David P. Pullman
Associate Professor, Physical
office: CSL 301
The emphasis of research in the Pullman lab is on the synthesis, structural and kinetic characterization, and manipulation of metal nanoparticles. Much of our work involves silver nanoparticles, which are now the most commercially prevalent nanoparticles on the market, due to their antimicrobial activity as well as their remarkable optical properties. We are predominantly an experimental group, but when needed, we use an integrated approach in which computational and theoretical studies help in guiding and then interpreting the experiments. Examples of current nanoparticle projects include the:
- Catalytic production of silver nanoparticles
- Synthesis of chemically stable and photostable silver nanoparticles for application in plasmonic devices
- Mechanism of production of citrate-capped silver nanoparticles via reduction of silver ions by NaBH4
- Catalysis of chemical reactions on silver nanoparticle surfaces
- Tuning of the antibacterial activity of silver nanoparticles via surface modification
- Kinetics of halide-induced decomposition and aggregation of silver nanoparticles
- Adsorption kinetics of amino acids and proteins
A second research area, which overlaps and informs some of the nanoparticle work, is the study of the kinetics and dynamics of chemical reactions that take place on well-defined crystalline surfaces. In this work, we utilize ultrahigh vacuum techniques to prepare and characterize samples, which are subsequently probed using sensitive analytical techniques, including molecular beam scattering, angle-resolved thermal desorption spectroscopy, Auger spectroscopy, and mass spectroscopy. Our principal work in this area has been in elucidating the mechanism of reactions involving hydrogen on the Si(100) surface. An example is the discovery of an exceptionally high kinetic order, roughly 9, for the recombinative desorption of molecular hydrogen from Si(100) surfaces that were previously saturated with atomic hydrogen. This order is among the highest ever measured for any chemical reaction. It is an apparent order, and interestingly, our data suggest it arises from two competing low-order desorption processes.
Our final area of investigation, inspired by experiments in our group, is to develop a detailed understanding of the origin of contrast in scanning tunneling microscope images of graphite and few-layer graphene. Although this has been considered a solved problem, persistent discrepancies between experiment and theory led us to revisit this issue. Using periodic density functional theory, we are exploring the possibility that defects of various types may account for the prominent asymmetric features often seen in experiment. This work is done in collaboration with Dra. Maria Guadalupe Moreno Armenta of the Centro de Nanosciencias y Nanotecnologia, Universidad Nacional Autónoma de México in Ensenada.
- Espinoza, M. Gabriela; Hinks, Mallory L.; Mendoza, Alexandra M.; et al., Kinetics of Halide-Induced Decomposition and Aggregation of Silver Nanoparticles J. Phys. Chem. C 2012, 116 8305-8313.
- Kottke, M.; Neuburger, M. L.; Fee, D.; et al., Observation of an exceptionally high apparent kinetic order in the thermal desorption of D-2 from the Si(100) surface Molec. Phys. 2012, 110 1953-1966.
- Zeinalipour-Yazdi CD, Pullman DP, Quantitative structure - Property relationships for longitudinal, transverse, and molecular static polarizabilities in polyynes Journal of Physical Chemistry B 2008, 112 7377-7386.
- Zeinalipour-Yazdi CD, Pullman DP, A new interpretation of the scanning tunneling microscope image of graphite Chemical Physics 2008, 348 233-236.
- Peterson KI, Pullman D, Lin W, et al., Microwave spectra and ab initio studies of Ar-propane and Ne-propane complexes: Structure and dynamics Journal of Chemical Physics 2007, 127 184306.