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The dispersive optical-model is applied to transfer reactions. A systematic study of $(d,p)$ reactions on closed-shell nuclei using the finite-range adiabatic reaction model is performed at several beam energies and results are compared to data as well as to predictions using a standard global optical-potential. Overall, we find that the dispersive optical-model is able to describe the angular distributions as well as or better than the global parameterization. In addition, it also constrains the overlap function. Spectroscopic factors extracted using the dispersive optical-model are generally lower than those using standard parameters, exhibit a reduced dependence on beam energy, and are more in line with results obtained from $(e,ep)$ measurements.
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The molecular algebraic model based on three and four alpha clusters is used to describe the inelastic scattering of alpha particles populating low-lying states in $^{12}$C and $^{16}$O. Optical potentials and inelastic formfactors are obtained by folding densities and transition densities obtained within the molecular model. One-step and multi-step processes can be included in the reaction mechanism calculation. In spite of the simplicity of the approach the molecular model with rotations and vibrations provides a reliable description of reactions where $alpha$-cluster degrees of freedom are involved and good results are obtained for the excitation of several low-lying states. Within the same model we briefly discuss the expected selection rules for the $alpha$-transfer reactions from $^{12}$C and $^{16}$O.
We provide a summary of new developments in the area of direct reaction theory with a particular focus on one-nucleon transfer reactions. We provide a status of the methods available for describing (d,p) reactions. We discuss the effects of nonlocality in the optical potential in transfer reactions. The results of a purely phenomenological potential and the optical potential obtained from the dispersive optical model are compared; both point toward the importance of including nonlocality in transfer reactions explicitly. Given the large ambiguities associated with optical potentials, we discuss some new developments toward the quantification of this uncertainty. We conclude with some general comments and a brief account of new advances that are in the pipeline.
Nucleon-knockout reactions on proton targets (p, pN ) have experienced a renewed interest due to the availability of inverse-kinematics experiment with exotic nuclei. Various theoretical descriptions have been used to describe these reactions, such as the Distorted-Wave Impulse Approximation (DWIA), the Faddeev-type formalism and the Transfer to the Continuum method. Our goal is to benchmark the observables computed with the Faddeev and Transfer to the Continuum formalisms in the intermediate energy regime relevant for the experimental (p, pn) and (p, 2p) studies. In this paper, we analyze the 11 Be(p,pn)10Be reaction for different beam energies, binding energies and orbital quantum numbers with both formalisms to assess their agreement for different observables. We obtain a good agreement in all cases considered, within 10%, when the input potentials are taken consistently and realistically.
An improved description of single neutron stripping from $^{34,36,46}$Ar beams at 33 MeV/nucleon by a hydrogen target is presented and the dependence on the neutron-proton asymmetry of the spectroscopic factors is further investigated. A finite range adiabatic model is used in the analysis and compared to previous zero range and local energy approximations. Full three-body Faddeev calculations are performed to estimate the error in the reaction theory. In addition, errors from the optical potentials are also evaluated. From our new spectroscopic factors extracted from transfer, it is possible to corroborate the neutron-proton asymmetry dependence reported from knockout measurements.
Both ($e$,$ep$) and ($p$,$2p$) reactions have been performed to study the proton single-particle character of nuclear states with its related spectroscopic factor. Recently, the dispersive optical model (DOM) was applied to the ($e$,$ep$) analysis revealing that the traditional treatment of the single-particle overlap function, distorted waves, and nonlocality must be further improved to achieve quantitative nuclear spectroscopy. We apply the DOM wave functions to the traditional ($p$,$2p$) analysis and investigate the consistency of the DOM spectroscopic factor that describes the ($e$,$ep$) cross section with the result of the ($p$,$2p$) analysis. Additionally, we make a comparison with a phenomenological single-particle wave function and optical potential. Uncertainty arising from a choice of $p$-$p$ interaction is also investigated. We implement the DOM wave functions to the distorted wave impulse approximation (DWIA) framework for ($p$,$2p$) reactions. DOM + DWIA analysis on $^{40}$Ca($p$,$2p$)$^{39}$K data generates a proton $0d_{3/2}$ spectroscopic factor of 0.560, which is meaningfully smaller than the DOM value of 0.71 shown to be consistent with the ($e$,$ep$) analysis. Uncertainties arising from choices of single-particle wave function, optical potential, and $p$-$p$ interaction do not explain this inconsistency. The inconsistency in the spectroscopic factor suggests there is urgent need for improving the description of $p$-$p$ scattering in a nucleus and the resulting in-medium interaction with corresponding implications for the analysis of this reaction in inverse kinematics.
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