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Systematic shell-model study of Rn isotopes with A=A= 207 to 216 and isomeric states

Bharti Bhoy [email protected] Department of Physics, Indian Institute of Technology Roorkee, Roorkee 247 667, India    Praveen C. Srivastava [email protected] Department of Physics, Indian Institute of Technology Roorkee, Roorkee 247 667, India
Abstract

We present systematic large-scale shell-model calculations for Rn isotopes with A=A= 207 to 216. For the 207-212Rn isotopes, we perform calculations with KHH7B interaction, while for 213-216Rn isotopes with KHPE and KHH7B interactions. The calculated energies and electromagnetic properties are compared with the available experimental data and predicted where experimental data are not available. We also suggest spins and parities of several unconfirmed states available from the recent experimental data. Comprehensive study of several isomeric states from the calculated shell-model configurations and half-lives is also reported.

pacs:
21.60.Cs, 21.30.Fe, 21.10.Dr, 27.20.+n, 27.30.+t

I INTRODUCTION

In the recent past, several experimental measurements have been done to study the structure and collectivity in the Pb region Brown2000 ; Butler ; T.Otsuka ; yosi ; Tang ; 210At ; 210Ra ; Ra196 ; 210Po ; 208Fr ; 206Bi ; Discovery1 ; Discovery2 ; prgati ; berry ; abinitio . Apart from this, different class of correlations such as pairing, quadrupole and octupole ones are recently reported Butlerjpg . Nuclei in the vicinity of N=126N=126 are very crucial to understand the astrophysical rr process in producing nuclei heavier than A \sim 190 Tang . A solvable model for octupole phonons for 208Pb is reported in Ref. isacker . Also, several isomeric states are observed in this region jain ; astier ; 203Tl ; phil . The level scheme of 212Rn with up to spins of 39\sim 39\hbar and excitation energies of about 13 MeV has recently been reported using 204Hg(13C,5n)212Rn reaction 212Rn1 . In this experiment, two new isomers with τ=25(2)ns\tau=25(2)ns and τ=12(2)ns\tau=12(2)ns were placed at 12.211 and 12.548 MeV, respectively. Theoretical results obtained by using semiempirical shell-model and deformed independent particle model (DIPM) are also reported. In another recent experiment at Legnaro National Laboratory in Italy 212Rn2 , a low-lying level scheme of 212Rn has been populated. In this experiment, several non-yrast states based on πh9/24\pi h_{9/2}^{4} and πh9/23f7/2\pi h_{9/2}^{3}f_{7/2} configurations have been identified. Also, a 3()3^{(-)} collective state at 2.121 MeV is proposed. This state is believed to be arising from mixing of the octupole vibration with a 33^{-} member of the πh9/23i13/2\pi h_{9/2}^{3}i_{13/2} multiplet.

There have been several theoretical studies done in this mass region Mcgrory ; Coraggio ; Caurier ; koji ; Teruya ; Yanase ; Naidja ; Wilson ; Wahid ; Anil . McGrory and Kuo Mcgrory have reported the structure of the nuclei 204-206Pb, 210-212Pb, 210Po, 211At, and 212Rn with few valence nucleons away from the 204Pb core using conventional nuclear shell-model several decades before. However, with the increase in the computational facility, it becomes feasible to perform shell-model calculations for nuclei having more valence nucleons. Shell-model results using a realistic effective interaction, derived from the Bonn-A nucleon-nucleon potential by using a GG-matrix folded-diagram approach for N=126N=126 isotones are reported by Coraggio et al. in Ref. Coraggio . The Strasbourg group has reported large-scale shell model results for Po-Pu with N=126N=126 using Kuo-Herling interaction in Ref. Caurier . Yoshinaga group has reported shell model results for nuclei around mass 210 Teruya and masses from 210 to 217 Yanase using effective interaction with an extended pairing plus quadrupole-quadrupole interaction.

The objective of the present study is to perform comprehensive shell-model calculations of 207-216Rn isotopes to cover nuclei below and above N=126N=126 shell gap. There is no systematic shell-model study available in the literature. From our shell-model study in two different model spaces, we have predicted the importance of different orbitals required to explain the high-spin states. Since there are several new experimental data available for high spin states and corresponding isomers, thus in our study, we have focused on high spin states. Our results also confirm several unconfirmed states from the experiment. The energy spectrum and electromagnetic properties are calculated and compared with the available experimental data. Isomeric states and respective half-lives in terms of the shell-model configurations and seniority are also presented. It is important to note that for the 212Rn shell-model results are available with the KHPE interaction 212Rn2 . However, we have done calculations with the KHH7B interaction to see the importance of including lower orbitals in the model space.

The outline of the paper is as follows. In Sec. II, the theoretical formalism of the present shell-model study is given. In Sec. III, we present the results obtained for the energy spectrum, electromagnetic properties, and half-lives for isomers and compare them with the available experimental data. Sec. IV contains a summary and conclusions of the present work.

II Formalism : SHELL-MODEL SPACE AND INTERACTIONS

Systematic studies have been carried out to understand the structure of Rn isotopes with AA = 207-216 considering two different sets of interactions and valence spaces. To diagonalize the matrices, the NUSHELLX Nushellx1 ; Nushellx2 and KSHELL Kshell codes have been employed for the shell-model calculations. Here we have taken two interactions for two different sets of isotopes, KHPE Warburton1 , and KHH7B pbpop . Our focus is mainly on the application of KHH7B on the whole Rn chain considered. To handle large dimensions, the KSHELL shell-model code is used. The highest dimension is 1.3 x 109 corresponding to ground state for 216Rn with the KHPE interaction. For A=213216A=213-216, we have used KHPE interaction, and calculations using KHH7B interaction have also been done using NUSHELLX code with truncation in the model space. Computationally it is challenging to perform shell model calculations without truncation in the Pb region.

One of the interactions we are using in our calculation is KHPE. The model space here consists of 1h9/2,2f7/2,2f5/2,3p3/2,3p1/2,1i13/21h_{9/2},2f_{7/2},2f_{5/2},3p_{3/2},3p_{1/2},1i_{13/2} proton orbitals and 1i11/2,2g9/2,2g7/2,3d5/2,3d3/2,4s1/2,1j15/21i_{11/2},2g_{9/2},2g_{7/2},3d_{5/2},3d_{3/2},4s_{1/2},1j_{15/2} neutron orbitals. The KHH7B residual interaction used by Poppelier and Glaudemans pbpop is the Surface Delta Interaction (SDI), which is the schematic interaction but gives the same results as the Kuo-Herling matrix elements Kuo1 ; Kuo2 . The effective realistic residual interaction of Kuo and Herling Kuo1 ; Kuo2 was derived from a free nucleon-nucleon potential of Hamada and Johnston Hamada with renormalization due to the finite extension of model space by the reaction matrix techniques developed by Kuo and Brown Kuo3 . In the present work, we have performed shell model calculations with KHPE interaction without any truncations. The full-fledged calculation with KHPE interaction is sufficient to explain low-lying states, but we need core-excitation for the explanation of high-lying states.

The KHH7B interaction consists of the four proton orbitals 2d5/2,2d3/2,3s1/2,1h11/22d_{5/2},2d_{3/2},3s_{1/2},1h_{11/2} below and three orbitals 1h9/2,2f7/2,1i13/21h_{9/2},2f_{7/2},1i_{13/2} above the ZZ = 82, and four neutron orbitals 2f5/2,3p3/2,3p1/2,1i13/22f_{5/2},3p_{3/2},3p_{1/2},1i_{13/2} below and three orbitals 2g9/2,1i11/2,1j15/22g_{9/2},1i_{11/2},1j_{15/2} above NN = 126 energy gap. In KHH7B interaction, the cross shell two-body matrix elements (TBMEs) were generated by the G-matrix potential (H7B) Hosaka , while the proton-neutron, hole-hole, and particle-particle TBMEs are taken from Kuo-Herling interaction Kuo1 as modified in the Ref. Warburton1 . Previously, shell model results using KHH7B interaction are reported in Wilson ; berry ; Wahid ; Anil . For KHH7B, we have completely filled proton orbitals below Z=82Z=82, while neutrons are only allowed to occupy the orbitals below N=126N=126 for A=207212A=207-212 and above N=126N=126 for A=213216A=213-216. In the Pb region, shell-model calculation taking into account core-excitation is very important. However, due to huge-dimension, we are unable to perform an appropriate calculation using core-excitation. It is essential to perform the shell-model calculation using KHH7B interaction without any truncation to see the role of lower orbitals. Further, we need to develop a new interaction, because existing interactions are very old. Although, we have limited experimental data to tune the effective interaction. In the Pb region, new data for both energy and electromagnetic properties are coming. In the future, it is possible to construct a new interaction with these data.

Refer to caption
Figure 1: Comparison between calculated and experimental NNDC energy levels for 208Rn.
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Figure 2: Comparison between calculated and experimental NNDC energy levels for 210Rn.
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Figure 3: Comparison between calculated and experimental NNDC , 212Rn2 energy levels for 212Rn.
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Figure 4: Comparison between calculated and experimental NNDC energy levels for 214Rn.
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Figure 5: Comparison between calculated and experimental NNDC energy levels for 216Rn.

III RESULTS AND DISCUSSION

In this section, the results of our calculations for the Rn isotopes are presented and compared with experimental data. In Figs. 1 to 5 results obtained for the 208,210,212,214,216Rn isotopes are shown in comparison with experimental data. Results for the 207,209,211,213,215Rn isotopes are given in Figs. 6 to 10. The configuration of the probability for dominant wave-function and corresponding seniority of isomeric states are reported in Table 1. The electromagnetic properties are reported in Tables 2 and 3. The calculated half-lives corresponding to the isomeric states are reported in comparison with the experimental data in Table 4.

III.1 Even Rn isotopes

Fig. 1 shows the shell-model energy spectrum of 208Rn in comparison with the experimental data, where all the observed levels up to 5.2 MeV excitation energy are reported. In the calculated low-energy spectrum, we get a much higher level density compared to experimental data. We report only those yrast and non-yrast shell-model states corresponding to the experimental levels. The shell-model is giving close energy values for energy levels up to 2.5 MeV for all the yrast states. In our calculation, the experimental (4,5,6)+{(4,5,6)^{+}} level at 1.580 MeV can be associated with either the 43+4_{3}^{+} or 61+6_{1}^{+} state. The calculated 51+5_{1}^{+} state is produced 300 keV higher than the experimental state at 1.580 MeV, and calculated 52+5_{2}^{+} is produced 500 keV higher than the experimental state at 1.658 MeV ( 4+{4}^{+}, 5+{5}^{+}). Therefore, we propose the assignment of calculated 51+5_{1}^{+} state to the closest experimental level at 1.658 MeV, excluding 5+{5}^{+} from the 1.580 MeV experimental state. For the negative parity state, the experimental (5,6+){(5^{-},6^{+})} level at 2.18 MeV can be associated with the calculated 515_{1}^{-} at 2.308 MeV.

The shell-model energy spectrum of 210Rn in comparison with the experimental data is shown in Fig. 2, where all the observed levels up to 5.2 MeV excitation energy are reported. Experimentally, the relative energies between the ground state and many excited states are unknown in 210Rn. The (81+)(8_{1}^{+}) state of these excited states is the lowest and observed at 1.665+x MeV. In this figure, these states are shown without any assumption of x ( i.e., x=0). The shell-model reproduces the energy levels well up to 4 MeV for both positive and negative parity states. Most of the levels in the case of 210Rn are tentative. Therefore, a one-to-one correspondence has been estimated with the experimental data. The second excited state in the calculation is produced as 2+{2}^{+}, 90 keV lower than the experimental energy value, which is an experimentally tentative (4)+({4})^{+} state. The calculated 41+4_{1}^{+} state is produced at 1.593 MeV close to the tentative experimental level (4)+({4})^{+} at 1.545 MeV. The calculated 61+6_{1}^{+}, 81+8_{1}^{+} and 82+8_{2}^{+} are confirming the tentative experimental states with a difference of a few keV. The last two calculated negative parity states, 18118_{1}^{-} and 19119_{1}^{-} are lower in energies with respect to the experimental data by 436 keV and 572 keV, respectively. These levels might arise from core-excitations, and in some cases, significant admixtures of configurations without and with core-excitation beyond Z=82Z=82 and N=126N=126 shell closure.

The shell-model energy spectrum of 212Rn in comparison with the experimental data is shown in Fig. 3, where all the observed levels up to 6.2 MeV excitation energy are reported. In this work, we have reproduced all the new states identified in 212Rn2 , with a satisfactory quantitative agreement between our results and experimental data. A direct one-to-one correspondence between states can be established up to 2.300 MeV in positive parity states. Here we observe similar trend in 208Rn, 210Rn and 212Rn isotopes: a small energy gap between the 61+{6_{1}}^{+} and 81+{8_{1}}^{+} states, and a large gap between 81+8_{1}^{+} and 82+8_{2}^{+} states are featured. Our calculation confirms the tentative experimental 63+6_{3}^{+} and 131+13_{1}^{+} states with a difference of only a few keV. The calculated 65+6_{5}^{+} and 121+12_{1}^{+} states are 111 keV and 144 keV higher than the experimental data, respectively. This state could be 65+{6_{5}}^{+} state. For high-lying states, the compression becomes notable, except for the calculated 202+20_{2}^{+} state and confirms this tentative state. The 18118_{1}^{-} state is 662 keV lower, and 19119_{1}^{-} state is 1.065 MeV higher than the experimental data. The description of these high-lying states requires the core-excitation and maybe some mixing between the single-particle states and core-excitation above Z=82Z=82. and N=126N=126 shell closure. In our calculation, the collective 313_{1}^{-} state at 2.856 MeV is 735 keV higher than the proposed experimental value, and arising from the configuration π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}). The single-particle orbitals with Δl\Delta l = 3, πf7/2πi13/2\pi{f_{7/2}}-\pi{i_{13/2}} and νg9/2νj15/2\nu{g_{9/2}}-\nu{j_{15/2}} in our model space and core-excitations across the two shell gaps at Z=82Z=82 and N=126N=126 are responsible for the structure of this octupole vibration. The KHPE (results as reported in Ref. 212Rn2 ) and KHH7B interactions are giving almost similar results because we have only four valence protons beyond Z=82 and N=126. This is reflected from the similar wave functions we have obtained from these two interactions.

The shell-model energy spectrum of 214Rn in comparison with the experimental data is shown in Fig. 4 with the two interactions KHPE and KHH7B, where all the observed levels up to 4.6 MeV excitation energy are reported. In 214Rn, many of the energy levels are unidentified in terms of the spin-parity. These levels are not included in our figure. However, we have tried to interpret the first two unidentified levels. The shell-model results from the KHPE interaction are slightly better than the KHH7B interaction, as shown in Fig. 4. Similar to other even Rn isotopes, a small energy gap is observed between the 61+6_{1}^{+} and 81+8_{1}^{+} states, and a large gap between 81+8_{1}^{+} and 82+8_{2}^{+} states. The spin-parities of the experimental states at 1.332 MeV and 1.800 MeV are not assigned. In the experimental data, the first state decays to the 21+2_{1}^{+} state at 0.695 MeV, and the second state decays to the first unidentified state at 1.332 MeV. The calculated 22+2_{2}^{+} state is at 1.558 MeV and 1.509 MeV from the KHPE and KHH7B interaction, respectively. The calculated 62+6_{2}^{+} state is at 1.883 MeV and 1.842 MeV from the KHPE and KHH7B interaction, respectively. From the comparison with neighboring nuclei 212Rn, 216Rn from both our calculation and experimental data, and considering our results for the above two mentioned states, we suggest the spin-parities of the experimental state at 1.332 MeV to be 22+2_{2}^{+} and state at 1.800 MeV to be 62+6_{2}^{+}. With both interactions the calculated 12112_{1}^{-} state is very close to the tentative experimental state with only few keV differences. The calculated negative parity states above 3.0 MeV are highly compressed. The 214Rn isotope is above the Z=82Z=82 and N=126N=126 shell-closure with 4 valence protons and 2 valence neutrons. Therefore, it is important to consider sufficient orbitals around the shell-closure for core-excitation and required configuration mixing. Due to limited computational facilities, we are not able to include all orbitals without truncation.

The shell-model energy spectrum of 216Rn in comparison with the experimental data is shown in Fig. 5 with two interactions KHPE and KHH7B up to 3.8 MeV excitation energy. Previously observed feature for a small energy gap between the 61+6_{1}^{+} and 81+8_{1}^{+} states, and a large gap between 81+8_{1}^{+} and 82+8_{2}^{+} states, are not observed here as prominently as in the other even Rn isotopes. However, as observed in the experiment, this pattern has vanished in 216Rn due to the enhancement of quadrupole collectivity. As we move from 214Rn to 216Rn, the number of valence particles increases beyond Z=82Z=82 and N=126N=126 shell closure, thus we need to include more orbitals in the model space apart from the core-excitation. Therefore, both the interactions are not being able to reproduce the levels in the whole energy range. Due to the model space requirement for any specific state, some levels are in good agreement with experimental data, while others could not be reproduced well. The spectrum of 216Rn looks like vibrational one because low-lying states from 0+0^{+} - 8+8^{+} are equally spaced . In the case of vibrational spectra, the quadrupole moment should be smaller. In the simplest version of the vibrational model, the quadrupole moment of the 2+2^{+} state is predicted to be zero. Our shell model results give an equal spacing of low-lying states, although results for quadrupole-moments are large. However, there is no experimental data available for the quadrupole moment.

Refer to caption
Figure 6: Comparison between calculated and experimental NNDC energy levels for 207Rn.
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Figure 7: Comparison between calculated and experimental NNDC energy levels for 209Rn.
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Figure 8: Comparison between calculated and experimental NNDC energy levels for 211Rn.
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Figure 9: Comparison between calculated and experimental NNDC energy levels for 213Rn.
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Figure 10: Comparison between calculated and experimental NNDC energy levels for 215Rn.
Table 1: Configurations of isomeric states in Rn isotopes with the probability of the dominant component of the configuration.
Nucleus JπJ^{\pi} Seniority Wave-function Probability
207Rn 13/21+13/2_{1}^{+} v=1v=1 ν(i13/2)1\nu(i_{13/2})^{-1} 25.28%\%
209Rn 13/21+13/2_{1}^{+} v=1v=1 ν(i13/2)1\nu(i_{13/2})^{-1} 26.33%\%
29/2129/2_{1}^{-} v=3v=3 π(h9/2)4ν(f5/2)1\pi(h_{9/2})^{4}\otimes\nu(f_{5/2})^{-1} 73.43%\%
35/21+35/2_{1}^{+} v=5v=5 π(h9/2)3(i13/2)ν(f5/2)1\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(f_{5/2})^{-1} 58.53%\%
π(h9/2)3(i13/2)ν(p1/2)1\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(p_{1/2})^{-1} 11.45%\%
41/2141/2_{1}^{-} v=5v=5 π(h9/2)2(i13/2)2ν(f5/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(f_{5/2})^{-1} 49.48%\%
π(h9/2)2(i13/2)2ν(p1/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(p_{1/2})^{-1} 17.27%\%
211Rn 17/2117/2_{1}^{-} v=3v=3 π(h9/2)4ν(p1/2)1\pi(h_{9/2})^{4}\otimes\nu(p_{1/2})^{-1} 69.04%\%
35/21+35/2_{1}^{+} v=5v=5 π(h9/2)3(i13/2)ν(p1/2)1\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(p_{1/2})^{-1} 85.45%\%
43/2143/2_{1}^{-} v=5v=5 π(h9/2)2(i13/2)2ν(f5/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(f_{5/2})^{-1} 91.30%\%
49/21+49/2_{1}^{+} v=5v=5 π(h9/2)2(i13/2)2ν(g9/2)\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(g_{9/2}) 61.78%\%
63/2163/2_{1}^{-} v=7v=7 π(h9/2)2(i13/2)2\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes 88.04%\%
ν(g9/2)(i11/2)(f5/2)1\nu(g_{9/2})(i_{11/2})(f_{5/2})^{-1}
213Rn 15/2115/2_{1}^{-} v=1v=1 ν(j15/2)\nu(j_{15/2}) 41.94%\%
21/21+21/2_{1}^{+} v=3v=3 π(h9/2)4ν(g9/2)\pi(h_{9/2})^{4}\otimes\nu(g_{9/2}) 51.79%\%
25/21+25/2_{1}^{+} v=3v=3 π(h9/2)4ν(g9/2)\pi(h_{9/2})^{4}\otimes\nu(g_{9/2}) 48.37%\%
31/2131/2_{1}^{-} v=3v=3 π(h9/2)3(i13/2)ν(g9/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2}) 63.64%\%
37/21+37/2_{1}^{+} v=5v=5 π(h9/2)3(f7/2)ν(g9/2)\pi(h_{9/2})^{3}(f_{7/2})\otimes\nu(g_{9/2}) 95.82%\%
43/2143/2_{1}^{-} v=5v=5 π(h9/2)3(i13/2)ν(g9/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2}) 92.94%\%
49/21+49/2_{1}^{+} v=5v=5 π(h9/2)2(i13/2)2ν(g9/2)\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(g_{9/2}) 91.62%\%
55/21+55/2_{1}^{+} v=5v=5 π(h9/2)(i13/2)3ν(j15/2)\pi(h_{9/2})(i_{13/2})^{3}\otimes\nu(j_{15/2}) 99.95%\%
208Rn 81+8_{1}^{+} v=2v=2 π(h9/2)4\pi(h_{9/2})^{4} 38.74%\%
10110_{1}^{-} v=2v=2 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}) 32.88%\%
16116_{1}^{-} v=2v=2 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}) 43.65%\%
210Rn 81+8_{1}^{+} v=2v=2 π(h9/2)4\pi(h_{9/2})^{4} 46.63%\%
11111_{1}^{-} v=2v=2 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}) 42.72%\%
141+14_{1}^{+} v=4v=4 π(h9/2)3(f7/2)\pi(h_{9/2})^{3}(f_{7/2}) 49.23%\%
17117_{1}^{-} v=4v=4 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}) 50.80%\%
201+20_{1}^{+} v=4v=4 π(h9/2)2(i13/2)2\pi(h_{9/2})^{2}(i_{13/2})^{2} 42.73%\%
212Rn 61+6_{1}^{+} v=2v=2 π(h9/2)4\pi(h_{9/2})^{4} 67.34%\%
81+8_{1}^{+} v=2v=2 π(h9/2)4\pi(h_{9/2})^{4} 68.42%\%
141+14_{1}^{+} v=4v=4 π(h9/2)3(f7/2)\pi(h_{9/2})^{3}(f_{7/2}) 98%\%
17117_{1}^{-} v=4v=4 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}) 99.59%\%
221+22_{1}^{+} v=6v=6 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes 80.48%\%
ν(p1/2)1(g9/2)\nu(p_{1/2})^{-1}(g_{9/2})
25125_{1}^{-} v=6v=6 π(h9/2)2(i13/2)2\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes 73.45%\%
ν(p1/2)1(g9/2)\nu(p_{1/2})^{-1}(g_{9/2})
214Rn 181+18_{1}^{+} v=4v=4 π(h9/2)3(i13/2)ν(g9/2)2\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2})^{2} 60%\%
221+22_{1}^{+} v=4v=4 π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes 83%\%
ν(g9/2)(j15/2)\nu(g_{9/2})(j_{15/2})

The seniority, configurations and half-life corresponding to different isomeric states for Rn isotopes as reported in Table 1 and Table 4 are discussed below. In spherical nuclei close to the magic number, the breaking of high-jj nucleon pairs produces isomeric states. The Rn isotopes considered in our calculations are spherical, thus it is possible to explain the isomers in terms of seniority quantum number. Seniority ν\nu is the number of particles not in pairs coupled to angular momentum JJ = 0. With shell-model, it is possible to extract information about seniority from the configurations. For the seniority isomer, the decay is hindered because of the same seniority of the initial and final states. Seniority isomers arise because E2E2 decay is hindered between the same seniority of the initial and final states. In the case of 208,210,212Rn isotopes, 8+8^{+} state is the seniority isomer with a very small B(E2B(E2; 8+8^{+} \rightarrow 6+6^{+}) value. This is because of the same seniority v=2v=2 for 8+8^{+} and 6+6^{+}, which is coming from π(h9/2)4\pi(h_{9/2})^{4} configuration.

In 208Rn, 210Rn and 212Rn the 81+8_{1}^{+} isomeric state is coming from π(h9/2)4\pi(h_{9/2})^{4} configuration, in increasing probability with mass number. The 81+8_{1}^{+} isomeric state is formed by purely h9/2h_{9/2} orbital with one pair breaking, thus ν\nu = 2. The half-life of this isomeric state is also reproduced very close to the experimental data with B(E2)B(E2) transition for all three isotopes. The 10110_{1}^{-} and 16116_{1}^{-} states are coming from the same configuration π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2}), and formed by one proton in h9/2h_{9/2}, i13/2i_{13/2} each coupled with one pair in h9/2h_{9/2} orbital, hence the seniority ν\nu = 2. These two states are generated by B(M1)B(M1) transition and half-lives for these states are reproduced well with the experimental data. In 210Rn, 11111_{1}^{-}[π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2})] isomeric state is formed by one proton in h9/2h_{9/2} and i13/2i_{13/2} orbitals each, thus ν\nu = 2. The 141+{14_{1}}^{+}[π(h9/2)3(f7/2)\pi(h_{9/2})^{3}(f_{7/2})] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital, and one proton in h9/2h_{9/2} and f7/2f_{7/2} orbitals each, thus ν\nu = 4. The half-life for this state is reproduced in the same order as the experimental data 76(7) ns, with a higher magnitude, as the B(E2)B(E2) transition value in our calculation is smaller than the experimental data. The 171{17_{1}}^{-}[π(h9/2)3(i13/2)\pi(h_{9/2})^{3}(i_{13/2})] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital, and one proton in h9/2h_{9/2} and i13/2i_{13/2} orbitals each, thus ν\nu = 4. The 201+20_{1}^{+}[π(h9/2)2(i13/2)2\pi(h_{9/2})^{2}(i_{13/2})^{2}] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) both the orbitals, thus ν\nu = 4. In 212Rn, the 61+6_{1}^{+} isomeric state is formed similar to the 81+8_{1}^{+} states in all even isotopes with the same seniority. The half-life of this state is almost the same as the experimental data, as our B(E2)B(E2) transition value and energy difference are reproduced very well. The 141+14_{1}^{+} and 17117_{1}^{-} isomeric states are similar as in the 210Rn, with almost double probability (98%\% and 99.59%\%, respectively) as these states are pure states. The half-lives for 141+14_{1}^{+} and 17117_{1}^{-} isomeric states are coming in the same order with higher magnitude because the calculated B(E2)B(E2) transition value is significantly less than the experimental data for the 141+14_{1}^{+} state, and our energy difference is very small for 17117_{1}^{-}. The 221+22_{1}^{+}[π(h9/2)3(i13/2)ν(p1/2)1(g9/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(p_{1/2})^{-1}(g_{9/2})] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital, and one proton in h9/2h_{9/2} and i13/2i_{13/2} orbitals each, and one neutron in p1/2p_{1/2} and g9/2g_{9/2} orbitals each, thus ν\nu = 6. The 25125_{1}^{-}[π(h9/2)2(i13/2)2ν(p1/2)1(g9/2)\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(p_{1/2})^{-1}(g_{9/2})] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) both the orbitals and one neutron in p1/2p_{1/2} and g9/2g_{9/2} orbitals each, thus ν\nu = 6. In 214Rn, the 181+{18_{1}}^{+}[π(h9/2)3(i13/2)ν(g9/2)2\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2})^{2}] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) or ν(g9/2)\nu(g_{9/2}) orbital, and one proton in h9/2h_{9/2} and i13/2i_{13/2} orbitals each, thus ν\nu = 4. The 221+22_{1}^{+} isomeric state is arising from the configuration π(h9/2)3(i13/2)ν(g9/2)(j15/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2})(j_{15/2}), and formed by one proton in h9/2h_{9/2} and i13/2i_{13/2} orbitals each, and one neutron in g9/2g_{9/2} and j15/2j_{15/2} orbitals each, thus ν\nu = 4. For this isomeric state, seniority reduces as compared to the 221+22_{1}^{+} state in 212Rn because of the role of j15/2j_{15/2} orbital. It is important to mention here that to calculate 49/21+49/2_{1}^{+} and 63/2163/2_{1}^{-} for 211Rn and 221+22_{1}^{+} and 25125_{1}^{-} for 212Rn, we have opened 2g9/2,1i11/22g_{9/2},1i_{11/2}, and 1j15/21j_{15/2} neutron orbitals, allowing two-particle excitation in each orbital (with restriction on other orbitals also). Corresponding wavefunctions are shown in Table 1, and the calculations are performed using the NUSHELLX code.

III.2 Odd Rn isotopes

Fig. 6 shows the shell-model energy spectrum of 207Rn in comparison with the experimental data, where all the observed levels up to 2.8 MeV excitation energy are reported. In 207Rn, most of the experimental levels above 1.5 MeV are not assigned with confirmed spin-parities. Therefore, we have calculated the same levels for both parities to see a resemblance between the experimental data and shell-model. For the known experimental states with both spin-parity, the shell-model reproduces the energy spectrum with good agreement. The calculated 3/213/2_{1}^{-} state is twice the energy of the experimental data. On the other hand, following the trend of our calculated spectrum, 100-200 keV range discrepancy in energy is negligible, and the experimental 3/213/2_{1}^{-} state is at a very small energy value of 0.123 MeV. The experimental state at 0.283 MeV can be associated with both 3/223/2_{2}^{-} and 1/211/2_{1}^{-} calculated states. Above 1.4 MeV, all the calculated states are compressed.

We can see from Fig. 6, our calculation can not predict precisely the unconfirmed experimental states, as they are equally likely be assigned in both the parities.

The shell-model energy spectrum of 209Rn in comparison with the experimental data is shown in Fig. 7, where all the observed levels up to 3.6 MeV excitation energy are reported. In 209Rn, the energy spectrum is dense for low-lying states, and the calculated spectrum has reproduced the experimental data with a quantitative agreement. We have calculated all of the low-lying experimental levels, but we have excluded few non-yrast calculated levels from Fig. 7, showing one-to-one feasibly neat correspondence with the experimental data. The calculated states are overpredicted up to 1.174 MeV experimental energy value and under predicted above this energy range for both the parities. In our calculation, the experimental level at 0.511 MeV is reproduced with large discrepancies 415 keV and 945 keV for 5/225/2_{2}^{-} and 3/243/2_{4}^{-} states, respectively, while 1/221/2_{2}^{-} is reproduced with 122 keV energy difference with respect to the experimental data. We suggest that this experimental level can be associated with either the 1/221/2_{2}^{-} or 5/225/2_{2}^{-} calculated state. For the experimental level at 0.867 MeV, the calculated state can be associated with 7/227/2_{2}^{-} or 9/229/2_{2}^{-}. Above \sim 1 MeV energy value, all the calculated states are compressed. The calculated 27/21+27/2_{1}^{+} state is lower in energy by 1 MeV with respect to the experimental data. The compression in energy in our calculated spectrum for high-spin states might be due to the need for core-excitation and significant configuration mixing with the higher orbitals beyond Z=82Z=82 and N=126N=126 shell closure. As the neutron number increases in odd Rn isotopes, the calculated 1/21{{1/2}_{1}}^{-}, 3/21{{3/2}_{1}}^{-} and 5/21{{5/2}_{1}}^{-} states show strong single-particle nature with the dominant configuration ν(p1/2)1\nu(p_{1/2})^{-1} (38%38\%), ν(p3/2)1\nu(p_{3/2})^{-1} (36%36\%) and ν(f5/2)1\nu(f_{5/2})^{-1} (39%39\%), respectively.

The shell-model energy spectrum of 211Rn in comparison with the experimental data is shown in Fig. 8, where all the observed levels up to 3.9 MeV excitation energy are reported. Experimentally, the relative energies between the ground state and many excited states are unknown in 211Rn. The (17/21)(17/2_{1}^{-}) state of these excited states is the lowest and observed at 1.578+x MeV. In this figure, these states are shown without any assumption of x ( i.e., x=0). Most of the levels in the case of 211Rn are tentative. For 211Rn, the shell-model spectrum reproduces very well the experimental data with an establishment of one-to-one correspondence in both positive and negative parity states, with good estimation for the tentative states. The calculated 5/215/2_{1}^{-} state is 147 keV higher than the experimental data, similar to other odd Rn isotopes for the first excited state. The tentative experimental state at 0.833 MeV is reproduced with only 31 keV energy difference in our calculation, suggesting this state as 3/213/2_{1}^{-}. In the case of positive parity, the calculated 9/21+9/2_{1}^{+} is over-predicted, while 31/21+31/2_{1}^{+} and 35/21+35/2_{1}^{+} states are lower in energies. This may be due to our model space is not enough for these high-spin states. For the negative parity, the calculated 1/21{{1/2}_{1}}^{-}, 3/21{{3/2}_{1}}^{-} and 5/21{{5/2}_{1}}^{-} states show strong single-particle nature with the dominant configuration ν(p1/2)1\nu(p_{1/2})^{-1}(48%48\%), ν(p3/2)1\nu(p_{3/2})^{-1}(42%42\%) and ν(f5/2)1\nu(f_{5/2})^{-1}(49%49\%), respectively. Due to the restrictions of orbitals in the KSHELL code, as mentioned before, the KHH7B interaction could not reproduce high-lying states.

The shell-model energy spectrum of 213Rn in comparison with the experimental data is shown in Fig. 9 with two interactions KHPE and KHH7B, where all the observed levels up to 3.5 MeV excitation energy are reported. Experimentally, the relative energies between the ground state and many excited states are unknown in 213Rn. The (25/21+)(25/2_{1}^{+}) state of these excited states is the lowest and observed at 1.664+x MeV. In this figure, these states are shown without any assumption of x ( i.e., x=0). In 213Rn, all levels are tentative, and many of the energy levels are unidentified in terms of the spin-parity. These unidentified levels are not included in the figure. Our calculation is supporting almost all of the tentative experimental states from both interactions. The shell-model results from the KHPE interaction are better than the KHH7B interaction for positive parity states, and the KHH7B interaction is slightly better for the negative parity states, as we can see in Fig. 9. This is due to the different model spaces in these interactions, which are responsible for generating the spectrum for positive or negative parity states. The 213Rn isotope is just above the Z=82Z=82 and N=126N=126 shell closure. Therefore the trend of a higher first excited state, as in other odd Rn isotopes, is not followed here as it is compressed because of collectivity. For the energy value up to 2.121 MeV, KHPE interaction gives overall good results, and KHH7B interaction gives compressed results. Above this energy range, KHPE interaction slightly overpredicts the states, but overall results agree with the with the experimental data, and KHH7B interaction gives highly compressed results. These compressed results from the KHH7B interaction indicate the importance of inclusion of the higher orbitals and core-excitation beyond Z=82Z=82 and N=126N=126 shell closure. The KHPE interaction results for high-lying states are overpredicted because we have not taken into account core-excitation. The states above 3.0 MeV are compressed from the KHPE interaction. The KHH7B interaction has reproduced quite well the spectrum for the negative parity states. We can see from Fig. 9, our calculation can not predict precisely the unconfirmed 27/2{27/2} experimental state, as this state is equally likely to be assigned in both the parities.

The shell-model energy spectrum of 215Rn in comparison with the experimental data is shown in Fig. 10 with the two interactions KHPE and KHH7B, where all the observed levels up to 2.3 MeV excitation energy are reported. In 215Rn, all levels are tentative except for the ground state. The shell-model result is supporting a few of the tentative experimental states from both the interactions. The first excited state is not confirmed experimentally. In our calculation, the 11/21+{{11/2}_{1}}^{+} state is coming as the first-excited state from both the interaction, which is an experimentally tentative second excited state. The calculated 7/21+{{7/2}_{1}}^{+} state has 119 keV and 246 keV difference and the 9/21+{{9/2}_{1}}^{+} state has 689 keV and 563 keV difference with the experimental value from KHPE and KHH7B interaction, respectively. Therefore, for the experimental state at 0.214 MeV, our calculation suggests the state as 7/21+{{7/2}_{1}}^{+}. For the experimental negative parity state at 0.291 MeV, our calculation overpredicts all three tentative spins with large energy value differences from the experimental data from both the interactions.

In all the Rn isotopes, we have observed that most of the low-lying states are collective because they show large configuration mixing. Some of these states are highly admixture of different configurations that have almost the same probability. On the other hand, the high-lying states are less collective, and many states in 212Rn are almost pure.

Table 2: The calculated B(E2)B(E2) values in units of W.u. for Rn isotopes using KHH7B interaction (SM) in comparison with the experimental data (Expt.) NNDC ; 207Rn ; 208Rn ; 209Rn ; 210Rn ; 211Rn ; 212Rn ; 213Rn ; 214Rn ; 215Rn ; 216Rn corresponding to epe_{p} = 1.5ee and ene_{n} = 0.5ee.
B(E2;JiJf{B(E2;J_{i}\rightarrow J_{f}})                B(E2;JiJf{B(E2;J_{i}\rightarrow J_{f}})
207Rn Expt. SM 208Rn Expt. SM
3/215/213/2_{1}^{-}\rightarrow 5/2_{1}^{-} NA 1.428 21+01+2_{1}^{+}\rightarrow 0_{1}^{+} NA 5.838
9/215/219/2_{1}^{-}\rightarrow 5/2_{1}^{-} NA 5.551 41+21+4_{1}^{+}\rightarrow 2_{1}^{+} 4.7(4) 0.1789
13/219/2113/2_{1}^{-}\rightarrow 9/2_{1}^{-} NA 1.347 61+41+6_{1}^{+}\rightarrow 4_{1}^{+} NA 0.124
17/21+13/21+17/2_{1}^{+}\rightarrow 13/2_{1}^{+} NA 7.655 81+61+8_{1}^{+}\rightarrow 6_{1}^{+} 0.187(7) 0.449
17/2113/2117/2_{1}^{-}\rightarrow 13/2_{1}^{-} NA 0.511 101+81+10_{1}^{+}\rightarrow 8_{1}^{+} NA 4.557
21/21+17/21+21/2_{1}^{+}\rightarrow 17/2_{1}^{+} NA 0.144 141+121+14_{1}^{+}\rightarrow 12_{1}^{+} 0.35(17) 5.177
209Rn Expt. SM 210Rn Expt. SM
1/215/211/2_{1}^{-}\rightarrow 5/2_{1}^{-} NA 0.808 21+01+2_{1}^{+}\rightarrow 0_{1}^{+} NA 5.286
3/215/213/2_{1}^{-}\rightarrow 5/2_{1}^{-} NA 0.325 41+21+4_{1}^{+}\rightarrow 2_{1}^{+} 1.8(2) 0.698
9/215/219/2_{1}^{-}\rightarrow 5/2_{1}^{-} NA 6.994 61+41+6_{1}^{+}\rightarrow 4_{1}^{+} 1.58(15) 0.963
13/219/2113/2_{1}^{-}\rightarrow 9/2_{1}^{-} NA 0.159 61+42+6_{1}^{+}\rightarrow 4_{2}^{+} 1.58(19) 1.752
23/2119/2123/2_{1}^{-}\rightarrow 19/2_{1}^{-} NA 1.954 81+61+8_{1}^{+}\rightarrow 6_{1}^{+} NA 0.351
25/2121/2125/2_{1}^{-}\rightarrow 21/2_{1}^{-} NA 5.028 101+81+10_{1}^{+}\rightarrow 8_{1}^{+} NA 3.937
27/2123/2127/2_{1}^{-}\rightarrow 23/2_{1}^{-} NA 1.774 121+101+12_{1}^{+}\rightarrow 10_{1}^{+} NA 2.734
29/2127/2129/2_{1}^{-}\rightarrow 27/2_{1}^{-} 0.66(15) 0.70 141+121+14_{1}^{+}\rightarrow 12_{1}^{+} 0.0248(23) 3.981×103\times 10^{-3}
211Rn Expt. SM 212Rn Expt. SM
5/211/215/2_{1}^{-}\rightarrow 1/2_{1}^{-} >>0.040 1.911 21+01+2_{1}^{+}\rightarrow 0_{1}^{+} NA 5.195
9/215/219/2_{1}^{-}\rightarrow 5/2_{1}^{-} NA 0.222 41+21+4_{1}^{+}\rightarrow 2_{1}^{+} 1.0540+44{}^{+44}_{-40} 1.234
13/219/2113/2_{1}^{-}\rightarrow 9/2_{1}^{-} NA 0.744 61+41+6_{1}^{+}\rightarrow 4_{1}^{+} 0.404+6{}^{+6}_{-4} 0.717
21/2117/2121/2_{1}^{-}\rightarrow 17/2_{1}^{-} >>0.030 1.744 81+61+8_{1}^{+}\rightarrow 6_{1}^{+} 0.117(7) 0.229
25/2121/2125/2_{1}^{-}\rightarrow 21/2_{1}^{-} >>0.036 0.926 101+81+10_{1}^{+}\rightarrow 8_{1}^{+} NA 3.294
29/2125/2129/2_{1}^{-}\rightarrow 25/2_{1}^{-} 0.073(17) 0.012 121+101+12_{1}^{+}\rightarrow 10_{1}^{+} 4.5229+32{}^{+32}_{-29} 3.115
29/2125/2229/2_{1}^{-}\rightarrow 25/2_{2}^{-} 1.9(6) 0.090 141+121+14_{1}^{+}\rightarrow 12_{1}^{+} 0.031936+45{}^{+45}_{-36} 5.236×103\times 10^{-3}
31/21+27/21+31/2_{1}^{+}\rightarrow 27/2_{1}^{+} >>0.0077 1.688 141+122+14_{1}^{+}\rightarrow 12_{2}^{+} 2.9(6) 2.624
35/21+31/21+35/2_{1}^{+}\rightarrow 31/2_{1}^{+} 2.3(5) 2.484 17115117_{1}^{-}\rightarrow 15_{1}^{-} 2.9415+17{}^{+17}_{-15} 2.942
213Rn Expt. SM 214Rn Expt. SM
13/21+9/21+13/2_{1}^{+}\rightarrow 9/2_{1}^{+} NA 4.645 21+01+2_{1}^{+}\rightarrow 0_{1}^{+} >>0.032 5.459
17/21+13/21+17/2_{1}^{+}\rightarrow 13/2_{1}^{+} NA 2.255 41+21+4_{1}^{+}\rightarrow 2_{1}^{+} >>0.28 5.069
21/21+17/21+21/2_{1}^{+}\rightarrow 17/2_{1}^{+} 1.68(16) 1.421 61+41+6_{1}^{+}\rightarrow 4_{1}^{+} 3.89+17{}^{+17}_{-9} 2.026
37/21+33/21+37/2_{1}^{+}\rightarrow 33/2_{1}^{+} 0.12(7) 2.329 81+61+8_{1}^{+}\rightarrow 6_{1}^{+} 3.81+3{}^{+3}_{-1} 0.251
37/21+33/22+37/2_{1}^{+}\rightarrow 33/2_{2}^{+} 4(3) 0.208 101+81+10_{1}^{+}\rightarrow 8_{1}^{+} 2.9(7) 2.905×103\times 10^{-3}
35/2131/2135/2_{1}^{-}\rightarrow 31/2_{1}^{-} NA 3.338 121+101+12_{1}^{+}\rightarrow 10_{1}^{+} >>0.0064 1.39×104\times 10^{-4}
215Rn Expt. SM 216Rn Expt. SM
11/2+9/2+11/2^{+}\rightarrow 9/2^{+} NA 0.022 2+0+2^{+}\rightarrow 0^{+} NA 9.740
13/2+9/2+13/2^{+}\rightarrow 9/2^{+} NA 3.733 4+2+4^{+}\rightarrow 2^{+} NA 15.237
15/2+11/2+15/2^{+}\rightarrow 11/2^{+} NA 3.531 6+4+6^{+}\rightarrow 4^{+} NA 7.499
17/2+13/2+17/2^{+}\rightarrow 13/2^{+} NA 4.226 8+6+8^{+}\rightarrow 6^{+} NA 0.331
19/2+15/2+19/2^{+}\rightarrow 15/2^{+} NA 0.344
21/2+17/2+21/2^{+}\rightarrow 17/2^{+} NA 2.087
Table 3: The calculated (with KHH7B) magnetic dipole moments μ\mu in units of μN\mu_{N} and electric quadrupole moments QQ in units of eeb for Rn isotopes (SM) in comparison with the experimental data (Expt.) NNDC ; 207Rn ; 208Rn ; 209Rn ; 210Rn ; 211Rn ; 212Rn ; 213Rn ; 214Rn ; 215Rn ; 216Rn . The effective charges are taken as epe_{p} = 1.5ee and ene_{n} = 0.5ee for quadrupole moment. The gyromagnetic ratios for magnetic moments are taken as glνg_{l}^{\nu} = 0.00, glπg_{l}^{\pi} = 1.00 for orbital angular momenta, and gsνg_{s}^{\nu} = -3.826, gsπg_{s}^{\pi} = 5.586 for spin angular momenta.
  μ(μN)\mu(\mu_{N})   Q(eb)   μ(μN)\mu(\mu_{N})   Q(eb)
207Rn Expt. SM Expt. SM 208Rn Expt. SM Expt. SM
1/211/2_{1}^{-} NA +0.4477 - - 21+2_{1}^{+} NA +0.6774 NA -0.0531
3/213/2_{1}^{-} NA -0.8955 NA +0.1165 41+4_{1}^{+} NA +1.4301 NA +0.4231
5/215/2_{1}^{-} +0.816(9) +0.9602 +0.220(22) +0.1432 61+6_{1}^{+} NA +3.5437 NA -0.0819
9/219/2_{1}^{-} N/A +1.6032 NA +0.1561 81+8_{1}^{+} +6.98(8) +4.7403 +0.39(5) -0.3628
13/21+13/2_{1}^{+} -0.903(3) -1.1908 NA +0.7427 101+10_{1}^{+} NA +5.6742 NA -0.3598
17/21+17/2_{1}^{+} N/A -0.4300 NA +0.7005 10110_{1}^{-} +10.77(10) +10.4988 NA -1.4264
209Rn Expt. SM Expt. SM 210Rn Expt. SM Expt. SM
1/211/2_{1}^{-} NA +0.6453 - - 21+2_{1}^{+} NA +0.3804 NA +0.3602
3/213/2_{1}^{-} NA -1.2722 NA +0.1773 41+4_{1}^{+} NA +2.3803 NA +0.1283
5/215/2_{1}^{-} +0.8388(4) +1.3379 +0.31(3) +0.3104 61+6_{1}^{+} NA +3.5861 NA -0.0529
9/219/2_{1}^{-} NA +2.0306 NA +0.5191 81+8_{1}^{+} +7.184(56) +4.8116 +0.31(4) -0.3766
13/21+13/2_{1}^{+} NA -1.7442 NA +0.6068 141+14_{1}^{+} +14.92(10) +12.0143 NA -1.1421
201+20_{1}^{+} +22.3 +20.8586 NA -1.7096
11111_{1}^{-} +12.16(11) +11.3682 NA -1.0208
17117_{1}^{-} +17.88(9) +15.0538 +0.86(10) -1.3051
211Rn Expt. SM Expt. SM 212Rn Expt. SM Expt. SM
1/211/2_{1}^{-} +0.601(7) +0.6420 - - 21+2_{1}^{+} NA +1.2235 NA +0.1411
3/213/2_{1}^{-} NA -1.6115 NA +0.1729 41+4_{1}^{+} +4.0(2) +2.3630 NA +0.1067
5/215/2_{1}^{-} NA +1.4613 NA +0.2598 61+6_{1}^{+} +5.45(5) +3.5227 NA -0.0553
9/219/2_{1}^{-} N/A +3.1991 NA +0.1127 81+8_{1}^{+} +7.15(2) +4.6982 NA -0.3126
17/2117/2_{1}^{-} +7.75(8) +5.4127 +0.18(2) -0.2953 141+14_{1}^{+} +15.0(4) +11.9660 NA -0.8948
43/2143/2_{1}^{-} +15.9(4) +21.3675 NA -1.4060 17117_{1}^{-} +17.9(2) +14.9328 NA -1.0475
35/21+35/2_{1}^{+} +17.80(21) +15.0728 NA -1.1457 19119_{1}^{-} NA +22.3372 NA -0.9955
213Rn Expt. SM Expt. SM 214Rn Expt. SM Expt. SM
9/21+9/2_{1}^{+} NA -1.7661 NA -0.4454 21+2_{1}^{+} NA +0.0252 NA +0.3038
11/21+11/2_{1}^{+} NA +1.6386 NA -0.5370 41+4_{1}^{+} NA -0.0127 NA +0.1857
13/21+13/2_{1}^{+} NA -0.4519 NA -0.2827 61+6_{1}^{+} NA +2.4739 NA -0.1133
17/21+17/2_{1}^{+} NA +0.7723 NA -0.3534 81+8_{1}^{+} NA -1.4036 NA -0.3693
21/21+21/2_{1}^{+} +4.73(11) +2.3722 NA -0.7344 101+10_{1}^{+} NA -0.0557 NA -0.9853
25/21+25/2_{1}^{+} +7.63(25) +4.9119 NA -0.7076 121+12_{1}^{+} NA NA -0.2969
15/2115/2_{1}^{-} NA -1.6079 NA -0.6745 11111_{1}^{-} NA -2.9506 NA -0.8147
31/2131/2_{1}^{-} +9.90(8) +3.9558 NA -0.6248 12112_{1}^{-} NA +0.0166 NA -1.0387
215Rn Expt. SM Expt. SM 216Rn Expt. SM Expt. SM
7/21+7/2_{1}^{+} N/A -1.3756 NA -0.5900 21+2_{1}^{+} NA NA +0.5094
9/21+9/2_{1}^{+} N/A -1.7551 NA -0.3608 41+4_{1}^{+} NA NA +0.5465
11/21+11/2_{1}^{+} N/A +1.5711 NA -0.9984 61+6_{1}^{+} NA +1.4068 NA -0.0274
13/21+13/2_{1}^{+} N/A -1.0438 NA -0.1496 81+8_{1}^{+} NA +4.7956 NA -0.4624
15/21+15/2_{1}^{+} N/A +1.7524 NA -0.4138 101+10_{1}^{+} NA -0.0161 NA -0.9063
17/21+17/2_{1}^{+} N/A -1.7198 NA -0.1408 121+12_{1}^{+} NA +1.8390 NA -0.5366
7/217/2_{1}^{-} N/A +0.9056 NA -0.1517 13113_{1}^{-} NA -0.0292 NA -1.6812
9/219/2_{1}^{-} N/A +0.8498 NA +0.0961 15115_{1}^{-} NA +1.2423 NA -1.1205
11/2111/2_{1}^{-} N/A -0.9523 NA -0.0738

In 207Rn and 209Rn, the 13/21+13/2_{1}^{+} isomeric state is formed by purely ν(i13/2)1\nu(i_{13/2})^{-1} configuration, thus ν\nu = 1. In 209Rn, the 29/2129/2_{1}^{-}[ π(h9/2)4ν(f5/2)1\pi(h_{9/2})^{4}\otimes\nu(f_{5/2})^{-1}] isomeric state is formed by one pair breaking of the π(h9/2)\pi(h_{9/2}) orbital and one unpaired neutron in f5/2f_{5/2}, thus ν\nu = 3. This isomeric state is coming from B(M1)B(M1)+B(E2)B(E2) transition, and our result for the half-life is 55.55 ns which is very close to the observed half-life. The 41/2141/2_{1}^{-} isomeric state in our calculation is coming from the configuration π(h9/2)2(i13/2)2ν(f5/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(f_{5/2})^{-1} with 49.48%\% probability, and also from the configuration π(h9/2)2(i13/2)2ν(p1/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(p_{1/2})^{-1} with 17.27%\% probability. This isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) orbital each, and one unpaired neutron in f5/2f_{5/2} or p1/2p_{1/2}, thus the seniority is ν\nu = 5. The 35/21+{35/2_{1}}^{+} isomeric state is arising from the configuration π(h9/2)3(i13/2)ν(f5/2)1\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(f_{5/2})^{-1} with 58.53%\%, and also from the configuration π(h9/2)3(i13/2)ν(p1/2)1\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(p_{1/2})^{-1} with 11.45%\% probability. In 211Rn, isomeric state 35/21+{35/2_{1}}^{+} is arising from the same configuration π(h9/2)3(i13/2)ν(p1/2)1\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(p_{1/2})^{-1} as 209Rn with an increased probability of 85.45%\%. This 35/21+{35/2_{1}}^{+} isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital and one unpaired proton in h9/2h_{9/2} and i13/2i_{13/2} orbital each and one unpaired neutron in f5/2f_{5/2} or p1/2p_{1/2} orbital, thus the seniority is ν\nu = 5. In 211Rn, the calculated half-life for 35/21+{35/2_{1}}^{+} isomeric state is 44.74 ns which is very close to the experimental half-life 40.2(14) ns because the B(E2)B(E2) value and corresponding energy difference for this state are well reproduced in our calculation with respect to the experimental data. The 17/21{17/2_{1}}^{-}[π(h9/2)4ν(p1/2)1\pi(h_{9/2})^{4}\otimes\nu(p_{1/2})^{-1}] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital and one unpaired neutron in p1/2p_{1/2} with seniority three (ν\nu = 3). In our calculation, the 43/2143/2_{1}^{-} isomeric state is arising from the configuration π(h9/2)2(i13/2)2ν(f5/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(f_{5/2})^{-1}, with 91.30%\% probability. This state is formed with one pair breaking in both the orbitals π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) and one unpaired neutron in f5/2f_{5/2} orbital, thus the seniority is ν\nu = 5. The isomeric state 49/21+49/2_{1}^{+} is arising from the configuration π(h9/2)2(i13/2)2ν(g9/2)\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(g_{9/2}), with 61.78%\% probability. This state is formed with one pair breaking in both the π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) orbitals, and one neutron in g9/2g_{9/2} orbital, thus the seniority is ν\nu = 5. The 63/2163/2_{1}^{-} isomeric state is coming from the configuration π(h9/2)2(i13/2)2ν(g9/2)(i11/2)(f5/2)1\pi(h_{9/2})^{2}(i_{13/2})^{2}\otimes\nu(g_{9/2})(i_{11/2})(f_{5/2})^{-1}, with 88.04%\% probability. This isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) orbital each, and one neutron in both the orbitals g9/2g_{9/2} and i11/2i_{11/2}, with one unpaired neutron in f5/2f_{5/2} orbital, thus the seniority is ν\nu = 7.

Table 4: The calculated half-life for Rn isotopes (SM) in comparison with the experimental data (Expt.) NNDC ; 207Rn ; 208Rn ; 209Rn ; 210Rn ; 211Rn ; 212Rn ; 213Rn ; 214Rn ; 215Rn ; 216Rn .
JπJ^{\pi} EγE_{\gamma} B(Eλ)B(E\lambda) or B(Eλ)B(E\lambda) B(Mλ)B(M\lambda) Expt. SM
(MeV) B(Mλ)B(M\lambda) (e2e^{2}fm) (μN2\mu_{N}^{2}fm2λ-2) T1/2 T1/2
208Rn
81+8_{1}^{+} 6×103\times 10^{-3} B(E2)B(E2) 32.90 487(12) ns 1076 ns
10110_{1}^{-} 0.296 B(M1)B(M1) 2×104\times 10^{-4} 11.8(7) ns 4.69 ns
16116_{1}^{-} 0.143 B(M1)B(M1) 0.0819 18.3(4) ns 0.03 ns
209Rn
29/2129/2_{1}^{-} 2.29×103\times 10^{-3} B(M1)B(M1)+B(E2)B(E2) 6×107\times 10^{7} 1.09×104\times 10^{4} 13.9(21) ns 55.55 ns
210Rn
81+8_{1}^{+} 0.019 B(E2)B(E2) 2.55×104\times 10^{4} 644(40) ns 344 ns
141+14_{1}^{+} 0.274 B(E2)B(E2) 1.82×101\times 10^{-1} 76(7) ns 1049 ns
231+23_{1}^{+} 0.843 B(E2)B(E2) 1.14×102\times 10^{-2} 1.04(7) ns 0.61 ns
231+23_{1}^{+} 0.445 B(E2)B(E2) 4.67×102\times 10^{-2} 1.04(7) ns 13.04 ns
211Rn
17/2117/2_{1}^{-} 0.015 B(E2)B(E2) 20.72 596 (28) ns 1660 ns
35/21+35/2_{1}^{+} 0.043 B(E2)B(E2) 185.39 40.2(14) ns 44.74 ns
212Rn
61+6_{1}^{+} 0.093 B(E2)B(E2) 53.91 118(14) ns 122 ns
81+8_{1}^{+} 8×103\times 10^{-3} B(E2)B(E2) 17.24 0.91(3) μ\mus 2.04 μ\mus
141+14_{1}^{+} 0.273 B(E2)B(E2) 0.40 7.4(9) ns 800 ns
17117_{1}^{-} 2×103\times 10^{-3} B(E2)B(E2) 187.04 28.9(14) ns 807 ns
213Rn
15/2115/2_{1}^{-} 0.478 B(M2)B(M2) 0.28×103\times 10^{3} 26(1) ns 4.84 ns
15/2115/2_{1}^{-} 1.158 B(E3)B(E3) 0.66×104\times 10^{4} 26(1) ns 64.79 ns
21/21+21/2_{1}^{+} 0.574 B(E3)B(E3) 0.24×101\times 10^{-1} 29(2) ns 2.29 s
21/21+21/2_{1}^{+} 0.08 B(E2)B(E2) 115.81 29(2) ns 61.81 ns
31/2131/2_{1}^{-} 0.269 B(E3)B(E3) 0.33×104\times 10^{4} 1.36(7) μ\mus 1559 μ\mus
31/2131/2_{1}^{-} 0.168 B(E3)B(E3) 0.17×105\times 10^{5} 1.36(7) μ\mus 1326 μ\mus
37/21+37/2_{1}^{+} 0.100 B(E2)B(E2) 281.99 26(1) ns 122.6 ns
37/21+37/2_{1}^{+} 0.078 B(E2)B(E2) 19.58 26(1) ns 369.6 ns
49/21+49/2_{1}^{+} 0.789 B(E3)B(E3) 0.82×101\times 10^{-1} 12(1) ns 7.50×102\times 10^{-2} s
214Rn
181+18_{1}^{+} 0.114 B(E2)B(E2) 5.7145 44(3) ns 894 ns

In 213Rn, the isomeric state 15/2115/2_{1}^{-} is formed by purely ν(j15/2)\nu(j_{15/2}) configuration, thus seniority ν\nu = 1. The B(M2)B(M2) and B(E3)B(E3) transitions are responsible for the isomeric nature of the 15/2115/2_{1}^{-} state. From both transition values, our calculation is giving satisfactory results for the half-life. The isomeric states 21/21+21/2_{1}^{+} and 25/21+25/2_{1}^{+} are arising from the configuration π(h9/2)4ν(g9/2)\pi(h_{9/2})^{4}\otimes\nu(g_{9/2}), having seniority ν\nu = 3 with one pair breaking in the π(h9/2)\pi(h_{9/2}) orbital and one neutron in the g9/2g_{9/2} orbital. The isomeric state 21/21+21/2_{1}^{+} is coming from both the transitions B(E2)B(E2) and B(E3)B(E3). The half-life obtained from the calculated B(E2)B(E2) value is satisfactory. Whereas the half-life results from B(E3)B(E3) value is coming in order of seconds, in contrast to the experimental half-life of 29(2) ns, this is because our calculation is not predicting B(E3)B(E3) value correctly. The 31/2131/2_{1}^{-}[π(h9/2)3(i13/2)ν(g9/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2})] isomeric state is formed by one proton in h9/2h_{9/2}, i13/2i_{13/2} orbitals each and one neutron in g9/2g_{9/2} orbital, thus ν\nu = 3. The calculated half-lives for this isomeric state are reproduced in the same order μ\mus as the experimental data 1.36(7) μ\mus but with very high magnitude, because of the inaccurate prediction of B(E3)B(E3) value, and also the energy differences are compressed by half in comparison with the experimental data. The 37/21+37/2_{1}^{+}[π(h9/2)3(f7/2)ν(g9/2)\pi(h_{9/2})^{3}(f_{7/2})\otimes\nu(g_{9/2})] isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital, and one proton in h9/2h_{9/2}, f7/2f_{7/2} orbitals each and one neutron in g9/2g_{9/2} orbital, thus ν\nu = 5. The half-life of 37/21+{37/2_{1}}^{+} state is in satisfactory agreement with the experimental data. Unlike 211Rn, the 43/21{43/2_{1}}^{-} isomeric state in 213Rn is arising from the configuration π(h9/2)3(i13/2)ν(g9/2)\pi(h_{9/2})^{3}(i_{13/2})\otimes\nu(g_{9/2}). This isomeric state is formed by one pair breaking in π(h9/2)\pi(h_{9/2}) orbital, and one proton in h9/2h_{9/2}, i13/2i_{13/2} orbitals each and one neutron in g9/2g_{9/2} orbital, thus ν\nu = 5. The 49/21+49/2_{1}^{+} isomeric state is formed with the same configuration and seniority (ν\nu = 5) as in 211Rn with increased probability of wave-function. The half-life for 49/21+49/2_{1}^{+} isomeric state was also produced in seconds because of the inaccurate B(E3)B(E3) value, while the experimental half-life is 12(1) ns. The isomeric state 55/21+{55/2_{1}}^{+}[π(h9/2)(i13/2)3ν(j15/2)\pi(h_{9/2})(i_{13/2})^{3}\otimes\nu(j_{15/2})] is formed by one pair breaking in π(i13/2)\pi(i_{13/2}) orbital, and one proton in h9/2h_{9/2}, i13/2i_{13/2} orbitals each and one neutron in j15/2j_{15/2} orbital, thus ν\nu = 5. In this way, we can see that for odd Rn isotopes π(h9/2)\pi(h_{9/2}) and π(i13/2)\pi(i_{13/2}) orbitals are responsible for forming most of the isomeric states. On the whole, the calculated half-life values are in good agreement with the experimental data. Previously, we have reported a shell-model study of isomeric states for fpfp shell nuclei and Sn isotopes in Refs. fp ; Sn . In the fpfp region f7/2f_{7/2} and g9/2g_{9/2} orbitals, in the Sn region g7/2g_{7/2}, d5/2d_{5/2} and h11/2h_{11/2} orbitals, while for the Pb region h9/2h_{9/2}, f7/2f_{7/2} and i13/2i_{13/2} orbitals are crucial. Our result corresponding to isomeric states for the Rn chain shows the importance of h9/2h_{9/2}, f7/2f_{7/2} and i13/2i_{13/2} orbitals. Several recent articles are available in the literature to explain seniority isomer for different nuclei within the framework of the nuclear shell-mode astier ; PRC85astier3 ; PRC87astier2 .

III.3 Electromagnetic properties

In this section, we have discussed the results of the B(E2)B(E2) values, magnetic moments, and quadrupole moments for Rn isotopes. For 207Rn, the experimental data for B(E2)B(E2) values are not available. In 208Rn, our calculated value for B(E2;41+21+)B(E2;4_{1}^{+}\rightarrow 2_{1}^{+}) is smaller than the experimental data. This may be because the 21+2_{1}^{+} and 41+4_{1}^{+} states show a large configuration mixing in our calculation. For B(E2;81+61+)B(E2;{8_{1}}^{+}\rightarrow{6_{1}}^{+}) transition, a small value is reproduced as the experimental data. In 208Rn, because of this small B(E2)B(E2) value, the 81+8_{1}^{+} state is an isomer with 487 (12) ns half-life NNDC . A large B(E2;141+121+)B(E2;14_{1}^{+}\rightarrow 12_{1}^{+}) value 5.177 W.u. is obtained in our calculation corresponding to a small experimental value 0.35(17) W.u. In theory, the 141+{14_{1}}^{+} and 121+{12_{1}}^{+} states consist of the same configuration [π(h9/2)4ν(f5/2)2\pi(h_{9/2})^{4}\nu(f_{5/2})^{-2}]. This is why the theoretical B(E2;141+121+)B(E2;14_{1}^{+}\rightarrow 12_{1}^{+}) value is large. The calculated magnetic and quadrupole moments are in good agreement with the experimental data, although, the sign is different for quadrupole moment in 208Rn. In 210Rn, the calculated B(E2;41+21+)B(E2;4_{1}^{+}\rightarrow 2_{1}^{+}) value is almost half of the experimental value. In our calculation, the 21+2_{1}^{+} and 41+4_{1}^{+} states come from the same configuration [π(h9/2)4\pi(h_{9/2})^{4}], but the 21+2_{1}^{+} state shows a large configuration mixing. This is the reason for the small B(E2)B(E2) value. Corresponding to the experimental B(E2;141+121+)B(E2;14_{1}^{+}\rightarrow 12_{1}^{+}) value 0.0248(23) W.u., our calculation reproduces a very small value which is 3.981×103\times 10^{-3} W.u. The 141+14_{1}^{+} state is with configuration [π(h9/2)3(f7/2)\pi(h_{9/2})^{3}(f_{7/2})] and the 121+12_{1}^{+} state is with configuration [π(h9/2)4\pi(h_{9/2})^{4}]. This difference in the configurations is responsible for the small B(E2)B(E2) value. This hindered decay shows the behaviour of the isomeric state 141+14_{1}^{+} in the 210Rn with 76(7) ns half-life NNDC .

In 211Rn, overall calculated B(E2)B(E2) values are in good agreement with the experimental data. The calculated magnetic and quadrupole moments are well reproduced with the experimental data, although the sign is different for the quadrupole moment of 17/2117/2_{1}^{-} state. In 212Rn, most of the B(E2)B(E2) values are well reproduced in our calculation. The largest discrepancy between the experimental and calculated value is seen in the B(E2;141+121+)B(E2;14_{1}^{+}\rightarrow 12_{1}^{+}) transition. In our calculation, the 121+12_{1}^{+} and 122+12_{2}^{+} states are coming from the configurations [π(h9/2)4\pi(h_{9/2})^{4}] and [π(h9/2)3(f7/2)\pi(h_{9/2})^{3}(f_{7/2})], respectively. Whereas 141+14_{1}^{+} state is coming from the [π(h9/2)3(f7/2)\pi(h_{9/2})^{3}(f_{7/2})] configuration. Due to this difference of the configurations, the small value is reproduced for B(E2;141+121+)B(E2;14_{1}^{+}\rightarrow 12_{1}^{+}) transition, and because of the same configuration, the calculated B(E2;141+122+)B(E2;14_{1}^{+}\rightarrow 12_{2}^{+}) value is large. In 212Rn, because of this hindered decay, our calculation supports the isomeric nature of 141+14_{1}^{+} state. The experimental half-life of this state is 7.4(9) ns NNDC , similar to the 141+14_{1}^{+} isomeric state in 210Rn. In 213Rn, the experimental B(E2;37/21+33/21+)B(E2;37/2_{1}^{+}\rightarrow 33/2_{1}^{+}) and B(E2;37/21+33/22+)B(E2;37/2_{1}^{+}\rightarrow 33/2_{2}^{+}) values are 0.12(7) W.u. and 4(3) W.u., respectively. The 33/21+33/2_{1}^{+} and 33/22+33/2_{2}^{+} states are calculated higher than the 37/21+37/2_{1}^{+} state in contrast to the experimental spectrum. The calculated B(E2)B(E2) value corresponding to B(E2;37/21+33/21+)B(E2;37/2_{1}^{+}\rightarrow 33/2_{1}^{+}), B(E2;37/21+33/22+)B(E2;37/2_{1}^{+}\rightarrow 33/2_{2}^{+}) transitions are 2.329 and 0.208 W.u., respectively. In our calculation, 37/21+37/2_{1}^{+} and 33/21+33/2_{1}^{+} states are arising from the configuration [π(h9/2)3(f7/2)ν(g9/2)\pi(h_{9/2})^{3}(f_{7/2})\nu(g_{9/2})], hence giving a large B(E2)B(E2) value. In contrast, the calculated B(E2;37/21+33/22+)B(E2;37/2_{1}^{+}\rightarrow 33/2_{2}^{+}) value is small as the 33/22+33/2_{2}^{+} state is coming from a different configuration [π(h9/2)4ν(g9/2)\pi(h_{9/2})^{4}\nu(g_{9/2})]. Therefore, the 33/21+33/2_{1}^{+} and 33/22+33/2_{2}^{+} states might be reversely calculated referring to the 37/21+37/2_{1}^{+} state, compared to the experimental data. In 214Rn, the calculation predicts large B(E2)B(E2) values for B(E2;21+01+)B(E2;{2_{1}}^{+}\rightarrow{0_{1}}^{+}) and B(E2;41+21+)B(E2;{4_{1}}^{+}\rightarrow{2_{1}}^{+}) transitions, whereas smaller B(E2)B(E2) values for B(E2;81+61+)B(E2;8_{1}^{+}\rightarrow 6_{1}^{+}), B(E2;101+81+)B(E2;10_{1}^{+}\rightarrow 8_{1}^{+}) and B(E2;121+101+)B(E2;12_{1}^{+}\rightarrow 10_{1}^{+}) transitions. In 214Rn, these states are coming from huge configuration mixing. On the whole, theoretical calculations for the electromagnetic properties reproduce the experimental data well. The B(E2)B(E2) values are small, corresponding to the transitions from the isomeric states with the shell-model. We have also reported electromagnetic properties for different states where experimental data are not available. Since our calculation is providing overall good agreement with the experimental data, our prediction might be helpful for a future experiment.

IV CONCLUSIONS

In the present study, we have performed systematic shell-model calculations for the 207-216Rn isotopes employing two different interactions KHH7B and KHPE, developed for the different model spaces. For 207-212Rn isotopes, we have used KHH7B interaction, while for 213-216Rn, we have performed calculations with KHH7B and KHPE interactions. The results of the KHH7B interaction are in reasonable agreement with the experimental data. The KHPE interaction is found to give a good description for the 213-216Rn isotopes. The cross-shell interaction KHH7B is found to give good agreements with the experimental data for the isotopes below N=126N=126 shell-gap. For higher mass isotopes 213-216Rn, it becomes crucial to consider sufficient orbitals below the shell-closure for low-lying states apart from the core-excitation. We have successfully reproduced all the new levels identified in the experiment for 212Rn 212Rn2 . Our calculation also supports many tentative levels in the energy spectrum for other Rn isotopes. We found that low-lying states are arising from large configuration mixing while high-lying states show less collective behavior. The isotopes near N=126N=126 shell closure show minor collective nature, and as we move far from the shell-closure, collectivity and configuration mixing increase very rapidly. This shows the importance of the inclusion of a sufficient model space in the 208Pb region to reproduce the energy spectrum correctly. We have calculated B(E2)B(E2) values, magnetic and quadrupole moments, and compared with the available experimental data. We have also reported shell model results where the experimental data are not available. This will be very useful to compare the upcoming experimental data.

We have also analyzed different isomeric states and calculated corresponding half-lives. The calculated B(E2)B(E2) value supports the behavior of these isomeric states so that the half-lives of these isomeric states are well reproduced. The isomeric states are described in terms of the shell-model configuration and seniority quantum number (vv). The orbitals h9/2h_{9/2} and i13/2i_{13/2} are responsible for the isomeric states in the Rn isotopes. The high-spin isomers in Rn isotopes are due to seniority (vv) = 1, 2, 3, 4, 5, 6 and 7.

ACKNOWLEDGEMENTS

We acknowledge financial support from MHRD, the Government of India, and a research grant from SERB (India), CRG/2019/000556. Shell-model calculations were performed at the Kalam and Prayag computational facilities at IIT-Roorkee. We would like to thank Prof. Larry Zamick for useful discussions.

References