No Arabic abstract
We develop a first principles, microscopic theory of impurity atom scattering from inhomogeneous quantum liquids such as adsorbed films, slabs, or clusters of He-4. The theory is built upon a quantitative, microscopic description of the ground state of both the host liquid as well as the impurity atom. Dynamic effects are treated by allowing all ground-state correlation functions to be time-dependent. Our description includes both the elastic and inelastic coupling of impurity motion to the excitations of the host liquid. As a specific example, we study the scattering of He-3 atoms from adsorbed He-4 films. We examine the dependence of ``quantum reflection on the substrate, and the consequences of impurity bound states, resonances, and background excitations for scattering properties. A thorough analysis of the theoretical approach and the physical circumstances point towards the essential role played by inelastic processes which determine almost exclusively the reflection probabilities. The coupling to impurity resonances within the film leads to a visible dependence of the reflection coefficient on the direction of the impinging particle.
Four light-mass nuclei are considered by an effective two-body clusterisation method; $^6$Li as $^2$H$+^4$He, $^7$Li as $^3$H$+^4$He, $^7$Be as $^3$He$+^4$He, and $^8$Be as $^4$He$+^4$He. The low-energy spectrum of each is determined from single-channel Lippmann-Schwinger equations, as are low-energy elastic scattering cross sections for the $^2$H$+^4$He system. These are presented at many angles and energies for which there are data. While some of these systems may be more fully described by many-body theories, this work establishes that a large amount of data may be explained by these two-body clusterisations.
Mixed $^3$He-$^4$He droplets created by hydrodynamic instability of a cryogenic fluid-jet may acquire angular momentum during their passage through the nozzle of the experimental apparatus. These free-standing droplets cool down to very low temperatures undergoing isotopic segregation, developing a nearly pure $^3$He crust surrounding a very $^4$He-rich superfluid core. Here, the stability and appearance of rotating mixed helium droplets are investigated using Density Functional Theory for an isotopic composition that highlights, with some marked exceptions related to the existence of the superfluid inner core, the analogies with viscous rotating droplets.
We use the next-to-leading-order (NLO) amplitude in an effective field theory (EFT) for ${}^3$He + ${}^4$He $rightarrow {}^7$Be + $gamma$ to perform the extrapolation of higher-energy data to solar energies. At this order the EFT describes the capture process using an s-wave scattering length and effective range, the asymptotic behavior of $^7$Be and its excited state, and short-distance contributions to the E1 capture amplitude. We use a Bayesian analysis to infer the multi-dimensional posterior of these parameters from capture data below 2 MeV. The total $S$-factor $S(0)= 0.578^{+0.015}_{-0.016}$ keV b at 68% degree of belief. We also find significant constraints on $^3$He-$^4$He scattering parameters.
We predict $s-$wave elastic cross-sections $sigma$ for low-energy atom-molecule collisions with kinetic energies up to 40 mK, for the $^4$He collision with weakly bound diatomic molecules formed by $^4$He with $^7$Li, $^6$Li and $^{23}$Na. Our scattering calculations are performed by using diatomic and triatomic molecular binding energies obtained from several available realistic models as input in a renormalized zero-range model, as well as a finite-range one-term separable potential in order to quantify the relevance of range corrections to our predictions. Of particular relevance for possible experimental realization, we show the occurrence of a zero in $sigma$ for the collision of cold $^4$He on $^4$He$-^{23}$Na molecule below 20 mK. Also our results for the elastic collision $^4$He on $^4$He$-^{6,7}$Li molecules suggest that $sigma$ varies considerably for the realistic models studied. As the chosen molecules are weakly bound and the scattering energies are very low, our results are interpreted on the light of the Efimov physics, which explains the model independent and robustness of our predictions, despite some sensitivity on the potential range.
We present systematic results, based on density functional calculations, for the structure and energetics of $^3$He and $^4$He nanodroplets doped with alkaline earth atoms. We predict that alkaline earth atoms from Mg to Ba go to the center of $^3$He drops, whereas Ca, Sr, and Ba reside in a deep dimple at the surface of $^4$He drops, and Mg is at their center. For Ca and Sr, the structure of the dimples is shown to be very sensitive to the He-alkaline earth pair potentials used in the calculations. The $5s5pleftarrow5s^2$ transition of strontium atoms attached to helium nanodroplets of either isotope has been probed in absorption experiments. The spectra show that strontium is solvated inside $^3$He nanodroplets, supporting the calculations. In the light of our findings, we emphasize the relevance of the heavier alkaline earth atoms for analyzing mixed $^3$He-$^4$He nanodroplets, and in particular, we suggest their use to experimentally probe the $^3$He-$^4$He interface.