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The photophysical properties of CdSe and ZnS(CdSe) semiconductor quantum dots in nonpolar and aqueous solutions with steady-state (absorption and emission) and time-resolved (timecorrelated single-photon-counting) spectroscopy are examined. The result reveals that even with heavily quenched CdSe solublized with mercapotacetic acid it is still possible to modulate the emission using a hole acceptor such as adenine.

Singlet fission is a process that occurs in select molecular systems wherein a singlet excited state divides its energy to form two triplet excitations on neighboring chromophores. While singlet fission has been largely studied in molecular crystals, colloidal nanoparticles offer the ability to investigate fission using liquid suspensions, allowing questions regarding the importance of molecular arrangement and charge transfer to be assessed. Herein, we report the synthesis of aqueous colloidal nanoparticles of 5,12-diphenyltetracene (DPT), a material recently demonstrated to undergo singlet fission in disordered films. Upon synthesis, nanoparticles display absorption features that lie between those of monomeric DPT and disordered DPT films. These features evolve over a few days in a manner that suggests an increase in the degree of association between neighboring molecules within the nanoparticles. Transient absorption and time-resolved emission experiments indicate that photoexcited DPT nanoparticles undergo fission, but produce a lower triplet yield than disordered films.

We use photoelectron emission spectroscopy with vacuum microjet technique and quantum chemistry calculations to investigate electronic structure and stability of aqueous phosphate anions. On the basis of the measured photoelectron spectra of sodium phosphates at different pH, we report the lowest vertical ionization energies of monobasic (9.5 eV), dibasic (8.9 eV), and tribasic (8.4 eV) anions. Electron binding energies were in tandem modeled with ab initio methods, using a mixed dielectric solvation model together with up to 64 explicitly solvating water molecules. We demonstrate that two solvation layers of explicit water molecules are needed to obtain converged values of vertical ionization energies (VIEs) within this mixed solvation model, leading to very good agreement with experiment. We also show that the highly charged PO(4)(3-) anion, which is electronically unstable in the gas phase, gains the electronic stability with about 16 water molecules, while only 2-3 water molecules are sufficient to stabilize the doubly charged phosphate anion. We also investigate the effect of ion pairing on the vertical ionization energy. In contrast to protonation (leading to a formation of covalent O-H bond), sodiation (leading to an anion···Na(+) ion pair) has only a weak effect on the electron binding energy.

We have simulated ionization of purine nucleic acid components in the gas phase and in a water environment. The vertical and adiabatic ionization processes were calculated at the PMP2/aug-cc-pVDZ level with the TDDFT method applied to obtain ionization from the deeper lying orbitals. The water environment was modeled via microsolvation approach and using a nonequilibrium polarizable continuum model. We have characterized a set of guanine tautomers and investigated nucleosides and nucleotides in different conformations. The results for guanine, i.e., the nucleic acid base with the lowest vertical ionization potential, were also compared to those for the other purine base, adenine. The main findings of our study are the following: (i) Guanine remains clearly the base with the lowest ionization energy even upon aqueous solvation. (ii) Water solvent has a strong effect on the ionization energetics of guanine and adenine and their derivatives; the vertical ionization potential (VIP) is lowered by about 1 eV for guanine while it is ∼1.5 eV higher in the nucleotides, overall resulting in similar VIPs for GMP(-), guanosine and guanine in water. (iii) Water efficiently screens the electrostatic interactions between nucleic acid components. Consequently, ionization in water always originates from the base unit of the nucleic acid and all the information about conformational state is lost in the ionization energetics. (iv) The energy splitting between ionization of the two least bound electrons increases upon solvation. (v) Tautomerism does not contribute to the width of the photoelectron spectra in water. (vi) The effect of specific short-range interactions with individual solvent molecules is negligible for purine bases, compared to the long-range dielectric effects of the aqueous medium.

The spectroscopy and dynamics of a novel molecular architecture that mimics natural light harvesting have been characterized. The deployment of 9,9-dimethyl-2-fluorenyl (DMF) chromophores in atactic macrocyclic poly(9,9-dimethyl-2-vinylfluorene) is similar to that in the light harvesting antenna LH2 of the purple photosynthetic bacteria. A variety of spectroscopic probes are used to study the dynamics in these novel polymer systems. The number of chromophores is tuned from 12-142 identical chromophore units. Steady-state absorption and emission measurements, time-resolved fluorescence, and ultrafast transient absorption anisotropy techniques provide evidence for distinct differences in the photophysics of matching molecular weight linear and cyclic polymers and of the occurrence of energy transfer in these polymers. There is direct evidence of energy transfer in these macrocycles manifested in the depolarization decay components, which are characterized by two exponentials and are substantially faster than observed for reorientation of the free DMF chromophore. The time constants for the macrocycles are 700-900 fs and 7-8 ps and are size dependent; the biexponential decay arises from conformational and stereochemical disorder and can be well described by a master equation simulation assuming Förster incoherent hopping on model polymer structures. The results suggest energy hopping between adjacent chromophores on a 1 ps time scale. The pathway for energy migration is shown to be primarily between nearest neighbors along the cyclic backbone, but there is a considerable spread in the site-to-site hopping rates. Small cycles adopt a pseudoplanar ring type arrangement of the chromophore transition dipoles as observed in bacterial light harvesting antenna, and it is found that the linear polymers also show similar short-range planarity of transition dipoles. Overall, it is found that such small macrocyclic polymers possess excellent characteristics for light harvesting among identical chromophores and behave as a circular photonic wire.