Patent Application
20150362433
Systems for performing molecular analysis can include the use of surface-enhanced Raman spectroscopy (SERS), enhanced fluorescence, enhanced luminescence, and plasmonic sensing, among others. With specific regard to SERS, Raman spectroscopy is a spectroscopic technique used in condensed matter physics and chemistry to study various low-frequency modes in molecular systems. In further detail, in a Raman spectroscopic, an approximately monochromatic beam of light of a particular wavelength range passes through a sample of molecules and a spectrum of scattered light is emitted. The spectrum of wavelengths emitted from the molecule is called a “Raman spectrum” and the emitted light is called “Raman scattered light.” A Raman spectrum can reveal electronic, vibrational, and rotational energies levels of a molecule. Different molecules produce different Ra-man spectrums that can be used like a fingerprint to identify molecules and even determine the structure of molecules. With this and other sensing techniques, enhancing device sensitivity, simplifying sensors, providing additional flexibility, etc., in such devices would be desirable.
Additional features and advantages of the invention will be apparent from the detailed description which follows, taken in conjunction with the accompanying drawings, which together illustrate, by way of example, features of the disclosure.
Reference will now be made to the exemplary embodiments illustrated, and specific language will be used herein to describe the same. It will nevertheless be understood that no limitation of the scope of the disclosure is thereby intended.
Raman spectroscopy can be used to study the transitions between molecular energy states when photons interact with molecules, which results in the energy of the scattered photons being shifted. The Raman scattering of a molecule can be seen as two processes. The molecule, which is at a certain energy state, is first excited into another (either virtual or real) energy state by the incident photons, which is ordinarily in the optical frequency domain. The excited molecule then radiates as a dipole source under the influence of the environment in which it sits at a frequency that may be relatively low (i.e., Stokes scattering), or that may be relatively high (i.e., anti-Stokes scattering) compared to the excitation photons. The Raman spectrum of different molecules or matters has characteristic peaks that can be used to identify the species. As such, Raman spectroscopy is a useful technique for a variety of chemical or bio-logical sensing applications. However, the intrinsic Raman scattering process is very inefficient, and rough metal surfaces, various types of nano-antennas, as well as waveguiding structures have been used to enhance the Raman scattering processes (i.e., the excitation and/or radiation process described above).
The Raman scattered light generated by a compound (or ion) adsorbed on or within a few nanometers of a structured metal surface can be over 100 times greater than the Raman scattered light generated by the same compound in solution or in the gas phase. This process of analyzing a compound is called surface-enhanced Raman spectroscopy (“SERS”). In recent years, SERS has emerged as a routine and powerful tool for investigating molecular structures and characterizing interfacial and thin-film systems, and even enables single-molecule detection. Engineers, physicists, and chemists continue to seek improvements in systems and methods for performing SERS.
Most SERS systems only enhance the electro-magnetic field at certain hot spots. While this can be desirable, in many cases, the analytes are spread evenly on the SERS substrate, such as by simple adsorption. However, only a small fraction of the analytes actually populates the hot spots.
It has been recognized that it would be advantageous to develop a chemical sensing device based on a new class of surface-enhanced Raman spectroscopy (SERS) structures. Specifically, the present devices can contain a plurality of elongated nanostructures affixed to a substrate with a free end having a metallic coating or cap. The present nanostructures can flex and trap molecules which can then be sensed using SERS techniques. Further, the present nanostructures generally include ligands attached to the metallic coating or cap that can provide selectivity and sensitivity previously unachieved.
It is noted that when discussing a chemical sensing device, a method detecting a target molecule, or a method of making a chemical sensing device, each of these discussions can be considered applicable to the other embodiment, whether or not they are explicitly discussed in the context of that embodiment. Thus, for example, in discussing a ligand for a chemical sensing device, such a ligand can also be used in a method of detecting a target molecule, and vice versa.
Thus, a chemical sensing device can include a substrate and an elongated nanostructure having an attachment end and a free end opposite the attachment end, the attachment end affixed to the substrate and the free end including a metal having a potential sensing ligand attached thereto via a covalent bond.
As used herein, the term “nanostructure” refers to any structure having dimensions of width or diameter less than 1 micron. As such, an elongated nanostructure can include structures that have an aspect ratio with a length at least two times longer than the shortest width. Examples can include nanocones, nanopyramids, nanorods, nanobars, nanofingers, nanopoles and nanograss, without limitation thereto. As used herein, the terms “nanocones,” “nanopyramids,” “nanorods,” “nanobars,” “nanopoles” and “nanograss,” refer to structures that are substantially: conical, pyramidal, rod-like, bar-like, pole-like and grass-like, respectively, which have nano-dimensions as small as a few tens of nanometers (nm) in height and a few nanometers in diameter, or width. For example, flexible columns may include nano-columns having the following dimensions: a diameter of 10 nm to 500 nm, a height of 20 nm to 2 micrometers (μm), and a gap between flexible columns of 20 nm to 500 nm. The terms of art, “substantially conical,” “substantially pyramidal,” “substantially rod-like,” “substantially bar-like,” “substantially pole-like” and “substantially grass-like,” refers to structures that have nearly the respective shapes of cones, pyramids, rods, bars, poles and grass-like asperities within the limits of fabrication with nanotechnology.
As used herein, the term “metallic cap” refers to nanostructures, including nanospheres, prolate nanoellipsoids, oblate nanoellipsoids, nanodisks, and nanoplates, having a width or diameter of 500 nm or less. In one example, the metallic cap may possess shape-induced magnetic anisotropy. As used herein, the terms “nanospheres,” “prolate nanoellipsoids,” “oblate nanoellipsoids,” “nanodisks,” and “nanoplates,” refer to structures that are substantially: spherical, prolate ellipsoidal, oblate ellipsoidal, disk-like, and plate-like, respectively, which have nano-dimensions as small as a few nanometers in size: height, diameter, or width. In addition, the terms “substantially spherical,” “substantially prolate ellipsoidal,” “substantially oblate ellipsoidal,” “substantially disk-like,” and “substantially and plate-like,” refers to structures that have nearly the respective shapes of spheres, prolate ellipsoids, oblate ellipsoids, disks, and plates within the limits of fabrication with nanotechnology.
Generally, the elongated nanostructure can include a non-metallic column with a metallic coating or metallic cap. In one example, the nanostructure can include a polymer, such as a resist, coated with a SERS-active metal, such as gold, silver, copper, platinum, aluminum, etc. or the combination of those metals in the form of alloys. Generally, the SERS active metal can be selectively coated on the tips of the non-metallic column or deposited thereon. In addition, the SERS active metal can be a multilayer structure, for example, 10 to 100 nm silver layer with 1 to 50 nm gold over-coating, or vice versa. Additionally, the SERS active metal can be further coated with a thin dielectric layer.
Generally, the use of a polymer can render the nanostructures sufficiently flexible to permit the bending so that the tips meet at the top of the structure. Examples of suitable polymers include, but are not limited to, polymethyl methacrylate (PMMA), polycarbonate, siloxane, polydimethylsiloxane (PDMS), photoresist, nanoimprint resist, and other thermoplastic polymers and UV curable materials including one or more monomers/oligomers/polymers. In another example, the nanostructures can include an inorganic material having sufficient flexibility to bend. Examples of such inorganic materials include silicon oxide, silicon, silicon nitride, alumina, diamond, diamond-like carbon, aluminum, copper, and the like.
The chemical sensing device generally includes potential sensing ligands attached to the metallic coating or cap. In one example, the potential sensing ligand can include an attachment functional group(A), a spacer group (B), and a potential sensing moiety (PS) according to Formula I:
A—B—PS (I) Formula I
where A is an organic functional group attached to the nanostructure, B is substituted or unsubstituted, linear or branched alkyl or aryl, and PS is an organic functional group capable of binding to a target molecule. The functional group can include any group that is capable of covalent bonding to the metal coating or cap. The potential sensing moiety can include any moiety that is capable of interacting (including ionic, coordinate, covalent bonding) with a target molecule. The spacer group generally includes any group of atoms that covalently bond the functional group to the potential sensing moiety. For example, in one aspect, the metal can include gold and the functional group can include a thiol that covalently bonds to the gold. The ligand can further include an alkyl spacer group with an amine potential sensing moiety. For example, without be limiting, 3-aminopropylthiol would qualify as such a ligand, although other aminoalkylthiols would also qualify. Various functional groups can include primary amines, secondary amines, tertiary amines, amides, nitriles, isonitriles, cyanates, isocyanates, thiocyanates, isothiocyanates, azides, thiols, thiolates, sulfides, sulfinates, sulfonates, phosphates, hydroxyls, alcoholates, phenolates, carbonyls, carboxylates, phosphines, phosphine oxides, phosphonic acids, phosphoramides and phosphates. Additionally, various potential sensing groups can include functional groups as discussed herein, alone, or in combination with more complex structures, e.g., methyl red dyes, carboxyfluorescein dyes, carboxyrhodamine dyes, cyanine dyes, crown-ethers, polyamines etc. Particularly, a list of examples of potential sensing groups includes 4-pyridinethiol, 3-pyridinethiol, 2-pyridinethiol, 4-pyridinemethanethiol, 3-pyridinemethanethiol, 2-pyridinemethanethiol, 4-pyridineethanethiol, 3-pyridineethanethiol, 2-pyridineethanethiol, 4-pyridinepropanethiol, 3-pyridinepropanethiol, 2-pyridinepropanethiol, 4-pyridinebutanethiol, 3-pyridinebutanethiol, 2-pyridinebutanethiol, 4-pyridinepentanethiol, 3-pyridinepentanethiol, 2-pyridinepentanethiol, etc.
The chemical sensing device generally includes a potential sensing ligand formulated to selectively bind a target molecule. The target molecule can be a metal ion, an organic compound, or a hydrogen ion. In one example, the target molecule is a metal ion and the potential sensing ligand is formulated to selectively bind the metal ion. In one example, the metal ions can include chromium, lead, mercury, zinc, calcium, sodium, hydrogen, potassium, arsonium, and mixtures thereof.
By using the present potential sensing ligands, the chemical sensing device can be sensitive enough to detect a target molecule; including a metal ion, an organic compound, or a hydrogen ion, at a concentration as low as 1 part-per-million (ppm). In one aspect, the sensitivity can be as low as 1 part-per-billion (ppb), and in one specific aspect, as low as 1 part-per-trillion (ppt).
Regarding sensitivity, the present chemical device can include a plurality of elongated nanostructures attached to a substrate forming an array. In one example, the array can include sub-arrays. In one aspect, the sub-arrays can each have individual selectivity for a target molecule. As such, one array can have selectivity for a plurality of target molecules. The chemical sensing device can be further configured to detect the target molecule from a liquid or gas.
Additionally, the chemical sensing device can further include a detector operatively coupled to the nanostructure. In one example, the detector can be a colorimeter, a reflectometer, a spectrometer, a spectrophotometer, a Raman spectrometer, an optical microscope, and/or an instrument for measuring luminescence.
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It is noted that, as used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise.
As used herein, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. Thus, no individual member of such list should be construed as a de facto equivalent of any other member of the same list solely based on their presentation in a common group without indications to the contrary.
Concentrations, amounts, and other numerical data may be expressed or presented herein in a range format. It is to be understood that such a range format is used merely for convenience and brevity and thus should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. As an illustration, a numerical range of “about 1 wt % to about 5 wt %” should be interpreted to include not only the explicitly recited values of about 1 wt % to about 5 wt %, but also include individual values and sub-ranges within the indicated range. Thus, included in this numerical range are individual values such as 2, 3.5, and 4 and sub-ranges such as from 1-3, from 2-4, and from 3-5, etc. This same principle applies to ranges reciting only one numerical value. Furthermore, such an interpretation should apply regardless of the breadth of the range or the characteristics being described.
The following examples illustrate embodiments of the disclosure that are presently known. Thus, these examples should not be considered as limitations of the invention, but are merely in place to teach how to make devices of the present disclosure. As such, a representative number of devices and their method of manufacture are disclosed herein.
Immobilizing a potential sensing moiety to a gold surface on a nanostructure can be carried out with surface modification by treating the gold nanostructure with chemical reagents. A reactant moiety A is introduced on the surface. Additionally, a reactant moiety B having a potential sensing (PS) moiety bound thereto is reacted with the reactant moiety A. For example, the modified substrate can be dipped into the solutions of potential sensing moieties bound to the reactant moiety B. The reactant moieties A and B react heterogeneously but neither react homogeneously to form a covalent bond between the substrate and the potential sensor moiety, thus immobilizing the potential chemical sensing moiety onto the gold coated nanostructure surface.
Surface modification of a gold nanostructure is performed with 3-aminopropylthiol providing a modified surface with a reactive amino group, which is reactive towards an activated ester. The modified gold nanostructure is then treated with a solution of the activated ester, where the activated ester includes a potential sensing moiety. The reaction between the activated ester and the amino group takes place, forming a covalent bond between the potential sensing molecular moiety and the gold nanostructure surface via the propylthiol linkage.
The present example sets for the preparation of a nanostructure modified with a pH indicator to sense acidity. First, commercially available methyl red is modified with DSC (N,N′-disuccinimidyl carbonate) in the presence of catalytic amount of 3-dimethylaminopyridine to give modified methyl red with reactive succinimidyl group. Second, a gold nanostructure is modified with the solution of 3-aminopropylthiol, generating a modified gold nanostructure with a reactive amino group on the surface. When the modified nanofinger is treated with the modified methyl red, a reaction between the surface and the dye takes place, forming a gold nanofinger attached with methyl red dye, which can be used for detecting proton ion H+.
Another approach is to first modify the potential sensing moiety with certain chemical reagents to form a modified potential sensing moiety with reactive groups, which are reactive towards gold nanostructure surfaces. For example, an activated ester having a potential sensing moiety can be treated with commercially available 3-aminopropylthiol, and the reaction between the amino group with the activated ester takes place, generating a modified potential sensing moiety coupled to a reactive thiol group, which is reactive towards gold nanostructure surface. When the untreated gold nanostructure is treated with the modified potential sensing moiety coupled to a reactive thiol group, a chemical reaction between the thiol group and gold surface takes place to form a chemical bond, thus immobilizing the potential sensing moiety on the gold nanostructure surface.
Reaction of methyl red dye with 3-aminopropylthiol in the presence of coupling reagent such as N,N′-dicyclohexylcarbodiimide (DCC) forms a modified methyl red with thiol group on the end, which is reactive towards a gold surface. When a gold nanostructure is treated with the modified methyl red, a covalent bond forms between the gold nanostructure and methyl red. Thus, the methyl dye is immobilized on the gold nanostructure surface, which can be used for detection of proton ions H+.
Nanostructures (referred to as “NS” in Scheme 1 below) can be used to detect metal ions, such as chromium (VI). As shown in Scheme 1: Reaction of 4-vinylpyridine with thiourea in the presence of p-toluenesulfonic acid gave intermediate 2. Treatment of intermediate 2 with ammonium hydroxide formed 4-pyridineethantiol 3, which can be converted into HCl salt 4. Upon careful neutralization of HCl salt 4 with a base, it can be self-assembled into a gold nanostructure (NS) surface. Since the pyridine can form a coordination bond with Cr (VI), it can be used for highly sensitive and selective detection of chromium (VI).
A gold nanostructure was prepared by treatment of the surface of the gold with 4-mercaptopyridine. A gold nanostructure was dipped without stirring into a solution of ethanol containing 4-mercaptopyridine for 24 hrs at room temperature, followed by being rinsed with pure ethanol solvent. In order to prepare a cationic pyridinium form of the functionalized 4-mercaptopyridine, the gold nanostructure was re-dipped in 0.1 M sulfuric acid for 30 min. The pyridinium-functionalized nanostructure was then exposed to varying amount of Cr(VI) as shown in
While the invention has been described with reference to certain examples, those skilled in the art will appreciate that various modifications, changes, omissions, and substitutions can be made without departing from the spirit of the invention. It is intended, therefore, that the invention be limited only by the scope of the following claims.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2013/023218 | 1/25/2013 | WO | 00 |
