TY - JOUR
T1 - Adsorption and Reaction of NO on Ni(100)
AU - Shen, Shikong
AU - Feulner, P.
AU - Umbach, E.
AU - Wurth, W.
AU - Menzel, D.
N1 - Funding Information:
supported by the Deutsche Forschungsgemeinschaft through Sonderforschungsbereich 128.
Funding Information:
We thank G. Michalk and H. Schlichting for the development of microcomputer based controlling and data processing devices which were decisive for the success of the experiments and for help during the early stages of the measurements. One of us, Shikong Shen, thanks the Alexander von Humboldt Foundation for a fellowship. This work has been
PY - 1987/11/1
Y1 - 1987/11/1
N2 - The adsorption, desorption and decomposition of NO on Ni (100) was studied with XPS, UPS, XAES, ΔΦ, temperature programmed thermal desorption (TPD) and LEED in the temperature range 80 to 1300 K. NO adsorbs molecularly on Ni (100) at low temperatures; dissociation occurs above 200 K. Up to ≈ 1/4 saturation coverage, only N2 desorbs in a second order peak around 1100 K. At saturation three NO desorption states at 350, 420 and 1200 K and two N2 peaks at 660 and 1020 K are observed for a heating rate ß of 5 K/s. Activation energies for desorption are obtained by TPD with variable ß. Coadsorption experiments show that the NO-TPD peak at 1200 K is due to recombination of N and O on the surface. The relative areas of some TPD maxima depend strongly on coadsorbed O-, C- and N-impurities. At 100 K, ΔΦ increases up to a maximum of 1.1 eV at 3/4 saturation coverage and drops to 1.0 eV at saturation. Complex LEED patterns are observed for saturated layers adsorbed below 200 K which change during heating. The nature of the observed binding and desorption states is discussed.
AB - The adsorption, desorption and decomposition of NO on Ni (100) was studied with XPS, UPS, XAES, ΔΦ, temperature programmed thermal desorption (TPD) and LEED in the temperature range 80 to 1300 K. NO adsorbs molecularly on Ni (100) at low temperatures; dissociation occurs above 200 K. Up to ≈ 1/4 saturation coverage, only N2 desorbs in a second order peak around 1100 K. At saturation three NO desorption states at 350, 420 and 1200 K and two N2 peaks at 660 and 1020 K are observed for a heating rate ß of 5 K/s. Activation energies for desorption are obtained by TPD with variable ß. Coadsorption experiments show that the NO-TPD peak at 1200 K is due to recombination of N and O on the surface. The relative areas of some TPD maxima depend strongly on coadsorbed O-, C- and N-impurities. At 100 K, ΔΦ increases up to a maximum of 1.1 eV at 3/4 saturation coverage and drops to 1.0 eV at saturation. Complex LEED patterns are observed for saturated layers adsorbed below 200 K which change during heating. The nature of the observed binding and desorption states is discussed.
UR - http://www.scopus.com/inward/record.url?scp=84926604171&partnerID=8YFLogxK
U2 - 10.1515/zna-1987-1118
DO - 10.1515/zna-1987-1118
M3 - Article
AN - SCOPUS:84926604171
SN - 0932-0784
VL - 42
SP - 1333
EP - 1345
JO - Zeitschrift fur Naturforschung - Section A Journal of Physical Sciences
JF - Zeitschrift fur Naturforschung - Section A Journal of Physical Sciences
IS - 11
ER -