اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدMapping the Evolution of Optically-Generated Rotational Wavepackets in a Room Temperature Ensemble of D$_2$
231
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
A coherent superposition of rotational states in D$_2$ has been excited by nonresonant ultrafast (12 femtosecond) intense (2 $times$ 10$^{14}$ Wcm$^{-2}$) 800 nm laser pulses leading to impulsive dynamic alignment. Field-free evolution of this rotational wavepacket has been mapped to high temporal resolution by a time-delayed pulse, initiating rapid double ionization, which is highly sensitive to the angle of orientation of the molecular axis with respect to the polarization direction, $theta$. The detailed fractional revivals of the neutral D$_2$ wavepacket as a function of $theta$ and evolution time have been observed and modelled theoretically.
قيم البحث
اقرأ أيضاً
Dynamic Nuclear Polarization (DNP) is a powerful suite of techniques that deliver multifold signal enhancements in NMR and MRI. The generated athermal spin states can also be exploited for quantum sensing and as probes for many-body physics. Typical
DNP methods require use of cryogens, large magnetic fields, and high power microwaves, which are expensive and unwieldy. Nanodiamond particles, rich in Nitrogen-Vacancy (NV) centers, have attracted attention as alternative DNP agents because they can potentially be optically hyperpolarized at room temperature. Indeed the realization of a miniature optical nanodiamond hyperpolarizer, where 13C nuclei are optically hyperpolarized has been a longstanding goal but has been technically challenging to achieve. Here, unravelling new physics underlying an optical DNP mechanism first introduced in [Ajoy et al., Sci. Adv. 4, eaar5492 (2018)], we report the realization of such a device in an ultracompact footprint and working fully at room temperature. Instrumental requirements are very modest: low polarizing fields, extremely low optical and microwave irradiation powers, and convenient frequency ranges that enable device miniaturization. We obtain best reported optical 13C hyperpolarization in diamond particles exceeding 720 times of the thermal 7T value (0.86% bulk polarization), corresponding to a ten-million-fold gain in NMR averaging time. In addition the hyperpolarization signal can be background-suppressed by over two-orders of magnitude and retained for multiple-minute long periods. Besides compelling applications in quantum sensing, and bright-contrast MRI imaging, this work paves the way for low-cost DNP platforms that relay the 13C polarization to liquids in contact with the high surface-area particles. This will ultimately allow development of miniature quantum-assisted NMR spectrometers for chemical analysis.
We demonstrate trapping of electrons in a millimeter-sized quadrupole Paul trap driven at 1.6~GHz in a room-temperature ultra-high vacuum setup. Cold electrons are introduced into the trap by ionization of atomic calcium via Rydberg states and stay c
onfined by microwave and static electric fields for several tens of milliseconds. A fraction of these electrons remain trapped longer and show no measurable loss for measurement times up to a second. Electronic excitation of the motion reveals secular frequencies which can be tuned over a range of several tens to hundreds of MHz. Operating a similar electron Paul trap in a cryogenic environment may provide a platform for all-electric quantum computing with trapped electron spin qubits.
We report quantum ground state cooling of a levitated nanoparticle in a room temperature environment. Using coherent scattering into an optical cavity we cool the center of mass motion of a $143$ nm diameter silica particle by more than $7$ orders of
magnitude to $n_x=0.43pm0.03$ phonons along the cavity axis, corresponding to a temperature of $12~mu$K. We infer a heating rate of $Gamma_x/2pi = 21pm 3$ kHz, which results in a coherence time of $7.6~mu$s -- or $15$ coherent oscillations -- while the particle is optically trapped at a pressure of $10^{-6}$ mbar. The inferred optomechanical coupling rate of $g_x/2pi = 71$ kHz places the system well into the regime of strong cooperativity ($C approx 5$). We expect that a combination of ultra-high vacuum with free-fall dynamics will allow to further expand the spatio-temporal coherence of such nanoparticles by several orders of magnitude, thereby opening up new opportunities for macrosopic quantum experiments.
We report the experimental verification of nonclassical correlations for a four-wave-mixing process in an ensemble of cold two-level atoms, confirming theoretical predictions by Du et al. in 2007 for the violation of a Cauchy-Schwarz inequality in th
e system, and obtaining $R = (1.98pm0.03) leq 1$. Quantum correlations are observed in a nano-seconds timescale, in the interference between the central exciting frequency and sidebands dislocated by the detuning to the atomic resonance. They prevail without filters over the noise background coming from linear scattering from the same optical transition. These correlations are fragile with respect to processes that disturb the phase of the atomic excitation, but are robust to variations in number of atoms and to increasing light intensities.
We use nominally forbidden electron-nuclear spin transitions in nitrogen-vacancy (NV) centers in diamond to demonstrate coherent manipulation of a nuclear spin ensemble using microwave fields at room temperature. We show that employing an off-axis ma
gnetic field with a modest amplitude($approx$ 0.01 T) at an angle with respect to the NV natural quantization axes is enough to tilt the direction of the electronic spins, and enable efficient spin exchange with the nitrogen nuclei of the NV center. We could then demonstrate fast Rabi oscillations on electron-nuclear spin exchanging transitions, coherent population trapping and polarization of nuclear spin ensembles in the microwave regime. Coupling many electronic spins of NV centers to their intrinsic nuclei offers full scalability with respect to the number of controllable spins and provides prospects for transduction. In particular, the technique could be applied to long-lived storage of microwave photons and to the coupling of nuclear spins to mechanical oscillators in the resolved sideband regime.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
