Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Ultrafast preparation and detection of entangled atoms.

ABSTRACT: Atoms can form a molecule by sharing their electrons in binding orbitals. These electrons are entangled. Is there a way to break a molecular bond and obtain atoms in their ground state that are spatially separated and still entangled? Here, we show that it is possible to prepare these spatially separated, entangled atoms on femtosecond time scales from single oxygen molecules. The two neutral atoms are entangled in the magnetic quantum number of their valence electrons. In a time-delayed probe step, we use nonadiabatic tunneling, which is a magnetic quantum number-sensitive ionization mechanism. We find a fingerprint of entanglement in the measured ionization probability as a function of the angle between the light's quantization axis and the molecular axis. This establishes a platform for further experiments that harness the time resolution of strong-field experiments to investigate spatially separated, entangled atoms on femtosecond time scales.

SUBMITTER: Eckart S

PROVIDER: S-EPMC10491222 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Ultrafast preparation and detection of entangled atoms.

Eckart Sebastian S Trabert Daniel D Rist Jonas J Geyer Angelina A Schmidt Lothar Ph H LPH Fehre Kilian K Kunitski Maksim M

Science advances 20230908 36

Atoms can form a molecule by sharing their electrons in binding orbitals. These electrons are entangled. Is there a way to break a molecular bond and obtain atoms in their ground state that are spatially separated and still entangled? Here, we show that it is possible to prepare these spatially separated, entangled atoms on femtosecond time scales from single oxygen molecules. The two neutral atoms are entangled in the magnetic quantum number of their valence electrons. In a time-delayed probe s ...[more]

PMID: 37683006

Similar Datasets

Creating heralded hyper-entangled photons using Rydberg atoms.

Project description:Entangled photon pairs are a fundamental component for testing the foundations of quantum mechanics, and for modern quantum technologies such as teleportation and secured communication. Current state-of-the-art sources are based on nonlinear processes that are limited in their efficiency and wavelength tunability. This motivates the exploration of physical mechanisms for entangled photon generation, with a special interest in mechanisms that can be heralded, preferably at telecommunications wavelengths. Here we present a mechanism for the generation of heralded entangled photons from Rydberg atom cavity quantum electrodynamics (cavity QED). We propose a scheme to demonstrate the mechanism and quantify its expected performance. The heralding of the process enables non-destructive detection of the photon pairs. The entangled photons are produced by exciting a rubidium atom to a Rydberg state, from where the atom decays via two-photon emission (TPE). A Rydberg blockade helps to excite a single Rydberg excitation while the input light field is more efficiently collectively absorbed by all the atoms. The TPE rate is significantly enhanced by a designed photonic cavity, whose many resonances also translate into high-dimensional entanglement. The resulting high-dimensionally entangled photons are entangled in more than one degree of freedom: in all of their spectral components, in addition to the polarization-forming a hyper-entangled state, which is particularly interesting in high information capacity quantum communication. We characterize the photon comb states by analyzing the Hong-Ou-Mandel interference and propose proof-of-concept experiments.

| S-EPMC8113235 | biostudies-literature

Manipulating frequency-bin entangled states in cold atoms.

Project description:Optical manipulation of entanglement harnessing the frequency degree of freedom is important for encoding of quantum information. We here devise a phase-resonant excitation mechanism of an atomic interface where full control of a narrowband single-photon two-mode frequency entangled state can be efficiently achieved. We illustrate the working physical mechanism for an interface made of cold (87)Rb atoms where entanglement is well preserved from degradation over a typical 100 μm length scale of the interface and with fractional delays of the order of unity. The scheme provides a basis for efficient multi-frequency and multi-photon entanglement, which is not easily accessible to polarization and spatial encoding.

| S-EPMC3909907 | biostudies-other

Experimental certification of millions of genuinely entangled atoms in a solid.

Project description:Quantum theory predicts that entanglement can also persist in macroscopic physical systems, albeit difficulties to demonstrate it experimentally remain. Recently, significant progress has been achieved and genuine entanglement between up to 2900 atoms was reported. Here, we demonstrate 16 million genuinely entangled atoms in a solid-state quantum memory prepared by the heralded absorption of a single photon. We develop an entanglement witness for quantifying the number of genuinely entangled particles based on the collective effect of directed emission combined with the non-classical nature of the emitted light. The method is applicable to a wide range of physical systems and is effective even in situations with significant losses. Our results clarify the role of multipartite entanglement in ensemble-based quantum memories and demonstrate the accessibility to certain classes of multipartite entanglement with limited experimental control.The presence of entanglement in macroscopic systems is notoriously difficult to observe. Here, the authors develop a witness which allow them to demonstrate entanglement between millions of atoms in a solid-state quantum memory prepared by the heralded absorption of a single photon.

| S-EPMC5640624 | biostudies-literature

Entangled photons enabled ultrafast stimulated Raman spectroscopy for molecular dynamics.

Project description:Quantum entanglement has emerged as a great resource for studying the interactions between molecules and radiation. We propose a new scheme of stimulated Raman scattering with entangled photons. A quantum ultrafast Raman spectroscopy is developed for condensed-phase molecules, to monitor the exciton populations and coherences. Analytic results are obtained, showing an entanglement-enabled time-frequency scale not attainable by classical light. The Raman signal presents an unprecedented selectivity of molecular correlation functions, as a result of the Hong-Ou-Mandel interference. Our work suggests a new paradigm of using an unconventional interferometer as part of spectroscopy, with the potential to unveil advanced information about complex materials.

| S-EPMC11247098 | biostudies-literature

Ultrafast hot-carrier cooling in quasi freestanding bilayer graphene with hydrogen intercalated atoms.

Project description:Femtosecond-THz optical pump probe spectroscopy is employed to investigate the cooling dynamics of hot carriers in quasi-free standing bilayer epitaxial graphene with hydrogen interacalation. We observe longer decay time constants, in the range of 2.6 to 6.4 ps, compared to previous studies on monolayer graphene, which increase nonlinearly with excitation intensity. The increased relaxation times are due to the decoupling of the graphene layer from the SiC substrate after hydrogen intercalation which increases the distance between graphene and substrate. Furthermore, our measurements show that the supercollision mechanism is not related to the cooling process of the hot carriers, which is ultimately achieved by electron optical phonon scattering.

| S-EPMC9846464 | biostudies-literature

High yield and ultrafast sources of electrically triggered entangled-photon pairs based on strain-tunable quantum dots.

Project description:Triggered sources of entangled photon pairs are key components in most quantum communication protocols. For practical quantum applications, electrical triggering would allow the realization of compact and deterministic sources of entangled photons. Entangled-light-emitting-diodes based on semiconductor quantum dots are among the most promising sources that can potentially address this task. However, entangled-light-emitting-diodes are plagued by a source of randomness, which results in a very low probability of finding quantum dots with sufficiently small fine structure splitting for entangled-photon generation (∼10(-2)). Here we introduce strain-tunable entangled-light-emitting-diodes that exploit piezoelectric-induced strains to tune quantum dots for entangled-photon generation. We demonstrate that up to 30% of the quantum dots in strain-tunable entangled-light-emitting-diodes emit polarization-entangled photons. An entanglement fidelity as high as 0.83 is achieved with fast temporal post selection. Driven at high speed, that is 400 MHz, strain-tunable entangled-light-emitting-diodes emerge as promising devices for high data-rate quantum applications.

| S-EPMC4686767 | biostudies-literature

Ultrafast Bisulfite Sequencing for Efficient and Accurate 5-Methylcytosine Detection in DNA and RNA

Project description:We present an ultrafast bisulfite sequencing (UBS-seq) method, which accelerates the bisulfite reaction by about 13-fold, resulting in minimal DNA damage and much lower background in all DNA sequences. This ultrafast BS protocol is also ideal for mapping of RNA 5-methylcytosine (m5C) because of much shorter reaction time and dramatically reduced RNA background. And allowed detection of m5C stoichiometry in highly structured RNA species.

2023-10-13 | GSE225614 | GEO

Detection of gas atoms with carbon nanotubes

Project description:Owning to their unparalleled sensitivity resolution, nanomechanical resonators have excellent capabilities in design of nano-sensors for gas detection. The current challenge is to develop new designs of the resonators for differentiating distinct gas atoms with a recognizably high sensitivity. In this work, the characteristics of impulse wave propagation in carbon nanotube-based sensors are investigated using molecular dynamics simulations to provide a new method for detection of noble gases. A sensitivity index based on wave velocity shifts in a single-walled carbon nanotube, induced by surrounding gas atoms, is defined to explore the efficiency of the nano-sensor. The simulation results indicate that the nano-sensor is able to differentiate distinct noble gases at the same environmental temperature and pressure. The inertia and the strengthening effects by the gases on wave characteristics of carbon nanotubes are particularly discussed, and a continuum mechanics shell model is developed to interpret the effects.

| S-EPMC3646270 | biostudies-literature

Coherence and resonance effects in the ultra-intense laser-induced ultrafast response of complex atoms.

Project description:Both coherent pumping and energy relaxation play important roles in understanding physical processes of ultra-intense coherent light-matter interactions. Here, using a large-scale quantum master equation approach, we describe dynamical processes of practical open quantum systems driven by both coherent and stochastic interactions. As examples, two typical cases of light-matter interactions are studied. First, we investigate coherent dynamics of inner-shell electrons of a neon gas irradiated by a high-intensity X-ray laser along with vast number of decaying channels. In these single-photon dominated processes, we find that, due to coherence-induced Rabi oscillations and power broadening effects, the photon absorptions of a neon gas can be suppressed resulting in differences in ionization processes and final ion-stage distributions. Second, we take helium as an example of multiphoton and multichannel interference dominated electron dynamics, by investigating the transient absorption of an isolated attosecond pulse in the presence of a femtosecond infrared laser pulse.

| S-EPMC4702093 | biostudies-other

S-Trap is an ultrafast sample preparation approach for shotgun proteomics

Project description:The success of shotgun proteomic analysis depends largely on how samples are prepared. Current approaches such as gel-, solution- or filter-based, although being extensively employed in the field, are time-consuming and less effective with respect to the repetitive sample processing, recovery, and overall yield. As an alternative, suspension trapping (S-Trap) filter is commercially available very recently in the format of single or 96-well filter plate. In contrast to conventional filter aided sample preparation (FASP) approach, which utilizes a molecular weight cutoff (MWCO) membrane as the filter and requires hours of processing before digestion-ready proteins can be obtained, S-Trap employs a three-dimensional porous material as filter media, and traps particulate protein suspension with subsequent depletion of interfering substances and in-filter digestion. Due to the large (sub-micron) pore size, each centrifugation cycle of S-Trap filter only takes around 1 minute, which significantly reduces the total processing time from approximately 3 hours by FASP to less than 15 minutes, suggesting an ultrafast sample preparation approach for shotgun proteomics. Here, for the first time, we comprehensively evaluate the performance of individual S-Trap filter and 96-well filter plate in the context of global protein identification and quantitation using whole cell lysate and clinically relevant sputum samples.

2019-03-28 | PXD010237 | Pride

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data