We experimentally investigated the rotationally resolved polarization characteristics of N$_2^+$ lasing at 391 and 428 nm using a pump-seed scheme. By varying the relative angle between the linear polarizations of the pump and seed, it is found that the polarizations of the P and R branches of 391-nm lasing are counter-rotated. By contrast, both branches of 428-nm lasing remain polarized along the pump. The origin of the puzzled abnormal polarization characteristics is found based on a complete physical model that simultaneously includes the transient photoionization and the subsequent coupling among the electronic, vibrational and rotational quantum states of ions.It suggests that the cascaded resonant Raman processes following ionization create negative coherence between the rotational states of $J$ and $J$+2 in the ionic ground state X$^2Σ_g^+(ν=0)$, which leads to mirror-symmetrical polarization for the P and R branches of 391-nm lasing. Both the experiment and theory indicate that the demonstrated rotational coherence plays an extremely pivotal role in clarifying the gain mechanism of N$_2^+$ lasing and opens up the route toward quantum optics under ultrafast strong fields.
Delayed cavity-free forward lasing at the wavelengths of 391 and 428 nm was observed in recent experiments in air or pure nitrogen pumped with an intense femtosecond laser pulse at wavelength of 800~nm. The mechanism responsible for the lasing is highly controversial. In this article we explain the delayed emission by the presence of long-lived polarizations coupling simultaneously ground state X$^2Σ_g^+$ to states A$^2Π_u$ and B$^2Σ_u^+$ of singly ionized nitrogen molecules N$_2^+$. Ionization of neutral nitrogen molecules in a strong laser field and subsequent ion excitation are described by…
Singly ionized nitrogen molecules in ambient air pumped by near-infrared femtosecond laser give rise to superradiant emission. Here we demonstrate coherent control of this superradiance by injecting a pair of resonant seeding pulses inside the nitrogen gas plasma. Strong modulation of the 391.4 nm superradiance with a period of 1.3 fs is observed when the delay between the two seeding pulses are finely tuned, pinpointing the essential role of macroscopic coherence in this lasing process. Based on this time-resolved method, the complex temporal evolution of the macroscopic coherence between two…
We simulate the pump-probe experiments of lasing in molecular nitrogen ions with particular interest on the effects of rotational wave-packet dynamics. Our computations demonstrate that the coherent preparation of rotational wave packets in N$_2^+$ by an intense short non-resonant pulse results in a modulation of the subsequent emission from $B^2Σ_u^+ \rightarrow X^2Σ_g^+$ transitions induced by a resonant seed pulse. We model the dynamics of such pumping and emission using density matrix theory to describe the N$_2^+$ dynamics and the Maxwell wave equation to model the seed pulse propagation.…
In standard lasers, light amplification requires population inversion between an upper and a lower state to break the reciprocity between absorption and stimulated emission. However, in a medium prepared in a specific superposition state, quantum interference may fully suppress absorption while leaving stimulated emission intact, opening the possibility of lasing without inversion. Here we show that lasing without inversion arises naturally during propagation of intense femtosecond laser pulses in air. It is triggered by the combination of molecular ionization and molecular alignment, both una…
Since the advent of x-ray free-electron lasers (XFELs), considerable efforts have been devoted to achieve x-ray pulses with better temporal coherence. Here, we put forward a scheme to generate fully coherent x-ray lasers (XRLs) based on population inversion in highly charged ions (HCIs), created by fast inner-shell photoionization using XFEL pulses in a laser-produced plasma. Numerical simulations show that one can obtain high-intensity, femtosecond x-ray pulses of relative bandwidths $Δω/ω=10^{-5}$ - $10^{-7}$ by orders of magnitude narrower than in XFEL pulses for wavelengths down to the sub…
We report the fluorescence emission which is driven by femtosecond laser pulses with a repetition rate of 100 MHz and a center wavelength of 1040 nm in a nitrogen gas jet. The experiment is performed in a femtosecond enhancement cavity coupled with high repetition rate laser for the first time to the best of our knowledge. In contrast to previous observation at low repetition rate with a nitrogen gas jet, where the 391 nm radiation was observed but the 337 nm emission was missing, the 337 nm emission is 3 times stronger than the 391 nm emission in our experiment. By examining the dependence of…
Ionization-free femtosecond UV pulse filamentation resulting from non-perturbative Kerr effect saturation due to transient photoexcitation of molecules
P.N. Lebedev Physical Institute of the Russian Academy of Sciences（俄罗斯科学院列别杰夫物理研究所）
Imaging changes in molecular geometries on their natural femtosecond timescale with sub-Angstrom spatial precision is one of the critical challenges in the chemical sciences, since the nuclear geometry changes determine the molecular reactivity. For photoexcited molecules, the nuclear dynamics determine the photoenergy conversion path and efficiency. We performed a gas-phase electron diffraction experiment using Megaelectronvolt (MeV) electrons, where we captured the rotational wavepacket dynamics of nonadiabatically laser-aligned nitrogen molecules. We achieved an unprecedented combination of…
The capability of generating two intense, femtosecond x-ray pulses with controlled time delay opens the possibility of performing time-resolved experiments for x-ray induced phenomena. We have applied this capability to study the photoinduced dynamics in diatomic molecules. In molecules composed of low-Z elements, \textit{K}-shell ionization creates a core-hole state in which the main decay mode is an Auger process involving two electrons in the valence shell. After Auger decay, the nuclear wavepackets of the transient two-valence-hole states continue evolving on the femtosecond timescale, lea…
Photoinduced quantum dynamics in molecules have hierarchical temporal structures with different energy scales that are associated with electron and nuclear motions. Femtosecond-to-attosecond transient absorption spectroscopy (TAS) using high-harmonic generation (HHG) with a photon energy below 300 eV has been a powerful tool to observe such electron and nuclear dynamics in a table-top manner. However, comprehensive measurements of the electronic, vibrational, and rotational molecular dynamics have not yet been achieved. Here, we demonstrate HHG-based TAS at the nitrogen K-edge (400 eV) for the…
We investigate experimentally the effect of quantum resonance in the rotational excitation of the simplest quantum rotor - a diatomic molecule. By using the techniques of high-resolution femtosecond pulse shaping and rotational state-resolved detection, we measure directly the amount of energy absorbed by molecules interacting with a periodic train of laser pulses, and study its dependence on the train period. We show that the energy transfer is significantly enhanced at quantum resonance, and use this effect for demonstrating selective rotational excitation of two nitrogen isotopologues, $ ^{…
