Abstract

The spectral behavior of single terrylene molecules at a hexadecane−silica interface structure is studied. Different sample preparation techniques indicate that molecules close to a silica substrate in a hexadecane matrix are subject to additional dephasing or spectral diffusion. The temperature activation of the homogeneous line width of these molecules shows much reduced activation energies as compared to those of molecules in bulk hexadecane. These low-lying activation energies may be attributed to surface phonon states or local phonon modes particular to the interface structure. With the aid of a low-temperature scanning confocal microscope, the distance of single terrylene molecules to the silica surface can be measured with a precision of 60 nm. A drastic increase of the homogeneous line width for molecules with distances less than 150 nm to the silica surface is found.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.