TY - JOUR
T1 - Nuclear resonant scattering experiment with fast time response
T2 - Photonuclear excitation of Hg 201
AU - Yoshimi, A.
AU - Hara, H.
AU - Hiraki, T.
AU - Kasamatsu, Y.
AU - Kitao, S.
AU - Kobayashi, Y.
AU - Konashi, K.
AU - Masuda, R.
AU - Masuda, T.
AU - Miyamoto, Y.
AU - Okai, K.
AU - Okubo, S.
AU - Ozaki, R.
AU - Sasao, N.
AU - Sato, O.
AU - Seto, M.
AU - Schumm, T.
AU - Shigekawa, Y.
AU - Stellmer, S.
AU - Suzuki, K.
AU - Uetake, S.
AU - Watanabe, M.
AU - Yamaguchi, A.
AU - Yasuda, Y.
AU - Yoda, Y.
AU - Yoshimura, K.
AU - Yoshimura, M.
N1 - Publisher Copyright:
© 2018 American Physical Society.
PY - 2018/2/8
Y1 - 2018/2/8
N2 - Nuclear resonant excitation and detection of its decay signal for the 26.27-keV level of Hg201 is demonstrated with high-brilliance synchrotron radiation (SR) and a fast x-ray detector system. This SR-based photonuclear excitation scheme, known as nuclear resonant scattering (NRS) in the field of materials science, is also useful for investigating nuclear properties, such as the half-lives and radiative widths of excited nuclear levels. To date, because of the limited time response of the x-ray detector, the nuclear levels to which this method could be applied have been limited to the one whose half-lives are longer than ∼1 ns. The faster time response of the NRS measurement makes possible NRS experiments on nuclear levels with much shorter half-lives. We have fabricated an x-ray detector system that has a time resolution of 56 ps and a shorter tail function than that reported previously. With the implemented detector system, the NRS signal of the 26.27-keV state of Hg201 could be clearly discriminated from the electronic scattering signal at an elapsed time of 1 ns after the SR pulse. The half-life of the state was determined as 629 ± 18 ps, which has better precision by a factor of three compared with that reported to date obtained from nuclear decay spectroscopy.
AB - Nuclear resonant excitation and detection of its decay signal for the 26.27-keV level of Hg201 is demonstrated with high-brilliance synchrotron radiation (SR) and a fast x-ray detector system. This SR-based photonuclear excitation scheme, known as nuclear resonant scattering (NRS) in the field of materials science, is also useful for investigating nuclear properties, such as the half-lives and radiative widths of excited nuclear levels. To date, because of the limited time response of the x-ray detector, the nuclear levels to which this method could be applied have been limited to the one whose half-lives are longer than ∼1 ns. The faster time response of the NRS measurement makes possible NRS experiments on nuclear levels with much shorter half-lives. We have fabricated an x-ray detector system that has a time resolution of 56 ps and a shorter tail function than that reported previously. With the implemented detector system, the NRS signal of the 26.27-keV state of Hg201 could be clearly discriminated from the electronic scattering signal at an elapsed time of 1 ns after the SR pulse. The half-life of the state was determined as 629 ± 18 ps, which has better precision by a factor of three compared with that reported to date obtained from nuclear decay spectroscopy.
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U2 - 10.1103/PhysRevC.97.024607
DO - 10.1103/PhysRevC.97.024607
M3 - Article
AN - SCOPUS:85042069932
SN - 2469-9985
VL - 97
JO - Physical Review C
JF - Physical Review C
IS - 2
M1 - 024607
ER -