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The Auxiliary Field Diffusion Monte Carlo method has been applied to simulate droplets of 7 and 8 neutrons. Results for realistic nucleon-nucleon interactions, which include tensor, spin--orbit and three--body forces, plus a standard one--body confining potential, have been compared with analogous calculations obtained with Greens Function Monte Carlo methods. We have studied the dependence of the binding energy, the one--body density and the spin--orbit splittings of $^7n$ on the depth of the confining potential. The results obtained show an overall agreement between the two quantum Monte Carlo methods, although there persist differences in the evaluation of spin--orbit forces, as previously indicated by bulk neutron matter calculations. Energy density functional models, largely used in astrophysical applications, seem to provide results significantly different from those of quantum simulations. Given its scaling behavior in the number of nucleons, the Auxiliary Field Diffusion Monte Carlo method seems to be one of the best candidate to perform {sl ab initio} calculations on neutron rich nuclei.
We present variational Monte Carlo calculations of the neutron matter equation of state using chiral nuclear forces. The ground-state wavefunction of neutron matter, containing non-perturbative many-body correlations, is obtained from auxiliary-field
Zirconia (zirconium dioxide) and hafnia (hafnium dioxide) are binary oxides used in a range of applications. Because zirconium and hafnium are chemically equivalent, they have three similar polymorphs, and it is important to understand the properties
We analyze recently-measured total reaction cross sections for 24-38Mg isotopes incident on 12C targets at 240 MeV/nucleon by using the folding model and antisymmetrized molecular dynamics(AMD). The folding model well reproduces the measured reaction
Quantum Monte Carlo (QMC) methods are some of the most accurate methods for simulating correlated electronic systems. We investigate the compatibility, strengths and weaknesses of two such methods, namely, diffusion Monte Carlo (DMC) and auxiliary-fi
Spin crossover molecules have recently emerged as a family of compounds potentially useful for implementing molecular spintronics devices. The calculations of the electronic properties of such molecules is a formidable theoretical challenge as one ha