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Register a new userCounterintuitive transitions between crossing energy levels
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We calculate analytically the probabilities for intuitive and counterintuitive transitions in a three-state system, in which two parallel energies are crossed by a third, tilted energy. The state with the tilted energy is coupled to the other two states in a chainwise linkage pattern with constant couplings of finite duration. The probability for a counterintuitive transition is found to increase with the square of the coupling and decrease with the squares of the interaction duration, the energy splitting between the parallel energies, and the tilt (chirp) rate. Physical examples of this model can be found in coherent atomic excitation and optical shielding in cold atomic collisions.
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Stimulated emission and absorption are two fundamental processes of light-matter interaction, and the coefficients of the two processes should be equal in general. However, we will describe a generic method to realize significant difference between the stimulated emission and absorption coefficients of two nondegenerate energy levels, which we refer to as nonreciprocal transition. As a simple implementation, a cyclic three-level atom system, comprising two nondegenerate energy levels and one auxiliary energy level, is employed to show nonreciprocal transition via a combination of synthetic magnetism and reservoir engineering. Moreover, a single-photon nonreciprocal transporter is proposed using two one dimensional semi-infinite coupled-resonator waveguides connected by an atom with nonreciprocal transition effect. Our work opens up a route to design atom-mediated nonreciprocal devices in a wide range of physical systems.
We prepare heralded single photons from a photon pair source based on non-degenerate four-wave mixing in a cold atomic ensemble via a cascade decay scheme. Their statistics shows strong antibunching with g(2)(0) < 0.03, indicating a near single photon character. In an optical homodyne experiment, we directly measure the temporal envelope of these photons and find, depending on the heralding scheme, an exponentially decaying or rising profile. The rising envelope will be useful for efficient interaction between single photons and microscopic systems like single atoms and molecules. At the same time, their observation illustrates the breakdown of a realistic interpretation of the heralding process in terms of defining an initial condition of a physical system.
Using resonant two-step laser excitation of trapped 232Th+ ions, we observe 43 previously unknown energy levels within the energy range from 7.3 to 8.3 eV. The high density of states promises a strongly enhanced electronic bridge excitation of the 229mTh nuclear state that is expected in this energy range. From the observation of resonantly enhanced three-photon ionization of Th+, the second ionization potential of thorium can be inferred to lie within the range between 11.9 and 12.3 eV. Pulsed laser radiation in a wide wavelength range from 237 to 289 nm is found to provide efficient photodissociation of molecular ions that are formed in reactions of Th+ with impurities in the buffer gas, leading to a significantly increased storage time for Th+ in the ion trap.
The low-frequency optical excitations of AA-stacked bilayer graphene are investigated by the tight-binding model. Two groups of asymmetric LLs lead to two kinds of absorption peaks resulting from only intragroup excitations. Each absorption peak obeys a single selection rule similar to that of monolayer graphene. The excitation channel of each peak is changed as the field strength approaches a critical strength. This alteration of the excitation channel is strongly related to the setting of the Fermi level. The peculiar optical properties can be attributed to the characteristics of the LL wave functions of the two LL groups. A detailed comparison of optical properties between AA-stacked and AB-stacked bilayer graphenes is also offered. The compared results demonstrate that the optical properties are strongly dominated by the stacking symmetry. Furthermore, the presented results may be used to discriminate AABG from MG, which can be hardly done by STM.
The coherent states that describe the classical motion of a mechanical oscillator do not have well-defined energy, but are rather quantum superpositions of equally-spaced energy eigenstates. Revealing this quantized structure is only possible with an apparatus that measures the mechanical energy with a precision greater than the energy of a single phonon, $hbaromega_text{m}$. One way to achieve this sensitivity is by engineering a strong but nonresonant interaction between the oscillator and an atom. In a system with sufficient quantum coherence, this interaction allows one to distinguish different phonon number states by resolvable differences in the atoms transition frequency. Such dispersive measurements have been studied in cavity and circuit quantum electrodynamics where experiments using real and artificial atoms have resolved the photon number states of cavities. Here, we report an experiment where an artificial atom senses the motional energy of a driven nanomechanical oscillator with sufficient sensitivity to resolve the quantization of its energy. To realize this, we build a hybrid platform that integrates nanomechanical piezoelectric resonators with a microwave superconducting qubit on the same chip. We excite phonons with resonant pulses of varying amplitude and probe the resulting excitation spectrum of the qubit to observe phonon-number-dependent frequency shifts $approx 5$ times larger than the qubit linewidth. Our result demonstrates a fully integrated platform for quantum acoustics that combines large couplings, considerable coherence times, and excellent control over the mechanical mode structure. With modest experimental improvements, we expect our approach will make quantum nondemolition measurements of phonons an experimental reality, leading the way to new quantum sensors and information processing approaches that use chip-scale nanomechanical devices.
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