اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدDirectional spinning of molecules with sequences of femtosecond pulses
171
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We present an analysis of two experimental approaches to controlling the directionality of molecular rotation with ultrashort laser pulses. The two methods are based on the molecular interaction with either a pair of pulses (a double kick scheme) or a longer pulse sequence (a chiral pulse train scheme). In both cases, rotational control is achieved by varying the polarization of and the time delay between the consecutive laser pulses. Using the technique of polarization sensitive resonance-enhanced multi-photon ionization, we show that both methods produce significant rotational directionality. We demonstrate that increasing the number of excitation pulses supplements the ability to control the sense of molecular rotation with quantum state selectivity, i.e. predominant excitation of a single rotational state. We also demonstrate the ability of both techniques to generate counter-rotation of molecular nuclear spin isomers (here, ortho- and para-nitrogen) and molecular isotopologues (here, 14N_2 and 15N_2).
قيم البحث
اقرأ أيضاً
We discuss finite-difference time-domain simulations of femtosecond pulses interacting with silver nanowires and nanoparticles. We show how localized hot spots near the metal surfaces can be generated and controlled in a spatiotemporal manner. The co
ntrol is made possible by chirping the pulses such that the effective frequency passes through surface plasmon resonances associated with different spatial regions of the nanostructure over the course of time. The response of such nanostructures to chirped pulses could provide a novel means of encoding or decoding optical signals.
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 nitrog
en 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 involved energy levels has been experimentally revealed, which is found to last for around 10 picoseconds in the low gas pressure range. These observations provide a new level of control on the air lasing based on nitrogen ions, which can find potential applications in optical remote sensing.
The ongoing development of intense high-harmonic generation (HHG) sources has recently enabled highly nonlinear ionization of atoms by the absorption of at least 10 extreme-ultraviolet (XUV) photons within a single atom [Senfftleben textit{et al.}, a
rXiv1911.01375]. Here we investigate the role that reshaping of the fundamental, few-cycle, near-infrared (NIR) driving laser within the 30-cm-long HHG Xe medium plays in the generation of the intense HHG pulses. Using an incident NIR intensity that is higher than what is required for phase-matched HHG, signatures of reshaping are found by measuring the NIR blueshift and the fluorescence from the HHG medium along the propagation axis. These results are well reproduced by numerical calculations that show temporal compression of the NIR pulses in the HHG medium. The simulations predict that after refocusing an XUV beam waist radius of 320 nm and a clean attosecond pulse train can be obtained in the focal plane, with an estimated XUV peak intensity of 9x10^15 W/cm^2. Our results show that XUV intensities that were previously only available at large-scale facilities can now be obtained using moderately powerful table-top light sources.
We exploit inverse Raman scattering and solvated electron absorption to perform a quantitative characterization of the energy loss and ionization dynamics in water with tightly focused near-infrared femtosecond pulses. A comparison between experiment
al data and numerical simulations suggests that the ionization energy of water is 8 eV, rather than the commonly used value of 6.5 eV. We also introduce an equation for the Raman gain valid for ultra-short pulses that validates our experimental procedure.
The directional control of molecular dissociation with the laser electric field waveform is a paradigm and was demonstrated for a variety of molecules. In most cases, the directional control occurs via a dissociative ionization pathway. The role of l
aser-induced coupling of electronic states in the dissociating ion versus selective ionization of oriented neutral molecules, however, could not be distinguished for even small heteronuclear molecules such as CO. Here, we introduce a technique, using elliptically polarized pump and linearly polarized two-color probe pulses that unambiguously distinguishes the roles of laser-induced state coupling and selective ionization. The measured photoelectron momentum distributions governed by the light polarizations allow us to coincidently identify the ionization and dissociation from the pump and probe pulses. Directional dissociation of CO+ as a function of the relative phase of the linearly polarized two-color pulse is observed for both parallel and orthogonally oriented molecules. We find that the laser-induced coupling of various electronic states of CO+ plays an important role for the observed directional bond breaking, which is verified by quantum calculations.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
