09:00-10:40 | Th1: Adsorbate and interface dynamics |
10:40-11:20 | Coffee break |
11:20-13:00 | Th2: STM-IETS and beyond |
13:00-15:30 | Lunch break (on your own) |
15:30-16:40 | Th3: Molecular films and 2D materials |
16:40-17:20 | Coffee break |
17:20-19:00 | Th4: Tip-enhanced vibrational spectroscopies |
20:30-23:00 | Conference dinner at Cofradía Vasca de Gastronomía, Old Town |
Chair: J. I. Pascual, San Sebastián, Spain
Invited talk
Tip-enhanced Raman spectroscopy
Departments of Chemistry, Biomedical Engineering, and Applied Physics Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113, USA
During the last few years, there has been an explosion of interest and activity in the field of plasmonics. The goal of plasmonics is to control and manipulate light on the nanometer length scale using the properties of the collective electronic excitations in noble metal films or nanoparticles, known as surface plasmons. An improved understanding of the interactions between adsorbed molecules and plasmonic nanostructures (i.e., molecular plasmonics) is having a significant impact in a number of research areas including electrochemistry, surface science, catalysis for energy conversion and storage, the materials science of nanoparticles, biomedical diagnostics, art conservation science, and nanolithography.
I will focus in on three recent advances in tip-enhanced Raman spectroscopy (TERS) which illustrate the power of this nanoscale vibrational spectroscopy. First, new insights into the nature of the relative intensity fluctuations in single molecule tip-enhanced Raman spectroscopy (SMTERS) will be discussed. Second, our current understanding of the adsorbate surface interactions involved in the low temperature (LT), ultrahigh vacuum (UHV) TERS of the Ag tip/Rhodamine 6G (R6G) /Ag(111) system will be described. Finally, an update on our new results in coupling ultrafast lasers with TERS. This last topic illuminates a path forward toward the goal of understanding chemistry at the space-time limit.