Three-state coherent control using narrowband and passband sequences.

In this work, we propose a comprehensive design for narrowband and passband composite pulse sequences by involving the dynamics of all states in the three-state system. The design is quite universal as all pulse parameters can be freely employed to modify the coefficients of error terms. Two modulation techniques, the strength and phase modulations, are used to achieve arbitrary population transfer with a desired excitation profile, while the system keeps minimal leakage to the third state. Furthermore, the current sequences are capable of tolerating inaccurate waveforms, detuning errors, and work well when rotating wave approximation is not strictly justified. Therefore, this work provides versatile adaptability for shaping various excitation profiles in both narrowband and passband sequences.

Effective non-adiabatic holonomic quantum computation of cavity modes via invariant-based reverse engineering.

In this paper, we propose a protocol to realize non-adiabatic holonomic quantum computation (NHQC) of cavity modes via invariant-based reverse engineering. Coupling cavity modes with an auxiliary atom trapped in a cavity, we derive effective Hamiltonians with the help of laser pulses. Based on the derived Hamiltonians, invariant-based reverse engineering is used to find proper evolution paths for NHQC. Moreover, the systematic-error-sensitivity nullified optimal control method is considered in the parameter selections, making the protocol insensitive to the influence of systematic errors of pulses. We also estimate the imperfections induced by random noise and decoherence. Numerical results show that the protocol holds robustness against these imperfections. Therefore, the protocol may provide useful perspectives to quantum computation with optical qubits in cavity quantum electrodynamics systems. This article is part of the theme issue 'Shortcuts to adiabaticity: theoretical, experimental and interdisciplinary perspectives'.

Opposite Sensing Response of Heterojunction Gas Sensors Based on SnO2-Cr2O3 Nanocomposites to H2 against CO and Its Selectivity Mechanism.

Metal oxide semiconductor (MOS) gas sensors show poor selectivity when exposed to mixed gases. This is a challenge in gas sensors and limits their wide applications. There is no efficient way to detect a specific gas when two homogeneous gases are concurrently exposed to sensing materials. The p-n nanojunction of xSnO2-yCr2O3 nanocomposites (NCs) are prepared and used as sensing materials (x/y shows the Sn/Cr molar ratio in the SnO2-Cr2O3 composite and is marked as SnxCry for simplicity). The gas sensing properties, crystal structure, morphology, and chemical states are characterized by employing an electrochemical workstation, an X-ray diffractometer, a transmission electron microscope, and an X-ray photoelectron spectrometer, respectively. The gas sensing results indicate that SnxCry NCs with x/y greater than 0.07 demonstrate a p-type behavior to both CO and H2, whereas the SnxCry NCs with x/y < 0.07 illustrate an n-type behavior to the aforementioned reduced gases. Interestingly, the SnxCry NCs with x/y = 0.07 show an n-type behavior to H2 but a p-type to CO. The effect of the operating temperature on the opposite sensing response of the fabricated sensors has been investigated. Most importantly, the mechanism of selectivity opposite sensing response is proposed using the aforementioned characterization techniques. This paper proposes a promising strategy to overcome the drawback of low selectivity of this type of sensor.

Sulfur-Rich Graphene Nanoboxes with Ultra-High Potassiation Capacity at Fast Charge: Storage Mechanisms and Device Performance.

It is a major challenge to achieve fast charging and high reversible capacity in potassium ion storing carbons. Here, we synthesized sulfur-rich graphene nanoboxes (SGNs) by one-step chemical vapor deposition to deliver exceptional rate and cyclability performance as potassium ion battery and potassium ion capacitor (PIC) anodes. The SGN electrode exhibits a record reversible capacity of 516 mAh g-1 at 0.05 A g-1, record fast charge capacity of 223 mA h g-1 at 1 A g-1, and exceptional stability with 89% capacity retention after 1000 cycles. Additionally, the SGN-based PIC displays highly favorable Ragone chart characteristics: 112 Wh kg-1at 505 W kg-1 and 28 Wh kg-1 at 14618 W kg-1 with 92% capacity retention after 6000 cycles. X-ray photoelectron spectroscopy analysis illustrates a charge storage sequence based primarily on reversible ion binding at the structural-chemical defects in the carbon and the reversible formation of K-S-C and K2S compounds. Transmission electron microscopy analysis demonstrates reversible dilation of graphene due to ion intercalation, which is a secondary source of capacity at low voltage. This intercalation mechanism is shown to be stable even at cycle 1000. Galvanostatic intermittent titration technique analysis yields diffusion coefficients from 10-10 to 10-12 cm2 s-1, an order of magnitude higher than S-free carbons. The direct electroanalytic/analytic comparison indicates that chemically bound sulfur increases the number of reversible ion bonding sites, promotes reaction-controlled over diffusion-controlled kinetics, and stabilizes the solid electrolyte interphase. It is also demonstrated that the initial Coulombic efficiency can be significantly improved by switching from a standard carbonate-based electrolyte to an ether-based one.

Effective discrimination of chiral molecules in a cavity.

We present a scheme to realize precise discrimination of chiral molecules in a cavity. Assisted by additional laser pulses, cavity fields can evolve into different coherence states with contrary-sign displacements according to the handedness of molecules. Consequently, the handedness of molecules can be read out with homodyne measurement on the cavity, and the successful probability is nearly unity without very strong cavity fields. Numerical results show that the scheme is insensitive to errors, noise, and decoherence. Therefore, the scheme may provide helpful perspectives for accurate discrimination of chiral molecules.

Effective pulse reverse-engineering for strong field-matter interaction.

In this Letter, we propose a scheme to control the evolution of a two-level quantum system in the strong-coupling regime, based on the idea of reverse engineering. A coherent control field is designed to drive the system along a user-predefined evolution trajectory without utilizing the rotating-wave approximation. As concrete examples, we show that complete population inversion, an equally weighted coherent superposition, and even oscillation-like dynamics can be achieved. Since there are no limitations on the coupling strength between the control field and matter, the scheme is attractive for applications such as accelerating desired system dynamics and fast quantum information processing.

Quantum state engineering by periodical two-step modulation in an atomic system.

By periodical two-step modulation, we demonstrate that the dynamics of a multilevel system can evolve even in a multiple large detunings regime and provide the effective Hamiltonian (of interest) for this system. We then illustrate this periodical modulation in quantum state engineering, including achieving direct transition from the ground state to the Rydberg state or the desired superposition of two Rydberg states without satisfying the two-photon resonance condition, switching between the Rydberg blockade regime and the Rydberg antiblockade regime, stimulating distinct atomic transitions by the same laser field, and implementing selective transitions in the same multilevel system. Particularly, it is robust against perturbation of control parameters. Another advantage is that the waveform of the laser field has a simple square-wave form, which is readily implemented in experiments. Thus, it offers us a novel method of quantum state engineering in quantum information processing.

Random composites of nickel networks supported by porous alumina toward double negative materials.

Random composites with nickel networks hosted randomly in porous alumina are proposed to realize double negative materials. The random composite for DNMs (RC-DNMs) can be prepared by typical processing of material, which makes it possible to explore new DNMs and potential applications, and to feasibly tune their electromagnetic parameters by controlling their composition and microstructure. Hopefully, various new RC-DNMs with improved performance will be proposed in the future.