Autodetachment of Diatomic Carbon Anions from Long-Lived High-Rotation Quartet States

被引:0
|
作者
Schmidt, Viviane C. [1 ]
Curik, Roman [2 ]
Oncak, Milan [3 ]
Blaum, Klaus [1 ]
George, Sebastian [1 ]
Goeck, Juergen [1 ]
Grieser, Manfred [1 ]
Grussie, Florian [1 ]
von Hahn, Robert [1 ]
Krantz, Claude [1 ]
Kreckel, Holger [1 ]
Novomy, Oldrich [1 ]
Spruck, Kaija [1 ]
Wolf, Andreas [1 ]
机构
[1] Max Planck Inst Kernphys, Saupfercheckweg 1, D-69117 Heidelberg, Germany
[2] ASCR, J Heyrovsky Inst Phys Chem, Dolejskova 3, Prague 18223, Czech Republic
[3] Leopold Franzens Univ Innsbruck, Inst Ionenphys & Angew Phys, Technikerstr 25-3, A-6020 Innsbruck, Austria
关键词
ELECTRON-MOLECULE COLLISIONS; ASSOCIATIVE DETACHMENT; ULTRAHIGH-RESOLUTION; C-2; SPECTROSCOPY; TRANSITION; RESONANCE; SPECTRUM; BEHAVIOR; COMPLEX;
D O I
10.1103/PhysRevLett.133.183001
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We show that strong molecular rotation drastically modifies the autodetachment of C-2 ions in the lowest quartet electronic state a4 Sigma & thorn;u . In the strong-rotation regime, levels of this state only decay by a process termed "rotationally assisted" autodetachment, whose theoretical description is worked out based on the nonlocal resonance model. For autodetachment linked with the exchange of six rotational quanta, the results reproduce a prominent, hitherto unexplained electron emission signal with a mean decay time near 3 ms, observed on stored C-2 ions from a hot ion source.
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页数:7
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