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Journal of Physics B Atomic Molecular and Optical Physics

Rates of blackbody radiation-induced transitions from Rydberg states of alkali atoms

Vitalii D Ovsiannikov, Igor L. Glukhov, E A Nekipelov

Published Sep 21, 2011• 29 citations
Publisher

Abstract

General properties are considered of three different terms in the imaginary part of the Stark effect on n S, n P and n D Rydberg states of alkali atoms in the field of environmental blackbody radiation with temperature in the ranges between T = 100 K and T = 3000 K. The terms are equal to the rates of decay P d nl ( T ), excitation P e nl ( T ) and ionization P ion nl ( T ) and may be separated and determined independently of each other. Corresponding numerical data calculated together with the rates of spontaneous decay P sp nl in the region of principal quantum numbers n from n = 10–1000 are transformed into fractional rates R d(e, ion) nl ( T ) = P d(e, ion) nl ( T )/ P nl sp . The asymptotic dependences on T and n display an essential difference between the fractional rates of ionization R ion nl ( T )∝ Tn 2/3 and the rates of decay (excitation) R d(e) nl ( T )∝ Tn , approximated by two different asymptotic formulae, one for R ion nl ( T ) and another one for R d(e) nl ( T ). The approximation polynomials with coefficients, determined from the curve-fitting polynomial interpolation procedure for three values of n between n = 15 and n = 150 at three values of temperature T = 100, 300, 1000 K, reproduce the calculated values with fractional departures below 2–3% in the regions from n = 10 to n = 1000 at temperatures from T = 100 K to T = 3000 K.

DOI
10.1088/0953-4075/44/19/195010

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General properties are considered of three different terms in the imaginary part of the Stark effect on n S, n P and n D Rydberg states of alkali atoms in the field of environmental blackbody radiation with temperature in the ranges between T = 100 K and T = 3000 K. The terms are equal to the rates of decay P d nl ( T ), excitation P e nl ( T ) and ionization P ion nl ( T ) and may be separated and determined independently of each other. Corresponding numerical data calculated together with the rates of spontaneous decay P sp nl in the region of principal quantum numbers n from n = 10–1000 are transformed into fractional rates R d(e, ion) nl ( T ) = P d(e, ion) nl ( T )/ P nl sp . The asymptotic dependences on T and n display an essential difference between the fractional rates of ionization R ion nl ( T )∝ Tn 2/3 and the rates of decay (excitation) R d(e) nl ( T )∝ Tn , approximated by two different asymptotic formulae, one for R ion nl ( T ) and another one for R d(e) nl ( T ). The approximation polynomials with coefficients, determined from the curve-fitting polynomial interpolation procedure for three values of n between n = 15 and n = 150 at three values of temperature T = 100, 300, 1000 K, reproduce the calculated values with fractional departures below 2–3% in the regions from n = 10 to n = 1000 at temperatures from T = 100 K to T = 3000 K.
New features of the blackbody-induced radiation processes on Rydberg atoms were discovered on the basis of numerical data for the blackbody-induced decay P d nl ( T ), excitation P e nl ( T ) and ionization P ion nl ( T ) rates of n S, n P and n D Rydberg states calculated together with the spontaneous decay rates P sp nl in neutral hydrogen, and singlet and triplet helium atoms for some values of the principal quantum number n from 10 to 500 at temperatures from T = 100 K to 2000 K. The fractional rates R d ( e , ion) nl ( T ) = P nl d ( e , ion) ( T )/ P sp nl equal to the ratio of the induced decay (excitation, ionization) rates to the rate of spontaneous decay were determined as functions of T and n in every series of states with a given angular momentum l = 0, 1, 2. The calculated data reveal an essential difference between the asymptotic dependence of the ionization rate P ion nl ( T ) and the rates of decay and excitation P d ( e ) nl ( T )∝ T / n 2 . The departures appear in each Rydberg series for n > 100 and introduce appreciable corrections to the formula of Cooke and Gallagher. Two different approximation formulae are proposed on the basis of the numerical data, one for R d ( e ) nl ( T ) and another one for R ion nl ( T ), which reproduce the calculated values in wide ranges of principal quantum number from n = 10 to 1000 and temperatures between T = 100 K and T = 2000 K with an accuracy of 2% or better. Modified Fues' model potential approach was used for calculating matrix elements of bound–bound and bound–free radiation transitions in helium.
Abstract The rates of blackbody-radiation(BBR)-induced transitions from excited n S, n P, n D and n F states into bound states and into continua of the group IIa ions Ca + , Sr + , Ba + at temperatures from T = 100 K to T = 3000 K are calculated in consecutive comparison of the Fues model potential (FMP) with quantum defect method (QDM). The temperature and binding-energy dependencies are determined and analytical asymptotic approximations are proposed for evaluating numerically the contributions of the bound states and continua to the Rydberg-level widths and positions. The general properties of n -dependence at the threshold and regularities of above-threshold ionization cross sections for states with high principal quantum numbers n are used for determining the rates of BBR-induced ionization. Relations are determined between deviations from general regularities for the sum rules of oscillator- strengths and specific non-local dependence of the FMP on optical-electron angular momentum. The QDM appears preferable in comparison with the FMP approach for calculating the amplitudes of radiation transitions from Rydberg states, and specifically sums of matrix-element-dependent terms over very large (in particular, infinite) numbers of discrete states. The fractional (related to natural decay) rates of BBR-induced decay into lower bound states, excitation into upper bound states and ionization transitions into the continuum are presented asymptotically with parameters tabulated for the S, P, D and F Rydberg states.
Once created, an ensemble of atoms in their identical Rydberg states immediately experiences significant variations of its structure and corresponding properties. The variation is caused by the inevitable radiation transitions of highly excited states into different states of higher or lower energies. In particular, the change of a uniform definite-state population for another kind of population of different states will change the long-range interaction between atoms, even transforming the van der Waals interaction, Δ E vdW =− C 6 / R 6 , into dipole–dipole interaction with a different dependence on the interatomic distance, Δ E d−d =− C 3 / R 3 . In this paper, the most important—dipole radiation transitions from Rydberg states to higher- or lower-energy | n ′ 1 P 1 ⟩ states—are considered, both spontaneous and induced by the blackbody radiation (BBR) of the environment. The total transition probability rate, which is usually determined as the natural width, equals the imaginary part of the Rydberg-state energy Γ n S /2=−Im E n S . The probabilities of the | n ′ 1 P 1 ⟩-state populations W n S ( n ′ P, T ), which depend on the BBR temperature T , on the lifetime scale are also rather important optical characteristics of the ensemble of the Rydberg-state atoms. The value of W n S ( n ′ P, T ) is determined as the ratio of a particular transition probability rate Γ n S→ n ′ P sp +Γ n S→ n ′ P BBR ( T ) to the sum of all possible radiative transition rates, which include spontaneous and BBR-induced rates, where the latter depend on the temperature T of the environment. Numerical values of W n S ( n ′ P, T ) are calculated and presented in wide regions of the principal quantum numbers n , n ′ , and BBR temperatures T .
We have studied ionization of alkali-metal Rydberg atoms by blackbody radiation (BBR). The results of theoretical calculations of ionization rates of Li, Na, K, Rb and Cs Rydberg atoms are presented. The calculations have been performed for n S, n P and n D states for principal quantum numbers n =8–65 at ambient temperatures of 77, 300 and 600 K. The calculations take into account the contributions of BBR-induced redistribution of population between Rydberg states prior to photoionization and field ionization by extraction electric field pulses. The obtained results show that these phenomena affect both the magnitude of the measured ionization rates and their n dependence. A Cooper minimum for BBR-induced transitions between bound Rydberg states of Li has been found. The calculated ionization rates are compared with our earlier measurements of BBR-induced ionization rates of Na n S and n D Rydberg states with n =8–20 at 300 K. Good agreement for all states except n S with n >15 is observed. Useful analytical formulae for quick estimates of BBR ionization rates of Rydberg atoms are presented. Application of BBR-induced ionization signal to measurements of collisional ionization rates is demonstrated.
General properties were determined and asymptotic approximation formulas for probabilities of spontaneous decay and photoionization cross-sections were derived on the basis of numerically calculated amplitudes of bound-bound and bound-free radiation transitions from Rydberg nS -, nP - and nD -states of alkali atoms with high principal quantum numbers, up to n = 1000. The departure of data from the asymptotic formulas for states with principal quantum numbers in the range between n = 10 and n = 2000 from originally calculated data does not exceed 0.1–1%, and may be useful for estimations of natural radiation widths for arbitrary high Rydberg levels.
We have studied ionization of alkali-metal Rydberg atoms by blackbody radiation (BBR). The results of theoretical calculations of ionization rates of Li, Na, K, Rb and Cs Rydberg atoms are presented. The calculations have been performed for nS, nP and nD states for principal quantum numbers n=8-65 at ambient temperatures of 77, 300 and 600 K. The calculations take into account the contributions of BBR-induced redistribution of population between Rydberg states prior to photoionization and field ionization by extraction electric field pulses. The obtained results show that these phenomena affect both the magnitude of the measured ionization rates and their n-dependence. A Cooper minimum for BBR-induced transitions between bound Rydberg states of Li has been found. The calculated ionization rates are compared with our earlier measurements of BBR-induced ionization rates of Na nS and nD Rydberg states with n=8-20 at 300 K. A good agreement for all states except nS with n> 15 is observed. Useful analytical formulas for quick estimates of BBR ionization rates of Rydberg atoms are presented. Application of BBR-induced ionization signal to