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The total energy of a single-hyperon hypernucleus can be written as [69–71]
$ \begin{array}{*{20}{l}} E=\int \mathrm{d}^3 \boldsymbol{r} \varepsilon(\boldsymbol{r}), \quad \varepsilon=\varepsilon_{N N}+\varepsilon_{\Lambda N}, \end{array} $
(1) where
$ \varepsilon_{N N} $ and$ \varepsilon_{\Lambda N} $ account for the nucleon-nucleon and hyperon-nucleon interactions, respectively. The energy-density functional depends on the one-body density$ \rho_{q } (\boldsymbol{r}) $ , kinetic density$ \tau_{q } (\boldsymbol{r}) $ , and spin-orbit current$ \boldsymbol{J}_q (\boldsymbol{r}) $ ,$ \begin{aligned}[b] \rho_q (\boldsymbol{r} ) =\;&\sum\limits_{i=1}^{N_q} n_q^i\left|\phi_q^i(\boldsymbol{r} ) \right|^2, \\ \tau_q (\boldsymbol{r} ) =\;&\sum\limits_{i=1}^{N_q} n_q^i\left|\nabla \phi_q^i(\boldsymbol{r} ) \right|^2, \\ \boldsymbol{J}_q (\boldsymbol{r} ) =\;&\sum\limits_{i=1}^{N_q} n_q^{i} \phi_q^{i\ast}\left(\nabla \phi_q^i(\boldsymbol{r} ) \times \sigma\right) / i, \end{aligned} $
(2) where
$ \phi_q^i $ (i = 1,...$ N_q $ ) are self-consistently calculated the single-particle wave functions of the$ N_q $ occupied states for the different particles q =n,$ p, $ and Λ. They satisfy the Schrödinger equation, obtained by the minimization of the total energy functional Eq. (1) according to the variational principle,$ \left[\nabla \cdot \frac{1}{2 m_q^*(\boldsymbol{r})} \nabla-V_q(\boldsymbol{r})+i \boldsymbol{W}_q(\boldsymbol{r}) \cdot(\nabla \times \boldsymbol{\sigma})\right] \phi_q^i(\boldsymbol{r})=e_q^i \phi_q^i(\boldsymbol{r}), $
(3) in which
$ \boldsymbol{W}_q(\boldsymbol{r}) $ is the spin–orbit interaction part for the nucleons as given in Refs. [72], while the spin-orbit force for the Λ hyperon is very small [73, 74] and it is ignored in the present study. The central mean-fields$ {V}_q(\boldsymbol{r}) $ , corrected by the effective-mass terms following the procedure described in Refs.[69, 71] are$ \begin{aligned}[b] V_N=\; & V_N^{\mathrm{SHF}}+\frac{\partial \varepsilon_{N \Lambda}}{\partial \rho_N} \\ & +\frac{\partial}{\partial \rho_N}\left(\frac{m_{\Lambda}}{m_{\Lambda}^*\left(\rho_N\right)}\right)\left(\frac{\tau_{\Lambda}}{2 m_{\Lambda}}-\frac{3}{5} \frac{\rho_{\Lambda}\left(3 \pi^2 \rho_{\Lambda}\right)^{2 / 3}}{2 m_{\Lambda}}\right), \end{aligned} $
(4) $ V_{\Lambda}=\frac{\partial\varepsilon_{N \Lambda}}{\partial \rho_{\Lambda}}-\left(\frac{m_{\Lambda}}{m_{\Lambda}^*\left(\rho_N\right)}-1\right) \frac{\left(3 \pi^2 \rho_{\Lambda}\right)^{2 / 3}}{2 m_{\Lambda}} . $
(5) The Skyrme force SLy5 [75, 76] is used for the nucleon-nucleon interaction
$ \varepsilon_{N N} $ , and the hyperon-nucleon interaction$ \varepsilon_{N \Lambda} $ is parameterized as (densities ρ given in units of fm$ ^{-3} $ , energy density ε in MeV fm$ ^{-3} $ ):$ \begin{aligned}[b] \varepsilon_{N \Lambda}\left(\rho_N, \rho_{\Lambda}\right)=\; & -\left(\varepsilon_1-\varepsilon_2 \rho_N+\varepsilon_3 \rho_N^2\right) \rho_N \rho_{\Lambda} \\ & +\left(\varepsilon_4-\varepsilon_5 \rho_N+\varepsilon_6 \rho_N^2\right) \rho_N \rho_{\Lambda}{ }^{5 / 3}, \end{aligned} $
(6) together with
$ \frac{m_{\Lambda}^*}{m_{\Lambda}}\left(\rho_N\right) \approx \mu_1-\mu_2 \rho_N+\mu_3 \rho_N^2-\mu_4 \rho_N^3 . $
(7) The parameter
$ \varepsilon_{1},...,\varepsilon_{6} $ in Eq. (6) and the Λ effective-mass$ \mu_i $ were determined in BHF calculations with the Nijmegen potential NSC97f [71, 77]. -
The nuclear cores considered in this work are almost spherical and the deformation can be neglected, therefore, the single channel Schrödinger equation in momentum representation can be written as:
$ \dfrac{\hbar^2k^2}{2\mu}\phi(k)+\int V_l(k,k')\phi(k')k'^2dk'=E\phi(k), $
(8) where the reduced mass
$ \mu=\dfrac{Am_N m_{\Lambda}}{Am_N+m_{\Lambda}} $ with A being the nucleon number of nuclear core, nucleon mass$ m_N $ being 938.918 MeV and Λ hyperon mass$ m_{\Lambda} $ being 1115.683 MeV. The potential in momentum space$ V_l(k,k') $ is obtained by the spherical potential$ V(r) $ extracted from the Skyrme-Hartree-Fock method:$ \begin{array}{*{20}{l}} V_l(k,k')=\dfrac{2}{\pi}\int j_l(kr)V(r)j_l(k'r)r^2dr, \end{array} $
(9) where
$ j_l $ represents the spherical Bessel function. Although the doubly-magic core nuclei considered in this work do exhibit deformation experimentally, the deformation is relatively small and these core nuclei can be regarded as near-spherical nuclei. Therefore, we employ a spherical hyperon-nucleus interaction$ V(r) $ in our theoretical framework. When deformation cannot be neglected, Eq.(8) will become a coupled equation.As mentioned, we can extract effective potential
$ V(r) $ between the nucleus and the single hyperon from SHF calculations, explicitly speaking, from the nucleon and hyperon density distributions. In this work, we select the Skyrme force SLy5 for nucleon-nucleon interaction and the Nijmegen potential NSC97f for hyperon-nucleon interaction. The Nijmegen potential NSC97f is chosen because it can successfully describe the binding energy of single hyperon in hypernuclei and also effectively accounts for the binding energy of multiple hyperons in multi-hyperon hypernuclei [30]. The SLy5 interaction is selected for nucleon-nucleon interactions due to its good performance in describing nuclear structure [75, 76]. Additionally, once the hyperon-nucleon interaction is determined, the choice of nucleon-nucleon interaction has a insignificant impact on the binding energies of hyperons [24].The integral function (8) can be converted into a equivalent matrix equation involving the summation over a finite set of mesh points
$ k_i $ in momentum space:$ \begin{array}{*{20}{l}} \dfrac{\hbar^2k_i^2}{2\mu}\phi(k_j)\delta_{i,j}+\sum \limits_j V_l(k_i,k_j)\phi(k_j)k_j^2\omega_j=E\phi(k_i), \end{array} $
(10) where
$ \omega_j $ represents the weight of j-th momentum mesh point. In our calculations the complex Gaussian-Legendre mesh is adopted and our contours consist of line segments in complex momentum space. Generally speaking, as long as the contour can enclose the discrete eigenstates we wish to obtain and the momentum cutoff$ k_{max} $ is sufficiently large, the shape of the contour has no effect on the final calculation result.In addition, one can also find that the contour
$ ke^{-i\theta} $ is exactly equivalent to complex scaling in coordinate space:$ \begin{array}{*{20}{l}} U(\theta)f({r})=\exp(i\dfrac{3}{2}\theta)f({r}\exp(i\theta)). \end{array} $
(11) However, when excessively large complex scaling angles are employed in the complex scaling method, the computation will become unstable. However, this issue does not exist for CMR. Therefore, CMR can exhibit better computational performance for broader resonant states.
In this work, we only address the resonance states of spherical hypernuclei through CMR. In the more general case of deformed potentials, coupling effects of higher excited energy levels could be very crucial, which is essential for analyzing deformed hypernuclei. Moreover, extending CMR to coupled-channel problems is also straightforward and convenient, which allows us to further discuss the impact of deformation effects on hyperon emission.
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The level density
$ \rho(\varepsilon) $ of the full Hamiltonian h is defined by:where
$ \varepsilon_i $ are eigenvalues of h, summation and integration are taken for discrete and continuous eigenvalues, respectively. This definition of the level density can also be expressed with the help of the Green's function:$ \begin{array}{*{20}{l}} \rho(\varepsilon)= -\dfrac{1}{\pi} {\rm{Im}}\left\{{\rm{Tr}}\left[\dfrac{1}{\varepsilon+i0-h}\right]\right\}. \end{array} $
(13) When the Hamiltonian is described by a sum of an asymptotic term
$ h_0 $ and the short-range interaction V, namely$ h=h_0+V $ , the CLD (denoted by$ \Delta(\varepsilon) $ ) for an energy ε is expressed with the density$ \rho(\varepsilon) $ obtained from the full Hamiltonian h and the level density$ \rho_0(\varepsilon) $ of continuum states obtained from the asymptotic Hamiltonian$ h_0 $ as:$ \begin{aligned}[b] \Delta(\varepsilon)=\;&\rho(\varepsilon)-\rho_0(\varepsilon)\\=\;&-\dfrac{1}{\pi}{\rm{Im}}\left[{\rm{Tr}}\left\{\dfrac{1}{\varepsilon+i0-h}-\dfrac{1}{\varepsilon+i0-h_0}\right\}\right]. \end{aligned} $
(14) Additionally,
$ \Delta(\varepsilon) $ is well known to be related to the scattering S-matrix$ S(\varepsilon) $ as:$ \Delta(\varepsilon)=\dfrac{1}{2\pi}{\rm{Im}}\dfrac{d}{d\varepsilon}\ln\{\det S(\varepsilon)\}, $
(15) for a single channel system, the scattering S-matrix can be expressed as:
$ S(\varepsilon)=e^{2i\delta(\varepsilon)} $ , where$ \delta(\varepsilon) $ is the scattering phase shift. In such case we can obtain the simplified CLD and the scattering phase shift$ \Delta(\varepsilon)=\dfrac{1}{\pi}\dfrac{d\delta}{d\varepsilon}, \quad \delta(\varepsilon)=\pi\int_{-\infty}^{\varepsilon}\Delta(\varepsilon')d\varepsilon'. $
(16) -
If the energy spectrum is obtained through N momentum mesh points in the CMR. The CMR-CLD can be expressed in the following form:
$ \begin{aligned}[b] \Delta_N^{CMR}(\varepsilon)=\;&\sum\limits_b^{N_B}\delta(\varepsilon-\varepsilon_b)+\dfrac{1}{\pi}\sum_r^{N_R^{CMR}}\dfrac{\Gamma_r/2}{(\varepsilon-\varepsilon_r)^2+\Gamma_r^2/4}\\&+\dfrac{1}{\pi}\sum\limits_C^{N_C^{CMR}=N-N_B-N_R^{CMR}}\dfrac{\epsilon_C^I}{(\varepsilon-\epsilon_C^R)^2+{\epsilon_C^I}^2}\\&-\dfrac{1}{\pi}\sum\limits_C^{N}\dfrac{\epsilon_C^{0I}}{(\varepsilon-\epsilon_C^{0R})^2+{\epsilon_C^{0I}}^2}, \end{aligned} $
(17) where
$ \varepsilon_b $ ,$ \varepsilon_r-i\Gamma_r/2 $ and$ \epsilon^R-i\epsilon^I $ are eigenvalues of the full Hamiltonian$ h=T+V $ ,$ \epsilon^{0R}-i\epsilon^{0I} $ are eigenvalues of asymptotic Hamiltonian$ h_0=T $ .$ N_B $ represents the number of the bound state and$ N_{R}^{CMR} $ represents the number of the resonant state.With Eq.(16) the phase shift within the N complex momentum mesh points in the CMR can be expressed as:
$ \begin{aligned}[b] \delta_N^{CMR}(\varepsilon)=\;&\pi\int_{-\infty}^{\varepsilon}\Delta_N^{CMR}(\varepsilon)\\& =N_B\pi+\sum\limits_{r=1}^{N_R^{CMR}}\int_0^{\varepsilon} d\varepsilon\dfrac{\Gamma_r/2}{(\varepsilon-\varepsilon_r)^2+\Gamma_r^2/4}\\&+\int_0^{\varepsilon} d\varepsilon[\sum\limits_{C=1}^{N_C^{CMR}}\dfrac{\epsilon_C^I}{(\varepsilon-\epsilon_C^R)^2+{\epsilon_C^I}^2}-\sum\limits_{C=1}^{N}\dfrac{\epsilon_C^{0I}}{(\varepsilon-\epsilon_C^{0R})^2+{\epsilon_C^{0I}}^2}]\\&=N_B\pi+\delta_R(\varepsilon)+\delta_C(\varepsilon), \end{aligned} $
(18) where the resonance and non-resonance phase shifts are given as:
$ \begin{array}{*{20}{l}} \delta_R(\varepsilon)=\sum\limits_{r=1}^{N_R^{CMR}}\delta_r(\varepsilon), \quad \delta_C(\varepsilon)=\sum\limits_{c=1}^{N_C^{CMR}}\delta_c(\varepsilon)-\sum\limits_{c=1}^{N}\delta_c^0(\varepsilon). \end{array} $
(19) -
Using the continuum level density, the scattering phase shifts can be conveniently obtained from the energy spectrum. To extract the information such as scattering length, effective range, resonance energies and so on from the phase shifts, we choose the effective range expansion to expand the phase shift
$ \delta_l $ through a power series in momentum k:$ \begin{aligned}[b] & C_l^2(\eta) k^{2l+1}\left[\cot(\delta_l)+\dfrac{2\eta H(\eta)}{C_0^2(\eta)}\right]\\=\;&-\dfrac{1}{a_l}+\dfrac{r_l k^2}{2}+P_l r_l^3k^4+{O}(k^6), \end{aligned} $
(20) where
$ a_l $ is the scattering length,$ r_l $ is the effective range, and$ P_l $ is the shape parameter of partial wave l. In this expression$ C_l^2(\eta) $ ,$ C_0^2(\eta) $ and$ H(\eta) $ are given by:$ \begin{aligned}[b] C_l^2(\eta)=\;&C_{l-1}^2(\eta)(1+\dfrac{\eta^2}{l^2}), \ C_0^2(\eta)=\frac{2\pi\eta}{e^{2\pi\eta}-1},\\ H(\eta)=\;&\sum\limits_{s=1}^{\infty}\frac{\eta^2}{s(s^2+\eta^2)}-\ln(\eta)-\gamma \\=\;&-\dfrac{i\pi}{e^{2\pi\eta}-1}+\Psi(i\eta)+\dfrac{1}{2i\eta}-\ln(i\eta) , \end{aligned} $
(21) where
$ \eta=\dfrac{Z_1Z_2e^2\mu}{\hbar^2k} $ ,$ \gamma=0.5772156649\cdots $ is the Euler's constant,$ \Psi(z) $ is the logarithmic derivative of the Γ function (Ψ function or digamma).In the case of neutral particle scattering, the effective range expansion reads:
$ \begin{array}{*{20}{l}} & k^{2l+1}\cot(\delta_l)=-\dfrac{1}{a_l}+\dfrac{r_l k^2}{2}+P_l r_l^3k^4+{O}(k^6). \end{array} $
(22) According to the form of the on-shell elements of T-matrix:
$ T(k,k)=\dfrac{(4\pi)^2}{2\mu k}\dfrac{1}{\cot(\delta_l(k))-i} $ , one can find that the resonance is the pole of the T-matrix and thus phase shift at complex momentum$ k_{res}=\dfrac{\sqrt{2\mu E_{res}}}{\hbar} $ of resonant state satisfies the condition$ \cot(\delta_l(k_{res}))=i $ . Therefore, through effective range expansion, the parametrization of the phase shift at$ k_{res} $ satisfies the following equation:$ \begin{array}{*{20}{l}} &-\dfrac{1}{a_l}+\dfrac{r_l k^2}{2}+P_l r_l^3k^4+{O}(k^6)=C_l^2(\eta) k^{2l+1}\left[i+\dfrac{2\eta H(\eta)}{C_0^2(\eta)}\right], \end{array} $
(23) for neutral particle scattering Eq.(23) becomes:
$ \begin{array}{*{20}{l}} &-\dfrac{1}{a_l}+\dfrac{r_l k^2}{2}+P_l r_l^3k^4+{O}(k^6)= ik^{2l+1}. \end{array} $
(24) -
Due to the considerably shorter lifetimes observed in hypernuclei compared to those of conventional atomic nuclei, it is thus assumed in studies of hypernuclear resonant states that their cores exist in deeply bound states. Accordingly, stable nuclei such as
$ {}^{16} $ O,$ {}^{40} $ Ca,$ {}^{48} $ Ca, and$ {}^{56} $ Ni have been designated as core nuclei for this purpose. Firstly, from calculations based on Skyrme-Hartree-Fock method, the effective interaction between hyperon and nuclear core can be extracted as$ V(r) $ . In practical computations only effective potential in a finite region$ r<r_{max} $ can be obtained in Skyrme-Hartree-Fock method. To provide potential in the entire coordinate space, we employ a Woods-Saxon form$ \dfrac{V_0}{1+e^{\frac{r-R}{a}}} $ to fit$ V(r) $ and utilize the analytical potential beyond$ r_{max} $ in Eq.(9).The effective hyperon-nucleus interactions
$ V(r) $ for$ {}^{17}_\Lambda $ O,$ {}^{41}_{\Lambda} $ Ca,$ {}^{49}_{\Lambda} $ Ca, and$ {}^{57}_\Lambda $ Ni are plotted in Fig. 1. For these nearly spherical nuclei, the deformation obtained from Skyrme-Hartree-Fock calculations is very small and can be neglected. Hence, we only need to consider single-channel scattering process. However, if the deformation is significant and cannot be ignored, then deformed potentials and the corresponding coupled-channel equations must be considered. It should also be noted that in the current calculations, we assume the energy level splitting induced by spin-orbit coupling is relatively small compared to the energy levels themselves, and thus we have neglected the influence of the spin-orbit coupling potential. However, if a more detailed discussion of the level splitting is required, we can derive a phenomenological spin-orbit coupling potential based on$ V(r) $ within the current framework.Figure 1. (color online) The effective potential between the hyperon and the nuclear core extracted from the Skyrme-Hartree-Fock method. Solid, dashed, dotted, and dash-dot line represent the effective potential
$ V(r) $ for$ {}^{17}_{\Lambda} $ O,$ {}^{41}_{\Lambda} $ Ca,$ {}^{49}_{\Lambda} $ Ca, and$ {}^{57}_{\Lambda} $ Ni, respectively.In the following, we illustrate the results of CMR-CLD and effective rang expansion by taking
$ {}^{17}_\Lambda $ O as an example. In solving the Schrödinger equation in momentum space the truncation of momentum is taken to be$ k_{max}=5 $ fm$ {}^{-1} $ , which is large enough to guarantee the stabilization of the numerical solutions. For CMR-CLD, as long as the contour encompasses the discrete eigenvalues, then these discrete eigenvalues are independent on the choice of the contour, furthermore, once the discrete eigenvalues can be accurately solved, the phase shifts obtained through continuum level density also do not depend on the contour shape.Figure 2 illustrates the complex momentum spectra and phase shifts obtained through CMR-CLD for
$ {}^{17}_\Lambda $ O with orbital angular momentum$ l=0 $ and$ l=1 $ . Both states with$ l=0 $ and$ l=1 $ are bound states, whose positions are marked on the positive imaginary axis in panel (a). Panel (b) shows the scattering phase shifts obtained with both CMR-CLD and conventional R-matrix method, where circular and square markers represent the P-wave and S-wave phase shifts obtained from R-matrix method, and solid and dashed lines correspond to the P-wave and S-wave phase shifts obtained from CMR-CLD. In the R-matrix calculation of scattering phase shifts, we adopt the conventional Lagrange functions over the interval$ (0,a) $ , with the channel radius a set to around 20 fm (large enough to neglect the short-range nuclear interaction) and the number of grid points set to about 50. The same parameters are used in the calculation of resonant states.Figure 2. (color online) (a) The complex momentum spectra of
$ {}^{17}_{\Lambda} $ O obtained from CMR. The square and circle markers correspond to the results for S-wave and P-wave, respectively. Two bound states are marked on the positive imaginary axis. (b) The phase shifts of$ {}^{17}_{\Lambda} $ O for S-wave and P-wave. The square and circle markers represent the phase shifts obtained by R-matrix method for S-wave and P-wave, respectively. The dashed and solid lines represent the phase shifts obtained by CMR-CLD for S-wave and P-wave, respectively.When considering higher angular momentum, the
$ l=2 $ state becomes a resonance due to the stronger repulsive centrifugal potential. As shown in Fig. 3(a), a resonance appears in the fourth quadrant of the complex momentum space. The square, diamond, and circular markers in panel (a) represent the complex momentum spectra obtained using three different contour shapes. It can be observed that the position of the resonant state remains almost unchanged regardless of the contour shape. In Fig. 3(b) the phase shifts of$ {}^{17}_\Lambda $ O for D-wave scattering are displayed, the triangle markers and solid line represent the results obtained by CMR-CLD and R-matrix, respectively. Similar calculations are performed for other systems and we display the phase shifts corresponding to the first resonant state of$ {}^{17}_\Lambda $ O,$ {}^{41}_{\Lambda} $ Ca,$ {}^{49}_{\Lambda} $ Ca, and$ {}^{57}_\Lambda $ Ni in Fig. 4. The solid lines represent results obtained using CMR-CLD, while the markers denote results obtained with the R-matrix method.Figure 3. (color online) (a)The complex momentum spectra of
$ {}^{17}_\Lambda $ O obtained from CMR. The square, circle and rhombus markers correspond to three different contours. The D-wave resonant state and its eigenenergy are marked in this panel. (b) The phase shifts of$ {}^{17}_\Lambda $ O for D-wave. The triangle markers represent the phase shifts obtained by R-matrix and the solid line represent the results obtained by CMR-CLD.Figure 4. (color online) The scattering phase shifts at the appearance of the first resonant state. Solid lines represent the calculations from CMR-CLD, while circle, square, diamond, upward triangle, downward triangle, and right triangle markers correspond to the results of R-matrix method for
$ {}^{17}_\Lambda $ O,$ {}^{41}_{\Lambda} $ Ca,$ {}^{49}_{\Lambda} $ Ca, and$ {}^{57}_\Lambda $ Ni, respectively.After obtaining the phase shifts through CMR-CLD, we can also extract physical quantities such as scattering length, complex resonant energy by using effective range expansion. For the D-wave scattering of
$ {}^{17}_\Lambda $ O, these extracted physical quantities are listed in Table 2. For other systems, the calculations are similar and the corresponding results are also listed in Table 2.Nuclear core l $ a_l^{CMR-CLD+ERE} $ (fm$ {}^{2l+1} $ )$ a_l^{R-matrix} $ (fm$ {}^{2l+1} $ )$ E_{res}^{R-matrix} $ (MeV)$ E_{res}^{CMR-CLD+ERE} $ (MeV)$ E_{res}^{CMR} $ (MeV)$ {}^{16} $ O2 −16.50 −16.49 4.70-1.84i 4.70-1.84i 4.70-1.84i $ {}^{40} $ Ca3 −53.02 −53.03 3.76-0.387i 3.76-0.387i 3.76-0.387i $ {}^{48} $ Ca3 −181.0 −180.9 1.61-0.0408i 1.61-0.0406i 1.61-0.0408i $ {}^{56} $ Ni4 −30.93 −30.98 7.46-0.951i 7.46-0.954i 7.46-0.951i Table 2. The complex resonant energy
$ E_{res} $ and scattering length$ a_l $ computed with CMR-CLD and R-matrix method. Here, the angular momentum l supports the first resonant state.$ a_{l}^{CMR-CLD+ERE} $ and$ E_{res}^{CMR-CLD+ERE} $ denote the scattering length and resonant energy obtained from CMR-CLD plus effective range expansion, respectively.$ E_{res}^{CMR} $ is the result calculated from pure CMR. Here, "pure" refers to extracting resonant energies solely from the momentum spectrum obtained from CMR. To ensure reliable resonance extraction, we have carefully selected an appropriate integral contour.$ a_{l}^{R-matrix} $ and$ E_{res}^{R-matrix} $ denote the scattering length and resonant energy obtained from R-matrix method, respectively. In the R-matrix calculations, the channel radius is set to be around 20 fm and about 50 Gaussian-Legendre grid points are used.Hypernuclei a (fm) R (fm) $ V_0 $ (MeV)$ {}^{17}_{\Lambda} $ O0.4264 3.103 −28.75 $ {}^{40}_{\Lambda} $ Ca0.4383 4.128 −30.46 $ {}^{48}_{\Lambda} $ Ca0.4630 4.388 −30.46 $ {}^{56}_{\Lambda} $ Ni0.4438 4.647 −30.18 Table 1. Parameters of the Woods-Saxon potentials. These parameters are derived by fitting the effective interaction obtained from the SHF method with the Woods-Saxon potential. In practical calculations, these parameters are used in the region where
$ r>r_{max} $ .The first column represents the nuclear core, the second column denotes the angular momentum l which supports the first resonant state, the third column indicates the scattering length
$ a_l $ obtained from CMR-CLD with effective range expansion, the fourth column displays the scattering length obtained from the R-matrix method, the fifth column shows the complex resonant energy$ E_{res} $ obtained from the R-matrix method and the sixth column shows$ E_{res} $ obtained from CMR-CLD plus effective range expansion, and$ E_{res} $ obtained by CMR are listed in the last column.Generally speaking, the positive or negative phase shift at a certain scattering energy indicates whether the interaction is attractive or repulsive. Due to the connection between phase shift
$ \delta_l(k) $ and scattering length$ a_l $ , namely$ \lim\limits_{k\rightarrow 0}\dfrac{k^{2l+1}}{\tan(\delta_l(k))}=-\dfrac{1}{a_l} $ , a negative scattering length corresponds to a positive scattering phase shift near zero energy, which indicates an attractive effect in this energy region, while a positive scattering length reflects a repulsive effect on the contrary. Moreover, qualitatively speaking, the larger (in absolute value) the scattering length, the stronger the attractive (or repulsive) effect near zero energy. This can also be partially reflected from Table 2: the larger absolute values of the scattering length correspond to smaller decay widths, namely indicating stronger attractive effect between Λ hyperon and nuclear core. However, it should be noted that such comparison should be based on the condition of equal angular momentum and thus the magnitude of scattering lengths can not be directly compared for different angular momentum cases.From Table 2, it is evident that the complex resonant energy obtained through CMR closely matches those obtained from the conventional R-matrix method. Additionally, the scattering length and complex resonant energy extracted through effective range expansion also exhibit good agreement with results obtained from the R-matrix method. These numerical results validate the reliability and accuracy of the CMR-CLD method in dealing with resonance problems for single hyperon hypernuclei in the case of spherical potential.
From the numerical results, we can find that for the single Λ hypernuclei considered, the decay width is approximately in the MeV range, which is much larger than the decay width derived from the weak decay lifetime of hypernucleus. Therefore, this indicates that the time involved in the emission process within the hypernucleus is much shorter than its weak decay lifetime and also much shorter than the half-life of a free Λ hyperon. These results suggest that even if the weak decay lifetime of the hypernucleus is pretty short, the emission process of the hyperon should also be considered and investigated.
Resonance of hypernuclei with complex momentum representation
- Received Date: 2024-09-03
- Available Online: 2025-04-01
Abstract: By combining the Skyrme-Hartree-Fock method with complex momentum representation (CMR), the resonant states of