Femtosecond Spectroscopy Research Articles

Ultrafast excited state dynamics of isocytosine unveiled by femtosecond broadband time-resolved spectroscopy combined with density functional theoretical study.

Isocytosine, having important applications in antivirus and drug development, is among the building blocks of Hachimoji nucleic acids. In this report, we present an investigation of the excited state dynamics of isocytosine in both protic and aprotic solvents, which was conducted by a combination of methods including steady-state spectroscopy, femtosecond broadband time-resolved fluorescence, and transient absorption. These methods were coupled with density functional and time-dependent density functional theory calculations. The results of our study provide the first direct evidence for a highly efficient nonradiative mechanism achieved through internal conversion from the ππ* state of the isocytosine keto-N(3)H form occurring within subpicoseconds and picoseconds following photo-excitation. Our study also unveils a crucial role of solvent, particularly solute-solvent hydrogen bonding, in determining the tautomeric composition and regulating the pathways and dynamics of the deactivation processes. The deactivation processes of isocytosine in the solvents examined are found to be distinct from those of cytosine and the case known for isocytosine in the gas phase mainly due to different tautomeric forms involved. Overall, our findings demonstrate the high photo-stability of isocytosine in the solution and showcase the remarkable effect of covalent modification in altering the spectral character and excited state dynamics of nucleobases.

Quantifying the Relaxation Dynamics of Higher Electronic Excited States in Perylene.

Gating logical operations through high-lying electronic excited states presents opportunities for developing ultrafast, subnanometer computational devices. A lack of molecular systems with sufficiently long-lived higher excited states has hindered practical realization of such devices, but recent studies have reported intriguing photophysics from high-lying excited states of perylene. In this work, we use femtosecond spectroscopy supported by quantum chemical calculations to identify and quantify the relaxation dynamics of monomeric perylene's higher electronic excited states. The 21B2u state is accessed through single-photon absorption at 250 nm, while the optically dark 21Ag state is excited via the 11B3u state. Population of either state results in subpicosecond relaxation to the 11B3u state, and we quantify 21Ag and 21B2u state lifetimes of 340 and 530 fs, respectively. These lifetimes are significantly longer than the singlet fission time constant from the perylene 21B2u state, suggesting that the higher electronic states of perylene may be useful for gating logical operations.

Observation of Electronic and Structural Interaction between Small Polaron and Host Material Using Femtosecond XUV Reflection Spectroscopy

Small polaron formation in transition metal oxides is believed to be a reaction bottleneck in many solar energy conversion applications. While polaron formation has been previously confirmed, the microscopic interaction between a small polaron and its host material is largely unexplored. Here, using femtosecond XUV reflection spectroscopy, we report the evidence of electronic and structural interaction between the small polaron and its host material in CuFeO2, a photoelectrode material for CO2 reduction. Initial small polaron formation is observed as a spectral blue shift occurring within the first 100 fs. After polaron formation, we observe an increased coherent oscillation signal around the polaron sites, which is attributed to polaron-induced optical phonons. This observation suggests that the polaron-associated local lattice distortion can launch optical phonons in neighboring unit cells. In addition to structural coupling, the electronic states in the host materials can also be modified during polaron formation. As an example, we report an increase of Fe oxidation states after photoexcitation. The population of these highly oxidized Fe atoms strongly correlates with polaron dynamics, suggesting that polaron can alter its surrounding electronic states in host materials.

(Invited) Ultrafast Charge Transfer Dynamics in WS2–Au Nanohybrid System Fabricated by Pulsed Laser Ablation in Liquid

Nanosheet semiconductor materials have attracted much attention in recent years due to their unique optical, electronic, and chemical properties for various applications such as photodetectors, light emitters, photocatalysts, and biosensors. We have fabricated tungsten disulfide (WS2) nanostructures by pulsed laser ablation in liquid. We applied nanosecond and femtosecond lasers and found the latter to be suitable for nanosheet fabrication [1]. Visible light response was enhanced by attaching gold nanoparticles (AuNPs) onto WS2 nanosheets [2]. The charge transfer dynamics in the WS2-Au nanohybrid system was characterized using femtosecond diffuse reflectance spectroscopy. The nanosheet structure was found to reduce the bulk carrier property. Furthermore, modification with AuNPs was found to enhance the formation of carriers trapped deeply in the WS2 nanosheets. These findings will be useful for the design of future metal-nanosheet semiconductor hybrid systems.Reference Pankaj Koinkar, Kohei Sasaki, Tetsuro Katayama and Akihiro Furube, International Journal of Modern Physics B, 35, 2140007 (2021)Tatsuki Kokufu, Daichi Nakayama, Tetsuro Katayama, Koinkar Pankaj, and Akihiro Furube, The 13th Asia-Pacific Conference on Near-Field Optics, OL30-A13 (2022)

Experimental demonstration of dyed water aerosol fluorescence stimulated by femtosecond laser postfilaments propagating in air.

We present the fluorescence spectra of single millimeter water droplets and micron-sized dyed water aerosol (rhodamine 6G) stimulated by a high-intensity femtosecond Ti:sapphire-laser pulse (carrier wavelength 792nm) upon its nonlinear propagation in air. The distinctive feature of our experimental measurements is that the droplet fluorescence is obtained in the area of plasma-free pulse propagation after the pulse filamentation has already been terminated (postfilamentation region). Our results significantly expand the working area of femtosecond laser-induced fluorescence spectroscopy for remote diagnostics of atmospheric aerosols.

Ultrafast Plasmonic Hot Hole Transfer and Plasmon Dynamics in a Dual Plasmonic Au@p‐Cu2−xSe Heterostructure

AbstractMetal‐semiconductor heterostructures have significant potential in harvesting plasmon induced hot charge carriers for photocatalytic and photovoltaic devices. Despite numerous studies, the field of hot hole transfer in heterostructures remains unexplored. In this work, the plasmon dynamics of a dual plasmonic core–shell Au@p‐Cu2−xSe heterostructure are investigated with the aid of femtosecond broadband pump probe spectroscopy. Ultrafast studies reveal that hot holes generated within the d and sp band after 400 and 800 nm excitations are injected from Au to copper selenide. Hot hole transfer substantially reduces the transient signal intensity and electron phonon relaxation time for Au plasmon. Increment in the transient signal intensity and slower kinetics for the semiconducting plasmon of Au@Cu2−xSe validate the hot hole transfer in the valence band of copper selenide. Fluence dependent studies reveal that d band hot holes extraction is more efficient than that of sp band hot holes.

Characterization of non-Boltzmann CN X2Σ+ behind shock waves in CH4-N2 via broadband ultraviolet femtosecond absorption spectroscopy.

This article describes the temporal evolution of rotationally and vibrationally non-Boltzmann CN X2Σ+ formed behind reflected shock waves in N2-CH4 mixtures at conditions relevant to atmospheric entry into Titan. A novel ultrafast (i.e., femtosecond) laser absorption spectroscopy diagnostic was developed to provide broadband (≈400 cm-1) spectrally resolved (0.02nm resolution) measurements of CN absorbance spectra belonging to its B2Σ+ ← X2Σ+ electronic system and its first four Δv = 0 vibrational bands (v″ = 0, 1, 2, 3). Measurements were acquired behind reflected shock waves in a mixture with 5.65% CH4 and 94.35% N2 at initial chemically and vibrationally frozen temperatures and pressures of 4400-5900K and 0.55-0.75bar, respectively. A six-temperature line-by-line absorption spectroscopy model for CN was developed to determine the rotational temperature of CN in v″ = 0, 1, 2, and 3, as well as two vibrational temperatures via least-squares fitting. The measured CN spectra revealed rotationally and vibrationally non-Boltzmann population distributions that strengthened with increasing shock speed and persisted for over 100 µs. The measured vibrational temperatures of CN initially increase in time with the increasing CN mole fraction and eventually exceed the expected post-shock rotational temperature of N2. The results suggest that strong chemical pumping is ultimately responsible for these trends and that, at the conditions studied, CN is primarily formed in high vibrational states within the A2Π or B2Σ+ state at characteristic rates, which are comparable to or exceed those of key vibrational equilibration processes.

Rydberg state dynamics and fragmentation mechanism of N,N,N',N'-tetramethylmethylenediamine.

The non-adiabatic relaxation processes and the fragmentation dynamics of Rydberg-excited N,N,N',N'-tetramethylmethylenediamine (TMMDA) are investigated using femtosecond time-resolved photoelectron imaging and time-resolved mass spectroscopy. Excitation at 208nm populates TMMDA in a charge-localized 3p state. Rapid internal conversion (IC) to 3s produces two charge-delocalized conformers with independent time constants and distinct population ratios. As the system explores the 3s potential surface, the structural evolution continues on a 1.55ps timescale, followed by a slower (12.1ps) relaxation to the ground state. A thorough comparison of the time-dependent mass and photoelectron spectra suggests that ionization out of the 3p state ends up with the parent ion, the vibrational energy of which is insufficient for the bond cleavage. On the contrary, by virtue of the additional energy acquired by IC from 3p, the internal energy deposited in 3s is available to break the C-N bond, leading to the fragment ion. The fragmentation is found to occur on the ion surface instead of the Rydberg surface.

Role of Substrate Binding Interactions on DNA Repair by Photolyase.

The repair of the cyclobutane pyrimidine dimer (CPD) lesion in DNA by photolyase is determined by its initial recognition, and the catalytic efficiency depends on a series of intermolecular electron-transfer (ET) processes. Here, we investigated the repair of a CPD structural isomer, replacing the deoxyribose with a pyranose sugar on the 5' site, and found a loss in binding efficiency and repair quantum yield. Using femtosecond spectroscopy, we characterized all elementary repair steps and observed a systemic slowdown of the four intermolecular ET reactions and the second bond splitting. Our observations and molecular dynamics simulations suggest that the sugar replacement disrupts the lesion binding configuration, weakening the electronic coupling between the cofactor and lesion and altering the stability of lesion intermediates. These findings highlight how the CPD photolyases have utilized the structural features of the CPD lesion and optimized its interactions with the cofactor and key active-site residues to maximize repair yields.

Imaging and controlling coherent phonon wave packets in single graphene nanoribbons

The motion of atoms is at the heart of any chemical or structural transformation in molecules and materials. Upon activation of this motion by an external source, several (usually many) vibrational modes can be coherently coupled, thus facilitating the chemical or structural phase transformation. These coherent dynamics occur on the ultrafast timescale, as revealed, e.g., by nonlocal ultrafast vibrational spectroscopic measurements in bulk molecular ensembles and solids. Tracking and controlling vibrational coherences locally at the atomic and molecular scales is, however, much more challenging and in fact has remained elusive so far. Here, we demonstrate that the vibrational coherences induced by broadband laser pulses on a single graphene nanoribbon (GNR) can be probed by femtosecond coherent anti-Stokes Raman spectroscopy (CARS) when performed in a scanning tunnelling microscope (STM). In addition to determining dephasing (~440 fs) and population decay times (~1.8 ps) of the generated phonon wave packets, we are able to track and control the corresponding quantum coherences, which we show to evolve on time scales as short as ~70 fs. We demonstrate that a two-dimensional frequency correlation spectrum unequivocally reveals the quantum couplings between different phonon modes in the GNR.

Revealing core-valence interactions in solution with femtosecond X-ray pump X-ray probe spectroscopy

Femtosecond pump-probe spectroscopy using ultrafast optical and infrared pulses has become an essential tool to discover and understand complex electronic and structural dynamics in solvated molecular, biological, and material systems. Here we report the experimental realization of an ultrafast two-color X-ray pump X-ray probe transient absorption experiment performed in solution. A 10 fs X-ray pump pulse creates a localized excitation by removing a 1s electron from an Fe atom in solvated ferro- and ferricyanide complexes. Following the ensuing Auger–Meitner cascade, the second X-ray pulse probes the Fe 1s → 3p transitions in resultant novel core-excited electronic states. Careful comparison of the experimental spectra with theory, extracts +2 eV shifts in transition energies per valence hole, providing insight into correlated interactions of valence 3d with 3p and deeper-lying electrons. Such information is essential for accurate modeling and predictive synthesis of transition metal complexes relevant for applications ranging from catalysis to information storage technology. This study demonstrates the experimental realization of the scientific opportunities possible with the continued development of multicolor multi-pulse X-ray spectroscopy to study electronic correlations in complex condensed phase systems.

Identification of tumor tissue in thin pathological samples via femtosecond laser-induced breakdown spectroscopy and machine learning

In the treatment of most newly discovered solid cancerous tumors, surgery remains the first treatment option. An important factor in the success of these operations is the precise identification of oncological safety margins to ensure the complete removal of the tumor without affecting much of the neighboring healthy tissue. Here we report on the possibility of applying femtosecond Laser-Induced Breakdown Spectroscopy (LIBS) combined with Machine Learning algorithms as an alternative discrimination technique to differentiate cancerous tissue. The emission spectra following the ablation on thin fixed liver and breast postoperative samples were recorded with high spatial resolution; adjacent stained sections served as a reference for tissue identification by classical pathological analysis. In a proof of principle test performed on liver tissue, Artificial Neural Networks and Random Forest algorithms were able to differentiate both healthy and tumor tissue with a very high Classification Accuracy of around 0.95. The ability to identify unknown tissue was performed on breast samples from different patients, also providing a high level of discrimination. Our results show that LIBS with femtosecond lasers is a technique with potential to be used in clinical applications for rapid identification of tissue type in the intraoperative surgical field.

Mechanism and Dynamics of Photodecarboxylation Catalyzed by Lactate Monooxygenase.

Photoenzymes are a rare class of biocatalysts that use light to facilitate chemical reactions. Many of these catalysts utilize a flavin cofactor to absorb light, suggesting that other flavoproteins might have latent photochemical functions. Lactate monooxygenase is a flavin-dependent oxidoreductase previously reported to mediate the photodecarboxylation of carboxylates to afford alkylated flavin adducts. While this reaction holds a potential synthetic value, the mechanism and synthetic utility of this process are unknown. Here, we combine femtosecond spectroscopy, site-directed mutagenesis, and a hybrid quantum-classical computational approach to reveal the active site photochemistry and the role the active site amino acid residues play in facilitating this decarboxylation. Light-induced electron transfer from histidine to flavin was revealed, which has not been reported in other proteins. These mechanistic insights enable the development of catalytic oxidative photodecarboxylation of mandelic acid to produce benzaldehyde, a previously unknown reaction for photoenzymes. Our findings suggest that a much wider range of enzymes have the potential for photoenzymatic catalysis than has been realized to date.

Quality assessment of the commercially available alcohol-based hand sanitizers with femtosecond thermal lens spectroscopy

Using femtosecond-pulse-induced thermal lens spectroscopy (FTLS), we report a novel method for the quality measurements of alcohol-based hand sanitizers (ABHS). To sustain its effectiveness, the ABHS must contain the recommended concentration of alcohol content. We diluted the hand sanitizer with water to reduce the quantity of alcohol in the mixture and then performed thermal measurements on it. We performed both dual-beam Z-scan and time-resolved TL measurements to identify the alcoholic content in the ABHS. The thermal lens (TL) signal of the solvent is capable of detecting any relative change in the alcohol content in the mixture. Our technique, therefore, emerges as a sensitive tool for quality testing of alcohol-based hand sanitizers.

Probing electron localization during molecular dissociation by femtosecond strong-field ion momentum spectroscopy

The study of molecular valence electron dynamics and their coupling with nuclear motion is one of the frontiers of ultrafast physics and ultrafast chemistry. With time-resolved strong-field ion momentum spectroscopy, we study electron valence and nucleus wavepacket evolution on a femtosecond timescale. Two orientation-dependent bond-breaks of N2O molecules from the same electronic state are studied, and the influence of orbital hybridization and polarization effect during molecular breaking is analyzed based on the measured time-resolved asymmetric Pzsum distributions, allowing a visual representation of electron localization during the dissociation of molecules into ions and atoms. Comparison of experimental and theoretical results on orientation-dependent dissociation dynamics allows us to understand how nuclear motions evolve during fragmentation and to control ultrafast molecular reactions.

Excited-State Dynamics of All the Mono-cis and the Major Di-cis Isomers of β-Apo-8'-Carotenal as Revealed by Femtosecond Time-Resolved Transient Absorption Spectroscopy.

Cis isomers of carotenoids play important roles in light harvesting and photoprotection in photosynthetic bacteria, such as the reaction center in purple bacteria and the photosynthetic apparatus in cyanobacteria. Carotenoids containing carbonyl groups are involved in efficient energy transfer to chlorophyll in light-harvesting complexes, and their intramolecular charge-transfer (ICT) excited states are known to be important for this process. Previous studies, using ultrafast laser spectroscopy, have focused on the central-cis isomer of carbonyl-containing carotenoids, revealing that the ICT excited state is stabilized in polar environments. However, the relationship between the cis isomer structure and the ICT excited state has remained unresolved. In this study, we performed steady-state absorption and femtosecond time-resolved absorption spectroscopy on nine geometric isomers (7-cis, 9-cis, 13-cis, 15-cis, 13'-cis, 9,13'-cis, 9,13-cis, 13,13'-cis, and all-trans) of β-apo-8'-carotenal, whose structures are well-defined, and discovered correlations between the decay rate constant of the S1 excited state and the S0-S1 energy gap, as well as between the position of the cis-bend and the degree of stabilization of the ICT excited state. Our results demonstrate that the ICT excited state is stabilized in polar environments in cis isomers of carbonyl-containing carotenoids and suggest that the position of the cis-bend plays an important role in the stabilization of the excited state.

Femtosecond exciton relaxation in chlorosomes of the photosynthetic green bacterium <i>Chloroflexus aurantiacus</i>

In the green bacteria Chloroflexus (Cfx.) aurantiacus, the process of photosynthesis begins with the absorption of light by chlorosomes, peripheral antennas consisting of thousands of bacteriochlorophyll c (BChl c) molecules combined into oligomeric structures. In this case, excited states are formed in BChl c, the energy of which migrates along the chlorosome towards the baseplate and further to the reaction center, where the primary charge separation occurs. Energy migration is accompanied by nonradiative electronic transitions between numerous exciton states, that is exciton relaxation. In this work, we studied the dynamics of exciton relaxation in Cfx. aurantiacus chlorosomes using difference femtosecond spectroscopy at cryogenic temperature (80 K). Chlorosomes were excited by 20 fs light pulses at wavelengths from 660 to 750 nm, and the difference (light-dark) kinetics were measured at a wavelength of 755 nm. Mathematical analysis of the data obtained revealed the kinetic components with characteristic time constants of 140, 220, and 320 fs responsible for the exciton relaxation. As the excitation wavelength decreased, the number of components and their relative contribution increased. Theoretical modeling of the results obtained was carried out on the base of the cylindrical model of BChl c aggregates. Nonradiative transitions between groups of exciton bands were ascribed by the system of kinetic equations. The model in which the energetic and structural disorder was taken into account turned out to be the most adequate.

Coherent Phonon-Mediated Many-Body Interaction in Monolayer WSe2

Due to the strong Coulomb interaction, the optical and electrical properties of two-dimensional transition metal dichalcogenides (TMDCs) are greatly determined by the emergence of many-body complexes such as excitons or trions. To fully realize the potential functionalities of these atomically thin materials, a comprehensive understanding of their many-body interaction mechanism is essential. Here, using the advanced femtosecond two-dimensional electronic spectroscopy technique combined with broadband transient absorption spectroscopy, a strong electron-exciton coupling effect in monolayer WSe2 following the ultrafast photoexcitation is revealed. We demonstrate that such many-body complexes can be generated effectively through the band-edge optical excitation, with a ∼1.5 ps stabilization process. The coherent optical phonon plays a dominant role in this electron-exciton interaction, and the coherence of the electron (exciton)-phonon coupling can last for ∼4.5 ps. This finding offers new insight into the formation mechanism of photoinduced many-body complexes in TMDCs.

Ferricyanide photo-aquation pathway revealed by combined femtosecond Kβ main line and valence-to-core x-ray emission spectroscopy

Reliably identifying short-lived chemical reaction intermediates is crucial to elucidate reaction mechanisms but becomes particularly challenging when multiple transient species occur simultaneously. Here, we report a femtosecond x-ray emission spectroscopy and scattering study of the aqueous ferricyanide photochemistry, utilizing the combined Fe Kβ main and valence-to-core emission lines. Following UV-excitation, we observe a ligand-to-metal charge transfer excited state that decays within 0.5 ps. On this timescale, we also detect a hitherto unobserved short-lived species that we assign to a ferric penta-coordinate intermediate of the photo-aquation reaction. We provide evidence that bond photolysis occurs from reactive metal-centered excited states that are populated through relaxation of the charge transfer excited state. Beyond illuminating the elusive ferricyanide photochemistry, these results show how current limitations of Kβ main line analysis in assigning ultrafast reaction intermediates can be circumvented by simultaneously using the valence-to-core spectral range.

Energy dissipation efficiency in the CP43 assembly intermediate complex of photosystem II

Photosystem II in oxygenic organisms is a large membrane bound rapidly turning over pigment protein complex. During its biogenesis, multiple assembly intermediates are formed, including the CP43-preassembly complex (pCP43). To understand the energy transfer dynamics in pCP43, we first engineered a His-tagged version of the CP43 in a CP47-less strain of the cyanobacterium Synechocystis 6803. Isolated pCP43 from this engineered strain was subjected to advanced spectroscopic analysis to evaluate its excitation energy dissipation characteristics. These included measurements of steady-state absorption and fluorescence emission spectra for which correlation was tested with Stepanov relation. Comparison of fluorescence excitation and absorptance spectra determined that efficiency of energy transfer from β-carotene to chlorophyll a is 39 %. Time-resolved fluorescence images of pCP43-bound Chl a were recorded on streak camera, and fluorescence decay dynamics were evaluated with global fitting. These demonstrated that the decay kinetics strongly depends on temperature and buffer used to disperse the protein sample and fluorescence decay lifetime was estimated in 3.2–5.7 ns time range, depending on conditions. The pCP43 complex was also investigated with femtosecond and nanosecond time-resolved absorption spectroscopy upon excitation of Chl a and β-carotene to reveal pathways of singlet excitation relaxation/decay, Chl a triplet dynamics and Chl a → β-carotene triplet state sensitization process. The latter demonstrated that Chl a triplet in the pCP43 complex is not efficiently quenched by carotenoids. Finally, detailed kinetic analysis of the rise of the population of β-carotene triplets determined that the time constant of the carotenoid triplet sensitization is 40 ns.