Photoinduced Electron Transfer Dynamics Research Articles

Ultrafast electron transfer of different vibronic states in flavodoxin

Understanding the ultrafast electron transfer (ET) processes involving various vibronic excitation in biological systems remains challenging and requires well-defined model proteins for in-depth studies. In this work, we selected three types of mutants with different ET lifetimes in flavodoxin to explore the excitation dependence of the photo-induced ET dynamics. For the ultrafast ET processes within the time window of intramolecular vibrational relaxation, with increasing excitation energies, we observed no change of ET lifetimes but with higher vibrational excitation in products, both of which can be attributed to the unique nature of ultrafast ET. For the slower ET, we did not find any dependence of product vibration excitation relative to the initial different excitation due to the complete vibrational relaxation. These results strongly indicate the vibrational energy can be propagated to the subsequent reactions during ultrafast ET processes.

Direct observation of chirality-induced spin selectivity in electron donor-acceptor molecules.

The role of chirality in determining the spin dynamics of photoinduced electron transfer in donor-acceptor molecules remains an open question. Although chirality-induced spin selectivity (CISS) has been demonstrated in molecules bound to substrates, experimental information about whether this process influences spin dynamics in the molecules themselves is lacking. Here we used time-resolved electron paramagnetic resonance spectroscopy to show that CISS strongly influences the spin dynamics of isolated covalent donor-chiral bridge-acceptor (D-Bχ-A) molecules in which selective photoexcitation of D is followed by two rapid, sequential electron-transfer events to yield D•+-Bχ-A•-. Exploiting this phenomenon affords the possibility of using chiral molecular building blocks to control electron spin states in quantum information applications.

Solvent effects on the photoinduced charge separation dynamics of directly linked zinc phthalocyanine-perylenediimide dyads: a nonadiabatic dynamics simulation with an optimally tuned screened range-separated hybrid functional.

Herein, we have employed a combination of the optimally tuned screened range-separated hybrid (OT-SRSH) functional, the polarizable continuum model (PCM), and nonadiabatic dynamics (NAMD) simulations to investigate the photoinduced dynamics of directly linked donor-acceptor dyads formed using zinc phthalocyanine (ZnPc) and perylenediimide (PDI), in which ZnPc is the donor while PDI is the acceptor. Our simulations aim to analyze the behavior of these dyads upon local excitation of the ZnPc moiety in the gas phase and in benzonitrile. Our findings indicate that the presence of a solvent can significantly influence the excited state dynamics of ZnPc-PDI dyads. Specifically, the polar solvent benzonitrile effectively lowers the vertical excitation energies of the charge transfer (CT) state from ZnPc to PDI. As a result, the energetic order of the locally excited (LE) states of ZnPc and the CT states is reversed compared to the gas phase. Consequently, the photoinduced electron transfer (PET) dynamics from ZnPc to PDI, which is absent in the gas phase, takes place in benzonitrile with a time constant of 10.4 ps. Importantly, our present work not only qualitatively agrees with experimental results but also provides in-depth insights into the underlying mechanisms responsible for the photoinduced dynamics of ZnPc-PDI. Moreover, this study emphasizes the importance of appropriately considering solvent effects in NAMD simulation of organic donor-acceptor systems, taking into account the distinct excited state dynamics observed in the gas phase and benzonitrile. Furthermore, the combination of the OT-SRSH functional, the PCM solvent model, and nonadiabatic dynamics simulations shows promise as a strategy for investigating the complex excited state dynamics of organic donor-acceptor systems in solvents. These findings will be valuable for the future design of novel organic donor-acceptor structures with improved performance.

Redfield Propagation of Photoinduced Electron Transfer Reactions in Vacuum and Solution.

Dynamical simulations of ultrafast electron transfer reactions are of utmost interest. To allow for energy dissipation directly into an external surrounding environment, a solvent coupling model has been deduced, implemented, and utilized to describe the photoinduced electron transfer dynamics within a model triad system herein. The model is based on Redfield theory, and the environment is represented by harmonic oscillators filled with bosonic quanta. To imitate real solvents, the oscillators have been equipped with frequencies and polarization lifetimes characteristic of the corresponding solvent. The population was found to transfer through the energetically lowest electron transfer route regardless of the medium. The condensed population transfer dynamics were observed to be highly dependent on the solvent parameters. In particular, an increase in the solvent coupling entailed a detainment in the population transfer from the initially prepared diabatic state and a promotion in the population transfer through the other electron transfer route. Two explanations based on the diagonal and off-diagonal matrix elements of the Kohn-Sham Fock matrix, respectively, have been provided. The lifetime of the populated partially charge-separated state was prolonged with increasing solvent polarity, and it was explained in terms of attractive interactions between the solvent's dipole moments and the fragments' charges. The high-frequency vibrational fine-structure in the correlation function was demonstrated to be important for the transfer dynamics, and the importance of dephasing effects in polar solvents was verified and precised to concern the optical polarization of the solvents.

Ultrafast Dynamics of Photoinduced Electron Transfer in Bay-Aryl-Substituted Perylene Diimide Derivatives.

Blends of donors and acceptors have been widely used in bulk-heterojunction solar cells to have exciton formation and charge separation by photoinduced electron transfer (PET). In this work, we have synthesized perylene diimide (PDI)-based materials having different aryl substituents at the bay positions (4-Anisyl-PDI, CBZ-N-Ph-PDI, and 4-Pyridyl-PDI) to understand the excited-state dynamics of electron transfer. The detailed photophysics was studied using steady-state as well as ultrafast dynamics of the excited states in different solvents. CBZ-N-Ph-PDI showed tremendous effects of the solvent on the electronic properties compared with the other two derivatives. The emission quantum yield of CBZ-N-Ph-PDI decreases drastically in dichloromethane and other polar solvents, indicating strong electron transfer. DFT calculations showed that in CBZ-N-Ph-PDI the HOMO is centered mostly on the N-phenylcarbazole and the LUMO is on the electron-poor PDI moieties. In addition, the energy levels of the HOMO and HOMO-1 in CBZ-N-Ph-PDI are estimated to be identical. The free energy change for charge separation (ΔGCS) was calculated using electrochemical and photophysical data and found to be negative for CBZ-N-Ph-PDI. The ground- and excited-state dipole moment ratios suggest that the excited state of 4-Pyridyl-PDI (1.90) is less polar than that of 4-Anisyl-PDI (3.67), which provides an idea of the lower possibility of charge separation in 4-Anisyl-PDI and 4-Pyridyl-PDI. Ultrafast photodynamics studies of 4-Anisyl-PDI, CBZ-N-Ph-PDI, and 4-Pyridyl-PDI showed fast electron transfer only in CBZ-N-Ph-PDI and not in the other PDI derivatives. It was also observed that electron transfer is faster in DCM and THF than in toluene. Ultrafast dynamics studies showed the presence of an equilibrium between electron transfer and decay from the singlet excited state. Ultrafast studies also showed the features of the N-phenylcarbazole cation and PDI anion, further confirming the intramolecular electron transfer in CBZ-N-Ph-PDI.

Electron transfer and spin-orbit coupling: Can nuclear motion lead to spin selective rates?

We investigate a spin-boson inspired model of electron transfer, where the diabatic coupling is given by a position-dependent phase, eiWx. We consider both equilibrium and nonequilibrium initial conditions. We show that, for this model, all equilibrium results are completely invariant to the signof W (to infinite order). However, the nonequilibrium results do depend on the signof W, suggesting that photo-induced electron transfer dynamics with spin-orbit coupling can exhibit electronic spin polarization (at least for some time).

Synergistic dynamics of photoionization and photoinduced electron transfer probed by laser flash photolysis and ultrafast fluorescence spectroscopy.

Photoionization (PI) and photoinduced electron transfer (PET) dynamics of coumarin 450 (C450) in micelles were investigated in the time domains of micro to femtoseconds using steady-state and time-resolved absorption and fluorescence spectroscopy. The PI of C450 occurs inside the micelles leads to the formation of C450 cation radical (CR) and hydrated electron, which is characterized by the respective transient absorption. The PI of C450 is monophotonic in nature and the yield is dependent on the charge of the micelles. The observation of amine CR in the transient absorption confirms the PET from amine to the excited state of C450 in micelles, which results in the quenching of both fluorescence intensity and lifetime. The decrease in femtosecond fluorescent decay of C450 and the absence of transient C450 radical anion in the presence of amine implies that the concerted ultrafast PET promoted PI and PET to the C450 CR-electron pair. The decrease in the time constant for the formation of relaxed state in the presence of amines is due to the ultrafast PET to the C450 CR-electron pair, which prevents the formation of a relaxed state through recombination at a longer time scale. In the present investigation, the recombination dynamics of the CR-electron pair is justified as one of the origins of the slow solvation in micelles. The influence of amine concentration on the decay of C450 CR indicates ET reaction between C450 CR and amine, which is further confirmed by the bleach recovery of C450 ground state in the presence of amine.

The spin-orbit interaction controls photoinduced interfacial electron transfer in fullerene-perovskite heterojunctions: C60versus C70.

Here, we used collinear and noncollinear density functional theory (DFT) methods to explore the interfacial properties of two heterojunctions between a fullerene (C60 and C70) and the MAPbI3(110) surface. Methodologically, consideration of the spin-orbit interaction has been proven to be required to obtain accurate energy-level alignment and interfacial carrier dynamics between fullerenes and perovskites in hybrid perovskite solar cells including heavy atoms (such as Pb atoms). Both heterojunctions are predicted to be the same type-II heterojunction, but the interfacial electron transfer process from MAPbI3 to C60 is completely distinct from that to C70. In the former, the interfacial electron transfer is slow because of the associated large energy gap, and the excited electrons are thus trapped in MAPbI3 for a while. In contrast, in the latter, the smaller energy gap induces ultrafast electron transfer from MAPbI3 to C70. These points are further supported by DFT-based nonadiabatic dynamics simulations including the spin-orbit coupling (SOC) effects. These gained insights could help rationally design superior fullerene-perovskite interfaces to achieve high power conversion efficiencies of fullerene-perovskite solar cells.

Electron-transfer behaviors between photoexcited metal complex and methyl viologen codoped in ionic nanospheres

In this study, we investigated photo-induced electron transfer (PET) dynamics from [Ru(bpy)3]2+ to MV2+ codoped in ionic nanospheres by picosecond time-resolved luminescence spectroscopy. The luminescence from [Ru(bpy)3]2+ was decreased with an increase of the MV2+ content in nanospheres, suggesting an electron transfer from the 3MLCT excited state of [Ru(bpy)3]2+ to MV2+. The fast decay component with the time-constant of 62 ns was found in the luminescence decay kinetics. This component is associated with a Perrin-type electron transfer and increases with an increase of the MV2+ content, suggesting the efficient Perrin-type electron transfer in the higher MV2+ content. In addition, the decay component of 280∼410 ns depending on a MV2+ concentration is explained by the dynamic-type electron transfer since the inverse lifetime of this component exhibits the linear dependence on the MV2+ content. The Perrin- and dynamic-type electron transfer rates were determined to be 1.4 × 107 s−1 and 7.8 × 10−3 nmol−1 mg μs−1, respectively. The PET efficiency was determined 70 % in ionic nanospheres containing 92 nmol/mg of [Ru(bpy)3]2+ and 152 nmol/mg of MV2+.

Chemical control of competing electron transfer pathways in iron tetracyano-polypyridyl photosensitizers.

Photoinduced intramolecular electron transfer dynamics following metal-to-ligand charge-transfer (MLCT) excitation of [Fe(CN)4(2,2′-bipyridine)]2− (1), [Fe(CN)4(2,3-bis(2-pyridyl)pyrazine)]2− (2) and [Fe(CN)4(2,2′-bipyrimidine)]2− (3) were investigated in various solvents with static and time-resolved UV-Visible absorption spectroscopy and Fe 2p3d resonant inelastic X-ray scattering (RIXS). This series of polypyridyl ligands, combined with the strong solvatochromism of the complexes, enables the 1MLCT vertical energy to be varied from 1.64 eV to 2.64 eV and the 3MLCT lifetime to range from 180 fs to 67 ps. The 3MLCT lifetimes in 1 and 2 decrease exponentially as the MLCT energy increases, consistent with electron transfer to the lowest energy triplet metal-centred (3MC) excited state, as established by the Tanabe–Sugano analysis of the Fe 2p3d RIXS data. In contrast, the 3MLCT lifetime in 3 changes non-monotonically with MLCT energy, exhibiting a maximum. This qualitatively distinct behaviour results from a competing 3MLCT → ground state (GS) electron transfer pathway that exhibits energy gap law behaviour. The 3MLCT → GS pathway involves nuclear tunnelling for the high-frequency polypyridyl breathing mode (hν = 1530 cm−1), which is most displaced for complex 3, making this pathway significantly more efficient. Our study demonstrates that the excited state relaxation mechanism of Fe polypyridyl photosensitizers can be readily tuned by ligand and solvent environment. Furthermore, our study reveals that extending charge transfer lifetimes requires control of the relative energies of the 3MLCT and the 3MC states and suppression of the intramolecular distortion of the acceptor ligand in the 3MLCT excited state.

Photoinduced electron transfer dynamics of AuNPs and Au@PdNPs supported on graphene oxide probed by dark-field hyperspectral microscopy.

The time scale for interfacial photoinduced electron transfer (PeT) in plasmonic nanoparticles is not well established and the details are still under debate. This has renewed the interest in studying the electron transfer effect from both experimental and theoretical points of view. We present a quantitative analysis of PeT in single spherical gold (Au) and gold@palladium core@shell (Au@Pd) nanoparticles supported on reduced graphene oxide (RGO) using dark-field hyperspectral microscopy (DFHM) and electrochemical impedance spectroscopy (EIS). By studying the plasmon bandwidth in the scattering spectra of single particles and by correlating it to the plasmon damping processes we showed that PeT occurs from the AuNPs to RGO in a 10 fs time scale with a quantum efficiency of 35%. The introduction of a Pd shell on the AuNPs decreases the PeT time, with transfer occurring in as little as 1.7 fs with quantum yield higher than 74%. Furthermore, EIS showed a smaller resistance for PeT on RGO/Au@PdNPs under green light illumination. Our results can improve the understanding of the chemical interface damping process due to PeT in plasmonic nanomaterials and can enable the design of more efficient plasmon enhanced photocatalysts.

Unsymmetrical Bis-Alkynyl Complexes Based on Co(III)(cyclam): Synthesis, Ultrafast Charge Separation, and Analysis.

Donor-bridge-acceptor (D-B-A) systems with a polarizable bridge can afford rapid photoinduced electron transfer dynamics that may be susceptible to rate modulation by infrared excitation. We describe the synthesis, characterization, and electronic structure of a class of readily assembled D-B-A structures linked by a cobalt cyclam bridge. The reaction between [Co(cyclam)Cl2]Cl and 4-ethynyl-N-isopropyl-1,8-naphthalimide (HC2NAPiPr) yields [Co(cyclam)(C2NAPiPr)Cl]Cl (1), which reacts with LiC2Y at -78 °C to afford [Co(cyclam)(C2NAPiPr)(C2D)]Cl with D as C6H4-4-NMe2 (2a), NAPiPr (2b), Ph (2c), and C6H4-4-N(4-MeOPh)2 (2d). Molecular structures of 1 and 2a were established using single-crystal X-ray diffraction, while the redox properties and fluorescence profiles of compounds 1 and 2 were examined using voltammetric and steady-state emission techniques, respectively. The electronic structures and photophysical properties of these compounds were studied using density functional theory and time-dependent density functional theory methods. The excited-state dynamics of compounds 1, 2a, and 2d were explored using femtosecond transient absorption spectroscopy with 400 nm excitation and detection in both the visible and mid-IR spectral regions. Formation of a long-lived excited state was complete within 20 ps of excitation in all three compounds. Ultrafast spectral changes observed in 2a and 2d within the first 20 ps indicated the formation of a charge separated state (CS state, D+-B-A-) with characteristic times of less than 0.1 and 0.25 ps, respectively. The CS state undergoes rapid charge recombination (8 ps in 2a and 4 ps in 2d). The CS dynamics is facilitated by the Co center, which mixes the bright NAP-centered electronic state with a pure CS state. The mixing strength depends on the donor energetics and conformation, which significantly influences the charge transfer dynamics in 2a and 2d.

Theoretical Insights into Interfacial Electron Transfer between Zinc Phthalocyanine and Molybdenum Disulfide.

A comprehensive understanding of interfacial charge transfer dynamics is critical for improving the optoelectronic efficiency of organic-transition metal dichalcogenide heterostructures. In this work we have employed density functional theory (DFT) and developed nonadiabatic dynamics simulation approaches to study the photoinduced electron transfer dynamics at the interface of zinc phthalocyanine (ZnPc) and molybdenum disulfide (MoS2). Our present results show that ZnPc is adsorbed in a parallel orientation on MoS2 through a weak van der Waals interaction. Photoirradiation excites an electron of ZnPc into its lowest unoccupied molecular orbital (LUMO), which is primarily located on ZnPc but has a tail on MoS2. This enhances the vibronic coupling between the LUMO of ZnPc and adiabatic states of MoS2, thereby benefiting the interfacial electron transfer. The LUMO of ZnPc is also calculated to be 0.27 eV higher than the conduction band minimum (CBM) of MoS2 so that the electron transfer from ZnPc to MoS2 is thermodynamically favorable. Further nonadiabatic dynamics simulations verify such ultrafast electron transfer and estimate its time scale of ca. 10 fs. In this process, the low-frequency out-of-plane vibration of MoS2, and low- and high-frequency in-plane and out-of-plane vibrations of ZnPc are found to play an important role in regulating this interfacial electron transfer. In-depth analysis also reveals that atomic motion induced changes of adiabatic states is a dominant factor leading to such ultrafast interfacial electron transfer. These insights could be useful for understanding charge transfer processes at interfaces of heterostructures.

Photoinduced electron transfer processes of (E)-9-(4-nitrostyryl)anthracene in non-polar solvent medium: generation of long-lived charge-separated states $$^{\S }$$ §

In the present study, photoinduced electron transfer (PET) dynamics between N,N-diethylaniline (DEA) and (E)-9-(4-nitrostyryl)anthracene ( $$\hbox {An-NO}_{2}$$ ) in a non-polar solvent medium {methylcyclohexane (MCH)}, has been investigated. The rate constant of back electron transfer ( $$\hbox {k}_{{\mathrm{BET}}}$$ ) for the $$\hbox {An-NO}_{2}$$ – DEA pair was $$\sim 3.8\times 10^{5}~\hbox {s}^{-1}$$ which is ca. 2 orders of magnitude less compared to the anthracene (An)-DEA (control) system. The results indicate that long-lived charge separated species can be generated using the design strategy used herein by achieving resonance stabilization of the excited state (acceptor) radical via conjugation. SYNOPSIS For N,N-diethylaniline/(E)-9-(4-nitrostyryl)anthracene donor-acceptor pair, the back electron transfer rate constant is $$\sim 2$$ orders of magnitude slower compared to N,N-diethylaniline/anthracene system. The results indicate that organic molecules with extended $$\uppi $$ -conjugation can be utilized for generating long-lived charge separated states via bimolecular PET, due to increased feasibility of charge delocalization.

Photoinduced electron transfer dynamics in dye-sensitized ZnO nanowire photoanodes

A photoanode using dye-sensitized ZnO nanowire (NW) is a good candidate for low-cost, colorful, light-weight and flexible solar cell material. We have synthesized a ZnO NW anode and a ZnO nanowire–nanoparticle (NWNP) anode, in which ZnO nanoparticles (NPs) are decollated on the surface of NWs. Photo-induced electron transfer dynamics from the excited state of sensitizer dye (D149) to the conduction band of ZnO NW and ZnO NWNP was clarified using femtosecond transient absorption spectroscopy. The decay of the single excited state ([Formula: see text]) of D149 was faster in ZnO NW than that of ZnO NWNP, indicating that NW is more suitable as an efficient electron acceptor.

Photoinduced Electron Transfer in Naphthalene Diimide End-Capped Thiophene Oligomers

A series of linear thiophene oligomers containing 4, 6, 8, 10, and 12 thienylene units were synthesized and end-capped with naphthalene diimide (NDI) acceptors with the objective to study the effect of oligomer length on the dynamics of photoinduced electron transfer and charge recombination. The synthetic work afforded a series of nonacceptor-substituted thiophene oligomers, Tn, and corresponding NDI end-capped series, TnNDI2 (where n is the number of thienylene repeat units). This paper reports a complete photophysical characterization study of the Tn and TnNDI2 series by using steady-state absorption, fluorescence, singlet oxygen sensitized emission, two-photon absorption, and nanosecond-microsecond transient absorption spectroscopy. The thermodynamics of photoinduced electron transfer and charge recombination in the TnNDI2 oligomers were determined by analysis of photophysical and electrochemical data. Excitation of the Tn oligomers gives rise to efficient fluorescence and intersystem crossing to a triplet excited state that is easily observed by nanosecond transient absorption spectroscopy. Bimolecular photoinduced electron transfer from the triplet states, 3Tn*, to N,N-dimethylviologen (MV2+) occurs, and by using microsecond transient absorption it is possible to assign the visible region absorption spectra for the one electron oxidized (polaron) states, Tn+•. The fluorescence of the TnNDI2 oligomers is quenched nearly quantitatively, and no long-lived transients are observed by nanosecond transient absorption. These findings suggest that rapid photoinduced electron transfer and charge recombination occurs, NDI-1(Tn)*-NDI → NDI-(Tn)+•-NDI-• → NDI-Tn-NDI. Preliminary femtosecond-picosecond transient absorption studies on T4NDI2 reveal that both forward electron transfer and charge recombination occur with k > 1011 s-1, consistent with both reactions being nearly activationless. Analysis with semiclassical electron transfer theory suggests that both reactions occur at near the optimum driving force where -ΔG ∼ λ.

How good is the generalized Langevin equation to describe the dynamics of photo-induced electron transfer in fluid solution?

The dynamics of unimolecular photo-triggered reactions can be strongly affected by the surrounding medium for which a large number of theoretical descriptions have been used in the past. An accurate description of these reactions requires knowing the potential energy surface and the friction felt by the reactants. Most of these theories start from the Langevin equation to derive the dynamics, but there are few examples comparing it with experiments. Here we explore the applicability of a Generalized Langevin Equation (GLE) with an arbitrary potential and a non-Markovian friction. To this end, we have performed broadband fluorescence measurements with sub-picosecond time resolution of a covalently linked organic electron donor-acceptor system in solvents of changing viscosity and dielectric permittivity. In order to establish the free energy surface (FES) of the reaction, we resort to stationary electronic spectroscopy. On the other hand, the dynamics of a non-reacting substance, Coumarin 153, provide the calibrating tool for the non-Markovian friction over the FES, which is assumed to be solute independent. A simpler and computationally faster approach uses the Generalized Smoluchowski Equation (GSE), which can be derived from the GLE for pure harmonic potentials. Both approaches reproduce the measurements in most of the solvents reasonably well. At long times, some differences arise from the errors inherited from the analysis of the stationary solvatochromism and at short times from the excess excitation energy. However, whenever the dynamics become slow, the GSE shows larger deviations than the GLE, the results of which always agree qualitatively with the measured dynamics, regardless of the solvent viscosity or dielectric properties. The method applied here can be used to predict the dynamics of any other reacting system, given the FES parameters and solvent dynamics are provided. Thus no fitting parameters enter the GLE simulations, within the applicability limits found for the model in this work.

Effect of Conjugation Length on Photoinduced Charge Transfer in π-Conjugated Oligomer-Acceptor Dyads.

A series of π-conjugated oligomer-acceptor dyads were synthesized that feature oligo(phenylene ethynylene) (OPE) conjugated backbones end-capped with a naphthalene diimide (NDI) acceptor. The OPE segments vary in length from 4 to 8 phenylene ethynene units (PEn-NDI, where n = 4, 6 and 8). Fluorescence and transient absorption spectroscopy reveals that intramolecular OPE → NDI charge transfer dominates the deactivation of excited states of the PEn-NDI oligomers. Both charge separation (CS) and charge recombination (CR) are strongly exothermic (ΔG0CS ∼ -1.1 and ΔG0CR ∼ -2.0 eV), and the driving forces do not vary much across the series because the oxidation and reduction potentials and singlet energies of the OPEs do not vary much with their length. Bimolecular photoinduced charge transfer between model OPEs that do not contain the NDI acceptors with methyl viologen was studied, and the results reveal that the absorption of the cation radical state (OPE+•) remains approximately constant (λ ∼ 575 nm) regardless of oligomer length. This finding suggests that the cation radical (polaron) of the OPE is relatively localized, effectively occupying a confined segment of n ≤ 4 repeat units in the longer oligomers. Photoinduced intramolecular electron transfer dynamics in the PEn-NDI series was investigated by UV-visible femtosecond transient absorption spectroscopy with visible and mid-infrared probes. Charge separation occurs on the 1-10 ps time scale with the rates decreasing slightly with increased oligomer length (βCS ∼ 0.15 Å-1). The rate for charge-recombination decreases in the sequence PE4-NDI > PE6-NDI ∼ PE8-NDI. The discontinuous distance dependence in the rate for charge recombination may be related to the spatial localization of the positive polaron state in the longer oligomers.

Through-Space Ultrafast Photoinduced Electron Transfer Dynamics of a C70-Encapsulated Bisporphyrin Covalent Organic Polyhedron in a Low-Dielectric Medium.

Ultrafast photoinduced electron transfer (PIET) dynamics of a C70-encapsulated bisporphyrin covalent organic polyhedron hybrid (C70@COP-5) is studied in a nonpolar toluene medium with fluorescence and transient absorption spectroscopies. This structurally rigid donor (D)-acceptor (A) molecular hybrid offers a new platform featuring conformationally predetermined cofacial D-A orientation with a fixed edge-to-edge separation, REE (2.8 Å), without the aid of covalent bonds. Sub-picosecond PIET (τET ≤ 0.4 ps) and very slow charge recombination (τCR ≈ 600 ps) dynamics are observed. The origin of these dynamics is discussed in terms of enhanced D-A coupling (V = 675 cm-1) and extremely small reorganization energy (λ ≈ 0.18 eV), induced by the intrinsic structural rigidity of the C70@COP-5 complex.

Photoinduced electron transfer from rylenediimide radical anions and dianions to Re(bpy)(CO)3 using red and near-infrared light.

A major goal of artificial photosynthesis research is photosensitizing highly reducing metal centers using as much as possible of the solar spectrum reaching Earth's surface. The radical anions and dianions of rylenediimide (RDI) dyes, which absorb at wavelengths as long as 950 nm, are powerful photoreductants with excited state oxidation potentials that rival or exceed those of organometallic chromophores. These dyes have been previously incorporated into all-organic donor-acceptor systems, but have not yet been shown to reduce organometallic centers. This study describes a set of dyads in which perylenediimide (PDI) or naphthalenediimide (NDI) chromophores are attached to Re(bpy)(CO)3 through either the bipyridine ligand or more directly to the Re center via a pyridine ligand. The chromophores are reduced with a mild reducing agent, after which excitation with long-wavelength red or near-infrared light leads to reduction of the Re complex. The kinetics of electron transfer from the photoexcited anions to the Re complex are monitored using transient visible/near-IR and mid-IR spectroscopy, complemented by theoretical spectroscopic assignments. The photo-driven charge shift from the reduced PDI or NDI to the complex occurs in picoseconds regardless of whether PDI or NDI is attached to the bipyridine or to the Re center, but back electron transfer is found to be three orders of magnitude slower with the chromophore attached to the Re center. These results will inform the design of future catalytic systems that incorporate RDI anions as chromophores.