Method and apparatus for enhanced nano-spectroscopic scanning
Apparatus and method for examining the identity of chemical groups in a sample are disclosed. The apparatus has a substrate having a plasmon resonant surface on which the sample is supported, a source of a beam of light, and a lens assembly having a tip region and a nanolens composed of one or more plasmon resonance particles (PRPs) on the tip region. The PRPs are arranged to produce near-field electromagnetic gap modes in a space between the nanolens and a confronting detection region on the substrate surface when the gap between the nanolens and substrate is 30 nm or less. A focusing mechanism in the apparatus operates to move the lens assembly toward and away from the substrate surface, with a gap of less than 30 nm, to produce electromagnetic gap modes that enhance the Raman spectroscopy signals produced by the sample in the detection region.
1. Apparatus for examining the identity of chemical groups in a sample attached to a surface, comprising
a substrate having a mirror surface on which the sample is supported, and which is formed of a plasmon resonant metal,
a source of a beam of light,
a lens assembly having a tip region and a nanolens composed of one or more plasmon resonance particles disposed on the tip region, and arranged thereon to produce, when the light beam is directed through the nanolens, near-field electromagnetic gap modes in a space between the nanolens and a confronting detection region on the substrate surface, in a gap between the nanolens and substrate that is 40 nm or less,
a focusing mechanism for moving the lens assembly toward and away from the substrate surface, with a gap of less than 40 nm, to produce electromagnetic gap modes that enhance the Raman spectroscopy signals produced by the sample in the detection region;
a detector for receiving light emitted by or scattered from the sample at the detection region, and for converting the received light into a gap-mode enhanced Raman spectrum, whereby the sample chemical group at the detection region can be identified, and
a translation mechanism for translating the lens assembly relative to said substrate, to position the lens assembly over different detection regions of the substrate.
2. The apparatus of claim 1 , wherein the nanolens in said assembly includes at least said three plasmon resonance particles arranged symmetrically about a central axis that is normal to the plane of the substrate surface, each particle is less than 200 nm in its largest dimension, and the distance across any pair of particles is substantially less than the wavelength of the light beam.
3. The apparatus of claim 2 , wherein said particles are spherical.
4. The apparatus of claim 2 , wherein said particles are ellipsoidal and arranged with their major axes oriented to intersect said central axis.
5. The apparatus of claim 2 , wherein said light source produces a beam of circularly polarized light whose plane of polarization is normal to said central axis.
6. The apparatus of claim 1 , wherein said lens assembly includes a cantilever beam having a tip region at its free end.
7. The apparatus of claim 6 , wherein said focusing mechanism includes a piezo-electric driver operatively coupled to said beam.
8. The apparatus of claim 7 , wherein said focusing mechanism is operative to bring said nanolens to a selected distance between 0.1 and 5 nm of the substrate surface.
9. The apparatus of claim 1 , wherein said translation mechanism includes a piezoelectronic drive.
10. The apparatus of claim 1 , for use in sequencing a linear strand of nucleic acid, by examining the chemical-group bases of the nucleic acid strand, wherein the substrate includes molecular anchors for holding the nucleic acid strand in a stretched linear condition, and the translation mechanism is operable to move the lens assembly along the length of the strand, for examining and identifying each base of the strand sequentially.
11. The apparatus of claim 10 for examining a plurality of substantially linear samples simultaneous, which includes a plurality of linearly aligned cantilever lens assemblies, each of whose position toward and away from the substrate surface can be individually controlled by a corresponding focusing mechanism associated with each lens assembly, and which are translated as a unit by a single translation mechanism.
12. The apparatus of claim 11 , for use in sequencing a plurality of linear strands of nucleic acid, by examining the chemical-group bases of the nucleic acid strands, wherein the substrate includes molecular anchors for holding each of the nucleic acid strands in a stretched linear condition, and the translation mechanism is operable to move the lens assembly along the lengths of the strands, for examining and identifying each base of the strands sequentially.
13. A method for examining the identity of chemical groups in a sample, comprising
attaching the sample to a substrate having a mirror surface on which the sample is supported, and which is formed of a plasmon resonant metal,
directing a beam of light onto a nanolens in a lens assembly having a tip region and a nanolens disposed on the tip region and composed of one or more plasmon resonance particles which are arranged on the tip region to produce near-field electromagnetic gap modes in a space between the nanolens and a confronting detection region on the substrate surface, when the gap between the nanolens and substrate is 30 nm or less,
moving the lens assembly toward or away from the substrate surface, with a spacing between the nanolens and substrate surface of less than 30 nm, to produce electromagnetic gap modes that enhance the Raman spectroscopy signals produced by the sample in the detection region;
receiving light emitted by or scattered from the sample at the detection region, and
converting the received light into a gap-mode enhanced Raman spectrum, whereby the sample chemical group at the detection region can be identified.
14. The method of claim 13 , wherein said moving is carried out to bring said nanolens to a selected gap distance between 0.1 and 5 nm of the substrate surface.
15. The method of claim 13 , wherein said directing includes directing the light beam onto a nanolens composed of at least said three plasmon resonance particles arranged symmetrically about a central axis that is normal to the plane of the substrate surface, each particle is less than 200 nm in its largest dimension, and the distance across any pair of particles is substantially less than the wavelength of the light beam.
16. The method of claim 15 , wherein said directing includes directing onto said lens, a beam of circularly polarized light whose plane of polarization is normal to said central axis.
17. The method of claim 15 , for use in sequencing a linear strand of nucleic acid, wherein said attaching includes stretching the strand linearly, and anchoring opposite end portions of the strands to said substrate, and which further includes translating the lens assembly with respect to the sample on the substrate, to position the nanolens adjacent successive chemical-group bases in the strand.
18. The method of claim 17 , for use in sequencing a plurality of linear strands of nucleic acid samples, wherein said attaching includes anchoring the samples in a plurality of parallel strands, and said translating includes translating the lens assembly with respect to the samples on the substrate, to position the nanolens adjacent successive chemical-group bases in each of the strands.