1 Introduction
Type I X-ray bursts (XRBs) are triggered by thermonuclear runaways in the accreted envelopes of neutron stars in close binary systems [1, 2]. During the thermonuclear runaway, the accreted envelope enriched in H and He can be transformed to matter strongly enriched in heavier species (up to A≃100 [3, 4]) via the rapid proton capture process (rp-process) [5-7]. The physical theory of the XRBs has been reviewed in Refs. [8-10].
The rp-process is mostly characterized by localized (p,γ)–(γ,p) equilibrium within particular isotonic chains near the proton drip-line. The abundance distribution within an isotonic chain exponentially depends on the difference in nuclear masses because the abundance ratio between two neighboring isotones is proportional to exp[Sp/kT], where Sp is the proton separation energy. In particular, isotonic chains with sufficiently small Sp values (relative to XRB temperatures at 1 GK and kT≈100 keV) need to be be known with a precision of at least ∼50–100 keV [6, 11]. To compare model predictions with observations of the light curves [12], reliable nuclear physical inputs, such as the precise Sp values and thermonuclear reaction rates, are needed for those nuclei along the rp-process path.
56Cu is a very important nucleus, because it is close to the waiting-point nucleus 56Ni and lies on the rp-process path [6, 12]. In this work, a new thermonuclear reaction rate is derived for 55Ni(p,γ)56Cu in the temperature region relevant to XRBs based on the recent experimental results of energy levels and proton separation energy of Sp = 579.8(7.1) keV in 56Cu, together with the shell-model calculation and mirror nuclear structure in 56Co.
2 Proton separation energy of Sp(56Cu)
Previously, four theoretical proton separation energy, Sp, values have been predicted for 56Cu, as Sp(56Cu) = 573±54 keV based on the charge-symmetry formula of Kelson–Garvey [13], 560±140 keV from Coulomb displacement energy (CDE) mass relation [14], 526±1 keV using the improved Kelson–Garvey (ImKG) mass relation, [15], and 647±88 keV based on the mirror symmetry and known data from beta-delayed proton spectroscopy [16]. Using the smoothness trends of the mass surface, analysis by atomic mass evaluations (AME) provided Sp(56Cu) values as 459±200 keV in AME85 [17], 560±140 keV in both AME95 [18] and AME03 [19], and 190±200 keV in AME12 [20]. The large uncertainty in the results is due to the theoretically estimated mass of 65Cu.
The first measurement of the nuclear mass of 65Cu was first performed in 2016, with a relative precision of (1–4)×10-7 using isochronous mass spectrometry (IMS) at the Cooler Storage Ring (CSRe), at the Institute of Modern Physics IMP in Lanzhou, China. Together with the unpublished mass excess value of ME(65Cu)=-38643(15) keV, the value of Sp(56Cu) = 596±15 keV was compiled into AME16 [21] (referenced as "private communication"). This experimental value was formally published in 2018 [22]; however, during the review process of this paper, a more accurate value of ME(65Cu)=-38626.7(7.1) keV was measured [23] using the Low-Energy Beam and Ion Trap (LEBIT) 9.4-T penning trap mass spectrometer in the National Superconducting Cyclotron Laboratory (NSCL) at the Michigan State University (MSU). Then, an accurate value of Sp = 579.8(7.1) keV was deduced. Based on the weighted average Sp values obtained from the MSU and IMP measurements, the value of Sp = 582.8(6.4) keV was adopted in their thermonuclear 55Ni(p,γ)56Cu rate calculations [23]. This shows that two experimental ME values agree well within the uncertainties, and the Sp values also agree well with the three theoretical predictions mentioned above, except for the highly accurate ImKG prediction with an uncertainty of ±1 keV [15].
In this work, in the reaction rate calculations we use the value of Sp = 579.8(7.1) keV derived at MSU, because the MSU mass value of 65Cu has been the most accurate value until now.
3 Previous results for reaction rates
The reaction rate of 55Ni(p,γ)56Cu was estimated for the first time by van Wormer et al. [24], based on the properties of 10 resonances in the mirror nucleus 56Co, at Sp = 459 keV determined by AME85. This rate is referred to as laur in the JINA Reaclib Database [25]. Later, Fisker et al. [26] performed a shell-model calculation at the value of Sp = 563 keV estimated by AME95. The following comments need to be added about the study by Fisker et al. [26]: (1) the direct-capture (DC) rate, expressed by Eq. (15) in the paper, need to be multiplied by a factor of two; (2) considering the 55Ni(p,γ)56Cu reaction, certain resonance strength values listed in Table I in the paper (p. 270) cannot be reproduced by the relationship of ωγ=ωΓpΓγ/(Γp+Γγ), based on their Γp and Γγ values; and (3) the resonant rate cannot be reproduced by the analytical formula in Eq. (7) in the paper using the listed strengths. Unfortunately, we cannot find the exact source of these errors. In addition, shell-model levels predicted by Fisker et al. for 56Cu (with excitation energy up to Ex = 3561 keV) were only valid for a temperature region up to ∼3.5 GK by considering the Gamow window. Therefore, the rates listed in Table II in Ref. [26] are typically underestimated above ∼3.5 GK. In the JINA Reaclib Database, the rate calculated by Fisker et al. [26] was revised at the value of Sp = 648 keV, and denoted as nfis.
Ex(56Cu, keV) | Er (keV)a | Jπ | T1/2 (ps)b | Γγ (eV)c | C2Sp(≤ll=1)d | C2Sp(≤ll=3)d | Γpe (eV) | ωγ (eV) | |
---|---|---|---|---|---|---|---|---|---|
Experimental energy levels in 56Cu obtained from Ong et al. [30] | ωγ ≈ ωΓp | ||||||||
826(3) | 246(7) | 4+ | gt;1.7 | 4.50×10-4f | 1.2×10-1 | 6.9×10-1 | 4.22×10-13(2.3) | 2.38×10-13 | |
1037(3) | 457(7) | 2+ | 0.12 |
3.80×10-3(0.1×10-3) | 6.4×10-1 | 1.6×10-1 | 3.13×10-6(1.4) | 9.78×10-7 | |
1224(4) | 644(8) | 5+ | 0.38 |
1.20×10-3(2.0×10-3) | 7.1×10-1 | 2.40×10-5(1.4) | 1.62×10-5 | ||
1224(4) | 644(8) | 3+ | 0.19 |
2.40×10-3(1.9×10-3) | 1.5×10-1 | 2.09×10-4(1.3) | 8.42×10-5 | ||
Experimental energy levels in 56Cu obtained from Orrigo et al. [31] with corrections | |||||||||
1411(13) | 831(15) | 0+ | 1580±60 | 2.89×10-7(16×10-7) | 3.8×10-2 | 2.28×10-5(1.4) | 1.78×10-8 | ||
1711(13) | 1131(15) | 1+ | 0.34 |
1.34×10-3(0.5×10-3) | 1.3×10-2 | 5.64×10-4(1.2) | 7.44×10-5 | ||
Estimated energy levels in 56Cu by mirror symmetry as discussed in the text | ωγ ≈ ωΓγ | ||||||||
1930(84) | 1350(84) | 3+ | 0.033 |
1.38×10-2(2.2×10-2) | 5.9×10-1 | 9.1×10-2 | 2.58×101(2.1) | 6.03×10-3 | |
2060(84) | 1480(84) | 2+ | 0.024±0.006 | 1.90×10-2(1.4×10-2) | 1.5×10-1 | 5.7×10-1 | 2.01×101(1.9) | 5.93×10-3 | |
2225(84) | 1645(84) | 2+ | 3.80×10-3 | 1.7×10-3 | 3.9×10-2 | 7.64×10-1(1.7) | 1.18×10-3 | ||
2283(84) | 1703(84) | 7+ | 1.20×10-4 | 9.9×10-3 | 5.53×10-2(1.8) | 1.12×10-4 | |||
2306(84) | 1726(84) | 3+ | 8.90×10-3 | 5.5×10-2 | 1.3×10-2 | 3.12×101(1.7) | 3.89×10-3 | ||
2357(84) | 1777(84) | 1+ | 9.80×10-3 | 1.0×10-2 | 8.65×10-2(1.8) | 1.65×10-3 | |||
2372(84) | 1792(84) | 6+ | 0.042±0.021 | 1.09×10-2(3.1×10-2) | 7.2×10-1 | 6.92×100(1.7) | 8.84×10-3 | ||
2470(84) | 1889(84) | 4+ | 0.016±0.009 | 2.85×10-2(5.3×10-2) | 6.3×10-1 | 1.3×10-1 | 8.74×102(1.6) | 1.60×10-2 | |
Levels in 56Cu calculated by the shell-model obtained from Ong et al. [30] | ωγ ≈ ωΓγ | ||||||||
2505(184g) | 1925(184) | 1+ | 2.00×10-2 | 7.3×10-3 | 1.52×10-1(2.9) | 3.31×10-3 | |||
2543(184g) | 1963(184) | 2+ | 9.20×10-3 | 1.6×10-2 | 7.5×10-3 | 3.06×101(2.5) | 2.87×10-3 | ||
2630(184g) | 2050(184) | 3+ | 9.60×10-3 | 8.8×10-3 | 3.6×10-3 | 2.48×101(2.4) | 4.20×10-3 | ||
2723(184g) | 2143(184) | 4+ | 9.90×10-3 | 2.3×10-2 | 2.0×10-2 | 9.55×101(2.2) | 5.57×10-3 | ||
2762(184g) | 2182(184) | 6+ | 1.50×10-2 | 5.0×10-2 | 3.40×100(2.4) | 1.21×10-2 | |||
2914(184g) | 2334(184) | 5+ | 1.70×10-2 | 1.1×10-2 | 1.0×10-2 | 9.50×101(2.0) | 1.17×10-2 |
T9 | Present rate | JINA Reaclib rates | ||||||
---|---|---|---|---|---|---|---|---|
Mean (579.8 keV) | Lower limit | Upper limit | nfis (648 keV) | rath (-448 keV) | thra (1919 keV) | laur (459 keV) | ths8 (648 keV) | |
0.10 | 4.59×10-19 | 2.32×10-19 | 1.42×10-18 | 1.69×10-20 | 7.07×10-27 | 1.20×10-20 | 3.37×10-21 | 2.29×10-20 |
0.15 | 4.56×10-15 | 3.36×10-15 | 1.00×10-14 | 2.82×10-15 | 1.04×10-18 | 7.15×10-16 | 3.06×10-15 | 6.09×10-16 |
0.20 | 5.42×10-12 | 3.82×10-12 | 8.80×10-12 | 3.07×10-12 | 8.58×10-15 | 4.17×10-13 | 3.15×10-12 | 3.53×10-13 |
0.30 | 2.09×10-08 | 1.60×10-08 | 2.96×10-08 | 9.45×10-09 | 8.73×10-11 | 1.04×10-09 | 1.34×10-08 | 9.17×10-10 |
0.40 | 1.52×10-06 | 1.31×10-06 | 1.97×10-06 | 9.64×10-07 | 1.33×10-08 | 1.47×10-07 | 1.77×10-06 | 1.17×10-07 |
0.50 | 2.49×10-05 | 2.23×10-05 | 3.07×10-05 | 2.06×10-05 | 3.66×10-07 | 5.01×10-06 | 3.69×10-05 | 3.41×10-06 |
0.60 | 1.79×10-04 | 1.61×10-04 | 2.16×10-04 | 1.85×10-04 | 4.03×10-06 | 7.16×10-05 | 2.85×10-04 | 4.20×10-05 |
0.70 | 7.50×10-04 | 6.78×10-04 | 9.01×10-04 | 9.69×10-04 | 2.53×10-05 | 5.75×10-04 | 1.22×10-03 | 2.97×10-04 |
0.80 | 2.21×10-03 | 1.99×10-03 | 2.65×10-03 | 3.52×10-03 | 1.08×10-04 | 3.07×10-03 | 3.62×10-03 | 1.43×10-03 |
0.90 | 5.08×10-03 | 4.62×10-03 | 6.12×10-03 | 9.89×10-03 | 3.53×10-04 | 1.21×10-02 | 8.36×10-03 | 5.23×10-03 |
1.00 | 9.86×10-03 | 9.08×10-03 | 1.20×10-02 | 2.30×10-02 | 9.39×10-04 | 3.77×10-02 | 1.63×10-02 | 1.55×10-02 |
1.10 | 1.70×10-02 | 1.58×10-02 | 2.09×10-02 | 4.62×10-02 | 2.14×10-03 | 9.83×10-02 | 2.82×10-02 | 3.91×10-02 |
1.20 | 2.71×10-02 | 2.55×10-02 | 3.40×10-02 | 8.36×10-02 | 4.31×10-03 | 2.22×10-01 | 4.49×10-02 | 8.65×10-02 |
1.30 | 4.10×10-02 | 3.88×10-02 | 5.26×10-02 | 1.40×10-01 | 7.88×10-03 | 4.47×10-01 | 6.72×10-02 | 1.73×10-01 |
1.40 | 5.97×10-02 | 5.69×10-02 | 7.96×10-02 | 2.19×10-01 | 1.33×10-02 | 8.19×10-01 | 9.63×10-02 | 3.16×10-01 |
1.50 | 8.48×10-02 | 8.14×10-02 | 1.18×10-01 | 3.30×10-01 | 2.11×10-02 | 1.39 | 1.33×10-01 | 5.40×10-01 |
2.00 | 3.92×10-01 | 3.87×10-01 | 6.32×10-01 | 1.68 | 1.10×10-01 | 8.83 | 4.95×10-01 | 3.71 |
In addition, certain theoretical rates based on the statistical model are available in the JINA Reaclib Database [25]. For instance, the rath, thra rates are obtained from statistical model calculations [27] using the finite-range droplet macroscopic (FRDM) [28](Sp = -448 keV) and the ETSFIQ mass models [29] (Sp = 1919 keV), respectively. The ths8 rate is the theoretical value by Rauscher [25] (Sp = 648 keV). These indicated that the rates from statistical models differ from one another by up to several orders of magnitude in the typical XRB temperature range. Therefore, experimental data for 56Cu, such as the Sp value and level structure information, are strongly required.
In 2017, the low-lying energy levels of 56Cu (Ex = 166, 572, 826, 1037, and 1224 keV) were obtained by in-beam γ-ray spectroscopy using the state-of-art Gamma-Ray Energy Tracking In-beam Nuclear Array (GRETINA) detector together with the S800 spectrograph at MSU [30]. With the newly obtained value of Sp = 639±82 keV using a more localized isobaric multiplet mass equation (IMME) fit, the 55Ni(p,γ)56Cu rate was calculated together with the shell-model results. In this study, this rate is denoted as ong.
As mentioned in the previous section, the high-precision mass measurement of 56Cu was performed at MSU in 2018 [23]: Valverde et al. obtained a weighted average value of Sp = 582.8(6.4) keV and applied it in the reaction rate calculations. In that study, the energy levels observed in Ref. [30] were utilized, and the resonance energies and corresponding proton width, Γp, were scaled to the revised Sp value. Although the reaction rates and the associated uncertainties were calculated and presented in a figure, no numerical rates were provided for the readers. In this study, this rate is denoted as valverde.
4 Energy levels in 56Cu
As mentioned in the previous section, Ong et al. [30] observed five low-lying energy levels, Ex = 166, 572, 826, 1037, and 1224 keV, in 56Cu, using in-beam γ-ray spectroscopy at MSU [30]. Orrigo et al. [31] performed a β-delayed-proton decay experiment of 56Zn at the Grand Accélérateur National d’Ions Lourds (GANIL), and observed six proton-decay branches. Based on these events, the level scheme of 56Cu was constructed in the range of Ex = 1391–3508 keV. The associated large uncertainty of 140 keV was due to the uncertainty of Sp=560±140 keV estimated by AME03 at that time. In this work, the excitation energies obtained by Orrigo et al. are shifted by 19.8 keV (i.e. to 579.8–560.0 keV) upward, to Ex = 1411, 1711, 2557, 2680, 3443, and 3528 keV, according to the new MSU ground-state mass of 56Cu applied here. The associated uncertainty in the level energies was reduced to 12.3 keV (in this study 13 keV was adopted), which could be attributed to that adopted at 10 keV proton energy, Ep, and 7.1 keV Sp value. The energy levels in 56Cu obtained experimentally and calculated by the shell-model are shown in Fig. 1. For comparison, the experimental data of the mirror nucleus 56Co are also shown, and the mirror assignments are suggested accordingly.
-201909/1001-8042-30-09-011/alternativeImage/1001-8042-30-09-011-F001.jpg)
Figure 1 shows an exceptional mirror symmetry of the excited states between 56Cu and 56Co. Therefore, the energies of the missing high-lying levels in 56Cu can be assumed identical to the corresponding energies in the mirror 56Co. Thus, for the missing levels in 56Cu, we calculated their resonant rates using the level energies from 56Co. To estimate the uncertainty in the level energies (Ex) of 56Cu calculated by this approach, the neighboring mirror pairs in the pf-shell region [32] were analyzed. Figure 2 shows the level energy difference between the mirror pairs of Tz = 1. The horizontal axis Emean indicates the average level energies of the mirror pairs, and the vertical axis represents the level energy difference. The root mean square (rms) value was found to be ∼84 keV. Thus, in this study, we assumed an uncertainty of ±84 keV in the energies estimated for the missing states in 56Cu, for which a provisional correspondence was demonstrated between the mirror 56Co and shell-model calculated levels, shown in Fig. 1 by the dotted blue lines. In addition, we also adopted these shell-model level energies for six states of Ex gt;2470 keV (see Table 1) in the reaction rate calculations, and an rms uncertainty of 184 keV was estimated for these calculated levels, based on the energy difference between the experimental and shell-model levels in 65Cu (the correspondence is shown in Table 1). However, their contribution to the total rate is negligible in the temperature region relevant to XRB, which is discussed in the next section.
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5 Revised reaction rate
For a typical (p,γ) reaction, the total rate consists of the resonant and DC rates of proton capture on the ground state, and all thermally excited states in the target nucleus are weighted with their individual population factors [35, 40]. Here, the excitation energies in 55Ni are rather high (Ex = 2089 keV for the first excited state), and therefore the contributions from the thermally populated excited states can be entirely neglected in the temperature region relevant to XRB. The DC rate is also negligible compared to the resonant rate as demonstrated in previous works [24, 26]. Thus, only the resonant rate (equivalent to the total rate) was calculated in the temperature region relevant to XRB. In this work, we calculated the 55Ni(p,γ)56Cu resonant rate using the most accurate experimental value of Sp(56Cu) = 579.8±7.1 keV [23], the recent experimental level energies in 56Cu, the mirror information for the missing high-lying states in 56Cu, and the previous shell-model results for six levels above Ex=2470 keV (see Table 1). A similar approach was used in Refs. [24, 34, 35].
The resonant 55Ni(p,γ)56Cu rate was calculated using Eq. (7) in Ref. [26], which is the well-known narrow resonance formalism given as [24, 34, 35]
where the unit of the resonant energy Er and the strength ωγ is in MeV. The Er value can be calculated by the relation of Er = Ex-Sp, where Ex denotes the level energies in 56Cu (see Sect. 4), and the MSU value is Sp(56Cu) = 579.8±7.1 keV. For the proton capture reaction, the reduced mass μ is defined by AT/(1+AT) (here, the target mass is AT = 55 for 55Ni). The resonant strength ωγ is defined as (Eq. (8) in Ref. [26])
where JT and J are the spins of the target (JT = 7/2 for the ground state of 55Ni) and resonant state, respectively. The Γp and Γγ parameters are the partial widths for the entrance and exit channels, respectively, and Γtot is the total decay width of a resonance (Γtot Γp + Γγ).
In this work, the gamma width Γγ for the part of the unbound state in 56Cu was calculated by the available half-lives T1/2 of the corresponding bound state in the mirror 56Co using Γγ = ln2× /T1/2, as shown in Table 1, where the previous shell-model gamma widths (Γγ) [30] are indicated in the parentheses of the corresponding Γγ column. It can be seen that the gamma widths calculated by the shell-model deviate from the mirror values by a factor of no more than ∼3, except for a factor of 5.5 for the 1.411 MeV (0+) state; however, this is not a noticeable parameter in the rate calculation, as discussed below. For the other remaining states listed in Table 1, the previous shell-model gamma widths (Γγ) [30] are adopted. In Ref. [30], the uncertainty for the calculated γ widths were estimated to be approximately a factor of two [37]. We conservatively estimated the uncertainty in the gamma widths adopted here as a factor of three; however, the uncertainties in the gamma widths obtained from the mirror half-lives T1/2 are less than a factor of two.
The proton widths were calculated by the appropriate scaling to those in Ref. [30] enabled by the energy difference of Er in the calculation of the penetrability factor P≤ll. The leading uncertainties in Γp are due to those in Er from the P≤ll factors, and they are significantly larger than those resulting from the uncertainty due to the choice of channel radius r0 and diffuseness a (∼20% [36]). In addition, the uncertainties in the C2S factors calculated by the shell-model are estimated to be ∼20% [37], which can be neglected in the present calculations. In Table 1, the corresponding uncertainties are indicated in the parentheses of the Γγ column. For example, the number 2.3 indicates an uncertainty factor of 2.3.
The resonant parameters for calculating the 55Ni(p,γ)56Cu reaction rate are listed in Table 1. The peak temperature in the recent hydrodynamic XRB models can be as high as ∼1.4 GK [11, 38, 39]. In this study, we consider the reaction rate that is valid for a temperature region up to 2 GK, corresponding to a Gamow peak of Er≈1.77 MeV with a width of Δ≈1.28 MeV [40]. Therefore, we believe that the resonances listed in Table 1 are sufficient for the description of the reaction rates of the relevant XRB region.
The percentage contributions of each resonance to the total resonant rate were calculated. Only five resonances contribute significantly to the total rate in the temperature region up to ∼2 GK: at Ex = 826, 1037, 1224, 1930, and 2060 keV. The contributions of these five special resonances to the total rate are shown in Fig. 3. Ong et al. provisionally assigned Ex = 1224 keV to either the Jπ = 3+ or the 5+ state. The cases of 3+ and 5+ are shown in Figs 3(a) and 3(b), respectively. Only three resonances, at Ex = 1037(2+), 1224(3+ or 5+), and 1930(3+) keV dominate most of the temperature region relevant to XRB (∼0.4–1.4 GK). If the Ex = 1224 keV state is of 3+, it nearly dominates the entire temperature region relevant to XRB. If the Ex = 1224 keV state is of 5+, the total rate can be reduced by a factor of ∼3 compared with the 3+ case. Thus, the experimental determination of the Jπ value is strongly required for the Ex = 1224 keV state. It should be noted, that other resonances can also have noticeable contribution, which are not shown in Fig. 3, by considering the uncertainties in their Er and ωγ values. A realistic reaction rate and the associated uncertainties were calculated and discussed in the following paragraph. It should be noted, that the rate by Ong et al. assumed the Ex = 1224 keV state as a doublet (with 3+ and 5+), which might not be correct, according to the mirror information and shell-model calculations. This assumption probably results in an overestimation of the rate by different degrees depending on the assignment of this state to 3+ or 5+. Here, for comparison we also adopt the same assumption.
-201909/1001-8042-30-09-011/alternativeImage/1001-8042-30-09-011-F003.jpg)
Table 2 summarizes the thermonuclear 55Ni(p,γ)56Cu rates calculated analytically using Eq. 1 with the resonant parameters listed in Table 1. The listed 1σ uncertainties (lower and upper limits) were calculated by a Monte-Carlo method, which simultaneously sampled the uncertainties in Er, Γp, and Γγ. Our (mean) rate can be parameterized very well by the standard format of [27]
with a fitting error less than 3.2% in the range of 0.1–2.0 GK.
Figure 4 shows a comparison of the rate in this study with two recently obtained results given in Refs. [23, 30]. It can be seen that our revised rate and associated uncertainties are rather different from those in the previous studies. The present uncertainties are significantly smaller than those by Ong et al. [30] mainly because we used a considerably more accurate experimental Sp value (and hence Er) in the reaction rate calculations. Here, two remarks need to be made: 1) The recommended rate and uncertainties listed in Table IV in the paper by Ong et al. are not in exact agreement with those shown in Fig. 6 in the same paper, and the exact reason for this is not known and 2) according to the method of rate calculation described by Valverde et al. [23], we cannot reproduce the rate shown in Fig. 4 in their paper in any form. They used Sp = 582.8(6.4) keV, which is only ∼3 keV higher than our value of Sp = 579.8(7.1) keV. Our rate is expected not to be very different from that by Valverde et al. In the work by Valverde et al., if it is assumed that they used the exactly same Γp and Γγ parameters (instead of the scaled ones), we need to be able to approximately reproduce their rate within one or two factor. This suggests that Valverde et al. presented an incorrect rate and associated uncertainties in the figure. As there are no numerical rates listed in their tables, the exact reason for this is not known. Our rates a re listed explicitly in Table 2.
-201909/1001-8042-30-09-011/alternativeImage/1001-8042-30-09-011-F004.jpg)
Figure 5 shows a comparison of the rate in this study with five different rates available in the JINA Reaclib Database: rath, thra, ths8, nifs, laur, ths8 rates. The uncertainties of the present rate are indicated by error bands in the figure. All rates for the 55Ni(p,γ)56Cu reaction are summarized in Table 2. It can be seen that neither the rates from the statistical model (rath, thra, ths8), nor that from the shell-model nifs, or the simple laur rate (based on the mirror information), agree with the rate in this study within the well-constrained uncertainties over the entire temperature region relevant to XRB. This implies that the experimental information of Sp, level structures, and 56Cu properties are very important to determine the 55Ni(p,γ)56Cu rate more accurately.
-201909/1001-8042-30-09-011/alternativeImage/1001-8042-30-09-011-F005.jpg)
6 Summary
The thermonuclear 55Ni(p,γ)56Cu rate was recalculated using the most accurate proton separation energy of Sp(56Cu) = 579.8±7.1 keV, the recent experimental levels in 56Cu, together with the shell-model calculation and the mirror nuclear structure in 56Co. Our revised rate deviates significantly from those available in the literature. To further reduce the uncertainties of the rate, the experimental determination of the Jπ value (3+ or 5+) is strongly required for the crucial Ex = 1224 keV state in 56Cu. In addition, we found that the previous reaction rate curve (Fig. 4 in Ref. [23]) is incorrect. Therefore, we recommend our revised rate to be incorporated in the future astrophysical network calculations, as it is based on a more fundamental experimental background. The astrophysical application of our revised rates in Type I XRB calculations is now under progress, which is beyond the scope of this work.
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