
Robert L. Byer
Stanford Univ., USA
2009 Frederic Ives Medal/Jarus W. Quinn Endowment Recipient
Ives Medal Lecture: TBA
Biography: Robert L. Byer has conducted research and taught classes on lasers and nonlinear optics at Stanford University since 1969. He has made extraordinary contributions to laser science and technology including the demonstration of the first tunable visible parametric oscillator, the development of the Q-switched unstable resonator Nd:YAG laser, remote sensing using tunable infrared sources, and precision spectroscopy using Coherent Anti Stokes Raman Scattering (CARS). Byer’s ongoing research includes development of nonlinear optical materials and laser diode pumped solid-state laser sources for applications to gravitational wave detection and to laser particle acceleration.
Currently the William R. Kenan Jr. Professor of Applied Physics, Byer has served as vice provost and dean of research at Stanford as well as chair of the Department of Applied Physics, director of the Edward L. Ginzton Laboratory, and Director of the Hansen Experimental Physics Laboratory. He is a founding member of the California Council on Science and Technology and served as chair from 1995–1999. He has been a member of the National Ignition Facility since 2000 and was a member of the Air Force Scientific Advisory Board from 2002–2006. He has served as president of both OSA and IEEE LEOS.
Byer has published more than 500 papers and holds 50 patents in the fields of lasers and nonlinear optics. He is a fellow of OSA, IEEE, APS, AAAS, and LEOS, and is a member of the National Academy of Engineering and the National Academy of Science. |

Robert W. Field
MIT, USA
2009 Arthur L. Schawlow Prize in Laser Science Recipient
Schawlow Prize Lecture: Acetylene: Just Large Enough
Abstract: What can acetylene (H-C≡C-H) do that a diatomic molecule cannot? It can undergo bond-breaking isomerization. The minimum energy isomerization path from acetylene to vinylidene is a very large-amplitude local-bend. How are large-amplitude motions encoded in a spectrum? At high vibrational excitation, anharmonic interactions between vibrational normal-modes become very strong and all of the textbook energy level patterns, upon which assignments are based, are shattered. Most vibrational eigenstates are complex, one might even say “ergodic,” mixtures of many normal-mode basis-states. However, large-amplitude-motion states comprise a tiny fraction of all eigenstates. How does one gain access to these rare large-amplitude states? How does one distinguish a large-amplitude state from an ergodic state in a spectrum? How does one use large-amplitude states to map the chemically interesting isomerization path on the S0 potential energy surface? Access is provided by a “local-bender pluck” state, which exploits anharmonic interactions on the S1 potential energy surface to escape Franck-Condon restrictions in the S1→S0 Stimulated Emission Pumping (SEP) spectrum. A relatively low trans-cis isomerization barrier on S1 provides spectroscopic access to eigenstates proximal to a high barrier on S0. Electronic properties (such as the electric dipole transition moment) serve as embedded reporters on the existence and extent of large-amplitude motions. However, electronic properties give rise to minuscule level splittings. How does one combine a survey over a wide spectral region in search of rare large-amplitude local-bender states yet simultaneously achieve the extremely high resolution necessary to read what the embedded reporter has written? Brooks Pate (University of Virginia) has developed “Chirped Pulse Microwave Spectroscopy (CPMW),” which combines the previously unimaginable combination of survey (10GHz), high-resolution (100kHz), and accurate relative-intensity (1 part in 104) capabilities. The CPMW scheme is perfectly suited to 20 Hz repetition rate pulsed supersonic jet molecular beams and Q-switched Nd:YAG pumped pulsed tunable lasers, upon which most small-molecule spectroscopists depend.
This research has been supported by the Department of Energy (Grant: DE-FG0287ER13671).
Biography: Robert W. Field majored in chemistry at Amherst College (AB thesis with Cooper H. Langford, 1965). He became a physical chemist in the research group of William Klemperer at Harvard University, where he discovered his affinity for multiple resonance spectroscopies and spectroscopic perturbations (PhD, 1972). As a post-doc with Herbert P. Broida and David O. Harris at University of California at Santa Barbara (1971–1974) he performed the first microwave-optical and optical-optical double resonance studies of diatomic molecules using tunable lasers and showed how to extract global insights into the electronic structure of the alkaline earth monoxides from the systematic study of spectroscopic perturbations. At MIT (Assistant Professor 1974, Associate Professor 1978, Professor 1982, Haslam and Dewey Professor 1999) his students and post-docs have continued to develop new laser spectroscopic techniques (most notably Stimulated Emission Pumping) with a goal of uncovering and exploiting unconventional patterns that encode the mechanisms of far-from-equilibrium molecular dynamics, particularly Intramolecular Vibrational Redistribution, Doorway-Mediated Intersystem Crossing, and energy exchange between a Rydberg electron and a molecular ion-core. He is a Fellow of the American Physical Society (APS), The Optical Society (OSA), the American Academy of Arts and Sciences, and the American Association for the Advancement of Science. He has received the Broida (1980) and Plyler (1988) Prizes of the APS, the Lippincott (1990) and Meggers (1996) Awards of the OSA, and the Bomem-Michelson Award of the Coblentz Society. His favorite molecules have been CO, CaF, and acetylene. His book (co-authored with Helene Lefebvre-Brion, 2004), “The Spectra and Dynamics of Diatomic Molecules,” is the user’s guide for both theorists and experimentalists. |