Patent Application
20180068756
The present invention relates to transparent, electrically-conductive solid materials, and methods and compositions for forming transparent, electrically-conductive solid materials, in particular, but not exclusively coatings. Such coatings may typically (but not exclusively) be used as part of substrates for electrical and opto-electrical devices, such as displays (for example, liquid crystal displays) or photovoltaic devices.
The provision of transparent electrically-conductive materials, such as coatings, is well-known to those skilled in the art. Such coatings are typically made from indium tin oxide (ITO) which is deposited under low pressure conditions. Deposition of ITO is therefore an expensive process requiring specialised equipment. ITO also tends to be brittle, and therefore may be unsuitable for use on flexible substrates. Furthermore, ITO has a relatively high optical absorbance and therefore ITO tends to be deposited in relatively thin layers in order that the ITO is transparent. It can be difficult to prepare such thin layers on relatively rough substrates. Indium is expensive and the mass of indium which is economically viable to mine is limited.
The increase in adoption of flexible screens and touch-screen displays provides challenges to the application of ITO. Several flexible conductive coatings have been proposed to those skilled in the art. For example, it is known to use conductive polymers or silver nanowires to form conductive coatings.
The present invention seeks to mitigate against one or more of the problems mentioned above.
In accordance with a first aspect of the present invention, there is provided a method of forming an electrically-conductive, transparent solid material, said method comprising:
The applicant has discovered that such a method may be effective in providing a transparent, optically-conductive solid material.
The term “liquid composition” indicates that the composition behaves like a liquid, not that all components thereof are liquid. It is anticipated that a substantial proportion of the liquid composition will be provided by components that are, themselves, liquid. For example, as mentioned below, optionally the matrix-forming material may be a liquid. Alternatively or additionally, the liquid composition may comprise a carrier liquid in which the matrix-forming material and plurality of nanowires are dispersed.
The solid material so produced may be in the form of a sheet, film or layer. Such a sheet, film or layer may optionally be of substantially uniform thickness, but this is not essential. The solid material so produced may be in the form of a free-standing film. For example, the method may comprise forming a free-standing film of said liquid composition and forming a solid free-standing film from the free-standing film of the liquid composition. “Free-standing” indicates that there is no underlying substrate which supports said film. A free-standing liquid film may be formed, for example, by dipping a loop into said liquid composition, with the film forming inside the loop.
The solid material so produced may be in the form of a coating. In this case, the method may comprise a method of forming an electrically-conductive, transparent coating on a surface of a first substrate, the method comprising contacting said surface with said liquid composition.
The solid material so produced typically comprises metal nanowires dispersed in a matrix, the matrix being formed from the matrix-forming material. The nature of the matrix and the matrix-forming material is discussed below.
Forming a solid material from said liquid composition may comprise initiating a liquid to solid phase transition. For example, the liquid composition may comprise one or more cross-linkers or gelling agents that, on heating or on exposure to a certain type of electromagnetic radiation, form a solid. Additionally or alternatively, the composition may, for example, comprise one or more monomers which react to form a solid polymer, for example, on exposure to a certain stimulus, such as exposure to a certain type of electromagnetic radiation, for example ultraviolet radiation.
The liquid composition may comprise a carrier liquid in which the matrix-forming material and plurality of metal nanowires are dispersed. In this case, forming a solid material from said liquid composition may additionally or alternatively comprise removing the carrier liquid to form said solid material.
The matrix-forming material may be a liquid. Additionally or alternatively, a carrier liquid may be provided, as mentioned above.
If a carrier liquid is present, the matrix-forming material may optionally be dissolved in the carrier liquid. Alternatively or additionally, the matrix-forming material may optionally be suspended in the carrier liquid.
The term “metal nanowire” refers to a metallic wire comprising one or more of elemental metal, metal alloys or metal compounds (such as metal oxides). For the avoidance of doubt, the term “metal nanowire” includes hollow wires and those which are not hollow. The metal nanowires may be made from any suitable metal, and may optionally comprise one or more of silver, gold, copper and nickel. The metal nanowires may optionally comprise one or more of silver and gold, and may optionally comprise silver (optionally in the absence of gold, nickel and copper). Silver nanowires may be particularly effective in providing electrically-conductive nanowires.
The metal nanowires may optionally have a mean aspect ratio (length/width) of at least 100:1, optionally at least 200:1, optionally at least 500:1, optionally from 200:1 to 3,000:1 and optionally from 250:1 to 2000:1. Nanowires with high aspect ratios may be particularly effective at forming electrically-conductive solid materials.
The metal nanowires optionally have a mean length of at least 10 microns, optionally at least 20 microns, optionally at least 30 microns, optionally no more than 100 microns and optionally from 20 to 50 microns. Nanowires having a mean length of from 20 to 50 microns may be particularly effective in forming electrically-conductive solid materials.
The metal nanowires optionally have a mean width of at least 10 nm, optionally at least 20 nm, optionally at least 30 nm, optionally of at least 40 nm, optionally no more than 100 nm and optionally from 30 to 70 nm.
The matrix-forming material may optionally be water-soluble. This facilitates the use of water as a carrier liquid. Water is non-toxic and inexpensive compared to other carrier liquids (although it has a relatively high boiling point and may therefore require more energy to remove). The liquid composition may optionally comprise one or more surfactants. Such surfactants may assist in dispersing the metal nanowires so that the solid material formed has the desired optical and electrical properties. For example, surfactants may assist in inhibiting the formation of metal nanowire aggregates having a size comparable to the wavelength of visible light. One or more low molecular weight surfactants may optionally be provided in the liquid composition. Low molecular weight surfactants optionally have a molecular mass of less than 2000, optionally less than 1000. Alternatively or additionally, the liquid composition may comprise one or more polymeric surfactants. Such polymeric surfactants may provide the matrix-forming material. Polymers which exhibit surfactant behaviour and which may also form the matrix include polyvinyl alcohol, for example. The liquid composition may comprise one or more polymeric surfactants in the absence of low molecular weight surfactants.
The matrix-forming material may optionally comprise one or more matrix-forming material precursors which form the matrix. Optionally, the matrix may comprise polymeric material, and said precursors may optionally comprise one or more monomers which form a polymer. For example, the one or more precursors may form the matrix on being exposed to a stimulus, such as heating, or exposure to electromagnetic radiation having certain characteristics.
The matrix may have a relative permittivity (measured at 1 MHz) of from 1.5 to 30, optionally from 1.5 to 25, optionally from 1.5 to 20, optionally from 1.5 to 15, optionally from 1.5 to 10, optionally from 1.5 to 6, optionally from 1.5 to 3, optionally from 3 to 30, optionally from 5 to 25 and optionally from 15 to 25.
Additionally or alternatively, the matrix-forming material may optionally comprise one or more polymers. The one or more polymers may optionally be water soluble. At least one of said polymers may optionally exhibit surfactant-like behaviour. At least one of said polymers may optionally be a polymeric surfactant. At least one of said polymers may optionally be a block co-polymer, optionally with a hydrophilic block and a hydrophobic block. Such block copolymers may display surfactant behaviour. At least one of said polymers may comprise repeat units comprising moieties capable of forming hydrogen bonds with water. Such polymers may also exhibit surfactant-like behaviour. At least one of said polymers may comprise repeat groups comprising ether linkages. These polymers may display surfactant behaviour. The one or more polymers may optionally be selected from one or more of the group consisting of a poly(alkenol); a polyether; and a block co-polymer comprising one or more blocks of poly(alkenol) or polyether, with one or more blocks of a polymer comprising repeat groups of a tertiary amine.
The mean thickness of the solid material (typically if the solid material is in the form of a coating) may optionally be at least 10 nm, optionally at least 50 nm, optionally at least 200 nm, optionally at least 500 nm, optionally at least 1 micron, optionally no more than 10 microns, optionally no more than 5 microns and optionally from 1 to 5 microns, optionally from 2 to 4 microns. The liquid composition and/or its method of deposition may be adapted to produce a solid material (especially a coating) having the mean thicknesses indicated above. The provision of a relatively thick matrix layer (at least 1 microns thick) may be beneficial in producing a relatively smooth surface, even when the underlying surface is rough.
If the method comprises the formation of a coating on a first substrate, then contacting the surface of the first substrate with the liquid composition may be performed using one or more of spin coating, dipping, spray coating and printing. Spin coating may optionally be used, for example, if a thinner coating is desired. Dipping, spray coating and printing may optionally be used for the production of thicker coatings. Printing includes, but is not limited to, screen printing, flexographic printing and aerosol jet printing.
If formation of the solid material comprises removal of the carrier liquid, then removal of the carrier liquid may optionally be performed by evaporation of the carrier liquid. This may optionally be effected by heating the liquid, for example, in an oven. The carrier liquid may optionally be evaporated by reducing the ambient pressure to which the carrier liquid is subjected. The carrier liquid may optionally be removed by heating the carrier liquid and reducing the ambient pressure to which the carrier liquid is subjected. If the liquid is heated, the temperature to which the liquid is heated will depend, inter alia, on the liquid itself and the ambient pressure to which the liquid is subjected. If the temperature is low, then evaporation of the carrier liquid will be relatively slow, which may be undesirable. If the temperature is high, then evaporation of the carrier liquid will be relatively rapid. Whilst this may be desirable, it may not be desirable to evaporate the liquid too quickly, because unwanted effects (such as babbling of the matrix), may occur. At atmospheric pressure, if the carrier liquid is water, then the carrier liquid may optionally be heated to at least 40° C., optionally at least 50° C., optionally at least 60° C., optionally no more than 80° C. and optionally no more than 70° C.
It may optionally be desirable to include in said liquid composition one of more of the following components; adhesion promoter, dye, corrosion inhibitor, refractive index modifier and viscosity modifier. Corrosion inhibitors may optionally comprise one or more of aromatic triazoles, imidazoles and thiazoles. Refractive index modifiers may optionally comprise silicon oxide. Viscosity modifiers may optionally comprise one or more of cellulose, cellulose derivatives, gums (such as xanthan gum) and glycols.
The liquid composition may optionally comprise no more than 10 wt % metal nanowires, optionally no more than 8 wt %, optionally no more than 6 wt %, optionally no more than 1 wt %, optionally no more than 0.8 wt %, optionally no more than 0.6 wt %, optionally at least 0.001 wt %, optionally at least 0.01 wt %, optionally at least 0.1 wt %, and optionally from 0.1 wt % to 0.6 wt % metal nanowires.
The liquid composition may optionally comprise no more than 10 wt % matrix-forming material, optionally no more than 8 wt %, optionally no more than 6 wt %, optionally at least 0.001 wt %, optionally at least 0.1 wt % and optionally from 0.1 wt % to 0.6 wt % matrix-forming material.
The liquid composition may optionally comprise at least 0.1 wt % metal nanowires and at least 0.1 wt % matrix-forming material, optionally when the matrix-forming material comprises a polymer (typically a polymer having surfactant properties, such as poly(vinyl alcohol)). The liquid composition may optionally comprise 0.1 to 0.6 wt % metal nanowires and 0.1 to 0.6 wt % matrix-forming material, optionally when the matrix-forming material comprises a polymer (typically a polymer having surfactant properties, such as poly(vinyl alcohol)).
The ratio of the weight of the matrix-forming material relative to the sum of the weight of the matrix-forming material and the metal nanowires may optionally be no more than 0.5:1, optionally no more than 0.4:1, optionally at least 0.05:1 and optionally from 0.05:1 to 0.4:1.
The ratio of the volume of the matrix-forming material relative to the sum of the volume of the matrix-forming material and the metal nanowires may optionally be no more than 0.9:1, optionally no more than 0.8:1, optionally no more than 0.7:1, optionally at least 0.05:1 and optionally from 0.05:1 to 0.6:1.
If the matrix-forming material comprises one or more polymers, then optionally at least one polymer has an average molecular weight (Mn) of at least 5000, optionally at least 10,000, optionally at least 20,000, optionally at least 50,000, optionally no more than 500,000 and optionally no more than 250,000. At least one polymer may optionally have a degree of polymerisation of at least 100, optionally at least 200, optionally at least 500, optionally at least 1000, optionally no more than 10,000 and optionally no more than 5000.
The carrier liquid, if present, is optionally an aqueous liquid i.e. it optionally comprises water. The carrier liquid may optionally be a polar liquid or comprise a mixture of polar liquids. The carrier liquid may comprise one or more of water, dimethyl sulfoxide, tetrahydrofuran, dimethylformamide, acetic acid, acetonitrile, ethanol, methanol and acetone. The carrier liquid may comprise water and/or a water-miscible liquid. The carrier liquid may have a polarity index of at least 4 (Burdick & Jackson polarity index).
If the method comprises the formation of a solid coating on a first substrate, then the method may optionally comprise transferring the coating from said first substrate to a second substrate. The method may optionally comprise contacting a surface of the second substrate with a surface of said coating, and moving said first substrate and said second substrate away from one another. Such movement comprises relative movement of the first and second substrates away from one another. One or both of the first and second substrates may be moved. For example, the first substrate may be kept still and the second substrate moved.
If the method comprises the formation of a coating on a first substrate, the first substrate (and second substrate, if present) may comprise a substrate for an electrical or opto-electrical device, such as a display (for example, a liquid crystal display) or a photovoltaic device. The first (and second, if present) substrate may be substantially rigid (for example, if the substrate is made from glass) or flexible (for example, if the substrate is made from a polymer). Said surface onto which the liquid composition is deposited may be provided by glass, for example, or may optionally be provided by a barrier layer, for example. Such barrier layers are typically applied to glass to inhibit the unwanted leaching of sodium ions.
The first substrate (and second substrate, if present) may be porous.
Those skilled in the art will understand the meaning of the term “electrically-conductive”. The sheet resistance of the solid material (particularly if the solid material is in the form of a coating) may optionally be no more than 1000 Ω/square, optionally no more than 500 Ω/square, optionally no more than 250 Ω/square, optionally no more than 100 Ω/square, optionally no more than 50 Ω/square, optionally at least 1 Ω/square, optionally from 1 to 100 Ω/square, optionally from 1 to 75 Ω/square and optionally from 5 to 60 Ω/square.
The meaning of the term “transparent” will be readily apparent to those skilled in the art. The percentage light transmission (typically measured using a UV-vis spectrometer in transmission mode in the visible region (390-750 nm wavelength light) against a reference substrate) of the solid material (particularly if formed as a coating) at a thickness of 2.5 microns is optionally at least 50%, optionally at least 60% and optionally at least 70%. The optical absorption coefficient of the solid material may optionally be no more than 0.1/micron, optionally no more than 0.08/micron and optionally no more than 0.06/micron. The optical absorption coefficient may be calculated using the Beer-Lambert law, using optical transmission measurements made using a UV-vis spectrometer in transmission mode in the visible region (390-750 nm wavelength light) against a reference substrate.
The solid material and liquid composition should optionally be arranged so that the amount of light scattered by the solid material is acceptable. Without wishing to be constrained by theory, it is believed that light scatter may be caused by the formation of metal nanowire aggregates which are of a similar size to the wavelength of incident light. Therefore, without wishing to be constrained by theory, it is understood that it is important to inhibit the formation in the liquid composition of such aggregates (for example, by limiting the formation of nanowire aggregates having a size of more than 400 nm by adding one or more surfactants to the liquid composition. The haze (a measure of light scatter) generated by the solid material (and particularly if the solid material is in the form of a coating) may be no more than 20%, optionally no more than 10%, optionally no more than 8%, optionally no more than 5% and optionally no more than 2%. Haze may be measured using a method well known to those skilled in the art, such as ASTM D1003-95.
Whilst not wishing to be constrained by theory, the applicant believes that the affinity of the matrix-forming material for the metal nanowires may be important to the electrical and optical properties of the solid material, particularly if the solid material is in the form of a coating. Certain matrix-forming materials have been observed to inhibit the formation of a conductive network of nanowires; for example, polyvinylpyrrolidone (PVP) appears to have a strong affinity for silver nanowires, and it is thought that PVP effectively forms an insulating layer around nanowires and inhibits the nanowire-nanowire contact which is necessary to form an electrically-conductive network. Whilst not wishing to be constrained by theory, it is believed that matrix-forming materials which have no affinity for the metal nanowires will lead to the formation of aggregates of nanowires; such aggregates may cause unwanted scattering of light as indicated above and may inhibit the formation of an effective electrically-conductive network of nanowires. The applicant believes that the matrix-forming material may optionally be selected to provide a solid material (particularly a coating) in which the aggregation of nanowires is on a length scale which is less than the wavelength of visible light. This may optionally be achieved by providing a matrix-forming material that has a weak electrostatic affinity for the metal nanowires, but provides strong steric stabilisation. Whilst not wishing to be bound by theory, the applicant understands that strong steric stabilisation may be obtained using a polymer of high molecular weight. The molecular weight of the polymer may optionally be greater than 500, optionally greater than 1000 and optionally greater than 5000.
The method is optionally arranged to provide a solid material and particularly a coating comprising metal nanowires distributed approximately uniformly throughout the thickness of the solid material (and particularly throughout the thickness of a coating). The density of the nanowires in the upper half of the solid material (and particularly in the upper half of a coating) may optionally be from 50-150% (optionally from 70-1.30%, optionally from 80 to 120%) of the density of the nanowires in the lower half of the solid material (and particularly in the lower half of a coating).
In accordance with a second aspect of the present invention, there is provided a transparent, electrically-conductive solid material produced in accordance with a method of the first aspect of the present invention. The solid material of the second aspect of the present invention may optionally have the properties of the solid material discussed above in relation to the method of the first aspect of the present invention. The solid material of the second aspect of the present invention is optionally a coating, as described in accordance with the method of the first aspect of the present invention.
In accordance with a third aspect of the present invention, there is provided an electrically-conductive transparent solid material comprising a plurality of metal nanowires dispersed within a matrix.
The solid material of the third aspect of the present invention may optionally comprise those features described above in relation to the method of the first aspect of the present invention. The nanowires and matrix of the solid material of the third aspect of the present invention may comprise those features described above in relation to the method of the first aspect of the present invention and/or the solid material of the second aspect of the present invention. For example, the matrix may optionally comprise one or more polymers. For example, the solid material may be in the form of a coating. For example, the mean thickness of the solid material may be at least 1 micron.
The ratio of the weight of the matrix-forming material relative to the sum of the weights of the matrix-forming material and the metal nanowires may optionally be no more than 0.5:1, optionally no more than 0.4:1, optionally at least 0.05:1 and optionally from 0.05:1 to 0.4:1.
The ratio of the volume of the matrix-forming material relative to the sum of the volumes of the matrix-forming material and the metal nanowires may optionally be no more than 0.9:1, optionally no more than 0.8:1, optionally no more than 0.7:1, optionally at least 0.05:1 and optionally from 0.05:1 to 0.6:1.
Those skilled in the art will understand the meaning of the term “electrically-conductive”. The sheet resistance of the solid material (particularly if the solid material is in the form of a coating) may optionally be no more than 1000 Ω/square, optionally no more than 500 Ω/square, optionally no more than 250 Ω/square, optionally no more than 100 Ω/square, optionally no more than 50 Ω/square, optionally at least 1 Ω/square, optionally from 1 to 100 Ω/square, optionally from 1 to 75 Ω/square and optionally from 5 to 60 Ω/square.
The meaning of the term “transparent” will be readily apparent to those skilled in the art. The percentage light transmission (typically measured using a UV-vis spectrometer in transmission mode in the visible region (390-750 nm wavelength light) against a reference substrate) of the solid material (particularly if the solid material is in the form of a coating) at a thickness of 2.5 microns is optionally at least 50%, optionally at least 60% and optionally at least 70%. The optical absorption coefficient of the solid material may be no more than 0.1/micron, optionally no more than 0.08/micron and optionally no more than 0.06/micron. The optical absorption coefficient may be calculated using the Beer-Lambert law, using optical transmission measurements made using a UV-vis spectrometer in transmission mode in the visible region (390-750 nm wavelength light) against a reference substrate.
The amount of light scattered by the solid material should optionally be acceptable. Without wishing to be constrained by theory, it is believed that light scatter may be caused by the formation of metal nanowires aggregates which are of a similar size to the wavelength of incident light. Therefore, without wishing to be constrained by theory, it is understood that it is important to inhibit the formation in the liquid composition of such aggregates (for example, by limiting the formation of nanowire aggregates having a size of more than 400 nm by adding one or more surfactants to the liquid composition which forms the solid material. The haze (a measure of light scatter) generated by the solid material may optionally be no more than 20%, optionally no more than 10%, optionally no more than 8%, optionally no more than 5% and optionally no more than 2%.
Whilst not wishing to be constrained by theory, the applicant believes that the affinity of the matrix-forming material for the metal nanowires may be important to the electrical and optical properties of the solid material. Certain matrix-forming materials have been observed to inhibit the formation of a conductive network of nanowires; for example, polyvinylpyrrolidone (PVP) appears to have a strong affinity for silver nanowires, and it is thought that PVP effectively forms an insulating layer around nanowires and inhibits the nanowire-nanowire contact which is necessary to form an electrically-conductive network. Whilst not wishing to be constrained by theory, it is believed that matrix-forming materials which have no affinity for the metal nanowires will lead to the formation of aggregates of nanowires; such aggregates may cause unwanted scattering of light and may inhibit the formation of an effective electrically-conductive network of nanowires. The applicant believes that the matrix-forming material may optionally be selected to provide a coating in which the aggregation of nanowires is on a length scale which is less than the wavelength of visible light. This may optionally be achieved by providing a matrix-forming material that has a weak electrostatic affinity for the metal nanowires, but provides strong steric stabilisation. Whilst not wishing to be bound by theory, the applicant understands that strong steric stabilisation may be obtained using a polymer of high molecular weight.
The metal nanowires may optionally be distributed approximately uniformly throughout the thickness of the solid material, particularly if the solid material is in the form of a coating. The density of the nanowires in the upper half of the solid material may optionally be from 50-150% (optionally from 70-130%, optionally from 80 to 120%) of the density of the nanowires in the lower half of the solid material, particularly if the solid material is in the form of a coating.
The solid material of the third aspect of the present invention may be made using the method of the first aspect of the present invention, and therefore the solid material of the third aspect of the present invention may comprise the features of the method of the first aspect of the present invention.
In accordance with a fourth aspect of the present invention there is provided a substrate provided with an electrically-conductive, transparent coating produced in accordance with a method of the first aspect of the present invention, or a substrate provided with an electrically-conductive, transparent coating according to the second or third aspect of the present invention.
The substrate may comprise a substrate for an electrical or opto-electrical device, such as a display (for example, a liquid crystal display) or a photovoltaic device. The substrate may be substantially rigid (for example, if the substrate is made from glass) or flexible (for example, if the substrate is made from a flexible polymer). Said surface onto which the liquid composition is deposited may be provided by glass, for example, or may optionally be provided by a barrier layer, for example. Such barrier layers are typically applied to glass to inhibit the unwanted leaching of sodium ions.
The substrate may be provided with those features typically provided to a substrate for an electrical or opto-electrical device. For example, the substrate may be provided with a plurality of electrically-conductive paths or tracks for transmitting electrical signals to said coating. The substrate may be provided with one or more spacers suitable for establishing a gap between two electrodes.
The substrate may be provided with one or more overlayers applied to said coating. For example, if the substrate is to form part of a liquid crystal device (such as a display), an alignment layer may be provided, such as a layer of a rubbed polymer (such as a polyamide or polyimide).
There is, in accordance with a fifth aspect of the present invention, a liquid composition for forming a transparent electrically-conductive solid material (particularly a coating), the liquid composition comprising a matrix-forming material and a plurality of metal nanowires. The liquid composition may comprise a carrier liquid, the matrix-forming material and the plurality of nanowires being dispersed in the carrier liquid. The liquid composition in accordance with the fifth aspect of the present invention may comprise those features described above in relation to the method of the first aspect of the present invention.
The prevent invention will now be described by way of example only with reference to the following figures of which:
A general example of a method in accordance with the present invention will now be described. Silver nanowires were made essentially as described in “Rapid synthesis of silver nanowires through a CuCl- or CuCl2-mediated polyol process”, K. E. Korte et al., J. Mat. Chem., 2008, vol. 18, pages 437-441. Instead of using an oil bath to heat the reaction (as described by Korte et al.), the applicant used a hot plate and glass wool. Optical transmission spectroscopy of aliquots of the reaction mixture in the UV-visible spectrum was used to monitor the progress of the reaction, a peak in absorption at about 400 nm indicating the presence of nanowires. The silver nanowires were characterised in several ways. The nanowires were deposited from suspension onto a substrate for examination using scanning electron microscopy (SEM). The SEM images allowed the size of the nanowires to be examined. Transmission electron microscopy was used to examine individual nanowires.
A suspension of nanowires in a carrier liquid was then prepared. A separate solution of polymer in the carrier liquid was prepared. An appropriate amount of the polymer solution was then combined with an appropriate amount of the suspension of nanowires to produce a liquid composition for depositing onto a substrate. The liquid composition was deposited onto a substrate (typically glass) using an off-the-shelf, low cost spray system to form a liquid layer on the substrate. The carrier liquid was then removed by heating the substrate and liquid layer to about 50° C.
The thickness of the coating was investigated using scanning electron microscopy (using a JEOL 840F).
The optical characteristics of the coating could be observed by eye and by measuring the optical transmission of the coating. This was performed using a UV-vis spectrometer in transmission mode in the visible region (390-750 nm wavelength light) against a reference substrate. The coating could also be examined using scanning electron microscopy.
The sheet resistance of the coating was measured using a 4-point probe, as is well known to those skilled in the art.
A 1 wt % suspension of silver nanowires in water was prepared. A 1 wt % solution of polyvinyl alcohol (PVA) in water was prepared. In the present example, the PVA was 99+% hydrolysed, having an average MW of 85000 to 124000 (Aldrich, UK). The PVA solution and the silver nanowire suspension were mixed in appropriate amounts to form the liquid composition for forming the coating. The coating was formed as described above in the general method.
The method of Example 1 was reproduced using methanol as the carrier liquid. The coatings produced were optically and electrically acceptable.
The method of Example 1 was reproduced using tetrahydrofuran as the carrier liquid. The coatings produced were optically and electrically acceptable.
The method of Example 1 was reproduced using iso-propyl alcohol as the carrier liquid. The coatings produced were optically and electrically acceptable, if the liquid composition comprising the carrier liquid, metal nanowires and the polymer was used quickly after preparation.
The method of Example 1 was reproduced using polyvinylpyrrolidone (Aldrich catalogue #85,656-8, MW of about 55000, Aldrich, UK) instead of PVA, but was unsuccessful. Whilst not wishing to be constrained by theory, it is thought that the polymer inhibits contact between metal nanowires, thereby inhibiting electrical conductivity. Furthermore, poor quality films were formed by spray coating.
The method of Example 1 was reproduced using PEDOT.ESS (Clevios P polymer, H.C.Starck GmbH, Germany) instead of PVA, but was relatively unsuccessful. Without wishing to be bound by theory, the applicant believes that the liquid used was too viscous.
The examples above illustrate the use of spray dispensing to form a liquid layer on a substrate. Those skilled in the art will realise that alternative methods for forming a layer may be used, for example, dipping or screen printing. Screen printing may be of particular benefit because screen printing permits effective deposition of the liquid composition through a screen onto substrates to generate patterning, for example, by providing strips or regions of coating separated by electrically-isolating gaps.
The examples above illustrate the use of polyvinyl alcohol as a polymer from which the layer is formed. Those skilled in the art will realise that other materials may be used. For example, alternative polymers could be used, such as other polymers which nave surfactant properties, such as polyethers, poly(methyl methacrylate) and substituted polystyrenes. Alternatively or additionally, other materials could be used, such as monomer or low molecular mass moieties which form polymers in the layer, for example, on exposure to a stimulus, such as illumination with UV or other suitable electromagnetic radiation.
The examples above describe the production of relatively thick films. Whilst this may be desirable in certain circumstances, it is possible to make thinner films, for example from 10 to 100 nm thick.
The examples above describe the deposition of coatings onto a substrate. Whilst this may be desirable in certain circumstances, it may be desirable to make a solid material which is not in the form of a coating but rather, for example, in the form of a free-standing film.
The examples above describe the use of a liquid composition comprising a carrier liquid which is subsequently removed, for example, by heating. Whilst this may be desirable in certain circumstances, it may be desirable not to have a carrier liquid, for instance, if the matrix-forming material itself is a liquid.
The examples above describe the use of silver nanowires. Those skilled in the art will realise that, additionally or alternatively, different metal nanowires may be used, for example, gold nanowires. Furthermore, additional conductive species, such as carbon nanostructures, could be added.
The examples above illustrate the use of a liquid composition comprising a polymer and metal nanowires to produce a conductive film. Those skilled in the art will realise that it would be possible to add further components to the liquid composition, such as one or more of a low molecular weight surfactant, an adhesion promoter, dye, a corrosion inhibitor, a refractive index modifier and a viscosity modifier.
Where in the foregoing description, integers or elements are mentioned which have known, obvious or foreseeable equivalents, then such equivalents are herein incorporated as if individually set forth. Reference should be made to the claims for determining the true scope of the present invention, which should be construed so as to encompass any such equivalents. It will also be appreciated by the reader that integers or features of the invention that are described as preferable, advantageous, convenient or the like are optional and do not limit the scope of the independent claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1209221.9 | May 2012 | GB | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14403018 | Nov 2014 | US |
| Child | 15702160 | US |
