ON THE ROLE OF POTENTIAL FEATURES IN FINE-STRUCTURE TRANSITIONS WITH APPLICATION TO H++F(P-2(1/2))-]H++F(P-2(3/2))
DSpace at IIT Bombay
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Title |
ON THE ROLE OF POTENTIAL FEATURES IN FINE-STRUCTURE TRANSITIONS WITH APPLICATION TO H++F(P-2(1/2))-]H++F(P-2(3/2))
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Creator |
PADMAVATHI, DA
MISHRA, MK RABITZ, H |
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Subject |
functional sensitivity analysis
structure-changing transitions quantum-mechanical treatment surface scattering data state atom collisions electronic states alkali atoms gas inversion energy |
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Description |
The first order functional sensitivity densities delta In sigma(1/2-->3/2)(E)/delta ln W-\A\(R) are employed to assess the role of structure in potential energy curves W-0(R) and W-0(R) involved in the fine-structure transition H+ + F(P-2(1/2))-->H+ + F(P-2(3/2)). The results reveal that the fine-structure transition cross-section draws on the W-0((2) Sigma) and W-1((2) Pi) potentials in a highly correlated fashion and a measurement of sigma 1/2-->3/2(E) for H+ + F will primarily allow information to be extracted only on the potential function difference W-0(R) - W-1(R) for moderate to large internuclear distances (R greater than or similar to 3 a(0)). While there is a marginal preference for the pi alignment in the region where splitting between the (2) Pi and (2) Sigma curves is equal to the fine-structure transition energy, the oscillatory nature of the sensitivity densities with respect to R indicates that the alignment effects may disappear upon averaging over many impact parameters. The results from both functional sensitivity and adiabatic analysis isolate the region of potential energy curves centered at R approximate to 7.8 a(0) where the potential function difference W-0(R) - W-1(R) is equal to the fine-structure splitting, to be of maximum significance to the collisional fine-structure transition in this system.
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Publisher |
ELSEVIER SCIENCE BV
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Date |
2011-07-26T00:06:45Z
2011-12-26T12:51:01Z 2011-12-27T05:37:18Z 2011-07-26T00:06:45Z 2011-12-26T12:51:01Z 2011-12-27T05:37:18Z 1994 |
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Type |
Article
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Identifier |
CHEMICAL PHYSICS, 179(3), 469-478
0301-0104 http://dx.doi.org/10.1016/0301-0104(94)87023-3 http://dspace.library.iitb.ac.in/xmlui/handle/10054/6825 http://hdl.handle.net/10054/6825 |
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Language |
en
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