Chemical Sensors Based on Plasmon Resonance in Graphene
US-2015369735-A1 · Dec 24, 2015 · US
US10801957B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10801957-B2 |
| Application number | US-201916566087-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 10, 2019 |
| Priority date | Sep 10, 2018 |
| Publication date | Oct 13, 2020 |
| Grant date | Oct 13, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method for molecular chirality detection is described. The method includes providing a substrate defining an array of hole-disks, each hole-disk coupled with an asymmetric optical cavity. Each asymmetric optical cavity having a back reflector separating a plasmonic pattern by an appropriate selection of thickness. The substrate is illuminated to simultaneously excite two degenerate localized surface plasmon modes producing a strong chiral near-field. The method may also include generating a characterization of chiral molecules on the substrate based on the strong chiral near-field. Substrates and detectors for molecular chirality detection are also described.
Opening claim text (preview).
What is claimed is: 1. A method, comprising: providing a substrate defining an array of hole-disks, each hole-disk coupled with an asymmetric optical cavity and each asymmetric optical cavity having a back reflector separating a plasmonic pattern by an appropriate selection of thickness; illuminating the substrate to simultaneously excite two degenerate localized surface plasmon modes; and producing a strong chiral near-field. 2. The method of claim 1 , wherein the substrate is a nanostructured square array of gold hole-disks and the back reflector comprises at least one of: gold or another high reflective metal. 3. The method of claim 2 , further comprising detecting background-free circular dichroism molecular chirality of a sample located on the substrate through near-field light-matter interaction with high signal to noise ratio. 4. An optical chip configured to perform the method of claim 2 in order to detect chirality of one of: drugs, proteins, DNAs, and other molecules. 5. A drug delivery chip configured to perform the method of claim 2 and configured to bring a target chiral sample into contact with the substrate, wherein the substrate is an achiral substrate. 6. The method of claim 1 , wherein illuminating the substrate comprises illuminating the substrate with circularly polarized light. 7. The method of claim 6 , wherein the substrate is an achiral substrate; and wherein illuminating the substrate by the circularly polarized light comprises changing a handedness of the circularly polarized light from right and left on the achiral substrate in order to switch a handedness of a chiral near-field between right and left enabling detection of both right and left handed chiral molecules on the achiral substrate. 8. The method of claim 1 , wherein the substrate is a plasmonic substrate, and wherein due to achiral symmetry, the plasmonic substrate suppresses the circular dichroism from the substrate, allowing detection of pure chiral signal from a sample molecule on the substrate. 9. A method of claim 1 , further comprising generating a characterization of chiral molecules for complex chiral assays, wherein the substrate comprises a thin film of the chiral molecules. 10. The method of claim 9 , wherein the complex chiral assays include at least one of: multiple molecules and control measurements. 11. The method of claim 9 , wherein the thin film comprises the chiral molecules embedded in a polymer matrix. 12. A chirality detector comprising: a substrate; a back reflector disposed on the substrate; and an array of hole-disks disposed in the substrate, each hole-disk coupled with an asymmetric optical cavity, wherein each asymmetric optical cavity is defined by the back reflector separating a plasmonic pattern by a given thickness. 13. The chirality detector of claim 12 , wherein the array of hole-disks is a nanostructured square array of hole-disks. 14. The chirality detector of claim 12 , wherein the array of hole-disks comprises gold hole-disks, and wherein the back reflector comprises gold. 15. The chirality detector of claim 12 , further comprising a thin film of chiral molecules. 16. The chirality detector of claim 15 , wherein the thin film comprises the chiral molecules embedded in a polymer matrix. 17. The chirality detector of claim 15 , further comprising a sensor configured to detect a pure chiral signal from the chiral molecules. 18. The chirality detector of claim 12 , wherein each hole-disk is disposed at approximately an optical center of the coupled asymmetric optical cavity. 19. The chirality detector of claim 12 , further comprising a source of circularly polarized light, the source configured to illuminate the array of hole-disks. 20. The chirality detector of claim 19 , further comprising optics configured to transform a Fourier-transform infrared spectroscopy signal into the circularly polarized light.
Polarisation-affecting properties (G01N21/19 takes precedence) · CPC title
using FTIR · CPC title
detecting the surface plasmon resonance of nanostructured metals, e.g. localised surface plasmon resonance · CPC title
Dichroism · CPC title
using infrared light (G01N21/39 takes precedence) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.