Ultrafast Internal Conversion Research Articles

Deuterium Isotope Effect on Internal Conversion of Ethylene Studied by Time-Resolved Photoelectron Spectroscopy.

The effect of deuterium isotopes on the internal conversion of ethylene is studied by using extreme ultraviolet time-resolved photoelectron spectroscopy. For deuterium-labeled ethylene, the time scale for ultrafast internal conversion is increased by a factor of approximately √2, in agreement with the results of ab initio multiple spawning calculations, indicating the essential role played by hydrogen motion in the conversion process. Following internal conversion, a metastable species with an electron binding energy of ∼9 eV is produced, and it decays with a time constant similar to that for both isotopologues.

Vibrational Motions in Ultrafast Electronic Relaxation of Pyrazine.

Ultrafast internal conversion via a conical intersection is ubiquitous in highly efficient photochemical reactions. Internal conversion from the 1ππ* to the 1nπ* state of pyrazine is the paradigm for this phenomenon; however, the relaxation occurs in such a short time (<20 fs) that the nuclear motion is difficult to observe in real time. The present study precisely measures the vibrational coherence transferred from the 1ππ* state to the 1nπ* state using time-resolved photoelectron spectroscopy with an unprecedented time resolution of 13.3 fs and reveals the key nuclear motions that drive the internal conversion.

Dual-Emissive Iridium(III) Complexes and Their Applications in Biological Sensing and Imaging.

Phosphorescent iridium(III) complexes are widely recognized for their unique properties in the excited triplet state, making them crucial for various applications including biological sensing and imaging. Most of these complexes display single phosphorescence emission from the lowest-lying triplet state after undergoing highly efficient intersystem crossing (ISC) and ultrafast internal conversion (IC) processes. However, in cases where these excited-state processes are restricted, the less common phenomenon of dual emission has been observed. This dual emission phenomenon presents an opportunity for developing biological probes and imaging agents with multiple emission bands of different wavelengths. Compared to intensity-based biosensing, where the existence and concentration of an analyte are indicated by the brightness of the probe, the emission profile response involves modifications in emission color. This enables quantification by utilizing the intensity ratio of different wavelengths, which is self-calibrating and unaffected by the probe concentration and excitation laser power. Moreover, dual-emissive probes have the potential to demonstrate distinct responses to multiple analytes at separate wavelengths, providing orthogonal detection capabilities. In this concept, we focus on iridium(III) complexes displaying fluorescence-phosphorescence or phosphorescence-phosphorescence dual emission, along with their applications as biological probes for sensing and imaging.

Signatures of Conical Intersections in Extreme Ultraviolet Photoelectron Spectra of Furan Measured with 15 fs Time Resolution.

Ultrafast internal conversion of furan upon deep UV excitation at 200 nm is studied by using extreme ultraviolet time-resolved photoelectron spectroscopy with a time resolution of 15 fs. Ballistic nuclear wavepacket motion from the 1B2(ππ*) state to the ground state is fully observed using 21.7 eV probe pulses. Through the performance of a comparison with the results of electronic structure calculations at the MS(3)-CASPT2(10,10)/cc-pVTZ level of theory, the photoelectron signals from the conical intersection regions are identified.

Mechanistic insights into the AIE properties of BF2 complexes of N-acetyl 2-aminobenzothiazoles as rotorless polyheteroaromatics

A series of four novel BF2 complexes of N-acetyl 2-aminobenzothiazoles featuring rigid rotorless polyheteroaromatic structures have been designed and synthesized. All of these compounds exhibited AIE properties with excellent solid-state fluorescence quantum yields up to 81.7%. Theoretical calculations revealed the characteristics of their ground-state structures and excitation processes. Their seemingly abnormal nonradiative decay in solutions was investigated from both direct vibrational relaxation and S0/S1 surface crossing perspectives by the two-channel model. The minimum energy conical intersection (MECI) located by SF-TDDFT method indicated that the CI is mainly induced by the deformation of the BF2 complex ring, leads to elevated energy level, and thus is not responsible for the fluorescence quenching. The potential energy curve (PEC) constructed along the distortion angle θ of BF2 complex ring showed that when θ reaches 50° (the dark-state region approaching MECI), the energy barrier is only 0.11 eV, suggesting that the deformed dark state could serve as an effective deactivation channel via ultrafast internal conversion (IC). Crystallographic analysis illustrated that the F atoms perpendicular to the polyheterocycle could effectively prohibit detrimental π-π stacking and enhance intermolecular interactions, thereby resulting in efficient solid-state emission.

Low- and high-frequency vibrations synergistically enhance singlet exciton fission through robust vibronic resonances.

Singlet exciton fission (SEF) is initiated by ultrafast internal conversion of a singlet exciton into a correlated triplet pair [Formula: see text]. The "reaction coordinates" for ultrafast SEF even in archetypal systems such as pentacene thin film remain unclear. Couplings between fast electrons and slow nuclei are ubiquitous across a range of phenomena in chemistry. Accordingly, spectroscopic detection of vibrational coherences in the [Formula: see text] photoproduct motivated investigations into a possible role of vibronic coupling, akin to that reported in several photosynthetic proteins. However, acenes are very different from chlorophylls with 10× larger vibrational displacements upon photoexcitation and low-frequency vibrations modulating intermolecular orbital overlaps. Whether (and if so how) these unique features carry any mechanistic significance for SEF remains a poorly understood question. Accordingly, synthetic design of new molecules aiming to mimic this process across the solar spectrum has broadly relied on tuning electronic couplings. We address this gap and identify previously unrecognized synergistic interplay of vibrations, which in striking contrast to photosynthesis, vitally enhances SEF across a broad, nonselective and, therefore, unavoidable range of vibrational frequencies. We argue that attaching mechanistic significance to spectroscopically observed prominent quantum beats is misleading. Instead, we show that vibronic mixing leads to anisotropic quantum beats and propose readily implementable polarization-based two-dimensional electronic spectroscopy experiments which uniquely distinguish vibrations which drive vibronic mixing and promote SEF, against spectator vibrations simply accompanying ultrafast internal conversion. Our findings introduce crucial ingredients in synthetic design of SEF materials and spectroscopy experiments aiming to decipher mechanistic details from quantum beats.

Intrinsic Photostability in Dithiolonaphthalimide Achieved by Disulfide Bond-Induced Excited-State Quenching.

Disulfide bridges common in proteins show excellent photostability achieved by ultrafast internal conversion and maintain the stability of the tertiary structure. When disulfide bonds exist in aromatic compounds, the rigid chemical structure may affect the cleavage and reforming dynamics of disulfide bonds. In this work, a model compound with a disulfide five-membered-ring structure, 4,5-dithiolo-N-(2,6-dimethylphenyl)-1,8-naphthalimide (DTDPNI), is selected to elaborate the effect of disulfide modification on the excited-state deactivation mechanism. Quantum chemical calculations show that the S-S stretching leads to a dramatic decrease in the energy gap between the S1 and S0 states, similar to the situation in 1,2-dithiane. Due to the efficient nonradiative process, the excited-state lifetime of DTDPNI resolved by ultrafast spectroscopy is determined to be ∼20 ps. It is found that the excellent photostability is achieved by ultrafast excited-state quenching induced by the S-S stretching, rather than the cleavage of the disulfide bond; even the disulfide bridge is in a very rigid aromatic molecular system.

Dynamic Role of the Intramolecular Hydrogen Bonding in the S1 State Relaxation Dynamics Revealed by the Direct Measurement of the Mode-Dependent Internal Conversion Rate of 2-Chlorophenol and 2-Chlorothiophenol.

The dynamic role of the intramolecular hydrogen bond in the S1 relaxation of cis-2-chlorophenol (2-CP) or cis-2-chlorothiophenol (2-CTP) has been investigated in a state-specific manner. Whereas ultrafast internal conversion is dominant for 2-CP, the H-tunneling competes with internal conversion for 2-CTP even at the S1 origin. The S0-S1 internal conversion rate of 2-CTP could be directly measured from the S1 lifetimes of 2-CTP-d1 (Cl-C6H4-SD) as the D-tunneling is kinetically blocked, allowing distinct estimations of tunneling and internal conversion rates with increasing the energy. The internal conversion rate of 2-CTP increases by two times at the out-of-plane torsional mode excitation, suggesting that the internal conversion is facilitated at the nonplanar geometry. It then sharply increases at ∼600 cm-1, indicating that the S1/S0 conical intersection is readily accessible at the extended C-Cl bond length. The strength of the intramolecular hydrogen bond should be responsible for the distinct dynamic behaviors of 2-CP and 2-CTP.

Ultrafast internal conversion and photochromism in gas-phase salicylideneaniline.

Salicylideneaniline (SA) is an archetypal system for excited-state intramolecular proton transfer (ESIPT) in non-planar systems. Multiple channels for relaxation involving both the keto and enol forms have been proposed after excitation to S1 with near-UV light. Here, we present transient absorption measurements of hot gas-phase SA, jet-cooled SA, and SA in Ar clusters using cavity-enhanced transient absorption spectroscopy (CE-TAS). Assignment of the spectra is aided by simulated TAS spectra, computed by applying time-dependent complete active space configuration interaction (TD-CASCI) to structures drawn from nonadiabatic molecular dynamics simulations. We find prompt ESIPT in all conditions followed by the rapid generation of the trans keto metastable photochrome state and fluorescent keto state in parallel. Increasing the internal energy increases the photochrome yield and decreases the fluorescent yield and fluorescent state lifetime observed in TAS. In Ar clusters, internal conversion of SA is severely hindered, but the photochrome yield is unchanged. Taken together, these results are consistent with the photochrome being produced via the vibrationally excited keto population after ESIPT.

Plasmon Energy Transfer Driven by Electrochemical Tuning of Methylene Blue on Single Gold Nanorods.

Plasmonic photocatalysis has attracted interest for its potential to generate energy-efficient reactions, but ultrafast internal conversion limits efficient plasmon-based chemistry. Resonance energy transfer (RET) to surface adsorbates offers a way to outcompete internal conversion pathways and also eliminate the need for sacrificial counter-reactions. Herein, we demonstrate RET between methylene blue (MB) and gold nanorods (AuNRs) using in situ single-particle spectroelectrochemistry. During electrochemically driven reversible redox reactions between MB and leucomethylene blue (LMB), we show that the homogeneous line width is broadened when spectral overlap between AuNR scattering and absorption of MB is maximized, indicating RET. Additionally, electrochemical oxidative oligomerization of MB allowed additional dipole coupling to generate RET at lower energies. Time-dependent density functional theory-based simulated absorption provided theoretical insight into the optical properties, as MB molecules were electrochemically oligomerized. Our findings show a mechanism for driving efficient plasmon-assisted processes by RET through the change in the chemical states of surface adsorbates.

Computational study of the adamantane cation: simulations of spectroscopy, fragmentation dynamics, and internal conversion

Diamondoids, of which adamantane (C_{10}H_{16}) is the simplest representative, constitute an intriguing class of carbon based nanomaterials with interesting chemical, mechanical and opto-electronic properties. While neutral diamondoids have been extensively studied for decades, their cationic counterparts were a subject of recent experimental investigations motivated by their potential role in astrochemistry. Here, we perform a computational study of the adamantane cation (C_{10}H_{16}^+) complementing the recent experimental findings. Specifically, we extend earlier theoretical work on vibrationally resolved electronic spectroscopy by accounting for the higher lying electronically excited states of the cation in the absorption and photoelectron spectra. We also perform adiabatic and nonadiabatic (surface hopping) molecular dynamics simulations to study (fast) fragmentation processes and electronic relaxation of C_{10}H_{16}^+. Our simulations reveal that after excitation with near-infrared–ultraviolet photons, the adamantane cation undergoes an ultrafast internal conversion to the ground (doublet) state (on a time scale of 10–100 fs depending on initial excitation energy) which can be followed by a fast fragmentation, predominantly H loss. The yield of the ultrafast hydrogen dissociation as a function of excitation energy is reported.

Photoexcited State Dynamics and Singlet Fission in Carotenoids.

We describe our simulations of the excited state dynamics of the carotenoid neurosporene, following its photoexcitation into the "bright" (nominally 11Bu+) state. To account for the experimental and theoretical uncertainty in the relative energetic ordering of the nominal 11Bu+ and 21Ag- states at the Franck-Condon point, we consider two parameter sets. In both cases, there is ultrafast internal conversion from the "bright" state to a "dark" singlet triplet-pair state, i.e., to one member of the "2Ag" family of states. For one parameter set, internal conversion from the 11Bu+ to 21Ag- states occurs via the dark, intermediate 11Bu- state. In this case, there is a cross over of the 11Bu+ and 11Bu- diabatic energies within 5 fs and an associated avoided crossing of the S2 and S3 adiabatic energies. After the adiabatic evolution of the S2 state from predominately 11Bu+ character to predominately 11Bu- character, there is a slower nonadiabatic transition from S2 to S1, accompanied by an increase in the population of the 21Ag- state. For the other parameter set, the 21Ag- energy lies higher than the 11Bu+ energy at the Franck-Condon point. In this case, there is cross over of the 21Ag- and 11Bu+ energies and an avoided crossing of the S1 and S2 energies, as the S1 state evolves adiabatically from being of 11Bu+ character to 21Ag- character. We make a direct connection from our predictions to experimental observables by calculating the time-resolved excited state absorption. For the case of direct 11Bu+ to 21Ag- internal conversion, we show that the dominant transition at ca. 2 eV, being close to but lower in energy than the T1 to T1* transition, can be attributed to the 21Ag- component of S1. Moreover, we show that it is the charge-transfer exciton component of the 21Ag- state that is responsible for this transition (to a higher-lying exciton state), and not its triplet-pair component. These simulations are performed using the adaptive tDMRG method on the extended Hubbard model of π-conjugated electrons. The Ehrenfest equations of motion are used to simulate the coupled nuclei dynamics. We next discuss the microscopic mechanism of "bright" to "dark" state internal conversion and emphasize that this occurs via the exciton components of both states. Finally, we describe a mechanism relying on torsional relaxation whereby the strongly bound intrachain triplet-pairs of the "dark" state may undergo interchain exothermic dissociation.

The effect of the intramolecular disorder on hot exciton dynamics in polymer solar cells.

In polymer solar cells (PSCs), the contribution of hot excitons to charge generation is strongly limited by their relatively low yield and ultrafast internal conversion (IC) process. In recent years, different strategies have been proposed to modulate the hot exciton dynamics, but a direct correlation between the microscopic properties of the polymer and hot exciton dynamics is still not completely clear. Here, we theoretically investigate the effect of intramolecular disorder, including the diagonal disorder (DD) and off-diagonal disorder (ODD), on the hot exciton dynamics based on the tight-binding model calculations. We find that the effect of ODD on the hot exciton yield is more significant than that of DD. In addition, we find that the IC relaxation time of hot excitons depends nonmonotonically on the intensity of DD and ODD, indicating that the intramolecular disorder can modulate the competitive relationship between the spontaneous dissociation of hot excitons and the IC process. This work provides a guide for promoting charge generation in PSCs dominated by hot exciton dissociation.

The Effect of Methylation on the Triplet-State Dynamics of 2-Thiouracil: Time-Resolved Photoelectron Spectroscopy of 2-Thiothymine.

The ultrafast internal conversion and intersystem crossing dynamics of 2-thiouracil (2TU) and 2-thiothymine (2TT) are studied using time-resolved photoelectron spectroscopy to investigate the effect of methylation on the deactivation mechanism. Like other thiobases, the triplet manifold is populated with high quantum yields via the lowest singlet excited state, which is dark in absorption. This study focuses on the lowest triplet state and the role of two minima, with sulfur-out-of-plane and slightly boat-like geometries, in the intersystem crossing dynamics back to the ground state.

The photoprotection mechanism in the black–brown pigment eumelanin

The natural black-brown pigment eumelanin protects humans from high-energy UV photons by absorbing and rapidly dissipating their energy before proteins and DNA are damaged. The extremely weak fluorescence of eumelanin points toward nonradiative relaxation on the timescale of picoseconds or shorter. However, the extreme chemical and physical complexity of eumelanin masks its photoprotection mechanism. We sought to determine the electronic and structural relaxation pathways in eumelanin using three complementary ultrafast optical spectroscopy methods: fluorescence, transient absorption, and stimulated Raman spectroscopies. We show that photoexcitation of chromophores across the UV-visible spectrum rapidly generates a distribution of visible excitation energies via ultrafast internal conversion among neighboring coupled chromophores, and then all these excitations relax on a timescale of ∼4 ps without transferring their energy to other chromophores. Moreover, these picosecond dynamics are shared by the monomeric building block, 5,6-dihydroxyindole-2-carboxylic acid. Through a series of solvent and pH-dependent measurements complemented by quantum chemical modeling, we show that these ultrafast dynamics are consistent with the partial excited-state proton transfer from the catechol hydroxy groups to the solvent. The use of this multispectroscopic approach allows the minimal functional unit in eumelanin and the role of exciton coupling and excited-state proton transfer to be determined, and ultimately reveals the mechanism of photoprotection in eumelanin. This knowledge has potential for use in the design of new soft optical components and organic sunscreens.

Revisiting the Dynamics of Triplet Formation in Anthraquinones.

Triplet formation pathways in 9,10-anthraquinone (AQ) and its hydroxy derivative, 1-hydroxyanthraquinone (HAQ), are studied theoretically. Dynamics simulations on the model singlet-triplet potential energy surfaces within the linear vibronic coupling framework are performed to elucidate possible internal conversion (IC) and intersystem crossing (ISC) pathways in these molecules. An ultrafast IC decay from the "bright" S4 to S1 followed by efficient ISC via S1-T4 and S1-T5 pathways fosters a high triplet quantum yield (ΦT = 0.90) in AQ. In HAQ, a new nonradiative channel of "barrierless" excited-state intramolecular proton transfer (ESIPT) opens up and competes with the IC decay to S1 upon photoexcitation to the "bright" S2. Extremely fast ESIPT on S2 reduces the efficiency of triplet formation via possible ISC pathways involving S1 and S2, resulting in a low ΦT (=0.17).

The ultrafast nonradiative processes and photodissociation dynamics investigation of S1 state in propanal.

The ultrafast nonradiative dynamics in the S1 electronic excited state and the corresponding photodissociation dynamics in propanal molecules have been studied with time-resolved photoelectron imaging and time-of-flight mass spectrometry at an excitation wavelength of 320nm. The population of the S1 state undergoes ultrafast internal conversion (IC) to the highly vibrationally hot S0 state in a timescale of <100fs and nonradiative deactivation by intersystem crossing (ISC) to triplet T1 state occurring with a time constant of about several hundreds of femtoseconds. The ISC process is then followed by the dissociation on the T1 surface because the excitation energy is higher than the dissociation barrier along the C-C(HO) bond length coordinate. The dissociation product of the CHO radical has an appearance time of about 540fs, which agrees well with the measured ISC relaxation time constant of 430fs. The CO molecule is proposed to form at about 170fs after the excitation, supporting the dissociation mechanism via the molecular channel following the IC decay of the S1 state. The energy of the first excited electronic state of the C3H6O+ is obtained to be 12.25eV.

Ultrafast Internal Conversion Dynamics through the on-the-Fly Simulation of Transient Absorption Pump-Probe Spectra with Different Electronic Structure Methods.

An on-the-fly surface-hopping simulation protocol is developed for the evaluation of transient absorption (TA) pump-probe (PP) signals of molecular systems exhibiting internal conversion to the electronic ground state. We study the nonadiabatic dynamics of azomethane and the associating TA PP spectra at three levels of the electronic-structure theory, OM2/MRCI, SA-CASSCF, and XMS-CASPT2. The impact of these methods on the population dynamics and time-resolved TA PP signals is substantially different. This difference is attributed to the strong non-Condon effects that must be taken into account for the proper understanding and interpretation of time-resolved TA PP signals of nonadiabatic polyatomic systems. This shows that the combination of the dynamical and spectral simulations definitely provides more accurate and detailed information on the microscopic mechanisms of photophysical and photochemical processes. Hence the simulation of time-resolved spectroscopic signals provides another important dimension to examine the accuracy of quantum chemistry methods.

Ultrafast internal conversion without energy crossing

Ultrafast (sub-picosecond) internal conversion can occur between electronic states without energetically accessible conical intersections. For that, the molecule must remain in a region of at least weak nonadiabatic coupling, multiplying the odds of a transition, each with a small probability. This phenomenon is discussed with a simple analytical model correlating the instantaneous probability to the lifetime.

Modeling the heating and cooling of a chromophore after photoexcitation.

The heating of a chromophore due to internal conversion and its cooling down due to energy dissipation to the solvent are crucial phenomena to characterize molecular photoprocesses. In this work, we simulated the ab initio nonadiabatic dynamics of cytosine, a prototypical chromophore undergoing ultrafast internal conversion, in three solvents—argon matrix, benzene, and water—spanning an extensive range of interactions. We implemented an analytical energy-transfer model to analyze these data and extract heating and cooling times. The model accounts for nonadiabatic effects, and excited- and ground-state energy transfer, and can analyze data from any dataset containing kinetic energy as a function of time. Cytosine heats up in the subpicosecond scale and cools down within 25, 4, and 1.3 ps in argon, benzene, and water, respectively. The time constants reveal that a significant fraction of the benzene and water heating occurs while cytosine is still electronically excited.