TY - JOUR
T1 - Time-dependent Hartree-Fock plus Langevin approach for hot fusion reactions to synthesize the Z=120 superheavy element
AU - Sekizawa, K.
AU - Hagino, K.
N1 - Funding Information:
We thank K. Washiyama and Y. Aritomo for useful discussions. This work used computational resources of the HPCI system (Oakforest PACS) provided by the Joint Center for Advanced High Performance Computing (JCAHPC) through the HPCI System Research Projects (Project No. hp180080). This work also used (in part) computational resources of the Cray XC40 System at Yukawa Institute for Theoretical Physics (YITP), Kyoto Univesity and the COMA (PACS-IX) System provided by Multidisciplinary Cooperative Research Program in Center for Computational Sciences, University of Tsukuba.
PY - 2019/5/22
Y1 - 2019/5/22
N2 - We develop a novel approach to fusion reactions for synthesis of superheavy elements, which combines the time-dependent Hartree-Fock (TDHF) method with a dynamical diffusion model based on the Langevin equation. In this approach, the distance of the closest approach for the capture process is estimated within the TDHF approach, which is then plugged into the dynamical diffusion model as an initial condition. We apply this approach to hot fusion reactions leading to formation of the element Z=120, that is, the Ca48+Fm254,257, V51+Bk249, and Cr54+Cm248 reactions. Our calculations indicate that the distances of the closest approach for these systems are similar to each other and thus the difference in the probabilities of evaporation residue formation among those reaction systems originates mainly from the evaporation process, which is sensitive to the fission barrier height and the excitation energy of a compound nucleus.
AB - We develop a novel approach to fusion reactions for synthesis of superheavy elements, which combines the time-dependent Hartree-Fock (TDHF) method with a dynamical diffusion model based on the Langevin equation. In this approach, the distance of the closest approach for the capture process is estimated within the TDHF approach, which is then plugged into the dynamical diffusion model as an initial condition. We apply this approach to hot fusion reactions leading to formation of the element Z=120, that is, the Ca48+Fm254,257, V51+Bk249, and Cr54+Cm248 reactions. Our calculations indicate that the distances of the closest approach for these systems are similar to each other and thus the difference in the probabilities of evaporation residue formation among those reaction systems originates mainly from the evaporation process, which is sensitive to the fission barrier height and the excitation energy of a compound nucleus.
UR - http://www.scopus.com/inward/record.url?scp=85066440925&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85066440925&partnerID=8YFLogxK
U2 - 10.1103/PhysRevC.99.051602
DO - 10.1103/PhysRevC.99.051602
M3 - Article
AN - SCOPUS:85066440925
VL - 99
JO - Physical Review C
JF - Physical Review C
SN - 2469-9985
IS - 5
M1 - 051602
ER -