnetic circular dichroism spectroscopy and demonstrate strong magneto-optical activity for the three hybridized states resulting from this coupling. The J-aggregates of two different nonmagnetic dyes interact with metal nanoparticles effectively, achieving magnetic properties due to the hybridization of electronic excitations in the threecomponent system.

Semiconductor quantum dots (QDs) are known for their ability to exhibit multiphoton emission caused by recombination of biexcitons (BX). However, the quantum yield (QY) of BX emission is low due to the fast Auger process. Plasmonic nanoparticles (PNPs) provide an attractive opportunity to accelerate BX radiative recombination. Here, we demonstrate the PNPs induced distance-controlled enhancement of BX emission of single QDs. Studying the same single QD before and after its integration with the PNPs, we observed a plasmon-mediated increase in the QY of BX emission. Remarkably, the enhancement of BX emission remains pronounced even at distances of 170 nm. We attribute this effect to efficient coupling, which results in the trade-off between resonance energy transfer from QD to gold nanorods and the Purcell effect at small QD-PNP separations and the predominant influence of the Purcell effect at longer distances. Our findings constitute a reliable approach to managing the efficiency of multiexciton emission over a wide span of distances, thus paving the way for new applications.

We report our recent results of research of plasmon-exciton interactions in Au and Au@Ag nanorods integrated with J-aggregates of cyanine dyes is presented. In all developed hybrid nanostructures, the anti-crossing behavior of the hybridized modes can be tracked using a number of spectroscopic techniques such as absorption, photoluminescence (PL) and magnetic circular dichroism (MCD).

Resonant interaction between excitonic transitions of molecules and localized electromagnetic field allows the formation of hybrid light–matter polaritonic states. This hybridization of the light and the matter states has been shown to significantly alter the intrinsic properties of molecular ensembles placed inside the optical cavity. Here, we have observed strong coupling of excitonic transition in a pair of closely located organic dye molecules demonstrating an efficient donor-to-acceptor resonance energy transfer with the mode of a tuneable open-access cavity. Analysing the dependence of the relaxation pathways between energy states in this system on the cavity detuning, we have demonstrated that predominant strong coupling of the cavity photon to the exciton transition in the donor dye molecule can lead not only to an increase in the donor–acceptor energy transfer, but also to an energy shift large enough to cause inversion between the energy states of the acceptor and the mainly donor lower polariton energy state. Furthermore, we have shown that the polariton-assisted donor–acceptor chromophores' role reversal or “carnival effect” not only changes the relative energy levels of the donor–acceptor pair, but also makes it possible to manipulate the energy flow in the systems with resonant dipole–dipole interaction and direct energy transfer from the acceptor to the mainly donor lower polariton state. Our experimental data are the first confirmation of the theoretically predicted possibility of polariton-assisted energy transfer reversal in FRET systems, thus paving the way to new avenues in FRET-imaging, remote-controlled chemistry, and all-optical switching.

Excitons in semiconductor quantum dots (QDs) feature high values of the two-photon absorption cross-sections (TPACSs), enabling applications of two-photon-excited photoluminescence (TPE PL) of QDs in biosensing and nonlinear optoelectronics. However, efficient TPE PL of QDs requires high-intensity laser fields, which limits these applications. There are two possible ways to increase the TPE PL of QDs: by increasing their photoluminescence quantum yield (PLQY) or by further increasing the TPACS. Plasmonic nanoparticles (PNPs) may act as open nanocavities for increasing the PLQY via the Purcell effect, but this enhancement is strictly limited by the maximum possible PLQY value of 100%. Here we directly investigated the effect of PNPs on the effective TPACS of excitons in QDs. We have found that effective TPACS of excitons in a QD–PMMA thin film can be increased by a factor of up to 12 near the linearly excited gold nanorods (GNRs). Using gold nanospheres (GNSs), in which plasmons cannot be excited in the infrared range, as a control system, we have shown that, although both GNSs and GNRs increase the recombination rate of excitons, the TPACS is increased only in the case of GNRs. We believe that the observed effect of TPACS enhancement is a result of the nonlinear interaction of the plasmons in GNRs with excitons in QDs, which we have supported by numerical simulations. The results show the way to the rational design of the spectral features of plasmon–exciton hybrids for using them in biosensing and nonlinear optoelectronics.

Reliable control of spontaneous radiation from quantum emitters, such as quantum dots (QDs), is an extremely important problem in quantum science, nanophotonics, and engineering. The QD photoluminescence (PL) may be enhanced near plasmon nanoparticles because of excitation field enhancement or the Purcell effect. However, both of these effects have their specific limitations. The excitation enhancement is usually accompanied by a decrease in the PL quantum yield (QY) due to the plasmon-induced energy transfer, and the Purcell effect cannot significantly enhance the PL of QDs with an initially high QY because of the obvious limitation of the QY by the value of 100%. Here, we have shown that the synergistic combination of excitation enhancement caused by silver nanospheres and the Purcell effect caused by silver nanoplates in the same QD-in-polymer hybrid thin-film nanostructure permits simultaneous increases in the radiative and excitation rates to be obtained. This overcomes the limitations of each individual effect and yields a synergistic PL increase (+1320%) greater than the sum of the PL enhancements determined by each effect alone (+70% and +360%).

Hybridized plexcitonic states have unique properties which have been widely studied in recent decades in many research fields targeted at both fundamental science and innovative applications. However, to make these applications come true one needs to ensure the stabilization and preservation of electronic states and optical transitions in hybrid nanostructures, especially under the influence of external stressors, in regimes, that have not yet been comprehensively investigated. The present work shows that the nanohybrid system, composed of plasmonic nanoparticles and J-aggregates of organic molecules, displays outstanding resistance to harsh environmental stressors such as temperature, pH and strong light irradiation as well as demonstrates long-term stability and processability of the nanostructures both in weak and strong coupling regimes. These findings contribute to a deeper understanding of the physicochemical properties of plexcitonic nanoparticles and may find important implications for the development of potential applications in optoelectronics, optical imaging and chemo-bio-sensing and, in general, in the field of optical materials science.

Efficient biexciton (BX) photoluminescence (PL) from quantum dots (QDs) paves the way to the generation of entangled photons and related applications. However, the quantum yield (QY) of BX PL is much lower than that for single excitons (EX) due to efficient Auger-like recombination. In the vicinity of plasmon nanoparticles, the recombination rates of EX and BX may be affected by the Purcell effect, fluorescence quenching, and the excitation rate enhancement. Here, the effect of the plasmon resonance spectral position on the EX and BX PL is experimentally studied in two cases: when the plasmon band overlaps with the excitation wavelength and when it coincides with the QDs PL band. In the first case, the EX and BX excitation efficiencies are significantly increased but the EX QY reduced. As a result, the BX-to-EX QY ratio is higher than 1 at plasmon–exciton systems separations shorter than 40 nm. In the second case, the radiative recombination rates are enhanced by several orders of magnitude, which led to an increase in BX QY over distances of up to 90 nm. Finally, these two effects are obtained in the same hybrid structure, with the resultant increase in both excitation efficiency and QY of BX PL.

Over the last two decades, scientists have been studying the properties and functions of materials within hundred nanometers in size. Nanotechnology is a very broad field which includes sciences as diverse as surface science, semiconductor physics, energy storage, microfabrication, molecular engineering. Its fast evolution has demonstrated that it holds the key to many of the technological advancements in a wide range of applications, such as nanomedicine, nanoelectronics, energy production, and consumer products, among others. Hence, nanotechnology is expected to have a significant impact on our society within de next decades with several challenges like the creation of new materials and devices with superior properties in order to implement them in future applications. Recently research community focuses on the understanding the physical properties of a new type of nanomaterial known as plexcitonic nanoparticle, a system that combines plasmonic (metal) and excitonic (molecular) components. A large number of proof-of-concept experiments over last year indicate that these hybrid systems offer properties that can outperform the properties of their corresponding components when use separately. Although the structural integrity of these systems is achieved in laboratory conditions, it is of questionable control while dealing with long-term use in real-world conditions, e.g., exposure to light of high intensity, extreme temperatures, or harsh chemical conditions. Therefore, in the present Master thesis we set an overreaching goal of the evaluation the structural integrity of hybrid plexcitonic nanoparticles under light exposure conditions, which is of paramount importance when pointing towards the use of these systems in photocatalysis or biosensing.

Studies of resonance interaction between matter and localized electromagnetic field in a cavity have recently attracted much interest because they offer the possibility of controllably modifying some of the fundamental material properties. However, despite the large number of such studies, these is no universal approach that would allow investigation of sets of different samples with wide variation of the main experimental parameters of the optical modes. In this work, the main optical parameters of a previously developed universal tunable microcavity cell, i.e., the Q factor and mode volume, as well as their dependence on the characteristics of cavity mirrors and spacing between them, are analyzed. The results obtained will significantly expand the scope of applications of resonance interaction between light and matter, including such effects as the enhancement of Raman scattering, long-range resonance nonradiative energy transfer, and modification of chemical reaction rates.

Resonance interaction between a localized electromagnetic field and excited states in molecules paves the way to control fundamental properties of a matter. In this study, we encapsulated organic molecules with relatively low unoriented dipole moments in the polymer matrix, placed them in tunable optical microcavity and realized, for the first time, controllable modification of the broad photoluminescence (PL) emission of these molecules in strong coupling regime at room temperature. Notably, while in most previous studies it was reported that the single mode dominates in the PL signal (radiation of the so-called branch of the lower polariton), here we report on the observation of two distinct PL peaks, evolution of which has been followed as the microcavity mode is detuned from the excitonic resonance. A significant Rabi splitting estimated from the modified PL spectra was as large as 225 meV. The developed approach can be used both in fundamental research of resonant light-mater coupling and its practical applications in sensing and development of coherent spontaneous emission sources using a combination of carefully designed microcavity with a wide variety of organic molecules.

Triethanolamine is a widely used model electron donor that enables a fast screening of the photocatalyst parameters in both, homogeneous and heterogeneous scenarios. We report a new role of triethanolamine in heterogeneous photoregeneration of cofactor molecules – nicotinamide adenine dinucleotide (NADH) – using state-of-the-art heterogeneous photocatalysts. In contrast to the common model involving the light-induced electrons and holes generation to reduce the substrate and oxidize triethanolamine simultaneously, we identified glycolaldehyde as a stable product of triethanolamine degradation capable of reducing NAD+. Triethanolamine, apart from playing a role of a precursor for reducing agent, maintains the alkalinity of the solution to drive the reduction. Our findings offer a fresh insight into the triethanolamine-assisted photocatalysis because glycolaldehyde as such have generally been neglected in mechanistic considerations. Moreover, a spatial and temporal decoupling of the photocatalyst from the substrate reduction reaction minimizes the product re-oxidation, thus implying a relevant feature for the real-world applications using a continuous flow setting.