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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 $^4$He$+^8$Be and $^4$He$+^{10}$Be 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 $^4$He$+^8$Be, the linear-chain states evolve to a triangular configuration and then to a more compact shape. In contrast, for $^4$He$+^{10}$Be, 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.
The soliton existence in sub-atomic many-nucleon systems is discussed. In many nucleon dynamics represented by the nuclear time-dependent density functional formalism, much attention is paid to energy and mass dependence of the soliton existence. In
The stability of the linear chain structure of three $alpha$ clusters for $^{12}$C against the bending and fission is investigated in the cranking covariant density functional theory, in which the equation of motion is solved on a 3D lattice with the
Time-dependent covariant density functional theory with the successful density functional PCPK1 is developed in a three-dimensional coordinate space without any symmetry restrictions, and benchmark calculations for the 16O + 16O reaction are performe
We present the basic concepts and recent developments in the time-dependent density functional theory (TDDFT) for describing nuclear dynamics at low energy. The symmetry breaking is inherent in nuclear energy density functionals (EDFs), which provide
We present an implementation of time-dependent density-functional theory (TDDFT) in the linear response formalism enabling the calculation of low energy optical absorption spectra for large molecules and nanostructures. The method avoids any explicit