Two-pulse events
In this analysis, we have studied selected events that contain two distinct pulses, named “two-pulse events”, within the 8 \(\upmu \)s long waveforms. The event selection criteria to remove PMT-induced noise events [27] is applied as a preselection on candidate events. We have developed an offline selection algorithm to identify the two-pulse events using the summed waveforms from the two PMTs of each crystal. These are smoothed by averaging 30 neighboring time bins into 60 ns bin-width values. Two-pulse events are identified as those where, in addition to the initial rising edge of a pulse, there is a second rising edge of at least 1 keV. The computed mean decay times in a 300 ns time window starting from each rising edge are required to be greater than 100 ns. In addition, we define the asymmetry between two PMT signals as \((Q_1 -Q_2)/(Q_1+Q_2)\) where \(Q_1\) and \(Q_2\) are charge measured by the two PMTs. We calculate the asymmetries for two identified pulses within 300 ns time windows from the rising edges. The asymmetry for each pulse is required to be less than 0.25. A total of 4258 candidate events from the five crystals are accepted. Figure 2 shows three examples of the selected two-pulse candidate events that occurred in three different crystals.
Because of the low rate for two-pulse events, this initial selection still contains noisy events that did not originate from two scintillation occurrences. These include PMT-induced noise pulses or afterpulses that mimic a second scintillation occurrence and tail fluctuations due to reflections inside the crystal as shown in Fig. 4. Further characterization of two-pulse events provides further discrimination of these noisy events.
Considering two (fast and slow) decay components of the scintillating crystals [28, 29], we characterize each pulse using a single rise time (\(\tau _r\)), two decay times (\(\tau _f\) and \(\tau _s\)), the starting time of the pulse (\(t_0\)), and the ratio of the slow-to-fast decay components (R):
$$\begin{aligned} \begin{aligned} F_{i} (t)&= \frac{1}{\tau _{f_i}} e^{-(t-t_{0_i})/\tau _{f_i}} + \frac{R_i}{\tau _{s_i}} e^{-(t-t_{0_i})/\tau _{s_i}} \\&\quad - \left( \frac{1}{\tau _{f_i}} +\frac{R_i}{\tau _{s_i}} \right) e^{(-t-t_{0_i})/\tau _{r_i}}, \end{aligned} \end{aligned}$$
(1)
Two-pulse events are modeled as \(F(t) = A_1 F_1 (t) + A_2 F_2 (t)\) where \(A_1\) and \(A_2\) represent the total charge, proportional to the energy, of each pulse. Here, we can evaluate the energy of the first pulse (E1), the second pulse (E2), and \(\Delta \)T (\(t_{0_2} - t_{0_1}\)). Mean decay times for two pulses calculated from the fit parameters are required to be greater than 150 ns and less than 400 ns for each pulse. Selected events are required to have a reduced \(\chi ^2\) less than 4. In total, 2576 events are selected as the two-pulse events from the 4258 candidate events. Figures 3 and 4 show examples of the fit results for the two-pulse candidate events that are categorized as two-pulse events and noisy events, respectively.
For a quantitative measurement of the isomeric states, we need to evaluate selection efficiencies that depend on E1, E2, and \(\Delta \)T, and this requires simulated waveforms of the two-pulse events. Since photon simulations of the NaI(Tl) crystals are still being developed for the COSINE-100 experiment, we briefly report qualitative results based on our observations. Two-pulse events with small \(\Delta \)T, small E1 or E2, and large E1/E2 ratio are preferentially eliminated by the initial selection of the candidate events. Furthermore, large E1/E2 ratio events are still contaminated by events with large tail fluctuations, even though applied selection criteria removed many of these events. Because of these limitations, we only study events with individual pulse energies in the range 2−30 keV.
Figure 5a shows a scatter plot of E1 and E2 for the 2–30 keV energy region, where there is a large population of the two-pulse events around E2 equal to about 6 keV. The one dimensional spectrum of E2 is shown in Fig. 5b, where there is a two-peak structure with peaks centered at around 6 keV and 20 keV. We model the E2 spectrum as two Gaussian functions summed with an exponential background. The exponential background describes the residual noisy events. The mean energies of the two peaks are determined to be: 6.11 ± 0.09 keV and 20.6 ± 0.5 keV, respectively, which closely match the 6.28 keV and 20.19 keV nuclear levels of \(^{228}\)Ac, as indicated in Fig. 1.
Figure 5c shows the E1 spectra for E2 values that are greater or less than 13 keV. The E2 spectra have energy distributions with shapes characteristic of mono-energetic emissions, while the E1 spectra have broader energy distributions that are characteristic of \(\beta \)-decay and match the decay scheme of \(^{228}\)Ra into \(^{228}\)Ac shown in Fig. 1. The data are consistent with the identification of both the 6.28 keV and 20.19 keV excited states of \(^{228}\)Ac as metastable isomers with lifetimes of \(\mathcal {O}(100\,\mathrm {ns})\). To confirm this hypothesis, we simulate the \(\beta \) spectra of \(^{228}\)Ra using a Geant4-based simulation that is the same as the one used for background modeling of the COSINE-100 detectors [22, 30]. We model the energy spectra of two \(\beta \)-decays: one with Q = 39.52 keV that decays into the 6.28 keV state and the other with Q = 25.61 keV that decays into the 20.19 keV state. These energy spectra are overlaid in Fig. 5c and show similar behaviors for energies greater than 5 keV. Some discrepancies can be explained at low energies due to the low efficiency of the small E1 events.
Distributions of \(\Delta \)T are shown in Fig. 5d together with results from exponential fits for only large \(\Delta \)T events. This is because the two-pulse selection strongly suppress small \(\Delta \)T events. Only events with \(\Delta \)T > 600 ns are fitted for the E2 < 13 keV distributions. Because two-pulse discrimination is more efficient for large E2 events, E2 > 13 keV events with \(\Delta \)T > 350 ns are fitted. The fitted lifetimes are 299 ± 11 ns and 115 ± 25 ns for the E2 = 6.28 keV and E2 = 20.19 keV states, respectively, where only statistical uncertainties are considered.
Three-pulse events
If we consider the level scheme of \(^{228}\)Ac as Fig. 1, the 20.19 keV state transits to the 6.67 keV state before decaying to the ground state. Because of \(\mathcal {O}(100\,\mathrm {ns})\) lifetime of the 20.19 keV state transition, the 20.19 keV to 6.67 keV transition must have the same lifetime. However, the number of two-pulse events with E2 > 13 keV is only a few percent of those with E2 < 13 keV. Considering the relative intensities of the \(^{228}\)Ra \(\beta \)-decay shown in Fig. 1, the observed isomeric transition of the 20.19 keV state is only \(\mathcal {O}(1\%)\) of the total \(\beta \)-decay to the 20.19 keV state. This may indicate that the 6.67 keV state is also an isomeric state. In this case, three distinct emissions have to occur, but at a rate that cannot be seen in the current analysis. Only \(\mathcal {O}(1\%)\) of these events would be accepted as the two-pulse events if the two final emissions occur so close in time that they cannot be distinguished in the NaI(Tl) crystal.
To identify the hypothesis of an isomeric 6.67 keV state, we have searched for events that contain three distinct pulses, named “three-pulse events”, within the 8 \(\upmu \)s window. Similar selections applied for the two-pulse events are used for the three-pulse events: \(F(t) = A_1 F_1(t) + A_2 F_2(t) + A_3 F_3(t)\) from Eq. 1. In total, 34 three-pulse events are selected. Figure 6 shows three examples of the fit results that occurred in three different crystals. Here, we evaluate the energy of the first pulse (E1), the second pulse (E2), and the third pulse (E3) and the time differences between first and second pulses (\(\Delta \)T1), and second and third pulses (\(\Delta \)T2). These quantities are indicated in the figure.
Figure 7a shows the E1 spectrum that is overlaid with \(\beta \) spectrum with Q = 25.61 keV corresponding to decays into the 20.19 keV state. Simulations and data show similar behavior for energies greater than 5 keV. The energy spectra of the E2 and E3 are presented in Fig. 7b, c, respectively. A Gaussian function with an exponential background fits the data well. The mean energies of E2 and E3 are determined as 13.8 ± 0.4 keV and 6.70 ± 0.37 keV, respectively. The obtained energy levels are well matched with \(^{228}\)Ac level scheme in Fig. 1. Figure 7d shows \(\Delta \)T1 and \(\Delta \)T2 distributions. We observe \(\mathcal {O}(100\,\mathrm {ns})\) lifetime not only for the 20.19 keV state but also for the 6.67 keV state.
Consistency check of \(^{228}\)Ra decays
As a cross-check of the \(^{228}\)Ac isomer hypothesis, we evaluate the level of \(^{228}\)Ra contamination in the NaI(Tl) crystals by measuring the rate of the two-pulse events with E2 around 6.28 keV. We select 6.28 keV state events by a requirement of E2 < 13 keV in Fig. 5b. In order to account for the selection inefficiencies, we performed an extrapolation of the modeling in Fig. 5c, d for low-energy and small \(\Delta \)T events. Here, we assume a relative \(\beta \) intensity of the 6.28 keV state as 10 % according to data in Fig. 1. Table 1 summarizes the measured \(^{228}\)Ra activities for the crystals that are compared with the results obtained from the standard background modeling of the COSINE-100 data [30]. The consistency of the results for the \(^{228}\)Ra contamination supports the interpretation that the observed two-pulse events originate from \(^{228}\)Ra decays to isomeric excited states of \(^{228}\)Ac.
Table 1 \(^{228}\)Ra contamination in the COSINE-100 crystals measured using the two-pulse events at 6.28 keV. These measurements are compared with the fit result from the background modeling of the COSINE-100 detector [30] We have also evaluated the time dependent rate for the two-pulse events shown in Fig. 8. A decreasing rate of two-pulse events is evident and an exponential fit with \(R(t)=A\exp (-t/\tau )\) is overlaid. Because initial purification of NaI powder [31, 32] and decomposition of impurities from the crystal growing process [15], amounts of \(^{232}\)Th and \(^{228}\)Ra can be in non-equilibrium depending on their chemical properties. A similar non-equilibrium status between \(^{238}\)U and \(^{226}\)Ra was previously observed in the NaI(Tl) crystal [15]. If crystallization effectively removes \(^{232}\)Th but not \(^{228}\)Ra, the initial \(^{228}\)Ra activity will be reduced with a lifetime of 3028 days that is consistent with the measured rate decrease with \(\tau \) = 2724 ± 903 days in Fig. 8. This also supports the interpretation that the observed two-pulse events originate from \(^{228}\)Ra decays.
Based on the two- and three-pulse events measured in the COSINE-100 data, we conclude that the excited states of \(^{228}\)Ac at the 6.28 keV, 6.67 keV, and 20.19 keV are isomers with lifetimes of \(\mathcal {O}(100\,\mathrm {ns})\).