Published August 1, 2013 | Version v1
Journal article

Surfaces of colloidal PbSe nanocrystals probed by thin-film positron annihilation spectroscopy

  • 1. Department of Radiation, Radionuclides and Reactors, Faculty of Applied Sciences, Delft University of Technology, Mekelweg 15, NL-2629 JB Delft (Netherlands)
  • 2. Physics Department, Northeastern University, Boston, Massachusetts 02115 (United States)
  • 3. Kavli Institute of Nanoscience, Faculty of Applied Sciences, Delft University of Technology, Lorentzweg 1, NL-2628 CJ Delft (Netherlands)
  • 4. Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, Julianalaan 136, NL-2628 BL Delft (Netherlands)
  • 5. Institut für Angewandte Physik und Messtechnik, Universität der Bundeswehr München, Werner-Heisenberg-Weg 39, D-85579 Neubiberg (Germany)
  • 6. Academy of Mining and Metallurgy AGH, PL-30059 Kraków (Poland)

Description

Positron annihilation lifetime spectroscopy and positron-electron momentum density (PEMD) studies on multilayers of PbSe nanocrystals (NCs), supported by transmission electron microscopy, show that positrons are strongly trapped at NC surfaces, where they provide insight into the surface composition and electronic structure of PbSe NCs. Our analysis indicates abundant annihilation of positrons with Se electrons at the NC surfaces and with O electrons of the oleic ligands bound to Pb ad-atoms at the NC surfaces, which demonstrates that positrons can be used as a sensitive probe to investigate the surface physics and chemistry of nanocrystals inside multilayers. Ab initio electronic structure calculations provide detailed insight in the valence and semi-core electron contributions to the positron-electron momentum density of PbSe. Both lifetime and PEMD are found to correlate with changes in the particle morphology characteristic of partial ligand removal

Additional details

Identifiers

Publishing Information

Journal Title
APL Materials
Journal Volume
1
Journal Issue
2
Journal Page Range
p. 022111-022111.7
ISSN
2166-532X
CODEN
AMPADS

Optional Information

Notes
(c) 2013 Author(s)