CN104934329B - Preparation method for ZnO-Thin Film Transistor (ZnO-TFT) based on flexible substrate material - Google Patents
Preparation method for ZnO-Thin Film Transistor (ZnO-TFT) based on flexible substrate material Download PDFInfo
- Publication number
- CN104934329B CN104934329B CN201510205191.XA CN201510205191A CN104934329B CN 104934329 B CN104934329 B CN 104934329B CN 201510205191 A CN201510205191 A CN 201510205191A CN 104934329 B CN104934329 B CN 104934329B
- Authority
- CN
- China
- Prior art keywords
- sample
- photoresist
- minutes
- flexible substrate
- acetone
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 150
- 239000000463 material Substances 0.000 title claims abstract description 75
- 238000002360 preparation method Methods 0.000 title claims abstract description 18
- 239000010409 thin film Substances 0.000 title claims description 27
- 238000000034 method Methods 0.000 claims abstract description 69
- 238000005516 engineering process Methods 0.000 claims abstract description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 96
- 229920002120 photoresistant polymer Polymers 0.000 claims description 88
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 80
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 60
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- 239000011787 zinc oxide Substances 0.000 claims description 40
- 239000008367 deionised water Substances 0.000 claims description 39
- 229910021641 deionized water Inorganic materials 0.000 claims description 39
- 238000005566 electron beam evaporation Methods 0.000 claims description 38
- 238000000151 deposition Methods 0.000 claims description 29
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 28
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 28
- 229910052710 silicon Inorganic materials 0.000 claims description 28
- 239000010703 silicon Substances 0.000 claims description 28
- 238000004140 cleaning Methods 0.000 claims description 22
- 230000008021 deposition Effects 0.000 claims description 22
- 238000000206 photolithography Methods 0.000 claims description 20
- 239000003292 glue Substances 0.000 claims description 19
- 229910052782 aluminium Inorganic materials 0.000 claims description 18
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 18
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 claims description 17
- 239000004642 Polyimide Substances 0.000 claims description 16
- 229920001721 polyimide Polymers 0.000 claims description 16
- 238000001035 drying Methods 0.000 claims description 15
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 235000012239 silicon dioxide Nutrition 0.000 claims description 14
- 239000010408 film Substances 0.000 claims description 13
- 238000001755 magnetron sputter deposition Methods 0.000 claims description 12
- 238000004544 sputter deposition Methods 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 10
- 229910001220 stainless steel Inorganic materials 0.000 claims description 10
- 239000010935 stainless steel Substances 0.000 claims description 10
- 238000004528 spin coating Methods 0.000 claims description 8
- 238000005137 deposition process Methods 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 238000005260 corrosion Methods 0.000 claims description 5
- 230000007797 corrosion Effects 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000007772 electrode material Substances 0.000 claims description 4
- 238000007664 blowing Methods 0.000 claims description 2
- 229960001296 zinc oxide Drugs 0.000 claims 10
- 238000004026 adhesive bonding Methods 0.000 claims 5
- 239000007788 liquid Substances 0.000 claims 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
- 238000005229 chemical vapour deposition Methods 0.000 claims 1
- 238000002242 deionisation method Methods 0.000 claims 1
- 230000005611 electricity Effects 0.000 claims 1
- 238000001704 evaporation Methods 0.000 claims 1
- 230000008020 evaporation Effects 0.000 claims 1
- 238000005286 illumination Methods 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 238000001459 lithography Methods 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 238000001259 photo etching Methods 0.000 claims 1
- 238000007747 plating Methods 0.000 claims 1
- 235000012431 wafers Nutrition 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 239000011701 zinc Substances 0.000 claims 1
- 238000004377 microelectronic Methods 0.000 abstract description 2
- 238000010586 diagram Methods 0.000 description 14
- 238000004506 ultrasonic cleaning Methods 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000011109 contamination Methods 0.000 description 8
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000007738 vacuum evaporation Methods 0.000 description 4
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical group [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000001552 radio frequency sputter deposition Methods 0.000 description 3
- 238000005530 etching Methods 0.000 description 2
- 238000005452 bending Methods 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D99/00—Subject matter not provided for in other groups of this subclass
Landscapes
- Thin Film Transistor (AREA)
- Cleaning Or Drying Semiconductors (AREA)
Abstract
Description
技术领域technical field
本发明属于微电子技术领域,具体涉及一种基于柔性衬底材料氧化锌薄膜晶体管(ZnO-Thin Film Transistor,ZnO-TFT)的制备方法。The invention belongs to the technical field of microelectronics, and in particular relates to a method for preparing a zinc oxide thin film transistor (ZnO-Thin Film Transistor, ZnO-TFT) based on a flexible substrate material.
背景技术Background technique
目前,柔性显示由于具有超薄、重量轻、省电、可折叠等良好的性能特点成为未来发展一个重要方向。基于柔性材料衬底薄膜晶体管(TFT)的制备是实现柔性功能器件的关键步骤。与以硅、玻璃等硬质衬底材料相比,柔性薄膜晶体管以塑料等柔性材料为基质,可以弯曲、缠绕,以及折成一定角度。应用于显示领域,可以卷成圆筒及其它形状,缩小体积到放入随身穿戴的衣物口袋当中。具有很较强的实际意义和很好的市场前景。At present, flexible display has become an important direction for future development due to its excellent performance characteristics such as ultra-thin, light weight, power saving, and foldable. Fabrication of thin-film transistors (TFTs) based on flexible material substrates is a key step in the realization of flexible functional devices. Compared with hard substrate materials such as silicon and glass, flexible thin film transistors are based on flexible materials such as plastics, which can be bent, wound, and folded at a certain angle. Applied in the field of display, it can be rolled into cylinders and other shapes, and reduced in size to be put into the pockets of clothes worn by people. It has strong practical significance and good market prospects.
其中,氧化锌以其较低生长温度,较好的化学稳定性,较低的制备成本,特别因其直接宽带隙较高(常温带隙为3.37eV)、且薄膜材料透明、可见光下稳定等优点,成为柔性衬底薄膜晶体管制备领域一个研究热点。Among them, zinc oxide is characterized by its lower growth temperature, better chemical stability, and lower preparation cost, especially because of its high direct wide band gap (band gap at room temperature is 3.37eV), and its thin film material is transparent and stable under visible light, etc. It has become a research hotspot in the field of thin film transistor fabrication on flexible substrates.
氧化锌薄膜晶体管具备诸多优点:具备可见光区的高稳定性,高场效应迁移率、较低的器件制备温度、高电流开关比、低阈值电压及可见光区的高透过率,成为继硅基薄膜晶体管之后,未来显示驱动领域极具发展潜力的新型显示驱动器件。Zinc oxide thin film transistors have many advantages: high stability in the visible light region, high field effect mobility, low device fabrication temperature, high current switching ratio, low threshold voltage and high transmittance in the visible light region. After the thin film transistor, a new type of display driving device with great development potential in the field of display driving in the future.
发明内容Contents of the invention
本发明提供一种基于柔性衬底材料氧化锌薄膜晶体管的制备方法,以解决柔性衬底材料在薄膜材料生长、器件制备过程中的弯曲、翘曲的问题。The invention provides a method for preparing a zinc oxide thin film transistor based on a flexible substrate material to solve the problems of bending and warping of the flexible substrate material during the growth of the thin film material and device preparation.
本发明采取的技术方案是:包括下列步骤:The technical scheme that the present invention takes is: comprise the following steps:
(一)硬质衬底和柔性衬底的清洗、吹干、烘干;所述硬质衬底材料为玻璃、硅片、或不锈钢片,所述柔性衬底材料为聚酰亚胺PI;(1) cleaning, drying, and drying of hard substrate and flexible substrate; the hard substrate material is glass, silicon wafer, or stainless steel sheet, and the flexible substrate material is polyimide PI;
(二)衬底粘合,所述衬底粘合材料为光刻胶;(2) substrate bonding, the substrate bonding material is photoresist;
(三)栅极材料沉积,所述栅极材料为铝,采用电子束蒸发方法EB制备;(3) gate material deposition, the gate material is aluminum, prepared by electron beam evaporation method EB;
(四)绝缘层材料沉积,所述绝缘层材料为SiO2,采用离子体增强化学气相沉积PECVD,Plasma Enhanced Chemical Vapor Deposition方法生长;(4) deposition of insulating layer material, the insulating layer material is SiO 2 , grown by plasma enhanced chemical vapor deposition PECVD, Plasma Enhanced Chemical Vapor Deposition method;
(五)氧化锌沟道层材料沉积,所述沟道层材料为ZnO,方法采用射频磁控溅射;(5) Zinc oxide channel layer material is deposited, and described channel layer material is ZnO, and method adopts radio frequency magnetron sputtering;
(六)源漏电极沉积,所述源漏电极材料为铝,利用光刻剥离技术,沉积方法采用真空蒸镀、电子束蒸发。(6) Deposition of source and drain electrodes, the material of the source and drain electrodes is aluminum, and the photolithography lift-off technique is used, and the deposition method adopts vacuum evaporation and electron beam evaporation.
所述步骤(一)将硬质衬底,25mm*25mm和柔性衬底聚酰亚胺2,20mm*20mm分别清洗,方法是:The step (1) cleans the hard substrate, 25mm*25mm and the flexible substrate polyimide 2, 20mm*20mm respectively, the method is:
(1)先将其放入丙酮溶液中在室温下超声清洗4分钟—6分钟,去除表面分子型沾污等;(1) First put it into an acetone solution and ultrasonically clean it at room temperature for 4-6 minutes to remove surface molecular contamination, etc.;
(2)然后置于乙醇溶液中在室温下超声清洗3—5分钟,去除表面残余丙酮;(2) Then place it in an ethanol solution and ultrasonically clean it for 3-5 minutes at room temperature to remove residual acetone on the surface;
(3)再用去离子水在室温下超声清洗3—5分钟,去除残余乙醇及离子型沾污;(3) Ultrasonic cleaning with deionized water at room temperature for 3-5 minutes to remove residual ethanol and ionic contamination;
(4)高纯氮气吹干,烘干炉90℃下干燥3—5分钟。(4) Blow dry with high-purity nitrogen, and dry in an oven at 90°C for 3-5 minutes.
所述步骤(二)衬底粘合包括:将硬质衬底固定在匀胶仪上,在硬质衬底中间位置滴光刻胶一,0.2ml—0.5ml,将清洗好的柔性材料衬底聚酰亚胺,置于光刻胶一上面,待玻璃衬底与柔性衬底通过光刻胶一全部接触后,启动匀胶仪,转速450—550转/分钟,时间30秒—120秒,使光刻胶一均匀铺在柔性衬底与硬质衬底之间,从而使柔性衬底与硬质衬底紧紧粘合在一起,柔性衬底被平整固定在硬质衬底表面,形成样品一。The step (2) substrate bonding includes: fixing the hard substrate on the glue homogenizer, dripping photoresist 1, 0.2ml-0.5ml in the middle of the hard substrate, lining the cleaned flexible material Bottom polyimide, placed on the photoresist one, after the glass substrate and the flexible substrate are fully contacted through the photoresist one, start the homogenizer, the speed is 450-550 rpm, and the time is 30 seconds-120 seconds , so that the photoresist is evenly spread between the flexible substrate and the hard substrate, so that the flexible substrate and the hard substrate are tightly bonded together, and the flexible substrate is fixed flat on the surface of the hard substrate, Form sample one.
所述步骤(三)栅极材料沉积包括:将样品一放入电子束蒸发装置生长室中,放置方向为柔性衬底朝下,用电子束蒸发方法镀铝在柔性衬底上作为栅极4,完成后,依次将其放入丙酮溶液、乙醇、去离子水中超声清洗3-5分钟,用去离子水冲洗,N2吹干,在此过程中,光刻胶一溶于丙酮溶液,从而,硬质衬底与其他部分分离开来。形成样品二。The step (3) gate material deposition includes: put the sample 1 into the growth chamber of the electron beam evaporation device, place the flexible substrate downward, and use the electron beam evaporation method to plate aluminum on the flexible substrate as the gate 4 , after completion, put it into acetone solution, ethanol, and deionized water for ultrasonic cleaning for 3-5 minutes, rinse with deionized water, and blow dry with N2 . During this process, the photoresist is dissolved in acetone solution, thereby , the hard substrate is separated from other parts. Form sample two.
所述步骤(四)绝缘层材料沉积包括:取4英寸洁净硅片,将样品二放置在硅片上面中间位置,样品二吸附于硅片表面,将带有样品二的硅片置于PECVD生长室底座。为避免绝缘层沉积过程中样品二受热发生卷曲、翘角等现象,影响绝缘层生长,取清洗干净的不锈钢片制成的模具一,模具一为方框形,内径15mm,框宽5mm,将模具一压在样品二上面,俯沉积二氧化硅绝缘层,形成样品三。The step (4) of insulating layer material deposition includes: taking a 4-inch clean silicon wafer, placing sample 2 on the middle position above the silicon wafer, sample 2 is adsorbed on the surface of the silicon wafer, and placing the silicon wafer with sample 2 on PECVD growth chamber base. In order to avoid curling and warping of the sample 2 during the deposition process of the insulating layer, which will affect the growth of the insulating layer, a mold 1 made of a cleaned stainless steel sheet is taken. The mold 1 is a square frame with an inner diameter of 15 mm and a frame width of 5 mm. Mold 1 is pressed on sample 2, and a silicon dioxide insulating layer is deposited downward to form sample 3.
所述步骤(五)氧化锌沟道层材料沉积包括,将样品三分别放入丙酮、乙醇、去离子水中依次超声清洗3-5分钟,再用去离子水冲洗,N2吹干,烘干炉90℃下干燥3—5分钟,将其置于磁控溅射仪的溅射台托盘上,上压模具二,内径为12mm,小于模具一内尺寸3mm,框宽为10mm,用螺丝将其固定在溅射台托盘上,悬挂托盘,沉积氧化锌沟道层,将其从托盘中取出,得到样品四。The step (5) of depositing the zinc oxide channel layer material includes placing sample 3 into acetone, ethanol, and deionized water for 3-5 minutes, followed by ultrasonic cleaning for 3-5 minutes, then rinsing with deionized water, blowing dry with N 2 , and drying Dry it in an oven at 90°C for 3-5 minutes, place it on the sputtering table tray of the magnetron sputtering instrument, press mold 2 on it, the inner diameter is 12mm, which is 3mm smaller than the inner dimension of mold 1, and the frame width is 10mm. It is fixed on the tray of the sputtering table, hangs the tray, deposits the zinc oxide channel layer, takes it out from the tray, and obtains sample 4.
所述步骤(六)源漏电极沉积包括,The step (6) source-drain electrode deposition includes,
(1)清洗,按照步骤(一)所述清洗方法,将样品四进行清洗;(1) Cleaning, according to the cleaning method described in step (1), sample four is cleaned;
(2)固定,按照步骤(二)所述粘合方法,利用光刻胶二将清洗后的样品四固定在硬质衬底表面,形成样品五;(2) Fixing, according to the bonding method described in step (2), utilize photoresist 2 to fix sample 4 after cleaning on the hard substrate surface, form sample 5;
(3)光刻-剥离方法,把沟道层刻蚀出多个制作单一薄膜晶体管器件的小岛区域,在小岛区域内的沟道层上刻蚀出源、漏电极区,在源、漏电极区沉积源、漏电极,具体如下:(3) Photolithography-stripping method, the channel layer is etched out a plurality of small island regions for making a single thin film transistor device, the source and drain electrode regions are etched on the channel layer in the small island region, and the source and drain electrode regions are etched. The source and drain electrodes are deposited in the drain electrode area, as follows:
①涂胶,将样品五固定在匀胶仪上,旋转,涂有反转特性的光刻胶三,转速500-1300转/分钟,时间3—5分钟,使光刻胶均匀地涂覆在沟道层的表面;①Glue coating, fix sample 5 on the glue homogenizer, rotate, and coat photoresist 3 with inversion characteristics, the speed is 500-1300 rpm, and the time is 3-5 minutes, so that the photoresist is evenly coated on the the surface of the channel layer;
②前烘,90℃下前烘、坚膜9分钟;②Pre-bake, pre-bake at 90°C and harden the film for 9 minutes;
③曝光,用光刻版一14覆盖,放置于曝光机下曝光,此时,图形覆盖部分,未受到光照,其余部分曝光;③ Exposure, cover with photolithography plate 14, place it under the exposure machine for exposure, at this time, the covered part of the pattern is not exposed to light, and the rest is exposed;
④显影,将其置于显影液中,曝光部分对应的光刻胶三溶于显影液,被去除,露出氧化锌;④Development, put it in the developer solution, the photoresist three corresponding to the exposed part is dissolved in the developer solution, is removed, and zinc oxide is exposed;
⑤腐蚀,用千分之一盐酸腐蚀,未被光刻胶保护的部分,即氧化锌部分被腐蚀掉,露出绝缘层二氧化硅,形成样品六;⑤ Corrosion, corroding with one-thousandth hydrochloric acid, the part not protected by the photoresist, that is, the zinc oxide part is corroded, exposing the insulating layer of silicon dioxide, forming sample 6;
⑥去胶,将样品六放入丙酮、乙醇、去离子水中依次超声清洗3-5分钟,光刻胶二、三溶于丙酮从而被剥离掉;⑥Remove glue, put sample 6 into acetone, ethanol, deionized water and ultrasonically clean it for 3-5 minutes in sequence, photoresist 2 and 3 are dissolved in acetone and stripped off;
⑦二次光刻,按照步骤(二)所述粘合方法,利用光刻胶四将清洗去胶后的样品六固定在硬质衬底表面;7. Secondary photolithography, according to the bonding method described in step (2), utilize photoresist 4 to fix sample 6 after cleaning and deglue on the hard substrate surface;
涂胶,按照步骤①所述方法,旋涂有反转特性的光刻胶五;Glue coating, according to the method described in step 1., spin-coating photoresist five with inversion characteristics;
前烘,90℃下前烘,坚膜9分钟;Pre-bake, pre-bake at 90°C, harden the film for 9 minutes;
曝光,用光刻版二17覆盖,对版后,图形与氧化锌重叠,俯视;Expose, cover with photolithography plate 2 17, after the plate is aligned, the graphics overlap with zinc oxide, and look down;
曝光后烘,110℃下加热9分钟,有反转特性的光刻胶五变成负胶;Baking after exposure, heating at 110°C for 9 minutes, the photoresist with inversion characteristics becomes a negative resist five times;
裸曝光;naked exposure;
显影,放入显影液中,负胶未曝光部分被显影液溶掉,曝光部分保留;Developing, put it into the developer solution, the unexposed part of the negative film is dissolved by the developer solution, and the exposed part remains;
用去离子水冲洗,形成样品七,得到即将沉积源、漏电极的区域;Rinse with deionized water to form sample 7 to obtain the area where the source and drain electrodes are about to be deposited;
⑧沉积源、漏电极,按照步骤2所述粘合方法,将样品七固定在硬质衬底上,放入电子束蒸发设备EB中,沉积源/漏电极金属铝;⑧ Deposit source and drain electrodes, according to the bonding method described in step 2, fix sample 7 on the hard substrate, put it into the electron beam evaporation equipment EB, and deposit the source/drain electrode metal aluminum;
⑨去胶,放入丙酮溶液浸泡1小时—2小时,超声2-3分钟,光刻胶四溶于丙酮从而硬质衬底被分离掉,沟道层表面光刻胶五连同其上的电极被丙酮去除,露出沟道层,再用乙醇、去离子水冲洗干净,N2气吹干。⑨Remove the glue, soak in acetone solution for 1 hour to 2 hours, ultrasonic for 2-3 minutes, the photoresist 4 dissolves in acetone and the hard substrate is separated, and the photoresist 5 on the surface of the channel layer together with the electrodes on it It was removed by acetone to expose the channel layer, rinsed with ethanol and deionized water, and dried with N 2 gas.
本发明优点是,在室温状态下即可制备、且工艺简便易行、成本低,可应用于柔性显示技术领域。The invention has the advantages that it can be prepared at room temperature, has simple and easy process and low cost, and can be applied in the technical field of flexible display.
附图说明Description of drawings
图1是在硬质衬底上滴光刻胶示意图;Fig. 1 is a schematic diagram of dropping photoresist on a hard substrate;
图2是柔性材料衬底聚酰亚胺PI示意图;Fig. 2 is the schematic diagram of flexible material substrate polyimide PI;
图3是样品一剖面图;Fig. 3 is a sectional view of a sample;
图4.1是在样品一上沉积栅极铝示意图;Figure 4.1 is a schematic diagram of depositing gate aluminum on sample 1;
图4.2是样品二的结构示意图;Figure 4.2 is a schematic diagram of the structure of sample 2;
图5.1是品二置于硅片之上俯视图;Figure 5.1 is a top view of the second product placed on the silicon wafer;
图5.2是样品二置于硅片之上俯剖面图;Figure 5.2 is a cross-sectional view of sample 2 placed on the silicon wafer;
图6.1是模具一立体示意图;Figure 6.1 is a three-dimensional schematic diagram of the mold;
图6.2是模具一俯视图;Figure 6.2 is a top view of the mold;
图7.1是利用模具一准备沉积二氧化硅绝缘层俯视图;Figure 7.1 is a top view of a silicon dioxide insulating layer prepared to be deposited using a mold;
图7.2是利用模具一准备沉积二氧化硅绝缘层剖面图;Figure 7.2 is a cross-sectional view of preparing to deposit a silicon dioxide insulating layer using mold one;
图8是样品三俯视图;Figure 8 is a three top view of the sample;
图9是样品三剖面图;Figure 9 is a three-sectional view of the sample;
图10.1是利用模具二准备沉积氧化锌沟道层俯视图;Figure 10.1 is a top view of the zinc oxide channel layer prepared to be deposited using the second mold;
图10.2是利用模具二准备沉积氧化锌沟道层剖面图;Figure 10.2 is a cross-sectional view of the zinc oxide channel layer prepared for deposition using the second mold;
图11是沉积氧化锌沟道层俯视图;Fig. 11 is a top view of deposited zinc oxide channel layer;
图12是样品四剖面图;Fig. 12 is a sample four sectional view;
图13.1是样品五俯视图;Figure 13.1 is a top view of sample 5;
图13.2是样品五剖面图;Figure 13.2 is a cross-sectional view of sample five;
图14是光刻版一示意图;Fig. 14 is a schematic diagram of a photolithography plate;
图15.1是样品六俯视图;Figure 15.1 is a top view of sample six;
图15.2是样品六剖面图;Figure 15.2 is a cross-sectional view of sample six;
图16.1是把沟道层刻蚀出多个制作单一薄膜晶体管器件的小岛区域剖面图;Figure 16.1 is a cross-sectional view of a plurality of small island regions where a single thin film transistor device is produced by etching the channel layer;
图16.2是把沟道层刻蚀出多个制作单一薄膜晶体管器件的小岛区域俯视图;Figure 16.2 is a top view of a plurality of small island regions where a single thin film transistor device is produced by etching the channel layer;
图17是光刻版二示意图;Fig. 17 is a schematic diagram of photolithography plate 2;
图18.1是光刻版二对版后俯视图;Figure 18.1 is the top view of the second pair of photolithographic plates;
图18.2是光刻版二对版后剖面图,为单一器件制备区域示意图;Figure 18.2 is a cross-sectional view of the second pair of photolithography plates, which is a schematic diagram of the preparation area of a single device;
图19是样品七剖面图,为单一器件制备区域示意图;Figure 19 is a cross-sectional view of sample seven, which is a schematic diagram of the preparation area of a single device;
图20.1是基于柔性衬底氧化锌薄膜晶体管器件结构的俯视图,单一器件示意图;Figure 20.1 is a top view of a device structure based on a flexible substrate zinc oxide thin film transistor, a schematic diagram of a single device;
图20.2是基于柔性衬底氧化锌薄膜晶体管器件结构的剖面图,单一器件示意图。Figure 20.2 is a cross-sectional view of a device structure based on a flexible substrate zinc oxide thin film transistor, and a schematic diagram of a single device.
具体实施方式detailed description
实施例1Example 1
包括下列步骤:Include the following steps:
(一)硬质衬底和柔性衬底的清洗、吹干、烘干;所述硬质衬底材料为玻璃、硅片、或不锈钢片,所述柔性衬底材料为聚酰亚胺PI;(1) cleaning, drying, and drying of hard substrate and flexible substrate; the hard substrate material is glass, silicon wafer, or stainless steel sheet, and the flexible substrate material is polyimide PI;
将硬质衬底1,25mm*25mm和柔性衬底聚酰亚胺2,20mm*20mm分别清洗,方法是:Clean the hard substrate 1, 25mm*25mm and the flexible substrate polyimide 2, 20mm*20mm respectively, the method is:
(1)先将其放入丙酮溶液中在室温下超声清洗4分钟,去除表面分子型沾污等;(1) First put it into an acetone solution and ultrasonically clean it for 4 minutes at room temperature to remove surface molecular contamination, etc.;
(2)然后置于乙醇溶液中在室温下超声清洗3分钟,去除表面残余丙酮;(2) Then place it in an ethanol solution and ultrasonically clean it for 3 minutes at room temperature to remove residual acetone on the surface;
(3)再用去离子水在室温下超声清洗5分钟,去除残余乙醇及离子型沾污;(3) Ultrasonic cleaning with deionized water at room temperature for 5 minutes to remove residual ethanol and ionic contamination;
(4)高纯氮气吹干,烘干炉90℃下干燥5分钟;(4) blow dry with high-purity nitrogen, and dry at 90° C. for 5 minutes in an oven;
(二)衬底粘合,所述衬底粘合材料为光刻胶;(2) substrate bonding, the substrate bonding material is photoresist;
将硬质衬底固定在匀胶仪上,在硬质衬底中间位置滴光刻胶一3,0.2ml,如图1所示,将清洗好的柔性材料衬底聚酰亚胺2,如图2所示,置于光刻胶一上面,待玻璃衬底与柔性衬底通过光刻胶一全部接触后,启动匀胶仪,转速450转/分钟,时间30秒,使光刻胶一均匀铺在柔性衬底与硬质衬底之间,从而使柔性衬底与硬质衬底紧紧粘合在一起,柔性衬底被平整固定在硬质衬底表面,形成样品一,样品一剖面图如图3所示;Fix the hard substrate on the homogenizer, drop 0.2ml of photoresist-3 in the middle of the hard substrate, as shown in Figure 1, put the cleaned flexible material substrate polyimide 2, such as As shown in Figure 2, place it on the photoresist one, and after the glass substrate and the flexible substrate are fully contacted through the photoresist one, start the homogenizer, the speed is 450 rpm, and the time is 30 seconds, so that the photoresist one Spread evenly between the flexible substrate and the hard substrate, so that the flexible substrate and the hard substrate are tightly bonded together, and the flexible substrate is flattened on the surface of the hard substrate to form sample 1, sample 1 The section view is shown in Figure 3;
(三)栅极材料沉积,所述栅极材料为铝Al,采用电子束蒸发方法EB、Electron-beam Evaporation制备;(3) gate material deposition, the gate material is aluminum Al, prepared by electron beam evaporation method EB, Electron-beam Evaporation;
将样品一放入电子束蒸发装置生长室中,放置方向为柔性衬底朝下,用电子束蒸发方法镀铝在柔性衬底上作为栅极4,如图4.1所示,完成后,依次将其放入丙酮溶液、乙醇、去离子水中超声清洗3分钟,用去离子水冲洗,N2吹干,在此过程中,光刻胶一溶于丙酮溶液,从而,硬质衬底与其他部分分离开来,形成样品二,如图4.2所示;Put the sample 1 into the growth chamber of the electron beam evaporation device with the flexible substrate facing down, and use the electron beam evaporation method to plate aluminum on the flexible substrate as the grid 4, as shown in Figure 4.1. Put it into acetone solution, ethanol, and deionized water for ultrasonic cleaning for 3 minutes, rinse with deionized water, and blow dry with N2 . During this process, the photoresist is dissolved in the acetone solution, so that the hard substrate and other parts Separated to form sample 2, as shown in Figure 4.2;
(四)绝缘层材料沉积,所述绝缘层材料为SiO2,采用离子体增强化学气相沉积PECVD,Plasma Enhanced Chemical Vapor Deposition方法生长;(4) deposition of insulating layer material, the insulating layer material is SiO 2 , grown by plasma enhanced chemical vapor deposition PECVD, Plasma Enhanced Chemical Vapor Deposition method;
取4英寸洁净硅片5,将样品二放置在硅片上面中间位置,样品二吸附于硅片表面,如图5.1,5.2所示,将带有样品二的硅片置于PECVD生长室底座,为避免绝缘层沉积过程中样品二受热发生卷曲、翘角等现象,影响绝缘层生长,取清洗干净的不锈钢片制成的模具一6,模具一为方框形,内径15mm,框宽5mm,如图6.1,6.2所示,将模具一压在样品二上面,俯视、剖面效果如图7.1、7.2所示,沉积二氧化硅绝缘层7,俯视如图8所示,形成样品三,样品三剖面图如图9;Take a 4-inch clean silicon wafer 5, place sample 2 on the middle position above the silicon wafer, sample 2 is adsorbed on the surface of the silicon wafer, as shown in Figure 5.1 and 5.2, place the silicon wafer with sample 2 on the base of the PECVD growth chamber, In order to avoid curling and warping of the sample 2 during the deposition process of the insulating layer, which would affect the growth of the insulating layer, a mold 6 made of cleaned stainless steel sheets was taken. The mold 1 was in the shape of a square frame with an inner diameter of 15 mm and a frame width of 5 mm. As shown in Figures 6.1 and 6.2, mold one is pressed on sample two, and the top view and section effects are shown in Figures 7.1 and 7.2, and a silicon dioxide insulating layer 7 is deposited, and the top view is shown in Figure 8, forming sample three and sample three The cross-sectional view is shown in Figure 9;
(五)氧化锌沟道层材料沉积,所述沟道层材料为ZnO,方法采用射频磁控溅射radio-frequency magnetron sputtering,RF-sputtering;(5) Zinc oxide channel layer material deposition, the channel layer material is ZnO, the method adopts radio-frequency magnetron sputtering radio-frequency magnetron sputtering, RF-sputtering;
将样品三分别放入丙酮、乙醇、去离子水中依次超声清洗3分钟,再用去离子水冲洗,N2吹干,烘干炉90℃下干燥3分钟,将其置于磁控溅射仪的溅射台托盘8上,上压模具二9,内径为12mm,小于模具一内尺寸3mm,框宽为10mm,用螺丝10将其固定在溅射台托盘上,如图10.1、10.2所示俯视、剖面示意图,悬挂托盘,沉积氧化锌沟道层11,图11所示为俯视图,工艺完成后,将其从托盘中取出,得到样品四,图12为样品四剖面图;Put sample three into acetone, ethanol, and deionized water for 3 minutes, then rinse with deionized water, blow dry with N2 , dry in a drying oven at 90°C for 3 minutes, and place it in a magnetron sputtering apparatus. On the tray 8 of the sputtering table, press mold 2 9 on it. The inner diameter is 12mm, which is 3mm smaller than the inner dimension of mold 1, and the frame width is 10mm. Fix it on the tray of the sputtering table with screws 10, as shown in Figure 10.1 and 10.2 Top view, schematic sectional view, hang the tray, deposit the zinc oxide channel layer 11, the top view is shown in Figure 11, after the process is completed, it is taken out from the tray to obtain sample 4, and Figure 12 is a sectional view of sample 4;
(六)源漏电极沉积,所述源漏电极材料为Al,利用光刻剥离技术,沉积方法采用真空蒸镀、电子束蒸发;(6) Source-drain electrode deposition, the source-drain electrode material is Al, using photolithography stripping technology, the deposition method adopts vacuum evaporation and electron beam evaporation;
(1)清洗,按照步骤(一)所述清洗方法,将样品四进行清洗;(1) Cleaning, according to the cleaning method described in step (1), sample four is cleaned;
(2)固定,按照步骤(二)所述粘合方法,利用光刻胶二12将清洗后的样品四固定在硬质衬底表面,形成样品五,如图13.1、13.2为样品五俯视图、剖面图;(2) Fixing, according to the bonding method described in step (2), use photoresist 2 12 to fix the cleaned sample 4 on the surface of the hard substrate to form sample 5, as shown in Figures 13.1 and 13.2 for the top view of sample 5, section view;
(3)光刻-剥离方法,把沟道层刻蚀出多个制作单一薄膜晶体管器件的小岛区域,在小岛区域内的沟道层上刻蚀出源、漏电极区,在源、漏电极区沉积源、漏电极,具体如下:(3) Photolithography-stripping method, the channel layer is etched out a plurality of small island regions for making a single thin film transistor device, the source and drain electrode regions are etched on the channel layer in the small island region, and the source and drain electrode regions are etched. The source and drain electrodes are deposited in the drain electrode area, as follows:
①涂胶,将样品五固定在匀胶仪上,旋转,涂有反转特性的光刻胶三13,转速500转/分钟,时间3分钟,使光刻胶均匀地涂覆在沟道层的表面;①Glue coating, fix sample 5 on the glue homogenizer, rotate, and coat photoresist 3 13 with inversion characteristics, the rotation speed is 500 rpm, and the time is 3 minutes, so that the photoresist is evenly coated on the channel layer s surface;
②前烘,90℃下前烘、坚膜9分钟;②Pre-bake, pre-bake at 90°C and harden the film for 9 minutes;
③曝光,用图形如图14所示光刻版一14覆盖,放置于曝光机下曝光,此时,图形覆盖部分,未受到光照,其余部分曝光;③ Exposure, covered with photolithography plate 14 as shown in Figure 14, placed under the exposure machine for exposure, at this time, the covered part of the pattern was not exposed to light, and the rest was exposed;
④显影,将其置于显影液中,曝光部分对应的光刻胶三溶于显影液,被去除,露出氧化锌;④Development, put it in the developer solution, the photoresist three corresponding to the exposed part is dissolved in the developer solution, is removed, and zinc oxide is exposed;
⑤腐蚀,用千分之一盐酸腐蚀,未被光刻胶保护的部分,即氧化锌部分被腐蚀掉,露出绝缘层二氧化硅,形成样品六,如图15.1小岛、15.2所示样品六;⑤ Corrosion, corroding with one-thousandth hydrochloric acid, the part not protected by the photoresist, that is, the zinc oxide part is corroded, exposing the insulating layer of silicon dioxide, forming sample 6, as shown in Figure 15.1 small island and sample 15.2 ;
⑥去胶,将样品六放入丙酮、乙醇、去离子水中依次超声清洗3-5分钟,光刻胶二、三溶于丙酮从而被剥离掉,如图16.1、16.2所示,图示为多个制作单一薄膜晶体管器件的小岛区域;⑥Remove the glue, put sample 6 into acetone, ethanol, and deionized water, and ultrasonically clean it for 3-5 minutes in sequence. A small island area for making a single thin film transistor device;
⑦二次光刻,按照步骤(二)所述粘合方法,利用光刻胶四15将清洗去胶后的样品六固定在硬质衬底表面;7. Secondary photolithography, according to the bonding method described in step (2), utilize photoresist 4 15 to fix sample 6 after cleaning and deglue on the hard substrate surface;
涂胶,按照步骤①所述方法,旋涂有反转特性的光刻胶五16;Glue coating, according to the method described in step 1., spin-coating photoresist 5 16 with inversion characteristics;
前烘,90℃下前烘,坚膜9分钟;Pre-bake, pre-bake at 90°C, harden the film for 9 minutes;
曝光,用图17所示光刻版二17覆盖,对版后,图形与氧化锌重叠,俯视、剖面示意如图18.1、18.2所示;Expose, cover with the photolithography plate 2 17 shown in Figure 17, after the plate is aligned, the graphics overlap with the zinc oxide, and the top view and cross-section are shown in Figures 18.1 and 18.2;
曝光后烘,110℃下加热9分钟,有反转特性的光刻胶五变成负胶;Baking after exposure, heating at 110°C for 9 minutes, the photoresist with inversion characteristics becomes a negative resist five times;
裸曝光;naked exposure;
显影,放入显影液中,负胶未曝光部分被显影液溶掉,曝光部分保留;Developing, put it into the developer solution, the unexposed part of the negative film is dissolved by the developer solution, and the exposed part remains;
用去离子水冲洗,形成样品七,得到即将沉积源、漏电极的区域,图19为一个制备单一薄膜晶体管器件所对应的示意图;Rinse with deionized water to form sample 7, and obtain the area where the source and drain electrodes are about to be deposited. Figure 19 is a schematic diagram corresponding to the preparation of a single thin film transistor device;
⑧沉积源、漏电极,按照步骤2所述粘合方法,将样品七固定在硬质衬底上,放入电子束蒸发设备EB(Electron-beam Evaporation)中,沉积源/漏电极金属铝18;⑧ Deposit source and drain electrodes, according to the bonding method described in step 2, fix sample 7 on the hard substrate, put it into the electron beam evaporation equipment EB (Electron-beam Evaporation), and deposit the source/drain electrode metal aluminum 18 ;
⑨去胶,放入丙酮溶液浸泡1小时,超声2分钟,光刻胶四溶于丙酮从而硬质衬底被分离掉,沟道层表面光刻胶五连同其上的电极被丙酮去除,露出沟道层,再用乙醇、去离子水冲洗干净,N2气吹干,即完成了器件制备,器件图形俯视、剖面如图20.1、20.2所示。⑨Remove the glue, soak in acetone solution for 1 hour, ultrasonic for 2 minutes, the photoresist 4 is dissolved in acetone and the hard substrate is separated, and the photoresist 5 on the surface of the channel layer and the electrodes on it are removed by acetone, exposing The channel layer was rinsed with ethanol and deionized water, and dried with N 2 gas to complete the device preparation. The top view and cross-section of the device are shown in Figures 20.1 and 20.2.
实施例2Example 2
包括下列步骤:Include the following steps:
(一)硬质衬底和柔性衬底的清洗、吹干、烘干;所述硬质衬底材料为玻璃、硅片、或不锈钢片,所述柔性衬底材料为聚酰亚胺PI;(1) cleaning, drying, and drying of hard substrate and flexible substrate; the hard substrate material is glass, silicon wafer, or stainless steel sheet, and the flexible substrate material is polyimide PI;
将硬质衬底1,25mm*25mm和柔性衬底聚酰亚胺2,20mm*20mm分别清洗,方法是:Clean the hard substrate 1, 25mm*25mm and the flexible substrate polyimide 2, 20mm*20mm respectively, the method is:
(1)先将其放入丙酮溶液中在室温下超声清洗5分钟,去除表面分子型沾污等;(1) First put it into an acetone solution and ultrasonically clean it for 5 minutes at room temperature to remove surface molecular contamination, etc.;
(2)然后置于乙醇溶液中在室温下超声清洗4分钟,去除表面残余丙酮;(2) Then place it in an ethanol solution and ultrasonically clean it for 4 minutes at room temperature to remove residual acetone on the surface;
(3)再用去离子水在室温下超声清洗4分钟,去除残余乙醇及离子型沾污;(3) Ultrasonic cleaning with deionized water at room temperature for 4 minutes to remove residual ethanol and ionic contamination;
(4)高纯氮气吹干,烘干炉90℃下干燥4分钟;(4) blow dry with high-purity nitrogen, and dry at 90°C for 4 minutes in a drying oven;
(二)衬底粘合,所述衬底粘合材料为光刻胶;(2) substrate bonding, the substrate bonding material is photoresist;
将硬质衬底固定在匀胶仪上,在硬质衬底中间位置滴光刻胶一3,0.35ml,如图1所示,将清洗好的柔性材料衬底聚酰亚胺2,如图2所示,置于光刻胶一上面,待玻璃衬底与柔性衬底通过光刻胶一全部接触后,启动匀胶仪,转速500转/分钟,时间75秒,使光刻胶一均匀铺在柔性衬底与硬质衬底之间,从而使柔性衬底与硬质衬底紧紧粘合在一起,柔性衬底被平整固定在硬质衬底表面,形成样品一,样品一剖面图如图3所示;Fix the hard substrate on the homogenizer, drop 0.35ml of photoresist-3 in the middle of the hard substrate, as shown in Figure 1, put the cleaned flexible material substrate polyimide 2, such as As shown in Figure 2, put it on the photoresist one, and after the glass substrate and the flexible substrate are fully contacted through the photoresist one, start the homogenizer, the speed is 500 rpm, and the time is 75 seconds, so that the photoresist one Spread evenly between the flexible substrate and the hard substrate, so that the flexible substrate and the hard substrate are tightly bonded together, and the flexible substrate is flattened on the surface of the hard substrate to form sample 1, sample 1 The section view is shown in Figure 3;
(三)栅极材料沉积,所述栅极材料为铝,采用电子束蒸发方法EB、Electron-beamEvaporation制备;(3) gate material deposition, the gate material is aluminum, prepared by electron beam evaporation method EB, Electron-beamEvaporation;
将样品一放入电子束蒸发装置生长室中,放置方向为柔性衬底朝下,用电子束蒸发方法镀铝在柔性衬底上作为栅极4,如图4.1所示,完成后,依次将其放入丙酮溶液、乙醇、去离子水中超声清洗4分钟,用去离子水冲洗,N2吹干,在此过程中,光刻胶一溶于丙酮溶液,从而,硬质衬底与其他部分分离开来,形成样品二,如图4.2所示;Put the sample 1 into the growth chamber of the electron beam evaporation device with the flexible substrate facing down, and use the electron beam evaporation method to plate aluminum on the flexible substrate as the grid 4, as shown in Figure 4.1. Put it into acetone solution, ethanol, and deionized water for ultrasonic cleaning for 4 minutes, rinse with deionized water, and blow dry with N2 . During this process, the photoresist is dissolved in the acetone solution, so that the hard substrate and other parts Separated to form sample 2, as shown in Figure 4.2;
(四)绝缘层材料沉积,所述绝缘层材料为SiO2,采用离子体增强化学气相沉积PECVD,Plasma Enhanced Chemical Vapor Deposition方法生长;(4) deposition of insulating layer material, the insulating layer material is SiO 2 , grown by plasma enhanced chemical vapor deposition PECVD, Plasma Enhanced Chemical Vapor Deposition method;
取4英寸洁净硅片5,将样品二放置在硅片上面中间位置,样品二吸附于硅片表面,如图5.1,5.2所示,将带有样品二的硅片置于PECVD生长室底座,为避免绝缘层沉积过程中样品二受热发生卷曲、翘角等现象,影响绝缘层生长,取清洗干净的不锈钢片制成的模具一6,模具一为方框形,内径15mm,框宽5mm,如图6.1,6.2所示,将模具一压在样品二上面,俯视、剖面效果如图7.1、7.2所示,沉积二氧化硅绝缘层7,俯视如图8所示,形成样品三,样品三剖面图如图9;Take a 4-inch clean silicon wafer 5, place sample 2 on the middle position above the silicon wafer, sample 2 is adsorbed on the surface of the silicon wafer, as shown in Figure 5.1 and 5.2, place the silicon wafer with sample 2 on the base of the PECVD growth chamber, In order to avoid curling and warping of the sample 2 during the deposition process of the insulating layer, which would affect the growth of the insulating layer, a mold 6 made of cleaned stainless steel sheets was taken. The mold 1 was in the shape of a square frame with an inner diameter of 15 mm and a frame width of 5 mm. As shown in Figures 6.1 and 6.2, mold one is pressed on sample two, and the top view and section effects are shown in Figures 7.1 and 7.2, and a silicon dioxide insulating layer 7 is deposited, and the top view is shown in Figure 8, forming sample three and sample three The cross-sectional view is shown in Figure 9;
(五)氧化锌沟道层材料沉积,所述沟道层材料为ZnO,方法采用射频磁控溅射radio-frequency magnetron sputtering,RF-sputtering;(5) Zinc oxide channel layer material deposition, the channel layer material is ZnO, the method adopts radio-frequency magnetron sputtering radio-frequency magnetron sputtering, RF-sputtering;
将样品三分别放入丙酮、乙醇、去离子水中依次超声清洗4分钟,再用去离子水冲洗,N2吹干,烘干炉90℃下干燥4分钟,将其置于磁控溅射仪的溅射台托盘8上,上压模具二9,内径为12mm,小于模具一内尺寸3mm,框宽为10mm,用螺丝10将其固定在溅射台托盘上,如图10.1、10.2所示俯视、剖面示意图,悬挂托盘,沉积氧化锌沟道层11,图11所示为俯视图,工艺完成后,将其从托盘中取出,得到样品四,图12为样品四剖面图;Put sample three into acetone, ethanol, and deionized water for 4 minutes, then rinse with deionized water, blow dry with N2 , and dry in a drying oven at 90°C for 4 minutes, then place it in a magnetron sputtering apparatus On the tray 8 of the sputtering table, press mold 2 9 on it. The inner diameter is 12mm, which is 3mm smaller than the inner dimension of mold 1, and the frame width is 10mm. Fix it on the tray of the sputtering table with screws 10, as shown in Figure 10.1 and 10.2 Top view, schematic sectional view, hang the tray, deposit the zinc oxide channel layer 11, the top view is shown in Figure 11, after the process is completed, it is taken out from the tray to obtain sample 4, and Figure 12 is a sectional view of sample 4;
(六)源漏电极沉积,所述源漏电极材料为Al,利用光刻剥离技术,沉积方法采用真空蒸镀、电子束蒸发;(6) Source-drain electrode deposition, the source-drain electrode material is Al, using photolithography stripping technology, the deposition method adopts vacuum evaporation and electron beam evaporation;
(1)清洗,按照步骤(一)所述清洗方法,将样品四进行清洗;(1) Cleaning, according to the cleaning method described in step (1), sample four is cleaned;
(2)固定,按照步骤(二)所述粘合方法,利用光刻胶二12将清洗后的样品四固定在硬质衬底表面,形成样品五,如图13.1、13.2为样品五俯视图、剖面图;(2) Fixing, according to the bonding method described in step (2), use photoresist 2 12 to fix the cleaned sample 4 on the surface of the hard substrate to form sample 5, as shown in Figures 13.1 and 13.2 for the top view of sample 5, section view;
(3)光刻-剥离方法,把沟道层刻蚀出多个制作单一薄膜晶体管器件的小岛区域,在小岛区域内的沟道层上刻蚀出源、漏电极区,在源、漏电极区沉积源、漏电极,具体如下:(3) Photolithography-stripping method, the channel layer is etched out a plurality of small island regions for making a single thin film transistor device, the source and drain electrode regions are etched on the channel layer in the small island region, and the source and drain electrode regions are etched. The source and drain electrodes are deposited in the drain electrode area, as follows:
①涂胶,将样品五固定在匀胶仪上,旋转,涂有反转特性的光刻胶三13,转速900转/分钟,时间3—5分钟,使光刻胶均匀地涂覆在沟道层的表面;①Glue coating, fix sample 5 on the glue homogenizer, rotate, and coat the photoresist 3 13 with inversion characteristics, the rotation speed is 900 rpm, and the time is 3-5 minutes, so that the photoresist is evenly coated on the groove the surface of the road layer;
②前烘,90℃下前烘、坚膜9分钟;②Pre-bake, pre-bake at 90°C and harden the film for 9 minutes;
③曝光,用图形如图14所示光刻版一14覆盖,放置于曝光机下曝光,此时,图形覆盖部分,未受到光照,其余部分曝光;③ Exposure, covered with photolithography plate 14 as shown in Figure 14, placed under the exposure machine for exposure, at this time, the covered part of the pattern was not exposed to light, and the rest was exposed;
④显影,将其置于显影液中,曝光部分对应的光刻胶三溶于显影液,被去除,露出氧化锌;④Development, put it in the developer solution, the photoresist three corresponding to the exposed part is dissolved in the developer solution, is removed, and zinc oxide is exposed;
⑤腐蚀,用千分之一盐酸腐蚀,未被光刻胶保护的部分,即氧化锌部分被腐蚀掉,露出绝缘层二氧化硅,形成样品六,如图15.1小岛、15.2所示样品六;⑤ Corrosion, corroding with one-thousandth hydrochloric acid, the part not protected by the photoresist, that is, the zinc oxide part is corroded, exposing the insulating layer of silicon dioxide, forming sample 6, as shown in Figure 15.1 small island and sample 15.2 ;
⑥去胶,将样品六放入丙酮、乙醇、去离子水中依次超声清洗4分钟,光刻胶二、三溶于丙酮从而被剥离掉,如图16.1、16.2所示,图示为多个制作单一薄膜晶体管器件的小岛区域;⑥Remove the glue, put the sample 6 into acetone, ethanol, and deionized water and ultrasonically clean it for 4 minutes in sequence, and the photoresist 2 and 3 are dissolved in acetone and stripped off, as shown in Figure 16.1 and 16.2. The island region of a single TFT device;
⑦二次光刻,按照步骤(二)所述粘合方法,利用光刻胶四15将清洗去胶后的样品六固定在硬质衬底表面;7. Secondary photolithography, according to the bonding method described in step (2), utilize photoresist 4 15 to fix sample 6 after cleaning and deglue on the hard substrate surface;
涂胶,按照步骤①所述方法,旋涂有反转特性的光刻胶五16;Glue coating, according to the method described in step 1., spin-coating photoresist 5 16 with inversion characteristics;
前烘,90℃下前烘,坚膜9分钟;Pre-bake, pre-bake at 90°C, harden the film for 9 minutes;
曝光,用图17所示光刻版二17覆盖,对版后,图形与氧化锌重叠,俯视、剖面示意如图18.1、18.2所示;Expose, cover with the photolithography plate 2 17 shown in Figure 17, after the plate is aligned, the graphics overlap with the zinc oxide, and the top view and cross-section are shown in Figures 18.1 and 18.2;
曝光后烘,110℃下加热9分钟,有反转特性的光刻胶五变成负胶;Baking after exposure, heating at 110°C for 9 minutes, the photoresist with inversion characteristics becomes a negative resist five times;
裸曝光;naked exposure;
显影,放入显影液中,负胶未曝光部分被显影液溶掉,曝光部分保留;Developing, put it into the developer solution, the unexposed part of the negative film is dissolved by the developer solution, and the exposed part remains;
用去离子水冲洗,形成样品七,得到即将沉积源、漏电极的区域,图19为一个制备单一薄膜晶体管器件所对应的示意图;Rinse with deionized water to form sample 7, and obtain the area where the source and drain electrodes are about to be deposited. Figure 19 is a schematic diagram corresponding to the preparation of a single thin film transistor device;
⑧沉积源、漏电极,按照步骤2所述粘合方法,将样品七固定在硬质衬底上,放入电子束蒸发设备EB(Electron-beam Evaporation)中,沉积源/漏电极金属铝18;⑧ Deposit source and drain electrodes, according to the bonding method described in step 2, fix sample 7 on the hard substrate, put it into the electron beam evaporation equipment EB (Electron-beam Evaporation), and deposit the source/drain electrode metal aluminum 18 ;
⑨去胶,放入丙酮溶液浸泡1.5小时,超声2.5分钟,光刻胶四溶于丙酮从而硬质衬底被分离掉,沟道层表面光刻胶五连同其上的电极被丙酮去除,露出沟道层,再用乙醇、去离子水冲洗干净,N2气吹干,即完成了器件制备,器件图形俯视、剖面如图20.1、20.2所示。⑨Remove the glue, soak in acetone solution for 1.5 hours, ultrasonic for 2.5 minutes, the photoresist 4 is dissolved in acetone and the hard substrate is separated, and the photoresist 5 on the surface of the channel layer and the electrodes on it are removed by acetone, exposing The channel layer was rinsed with ethanol and deionized water, and dried with N 2 gas to complete the device preparation. The top view and cross-section of the device are shown in Figures 20.1 and 20.2.
实施例3Example 3
包括下列步骤:Include the following steps:
(一)硬质衬底和柔性衬底的清洗、吹干、烘干;所述硬质衬底材料为玻璃、硅片、或不锈钢片,所述柔性衬底材料为聚酰亚胺PI;(1) cleaning, drying, and drying of hard substrate and flexible substrate; the hard substrate material is glass, silicon wafer, or stainless steel sheet, and the flexible substrate material is polyimide PI;
将硬质衬底1,25mm*25mm和柔性衬底聚酰亚胺2,20mm*20mm分别清洗,方法是:Clean the hard substrate 1, 25mm*25mm and the flexible substrate polyimide 2, 20mm*20mm respectively, the method is:
(1)先将其放入丙酮溶液中在室温下超声清洗6分钟,去除表面分子型沾污等;(1) First put it into an acetone solution and ultrasonically clean it for 6 minutes at room temperature to remove surface molecular contamination, etc.;
(2)然后置于乙醇溶液中在室温下超声清洗5分钟,去除表面残余丙酮;(2) Then place it in an ethanol solution and ultrasonically clean it for 5 minutes at room temperature to remove residual acetone on the surface;
(3)再用去离子水在室温下超声清洗5分钟,去除残余乙醇及离子型沾污;(3) Ultrasonic cleaning with deionized water at room temperature for 5 minutes to remove residual ethanol and ionic contamination;
(4)高纯氮气吹干,烘干炉90℃下干燥5分钟;(4) blow dry with high-purity nitrogen, and dry at 90° C. for 5 minutes in an oven;
(二)衬底粘合,所述衬底粘合材料为光刻胶;(2) substrate bonding, the substrate bonding material is photoresist;
将硬质衬底固定在匀胶仪上,在硬质衬底中间位置滴光刻胶一3,0.5ml,如图1所示,将清洗好的柔性材料衬底聚酰亚胺2,如图2所示,置于光刻胶一上面,待玻璃衬底与柔性衬底通过光刻胶一全部接触后,启动匀胶仪,转速550转/分钟,时间120秒,使光刻胶一均匀铺在柔性衬底与硬质衬底之间,从而使柔性衬底与硬质衬底紧紧粘合在一起,柔性衬底被平整固定在硬质衬底表面,形成样品一,样品一剖面图如图3所示;Fix the hard substrate on the homogenizer, drop photoresist 1, 0.5ml in the middle of the hard substrate, as shown in Figure 1, and clean the flexible material substrate polyimide 2, such as As shown in Figure 2, place it on the photoresist one, and after the glass substrate and the flexible substrate are fully contacted through the photoresist one, start the homogenizer, the speed is 550 rpm, and the time is 120 seconds, so that the photoresist one Spread evenly between the flexible substrate and the hard substrate, so that the flexible substrate and the hard substrate are tightly bonded together, and the flexible substrate is flattened on the surface of the hard substrate to form sample 1, sample 1 The section view is shown in Figure 3;
(三)栅极材料沉积,所述栅极材料为铝,采用电子束蒸发方法EB、Electron-beamEvaporation制备;(3) gate material deposition, the gate material is aluminum, prepared by electron beam evaporation method EB, Electron-beamEvaporation;
将样品一放入电子束蒸发装置生长室中,放置方向为柔性衬底朝下,用电子束蒸发方法镀铝在柔性衬底上作为栅极4,如图4.1所示,完成后,依次将其放入丙酮溶液、乙醇、去离子水中超声清洗5分钟,用去离子水冲洗,N2吹干,在此过程中,光刻胶一溶于丙酮溶液,从而,硬质衬底与其他部分分离开来,形成样品二,如图4.2所示;Put the sample 1 into the growth chamber of the electron beam evaporation device with the flexible substrate facing down, and use the electron beam evaporation method to plate aluminum on the flexible substrate as the grid 4, as shown in Figure 4.1. Put it into acetone solution, ethanol, and deionized water for ultrasonic cleaning for 5 minutes, rinse with deionized water, and blow dry with N2 . During this process, the photoresist is dissolved in acetone solution, so that the hard substrate and other parts Separated to form sample 2, as shown in Figure 4.2;
(四)绝缘层材料沉积,所述绝缘层材料为SiO2,采用离子体增强化学气相沉积PECVD,Plasma Enhanced Chemical Vapor Deposition方法生长;(4) deposition of insulating layer material, the insulating layer material is SiO 2 , grown by plasma enhanced chemical vapor deposition PECVD, Plasma Enhanced Chemical Vapor Deposition method;
取4英寸洁净硅片5,将样品二放置在硅片上面中间位置,样品二吸附于硅片表面,如图5.1,5.2所示,将带有样品二的硅片置于PECVD生长室底座,为避免绝缘层沉积过程中样品二受热发生卷曲、翘角等现象,影响绝缘层生长,取清洗干净的不锈钢片制成的模具一6,模具一为方框形,内径15mm,框宽5mm,如图6.1,6.2所示,将模具一压在样品二上面,俯视、剖面效果如图7.1、7.2所示,沉积二氧化硅绝缘层7,俯视如图8所示,形成样品三,样品三剖面图如图9;Take a 4-inch clean silicon wafer 5, place sample 2 on the middle position above the silicon wafer, sample 2 is adsorbed on the surface of the silicon wafer, as shown in Figure 5.1 and 5.2, place the silicon wafer with sample 2 on the base of the PECVD growth chamber, In order to avoid curling and warping of the sample 2 during the deposition process of the insulating layer, which would affect the growth of the insulating layer, a mold 6 made of cleaned stainless steel sheets was taken. The mold 1 was in the shape of a square frame with an inner diameter of 15 mm and a frame width of 5 mm. As shown in Figures 6.1 and 6.2, mold one is pressed on sample two, and the top view and section effects are shown in Figures 7.1 and 7.2, and a silicon dioxide insulating layer 7 is deposited, and the top view is shown in Figure 8, forming sample three and sample three The cross-sectional view is shown in Figure 9;
(五)氧化锌沟道层材料沉积,所述沟道层材料为ZnO,方法采用射频磁控溅射radio-frequency magnetron sputtering,RF-sputtering;(5) Zinc oxide channel layer material deposition, the channel layer material is ZnO, the method adopts radio-frequency magnetron sputtering radio-frequency magnetron sputtering, RF-sputtering;
将样品三分别放入丙酮、乙醇、去离子水中依次超声清洗5分钟,再用去离子水冲洗,N2吹干,烘干炉90℃下干燥5分钟,将其置于磁控溅射仪的溅射台托盘8上,上压模具二9,内径为12mm,小于模具一内尺寸3mm,框宽为10mm,用螺丝10将其固定在溅射台托盘上,如图10.1、10.2所示俯视、剖面示意图,悬挂托盘,沉积氧化锌沟道层11,图11所示为俯视图,工艺完成后,将其从托盘中取出,得到样品四,图12为样品四剖面图;Put sample three into acetone, ethanol, and deionized water for 5 minutes, then rinse with deionized water, blow dry with N2 , and dry in a drying oven at 90°C for 5 minutes, then place it in a magnetron sputtering apparatus On the tray 8 of the sputtering table, press mold 2 9 on it. The inner diameter is 12mm, which is 3mm smaller than the inner dimension of mold 1, and the frame width is 10mm. Fix it on the tray of the sputtering table with screws 10, as shown in Figure 10.1 and 10.2 Top view, schematic sectional view, hang the tray, deposit the zinc oxide channel layer 11, the top view is shown in Figure 11, after the process is completed, it is taken out from the tray to obtain sample 4, and Figure 12 is a sectional view of sample 4;
(六)源漏电极沉积,所述源漏电极材料为Al,利用光刻剥离技术,沉积方法采用真空蒸镀、电子束蒸发;(6) Source-drain electrode deposition, the source-drain electrode material is Al, using photolithography stripping technology, the deposition method adopts vacuum evaporation and electron beam evaporation;
(1)清洗,按照步骤(一)所述清洗方法,将样品四进行清洗;(1) Cleaning, according to the cleaning method described in step (1), sample four is cleaned;
(2)固定,按照步骤(二)所述粘合方法,利用光刻胶二12将清洗后的样品四固定在硬质衬底表面,形成样品五,如图13.1、13.2为样品五俯视图、剖面图;(2) Fixing, according to the bonding method described in step (2), use photoresist 2 12 to fix the cleaned sample 4 on the surface of the hard substrate to form sample 5, as shown in Figures 13.1 and 13.2 for the top view of sample 5, section view;
(3)光刻-剥离方法,把沟道层刻蚀出多个制作单一薄膜晶体管器件的小岛区域,在小岛区域内的沟道层上刻蚀出源、漏电极区,在源、漏电极区沉积源、漏电极,具体如下:(3) Photolithography-stripping method, the channel layer is etched out a plurality of small island regions for making a single thin film transistor device, the source and drain electrode regions are etched on the channel layer in the small island region, and the source and drain electrode regions are etched. The source and drain electrodes are deposited in the drain electrode area, as follows:
①涂胶,将样品五固定在匀胶仪上,旋转,涂有反转特性的光刻胶三13,转速1300转/分钟,时间5分钟,使光刻胶均匀地涂覆在沟道层的表面;①Glue coating, fix sample 5 on the homogenizer, rotate it, and coat the photoresist 3 13 with inversion characteristics, the rotation speed is 1300 rpm, and the time is 5 minutes, so that the photoresist is evenly coated on the channel layer s surface;
②前烘,90℃下前烘、坚膜9分钟;②Pre-bake, pre-bake at 90°C and harden the film for 9 minutes;
③曝光,用图形如图14所示光刻版一14覆盖,放置于曝光机下曝光,此时,图形覆盖部分,未受到光照,其余部分曝光;③ Exposure, covered with photolithography plate 14 as shown in Figure 14, placed under the exposure machine for exposure, at this time, the covered part of the pattern was not exposed to light, and the rest was exposed;
④显影,将其置于显影液中,曝光部分对应的光刻胶三溶于显影液,被去除,露出氧化锌;④Development, put it in the developer solution, the photoresist three corresponding to the exposed part is dissolved in the developer solution, is removed, and zinc oxide is exposed;
⑤腐蚀,用千分之一盐酸腐蚀,未被光刻胶保护的部分,即氧化锌部分被腐蚀掉,露出绝缘层二氧化硅,形成样品六,如图15.1小岛、15.2所示样品六;⑤ Corrosion, corroding with one-thousandth hydrochloric acid, the part not protected by the photoresist, that is, the zinc oxide part is corroded, exposing the insulating layer of silicon dioxide, forming sample 6, as shown in Figure 15.1 small island and sample 15.2 ;
⑥去胶,将样品六放入丙酮、乙醇、去离子水中依次超声清洗5分钟,光刻胶二、三溶于丙酮从而被剥离掉,如图16.1、16.2所示,图示为多个制作单一薄膜晶体管器件的小岛区域;⑥Remove the glue, put the sample 6 into acetone, ethanol, and deionized water, and ultrasonically clean it for 5 minutes in sequence. The island region of a single TFT device;
⑦二次光刻,按照步骤(二)所述粘合方法,利用光刻胶四15将清洗去胶后的样品六固定在硬质衬底表面;7. Secondary photolithography, according to the bonding method described in step (2), utilize photoresist 4 15 to fix sample 6 after cleaning and deglue on the hard substrate surface;
涂胶,按照步骤①所述方法,旋涂有反转特性的光刻胶五16;Glue coating, according to the method described in step 1., spin-coating photoresist 5 16 with inversion characteristics;
前烘,90℃下前烘,坚膜9分钟;Pre-bake, pre-bake at 90°C, harden the film for 9 minutes;
曝光,用图17所示光刻版二17覆盖,对版后,图形与氧化锌重叠,俯视、剖面示意如图18.1、18.2所示;Expose, cover with the photolithography plate 2 17 shown in Figure 17, after the plate is aligned, the graphics overlap with the zinc oxide, and the top view and cross-section are shown in Figures 18.1 and 18.2;
曝光后烘,110℃下加热9分钟,有反转特性的光刻胶五变成负胶;Baking after exposure, heating at 110°C for 9 minutes, the photoresist with inversion characteristics becomes a negative resist five times;
裸曝光;naked exposure;
显影,放入显影液中,负胶未曝光部分被显影液溶掉,曝光部分保留;Developing, put it into the developer solution, the unexposed part of the negative film is dissolved by the developer solution, and the exposed part remains;
用去离子水冲洗,形成样品七,得到即将沉积源、漏电极的区域,图19为一个制备单一薄膜晶体管器件所对应的示意图;Rinse with deionized water to form sample 7, and obtain the area where the source and drain electrodes are about to be deposited. Figure 19 is a schematic diagram corresponding to the preparation of a single thin film transistor device;
⑧沉积源、漏电极,按照步骤2所述粘合方法,将样品七固定在硬质衬底上,放入电子束蒸发设备EB(Electron-beam Evaporation)中,沉积源/漏电极金属铝18;⑧ Deposit source and drain electrodes, according to the bonding method described in step 2, fix sample 7 on the hard substrate, put it into the electron beam evaporation equipment EB (Electron-beam Evaporation), and deposit the source/drain electrode metal aluminum 18 ;
⑨去胶,放入丙酮溶液浸泡2小时,超声3分钟,光刻胶四溶于丙酮从而硬质衬底被分离掉,沟道层表面光刻胶五连同其上的电极被丙酮去除,露出沟道层,再用乙醇、去离子水冲洗干净,N2气吹干,即完成了器件制备,器件图形俯视、剖面如图20.1、20.2所示。⑨Remove the glue, soak in acetone solution for 2 hours, ultrasonic for 3 minutes, the photoresist 4 is dissolved in acetone and the hard substrate is separated, the photoresist 5 on the surface of the channel layer and the electrodes on it are removed by acetone, exposing The channel layer was rinsed with ethanol and deionized water, and dried with N 2 gas to complete the device preparation. The top view and cross-section of the device are shown in Figures 20.1 and 20.2.
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510205191.XA CN104934329B (en) | 2015-04-28 | 2015-04-28 | Preparation method for ZnO-Thin Film Transistor (ZnO-TFT) based on flexible substrate material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510205191.XA CN104934329B (en) | 2015-04-28 | 2015-04-28 | Preparation method for ZnO-Thin Film Transistor (ZnO-TFT) based on flexible substrate material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104934329A CN104934329A (en) | 2015-09-23 |
| CN104934329B true CN104934329B (en) | 2017-03-22 |
Family
ID=54121438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510205191.XA Expired - Fee Related CN104934329B (en) | 2015-04-28 | 2015-04-28 | Preparation method for ZnO-Thin Film Transistor (ZnO-TFT) based on flexible substrate material |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN104934329B (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105470390B (en) * | 2015-11-23 | 2017-12-15 | 苏州大学 | Method for constructing large-area, flexible and wearable organic nanowire field effect transistor array by taking adhesive tape as substrate |
| CN106683998A (en) * | 2016-11-28 | 2017-05-17 | 中国电子科技集团公司第四十八研究所 | Flexible substrate pretreatment process |
| CN108962759B (en) * | 2018-07-15 | 2019-07-30 | 吉林建筑大学 | A kind of preparation method of zinc oxide thin-film transistor |
| CN108987529B (en) * | 2018-07-15 | 2019-09-24 | 吉林建筑大学 | A kind of preparation method of flexibility zinc oxide photistor |
| CN110047976B (en) * | 2019-04-30 | 2020-11-06 | 吉林建筑大学 | Preparation method of solar blind ultraviolet photosensitive transistor |
| CN113808921A (en) * | 2021-07-26 | 2021-12-17 | 天津大学 | Manufacturing method of flexible electronic device with characteristic dimension in submicron order |
| CN115996622B (en) * | 2022-12-07 | 2025-12-02 | 三序光学科技(苏州)有限公司 | A flexible photoelectric-pole-electric integrated sensor and its fabrication method |
| CN118550153B (en) * | 2024-06-26 | 2025-11-28 | 湖南大学 | Efficient batch preparation process for flexible photoetching mask plate |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8728861B2 (en) * | 2011-10-12 | 2014-05-20 | The United States Of America As Represented By The Secretary Of The Air Force | Fabrication method for ZnO thin film transistors using etch-stop layer |
| CN102496562B (en) * | 2011-11-30 | 2014-01-01 | 中国科学院半导体研究所 | A method of adhering a flexible film material to a glass substrate |
| CN103413833B (en) * | 2013-07-09 | 2016-04-20 | 复旦大学 | A kind of flexible zno-based thin-film transistor and preparation method thereof |
| CN103456900B (en) * | 2013-08-20 | 2016-07-06 | Tcl集团股份有限公司 | The manufacture method of flexible display apparatus |
-
2015
- 2015-04-28 CN CN201510205191.XA patent/CN104934329B/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN104934329A (en) | 2015-09-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104934329B (en) | Preparation method for ZnO-Thin Film Transistor (ZnO-TFT) based on flexible substrate material | |
| CN101330010A (en) | A method of making T-type HBT emitter/HEMT grid | |
| CN102881571B (en) | Active layer ion implantation method and active layer ion implantation method for thin-film transistor | |
| CN103715096A (en) | Thin film thyristor and manufacturing method thereof and array substrate and manufacturing method thereof | |
| WO2015149469A1 (en) | Preparation method of array substrate, array substrate and display device | |
| WO2015143745A1 (en) | Manufacturing method of array substrate | |
| CN107104044A (en) | A kind of preparation method of method for making its electrode and array base palte | |
| CN114613666A (en) | A kind of long-life chromium plate photolithography mask and preparation method thereof | |
| WO2013181915A1 (en) | Tft array substrate, method of fabricating same, and display device | |
| CN102420183B (en) | Manufacturing method of TFT (Thin Film Transistor) array substrate and TFT array substrate | |
| CN102779942A (en) | Organic thin film transistor array substrate and manufacturing method thereof | |
| CN115893305A (en) | Method for improving Lift-Off process graphic abnormity | |
| CN104617049B (en) | A kind of array base palte and preparation method thereof, display device | |
| CN103996618B (en) | Manufacturing method for TFT electrode lead | |
| CN102117767A (en) | Fully transparent TFT (Thin Film Transistor) active matrix manufacturing method based on colloidal sol mode | |
| CN103487160A (en) | Method for manufacturing Pt resistor temperature sensor | |
| CN108987529B (en) | A kind of preparation method of flexibility zinc oxide photistor | |
| CN103840243A (en) | Flexible coplanar waveguide manufacturing method | |
| CN103123912A (en) | Method for manufacturing top gate TFT (thin film transistor) array substrate | |
| CN106803485A (en) | A kind of thin film transistor (TFT) and preparation method thereof, display | |
| CN102956505B (en) | Manufacture method for switching tube and array substrate | |
| CN113917784A (en) | A multi-variable mask for all-solid-state memory transistors with top-gate structure based on overlay technology | |
| CN114229838B (en) | Graphene device, multilayer film, and manufacturing method and application thereof | |
| JPH03102324A (en) | Production of thin-film transistor | |
| CN106024707B (en) | Array substrate and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20170322 |