Integral neutronics experiments have been investigated at Institute of Modern Physics, Chinese Academy of Sciences (IMP, CAS) in order to validate evaluated nuclear data related to the design of Chinese Initiative Accelerator Driven Systems (CIADS).
In present paper, the accuracy of evaluated nuclear data for Tungsten has been examined by comparing measured leakage neutron spectra with calculated ones. Leakage neutron spectra from the irradiation of D-T neutrons on Tungsten slab sample were experimentally measured at 60$^{circ}$ and 120$^{circ}$ by using a time-of-flight method. Theoretical calculations are carried out by Monte Carlo neutron transport code MCNP-4C with evaluated nuclear data of the ADS-2.0, ENDF/B-VII.0, ENDF/B-VII.1, JENDL-4.0 and CENDL-3.1 libraries. From the comparisons, it is found that the calculations with ADS-2.0 and ENDF/B-VII.1 give good agreements with the experiments in the whole energy regions at 60$^{circ}$, while a large discrepancy is observed at 120$^{circ}$ in the elastic scattering peak, caused by a slight difference in the oscillation pattern of the elastic angular distribution at angles larger than 20$^{circ}$. However, the calculated spectra using data from ENDF/B-VII.0, JENDL-4.0 and CENDL-3.1 libraries showed larger discrepancies with the measured ones, especially around 8.5-13.5 MeV. Further studies are presented for these disagreements.
We report on the local electronic structure of oxygen incorporated FeTe and FeSe films and how this relates to superconductivity observed in these films. In the case of FeTe, intially grown films are measured to be non-superconducting, but become sup
erconducting following oxygen incorporation. In FeSe the opposite happens, initially grown films are measured to be superconducting, but experience a quenching of superconductivity following oxygen incorporation. Total Fluorescence Yield (TFY) X-ray absorption experiments show that oxygen incorporation changes the initial Fe valence state in both the initially grown FeTe and FeSe films to mainly Fe3+ in the oxygen incorporated films. In contrast we observe that while Te moves to a mixed Te0/Te4+ valence state, the Se always remains Se0. This work highlights how different responses of the electronic structure by the respective chalcogenides to oxidation could be related to the mechanisms which are inducing superconductivity in FeTe and quenching superconductivity in FeSe.
