Systematic shell-model study of Rn isotopes with 207 to 216 and isomeric states
Abstract
We present systematic large-scale shell-model calculations for Rn isotopes with 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.+tI 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 are very crucial to understand the astrophysical process in producing nuclei heavier than A 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 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 and 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 and configurations have been identified. Also, a collective state at 2.121 MeV is proposed. This state is believed to be arising from mixing of the octupole vibration with a member of the 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 -matrix folded-diagram approach for isotones are reported by Coraggio et al. in Ref. Coraggio . The Strasbourg group has reported large-scale shell model results for Po-Pu with 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 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 = 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 , 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 proton orbitals and 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 below and three orbitals above the = 82, and four neutron orbitals below and three orbitals above = 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 , while neutrons are only allowed to occupy the orbitals below for and above for . 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.





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 level at 1.580 MeV can be associated with either the or state. The calculated state is produced 300 keV higher than the experimental state at 1.580 MeV, and calculated is produced 500 keV higher than the experimental state at 1.658 MeV ( , ). Therefore, we propose the assignment of calculated state to the closest experimental level at 1.658 MeV, excluding from the 1.580 MeV experimental state. For the negative parity state, the experimental level at 2.18 MeV can be associated with the calculated 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 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 , 90 keV lower than the experimental energy value, which is an experimentally tentative state. The calculated state is produced at 1.593 MeV close to the tentative experimental level at 1.545 MeV. The calculated , and are confirming the tentative experimental states with a difference of a few keV. The last two calculated negative parity states, and 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 and 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 and states, and a large gap between and states are featured. Our calculation confirms the tentative experimental and states with a difference of only a few keV. The calculated and states are 111 keV and 144 keV higher than the experimental data, respectively. This state could be state. For high-lying states, the compression becomes notable, except for the calculated state and confirms this tentative state. The state is 662 keV lower, and 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 . and shell closure. In our calculation, the collective state at 2.856 MeV is 735 keV higher than the proposed experimental value, and arising from the configuration . The single-particle orbitals with = 3, and in our model space and core-excitations across the two shell gaps at and 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 and states, and a large gap between and 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 state at 0.695 MeV, and the second state decays to the first unidentified state at 1.332 MeV. The calculated state is at 1.558 MeV and 1.509 MeV from the KHPE and KHH7B interaction, respectively. The calculated 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 and state at 1.800 MeV to be . With both interactions the calculated 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 and 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 and states, and a large gap between and 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 and 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 - 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 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.





Nucleus | Seniority | Wave-function | Probability | |
207Rn | 25.28 | |||
209Rn | 26.33 | |||
73.43 | ||||
58.53 | ||||
11.45 | ||||
49.48 | ||||
17.27 | ||||
211Rn | 69.04 | |||
85.45 | ||||
91.30 | ||||
61.78 | ||||
88.04 | ||||
213Rn | 41.94 | |||
51.79 | ||||
48.37 | ||||
63.64 | ||||
95.82 | ||||
92.94 | ||||
91.62 | ||||
99.95 | ||||
208Rn | 38.74 | |||
32.88 | ||||
43.65 | ||||
210Rn | 46.63 | |||
42.72 | ||||
49.23 | ||||
50.80 | ||||
42.73 | ||||
212Rn | 67.34 | |||
68.42 | ||||
98 | ||||
99.59 | ||||
80.48 | ||||
73.45 | ||||
214Rn | 60 | |||
83 | ||||
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- 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 is the number of particles not in pairs coupled to angular momentum = 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 decay is hindered between the same seniority of the initial and final states. In the case of 208,210,212Rn isotopes, state is the seniority isomer with a very small ; ) value. This is because of the same seniority for and , which is coming from configuration.
In 208Rn, 210Rn and 212Rn the isomeric state is coming from configuration, in increasing probability with mass number. The isomeric state is formed by purely orbital with one pair breaking, thus = 2. The half-life of this isomeric state is also reproduced very close to the experimental data with transition for all three isotopes. The and states are coming from the same configuration , and formed by one proton in , each coupled with one pair in orbital, hence the seniority = 2. These two states are generated by transition and half-lives for these states are reproduced well with the experimental data. In 210Rn, [] isomeric state is formed by one proton in and orbitals each, thus = 2. The [] isomeric state is formed by one pair breaking in orbital, and one proton in and orbitals each, thus = 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 transition value in our calculation is smaller than the experimental data. The [] isomeric state is formed by one pair breaking in orbital, and one proton in and orbitals each, thus = 4. The [] isomeric state is formed by one pair breaking in and both the orbitals, thus = 4. In 212Rn, the isomeric state is formed similar to the 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 transition value and energy difference are reproduced very well. The and 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 and isomeric states are coming in the same order with higher magnitude because the calculated transition value is significantly less than the experimental data for the state, and our energy difference is very small for . The [] isomeric state is formed by one pair breaking in orbital, and one proton in and orbitals each, and one neutron in and orbitals each, thus = 6. The [] isomeric state is formed by one pair breaking in and both the orbitals and one neutron in and orbitals each, thus = 6. In 214Rn, the [] isomeric state is formed by one pair breaking in or orbital, and one proton in and orbitals each, thus = 4. The isomeric state is arising from the configuration , and formed by one proton in and orbitals each, and one neutron in and orbitals each, thus = 4. For this isomeric state, seniority reduces as compared to the state in 212Rn because of the role of orbital. It is important to mention here that to calculate and for 211Rn and and for 212Rn, we have opened , and 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 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 state is at a very small energy value of 0.123 MeV. The experimental state at 0.283 MeV can be associated with both and 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 and states, respectively, while 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 or calculated state. For the experimental level at 0.867 MeV, the calculated state can be associated with or . Above 1 MeV energy value, all the calculated states are compressed. The calculated 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 and shell closure. As the neutron number increases in odd Rn isotopes, the calculated , and states show strong single-particle nature with the dominant configuration (), () and (), 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 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 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 . In the case of positive parity, the calculated is over-predicted, while and 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 , and states show strong single-particle nature with the dominant configuration (), () and (), 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 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 and 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 and 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 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 state is coming as the first-excited state from both the interaction, which is an experimentally tentative second excited state. The calculated state has 119 keV and 246 keV difference and the 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 . 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.
) | ) | ||||
---|---|---|---|---|---|
207Rn | Expt. | SM | 208Rn | Expt. | SM |
NA | 1.428 | NA | 5.838 | ||
NA | 5.551 | 4.7(4) | 0.1789 | ||
NA | 1.347 | NA | 0.124 | ||
NA | 7.655 | 0.187(7) | 0.449 | ||
NA | 0.511 | NA | 4.557 | ||
NA | 0.144 | 0.35(17) | 5.177 | ||
209Rn | Expt. | SM | 210Rn | Expt. | SM |
NA | 0.808 | NA | 5.286 | ||
NA | 0.325 | 1.8(2) | 0.698 | ||
NA | 6.994 | 1.58(15) | 0.963 | ||
NA | 0.159 | 1.58(19) | 1.752 | ||
NA | 1.954 | NA | 0.351 | ||
NA | 5.028 | NA | 3.937 | ||
NA | 1.774 | NA | 2.734 | ||
0.66(15) | 0.70 | 0.0248(23) | 3.981 | ||
211Rn | Expt. | SM | 212Rn | Expt. | SM |
0.040 | 1.911 | NA | 5.195 | ||
NA | 0.222 | 1.05 | 1.234 | ||
NA | 0.744 | 0.40 | 0.717 | ||
0.030 | 1.744 | 0.117(7) | 0.229 | ||
0.036 | 0.926 | NA | 3.294 | ||
0.073(17) | 0.012 | 4.52 | 3.115 | ||
1.9(6) | 0.090 | 0.0319 | 5.236 | ||
0.0077 | 1.688 | 2.9(6) | 2.624 | ||
2.3(5) | 2.484 | 2.94 | 2.942 | ||
213Rn | Expt. | SM | 214Rn | Expt. | SM |
NA | 4.645 | 0.032 | 5.459 | ||
NA | 2.255 | 0.28 | 5.069 | ||
1.68(16) | 1.421 | 3.8 | 2.026 | ||
0.12(7) | 2.329 | 3.8 | 0.251 | ||
4(3) | 0.208 | 2.9(7) | 2.905 | ||
NA | 3.338 | 0.0064 | 1.39 | ||
215Rn | Expt. | SM | 216Rn | Expt. | SM |
NA | 0.022 | NA | 9.740 | ||
NA | 3.733 | NA | 15.237 | ||
NA | 3.531 | NA | 7.499 | ||
NA | 4.226 | NA | 0.331 | ||
NA | 0.344 | ||||
NA | 2.087 |
Q(eb) | Q(eb) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
207Rn | Expt. | SM | Expt. | SM | 208Rn | Expt. | SM | Expt. | SM | |
NA | +0.4477 | - | - | NA | +0.6774 | NA | -0.0531 | |||
NA | -0.8955 | NA | +0.1165 | NA | +1.4301 | NA | +0.4231 | |||
+0.816(9) | +0.9602 | +0.220(22) | +0.1432 | NA | +3.5437 | NA | -0.0819 | |||
N/A | +1.6032 | NA | +0.1561 | +6.98(8) | +4.7403 | +0.39(5) | -0.3628 | |||
-0.903(3) | -1.1908 | NA | +0.7427 | NA | +5.6742 | NA | -0.3598 | |||
N/A | -0.4300 | NA | +0.7005 | +10.77(10) | +10.4988 | NA | -1.4264 | |||
209Rn | Expt. | SM | Expt. | SM | 210Rn | Expt. | SM | Expt. | SM | |
NA | +0.6453 | - | - | NA | +0.3804 | NA | +0.3602 | |||
NA | -1.2722 | NA | +0.1773 | NA | +2.3803 | NA | +0.1283 | |||
+0.8388(4) | +1.3379 | +0.31(3) | +0.3104 | NA | +3.5861 | NA | -0.0529 | |||
NA | +2.0306 | NA | +0.5191 | +7.184(56) | +4.8116 | +0.31(4) | -0.3766 | |||
NA | -1.7442 | NA | +0.6068 | +14.92(10) | +12.0143 | NA | -1.1421 | |||
+22.3 | +20.8586 | NA | -1.7096 | |||||||
+12.16(11) | +11.3682 | NA | -1.0208 | |||||||
+17.88(9) | +15.0538 | +0.86(10) | -1.3051 | |||||||
211Rn | Expt. | SM | Expt. | SM | 212Rn | Expt. | SM | Expt. | SM | |
+0.601(7) | +0.6420 | - | - | NA | +1.2235 | NA | +0.1411 | |||
NA | -1.6115 | NA | +0.1729 | +4.0(2) | +2.3630 | NA | +0.1067 | |||
NA | +1.4613 | NA | +0.2598 | +5.45(5) | +3.5227 | NA | -0.0553 | |||
N/A | +3.1991 | NA | +0.1127 | +7.15(2) | +4.6982 | NA | -0.3126 | |||
+7.75(8) | +5.4127 | +0.18(2) | -0.2953 | +15.0(4) | +11.9660 | NA | -0.8948 | |||
+15.9(4) | +21.3675 | NA | -1.4060 | +17.9(2) | +14.9328 | NA | -1.0475 | |||
+17.80(21) | +15.0728 | NA | -1.1457 | NA | +22.3372 | NA | -0.9955 | |||
213Rn | Expt. | SM | Expt. | SM | 214Rn | Expt. | SM | Expt. | SM | |
NA | -1.7661 | NA | -0.4454 | NA | +0.0252 | NA | +0.3038 | |||
NA | +1.6386 | NA | -0.5370 | NA | -0.0127 | NA | +0.1857 | |||
NA | -0.4519 | NA | -0.2827 | NA | +2.4739 | NA | -0.1133 | |||
NA | +0.7723 | NA | -0.3534 | NA | -1.4036 | NA | -0.3693 | |||
+4.73(11) | +2.3722 | NA | -0.7344 | NA | -0.0557 | NA | -0.9853 | |||
+7.63(25) | +4.9119 | NA | -0.7076 | NA | NA | -0.2969 | ||||
NA | -1.6079 | NA | -0.6745 | NA | -2.9506 | NA | -0.8147 | |||
+9.90(8) | +3.9558 | NA | -0.6248 | NA | +0.0166 | NA | -1.0387 | |||
215Rn | Expt. | SM | Expt. | SM | 216Rn | Expt. | SM | Expt. | SM | |
N/A | -1.3756 | NA | -0.5900 | NA | NA | +0.5094 | ||||
N/A | -1.7551 | NA | -0.3608 | NA | NA | +0.5465 | ||||
N/A | +1.5711 | NA | -0.9984 | NA | +1.4068 | NA | -0.0274 | |||
N/A | -1.0438 | NA | -0.1496 | NA | +4.7956 | NA | -0.4624 | |||
N/A | +1.7524 | NA | -0.4138 | NA | -0.0161 | NA | -0.9063 | |||
N/A | -1.7198 | NA | -0.1408 | NA | +1.8390 | NA | -0.5366 | |||
N/A | +0.9056 | NA | -0.1517 | NA | -0.0292 | NA | -1.6812 | |||
N/A | +0.8498 | NA | +0.0961 | NA | +1.2423 | NA | -1.1205 | |||
N/A | -0.9523 | NA | -0.0738 |
In 207Rn and 209Rn, the isomeric state is formed by purely configuration, thus = 1. In 209Rn, the [ ] isomeric state is formed by one pair breaking of the orbital and one unpaired neutron in , thus = 3. This isomeric state is coming from + transition, and our result for the half-life is 55.55 ns which is very close to the observed half-life. The isomeric state in our calculation is coming from the configuration with 49.48 probability, and also from the configuration with 17.27 probability. This isomeric state is formed by one pair breaking in and orbital each, and one unpaired neutron in or , thus the seniority is = 5. The isomeric state is arising from the configuration with 58.53, and also from the configuration with 11.45 probability. In 211Rn, isomeric state is arising from the same configuration as 209Rn with an increased probability of 85.45. This isomeric state is formed by one pair breaking in orbital and one unpaired proton in and orbital each and one unpaired neutron in or orbital, thus the seniority is = 5. In 211Rn, the calculated half-life for isomeric state is 44.74 ns which is very close to the experimental half-life 40.2(14) ns because the value and corresponding energy difference for this state are well reproduced in our calculation with respect to the experimental data. The [] isomeric state is formed by one pair breaking in orbital and one unpaired neutron in with seniority three ( = 3). In our calculation, the isomeric state is arising from the configuration , with 91.30 probability. This state is formed with one pair breaking in both the orbitals and and one unpaired neutron in orbital, thus the seniority is = 5. The isomeric state is arising from the configuration , with 61.78 probability. This state is formed with one pair breaking in both the and orbitals, and one neutron in orbital, thus the seniority is = 5. The isomeric state is coming from the configuration , with 88.04 probability. This isomeric state is formed by one pair breaking in and orbital each, and one neutron in both the orbitals and , with one unpaired neutron in orbital, thus the seniority is = 7.
or | Expt. | SM | ||||
(MeV) | (fm2λ) | (fm2λ-2) | T1/2 | T1/2 | ||
208Rn | ||||||
6 | 32.90 | 487(12) ns | 1076 ns | |||
0.296 | 2 | 11.8(7) ns | 4.69 ns | |||
0.143 | 0.0819 | 18.3(4) ns | 0.03 ns | |||
209Rn | ||||||
2.29 | + | 6 | 1.09 | 13.9(21) ns | 55.55 ns | |
210Rn | ||||||
0.019 | 2.55 | 644(40) ns | 344 ns | |||
0.274 | 1.82 | 76(7) ns | 1049 ns | |||
0.843 | 1.14 | 1.04(7) ns | 0.61 ns | |||
0.445 | 4.67 | 1.04(7) ns | 13.04 ns | |||
211Rn | ||||||
0.015 | 20.72 | 596 (28) ns | 1660 ns | |||
0.043 | 185.39 | 40.2(14) ns | 44.74 ns | |||
212Rn | ||||||
0.093 | 53.91 | 118(14) ns | 122 ns | |||
8 | 17.24 | 0.91(3) s | 2.04 s | |||
0.273 | 0.40 | 7.4(9) ns | 800 ns | |||
2 | 187.04 | 28.9(14) ns | 807 ns | |||
213Rn | ||||||
0.478 | 0.28 | 26(1) ns | 4.84 ns | |||
1.158 | 0.66 | 26(1) ns | 64.79 ns | |||
0.574 | 0.24 | 29(2) ns | 2.29 s | |||
0.08 | 115.81 | 29(2) ns | 61.81 ns | |||
0.269 | 0.33 | 1.36(7) s | 1559 s | |||
0.168 | 0.17 | 1.36(7) s | 1326 s | |||
0.100 | 281.99 | 26(1) ns | 122.6 ns | |||
0.078 | 19.58 | 26(1) ns | 369.6 ns | |||
0.789 | 0.82 | 12(1) ns | 7.50 s | |||
214Rn | ||||||
0.114 | 5.7145 | 44(3) ns | 894 ns |
In 213Rn, the isomeric state is formed by purely configuration, thus seniority = 1. The and transitions are responsible for the isomeric nature of the state. From both transition values, our calculation is giving satisfactory results for the half-life. The isomeric states and are arising from the configuration , having seniority = 3 with one pair breaking in the orbital and one neutron in the orbital. The isomeric state is coming from both the transitions and . The half-life obtained from the calculated value is satisfactory. Whereas the half-life results from 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 value correctly. The [] isomeric state is formed by one proton in , orbitals each and one neutron in orbital, thus = 3. The calculated half-lives for this isomeric state are reproduced in the same order s as the experimental data 1.36(7) s but with very high magnitude, because of the inaccurate prediction of value, and also the energy differences are compressed by half in comparison with the experimental data. The [] isomeric state is formed by one pair breaking in orbital, and one proton in , orbitals each and one neutron in orbital, thus = 5. The half-life of state is in satisfactory agreement with the experimental data. Unlike 211Rn, the isomeric state in 213Rn is arising from the configuration . This isomeric state is formed by one pair breaking in orbital, and one proton in , orbitals each and one neutron in orbital, thus = 5. The isomeric state is formed with the same configuration and seniority ( = 5) as in 211Rn with increased probability of wave-function. The half-life for isomeric state was also produced in seconds because of the inaccurate value, while the experimental half-life is 12(1) ns. The isomeric state [] is formed by one pair breaking in orbital, and one proton in , orbitals each and one neutron in orbital, thus = 5. In this way, we can see that for odd Rn isotopes and 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 shell nuclei and Sn isotopes in Refs. fp ; Sn . In the region and orbitals, in the Sn region , and orbitals, while for the Pb region , and orbitals are crucial. Our result corresponding to isomeric states for the Rn chain shows the importance of , and 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 values, magnetic moments, and quadrupole moments for Rn isotopes. For 207Rn, the experimental data for values are not available. In 208Rn, our calculated value for is smaller than the experimental data. This may be because the and states show a large configuration mixing in our calculation. For transition, a small value is reproduced as the experimental data. In 208Rn, because of this small value, the state is an isomer with 487 (12) ns half-life NNDC . A large value 5.177 W.u. is obtained in our calculation corresponding to a small experimental value 0.35(17) W.u. In theory, the and states consist of the same configuration []. This is why the theoretical 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 value is almost half of the experimental value. In our calculation, the and states come from the same configuration [], but the state shows a large configuration mixing. This is the reason for the small value. Corresponding to the experimental value 0.0248(23) W.u., our calculation reproduces a very small value which is 3.981 W.u. The state is with configuration [] and the state is with configuration []. This difference in the configurations is responsible for the small value. This hindered decay shows the behaviour of the isomeric state in the 210Rn with 76(7) ns half-life NNDC .
In 211Rn, overall calculated 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 state. In 212Rn, most of the values are well reproduced in our calculation. The largest discrepancy between the experimental and calculated value is seen in the transition. In our calculation, the and states are coming from the configurations [] and [], respectively. Whereas state is coming from the [] configuration. Due to this difference of the configurations, the small value is reproduced for transition, and because of the same configuration, the calculated value is large. In 212Rn, because of this hindered decay, our calculation supports the isomeric nature of state. The experimental half-life of this state is 7.4(9) ns NNDC , similar to the isomeric state in 210Rn. In 213Rn, the experimental and values are 0.12(7) W.u. and 4(3) W.u., respectively. The and states are calculated higher than the state in contrast to the experimental spectrum. The calculated value corresponding to , transitions are 2.329 and 0.208 W.u., respectively. In our calculation, and states are arising from the configuration [], hence giving a large value. In contrast, the calculated value is small as the state is coming from a different configuration []. Therefore, the and states might be reversely calculated referring to the state, compared to the experimental data. In 214Rn, the calculation predicts large values for and transitions, whereas smaller values for , and 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 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 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 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 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 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 (). The orbitals and are responsible for the isomeric states in the Rn isotopes. The high-spin isomers in Rn isotopes are due to seniority () = 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.
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