Abstract
The time-dependent covariant density functional theory in 3D lattice space has been developed and applied to investigate the microscopic dynamics of the linear-chain cluster states for carbon isotopes in the reactions HeBe and HeBe without any symmetry assumptions. By examining the density distribution and its time evolutions, the structure and dynamics of the linear-chain states are analyzed, and the quasiperiodic oscillations of the clusters are revealed. For HeBe, the linear-chain states evolve to a triangular configuration and then to a more compact shape. In contrast, for HeBe, the lifetime of the linear-chain states is much more prolonged due to the dynamical isospin effects by the valence neutrons which slow down the longitudinal oscillations of the clusters and persist the linear-chain states. The dependence of the linear chain survival time and dynamical isospin effects on impact parameters have been illustrated as well.
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