Мобильная версия

Доступно журналов:

3 288

Доступно статей:

3 891 637

 

Скрыть метаданые

Автор A R Burns
Автор D R Jennison
Автор E B Stechel
Дата выпуска 1990-06-01
dc.description The electronically-stimulated dissociation of NO<sub>2</sub> on Pt(111) has been studied through state-selective, time-of-flight detection of the NO product above the surface. The NO leaves as a direct dissociation product resulting from 5-800 eV electron impact, whereas the O atom remains on the surface. The quantum-resolved analysis of the NO reveals fundamental aspects of the stimulated surface process such as dominant excitation channels and dynamics. Because of rapid decay via resonant tunneling from substrate levels, the 3 eV shallow valence excitations prominent in gas-phase photodissociation of NO<sub>2</sub> have lifetimes that are too short to produce observable dissociation on the metal surface. Instead, we find a 10-15 eV threshold which corresponds to ionization of 3b<sub>2</sub> and double ionization of 1a<sub>2</sub> levels which cannot be resonantly filled by substrate electrons and thus have the longest lifetimes relative to Auger decay. Screening of the hole(s) by the metal through the 6a<sub>1</sub> orbital of the molecule not only determines the lifetime, but is found to influence the extent of internal excitation in the NO product.
Формат application.pdf
Издатель Institute of Physics Publishing
Название Quantum-resolved analysis of electronically-stimulated NO<sub>2</sub> dissociation on Pt(111)
Тип paper
DOI 10.1088/0031-8949/41/6/037
Electronic ISSN 1402-4896
Print ISSN 0031-8949
Журнал Physica Scripta
Том 41
Первая страница 882
Последняя страница 886
Аффилиация A R Burns; Sandia National Laboratories, Division 1151, Albuquerque, New Mexico 87185, USA
Аффилиация D R Jennison; Sandia National Laboratories, Division 1151, Albuquerque, New Mexico 87185, USA
Аффилиация E B Stechel; Sandia National Laboratories, Division 1151, Albuquerque, New Mexico 87185, USA
Выпуск 6

Скрыть метаданые