As a demonstration, Oliver, Lewis and Fleming used their 2D-EV spectroscopy technique to study the excited-state relaxation dynamics of DCM dye dissolved in a deuterated solvent. DCM is considered a model "push-pull" emitter meaning it contains both electron donor and acceptor groups - but with a long-standing question as to how it fluoresces back to the ground energy state.
"From 2D-EV spectra, we elucidate a ballistic mechanism on the excited state potential energy surface whereby molecules are almost instantaneously projected uphill in energy toward a transition state between locally excited and charge-transfer states before emission," Oliver says. "The underlying electronic dynamics, which occur on the hundreds of femtoseconds time-scale, drive the far slower ensuing nuclear motions on the excited state potential surface, and serve as an excellent illustration for the unprecedented detail that 2D-EV will afford to photochemical reaction dynamics."
One example of how 2D-EV might be applied is in the study of rhodopsin, the pigment protein in the retina of the eye that is the primary light detector for vision, and carotenoids, the family of pigment proteins, such as chlorophyll, found in green plants and certain bacteria that absorb light for photosynthesis.
"The nonradiative energy transfer in rhodopsin and carotenoids is thought to involve the breakdown of one of the most widely used approximations of quantum mechanics, the Born-Oppenheimer approximation, which states that since motion of electrons are far faster than nuclei, as represented by vibrational motion, the nuclei respond to changes in electronic states," Oliver says. "With 2D-EV, we will be able to directly correlate the degrees of electronic and vibrational freedom and track their evolution as a function of time. It's a chicken and egg kind of problem: Do the electrons or nuclei move first? 2D-EV will give us insight
|Contact: Lynn Yarris|
DOE/Lawrence Berkeley National Laboratory