Fabrication of flexible conductive films, with semiconductive material, formed with rubbing-in technology for elastic or deformable devices
10994387 ยท 2021-05-04
Assignee
Inventors
- Muhammad Tariq Saeed Chani (Jeddah, SA)
- Abdullah Mohamed Asiri (Jeddah, SA)
- Hasan Karimov (Jeddah, SA)
Cpc classification
B29C70/882
PERFORMING OPERATIONS; TRANSPORTING
B32B25/04
PERFORMING OPERATIONS; TRANSPORTING
H01B1/24
ELECTRICITY
International classification
B29C71/00
PERFORMING OPERATIONS; TRANSPORTING
H01L23/498
ELECTRICITY
B32B25/04
PERFORMING OPERATIONS; TRANSPORTING
Abstract
Rubber composites with regions doped with conductive material, e.g., carbon nanotubes, and patterned regions doped with both conductive material and semiconductive material, e.g., carbon nanotubes and polcrystalline silicon are created with rubbing-in technology. The composites provide for a deformable and elastic composite which maintains semiconductor operations under stress, and can be used for filtering, determining compressive force, and a variety of other applications.
Claims
1. A method for preparing a deformable, semiconductive, composite, comprising: stretching a rubber substrate; applying a first powder of a first conductive material to a surface of the substrate while the rubber substrate is stretched; rubbing the first powder of the conductive material into the surface of the substrate using a loading device which applies pressure on the first powder against the surface and which moves in a plurality of directions across the surface, wherein rubbing produces an embedded region of the conductive material in the surface of the rubber substrate, wherein rubbing the first powder is performed while the rubber substrate is stretched; removing one or more portions of the embedded region so as to remove the conductive material in the one or more portions and associated rubber in the one or more portions of the embedded region so as to expose one or more regions of the rubber substrate where the one or more portions were removed; applying a second powder comprising a second conductive material and a semiconductive material in the one or more regions of the rubber substrate where the one or more portions were removed while the rubber substrate is stretched; rubbing the second powder into the one or more regions of the rubber substrate where the one or more portions were removed using the loading device which applies pressure on the second powder against the surface and which moves in a plurality of directions across the surface, wherein rubbing the second powder is performed while the rubber substrate is stretched; and relaxing the stretch on the rubber substrate to produce the deformable, semiconductive, composite, wherein the deformable, semiconductive composite, comprises a first portion which is rubber which is not doped with the first conductive material, the second conductive material, or the semiconductive material, a second portion which comprises rubber doped with the first conductive material, and one or more third portions which comprises rubber doped with the second conductive material and the semiconductive material.
2. The method of claim 1 wherein the first conductive material and the second conductive material are the same and are carbon nanotubes.
3. The method of claim 2 wherein the semiconductive material is polycrystalline silicon.
4. The method of claim 3 wherein the carbon nanotubes have a mean diameter of 5 to 50 nm and a mean length of 75 to 250 nm.
5. The method of claim 3 wherein the polycrystalline silicon is in particulate form with particles having a mean particle size of 7.5 to 15 m.
6. The method of claim 3 wherein the carbon nanotubes are 20 to 80% by weight and the polycrystalline silicon is 80 to 20% by weight of the second powder.
7. The method of claim 6 wherein each of the carbon nanotubes and polycrystalline silicon are present in the second powder at approximately 50% by weight.
8. The method of claim 3 wherein the two rubbing steps embed the carbon nanotubes and polycrystalline silicon to a depth of 5 to 20 m in the surface of the rubber substrate.
9. The method of claim 1 wherein the first and second rubbing procedures are independently performed using a rubbing pressure of 5 to 75 gf/cm2.
10. The method of claim 9 where in the first and second rubbing steps are independent performed at 5 to 50 Hz for 5 to 30 seconds.
11. The method of claim 1 wherein the rubber substrate is a styrene-butadiene rubber.
12. The method of claim 1 wherein the semiconductive material is an inorganic semiconductor.
13. The method of claim 12 wherein the inorganic semiconductor is polycrystalline silicon.
14. The method of claim 1 further comprising the step of repeating the each of the steps on a second surface of the rubber substrate.
Description
DESCRIPTION OF THE DRAWINGS
(1) The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawings will be provided by the Office upon request and payment of the necessary fee.
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DETAILED DESCRIPTION
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(14) In the rubbing-in technology, the conducting powder or conducting/semiconducting powder placed on a surface of the rubber substrate is rubbed into the surface of the substrate using a pressing/sliding unit that applies a downward force or load against the surface of the rubber substrate, and which moves in any of multiple directions across the surface of the rubber substrate while applying the downward force.
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(16) The conductive powder rubbed into the surface of the rubber can be any of a variety of materials including carbon nanotubes (CNT), graphene, and carbon powder. CNTs, as are shown in
(17) The semiconductive powder rubbed into the surface of the rubber can be any of a variety of materials including an inorganic semiconductor such as polycrystalline silicon (p-Si), germanium (Ge), and gallium arsenide. Good results can be achieved with p-Si in particulate form with particles having a mean particle size of 7.5 to 15 m.
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(19) The patterned composite of
(20) To demonstrate the utility of the invention a plurality of samples similar to those shown in
(21) The deformable composite samples based on CNT and p-Si built-in rubber were fabricated using rubbing-in technology. The effect of humidity up to 90% RH, temperature up to 60 C. and frequency of applied voltage in the interval of 1-200 kHz on the impedance of the samples were investigated
(22) A p-Si wafer and CNTs (carbon nanotubes) powder were purchased from Sun Nanotek Co. LTD. The diameter of the multiwalled carbon nanotubes was 10 to 30 nm, while their length was in the range of 100 to 200 nm. The silicon power was prepared from by grinding the p-Si crystalline wafer with following specification: sizes 6-inch (15.6 cm15.6 cm), p-type (Boron doped), thickness: 180 m, resistivity: 1.8 ohm/cm, doping concentration: 8e.sup.15, textured both sides (random pyramid) and crystal orientation: <100>. The particle size of the p-Si powder was mostly in the range of 9 m to 12 m.
(23) Rubbing-in technology as described above was used to fabricate the rubber-CNT and rubber-CNT-p-Si conductive films. A polished metallic surface which holds the rubber substrate in an extended (stretched) position was prepared. To form the composite the conducting/semiconducting powder is poured on to the stretched rubber substrate. A round shaped polished metallic block is used to rub the powder on the rubber surface using a special mechanism which controls the frequency and direction of the block. By this process the powder penetrates into the enlarged pores of the rubber and form a composite layer with rubber, which can be used for device fabrication. The rubber-conducting/semiconducting power composite layer can be formed on both surfaces of the rubber substrate.
(24) Samples of various dimensions (length: 2 cm to 3 cm, width: 1.5 cm to 2 cm, thickness: 1 mm to 2 mm can be prepared on the fabricated set-up. The samples are strained normally about 15 to 20%. Depending upon the sample's requirements, a range of loads (10 gf/cm.sup.2 to 20 gf/cm.sup.2) may be applied using various rubbing blocks. The frequency of the rubbing blocks varies from 10 to 20 Hz. The duration of the sample preparation was 15-20 s on average.
(25) Exemplary deformable composite samples based on CNT and p-Si built-in rubber were fabricated. A 2 cm3 cm rubber sheet of thickness of 1-2 mm was stretched up to 15-20% in two directions: length and width of the sample. While holding the sample in the strained position, carbon nanotubes (CNTs) powder was applied using the above-mentioned rubbing-in technology. The depth of the formed rubber-CNTs composite layer was 8-12 m.
(26) In the middle of the sample, a gap of 2 cm in length and 0.5 cm in width was made by removing rubber-CNT layer down to the pure rubber surface. This gap was filled by the mixture of CNT-p-Si powders (50/50 wt. %) (this ratio can be varied considerably, e.g., from 80/20 wt % to 20/80 wt %). To incorporate the CNT-p-Si mixture in the rubber substrate, the same procedure (rubbing-in) was applied. All samples were fabricated at pressure of 40 g/cm.sup.2. Figure shows the schematic diagram of fabricated sample. In the prepared samples the rubber-CNTs-p-Si composite played the role of the sensitive material.
(27) A digital multi-meter DT-4253-Hioki was used for the measurement of current and voltages (I-V) characteristics. All experiments were conducted at room temperature conditions. The uniaxial compressive displacements or pressure were applied along the length of the rectangular prism sample by use of the micrometer mechanism or weights in special experimental arrangement. Processes of application of compressive forces on the rubber sample are shown in
(28) X-ray diffraction of the samples were conducted with Philips PW1830 X-ray diffraction system in Bragg-Brentano (-2) scan mode using Cu-K radiation source at room temperature. Each sample was run three times and found repeatable results. The X-ray diffractograms of original rubber, CNTs powder, silicon powder, and rubber-CNTs+silicon composite, are presented in
(29) The XRD pattern of rubber shows notable high intensity Bragg's diffraction peaks at 2 of 23.1, 29.4 and 36, respectively. These peaks and other peaks present in the rubber X-ray diffraction pattern are characteristics of polyvinyl chloride which correspond to high amount of structural arrangement (order) in its polymeric chain. In CNTs powder diffractogram, the broad and major peak of CNTs was observed around 26.2 (002) which is attributed to the hexagonal graphite structure, having high electrical conductivities. This peak is consistent with standard x-ray diffraction data (ICSD code: 031170). One additional peak is also observed at 38.4 as a result of a different functional group attached to the CNTs. A broad peak of CNTs consistent with other studies (see Lu Scientific Reports 5, 16584 (2015)10.1038/srep16584) was also observed at 2 of 44.3 (101). A sharp peak of p-type silicon powder was observed at 20=68.9. In rubber-CNTs+silicon composite diffractogram, the additional peak of CNTs and silicon powder was observed around 20 of 26.2 and 68.9.
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(32) Comparison of the results in the top and bottom graphs of
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(35) The non-linearity coefficient (a) can be calculated by the following expression (see Khan World Applied Sciences Journal (2016) 24:1261-1268):
=(log(I.sub.2/I.sub.1)/log(V.sub.2/V.sub.1)(1)
(36) It can be determined also by the following expression
=dIV.sub.o/I.sub.odV(2)
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(38) The effect of the compressive displacement to the resistance was determined (See
(39) Sensitivity (S) of the displacement sensor can be found by the following expression:
S=dZ100%/ZdD(3)
where Z is impedance and D is displacement. It was found that S=0.03%/m at frequency of 1 kHz. The deformable composite can be used for fabrication of displacement sensor or flexible resistor and impedance.
(40) By use of this composite sample in electronic circuits, in principle, it is possible to fabricate low or high pass filters. The impedance of the sample can be represented as parallel connection of the resistor and capacitor (
Z=R/(1+jRC)(4)
(41) In summary, rubbing-in technology was used to fabricate the rubber-CNT-p-Si nanocomposite-based flexible conductive films. The effect of humidity up to 90%, temperature up to 60 C., frequency of applied voltage in the interval of (1-200) kHz, on the impedance of the samples were investigated. It was also revealed that the impedance of the rubber-CNTs-p-Si composite at 1 kHz was practically independent of temperature. At 10 kHz, 100 kHz and 200 kHz impedances of the composites decreased up to 9% when temperature increased from 23 C. up to 60 C. The temperature dependences of impedances of the p-Si crystal strips in average increased on 8-9% with the increase of the temperature and showed minimum at 25 C. As relative humidity was changed in the interval of (47-90) % the impedances of the composites decreased in the average on 5% of the values. On increasing displacement (compressive) up to 300 m the impedance decreases from 4% to 9% depending on the frequencies: at lower frequencies the changes were higher than in higher frequencies. The impedances of the sample decreased sharply with increase of the frequency that potentially can be used for fabrication of the filters. The I-V characteristics of the CNT and p-Si composite samples and p-Si crystal samples as well were non-linear. The non-linearity coefficients of the I-V characteristics were equal to 3.1 and 2.5 for composite and p-Si crystal samples accordingly. The elastic composite based on rubber, CNT and p-Si can be used as a compressive displacement sensor and for the demodulation of the frequency-modulated signals. Testing showed the semiconductive composite had a current-voltage nonlinearity coefficient beta of 1.25 to 1.75, an impedance of 90 to 150 M/cm at 30 to 70 C. at 1 kHz, and an impedance at 1 kHz which decreases by 0.03% per m of compressive displacement compared to an uncompressed impedance at 1 kHz.