TY - JOUR
T1 - Decomposition of N2O on Ni(755) and the character of the atomic oxygen deposited at step sites
AU - Orita, Hideo
AU - Kondoh, Hiroshi
AU - Nozoye, Hisakazu
PY - 1998/1/1
Y1 - 1998/1/1
N2 - Adsorption and reaction of N2O on a stepped Ni(755) surface have been investigated by temperature-programmed desorption (TPD). The decomposition of adsorbed N2O occurs exclusively at the step sites on Ni(755) below 200 K during TPD ramp, yielding gaseous N2 and leaving atomic oxygen there. The amount of the atomic oxygen is controlled easily by changing the exposure of N2O. The character of the atomic oxygen has been studied by using decomposition of cycloheptane as a probe reaction. All the atomic oxygen generated in situ from coadsorbed N2O can react with carbon atoms produced from the decomposition of cycloheptane, resulting in desorption of CO around 600 K upon heating. However, two thirds of the predeposited atomic oxygen cannot be desorbed as CO upon heating up to 723 K. The predeposited atomic oxygen becomes inactive during the predeposition process and probably interacts with the step sites more strongly.
AB - Adsorption and reaction of N2O on a stepped Ni(755) surface have been investigated by temperature-programmed desorption (TPD). The decomposition of adsorbed N2O occurs exclusively at the step sites on Ni(755) below 200 K during TPD ramp, yielding gaseous N2 and leaving atomic oxygen there. The amount of the atomic oxygen is controlled easily by changing the exposure of N2O. The character of the atomic oxygen has been studied by using decomposition of cycloheptane as a probe reaction. All the atomic oxygen generated in situ from coadsorbed N2O can react with carbon atoms produced from the decomposition of cycloheptane, resulting in desorption of CO around 600 K upon heating. However, two thirds of the predeposited atomic oxygen cannot be desorbed as CO upon heating up to 723 K. The predeposited atomic oxygen becomes inactive during the predeposition process and probably interacts with the step sites more strongly.
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U2 - 10.1006/jcat.1998.2101
DO - 10.1006/jcat.1998.2101
M3 - Article
AN - SCOPUS:0001181842
SN - 0021-9517
VL - 177
SP - 217
EP - 223
JO - Journal of Catalysis
JF - Journal of Catalysis
IS - 2
M1 - CA982101
ER -