Related Experiment Video

Updated: Feb 15, 2026

Determination of the Excitation and Coupling Rates Between Light Emitters and Surface Plasmon Polaritons
07:39

Determination of the Excitation and Coupling Rates Between Light Emitters and Surface Plasmon Polaritons

Published on: July 21, 2018

7.3K

Optical spin Hall effect of polariton condensation in organic crystal microcavities

Shida Feng, Jun Cui, Xiaohong Zhang

    Optics Letters
    |February 13, 2026
    PubMed

    More Related Videos

    Effect of Bending on the Electrical Characteristics of Flexible Organic Single Crystal-based Field-effect Transistors08:43

    Effect of Bending on the Electrical Characteristics of Flexible Organic Single Crystal-based Field-effect Transistors

    Published on: November 7, 2016

    8.5K
    Spectral and Angle-Resolved Magneto-Optical Characterization of Photonic Nanostructures08:01

    Spectral and Angle-Resolved Magneto-Optical Characterization of Photonic Nanostructures

    Published on: November 21, 2019

    7.7K

    Related Concept Videos

    The Hall Effect01:30

    The Hall Effect

    Edwin H. Hall, in the year 1879, devised an experiment that could be used to identify the polarity of the predominant charge carriers in a conducting material. From a historical perspective, this experiment was the first to demonstrate that the charge carriers in most metals are negative.
    4.5K
    Aldol Condensation vs Claisen Condensation01:33

    Aldol Condensation vs Claisen Condensation

    Aldol condensation is an acid or base-catalyzed condensation between aldehydes or ketones to give an α,ꞵ-unsaturated carbonyl compound. A base-promoted condensation between ester molecules to produce a ꞵ-ketoester is known as the Claisen condensation. In the presence of a base, both reactions involve deprotonation of the acidic α hydrogen to produce the corresponding enolates. The nucleophilic enolates attack their respective nonenolized carbonyl compound forming a tetrahedral...
    8.0K
    Phase Transitions: Vaporization and Condensation02:39

    Phase Transitions: Vaporization and Condensation

    The physical form of a substance changes on changing its temperature. For example, raising the temperature of a liquid causes the liquid to vaporize (convert into vapor). The process is called vaporization—a surface phenomenon. Vaporization occurs when the thermal motion of the molecules overcome the intermolecular forces, and the molecules (at the surface) escape into the gaseous state. When a liquid vaporizes in a closed container, gas molecules cannot escape. As these gas phase molecules...
    21.6K
    NMR Spectroscopy: Spin–Spin Coupling01:08

    NMR Spectroscopy: Spin–Spin Coupling

    The spin state of an NMR-active nucleus can have a slight effect on its immediate electronic environment. This effect propagates through the intervening bonds and affects the electronic environments of NMR-active nuclei up to three bonds away; occasionally, even farther. This phenomenon is called spin–spin coupling or J-coupling. Coupling interactions are mutual and result in small changes in the absorption frequencies of both nuclei involved. While nuclei of the same element are involved...
    3.3K
    Spin–Spin Coupling: One-Bond Coupling01:17

    Spin–Spin Coupling: One-Bond Coupling

    Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
    1.5K
    Spin–Spin Coupling Constant: Overview01:08

    Spin–Spin Coupling Constant: Overview

    In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
    Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
    1.5K