Search

Glioblastoma WHO IV belongs to a group of brain tumors that are still incurable. A promising treatment approach applies photodynamic therapy (PDT) with hypericin as a photosensitizer. To generate a comprehensive understanding of the photosensitizer-tumor interactions, the first part of our study is focused on investigating the distribution and penetration behavior of hypericin in glioma cell spheroids by fluorescence microscopy. In the second part, fluorescence lifetime imaging microscopy (FLIM) was used to correlate fluorescence lifetime (FLT) changes of hypericin to environmental effects inside the spheroids. In this context, 3D tumor spheroids are an excellent model system since they consider 3D cell–cell interactions and the extracellular matrix is similar to tumors in vivo. Our analytical approach considers hypericin as probe molecule for FLIM and as photosensitizer for PDT at the same time, making it possible to directly draw conclusions of the state and location of the drug in a biological system. The knowledge of both state and location of hypericin makes a fundamental understanding of the impact of hypericin PDT in brain tumors possible. Following different incubation conditions, the hypericin distribution in peripheral and central cryosections of the spheroids were analyzed. Both fluorescence microscopy and FLIM revealed a hypericin gradient towards the spheroid core for short incubation periods or small concentrations. On the other hand, a homogeneous hypericin distribution is observed for long incubation times and high concentrations. Especially, the observed FLT change is crucial for the PDT efficiency, since the triplet yield, and hence the O2 activation, is directly proportional to the FLT. Based on the FLT increase inside spheroids, an incubation time > 30 min is required to achieve most suitable conditions for an effective PDT. Graphical abstract

Photosynthesis is one the most important biological processes on earth, producing life-giving oxygen, and is the basis for a large variety of plant products. Measurable properties of photosynthesis provide information about its biophysical state, and in turn, the physiological conditions of a photoautotrophic organism. For instance, the chlorophyll fluorescence intensity of an intact photosystem is not constant as in the case of a single fluorescent dye in solution but shows temporal changes related to the quantum yield of the photosystem. Commercial photosystem analyzers already use the fluorescence kinetics characteristics of photosystems to infer the viability of organisms under investigation. Here, we provide a novel approach based on an optical Fabry–Pérot microcavity that enables the readout of photosynthetic properties and activity for an individual cyanobacterium. This approach offers a completely new dimension of information, which would normally be lost due to averaging in ensemble measurements obtained from a large population of bacteria.

We investigate the time-resolved photoelectric response of WSe

Surface charging effects at metal-molecule interfaces, for example, charge transfer, charge transport, charge injection, and so on, have a strong impact on the performance of organic electronics. Only having molecules bound or adsorbed on different metals results in a doping-like behavior at the interface by the different work functions of the metals and creates hybrid surface states, which strongly affect the efficiencies. With the ongoing downsizing and thinning of the organic components, the impact of the interface will even further increase. However, most of the investigations only monitor the interface without the additional charging effects from applying a voltage to the interface. In this work we present a spectroscopic approach based on tip-enhanced Raman spectroscopy (TERS) to study metal-molecule interfaces with an applied voltage simulating the electric field strength in real devices. We monitor how an intrinsic inductive effect of partial functional groups in molecules can shift the molecular electron density (ED) distribution when a bias voltage is applied. Therefore, we choose two molecules as model systems, which are similar in size and binding condition to a smooth gold surface, but with different electronic structure. By placing the tip 1 nm over the molecular surface at a fixed position and changing the applied bias voltage, we record electric-field-dependent tip-enhanced Raman spectra. Specific vibrational bands exhibit voltage-dependent intensity changes related to the shift of the local ED inside the molecules. We believe this experiment is valuable to gain deeper insights into charged metal-molecule interfaces.

Strong coupling between vibrational transitions and a vacuum field of a cavity mode leads to the formation of vibrational polaritons. These hybrid light-matter states have been widely explored because of their potential to control chemical reactivity. However, the possibility of altering Raman scattering through the formation of vibrational polaritons has been rarely reported. Here, we present the Raman scattering properties of different molecules under vibrational strong coupling conditions. The polariton states are clearly observed in the IR transmission spectra of the coupled system for benzonitrile and methyl salicylate in liquid phase and for polyvinyl acetate in a solid polymer film. However, none of the studied systems exhibits a signature of the polariton states in the Raman spectra. For the solid polymer film, we have used cavities with different layer structures to investigate the influence of vibrational strong coupling on the Raman spectra. The only scenario where alterations of the Raman spectra are observed is for a thin Ag layer being in direct contact with the polymer film. This shows that, even though the system is in the vibrational strong coupling regime, changes in the Raman spectra do not necessarily result from the strong coupling, but are caused by the surface enhancement effects.

Fibronectin coating increases implant biocompatibility by enhancing surface endothelialization via integrin-mediated binding. Surface properties determine the fibronectin orientation and conformation, dictating which ligands are presented, and therefore altering the bioactivity of an implant surface. In this study, polyurethane was treated with oxygen plasma, which allowed for a simultaneous modification of the surface chemistry and topography to modulate fibronectin adsorption. By varying the parameters of the treatment, human plasma fibronectin adsorbed on the surfaces in different conformations, orientations, and binding affinities, which was investigated by atomic force microscopy, fluorescence microscopy, monoclonal and polyclonal antibody staining and reflectometric interference spectroscopy. Apart from the most hydrophilic rough surfaces, the adsorbed fibronectin showed a lower binding affinity and less conformational change on the more hydrophilic surfaces. A large amount of exposed fibronectin-cell binding was detected on the rough treated and the smooth untreated surfaces. Primary isolated human umbilical vein and human microvascular endothelial cells showed a significantly higher cell adherence on the absorbed fibronectin with a low binding affinity and low conformational changes. Significant differences in the formation of mature focal adhesions and the reorganization of F-actin were identified on the rough treated and the smooth untreated surfaces. Our data suggest that oxygen plasma treatment is a reliable technique for the modulation of fibronectin adsorption in order to adjust fibronectin bioactivity and impact cell responses to implant surfaces.

Tip-enhanced Raman spectroscopy is combined with polarization angle-resolved spectroscopy to investigate the nanometre-scale structural properties of core-shell silicon nanowires (crystalline Si core and amorphous Si shell), which were synthesized by platinum-catalyzed vapor-liquid-solid growth and silicon overcoating by thermal chemical vapour deposition. Local changes in the fraction of crystallinity are characterized for those silicon nanowires at an optical resolution of about 300 nm. Furthermore, we are able to resolve the variations in the intensity ratios between the crystalline Si and the amorphous Si Raman peaks by applying tip-enhanced Raman spectroscopy, at sample positions being eight nanometers apart. The local crystallinity revealed using confocal Raman spectroscopy and tip-enhanced Raman spectroscopy agree well with the high-resolution transmission electron microscopy measurements. Additionally, the polarizations of Raman scattering and the photoluminescence signal from the tip-sample nanogap are explored by combining polarization angle-resolved emission spectroscopy with tip-enhanced optical spectroscopy. Our work demonstrates the significant potential of resolving local structural properties of Si nanomaterials at the sub-10 nanometer scale using tip-enhanced Raman techniques.

This work fundamentally investigates how the second harmonic generation (SHG) from commercial nonlinear crystals can be boosted by the addition of individual optical nanoantennas. Frequency conversion plays an important role in modern non-linear optics, and nonlinear crystals have become a widely used building block for non-linear processes. Still, SHG remains hampered by limited conversion efficiency. To strengthen SHG from the crystal surface, we investigate the interaction of LiNbO3 crystals with individual gold nanodiscs. The scattered intensities and resonance frequencies of the nanodiscs are analyzed by dark-field spectroscopy and simulations. Subsequently, the discs on LiNbO3 are excited by a pulsed femtosecond laser in a parabolic mirror setup. Comparing the SHG at the position of a single nanodisc at resonance on the crystal with that of the unstructured crystal and of gold nanodiscs on a reference substrate, local SHG enhancement of up to a factor of three was achieved in the focal volume through the presence of the antenna.

Hypericin tautomerization that involves the migration of the labile protons is believed to be the primary photophysical process relevant to its light-activated antiviral activity. Despite the difficulty in isolating individual tautomers, it can be directly observed in single-molecule experiments. We show that the tautomerization of single hypericin molecules in free space is observed as an abrupt flipping of the image pattern accompanied with fluorescence intensity fluctuations, which are not correlated with lifetime changes. Moreover, the study can be extended to a λ/2 Fabry-Pérot microcavity. The modification of the local photonic environment by a microcavity is well simulated with a theoretical model that shows good agreement with the experimental data. Inside a microcavity, the excited state lifetime and fluorescence intensity of single hypericin molecules are correlated, and a distinct jump of the lifetime and fluorescence intensity reveals the temporal behavior of the tautomerization with high sensitivity and high temporal resolution. The observed changes are also consistent with time-dependent density functional theory calculations. Our approach paves the way to monitor and even control reactions for a wider range of molecules at the single molecule level.

We investigate the time-resolved photoelectric response of WSe$_2$ crystals on common glass and flexible polyimide substrates to determine the effect of the dielectric environment on the speed of the photodetectors. We show that varying the substrate material can alter the speed-limiting mechanism: while the detectors on polyimide are RC limited, those on glass are limited by slower excitonic diffusion processes. We attribute this to a shortening of the depletion layer at the metal electrode/WSe2 interface caused by the higher dielectric screening of glass compared to polyimide. The photodetectors on glass show a tunable bandwidth which can be increased to 2.6 MHz with increasing the electric field., Comment: 27 pages, 13 figures

Gold bipyramids (AuBPs) attract significant attention due to the large enhancement of the electric field around their sharp tips and well-defined tunability of their plasmon resonances. Excitation ...

The quantum optical phenomena, such as single photon emission, in two-dimensional (2D) transition metal dichalcogenides (TMDCs) have triggered extensive researches on 2D material-based quantum optics and devices. By far, most reported quantum optical emissions in TMDCs are based on atomic defects in the material or the local confinement of excitons by introducing local stain or potential. In contrast, energy transfer between two materials could also manipulate the photon emission behaviors in materials, even at the single photon level. Along with the single-photon emission nature of zero-dimensional (0D) quantum dots (QDs) at room temperature, constructing a 0D-2D hybrid heterostructure may provide an effective way to regulate the quantum states related optical emissions of TMDCs. Here, we report on fluorescence blinking, a quantum phenomenon, from MoS2 atomic layers in QD/ MoS2 heterostructure at room temperature. We demonstrate the single-photon nature of the QDs in heterostructures by second-order photon correlation measurements. Based on the transient PL spectroscopy and PL time trajectories, we attribute the fluorescence blinking behavior in MoS2 to the single photon energy transfer from QD to MoS2. Our work opens the possibility to achieve correlated quantum emitters in TMDCs at room temperature by controlling the energy transfer between QD and TMDCs.

The first step in photosynthesis is an extremely efficient energy transfer mechanism that led to the debate to which extent quantum coherence may be involved in the energy transfer between the photosynthetic pigments. In search of such a coherent behavior, we have embedded living cyanobacteria between the parallel mirrors of an optical microresonator irradiated with low intensity white light. As a consequence, we observe vacuum Rabi splitting in the transmission and fluorescence spectra as a result of strong light matter coupling of the chlorophyll a molecules in the photosystems (PSs) and the cavity modes. The Rabi-splitting scales with the number of the PSs chlorophyll a pigments involved in strong coupling indicating a delocalized polaritonic state. Our data provide evidence that a delocalized polaritonic state can be established between the chlorophyll a molecule of the PSs in living cyanobacterial cells at ambient conditions in a microcavity.

We correlate spatially resolved fluorescence (-lifetime) measurements with X-ray nanodiffraction to reveal surface defects in supercrystals of self-assembled cesium lead halide perovskite nanocrystals and study their effect on the fluorescence properties. Upon comparison with density functional modeling, we show that a loss in structural coherence, an increasing atomic misalignment between adjacent nanocrystals, and growing compressive strain near the surface of the supercrystal are responsible for the observed fluorescence blueshift and decreased fluorescence lifetimes. Such surface defect-related optical properties extend the frequently assumed analogy between atoms and nanocrystals as so-called quasi-atoms. Our results emphasize the importance of minimizing strain during the self-assembly of perovskite nanocrystals into supercrystals for lighting application such as superfluorescent emitters.

Tautomerization is an intramolecular chemical reaction defined as structural interconversion of a molecule between two isomers separated by a low energy barrier. Tautomerization in free base phthalocyanines, porphyrins or porphycenes has fascinated and attracted chemists and physicists alike over the last decades for its fundamental importance in various chemical and biological systems and many applications in technology [1,2]. Particularly interesting is the reaction rate which can range over orders of magnitude depending on the temperature and the local environment. In solution, this reaction in porphycenes occurs usually in several picoseconds or even faster, as determined via anisotropy studies by ultrafast transient absorption spectroscopy [3] and in porphyrins at cryogenic temperatures it can last for hours or days as determined form the live time of narrow spectral holes photochemically burned in the inhomogeneously broadened absorption band with a narrow band laser [4]. However, a spectacular and unexpected observation has been made by optical single molecule imaging and spectroscopy [5]. Examining a large number of single molecules embedded at low concentration in various polymer matrices at room temperature has revealed unquestionably that the rate in these molecules can vary dramatically over time such that tautomerization can be frozen for seconds and longer under ambient conditions[6]. The interconversion of the inner protons of phthalocyanine changes the orientation of the transition dipole moment by 90o degrees with respect to the molecular structure. Hence, if these molecules are embedded with a fixed orientation in a transparent solid polymer film at high dilution and tautomerization is frozen, the orientation of their transition dipole moments can be determined by polarization spectroscopy. Here we report on our recent experimental and theoretical studies of monitoring tautomerization by fluorescence imaging of single molecules of phthalocyanines, porphyrins, or porphycenes excited in the tightly focused azimuthally and radially polarized laser beam with a sample scanning confocal optical microscope equipped with single photon counting electronics and a fluorescence spectrometer. This technique has been used to determine the transition dipole moment orientation of single molecules, the polarizability of plasmonic nanoparticles or the dimensionality of single quantum dots. Different diffraction limited fluorescence intensity patterns are observed for molecules that undergo tautomerization and for those that do not. The latter corresponds to a molecule with a fixed transition dipole moment direction, whereas the tautomerizing molecule can be treated as the superposition of two emitters with different transition dipole moment orientations. Previous studies have shown that tautomerization in porphyrins or phthalocyanines can occur via ground state tunneling and is frozen at low temperatures, particularly at cryogenic temperatures. The structural heterogeneity in a polymer matrix leads to a distribution of asymmetrically distorted ground state double well potential and hence can lead to long residence times in the deeper energy minimum. However, even at helium temperatures tautomerization can be induced by electronic excitation to the first excited state, making photochemical spectral hole-burning possible. Recently we could demonstrate in a single-molecule study that the tautomerization rate of phthalocyanine tetrasulfonate embedded in a thin PVA-film at room temperature could be controlled in a tunable λ/2 Fabry Perot resonator by weak coupling between the electronically excited state and the vacuum electromagnetic field of a resonant cavity mode. References: [1] S.Völker, J.H.Van der Waals; Mol. Phys. 32, 1703-1718, 1976. [2] J.G. Radziszewski, J. Waluk, J. Michl; Chem. Phys, 136, 165-180, 1989. [3] P. Fita, N. Urbanska, C. Radewicz, J. Waluk, Chem. Eur. J. 15, 4851-4856, 2009. [4] L. Kador, G. Schulte, D. Haarer; J. Phys.Chem 90, 1264-1270, 1986. [5] H. Piwoński, C. Stupperich, A. Hartschuh, J. Sepioł, A. Meixner, J. Waluk; J. Am. Chem. Soc. 127, 5302-5304, 2005. [6] A.M. Chizhik, R.Jäger, A.I. Chizhik, S. Bär, H.G. Mack, M. Sackrow, C.Stanciu, A. Lyubimtsev, M.Hanack, A.J.Meixner; Phys.Chem.Chem.Phys 13, 1722-1733, 2011. [7] H. Piwonski, A. Hartschuh, N. Urbanska, M. Pietraszkiewcz, J.Sepiol, A.Meixner, J. Waluk; J. Phys. Chem. C113, 11514-11519, 2009. [8] L. Piatkowski, Ch. Schanbacher, F. Wackenhut, A. Jamrozik, A.J. Meixner, J. Waluk; J. Phys. Chem. Lett. 9, 1211-1215, 2018. [9] W. M. Takele, F. Wackenhut, Q. Liu, L. Piatkowski, J. Waluk, A. J. Meixner; J. Phys. Chem. C125, 14932-14939, 2021. Figure 1

Tautomerization is a fast chemical reaction where structures of the reactants differ only in the position of a proton and a double bond. Tautomerization often occurs in natural substances and is a fundamental process in organic- and biochemistry. However, studying the optical properties of tautomeric species is challenging due to ensemble averaging. Many molecules, such as porphines, porphycenes or phenanthroperylene quinones, exhibit a reorientation of the transition dipole moment (TDM) during tautomerization, which can be directly observed in a single molecule experiment. A prominent phenanthroperylene quinone is hypericin showing antiviral, antidepressive, and photodynamical properties. Here, we study single hypericin molecules by using confocal microscopy combined with higher order laser modes. Observing abrupt flipping of the image pattern allows to draw conclusions about the coexistence of different tautomers and their conversion path. Time-dependent density functional theory calculations show that hypericin is cycling between the four most stable tautomers. This approach allows to unambiguously assign a TDM orientation to a specific tautomer and enables to determine the chemical structure in situ. Additionally, tautomerization can not only be observed by the image pattern orientation, but also as intermittency in the fluorescence emission of a single molecule. Time correlated single photon counting enables to determine the excited state lifetimes of the hypericin tautomers. Our approach is not only limited to hypericin, but can be applied to other molecules showing a TDM reorientation during tautomerization, helping to get a deeper understanding of this important process.

CdSe nanocrystals and aggregates of an aryleneethynylene derivative are assembled into a hybrid thin film with dual fluorescence from both fluorophores. Under continuous excitation, the nanocrystals and the molecules exhibit anticorrelated fluorescence intensity variations, which become periodic at low temperature. We attribute this to a structure-dependent aggregation-induced emission of the aryleneethynylene derivative, which impacts the rate of excitation energy transfer between the molecules and nanocrystals. This work highlights that combining semiconductor nanocrystals with molecular aggregates, which exhibit aggregation-induced emission, can result in emerging optical properties.

In SERS and TERS charge transfer can lead to the chemical signal enhancement. STM assisted TERS allows for applying DC electric fields between tip and sample comparably high to the fields experienced by molecules in regular devices. The influence of DC electric fields on tip enhanced Raman spectra has been reported by various authors who discussed different aspects such as reorientation of molecules, intensity changes and energy level shifts. Here we report on our progress towards a better understanding of a scanning DC electric field on tip enhanced Raman spectra of small molecules directly bound to the metallic substrate.