A portion of the disclosure of this patent document contains material which is subject to copyright or mask work protection. The copyright or mask work owner has no objection to the facsimile reproduction by anyone of the patent document or the patent disclosure, as it appears in the Patent and Trademark Office patent file or records, but otherwise reserves all copyright or mask work rights whatsoever.
This disclosure relates to producing ultra-small metal structures using a combination of various coating, etching and electroplating processing techniques using a conductive polymer preferably on a non-conductive or semi-conductive substrate.
In its broadest form, the process disclosed herein produces ultra-small structures with a range of sizes described as micro- or nano-sized. The processing begins with a non-conductive substrates (e.g., glass, oxidized silicon, plastics and many others) or a semi-conductive substrate (e.g., doped silicon, compound semiconductor materials (GaAs, InP, GaN, . . . )) on which a layer of a conductive polymer (CP) is applied or coated. Alternatively, a hard substrate such as metal plates or sheets (e.g., aluminum, copper, iron alloys), ceramic materials can be used. A second mask layer is formed on that conductive polymer layer, the second layer comprising a layer of a non-conductive polymer or a photoresist (PR) material. The second layer is then patterned using one or more conventional processes, such as an exposure process, in which subsequent developing will remove selected unwanted portions of the second mask layer thereby exposing portions of the underlying conductive polymer layer. Then, the now exposed portions of the first conductive polymer layer can be etched away where there is no material of the second layer acting as a mask or a protective layer. This etching of the CP layer is preferably accomplished by use of chemical etching or Reactive Ion Etching (RIE) techniques, as are described in the above mentioned '407 application, to develop a final pattern in the CP layer. Alternatively, it is also with the scope of this invention to etch only portions of the full depth of the conductive polymer layer or to also develop the ultra small structure directly on the conductive polymer layer itself.
Following the foregoing steps that can include the patterning of one or both the CP and PR layers, portions thereof, or even where the conductive layer has not be etched. The now patterned base structure will be positioned in an electroplating bath and a desired metal will be deposited into the holes formed in either or both the first and second layers and on the layers exposed by one or more of the prior etching processing steps. Thereafter, the PR and CP layers can be removed leaving formed metal structures on the non-conductive substrate exhibiting an ultra small size, or alternatively the PR layer will be removed leaving the formed metal structures lying directly on the conductive polymer layer. Alternatively, the PR or CP or both layers can be left in place if they do not interfere with the ultimate function of the ultra small structures.
Electroplating is well known and is fully described in the above referenced '407 application.
Ultra-small structures encompass a range of structure sizes sometimes described as micro- or nano-sized. Objects with dimensions measured in ones, tens or hundreds of microns are described as micro-sized. Objects with dimensions measured in ones, tens or hundreds of nanometers or less are commonly designated nano-sized. Ultra-small hereinafter refers to structures and features ranging in size from hundreds of microns in size to ones of nanometers in size.
Ultra-small three-dimensional surface structures can be formed in which the structures are compact, nonporous and exhibit smooth vertical surfaces. Examples of the desired ultra-small structures, and their uses, are set forth in the '476 application and the '477 application.
The ability to build three-dimensional structures with smooth dense sidewalls employing the similar processing offers advantages to device designers. For example, smooth dense sidewalls increase the efficiency of optical device function. It may also be beneficial in some micro-fluidic applications.
The invention is better understood by reading the following detailed description with reference to the accompanying drawings in which:
FIGS. 12(a)-12(b) are plots of typical voltage waveform according to embodiments of the present invention.
The conductive polymer layer 12 can be applied by conventional spin coating techniques, an evaporation process, or other suitable coating techniques that are familiar to those skilled in the art. Indeed, any process that can deposit a coating of the conductive polymer material can be used. Examples of suitable conductive materials include polypheneylene (PPV), methano [70] fullerene, (MDMO), Poly(3-methylthiophene) (pMeT), Poly(dithiono[3,4-b:3′,4′-d]thiophene) (pDTT1), Poly(3-p-fluorophenylthiophene) (pFPT), PEDT- Poly(ethylene-dioxythiophene), Plyaniline, Polythiophene, and Polypyrrole.
Thereafter, as shown in
As shown in
Where the full depth of the CP layer 12 has been removed, thereby exposing the underlying substrate layer 10, it is also possible, and within the scope of this invention, to provide an adhesion or barrier layer on the substrate 10 in the form of a thin film or layer 30, shown by a dotted line, prior to plating. This thin film or layer 30 can be deposited, for example, by e-beam evaporation or other similar techniques that will deposit the desired thin film or layer 30. That thin film or layer 30, an adhesion or barrier layer, can be, for example, a thin nickel layer. It should also be understood that the thin film or adhesion layer 30 should be thin enough so that the thin film or layer 30 does not short the side walls of the CP layer 12 to the top of the structure.
Alternatively, only a portion of the full depth of the CP layer 12 can be removed, as is shown by the dotted horizontal line 24 in
An alternative process is shown in
In addition, the CP layer can also be further etched and removed leaving the desired feature or structure 34 on a portion of the CP layer 12 lying directly under the structure 34 as shown in
Waveform functions on the personal computer 101 are drawn using a standard program included with function generator 102. After the personal computer 101 downloads the waveforms to the function generator 102, the function generator sets characteristics such as amplitude, period, and offset of its electrical output signal. The output of function generator 102 is sent to the current amplifier 108 along cables 106 and 107. The cables 106 and 107 may be, e.g., standard USB cables.
In cases where the output current of the function generator is insufficient to carry out the plating, an amplifier 108 can be introduced between the function generation and the plating bath 112. Amplifier 108 increases the output current of the function generator 102, making it sufficient to carry out the plating without experiencing a voltage drop. Current amplifier 108 maintains an appropriate voltage in plating bath 112 as deposition occurs. Any DC voltage offset introduced by an imperfect amplifier can be corrected by programming an opposite DC offset from the function generator.
Time between pulses is controlled via a program that triggers the function generator output. This program is also used to start and stop the plating.
The output signal from the current amplifier 108 is provided to electrode switch 111 on cable 109. Analog input-output (I/O) card 105 sends a signal to electrode switch 111 via cable/line 114. Analog input-output card 105 is controlled by an output signal from the computer 101.
Electrode switch 111 generates an output signal that is sent to timer 116 (via cable 115). The signal output from timer 116 is connected to anode 117 in the plating bath 112. In currently preferred embodiments, the anode is a silver (Ag) metal plate or a nickel (Ni) metal plate, but there is no requirement that the anode consist of silver, nickel, or other materials, including (without limitation) copper (Cu), aluminum (Al), gold (Au) and platinum (Pt) may be used and are contemplated by the invention.
A second output signal is sent from current amplifier 108 via cable 110 (which may be, e.g., a USB cable) to sample 113 (which comprises the surface/non-conductive substrate to be coated/plated by the metal on the anode 117). Sample 113 is the cathode. In presently preferred embodiments, non-conductive substrates are rectangular and are about 1 cm by 2 cm. There is no requirement that the non-conductive substrate be any minimum or maximum size.
An agitation mechanism such as agitation pump 118 is attached to plating bath 112. Agitation of the liquid in the bath 112 speeds up the deposition rate. The pump 118 agitates the solution, thereby moving the solution around the plating bath 112. The plating bath 112 is preferably large enough to permit even flow of the solution over the non-conductive substrate.
The effect of agitation depends on the size and shape of the device being plated. In some cases, agitation reduces the plating time to thirty seconds on some of the smaller devices and down to ninety seconds on larger ones. Agitation also facilitates uniform thicknesses on all the devices across the non-conductive substrate leading to higher yields. There are other known ways of agitation, including using an air pump to aerate the solution with air or another gas. For some applications, agitation may not-be preferred at all.
An appropriate plating solution is placed into plating bath 112. In presently preferred embodiments, a silver plating solution is used. In the currently preferred embodiment the solution is Caswell's Silver Brush & Tank Plating Solution.
To ensure that the plating bath 112 is getting the desired period and amplitude, an oscilloscope 121 can be connected directly to the plating bath.
In the plating process, the voltage applied on the sample 113 is pulsed. FIGS. 12(a)-12(b) show a plot of a typical voltage waveform. In FIGS. 12(a)-12(b), the percentage of the total voltage applied on the sample is plotted versus time. In this waveform, a positive voltage pulse of between five and six volts is applied on the sample, and after some rest time, the voltage is reversed to a negative voltage. Plating occurs as the voltage applied on the substrate is negative-referenced to the counter electrode. It should be noted that
During the intervals when the voltage is positive, material is removed from the structures. The optimum values of parameters such as peak voltage, pulse widths, and rest times will vary depending upon the size, shape and density of the devices on the substrate that are being plated, temperature and composition of the bath, and other specifications of the particular system to which this technique is applied.
In some embodiments, a series of plating pulses including at least one positive voltage pulse and at least one negative voltage pulse, are applied. Preferably each voltage pulse is for an ultra-short period. As used herein, an “ultra-short period” is a period of less than one microsecond, preferably less than 500 ns, and more preferably less than or equal to 400 ns. Preferably there is a rest period between each of the pulses in the pulse series. In presently preferred embodiments of the invention, the series of plating pulses is repeated at least once, after an inter-series rest time. Preferably the inter-series rest time is 1 microsecond or greater. In some embodiments of the present invention, the inter-series rest time is between 1 microsecond and 500 ms. As used herein, the term “ultra-short voltage pulse” refers to a voltage pulse that lasts for an ultra-short period—i.e., a voltage pulse (positive or negative) that lasts less than one microsecond, preferably less than 500 ns, and more preferably less than or equal to 400 ns.
While the invention has been described in connection with what is presently considered to be the most practical and preferred embodiment, it is to be understood that the invention is not to be limited to the disclosed embodiment, but on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.
This application is related to U.S. patent applications Ser. No. 11/243,476 (the '476 application), filed on Oct. 5, 2005, and entitled “Structures and Methods For Coupling Energy From An Electromagnetic Wave,” Ser. No. 11/243,477 (the '477 application), filed on Oct. 5, 2005, and entitled “Electron Beam Induced Resonance,” Ser. No. 11/203,407 (the '407 application), filed on Aug. 15, 2005, and entitled “Method of Patterning Ultra-Small Structures,” and Ser. No. 10/917,511 (the '511 application), filed on Aug. 13, 2004, and entitled “Patterning Thin Metal Films by Dry Reactive Ion Etching.” Each of these applications is commonly owned at the time of filing this application, and the entire contents of each are fully incorporated herein by reference.