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Journal of the Optical Society of America B

Isotope selective three-step photoionization of 176Lu

Manda V. Suryanarayana

Published Nov 18, 2020• 24 citations
Publisher

Abstract

Numerical computations of ionization efficiency and isotope selectivity of 176 L u have been carried out for the following three-step ladder type photoionization scheme, 5 d 6 s 2 2 D 3 / 2 ( 0.0 c m − 1 ) − − − ⟶ 540.4068 n m ⁡ 5 d 6 s 6 p 4 F 5 / 2 o ( 18504.58 c m − 1 ) − − − ⟶ 535.0626 n m 5 d 6 s 7 s 4 D 3 / 2 ( 37193.98 c m − 1 ) − − − ⟶ 618.0061 n m 53375 c m − 1 A u t o i o n i z a t i o n S t a t e → L u + , by invoking the density matrix formalism for the laser–atom interactions. Equations of motion have been derived for the odd isotopes by inclusion of hyperfine levels. The line shapes and their effect on the ionization efficiency and isotope selectivity have been discussed in detail. The effects of power of excitation and ionization lasers, spectral bandwidths, pulse delays, Doppler broadening of the atomic ensemble on the ionization efficiency, and degree of enrichment have been presented. Optimum conditions for the power of excitation, detunings, and other system parameters for the selective yet efficient photoionization of 176 L u have been identified.

DOI
10.1364/josab.409409

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Numerical computations of ionization efficiency and isotope selectivity of 176 L u have been carried out for the following three-step ladder type photoionization scheme, 5 d 6 s 2 2 D 3 / 2 ( 0.0 c m − 1 ) − − − ⟶ 540.4068 n m ⁡ 5 d 6 s 6 p 4 F 5 / 2 o ( 18504.58 c m − 1 ) − − − ⟶ 535.0626 n m 5 d 6 s 7 s 4 D 3 / 2 ( 37193.98 c m − 1 ) − − − ⟶ 618.0061 n m 53375 c m − 1 A u t o i o n i z a t i o n S t a t e → L u + , by invoking the density matrix formalism for the laser–atom interactions. Equations of motion have been derived for the odd isotopes by inclusion of hyperfine levels. The line shapes and their effect on the ionization efficiency and isotope selectivity have been discussed in detail. The effects of power of excitation and ionization lasers, spectral bandwidths, pulse delays, Doppler broadening of the atomic ensemble on the ionization efficiency, and degree of enrichment have been presented. Optimum conditions for the power of excitation, detunings, and other system parameters for the selective yet efficient photoionization of 176 L u have been identified.
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Ytterbium enriched in 176Yb is used for the production of the 177Lu radioisotope, which has applications in cancer treatment. We have theoretically studied the two-step resonant, three-step photoionization of the 176Yb isotope using the density-matrix approach. To simulate experimentally realistic conditions, the Doppler averaging, magnetic sublevel degeneracy, time-varying Rabi frequencies, ionization rate, angular divergence, and laser bandwidth have all been incorporated into the theoretical model. Calculations have been carried out to identify the optimized Rabi frequencies for evaluating the separation factor. The effect of the laser line shape on the excitation profile has also been thoroughly studied. We could obtain large separation factors of ~5000 for the 176Yb isotope, and the excitation conditions identified in this work may be utilized in the separation of the desired isotope.
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Abstract We propose a novel and simple method for the laser isotope separation of 176Lu a precursor for the production of 177Lu medical isotope. The physics of the laser-atom interaction has been studied through the dynamics of the atomic level populations using the density matrix formalism. It has been shown that a combination of cw excitation lasers and pulsed ionization laser can be used for the laser isotope separation of 176Lu. The optimum conditions for the efficient and selective separation of 176Lu have been derived by studying the time evolution of level population under laser excitation. It has also been shown that, it might be possible to produce ~ 100% enriched 176Lu isotope at a rate of 5 mg/h, which is higher than all previously reported methods so far. The isotope separation process proposed can be easily adopted using off-the-shelf lasers, for similar atomic systems.
Abstract The enriched 160 Gd isotope is an important target nucleus for the production of the next-generation β -emitting therapeutic nuclide 161 Tb. To address the limitation that the J = 2 → 2 → 1 → 0 polarization ionization path, although suitable for separating odd Gd isotopes with parallel linearly polarized lasers, cannot be used to enrich even Gd isotopes, we propose an efficient and highly selective ionization scheme for 160 Gd. Based on the density matrix theory, a general four-color, three-step ionization model was established by taking into account magnetic sublevel degeneracy and hyperfine structure. Numerical calculations of photoionization dynamics were performed to optimize laser parameters such as polarization, power density, and frequency detuning, with the aim of enhancing the ionization yield and isotopic abundance of 160 Gd. The results show that, in the absence of Doppler broadening, the ionization yield obtained with orthogonal linear polarization is higher than that obtained with parallel linear polarization in both three-color, three-step and four-color, three-step schemes. To maximize ionization yield, resonant excitation is required in the three-color, three-step scheme, whereas detuned excitation is needed in the four-color, three-step schemes to mitigate the population trapping effect. When Doppler broadening is taken into account, the selective photoionization performance depends on the residual Doppler broadening and on the number of laser beams passing through the atomic vapor. The calculations indicate that the optimal ionization scheme, namely the four-color, three-step scheme with parallel linear polarization, detuned excitation, saturation power density, and a bandwidth of 0.5 GHz, can achieve a 160 Gd abundance exceeding 98% at a residual Doppler broadening of 0.45 GHz, thereby meeting the application requirements.