Naomi Ginsberg

Naomi Ginsberg

Assistant Professor

Office: D64 Hildebrand
Main: (510) 643-9153

Research Area(s): Atomic, Molecular and Optical PhysicsBiophysicsCondensed Matter Physics And Materials Science


Naomi S. Ginsberg received a B.A.Sc. degree in Engineering Science from the University of Toronto in 2000 and a Ph.D. in Physics from Harvard University in 2007. She held a Glenn T. Seaborg Postdoctoral Fellowship at Lawrence Berkeley National Laboratory until her appointment as Assistant Professor in the Chemistry department at UC Berkeley in 2010. Naomi joined the Physics faculty in 2011. She currently holds the Cupola Era Endowed Chair in the College of Chemistry, is a Faculty Scientist in the Physical Biosciences Division at Lawrence Berkeley National Laboratory, and is the recipient of a David and Lucile Packard Fellowship in Science and Engineering (2011). Naomi's research is in the areas of Atomic, Molecular and Optical Physics, Biophysics, Condensed Matter Physics and Materials Science.

Research Interests

Work in the Ginsberg Group is motivated by the need to spatially and temporally resolve the complex dynamics of nanoscale processes, such as photosynthetic light harvesting. We use multiple approaches, separately and in combination, including ultrafast spectroscopy, light microscopy, and cathodoluminescence electron mocroscopy.

Current Projects
I. Mapping spatio-temporal photoexcitation trajectories onto the architecture of photosynthetic light harvesters

In photosynthesis, solar-to-chemical energy conversion begins with chlorophyll photoexcitation and its ultrafast energy transfer through a heterogeneous network of integral membrane pigment-protein complexes. The ultimate destination is the reaction center protein, where the excitation leads to charge separation that triggers transduction to chemical fuels. Remarkably, nearly every photoexcitation leads to charge separation, yet the reason for this high quantum efficiency is unclear.

We seek to uncover the underlying mechanisms of this targeted excitation energy transfer by probing photosynthetic membranes and synthesized mimics such as polymers, molecular crystals, and inorganic nanostructures intended for photovoltaic applications. Photoexcitations can travel many tens of nanometers without being quenched and do so much faster than typical molecular fluorescence lifetimes. By borrowing elements from fluorescence microscopy and ultrafast spectroscopy, we are interested in dynamically mapping distributions of traveling photoexcitations as a function of energy, space, and time.

Specifically in photosynthesis, we have only begun to learn the means by which molecular arrangement, the resulting Coulomb coupling between chlorophylls, and protein-induced energy fluctuations cooperatively yield high quantum efficiency transport. A more profound understanding is critical to unlocking nature's strategies for successful light harvesting. Artificial devices tend to suffer from limited excitation diffusion lengths prior to charge separation but can be more robust to photodamage. By observing dynamics in both naturally occurring and 'man-made' light harvesters, we will be poised to compare and contrast them and to mitigate their weaknesses.

II. Near-field cathodoluminescence microscopy

The demands for and on high-resolution imaging systems continue to increase with our eagerness to visualize ever smaller features of live cells and molecular interactions. Each imaging platform involves tradeoffs between resolution, working distance, sample environment, sensitivity, and molecular specificity. With these in mind, we are interested in imaging aqueous samples at high resolution using the near-field cathodoluminescence of thin-film phosphors. This technique will achieve controllable brightness and spectral selectivity and will approach the resolution and speed of electron microscopy, without the complications of mechanical scanning at close range or sample fixation.

Cathodoluminescence is the electron-beam induced generation of optical excitations in materials, by analogy to photoluminescence (light-induced) or electroluminescence (electronically-induced). It is an attractive alternative to visualizing the underlying mechanisms of complex molecular phenomena. The key idea in our studies is to leverage the focusing ability of electron optics to make nanoscopic scanned optical spots that can be used for a broad range of imaging applications. This will reveal information about the optical properties of nano phosphors alongside the interactions of small molecules and proteins in solution.

By bringing our excited optical spots very close to encapsulated aqueous samples, we are interested in revisiting optical probes of distance, binding, and aggregation such as Forster resonance energy transfer (FRET) and fluorescence correlation spectroscopy (FCS). This makes it possible to explore the effects of heterogeneity that may be washed out with diffraction-limited observation volumes and to work in the single-molecule regime at high concentrations. We are also interested in using this novel light source to perform precise fluorescence recovery after photobleaching (FRAP) diffusion studies of photosynthetic and other membrane structures at unprecedentedly small length scales.


Professor Naomi Ginsberg's publications can be found here.