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Single-field slice-imaging with a movable repeller: Photodissociation of N2O from a hot nozzle.
- Source :
- Journal of Chemical Physics; 8/7/2014, Vol. 141 Issue 5, p1-8, 8p, 2 Diagrams, 6 Graphs
- Publication Year :
- 2014
-
Abstract
- We present a new photo-fragment imaging spectrometer, which employs a movable repeller in a single field imaging geometry. This innovation offers two principal advantages. First, the optimal fields for velocity mapping can easily be achieved even using a large molecular beam diameter (5 mm); the velocity resolution (better than 1%) is sufficient to easily resolve photo-electron recoil in (2 + 1) resonant enhanced multiphoton ionization of N<subscript>2</subscript> photoproducts from N<subscript>2</subscript>O or from molecular beam cooled N<subscript>2</subscript>. Second, rapid changes between spatial imaging, velocity mapping, and slice imaging are straightforward. We demonstrate this technique's utility in a re-investigation of the photodissociation of N<subscript>2</subscript>O. Using a hot nozzle, we observe slice images that strongly depend on nozzle temperature. Our data indicate that in our hot nozzle expansion, only pure bending vibrations - (0, v<subscript>2</subscript>,0) - are populated, as vibrational excitation in pure stretching or bend-stretch combination modes are quenched via collisional near-resonant V-V energy transfer to the nearly degenerate bending states. We derive vibrationally state resolved absolute absorption cross-sections for (0, v<subscript>2</subscript> < 7, 0). These results agree well with previous work at lower values of v<subscript>2</subscript>, both experimental and theoretical. The dissociation energy of N<subscript>2</subscript>O with respect to the O(¹D) + N<subscript>2</subscript>¹Σ<subscript>g</subscript><superscript>+</superscript> asymptote was determined to be 3.65 ± 0.02 eV. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00219606
- Volume :
- 141
- Issue :
- 5
- Database :
- Complementary Index
- Journal :
- Journal of Chemical Physics
- Publication Type :
- Academic Journal
- Accession number :
- 97430429
- Full Text :
- https://doi.org/10.1063/1.4891469