Related Experiment Video
Updated: Feb 6, 2026

11:33
Dissection of Local Ca2+ Signals in Cultured Cells by Membrane-targeted Ca2+ Indicators
Published on: March 22, 2019
9.5K
Crossing-free on-chip 2 × 2 polarization-transparent switch with signals regrouping function
Optics Letters
|August 15, 2018
Summary
We developed a novel on-chip switch for polarization-division multiplexing (PDM) signals. This device reduces losses and complexity, enabling efficient signal routing and regrouping for advanced optical communication.
Area of Science:
- Photonics and Optical Engineering
- Integrated Optics
- Telecommunications
Background:
- Polarization-division multiplexing (PDM) is crucial for increasing optical communication capacity.
- Existing PDM switches often suffer from high insertion losses and complexity due to waveguide crossings.
- Efficient and flexible switching of PDM signals is essential for advanced optical networks.
Purpose of the Study:
- To propose and demonstrate an on-chip 2x2 polarization-transparent switch.
- To handle two-group PDM signals simultaneously.
- To reduce insertion losses and device complexity compared to conventional PDM switches.
Main Methods:
- Introduction of a polarization-transparent power splitter/combiner (PPS/PPC) to avoid waveguide crossings.
- Independent switching and routing of each input polarization tributary.
- Experimental characterization of the switch's performance, including polarization extinction ratio and insertion loss.
Main Results:
- Demonstration of an on-chip 2x2 polarization-transparent switch.
- Achieved a polarization extinction ratio greater than 15 dB.
- Observed reasonable insertion losses with less than 1 dB power penalties for all measured paths, indicated by clear eye diagrams.
Conclusions:
- The proposed PPS/PPC based switch effectively reduces insertion losses and complexity.
- The switch enables both basic switching and precise four-channel signal regrouping for dual-group PDM signals.
- This technology offers a complete and non-redundant switching functionality for optical communication systems.
Related Concept Videos
meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H
6.7K
All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...
6.7K
2° Amines to N-Nitrosamines: Reaction with NaNO2
5.5K
Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
5.5K
SN2 Reaction: Kinetics
10.3K
Kinetic Studies and Significance
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
10.3K
SN2 Reaction: Mechanism
17.5K
The kinetic studies of SN2 reactions suggest an essential feature of its mechanism: it is a single-step process without intermediates. Here, both the nucleophile and the substrate participate in the rate-determining step.
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
17.5K
SN2 Reaction: Transition State
12.0K
An SN2 reaction of an alkyl halide is a single-step process in which bond formation between the nucleophile and the substrate and bond breaking between the substrate and the halide occurs simultaneously through a transition state without forming an intermediate.
When the nucleophile approaches the electrophilic carbon with its lone pairs, the halide acts as a leaving group and moves away with the electron-pair bonded to the carbon. Dotted partial bonds represent the bonds being formed or broken...
When the nucleophile approaches the electrophilic carbon with its lone pairs, the halide acts as a leaving group and moves away with the electron-pair bonded to the carbon. Dotted partial bonds represent the bonds being formed or broken...
12.0K
SN2 Reaction: Stereochemistry
11.8K
In an SN2 reaction, the nucleophilic attack on the substrate and departure of the leaving group occurs simultaneously through a transition state. As the nucleophile approaches the substrate from the back-side, the configuration of the substrate carbon changes from tetrahedral to trigonal bipyramidal and then back to tetrahedral, leading to an inversion in the configuration of the product.
If the substrate is an achiral molecule at the α-carbon, the inversion of configuration is not...
If the substrate is an achiral molecule at the α-carbon, the inversion of configuration is not...
11.8K

