Excitation of a bound state in the continuum (BIC) through scattering is problematic since it is by definition uncoupled. Here, we consider a type of dressed BIC and show that it can be excited in a nonlinear system through multiphoton scattering and delayed quantum feedback. The system is a semi-infinite waveguide with linear dispersion coupled to a qubit, in which a single-photon, dressed BIC is known to exist. We show that this BIC can be populated via multiphoton scattering in the non-Markovian regime, where the photon delay time (due to the qubit-mirror distance) is comparable with the qubit's decay. A similar process excites the BIC existing in an infinite waveguide coupled to two distant qubits, thus yielding stationary entanglement between the qubits. This shows, in particular, that single-photon trapping via multiphoton scattering can occur without band edge effects or cavities, the essential resource being instead the delayed quantum feedback provided by a single mirror or the emitters themselves.
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http://dx.doi.org/10.1103/PhysRevLett.122.073601 | DOI Listing |
Adv Funct Mater
October 2024
Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720, USA.
Traditional deep fluorescence imaging has primarily focused on red-shifting imaging wavelengths into the near-infrared (NIR) windows or implementation of multi-photon excitation approaches. Here, we combine the advantages of NIR and multiphoton imaging by developing a dual-infrared two-photon microscope to enable high-resolution deep imaging in biological tissues. We first computationally identify that photon absorption, as opposed to scattering, is the primary contributor to signal attenuation.
View Article and Find Full Text PDFNanoscale
December 2024
Department of Chemistry, University at Buffalo, SUNY, New York 14260, USA.
Multiphoton upconversion lasing in scattering gain media has attracted considerable attention in recent years. LAPONITE® is a scattering medium consisting of 2-D nano-discs that can be dispersed as a transparent solution in aqueous media and forms a gel at high concentration. In this paper, we demonstrate two-photon pumped upconversion regular lasing along forward and backward directions as well as random lasing along all other directions.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Department of Chemistry, Aarhus University, Langelandsgade 140, 8000 Aarhus C, Denmark.
Vibrational wave packets are created in the lowest triplet state 13Σu+ of K2 and Rb2 residing on the surface of helium nanodroplets, through non-resonant stimulated impulsive Raman scattering induced by a moderately intense near-infrared laser pulse. A delayed, intense 50-fs laser pulse doubly ionizes the alkali dimers via multiphoton absorption and thereby causes them to Coulomb explode into a pair of alkali ions Ak+. From the kinetic energy distribution P(Ekin) of the Ak+ fragment ions, measured at a large number of delays, we determine the time-dependent internuclear distribution P(R, t), which represents the modulus square of the wave packet within the accuracy of the experiment.
View Article and Find Full Text PDFNanoscale Horiz
December 2024
Department of Chemistry and Centre for Atomic Engineering of Advanced Materials, Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Institutes of Physical Science and Information Technology and Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials, Anhui University, Hefei, Anhui, 230601, China.
Recent developments in optical imaging techniques, particularly multi-photon excitation microscopy that allows studies of biological interactions at a deep cellular level, have motivated intensive research in developing multi-photon absorption fluorophores. Biological tissues are optically transparent in the near-infrared region. Therefore, fluorophores that can absorb light in the near-infrared (NIR) region by multi-photon absorption are particularly useful in bio-imaging.
View Article and Find Full Text PDFJ Phys Chem Lett
November 2024
Department of Chemistry and Center for Advanced Light Source, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Nitrogen bond activation is a pivotal process in chemistry, with bond excitation being fundamental to understanding the underlying mechanisms, making the preparation of molecules in specific quantum states crucial. Here we report the first overtone excitation of the N molecule from XΣ( = 0, = 0, 1, and 2) to XΣ( = 2, = 0, 1, 2, and 3) using the stimulated Raman pumping (SRP) method in a pulsed molecular beam. N was detected using 2+1 resonance-enhanced multiphoton ionization through the a″Σ state.
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