TY - DATA T1 - AXE gain curves (a) and AXE (full) and fluorescence (protect {----}) spectra at z = 5 mm computed for vibrational initial states νg = 0 (b) and νg = 2 (c) at the C 1s−1 → X lasing transition, 〈cos 2ζ〉 = 0.64 PY - 2013/08/13 AU - Victor Kimberg AU - Song Bin Zhang AU - Nina Rohringer UR - https://iop.figshare.com/articles/figure/_AXE_gain_curves_a_and_AXE_span_class_inline_eqn_span_class_tex_span_class_texImage_img_src_http_ej_/1012422 DO - 10.6084/m9.figshare.1012422.v1 L4 - https://ndownloader.figshare.com/files/1480244 KW - CO molecule KW - moment polarization KW - radiation KW - C 1 KW - lasing efficiency KW - vibrational quantum state KW - fluorescence band KW - emission KW - core ionization KW - pulse duration KW - pulse parameters KW - 30 fs KW - xfel KW - transition KW - source KW - alignment KW - axe KW - C K KW - Atomic Physics KW - Molecular Physics N2 - Figure 7. AXE gain curves (a) and AXE (\full) and fluorescence (\protect {----}) spectra at z = 5 mm computed for vibrational initial states νg = 0 (b) and νg = 2 (c) at the C 1s−1 → X lasing transition, 〈cos 2ζ〉 = 0.64. The XFEL pump pulse parameters are the same as in figure 5. Abstract We theoretically demonstrate the feasibility of x-ray lasing in the CO molecule by the core ionization of the C K- and O K-shell by x-ray free-electron laser sources. Our numerical simulations are based on the solution of generalized Maxwell–Bloch equations, accounting for the electronic and nuclear degrees of freedom. The amplified x-ray emission pulses have an extremely narrow linewidth of about 0.1 eV and a pulse duration shorter than 30 fs. We compare x-ray lasing transitions to the three lowest electronic states of singly ionized CO. The dependence of the lasing efficiency on the spectral width of the x-ray fluorescence band, value and orientation of the electronic transition dipole moment, lifetime of the core-excited state and the duration of the pump pulse is analysed. Using a pre-aligned molecular ensemble substantially increases the amplified emission. Moreover, by controlling the molecular alignment and thereby the alignment of the transition dipole moment polarization, the control of the emitted x-ray radiation is achievable. Preparing the initial vibrational quantum state, the x-ray emission frequency can be tuned within the fluorescence band. The present scheme is applicable to other diatomic systems, thereby extending the spectral range of coherent x-ray radiation sources based on stimulated x-ray emission on bound transitions. ER -