portrait portrait

The 15th International Conference on

Vibrations at Surfaces

June 22-26, 2015 ▪ Donostia-San Sebastián, Spain

Donostia Igeldotik

Program

OverviewMondayTuesdayWednesdayThursdayFriday

Thursday June 25

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

Th2: STM-IETS and beyond

Chair: M. Alducin, San Sebastián, Spain

11:20-11:50 Y. Jiang, Beijing, China
Probing nuclear quantum effects in water with scanning tunneling microscopy and spectroscopy
11:50-12:20 J. Repp, Regensburg, Germany
Symmetry dependence of vibration-assisted tunneling
12:20-12:40 F. Schwartz, Ilmenau, Germany
Electronic and vibrational states of single Tin-Phthalocyanine molecules – a numerical STM study
12:40-13:00 P. Jelínek, Prague, Czech Republic
The origin of high-resolution IETS-STM images of organic molecules with functionalized tips

Invited talk

Probing nuclear quantum effects in water with scanning tunneling microscopy and spectroscopy

Y. Jiang

International Center for Quantum Materials, School of Physics, Peking University, Beijing 100871, P. R. China

Quantum behaviors of protons in terms of tunneling and zero-point motion have significant effects on water properties, structure, and dynamics even at room and at higher temperature. In spite of tremendous theoretical and experimental efforts, accurate and quantitative description of the nuclear quantum effects (NQEs) in water is still challenging, due to the difficulty of accessing the internal degrees of freedom of water molecules. Using a low-temperature scanning tunneling microscope (STM), we are able to resolve in real space the internal structure, that is, the O-H directionality, of individual water molecules adsorbed on a solid surface [1,2]. The key steps are decoupling electronically the water from the metal substrate by inserting an insulating NaCl layer and gating the molecular density of states of water around the Fermi level via tip-water coupling. These techniques allow us not only to directly visualize the many-body quantum tunneling of protons within the H-bonded network [3], but also to quantify the impact of quantum fluctuation on the strength of hydrogen bonds by resonantly enhanced inelastic electron tunneling spectroscopy (IETS) [4]. Our work opens up the possibility of exploring the quantum nature of hydrogen bonds at single-bond limit.

[1] J. Guo, X. Z. Meng, J. Chen, J. B. Peng, J. M. Sheng, X. Z. Li, L. M. Xu, J. R. Shi, E. G. Wang*, Y. Jiang*, "Real-space imaging of interfacial water with submolecular resolution", Nature Materials 13, 184 (2014)

[2] J. Chen, J. Guo, X. Z. Meng, J. B. Peng, J. M. Sheng, L. M. Xu, Y. Jiang*, X. Z. Li*, E. G. Wang, "An unconventional bilayer ice structure on a NaCl(001) film", Nature Communications 5, 4056 (2014)

[3] X. Meng, J. Guo, J. Peng, J. Chen, Z. Wang, J. R. Shi, X. Z. Li, E. G. Wang*, Y. Jiang*, "Direct visualization of concerted proton tunnelling in a water nanocluster", Nature Physics 11, 235 (2015)

[4] J. Guo, J.-T. Lü, J. Chen, J. Peng, X. Meng, Z. Wang, Z. Lin, X.-Z. Li*, E.-G. Wang*, Y. Jiang*, "Probing nuclear quantum effects on hydrogen-bonding strength at single bond limit", to be submitted