2003
DOI: 10.1016/s1386-1425(02)00396-7
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The structure of the lowest electronic Rydberg state of CdAr complex determined by laser double resonance method in a supersonic jet-expansion beam

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Cited by 15 publications
(30 citation statements)
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“…Furthermore, the potential barrier becomes smaller when going from Rg = Ne [5] through Ar [3] to Kr [2]. However, the barrier converts gradually into an outer shallow minimum which eventually vanishes at yet larger R. A similar conclusion, with respect to the complex shape of the E 3 R + -state potential in HgNe and HgAr, was drawn in [6][7][8][9], and it was based entirely on experimental observations and simulations of the spectra.…”
Section: Introductionmentioning
confidence: 87%
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“…Furthermore, the potential barrier becomes smaller when going from Rg = Ne [5] through Ar [3] to Kr [2]. However, the barrier converts gradually into an outer shallow minimum which eventually vanishes at yet larger R. A similar conclusion, with respect to the complex shape of the E 3 R + -state potential in HgNe and HgAr, was drawn in [6][7][8][9], and it was based entirely on experimental observations and simulations of the spectra.…”
Section: Introductionmentioning
confidence: 87%
“…Studies of ZnAr [1], CdKr [2], CdAr [3,4], CdNe [5], HgAr [6][7][8], HgNe [6,9] performed using an optical-optical double resonance (OODR) and free-jet expansion methods allowed exploring a structure of the E 3 R + (n 3 S 1 )-state interatomic potentials (n = 6 and 7 6 n 6 10 for Cd and Hg, respectively) in relatively large range of interatomic separations R. To facilitate the excitation process, two intermediate, A 3 P 0 þ (5 3 P 1 ) and B 3 R þ 1 (5 3 P 1 ), electronic energy states were employed. The findings for CdAr and HgAr were supplemented by those of Bennett and Breckenridge [10] who investigated the E 3 R + (6 3 S 1 ) state using method of laser vaporization in a free-jet expansion beam being a source of the b 3 G 2 intermediate state.…”
Section: Introductionmentioning
confidence: 99%
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