Laser-induced carbon nanostructures
Producing a food testing sensor electrode, using a first laser beam to irradiate an encapsulated, sub-surface region of a carbon pre-cursor material below a surface of the carbon pre-cursor material, the first laser beam selected to create carbon foam in the sub-surface region and a carbon-based material above the carbon foam; and a second laser beam to remove or ablate the carbon-based material sitting above the carbon foam, the second laser beam being to expose or alter at least some of the carbon foam, to produce a resultant carbon foam material; and functionalising the resultant carbon foam material by adding a receptor or recognition element that is specific to a target or analyte to the resultant carbon foam material or a linker that is attached to the resultant carbon foam material; and providing the functionalised carbon foam material for use as a sensor electrode in an assay device.
1 . A method of producing a food testing sensor electrode, comprising the steps of:
(a) using a first laser beam configured to irradiate an encapsulated, sub-surface region of a carbon pre-cursor material below a surface of the carbon pre-cursor material, parameters of the first laser beam being selected to create carbon foam in that encapsulated, sub-surface region and a carbon-based material above the carbon foam; and
(b) using a second laser beam configured to remove or ablate the carbon-based material sitting above the carbon foam, parameters of the second laser beam being selected to expose or alter at least some of the carbon foam, to produce a resultant carbon foam material; and
(c) functionalising the resultant carbon foam material by adding a receptor or recognition element that is specific to a target or analyte to the resultant carbon foam material or a linker that is attached to the resultant carbon foam material;
(d) providing the functionalised carbon foam material for use as a sensor electrode in an assay device, configured for food testing.
2 . The method of claim 1 in which the first laser beam operates at a first band and the second laser beam operates at a second band.
3 . The method of claim 1 in which the parameters of the first laser beam that irradiates the sub-surface, encapsulated region include one or more of: intensity, wavelength, pulse frequency, pulse duration, pulse profile, scanning speed, focal distance, heat generated at the sub-surface, encapsulated region, and in which varying the laser parameters of the first laser beam alters the carbon foam properties, enabling the resultant carbon foam material to be produced with properties that are optimised for different applications.
4 . The method of claim 3 in which varying the laser parameters of the first laser beam alters one or more of the following resultant carbon foam material properties or parameters: type of carbon nanostructures present, size of defects, distribution of defects, extent of defects, type of defects, size of the Raman D and 2D peaks, relative size of the Raman D and 2D peaks, thickness or depth, flexibility, adhesion, porosity, electrical conductivity, capacitance, absorption of organic solvents and water-based solutions, hydrophilicity, EMI shielding, electrode quality, carbon foam material wettability, carbon foam material contact angle, carbon foam material anti-fouling.
5 . The method of claim 1 in which no substantial gas escape pathways to a surface of the carbon pre-cursor material are created by the first laser beam.
6 . The method of claim 1 in which the first laser beam has a wavelength with very low absorbance by the carbon pre-cursor material.
7 . The method of claim 1 in which the sub-surface, encapsulated region has a thickness of between 10 μm and 200 μm.
8 . The method of claim 1 in which the carbon pre-cursor material is made substantially of one of the following: thermosetting material, one or more polymers.
9 . The method of claim 1 in which a surface of the carbon pre-cursor material is positioned on or adjacent to a substrate and in which the surface of the carbon pre-cursor material is converted to a disorganised, amorphous, non-graphene substance by the first laser beam and that disorganised, amorphous, non-graphene substance adheres or bonds to the substrate and hence indirectly attaches the carbon foam to the substrate.
10 . The method of claim 1 in which the carbon-based material created above the carbon foam by the first laser beam is a disorganised, amorphous, non-graphene substance.
11 . The method of claim 1 in which the parameters of the second laser beam include one or more of: intensity, wavelength, pulse frequency, pulse duration, pulse profile, scanning speed, focal distance, and heat generated at the sub-surface or encapsulated region; in which varying the second laser parameters alters the resultant carbon foam material properties, enabling the resultant carbon foam material to be produced with properties that are optimised for different applications;
and in which varying the laser parameters of the second laser beam alters one or more of the following resultant carbon foam material properties or parameters: type of carbon nanostructures present, size of defects, distribution of defects, extent of defects, type of defects, of the Raman D and 2D peaks, relative size of the Raman D and 2D peaks, thickness or depth, flexibility, adhesion, porosity, electrical conductivity, capacitance, absorption of organic solvents and water-based solutions, hydrophilicity, EMI shielding, electrode quality, carbon foam material wettability, carbon foam material contact angle, carbon foam material anti-fouling.
12 . The method of claim 1 in which the second laser beam alters the carbon foam to the resultant carbon foam material as part of the process of exposing the carbon foam.
13 . The method of claim 1 in which the second laser beam alters the morphology of the carbon foam as part of the process of creating the resultant carbon foam material and exposing the resultant carbon foam material.
14 . The method of claim 1 in which the resultant carbon foam material is or includes one or both of the following: a multilayer twisted or turbostratic carbon foam, and a non-graphene carbon foam.
15 . The method of claim 1 in which the resultant carbon foam material is between approximately 50 μm to 300 μm in thickness.
16 . The method of claim 1 in which the resultant carbon foam material is or includes a carbon foam with a spatial distribution of defects or vacancy position basal plane defects leading to electrochemical reactivity.
17 . The method of claim 1 in which the resultant carbon foam material has a contact angle of below 20°.
18 . The method of claim 1 including the step of using computer-controlled laser scanning for the first and the second laser beams.
19 . The method of claim 1 including the step of using reel-to-reel or reel-to-sheet production systems to pass reels or sheets of the carbon pre-cursor material past computer-controlled laser scanning that delivers the first and the second laser beams.
20 . The method of claim 1 when used for manufacturing, in one manufacturing facility, a sensor including sensor electrodes, each sensor electrode comprising the resultant carbon foam material, and the method includes the further step of adding, at the same or a different manufacturing facility, functionalised groups to a working electrode of the sensor electrodes.
21 . The method of claim 1 in which the resultant carbon foam material is functionalised as a sensor by adding a receptor that is specific to a target or analyte, and a linker that enables the receptor to attach to the carbon foam, and the receptor is selected from the following: crown ethers, catalysts, boric acids, ligands, aptamers, proteins, enzymes, antibodies, antigens, microorganisms, nucleic acids, fatty acids, fatty acid esters, molecularly imprinted polymers, metal-organic frameworks, polypeptides or oligopeptides capable of forming a ligand binding, cells, cell organelles, or other cellular components, or mixtures thereof.
22 . The method of claim 1 when used for manufacturing a sensor including sensor electrodes, each sensor electrode comprising the resultant carbon foam material and where the method includes printing electrical connection tracks over each sensor electrode and at least partly covering each sensor electrode and connection tracks with a printed dielectric.
23 . The method of claim 22 where each sensor electrode is formed onto an electrical connection track that has been previously printed on to the carbon pre-cursor material.
24 . The method of claim 22 where each sensor electrode is formed onto previously printed electrical connection tracks, a dielectric layer and a reference electrode.
25 . The method of claim 22 where each sensor electrode has a bottom face or base and electrical connections are positioned on the bottom face or base.
26 . The method of claim 22 where each sensor electrode is positioned in a layer below one or more sample wells, and electrode connections are positioned in layer below each sensor electrode.
27 . The method of claim 22 where each sensor electrode is formed in a multi-layer structure, in which an upper layer or layers includes one or more sample wells and a microfluidics channel, and one or more sensor electrodes are positioned below these upper layer or layers to receive a test fluid distributed by the microfluidics channel, and electrode connections to the or each sensor electrodes are positioned in a layer below the or each sensor electrode.
28 . The method of claim 1 , in which the assay device is an electrochemical assay device.
29 . The method of claim 20 , in which the sensor electrodes include a working electrode or a counter electrode.
30 . The method of claim 22 , in which the sensor electrodes include a working electrode or a counter electrode, and in which the printed dielectric is a screen printed dielectric.