Metal atom (Zn, Cd and Mg) luminescence in solid neon

Luminescence spectroscopy of the metal atoms Mg, Zn and Cd isolated in solid neon is recorded using pulsed synchrotron radiation excitation of the ns¹ np¹ ¹P₁–ns² ¹S₀ resonance (n = 3, 4 and 5 respectively) transitions. Two features, a dominant band and a red-shoulder, are identified in the UV abs...

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Збережено в:
Бібліографічні деталі
Дата:2012
Автори: Healy, B., Kerins, P., McCaffrey, J. G.
Формат: Стаття
Мова:English
Опубліковано: Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України 2012
Назва видання:Физика низких температур
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Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/117420
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Metal atom (Zn, Cd and Mg) luminescence in solid neon / B. Healy, P. Kerins, J. G. McCaffrey // Физика низких температур. — 2012. — Т. 38, № 8. — С. 860-870. — Бібліогр.: 33 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Резюме:Luminescence spectroscopy of the metal atoms Mg, Zn and Cd isolated in solid neon is recorded using pulsed synchrotron radiation excitation of the ns¹ np¹ ¹P₁–ns² ¹S₀ resonance (n = 3, 4 and 5 respectively) transitions. Two features, a dominant band and a red-shoulder, are identified in the UV absorption spectra of Zn/Ne and Cd/Ne. Excitation of these features yields distinct emission bands with the red-shoulder absorption producing the smaller, Stokes-shifted emission. Nanosecond decaytime measurements, made with the time correlated single photon counting technique indicate the emission bands arise from the spin singlet ¹P₁ → ¹S₀ transition. Hence, it is concluded the duplication of absorption and emission features in the Cd/Ne and Zn/Ne systems arises from metal atom occupancy in two distinct sites. In contrast, Mg/Ne luminescence consists of single excitation and emission bands, indicative of occupancy in just one site. The occurrence of distinct photophysical characteristics of the linewidths, Stokes shift and lifetimes in the Mg/Ne system, compared with those recorded for Zn/Ne and Cd/Ne, is rationalised in terms of a different site occupancy for atomic Mg. Accurate interaction potentials for the ground states of the M·Ne diatomics are used to analyse site occupancies and interpret this contrasting behavior.