Method of component assembly on a substrate
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.
1. A method for fabricating a sensor structure, the method comprising the steps of:
providing a first Bragg mirror;
providing a second Bragg mirror as a free-standing component; and
providing 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 method as claimed in claim 1 , wherein the first Bragg mirror is formed on a first substrate.
3. The method as claimed in claim 1 , further comprising derivatizing a surface of at least one of the first and second Bragg mirrors prior to providing the stimuli responsive material disposed between the first and second Bragg mirrors.
4. The method as claimed in claim 1 , wherein providing the second Bragg mirror as a free-standing component further comprises the steps of
forming the second Bragg mirror on a further substrate; and
lifting off the second Bragg mirror from the substrate prior to assembling the second Bragg mirror on the first Bragg mirror.
5. The method as claimed in claim 1 , the method further comprising the step of anodizing crystalline silicon in ethanolic hydrofluoric acid solution with a step function to yield alternating layers of high and low refractive index with an optical thickness to form the Bragg mirrors.
6. The method of claim 1 , wherein the stimuli responsive material comprises at least one of gelatin, an extracellular matrix biopolymer, a protein, an oligosaccharide, a proteoglycan, a recombinant polypeptide, a synthetic polypeptides, a nucleic acid, a synthetic co-polymer system, a small molecule and nano-object encapsulated polymer, a pNIPAM, a lipids, a carbohydrate, cellulose, a cell, plant tissue, animal tissue, a polymer, a hydrogel, a microorganisms, a nanoparticle, or a nanowire.
7. The method of claim 1 , further comprising derivatizing a surface of at least one of the first and second Bragg mirrors using at least one of a succininide ester, a carboxylic acid, an amine, a maleimide, an epoxide, an azide, an alkynes, an alcohols, a carbodiimide, an aldehyde, a diazonium, an imines, an acid chloride, a disulfide, or an anhydrides.
8. The method 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.
9. The method of claim 1 , wherein a stimuli for the stimuli responsive material comprises at least one of a biomolecule, a chemical, a temperature, light, a pH, a voltage, or a mechanical force.
10. The method of claim 1 , wherein providing the first and second Bragg mirrors comprises providing the first and second Bragg mirrors such that at least one of the first and second Bragg mirrors are responsive to a further stimuli.
11. The method of claim 1 , wherein at least one of the first and second Bragg mirrors comprise PSi nanoporous structures.
12. A method of fabricating a light emitting device, the method comprising the steps of:
providing a first Bragg mirror;
providing a second Bragg mirror as a free-standing component; and
providing a light emitting material disposed at an interface 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.
13. The method of claim 12 , wherein the light emitting material comprises at least one of a biorecognition element, a complementary biomolecular species, and quantum dots.
14. The method of claim 12 , wherein the light emitting material comprises a mixture of at least one biorecognition elements, at least one complementary biomolecular species, and quantum dots, wherein the binding interaction comprises the quantum dots being bound via pairs of the biorecognition elements and the complementary species.
15. The method of claim 14 , wherein the binding interaction further comprises the at least one biorecognition elements, the at least one complementary biomolecular species, and the quantum dots diffusing into respective interfacial regions of the first and second Bragg mirrors.
16. The method of claim 14 , wherein the quantum dots comprise II-VI semiconductor quantum dots or III-V semiconductor quantum dots.
17. The method of claim 12 , wherein the light emitting material comprises at least one of different types of QDs in different lateral areas within a layer or different types of QDs in different layers.
18. The method of claim 12 , further comprising forming an optical cavity at the interface between the first and second Bragg mirrors.
19. The method of claim 12 , wherein the light emitting material further comprises a gain material for facilitating lasing.
20. The method of claim 19 , wherein a thickness of the optical cavity matches an emission wavelength of the light emitting material.