Broadly speaking, our group develops and utilizes new light sources and techniques to follow the motions of molecular systems in real-time. Developing new technologies and physics ideas go hand in hand with gaining insight into chemical dynamics. We have built two novel instruments in the lab, one for Cavity-Enhanced Transient Absorption Spectroscopy (CETAS), and another for XUV Time-Resolved Photoelectron Spectroscopy (TRPES). Both are based on upon our home-built frequency comb lasers.
Frequency comb lasers, recognized with the 2005 Nobel prize in physics, have revolutionized atomic clocks and precision measurement. However, their enormous potential for ultrafast time-resolved measurements has been largely unexplored. The exquisite coherence of the pulse train of a frequency comb enables the signals from successive pulses to be coherently added and stored. This leads to orders of magnitude improvement in the attainable signal to noise of time-resolved experiments, enabling new and exciting directions that simultaneously push the boundaries of our ability to probe matter in the time and frequency domains. Now mature in the visible and near-infrared, recent breakthroughs have pushed frequency comb technology into more spectroscopically interesting regions of the electromagnetic spectrum. Mid-IR combs enable the probing and excitation of vibrational dynamics and UV combs enable the probing of electronic dynamics.
Our frequency comb lasers are based on Ytterbium (Yb) doped optical fibers. The small quantum defect, high doping, and the availability of double clad large-mode-area photonic crystal fibers makes Yb ideal for scaling to high average power. We have built in our lab a 100 W Yb:fiber laser for generating high order harmonics at high repetition rate.
Cavity-Enhanced High Harmonic Generation
High harmonic generation (HHG) can be used to generate ultrashort pulses of extreme ultraviolet (XUV) and soft x-ray light. These photon energies are ideal for performing photoelectron spectroscopy from surfaces and probing absorption edges of soft matter. However, due to limitations in laser power, most high-harmonic generation systems run at repetition rates around 1-10 kHz. We generate harmonics at repetition rates around 100 MHz, using the technique of cavity-enhanced high-order harmonic generation. In the cavity enhancement technique, a frequency comb laser is resonantly enhanced in Fabry-Perót resonator whose repetition rate and carier-envelope offset frequency are matched to that of the laser. These sources are now among the worlds brightest XUV sources.
Repetition-rate is particularly critical when recording electron signals from surfaces, where space-charge puts severe limitations on the number of electrons per pulse from the sample. In collaboration with the White group, we have built a beamline to couple our cavity-enhanced HHG source to a UHV chamber for TRPES from surfaces.
Time Resolved Photocatalysis
Photo-induced charge transfer processes at molecule-semiconductor interfaces are central to a wide range of technological applications including solar energy conversion, heterogeneous photocatalysis, and organic optoelectronics. In general, these photoreactions involve a number of elementary steps including charge carrier (e−/h+) excitation and thermalization, interfacial charge transfer, adsor- bate intramolecular relaxation, and subsequent reaction. The overall efficiency of photoconversion is determined by the complex interplay between these elementary processes, and identifying the rate limiting steps can ultimately provide the insight needed to improve efficiency.
Although modern time-resolved spectroscopic techniques have focused on some individual aspects of semiconductor photoconversion, the dynamics of molecular photoreactions on semiconductor surfaces remains largely unexplored. We have recently connected our beamline to a UHV surface science chamber and are preparing for TRPES experiments.
First experiments will focus on photo-oxidation reactions on TiO2 surfaces, which are important for both industrial and environmental applications.
Cavity-Enhanced Ultrafast Spectroscopy
Ultrafast spectroscopy is widely applied to a range of systems from molecules in solution to isolated molecules in the gas phase. However, measurements in the gas phase are almost always done using photoionization, due to the very high sensitivity of charged particle detection, whereas measurements in solution are restricted to measuring absorbed or nonlinear scattered light. Photoionization of gas phase clusters is also problematic due to cluster fragmentation. Comparison of gas phase, cluster, and solution phase data is thus often highly nontrivial.
We have developed techniques using frequency combs and Fabry-Perót resonators to achieve a large sensitivity in transient absorption spectroscopy and 2D spectroscopy, so that light signals can be recorded from dilute molecular beams. We have demonstrated detection limits as low as ΔOD = 2×10¯¹º. This allows the direct comparison of solution-phase and gas-phase data, and more importantly allows ultrafast vibrational spectroscopy to be applied to gas-phase and cluster systems.
Vibrational Dynamics of Clusters
While hydrogen bonding is a ubiquitous theme in Chemistry, the hydrogen bond is actually a complicated subject. Many interactions contribute to hydrogen bonding, including electrostatic forces, polarization, dispersion forces, and also a component of covalent bonding.
The complexities of the hydrogen bond play a major role in the difficulties in the theo- retical description of liquid water. Water, nature’s most important solvent, makes extensive use of the hydrogen bond and plays a central role in chemistry and biology. Water mediates the interactions between molecules, altering energy levels of solvated species, modifying po- tential energy profiles along reaction coordinates , and facilitates efficient proton transport through ion channels and interfaces
Using cavity-enhanced techniques, we can follow vibrational energy flow in small gas-phase hydrogen bonded clusters, such as water. These studies allow us to build up the liquid “one molecule at a time” and gain a very systematic understanding of the vibrational couplings between bonds.