Scalable narrow linewidth high power laser for barium ion optical qubits.

The linewidth of a laser plays a pivotal role in ensuring the high fidelity of ion trap quantum processors and optical clocks. As quantum computing endeavors scale up in qubit number, the demand for higher laser power with ultra-narrow linewidth becomes imperative, and leveraging fiber amplifiers emerges as a promising approach to meet these requirements. This study explores the effectiveness of thulium-doped fiber amplifiers (TDFAs) as a viable solution for addressing optical qubit transitions in trapped barium ion qubits. We demonstrate that by performing high-fidelity gates on the qubit while introducing minimal intensity noise, TDFAs do not significantly broaden the linewidth of the seed lasers. We employed a Voigt fitting scheme in conjunction with a delayed self-heterodyne method to accurately measure the linewidth independently, corroborating our findings through quadrupole spectroscopy with trapped barium ions. Our results show linewidth values of 160 ± 15 Hz and 156 ± 16 Hz, respectively, using these two methods, underscoring the reliability of our measurement techniques. The slight variation within the error-bars of the two methods can be attributed to factors such as amplified spontaneous emission in the TDFA or the influence of 1/f noise within the heterodyne setup delay line. These contribute to advancing our understanding of laser linewidth control in the context of ion trap quantum computing as well as stretching the availability of narrow linewidth, high-power tunable lasers beyond the C-band.

Macroporous Ceramic Monolith from Nanoparticle-Polyelectrolyte-Stabilized Pickering Emulsions.

In this work, we present a simple and scalable approach for fabricating porous ceramic from emulsions stabilized by a binary mixture of oppositely charged nanoparticles and a polyelectrolyte. The electrostatic heteroaggregation is exploited to form weakly charged particle-polyelectrolyte complexes (PPCs) that readily stabilize oil-in-water emulsions. The concentration of surface-active PPCs is varied to obtain Pickering emulsion gels that can be processed and converted into the macroporous ceramic structure. The polyelectrolyte in the binary mixture not only enables the adsorption of particles to the oil-water interface and renders processability of the emulsions but also acts as a binder. Nearly one-to-one correspondence between the microstructure of the green ceramic obtained after the evaporation of solvents from the gel-like emulsions and the parent emulsions is observed. The green ceramic is further sintered under controlled conditions to obtain a porous ceramic monolith. We demonstrate that the microstructure and the pore size distribution in the final ceramic can be altered by tuning the composition of the individual species used in the emulsion formulation, i.e., by optimization of the particle-polyelectrolyte ratio used in the processing route.

Semi-batch and continuous production of Pickering emulsion via direct contact steam condensation.

We propose a versatile strategy for the production of highly stable water in oil Pickering emulsion by direct contact condensation of steam. In contrast to conventional methods that use mechanical energy for creating drops, the condensation of steam brought in contact with a non-aqueous colloidal dispersion is exploited to produce Pickering emulsions in two modes of operation, namely, semi-batch and continuous. As steam that comes in contact with oil condenses into water drops, the particles adsorb to the interface and thus arrest drop-drop coalescence. The adsorption of particles on the drop's surface imparts kinetic stability to the emulsions. The dependence of size of the emulsions as a function of parameters such as steam temperature, flow rate, particle type and particle concentration is investigated. We show that the tailoring of these parameters allows a precise control over droplet size distribution. The flexibility of continuous mode of operation makes it a potential technique for large scale production of emulsions suited for many applications.

Resonantly Pumped Bright-Triplet Exciton Lasing in Cesium Lead Bromide Perovskites.

The surprising recent observation of highly emissive triplet-states in lead halide perovskites accounts for their orders-of-magnitude brighter optical signals and high quantum efficiencies compared to other semiconductors. This makes them attractive for future optoelectronic applications, especially in bright low-threshold nanolasers. While nonresonantly pumped lasing from all-inorganic lead-halide perovskites is now well-established as an attractive pathway to scalable low-power laser sources for nano-optoelectronics, here we showcase a resonant optical pumping scheme on a fast triplet-state in CsPbBr3 nanocrystals. The scheme allows us to realize a polarized triplet-laser source that dramatically enhances the coherent signal by 1 order of magnitude while suppressing noncoherent contributions. The result is a source with highly attractive technological characteristics, including a bright and polarized signal and a high stimulated-to-spontaneous emission signal contrast that can be filtered to enhance spectral purity. The emission is generated by pumping selectively on a weakly confined excitonic state with a Bohr radius ∼10 nm in the nanocrystals. The exciton fine-structure is revealed by the energy-splitting resulting from confinement in nanocrystals with tetragonal symmetry. We use a linear polarizer to resolve 2-fold nondegenerate sublevels in the triplet exciton and use photoluminescence excitation spectroscopy to determine the energy of the state before pumping it resonantly.

Porous Ceramics via Processable Pickering Emulsion Stabilized by Oppositely Charged Colloids.

We report a method to produce processable Pickering emulsions in which electrostatic heteroaggregation of oppositely charged fumed silica and alumina particles is exploited. The ability of weakly charged heteroaggregates to adsorb to the oil-water interface favors the formation of highly stable emulsions. A control over the microstructure and rheology of the Pickering emulsion is demonstrated by tuning parameters such as composition, pH, and total concentration of particles. The Pickering emulsions formed under optimal conditions are found to be gel-like and are excellent templates for the fabrication of porous ceramics. Furthermore, the porous mullite ceramic structure which has exceptional thermal and chemical resistance under harsh environments is obtained by drying and sintering of the emulsion template. The phase evolution, microstructure, and porosity of the resulting ceramic are characterized.

Squeezing Enhances Quantum Synchronization.

It is desirable to observe synchronization of quantum systems in the quantum regime, defined by the low number of excitations and a highly nonclassical steady state of the self-sustained oscillator. Several existing proposals of observing synchronization in the quantum regime suffer from the fact that the noise statistics overwhelm synchronization in this regime. Here, we resolve this issue by driving a self-sustained oscillator with a squeezing Hamiltonian instead of a harmonic drive and analyze this system in the classical and quantum regime. We demonstrate that strong entrainment is possible for small values of squeezing, and in this regime, the states are nonclassical. Furthermore, we show that the quality of synchronization measured by the FWHM of the power spectrum is enhanced with squeezing.

An exacting transition probability measurement - a direct test of atomic many-body theories.

A new protocol for measuring the branching fraction of hydrogenic atoms with only statistically limited uncertainty is proposed and demonstrated for the decay of the P3/2 level of the barium ion, with precision below 0.5%. Heavy hydrogenic atoms like the barium ion are test beds for fundamental physics such as atomic parity violation and they also hold the key to understanding nucleo-synthesis in stars. To draw definitive conclusion about possible physics beyond the standard model by measuring atomic parity violation in the barium ion it is necessary to measure the dipole transition probabilities of low-lying excited states with a precision better than 1%. Furthermore, enhancing our understanding of the barium puzzle in barium stars requires branching fraction data for proper modelling of nucleo-synthesis. Our measurements are the first to provide a direct test of quantum many-body calculations on the barium ion with a precision below one percent and more importantly with no known systematic uncertainties. The unique measurement protocol proposed here can be easily extended to any decay with more than two channels and hence paves the way for measuring the branching fractions of other hydrogenic atoms with no significant systematic uncertainties.

Hierarchical radioscopy using polychromatic and partially coherent hard synchrotron radiation.

Pushing synchrotron x-ray radiography to increasingly higher image-acquisition rates (currently up to 100,000 fps) while maintaining spatial resolutions in the micrometer range implies drastically reduced fields of view. As a consequence, either imaging a small subregion of the sample with high spatial resolution or only the complete specimen with moderate resolution is applicable. We introduce a concept to overcome this limitation by making use of a semi-transparent x-ray detector positioned close to the investigated sample. The hard x-rays that pass through the sample either create an image on the first detector or keep on propagating until they are captured by a second x-ray detector located further downstream. In this way, a process can be imaged simultaneously in a hierarchical manner within a single exposure and a projection of the complete object with moderate resolution as well as a subregion with high resolution are obtained. As a proof-of-concept experiment, image sequences of an evolving liquid-metal foam are shown, employing frame rates of 1000 images/s (1.2 µm pixel size) and 15,000 images/s (18.1 µm pixel size) for the first and second detector, respectively.

Photon correlation versus interference of single-atom fluorescence in a half-cavity.

Photon correlations are investigated for a single laser-excited ion trapped in front of a mirror. Varying the relative distance between the ion and the mirror, photon correlation statistics can be tuned smoothly from an antibunching minimum to a bunchinglike maximum. Our analysis concerns the non-Markovian regime of the ion-mirror interaction and reveals the field establishment in a half-cavity interferometer.