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Molecular hydrogen allows cooling in primordial gas, facilitating its collapse into Population III stars within primordial halos. Lyman–Werner (LW) radiation from these stars can escape the halo and delay further star formation by destroying H2 in other halos. As cosmological simulations show that increasing the background LW field strength increases the average halo mass required for star formation, we perform follow-up simulations of selected halos to investigate the knock-on effects this has on the Population III IMF. We follow 5 halos for each of the J21  = 0, 0.01, and 0.1 LW field strengths, resolving the pre-stellar core density of 10−6 g cm−3 (1018 cm−3) before inserting sink particles and following the fragmentation behaviour for hundreds of years further. We find that the mass accreted onto sinks by the end of the simulations is proportional to the mass within the ∼10−2 pc molecular core, which is not correlated to the initial mass of the halo. As such, the IMFs for masses above the brown dwarf limit show little dependence on the LW strength, although they do show variance in the number of low-mass clumps formed. As the range of background LW field strengths tested here covers the most likely values from literature, we conclude that the IMF for so-called Pop III.2 stars is not significantly different from the initial population of Pop III.1 stars. The primordial IMF therefore likely remains unchanged until the formation of the next generation of Population II stars.

 

Neutron-capture cross sections of neutron-rich nuclei are calculated using a Hauser–Feshbach model when direct experimental cross sections cannot be obtained. A number of codes to perform these calculations exist, and each makes different assumptions about the underlying nuclear physics. We investigated the systematic uncertainty associated with the choice of Hauser-Feshbach code used to calculate the neutron-capture cross section of a short-lived nucleus. The neutron-capture cross section for$$^{73}\hbox {Zn}$$${}^{73}\text{Zn}$(n,$$\gamma $$$\gamma$)$$^{74}\hbox {Zn}$$${}^{74}\text{Zn}$was calculated using three Hauser-Feshbach statistical model codes: TALYS, CoH, and EMPIRE. The calculation was first performed without any changes to the default settings in each code. Then an experimentally obtained nuclear level density (NLD) and$$\gamma $$$\gamma$-ray strength function ($$\gamma \hbox {SF}$$$\gamma \text{SF}$) were included. Finally, the nuclear structure information was made consistent across the codes. The neutron-capture cross sections obtained from the three codes are in good agreement after including the experimentally obtained NLD and$$\gamma \hbox {SF}$$$\gamma \text{SF}$, accounting for differences in the underlying nuclear reaction models, and enforcing consistent approximations for unknown nuclear data. It is possible to use consistent inputs and nuclear physics to reduce the differences in the calculated neutron-capture cross section from different Hauser-Feshbach codes. However, ensuring the treatment of the input of experimental data and other nuclear physics are similar across multiple codes requires a careful investigation. For this reason, more complete documentation of the inputs and physics chosen is important.

 

Abstract Fully internal and motional state controlled and individually manipulable polar molecules are desirable for many quantum science applications leveraging the rich state space and intrinsic interactions of molecules. While prior efforts at assembling molecules from their constituent atoms individually trapped in optical tweezers achieved such a goal for exactly one molecule (Zhang J T et al 2020 Phys. Rev. Lett. 124 253401; Cairncross W B et al 2021 Phys. Rev. Lett. 126 123402; He X et al 2020 Science 370 331–5), here we extend the technique to an array of five molecules, unlocking the ability to study molecular interactions. We detail the technical challenges and solutions inherent in scaling this system up. With parallel preparation and control of multiple molecules in hand, this platform now serves as a starting point to harness the vast resources and long-range dipolar interactions of molecules.