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Benjamin Schwartz, Ph.D.

Website:

Benjamin Schwartz's Home Page.

Email Address:

schwartz@chem.ucla.edu

Work Email Address:

schwartz@chem.ucla.edu

Laboratory Address:

Young Hall 2072

Work Address:

Young Hall 2077A

Lab Number:

1 (310) 206-6418

Work Phone Number:

1 (310) 206-4113
Vice Chair of Education, Chemistry and Biochemistry
Professor
Chemistry and Biochemistry, Physical Chemistry
Member
California NanoSystems Institute

A Short Biography:

Professor Schwartz received his bachelor's degree with a double major in physics and chemistry from the University of Michigan in 1986, and went on to receive his Ph.D in physical chemistry from the University of California, Berkeley in 1992, working with Prof. Charles B. Harris. Professor Schwartz then spent 2.5 years working as an NSF postdoctoral fellow at the University of Texas at Austin with Prof. Peter J. Rossky, and an additional 1.5 years working as a postdoctoral fellow at the University of California, Santa Barbara with Nobel Laureate Alan J. Heeger. Prof. Schwartz joined the UCLA faculty in 1997 as an assistant professor, reached the rank of associate professor in 2002 and reached his current rank of full professor in 2004.

Awards and Honors:

Institute for Polymers and Organic Solids, UC Santa Barbara Postdoctoral Fellow (1995-1996) ; University of Texas at Austin NSF Postdoctoral Fellowship in Chemistry (1993-1995) ; Camille Dreyfus Teacher-Scholar Award ; Hanson-Dow Award for Excellence in Teaching ; Research Corporation Cottrell Scholar Award ; Seaborg Award ; ACS APS Journal of Physical Chemistry Senior Editor for Journal of Physical Chemistry

Research Interest:

Research in the Schwartz group is aimed a building a molecular-level understanding of chemical reactivity in complex environments by studying condensed-phase chemical reaction dynamics using both experimental and theoretical techniques: femtosecond laser spectroscopies and mixed quantum/classical molecular dynamics simulations. Projects fall into two main areas: studies of how solvent motions control the rates and even the choice of products in solution-phase chemical reactions, and investigations into the electronic structure and optoelectronic behavior of semiconducting conjugated polymers.

Our first main area centers on solvent effects on chemical reactivity. We use femtosecond pump-probe spectroscopies to experimentally monitor the course of solution-phase chemical reactions in real time, allowing us to "watch" the motions of solvent molecules responding to chemical changes of reacting solutes, monitor the flow of energy between reacting species and the solvent, and identify the motion of electrons during charge transfer reactions. These experiments are accompanied by computer simulations, which make use of sophisticated algorithms allowing for quantum dynamics in the absence of the Born-Oppenheimer approximation (see Figure 1). Projects range from studies of model systems such as solvated metal anions or solvated electrons to investigations of large organic molecules with complex photochemistry. Simulations are done in close connection to the femtosecond experiments, so that experimental results drive new simulations and vice-versa, providing students in the group with an opportunity to do both experimental and theoretical work.

Our second main area of research is focused on the electronic structure of conjugated polymers, which have enormous commercial potential for use in light-emitting diodes, displays and photodetectors. Upon photoexcitation, the electrons and holes created in semiconducting polymers interact with their environment, leading to relaxation processes on multiple time scales; many of the important dynamical issues are qualitatively similar to the solution phase reactions discussed above. One of the main focuses in our group is the study of how excitations on neighboring conjugated polymer chains interact. By combining information from femtosecond and steady-state spectroscopies, scanning force microscopy, and the behavior of polymer light-emitting or photovoltaic devices, we can identify and potentially eliminate undesirable electronic properties. Projects include: studies of energy transfer and lasing behavior in inorganic/conjugated polymer composite materials (see Figure 2); studies of the electronic processes that take place in conjugated polymer/fullerene bulk heterojunction solar cells; and characterization of polymer-metal electrode interfaces using non-linear spectroscopies such as second harmonic generation. This work provides students the opportunity to learn fundamental photophysics, polymer processing techniques, and semiconductor device construction.


Detailed Biography:

Professor Schwartz joined the faculty at UCLA in 1997, which he established a research program aimed at building a molecular-level picture of chemical reaction dynamics in the condensed phase. The Schwartz group is one of the few pursing both experimental and theoretical approaches to solving chemical reaction dynamics problems. The experimental techniques focus largely on femtosecond spectroscopies, and particularly 3-pulse pump-probe experiments that allow for direct examination of transient species such as the excited states of conjugated polymers or reactive solvated atoms and electrons. The theoretical techniques include both the development and application of new algorithms for dealing with the breakdown of the Born-Oppenheimer approximation in mixed quantum/classical simulations and the development of new methods for deriving the pseudopoentials used in such simulations. Prof. Schwartz has served as the department's curriculum committee chair from 2003-2005 and has been serving as the department's graduate advisor since 2005; Prof. Schwartz was also the department's elected representative to the College Faculty Executive Committee from 2003-2007. Prof. Schwartz is also currently a Senior Editor for the Journal of Physical Chemistry, and serves on the advisory boards of several other journals. Prof. Schwartz has authored over 100 refereed publications during his career.

Publications:

Larsen, R. E. Schwartz, B. J.   Full configuration interaction computer simulation study of the thermodynamic and kinetic stability of hydrated dielectrons J Phys Chem B Condens Matter Mater Surf Interfaces Biophys, 2006; 110(2): 1006-14.
T. Mitsumori, I. M. Craig, I. B. Martini, B. J. Schwartz and F. Wudl   "Synthesis and Color Tuning Properties of Blue Highly Fluorescent Vinyl Polymers Containing a Pendant Pyrrolopyridazine", Macromol., 2005; 38: 4698-704.
M. J. Bedard-Hearn, R. E. Larsen and B. J. Schwartz.   "The Role of Solvent Structure in the Absorption Spectrum of Solvated Elections: Mixed Quantum/Classical Simulations in Tetrahydrofuran (THF)", J. Chem. Phys., 2005; 122(134506): 1-11.
I. B. Martini, E. R. Barthel and B. J. Schwartz.   "Building a Molecular-Level Picture of the Ultrafast Dynamics of the Charge-Transfer-to-Solvent Reaction of Sodide (Na-)", Pure Appl. Chem., 2004; 76: 1809-1825.
I. B. Martini, et al.   "Evidence for the Direct Production of Interchain Species in Conjugated Polymer Films: The Ultrafast Stimulated Emission and Fluorescence Dynamics of MEH-PPV", Phys. Rev. B, 2004; 69(3)(035204): 1-12.
I. B. Martini and B. J. Schwartz   "Exciton-exciton Annihilation and the Production of Interchain Species in Conjugated Polymer Films", Polym. Preprints, 2004; 45: 201-2.
R. E. Larsen and B. J. Schwartz   "Mixed Quantum/Classical Molecular Dynamics Simulations of the Hydrated Dielectron: The Role of Exchange in Condensed-Phase Structure, Dynamics and Spectroscopy", J. Phys. Chem., 2004; 108(31): 11760-73.
M. C. Cavanagh, I. B. Martini and B. J. Schwartz   "Revisiting the Pump-Probe Polarized Hole-Burning of the Hydrated Electron: Is its Absorption Spectrum Inhomogeneously Broadened?", Chem. Phys. Lett., 2004; 396(4-6): 359-66.
R. E. Larsen and B. J. Schwartz.   "An Efficient Real-Space Configuration-Interaction Method for Simulation of Multi-Electron Mixed Quantum/Classical Non-Adiabatic Dynamics in the Condensed Phase", J. Chem. Phys., 2003; 119(15): 7672-7684.
I. B. Martini, E. R. Barthel and B. J. Schwartz   "Control of an Electron Transfer Reaction Using a Sequence of Femtosecond Laser Pulses", Ultrafast Phenomena XIII, M. Murnane, N. Scherer, R. J. D. Miller and A. M. Weiner (Eds.), 2003; 487-9.
P. G. Conrad II, P. T. Nishimura, D. Aherne, B. J. Schwartz, D. Wu, N. Fang, X. Zhang, J. Roberts, and K. J. Shea   "Functional Molecularly Imprinted Polymer Microstructures Fabricated Using Microstereolithographic Techniques", Adv. Mat., 2003; 15(18): 1541-4.
M. J. Bedard-Hearn, R. E. Larsen and B. J. Schwartz   "Hidden Breakdown of Linear Response: Projections of Molecular Motions in Non-Equilbrium Simulations of Solvation Dynamics", J. Phys. Chem. A., 2003; 107(24): 4773-7.
E. R. Barthel and B. J. Schwartz   "Mapping the Conduction Band Under CTTS Transitions: The Photodetachment Quantum Yield of Sodide (Na¯) in Tetrahydrofuran", Chem. Phys. Lett., 2003; 375(3-4): 435-43.
X. Yin, N. Fang, X. Zhang, I. B. Martini and B. J. Schwartz   "Near-Field Multiphoton Nanolithography Using an Apertureless Near-Field Probe", Proc. SPIE, 2003; 5211: 96-103.
C. F.-K. Shen, G. Sommez, A. D. Smith, B. J. Schwartz, Y. Rubin and F. Wudl   "Photocurrent Generated with a Homoconjugated Bisfulleroid Polymer", Polym. Preprints, 2003; 44: 348-9.
E. R. Barthel, I. B. Martini, E. Keszei and B. J. Schwartz   "Solvent Effects on the Ultrafast Dynamics and Spectroscopy of the Charge-Transfer-to-Solvent (CTTS) Reaction of Sodide", J. Chem. Phys., 2003; 118: 5916-31.
C. J. Smallwood, W. B. Bosma, R. E. Larsen and B. J. Schwartz   "The Role of Symmetry in Charge-Transfer-to-Solvent Reactions: Quantum Non-Adiabatic Computer Simulation of Photoexcited Sodium Anions", J. Chem. Phys. , 2003; 119(21): 11263-77.
M. J. Bedard-Hearn, R. E. Larsen and B. J. Schwartz   "Understanding Nonequilibrium Solvent Motions Through Molecular Projections: Computer Simulations of Solvation Dynamics in Liquid Tetrahydrofuran (THF)", J. Phys. Chem. B, 2003; 107(51): 14464-75.
T.-Q. Nguyen and B. J. Schwartz   "Ionomeric Control of Interchain Interactions, Morphology and the Electronic Properties of Conjugated Polymer Solutions and Films", J. Chem. Phys., 2002; 116(18): 8198-208.
R. D. Schaller, P. T. Snee, J. C. Johnson, L. F. Lee, K. R. Wilson, L. H. Haber, R. J. Saykally, T.-Q. Nguyen and B. J. Schwartz   "Nanoscopic interchain aggregate domain formation in conjugated polymer films studied by third harmonic generation (THG) near-field scanning optical microscopy (NSOM)", J. Chem. Phys., 2002; 117(14): 6688-98.
X. Yin, N. Fang, X. Zhang, I. B. Martini and B. J. Schwartz   "Near-Field Two-Photon Nanolithography Using an Apertureless Optical Probe", Appl. Phys. Lett., 2002; 81(19): 3663-5.
I. B. Martini and B. J. Schwartz   "On the Insensitivity of the Non-Adiabatic Relaxation of Solvated Electrons to the Details of their Local Solvent Environment", Chem. Phys. Lett., 2002; 360(1-2): 22-30.
R. D. Schaller, L. F. Lee, J. C. Johnson, L. H. Haber, R. J. Saykally, J. Vieceli, I. Benjamin, T.-Q. Nguyen and B. J. Schwartz   "The Nature of Interchain Excitations in Conjugated Polymers: Near-Field Optical Studies of Spatially-Varying Solvatochromism in Annealed MEH-PPV Films", J. Phys. Chem. B, 2002; 106(37): 9496-506.
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