Density-functional study of Cu atoms, monolayers, and coadsorbates on polar ZnO surfaces

Physics – Condensed Matter – Materials Science

Scientific paper

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

6 pages with 2 postscript figures embedded. Uses REVTEX and epsf macros

Scientific paper

10.1103/PhysRevB.69.235420

The structure and electronic properties of single Cu atoms, copper monolayers and thin copper films on the polar oxygen and zinc terminated surfaces of ZnO are studied using periodic density-functional calculations. We find that the binding energy of Cu atoms sensitively depends on how charge neutrality of the polar surfaces is achieved. Bonding is very strong if the surfaces are stabilized by an electronic mechanism which leads to partially filled surface bands. As soon as the surface bands are filled (either by partial Cu coverage, by coadsorbates, or by the formation of defects), the binding energy decreases significantly. In this case, values very similar to those found for nonpolar surfaces and for copper on finite ZnO clusters are obtained. Possible implications of these observations concerning the growth mode of copper on polar ZnO surfaces and their importance in catalysis are discussed.

No associations

LandOfFree

Say what you really think

Search LandOfFree.com for scientists and scientific papers. Rate them and share your experience with other people.

Rating

Density-functional study of Cu atoms, monolayers, and coadsorbates on polar ZnO surfaces does not yet have a rating. At this time, there are no reviews or comments for this scientific paper.

If you have personal experience with Density-functional study of Cu atoms, monolayers, and coadsorbates on polar ZnO surfaces, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Density-functional study of Cu atoms, monolayers, and coadsorbates on polar ZnO surfaces will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFWR-SCP-O-719859

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.