GAS SENSOR WITH SUPERLATTICE STRUCTURE

Abstract

A gas sensor has a microstructure sensing element which comprises a plurality of interconnected units wherein the units are formed of connected graphene tubes. The graphene tubes may be formed by photo-initiating the polymerization of a monomer in a pattern of interconnected units to form a polymer microlattice, removing unpolymerized monomer, coating the polymer microlattice with a metal, removing the polymer microlattice to leave a metal microlattice, depositing graphitic carbon on the metal microlattice, converting the graphitic carbon to graphene, and removing the metal microlattice.

Claims

1. A gas sensor having a microstructure sensing element comprising: a plurality of interconnected units including at least a first unit formed of first graphene tubes; and a second unit formed of second graphene tubes, wherein one or more of the second graphene tubes are connected to one or more of the first graphene tubes.

2. The gas sensor having a microstructure sensing element recited in claim 1 wherein the graphene tubes are arranged in an ordered structure and form symmetric patterns that repeat along the principal directions of three-dimensional space.

3. The gas sensor having a microstructure sensing element recited in claim 1 wherein the graphene tubes form a rigid structure.

4. The gas sensor having a microstructure sensing element recited in claim 1 wherein the plurality of interconnected units forms a microlattice.

5. The gas sensor having a microstructure sensing element recited in claim 1 wherein the graphene tubes are hollow.

6. The gas sensor having a microstructure sensing element recited in claim 1 wherein the graphene tubes are interconnected by chemical electronic bonds.

7. A method of forming a sensor element for a gas sensor comprising: photo-initiating the polymerization of a monomer in a pattern of interconnected units to form a polymer microlattice; removing unpolymerized monomer; coating the polymer microlattice with a metal; removing the polymer microlattice to leave a metal microlattice; depositing graphitic carbon on the metal microlattice; converting the graphitic carbon to graphene; and removing the metal microlattice.

8. The method recited in claim 7 wherein photo-initiating the polymerization of the monomer comprises passing collimated light through a photomask.

9. The method recited in claim 7 wherein photo-initiating the polymerization of the monomer comprises multi-photon lithography.

10. The method recited in claim 7 wherein coating the polymer microlattice with a metal comprises the electroless deposition of copper.

11. The method recited in claim 7 wherein coating the polymer microlattice with a metal comprises the electroless deposition of nickel.

12. The method recited in claim 7 wherein the polymer microlattice comprises polystyrene.

13. The method recited in claim 7 wherein the polymer microlattice comprises poly(methyl methacrylate).

14. A gas sensor having a graphene microstructure sensor element prepared by the process comprising the steps of: photo-initiating the polymerization of a monomer in a pattern of interconnected units to form a polymer microlattice; removing unpolymerized monomer; coating the polymer microlattice with a metal; removing the polymer microlattice to leave a metal microlattice; depositing graphitic carbon on the metal microlattice; converting the graphitic carbon to graphene; and removing the metal microlattice.

15. The gas sensor recited in claim 14 wherein photo-initiating the polymerization of the monomer comprises passing collimated light through a photomask.

16. The gas sensor recited in claim 14 wherein photo-initiating the polymerization of the monomer comprises multi-photon lithography.

17. The gas sensor recited in claim 14 wherein coating the polymer microlattice with a metal comprises the electroless deposition of copper.

18. The gas sensor recited in claim 14 wherein coating the polymer microlattice with a metal comprises the electroless deposition of nickel.

19. The gas sensor recited in claim 14 wherein the polymer microlattice comprises polystyrene.

20. The gas sensor recited in claim 14 wherein the polymer microlattice comprises poly(methyl methacrylate).

Description

DETAILED DESCRIPTION

[0017] Although graphene is an effective gas sensor (having low density of states (DOS) and carrier concentration plus reversible chemical doping), it has certain limitations when used in the 2D form. These limitations include: substrate effects including a lack of structural stability when suspended; and, a limited surface area (a single face) available for gas detection.

[0018] It has been found that an organic/inorganic superstructure may be used as a template for the formation of a 3D metal superstructure that may then be used to grow graphitic carbon on the surface of the metal. The template may be fabricated through a self-propagating photopolymer waveguide technique (see, e.g., Xiaoyu Zheng et. al., Ultralight, Ultrastiff Mechanical Metamaterials; Science 344 (2014) 1373-1377 and T. A. Schaedler, et al., Ultralight Metallic Microlattices; Science 334 (2011) 962-965) in which an interconnected 3D photopolymer lattice may be produced upon exposure of an appropriate liquid photomonomer to collimated UV light through a specifically designed mask that contains openings with certain spacing and size. The fabricated microlattice may then be coated by electroless copper or other suitable metal (e.g. Ni, Co, Au, Ag, Cu, and alloys thereof) followed by etching away the organic polymeric matrix (scaffold). The resulting metal-based microlattice may be then used as a template to grow the graphitic carbon. The thickness of the electroless plated metal may be controlled in the range of nanometer to micrometer by adjusting the plating time, temperature, and/or plating chemistry.

[0019] FIG. 1A schematically illustrates an exemplary fabrication process of organic polymeric microlattices (scaffolds) prior to coating with electroless plating.

[0020] The present disclosure is of a gas sensor having as its sensing element a periodically structured carbon nanostructure. The carbon nanostructures of the prior art are irregular and have much larger dimensions than those which may be achieved using the methodology disclosed herein.

[0021] The present process may be used to create a regular array, and the superstructure dimensions (unit) and structure may be optimized for strength, thermal and other fundamental properties.

[0022] There are several aspects of this procedure that are noteworthy: [0023] it provides a regular structure with defined dimensions; [0024] it can form very thin metal (e.g. Ni, Co, Cu, Ag, Au) microlattices; [0025] it enables the formation of graphitic carbon on very thin metals by a surface-limited process for very thin metal wires or tubes.

[0026] The present process uses a polymeric structure as a template for such fabrication with the subsequent formation of a metal superstructure that may then be exposed to a hydrocarbon (e.g. methane, ethylene, acetylene, benzene) to form graphitic carbon, followed by etching of the metal from under the graphitic carbon using appropriate etchants such as, for example, FeCl.sub.3 or potassium permanganate.

[0027] Collimated light through a photomask or multi-photon lithography may be used in a photo-initiated polymerization to produce a polymer microlattice comprised of a plurality of interconnected units. Exemplary polymers include polystyrene and poly(methyl methacrylate) (PMMA). Once polymerized in the desired pattern, the remaining un-polymerized monomer may be removed.

[0028] The polymer structure (polymer scaffold) may then be plated with a suitable metal using an electroless plating process.

[0029] Electroless nickel plating (EN) is an auto-catalytic chemical technique that may be used to deposit a layer of nickel-phosphorus or nickel-boron alloy on a solid workpiece, such as metal, plastic, or ceramic. The process relies on the presence of a reducing agent, for example hydrated sodium hypophosphite (NaPO.sub.2H.sub.2H.sub.2O) which reacts with the metal ions to deposit metal. Alloys with different percentages of phosphorus, ranging from 2-5 (low phosphorus) to up to 11-14 (high phosphorus) are possible. The metallurgical properties of the alloys depend on the percentage of phosphorus.

[0030] Electroless plating has several advantages over electroplating. Free from flux-density and power supply issues, it provides an even deposit regardless of workpiece geometry, and with the proper pre-plate catalyst, may deposit on non-conductive surfaces. In contradistinction, electroplating can only be performed on electrically conductive substrates.

[0031] Before performing electroless plating, the material to be plated must be cleaned by a series of chemicals; this is known as the pre-treatment process. Failure to remove unwanted soils from the part's surface results in poor plating. Each pre-treatment chemical must be followed by water rinsing (normally two to three times) to remove chemicals that may adhere to the surface. De-greasing removes oils from surfaces, whereas acid cleaning removes scaling.

[0032] Activation may be done with an immersion into a sensitizer/activator solutionfor example, a mixture of palladium chloride, tin chloride, and hydrochloric acid. In the case of non-metallic substrates, a proprietary solution is often used.

[0033] The pre-treatment required for the deposition of metals on a non-conductive surface usually consists of an initial surface preparation to render the substrate hydrophilic. Following this initial step, the surface may be activated by a solution of a noble metal, e.g., palladium chloride. Electroless bath formation varies with the activator. The substrate is then ready for electroless deposition.

[0034] The reaction is accomplished when hydrogen is released by a reducing agent, normally sodium hypophosphite (with the hydrogen leaving as a hydride ion) or thiourea, and oxidized, thus producing a negative charge on the surface of the part. The most common electroless plating method is electroless nickel plating, although silver, gold and copper layers can also be applied in this manner.

[0035] In principle any hydrogen-based reducing agent can be used although the redox potential of the reducing half-cell must be high enough to overcome the energy barriers inherent in liquid chemistry. Electroless nickel plating most often employs hypophosphite as the reducer while plating of other metals like silver, gold and copper typically makes use of low-molecular-weight aldehydes.

[0036] A benefit of this approach is that the technique can be used to plate diverse shapes and types of surfaces.

[0037] As illustrated in FIG. 1B, the organic polymeric microlattice may be electrolessly plated with metal followed by dissolving out the organic polymer scaffold. The resulting metal-based microlattice may then be coated with a thin layer of immersion tin in order to prevent the metal from oxidizing during the subsequent process which may include a heat treatment. In an example, a copper/nickel super-lattice is used. The fabricated metal-based microlattice may be used as a template to synthesize a graphitic carbon superstructure. The metal may then be etched out to produce a graphene microstructure comprising a plurality of interconnected units wherein the units are formed of graphene tubes that are connected by chemical electronic bonds (as distinguished from van der Waals forces which may cause carbon nanotubes to agglomerate).

[0038] As illustrated in FIGS. 3 and 4, a 3D graphene microstructure comprising a plurality of interconnected units wherein the units are formed of connected graphene tubes may have sufficient structural rigidity to fabricate a gas sensor having a channel below the layer of graphene (see FIG. 3) thereby improving the sensitivity of the gas sensor by exposing both surfaces of the graphene element to the gas molecules. Alternatively, as illustrated in FIG. 4, if the sensor element comprises a 3D graphene super-lattice structure supported on the dielectric-coated substrate, enhanced sensitivity may obtain because of its gas permeability and increased surface area.

[0039] Modifications are possible in the described embodiments, and other embodiments are possible, within the scope of the claims.