Anharmonic resonance absorption of short laser pulses in clusters: A molecular dynamics simulation study

Abstract

Linear resonance (LR) absorption of an intense 800~nm laser light in a nano-cluster requires a long laser pulse > 100~fs when Mie-plasma frequency ($\omegaMie$) of electrons in the expanding cluster matches the laser frequency~($\omega$). For a short duration of the pulse the condition for LR is not satisfied. In this case, it was shown by a model and particle-in-cell (PIC) simulations [Phys. Rev. Lett. 96, 123401 (2006)] that electrons absorb laser energy by anharmonic resonance (AHR) when the position-dependent frequency $\Omega[r(t)]$ of an electron in the self-consistent anharmonic potential of the cluster satisfies $\Omega[r(t)]=\omega$. However, AHR remains to be a debate and still obscure in multi-particle plasma simulations. Here, we identify AHR mechanism in a laser driven cluster using molecular dynamics (MD) simulations. By analyzing the trajectory of each MD electron and extracting its $\Omega[r(t)]$ in the self-generated anharmonic plasma potential it is found that electron is outer ionized {\em only} when AHR is met. An anharmonic oscillator model, introduced here, brings out most of the features of MD electrons while passing the AHR. Thus, we not only bridge the gap between PIC simulations, analytical models and MD calculations for the first time but also unequivocally prove that AHR processes is a universal dominant collisionless mechanism of absorption in the short pulse regime or in the early time of longer pulses in clusters.