Direct observation of multistep energy transfer in LHCII with fifth-order 3D electronic spectroscopy.

During photosynthesis, sunlight is efficiently captured by light-harvesting complexes, and the excitation energy is then funneled towards the reaction centre. These photosynthetic excitation energy transfer (EET) pathways are complex and proceed in a multistep fashion. Ultrafast two-dimensional electronic spectroscopy (2DES) is an important tool to study EET processes in photosynthetic complexes.

Interplay of hole transfer and host-guest interaction in a molecular dyad and triad: ensemble and single-molecule spectroscopy and sensing applications.

A new molecular dyad consisting of a Cy5 chromophore and ferrocene (Fc) and a triad consisting of Cy5, Fc, and β-cyclodextrin (CD) are synthesized and their photophysical properties investigated at both the ensemble and single-molecule levels. Hole transfer efficiency from Cy5 to Fc in the dyad is reduced upon addition of CD. This is due to an increase in the Cy5-Fc separation (r) when the Fc is encapsulated in the macrocyclic host.

Pathways of energy transfer in LHCII revealed by room-temperature 2D electronic spectroscopy.

We present here the first room-temperature 2D electronic spectroscopy study of energy transfer in the plant light-harvesting complex II, LHCII. Two-dimensional electronic spectroscopy has been used to study energy transfer dynamics in LHCII trimers from the chlorophyll b Qy band to the chlorophyll a Qy band. Observing cross-peak regions corresponding to couplings between different excitonic states reveals partially resolved fine structure at the exciton level that cannot be isolated by pump-probe or linear spectroscopy measurements alone.

Fifth-order three-dimensional electronic spectroscopy using a pump-probe configuration.

We present the theoretical details and experimental demonstration of fifth-order three-dimensional (3D) electronic spectroscopy using a pump-probe beam geometry. This is achieved using a pulse shaper and appropriate phase cycling schemes. We show how 8-step and 27-step phase cycling schemes can measure purely absorptive 3D spectra as well as 3D spectra for the individual fifth-order processes that contribute to the purely absorptive spectrum.

Measuring the spectral diffusion of chlorophyll a using two-dimensional electronic spectroscopy.

Ultrafast two-dimensional electronic spectroscopy has been used to study the spectral diffusion of the Qy transition of chlorophyll a in methanol. The two time frequency-fluctuation correlation function (FFCF) of the transition has been measured using the center line slope method, together with optimized fitting of the linear spectrum. The FFCF was measured to decay over four time scales.

Purely absorptive fifth-order three-dimensional electronic spectroscopy.

We demonstrate a method to measure a purely absorptive fifth-order three-dimensional (3D) electronic spectrum based on a pulse-shaper assisted pump-probe beam geometry setup. The 3D spectra are measured as a function of two independently controlled population times. With phase-cycling and data processing, purely absorptive 3D spectra of chlorophyll a are obtained.

Time resolved velocity map imaging of H-atom elimination from photoexcited imidazole and its methyl substituted derivatives.

The photoresistive properties of DNA bases, amino acids and corresponding subunits have received considerable attention through spectroscopic studies in recent years. One photoresistive property implicates the participation of (1)πσ* states, allowing electronically excited states to evolve either back to the electronic ground state or undergo direct dissociation along a heteroatom-hydride (X-H) coordinate. To this effect, time-resolved velocity map imaging (TR-VMI) studies of imidazole (a subunit of both adenine and histidine) and methylated derivatives thereof have been undertaken, with the goal of understanding the effects of increasing molecular complexity, through methylation, on the dynamics following photoexcitation at 200 nm.

Time-resolved velocity map ion imaging study of NH(3) photodissociation.

Following excitation of the A state nu(2) (')=4 mode in ammonia, we show how the time scale to dissociation of the N-H bond depends on the internal energy imparted to the NH(2) photofragment. Using a combination of femtosecond pump/probe spectroscopy and velocity map ion imaging techniques, the time and energy resolved H-atom elimination can be directly related to the nonadiabatic nature of the photodissociation for high kinetic energy H atoms with evidence for adiabatic dynamics to dissociation giving the lowest energy H atoms. Extrapolation of the time scales for dissociation versus internal energy of the NH(2) photofragment implies that dissociation to the vibrationless ground state of NH(2) occurs in <50 fs, in very good agreement with frequency resolved measurements.