Light-directed electrochemical patterning of copper structures

Abstract

A method creating a patterned film with cuprous oxide and light comprising the steps of electrodepositing copper from a solution onto a substrate; illuminating selected areas of said deposited copper with light having photon energies above the band gap energy of 2.0 eV to create selected illuminated sections and non-illuminated sections; and stripping non-illuminated sections leaving said illuminated sections on the substrate. An additional step may include galvanically replacing the copper with one or more noble metals.

Claims

1. A method of creating a pattern on a substrate using electrodeposition and light comprising the steps of: on selected areas of said substrate, depositing material by electrodeposition and by illumination to create a deposition rate of material that is greater than in the non-illuminated areas; and reversing the polarity while maintaining the illumination of said selected areas to cause said non-illuminated areas to have a higher rate of dissolution than said selected areas.

2. The method of claim 1 wherein said deposited material is copper.

3. The method of claim 1 wherein said illumination is changed by time to create three-dimensional patterns.

4. The method of claim 1 wherein said illumination is changed by intensity to create three-dimensional patterns.

5. The method of claim 1 wherein said illumination is changed by color of the illumination to create three-dimensional patterns.

6. The method of claim 1 wherein said illumination is changed by a combination of color of the illumination, time or intensity to create three-dimensional patterns.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

(1) In the drawings, which are not necessarily drawn to scale, like numerals may describe substantially similar components throughout the several views. Like numerals having different letter suffixes may represent different instances of substantially similar components. The drawings illustrate generally, by way of example, but not by way of limitation, a detailed description of certain embodiments discussed in the present document.

(2) FIG. 1 is a schematic of a deposition procedure that may be used for an embodiment of the present invention.

(3) FIG. 2A provides an example of direct illuminated writing of black cuprous oxide (illuminated area) and plain, yellow cuprous oxide (masked area) via potentiostatic electrodeposition for an embodiment of the present invention.

(4) FIG. 2B illustrates a reflection image of direct illuminated writing of cuprous oxide (illuminated area) with cathodic electrodeposition/anodic dissolution for an embodiment of the present invention.

(5) FIG. 2C illustrates a back-illuminated image of direct illuminated writing of cuprous oxide (illuminated area) with cathodic electrodeposition/anodic dissolution for an embodiment of the present invention.

(6) FIG. 3A is a schematic of the photolithographic patterning of Cu.sub.2O on a conductive surface for an embodiment present invention.

(7) FIG. 3B depicts the galvanic replacement of Cu.sub.2O with Au, Ag, or other noble metals that spontaneously form on the surface while oxidizing the Cu.sub.2O back to soluble Cu2+ ions for an embodiment present invention.

(8) FIG. 4A shows a time series of Cu 2p and spectra for Cu.sub.2O films submerged in a Galvanic replacement reaction (GRR).

(9) FIG. 4B shows a time series of Au 4f XPS spectra for Cu.sub.2O films submerged in 5 mM NaAuCl4 GRR solution for an embodiment present invention.

(10) FIG. 5A is a comparison of Cu 2p spectra for Cu.sub.2O films submerged in an aqueous buffer for an embodiment present invention.

(11) FIG. 5B is a comparison of Au 4f XPS spectra for Cu.sub.2O films submerged in an aqueous buffer for an embodiment present invention.

(12) FIG. 6A is a SEM micrograph of the nanoscale of GRR-deposited Au on Cu2O after 5-minute exposure for an embodiment present invention.

(13) FIG. 6B is a SEM micrograph of the nanoscale microstructure of GRR-deposited Au on Cu2O after 5-minute exposure for an embodiment present invention.

(14) FIG. 7A illustrates GRR-deposited Au on Cu.sub.2O without illumination as shown in FIG. 4A.

(15) FIG. 7B illustrates GRR-deposited Au on Cu.sub.2O with 455 nm LED illumination but without NaAuCl4 in the solution for an embodiment present invention.

(16) FIG. 7C illustrates GRR-deposited Au on Cu.sub.2O and with 455 nm LED illumination and with NaAuCl4 in the solution for an embodiment present invention.

DETAILED DESCRIPTION OF THE INVENTION

(17) Detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention, which may be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for teaching one skilled in the art to variously employ the present invention in virtually any appropriately detailed method, structure or system. Further, the terms and phrases used herein are not intended to be limiting, but rather to provide an understandable description of the invention.

(18) As shown in FIG. 1, in one embodiment of the present invention, cuprous oxide (Cu.sub.2O) 100 can be electrodeposited from a solution of copper sulfate by using a potentiostat 102, light source 110 which may be a light emitting diode that is used to create a light pattern 112, electrolyte solution 114, and mask 116A-116E which may be transparent. Also provided are electrode 120, which may be transparent or non-transparent, reference electrode (RE) 122, and counter electrode (CE) 124.

(19) In a preferred embodiment, cuprous oxide (Cu.sub.2O) can be electrodeposited from a solution of copper sulfate and lactic acid, adjusted to basic pH (9-13) with sodium hydroxide. The electrodeposition is carried out on a conductive substrate like fluorine-doped tin oxide on glass, metal-coated substrates like evaporated gold on glass, or a silicon wafer as well as other substrates to which the metal will adhere.

(20) As shown, a cathodic potential is applied to the electrode in solution (roughly −0.4V vs. Ag/AgCl reference electrode) to reduce the copper ions in solution and form the solid Cu.sub.2O phase as a thin-film coating on the surface of the electrode. Cuprous oxide is synthesized as its hole-doped, p-type photoactive phase in this process. Moreover, it is a photocathode, meaning that the minority carrier electrons that are transferred at the interface to drive the electrodeposition can also be excited by light absorption to drift to the interface.

(21) It has been found that the electrons are energetic enough to reduce Cu.sub.2O on the surface to Cu as a method of photodoping. As a result, the regions of the thin film grown under illumination are visibly and chemically different than the regions grown without illumination as shown in FIGS. 2A-2C.

(22) FIG. 2A provides an example of direct illuminated writing of black cuprous oxide (illuminated area) 200 and plain, yellow cuprous oxide (masked area) 202 via potentiostatic electrodeposition for an embodiment of the present invention. FIG. 2B illustrates a reflection image of direct illuminated writing of cuprous oxide (illuminated area) 210 with cathodic electrodeposition/anodic dissolution for an embodiment of the present invention.

(23) FIG. 2C illustrates a back-illuminated image of direct illuminated writing of cuprous oxide (illuminated area) 220 with cathodic electrodeposition/anodic dissolution for an embodiment of the present invention. As a result, the methods provided by the present invention provide methods to grow copper structures patterned by illumination.

(24) The electrode can be switched between the cathodic (depositing) potential and a slightly anodic (dissolving) potential. The illumination of the pattern may occur during, before or in-between switching. Due to the photodoping of grown films, the areas under illumination or that have been illuminated, during this potential step procedure remain while the areas not under illumination or not subject to illumination are stripped away by dissolution.

(25) Patterning the light via a transparency mask allows for the patterning of regions of photodoped Cu.sub.2O, and therefore the two-dimensional structure of the thin film on the electrode surface. In one embodiment, the conductive interface may be a transparent fluorine-doped tin oxide on glass electrode.

(26) A number of different methods may be used to create the patterns. In the embodiment shown in FIG. 1, pattern 100 is formed on a first surface of substrate 120 while mask 116 is located on an opposingly located second surface. For this embodiment, light source 110 and mask 116 are used to create patterns of light that are transmitted through transparent substrate 120. This creates the illumination patterns that alter the Cu.sub.2O. In other words, the backside of the substrate is illuminated for this embodiment. Patterns may then be created as described above.

(27) As shown in FIG. 3A, pattern 300 may be created from illuminating the front side of the substrate 306. For this embodiment, patterning from the front allows for the use of non-transparent substrates and also allows for the patterning to occur on the growing interface 304. To promote the growth of the Cu.sub.2O pattern, mask 310 needs to be located a spaced distance away from growing surface 304 so as to not block the solution from reaching surface 304. Patterns may then be created as described above.

(28) In yet another embodiment of the present invention, a projector may be used to create the illumination patterns from either the front side or backside. This would eliminate the need to use mask 116 or 301. Patterns may then be created as described above. In other embodiments, the projection source can be used to produce a time-dependent, two-dimensional illumination pattern (like an image) that changes while the film is grown to add three-dimensional structure to the film. Under constant cathodic electrodeposition potential, changing the illumination patterns, by time, intensity, color of the illumination, or any combination of these three illumination parameters as a dynamical illumination image creates a three-dimensional, photodoped “black” Cu.sub.2O structure into the thin film. Under the cathodic electrodeposition/anodic dissolution work cycle, this can result into a printed three-dimensional structure of Cu.sub.2O on the electrode surface. In either case, portions of the deposited film can be removed by chemical dissolution or through electrochemical stripping during growth to produce a thin film patterned in three dimensions. This method could be used to grow three-dimensional templates (like stamps or molds), structured electrocatalysts, three-dimensional circuits, metamaterials (nanostructured materials with non-intuitive optical properties, like negative refractive index or generation of strange polarizations), or nanotextured, low-friction tribological surfaces.

(29) FIGS. 3A and 3B also show a two-step scheme for the solution-phase light-directed patterning of noble metal surfaces based on the photolithographic properties of Cu.sub.2O for another embodiment of the present invention. As shown in FIG. 3A, photolithographic patterning of Cu.sub.2O 300 and 302 on a conductive surface 304 and substrate 306 may be accomplished as described above through the use of a mask and illumination source.

(30) The patterned film may be fabricated, in a preferred embodiment, with an electrochemical duty cycle of cathodic Cu.sub.2O deposition followed by anodic dissolution. The remaining Cu.sub.2O is the portion of the film that was exposed to light during growth. The steps of depositing, illuminating and dissolution may be repeated.

(31) The second step of the embodiment is shown in FIG. 3B. As shown, this step utilizes the galvanic replacement of Cu.sub.2O 300 and 302 with Au, Ag, or other noble metals 350A-350F that spontaneously form on the surface while oxidizing the Cu.sub.2O back to soluble Cu2+ ions.

(32) The present invention may be used to fabricate integrated circuits, print interconnections between electrical components, perform three-dimensional patterning of circuits, provide direct write lithography masks, pattern semiconductor structures for photovoltaics or photoelectrochemical cells, electrocatalyst patterning, controlling the composition of multi-metal electrocatalysts, photodoping Cu2O to form electrodeposited PN junctions for electrical diodes and photovoltaics, microelectrode patterning for dry cell batteries (via low temp oxidation to CuO).

(33) In still other embodiments, the present invention provides a method to pattern the local doping/chemistry of thin films of cuprous oxide with light. By illuminating cuprous oxide with photon energies above the band gap energy of 2.0 eV, the illuminated area of the cuprous oxide thin film is increasingly darkened with increasing intensity during electrodeposition. By stepwise scanning of the electrode potential, the area of the thin film not under illumination can be stripped from the electrode, leaving the remaining illuminated areas on the electrode or conductive surface. This process allows for directly writing copper-based structures on electrodes to either pattern regions of Cu.sub.2O semiconductor or to pattern conductive Cu patterns for circuits. The Cu patterns may then be replaced with one or more noble metals as described above.

(34) In one application of the the present invention, Cu.sub.2O films were submerged in 5 mM NaAuCl4 GRR solution (pH 2.7) for 0 s, 10 s, 1 min, 2 min, and 60 min. The Cu 2p spectra show that the starting Cu.sub.2O surface quickly oxidizes to CuO. Eventually all of the CuO/Cu.sub.2O dissolves as indicated by the lack of the Cu XPS features after 60 min. A Cu.sub.2O film that was air-annealed (400 C for 1 hour) to CuO still showed the CuO XPS features after 60 minutes in the Au solution. The Au 4f spectra show that Au begins to deposit within the first 10 s of exposure and increases intensity. The CuO film shows no Au deposition after 60 minutes.

(35) FIGS. 5A and 5B are comparisons of Cu 2p and Au 4f XPS spectra for Cu.sub.2O films submerged in an aqueous buffer (pH 2.7) with 10 s, 1 min and without NaAuCl4. Plain, unexposed Cu.sub.2O is shown for reference. The Cu 2p spectra show that without NaAuCl4 in the solution, the Cu.sub.2O surface maintains its oxidation state through dissolution. The solid-state oxidation to CuO only occurs in the presence of AuCl4(−) reduction.

(36) FIGS. 6A and 6B are SEM micrographs of the nanoscale morphology and microstructure of GRR-deposited Au on Cu.sub.2O after a 5-minute exposure.

(37) FIG. 7A illustrates GRR-deposited Au on Cu.sub.2O without illumination as shown in FIG. 4A. FIG. 7B illustrates GRR-deposited Au on Cu.sub.2O with 455 nm LED illumination but without NaAuCl4 in the solution. FIG. 7C illustrates GRR-deposited Au on Cu.sub.2O and with 455 nm LED illumination and with NaAuCl4 in the solution.

(38) In yet other embodiments, the present invention provides methods for creating patterns by electrodeposition that are not limited to Cu.sub.2O, but include other materials that may be deposited by electrodeposition. In a preferred method, a film of photoactive material having an electrodeposition polarity that matches its photoactive polarity is deposited in two ways. First by electrodeposited and by the application of light. The light acts as an additional bias which results in additional deposition of material. Thus, in areas of the illumination, the deposition rate of material is greater that in the non-illuminated areas, creating a pattern of areas with more deposited material as compared to the non-illuminated areas.

(39) In circumstances where the desired pattern is to include areas of deposited material and areas where there is no deposited material, the illumination may be continued during the reversal of the polarity. Reversing the polarity causes dissolution of the deposited material. Non-illuminated areas have a higher rate of dissolution than the illuminated areas since the illumination reverses or retards the magnitude of the reverse polarity. Thus, non-illuminated areas are stripped of deposited material at a higher rate and will have all material removed prior to the removal of all material from the illuminated areas.

(40) While the foregoing written description enables one of ordinary skill to make and use what is considered presently to be the best mode thereof, those of ordinary skill will understand and appreciate the existence of variations, combinations, and equivalents of the specific embodiment, method, and examples herein. The disclosure should therefore not be limited by the above described embodiments, methods, and examples, but by all embodiments and methods within the scope and spirit of the disclosure.