Sensing chip, sensing chip manufacturing method, sensing kit, measuring method and measuring device
US-2024319093-A1 · Sep 26, 2024 · US
US9347940B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9347940-B2 |
| Application number | US-201414250872-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 11, 2014 |
| Priority date | Nov 1, 2007 |
| Publication date | May 24, 2016 |
| Grant date | May 24, 2016 |
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 of component assembly on a substrate, and an assembly of a bound component on a substrate. The method comprises the steps of forming a free-standing component having an optical characteristic; providing a pattern of a first binding species on the substrate or the free standing component; and forming a bound component on the substrate through a binding interaction via the first binding species; wherein the bound component exhibits substantially the same optical characteristic compared to the free-standing component.
Opening claim text (preview).
What is claimed is: 1. A sensor structure comprising: a first Bragg mirror; a second Bragg mirror that is a free-standing component; and a stimuli responsive material disposed between the first and second Bragg mirrors; wherein the second Bragg mirror is assembled on the first Bragg mirror by a binding interaction via the stimuli responsive material. 2. The sensor structure of claim 1 , wherein the stimuli responsive material is disposed between the first and second Bragg mirrors such that infiltration of the stimuli responsive material is prevented. 3. The sensor structure of claim 2 , wherein derivatisation of a surface of at least one of the first Bragg mirror, the second Bragg mirror, or both was performed prior to deposition of the stimuli responsive material. 4. The sensor structure of claim 1 , wherein a stimulus for the stimuli responsive material comprises one or a group of a biomolecule, a chemical, a temperature, light, a pH, a voltage, or a mechanical force. 5. The sensor structure of claim 1 , wherein the stimuli responsive material comprises one or more of gelatin, extracellular matrix biopolymers, proteins, oligosaccharides, proteoglycans, recombinant polypeptides, synthetic polypeptides, nucleic acids, synthetic co-polymer systems, small molecule and nano-object encapsulated polymers, pNIPAM, lipids, carbohydrates, cellulose, cells, plant or animal tissue, polymers of any type, hydrogels, microorganisms, nanoparticles, or nanowires. 6. The sensor structure of claim 1 , wherein one or both of the first Bragg mirror and the second Bragg mirror is configured to be responsive to a further stimulus. 7. The sensor structure of claim 1 , wherein one or both of the first and second Bragg mirrors comprises PSi nanoporous structures. 8. The sensor structure of claim 1 , wherein the first Bragg mirror is formed on a substrate. 9. The sensor structure of claim 8 , wherein the substrate and the second Bragg mirror are lattice mismatched. 10. The sensor structure of claim 1 , wherein the first Bragg mirror exhibits substantially the same optical characteristic as the second Bragg mirror. 11. A light emitting device comprising: a first Bragg mirror; a second Bragg mirror that is a free-standing component; and a light emitting material disposed between the first and second Bragg mirrors; wherein the second Bragg mirror is assembled on the first Bragg mirror by a binding interaction via the light emitting material. 12. The light emitting device of claim 11 , wherein the light emitting material comprises at least one of a biorecognition element, a complementary biomolecular species, or quantum dots. 13. The light emitting device of claim 11 , wherein the light emitting material comprises a mixture of at least one biorecognition element, at least one complementary biomolecular species, and quantum dots, and wherein a binding interaction in the light emitting material includes the quantum dots being bound via pairs of the at least one biorecognition element and the at least one complementary biomolecular species. 14. The light emitting device of claim 13 , wherein the second Bragg mirror is assembled on the first Bragg mirror by the binding interaction of the at least one biorecognition element, the at least one complementary biomolecular species, and the quantum dots diffusing into respective interfacial regions of the first and second Bragg mirrors. 15. The light emitting device of claim 13 , wherein the quantum dots comprise II-VI semiconductor quantum dots or III-V semiconductor quantum dots. 16. The light emitting device of claim 11 , wherein the light emitting material comprises at least one of different types of quantum dots in different lateral areas within a layer or different types of quantum dots in different layers. 17. The light emitting device of claim 11 , wherein the light emitting material further comprises a gain material configured to facilitate lasing. 18. The light emitting device of claim 11 , further comprising an optical cavity disposed at the interface between the first and second Bragg mirrors. 19. The light emitting device of claim 18 , wherein a thickness of the optical cavity corresponds with an emission wavelength of the light emitting material. 20. The light emitting device of claim 11 , wherein the first Bragg mirror is formed on a substrate.
forming resonant cavity structures · CPC title
within the light-emitting regions, e.g. having quantum confinement structures · CPC title
Multilayer mirrors, i.e. having two or more reflecting layers (G02B5/0883, G02B5/0891 take precedence) · CPC title
involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings · CPC title
Aligning microparts · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.