| Literature DB >> 29178528 |
Li-Qing Zheng1, Xing Wang1, Feng Shao1, Martin Hegner2, Renato Zenobi1.
Abstract
An understanding of the photoisomerization mechanism of molecules bound to a metal surface at the molecular scale is required for designing photoswitches at surfaces. It has remained a challenge to correlate the surface structure and isomerization of photoswitches at ambient conditions. Herein, the photoisomerization of a self-assembled monolayer of azobenzene-thiol molecules on a Au surface was investigated using scanning tunneling microscopy and tip-enhanced Raman spectroscopy. The unique signature of the cis isomer at 1525 cm-1 observed in tip-enhanced Raman spectra was clearly distinct from the trans isomer. Furthermore, tip-enhanced Raman images of azobenzene thiols after ultraviolet and blue light irradiation are shown with nanoscale spatial resolution, demonstrating a reversible conformational change. Interestingly, the cis isomers of azobenzene-thiol molecules were preferentially observed at Au grain edges, which is confirmed by density functional theory.Entities:
Keywords: azobenzene thiols; grain edges; photoisomerization; substrate-mediated charge transfer; tip-enhanced Raman spectroscopy
Year: 2017 PMID: 29178528 DOI: 10.1002/anie.201710443
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336