English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Luminescence and Configurations of Perylene Dimers in a Langmuir-Blodgett Film

MPS-Authors
/persons/resource/persons242687

Mahrt,  Jürgen
Theory, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22242

Willig,  Frank
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22143

Storck,  Winfried
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons268002

Weiss,  D.
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons254938

Kietzmann,  Reinhard
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons262166

Schwarzburg,  K.
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons268004

Tufts,  B.
Fritz Haber Institute, Max Planck Society;

/persons/resource/persons268006

Trösken,  B.
Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Mahrt, J., Willig, F., Storck, W., Weiss, D., Kietzmann, R., Schwarzburg, K., et al. (1994). Luminescence and Configurations of Perylene Dimers in a Langmuir-Blodgett Film. The Journal of Physical Chemistry, 98(7), 1888-1894. doi:10.1021/j100058a029.


Cite as: https://hdl.handle.net/21.11116/0000-0009-A242-5
Abstract
The photoemission electron microscope (PEEM) makes it possible to image a surface via its work function. On a CO-covered Pt(100) surface, we prepared oxygen islands which appear dark in the PEEM image due to their higher work function. As the surface is heated to temperatures above 650 K we observe the conversion of these dark islands into very bright ones with work functions much lower than even that of the clean surface arising from an inverted dipole moment of oxygen atoms beneath the surface. We found an activation energy for this conversion of about 15 kcal/mol. Partially transformed oxygen islands were used to study the reactivity and the formation of this species further. CO and H2 both react with subsurface oxygen rather slowly, while at the interface between the subsurface and the chemisorbed phase, both adsorbents accelerate the conversion of parts of the remaining oxygen atoms towards the subsurface state. In contrast, additional oxygen adsorption does not contribute to a further transformation. We propose a qualitative microscopic model for the formation of subsurface oxygen based on experimental evidence.