CN102280163B - Infrared transparent conductive film and preparation method thereof - Google Patents
Infrared transparent conductive film and preparation method thereof Download PDFInfo
- Publication number
- CN102280163B CN102280163B CN 201110133106 CN201110133106A CN102280163B CN 102280163 B CN102280163 B CN 102280163B CN 201110133106 CN201110133106 CN 201110133106 CN 201110133106 A CN201110133106 A CN 201110133106A CN 102280163 B CN102280163 B CN 102280163B
- Authority
- CN
- China
- Prior art keywords
- sapphire
- film
- photoresist
- sample
- sio
- 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
Landscapes
- Investigating Or Analysing Materials By Optical Means (AREA)
Abstract
The invention discloses an infrared transparent conductive film and a preparation method thereof. The preparation method comprises the following steps of: covering an Au grating film layer with thickness of 20-30 nm, period of 500-700 microns and line width of 2.0-4.0 microns on a SiO2 reflection reducing film of a sapphire sample or the sapphire surface, and forming an infrared transparent conductive film by the steps of coating photoresist, pre-baking, exposing, after-baking, depositing the Au film and removing photoresist. The period of the Au grating film is far longer than the wavelength of the infrared light, so the Au grating film has little influence on the infrared optical performance. Meanwhile, the period of the Au grating film is far shorter than the wavelength of the electromagnetic wave, so the Au grating film has good electromagnetic shielding function. Therefore, the Au grating film can be used as the infrared transparent conductive film of the sapphire. In combination with the SiO2-plated infrared reflection-reducing film, the purpose of simultaneously effectively improving the infrared transmissivity and the electromagnetic shielding function of the sapphire substrate can be achieved.
Description
Technical field
The present invention relates to material science, specifically a kind of infrared transparent conductive film and preparation method thereof.
Background technology
At present, infrared acquisition and guidance technology almost have been applied to various military combat platforms.Infrared Detectors window/head-shield is separated infrared sensing/imaging system and external environment, and system is played protective effect.Detector window/the hood material that can be used as 3~5 μ m medium-wave infrared wave bands has yittrium oxide, spinelle, nitrogen oxygen aluminium, sapphire etc.Wherein, sapphire has very high hardness, mechanical strength and high temperature stability performance, can bear the thermal shock power that the New Generation Missile high-speed flight produces, and its see through band from ultraviolet, can see infrared, it is wider to see through wave band, can be fit to the multiple aiming means requirements such as optics, electronics.Thereby, sapphire be as medium-wave infrared window and head-shield the optimal candidate material (Yin Shengxi, Chu Jianxin. " the novel method of attachment of sapphire dome and metal body is studied ". aviation Precision Manufacturing Technology, 2010,46 (1): 54~57).
The demand for development Infrared Detectors window/hood material of modern military and space technology is except will having good infrared transmittivity, also want to bear the bump of the solids such as free dust in high temperature, high pressure, thermal shock, the atmosphere and hail, possess the performance of anti-electromagnetic interference.Be limited to technology and the level of processing of Artificial Growth sapphire single-crystal material, sapphire infrared transmittivity can't satisfy actual operation requirements.In addition, the electromagnetic shielding efficiency of sapphire material itself is very low, is easy to be subject to electromagnetic interference, makes its service behaviour undesirable deviation (service behaviour is by " degradation " in other words) occur.The electronic equipment of detection system inside can produce electromagnetic radiation and might become the clue that the enemy scouts on the other hand, thereby military target is exposed.Thereby how effectively improving sapphire infrared transmittivity and electromagnetic shielding efficiency has become sapphire and has been applied in one of key technology on infrared window/head-shield.
U.S. air-sea tactical operations center adopts radio frequency magnetron sputtering method to prepare individual layer SiO in Sapphire Substrate
2Film and three layers of SiO
2/ Si
3N
4/ SiO
2Laminated film (L.F.Johnson, M.B.Moran. " Compressive Coatings for Strengthened Sapphire " .Proc.of the International Society for Optical Engineering on Window and Dome Technologies and Materials VI, April 1999, Orlando, Florida.) for improving sapphire infrared transmittivity.This studies show that SiO
2Film and SiO
2/ Si
3N
4/ SiO
2Film system can improve sapphire infrared transmittivity significantly.Applicant and the member of seminar have prepared SiO in Sapphire Substrate
2Film and SiO
2/ Si
3N
4(the L.P.Feng of duplicature system, Z.T.Liu. " Characteristics of Silicon Dioxide Films Prepared on Sapphire " .Material Science and Engineering B, 2005,122 (1): 7~11.L.P.Feng, Z.T.Liu, Q.Li, W.Song. " Investigation of SiO
2/ Si
3N
4Films prepared on sapphire by r.f.magnetron reactive sputtering " .Applied Surface Science, 2006,252 (12): 4064~4070.), SiO is found in research
2Film and SiO
2/ Si
3N
4Sapphire infrared transmittivity all can improve in duplicature system.But, SiO
2Film, SiO
2/ Si
3N
4/ SiO
2Film system and SiO
2/ Si
3N
4Film system all can not improve sapphire electromagnetic shielding efficiency.
Summary of the invention
In order to overcome the low problem of sapphire electromagnetic shielding efficiency in the prior art, the present invention is being coated with SiO
2A kind of infrared transparent conductive film and preparation method thereof is proposed on the Sapphire Substrate of anti-reflection film.
The technical scheme that the present invention takes is: plate SiO in Sapphire Substrate
2Anti-reflection film forms the sapphire sample; SiO at the sapphire sample
2On the anti-reflection film or sapphire surface cover layer of Au net grid film, form infrared transparent conductive film.The thickness of described Au net grid film is 20~30nm, and the cycle of Au net grid film is 500~700 μ m, and the live width of Au net grid film is 2.0~4.0 μ m.
The present invention also proposes a kind of method for preparing infrared transparent conductive film, may further comprise the steps:
Step 1 is cleaned the sapphire sample.To being coated with SiO
2The sapphire sample of anti-reflection film cleans.The process conditions of cleaning are: the sapphire sample is placed on uses Ultrasonic Cleaning in the deionized water first, hyperacoustic power is 100~200W, and hyperacoustic frequency is 20~24kHz, and scavenging period is 2~4 minutes; Then the sapphire sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, hyperacoustic power is 100~200W, and hyperacoustic frequency is 20~24kHz, and scavenging period is 3~5 minutes, the sapphire sample that obtains cleaning up.
Step 2, resist coating.Adopt photoresist spinner at the SiO of the sapphire sample that cleans up
2Resist coating on the film.The process conditions of resist coating are: at room temperature, drip the photoresist of 3~5ml at SiO
2On the film, the rotary speed of glue spreader is 3400~3500r/min, and rotational time is 47~53s, obtains scribbling the sapphire sample of photoresist.
Step 3, front baking.The sapphire sample that scribbles photoresist is put into baking oven carry out front baking.The process conditions of front baking are: pre-bake temperature is 105~110 ℃, and the front baking temperature retention time is 116~120s; Described sapphire sample is taken out air cooling to room temperature, obtain the sapphire sample that scribbles photoresist through front baking.
Step 4, exposure.Adopt mask aligner that the sapphire sample that scribbles photoresist through front baking is exposed.The process conditions of exposure are: will have the cycle is 500~700 μ m, and live width is the photoresist surface that the mask of 2.0~4.0 μ m is pressed in described sapphire sample, and the time for exposure is 38~42s, obtains the sapphire sample that scribbles photoresist through overexposure.
Step 5 is developed.The sapphire sample that scribbles photoresist through overexposure is developed.The process conditions of developing are: at room temperature, get concentration and be developing solution 20~30ml of 3~4%, described sapphire sample is put into developing solution develop, developing time is 90~96s, obtains the sapphire sample that scribbles photoresist through developing.
Step 6, rear baking.Baking after will putting into baking oven and carry out through the sapphire sample that scribbles photoresist that develops.The process conditions of rear baking are: the temperature of rear baking is 108~112 ℃, and the temperature retention time of rear baking is 120~126s, then described sapphire sample is taken out air cooling to room temperature, obtains the sapphire sample that scribbles photoresist that dries by the fire through later.
Step 7, deposition Au film.Adopt radio frequency magnetron sputtering method at the sapphire sample deposition Au film that scribbles photoresist through later baking.The process conditions of rf magnetron sputtering are: sputtering power is 86~90W, the Ar throughput is 13.0~15.0SCCM, underlayer temperature is room temperature, target-substrate distance is 6.0~6.2cm, sputtering pressure is 0.2~0.3Pa, sedimentation time 5~7min obtains being coated with the sapphire sample that scribbles photoresist of Au net grid film.
Step 8 is removed photoresist.The sapphire sample that scribbles photoresist that is coated with Au net grid film is removed photoresist.Go the process conditions of photoresist to be: the sapphire sample that scribbles photoresist that will be coated with Au net grid film is put into the glue-dispenser Ultrasonic Cleaning, hyperacoustic power is 200~300W, hyperacoustic frequency is 20~24kHz, scavenging period is 4~6 minutes, obtains removing the sapphire sample that photoresist is coated with Au net grid film.
Step 9 is cleaned.The sapphire sample that is coated with Au net grid film is cleaned.The process conditions of cleaning are: the sapphire sample that will be coated with Au net grid film is placed on uses Ultrasonic Cleaning in the deionized water, hyperacoustic power is 200~300W, hyperacoustic frequency is 20~24kHz, scavenging period is 6~8 minutes, the sapphire sample that then will be coated with Au net grid film is placed on uses Ultrasonic Cleaning in the absolute ethyl alcohol, hyperacoustic power is 200~300W, and hyperacoustic frequency is 20~24kHz, scavenging period is 6~8 minutes, obtains infrared transparent conductive film.
The present invention is being coated with SiO
2Deposition Au net grid film on the Sapphire Substrate of anti-reflection film.Because the cycle of Au net grid film is much larger than infrared light wavelength, so Au net grid film is little to the infrared optics performance impact; Simultaneously again since the cycle of Au net grid film much smaller than electromagnetic wavelength, so Au net grid film has good electro-magnetic screen function.Thereby Au net grid film can be used as sapphire infrared transparent conductive film.In conjunction with the SiO that is coated with
2The infrared anti-reflection film can realize effectively improving simultaneously infrared transmittivity and the electromagnetic shielding efficiency of Sapphire Substrate.
Table 1 for before the embodiment one described same Sapphire Substrate plated film, the two-sided SiO that is coated with
2Behind the anti-reflection film, the two-sided SiO that is coated with
2Anti-reflection film and single face are coated with electromagnetic shielding efficiency and the infrared transmission performance contrast behind the Au net grid film.
The average infrared transmittivities of electromagnetic shielding efficiency (dB) 3~4.5 mu m ranges (%)
Sapphire Substrate 0.13 86.8
SiO
2/ sapphire/SiO
20.10 96.7
Au net grid/SiO
2/ sapphire/SiO
27.12 95.7
The invention will be further described below in conjunction with embodiment.
Embodiment
Embodiment one
Present embodiment is a kind of at the two-sided SiO of being coated with
2The SiO on arbitrary surface of the sapphire sample of anti-reflection film
2Cover again layer of Au net grid film on the film, form infrared transparent conductive film.Desired Au net grid and the SiO of being coated with
2It is 7.12dB that the sapphire of anti-reflection film has electromagnetic shielding efficiency, and the average infrared transmittivity in 3~4.5 mum wavelength scopes is 95.7%.
Upper surface and lower surface in Sapphire Substrate plate respectively SiO
2Anti-reflection film forms the sapphire sample.In the present embodiment, it is the upper surface covering layer of Au net grid film at the sapphire sample.Be plated in the SiO on the Sapphire Substrate
2The thickness of film is 650nm, and refractive index is 1.41; The thickness of Au net grid film is 20nm, and the cycle of Au net grid film is 700 μ m, and the live width of Au net grid film is 2.0 μ m.
The concrete preparation process of present embodiment is:
Step 1 is cleaned the sapphire sample.To the two-sided SiO that is coated with
2The sapphire sample of anti-reflection film, i.e. SiO
2/ sapphire/SiO
2Sample cleans.The process conditions of cleaning are: first with SiO
2/ sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the deionized water, and hyperacoustic power is 200W, and hyperacoustic frequency is 24kHz, and scavenging period is 2 minutes, then with SiO
2/ sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, and hyperacoustic power is 200W, and hyperacoustic frequency is 24kHz, and scavenging period is 3 minutes, the SiO that obtains cleaning up
2/ sapphire/SiO
2Sample.
Step 2, resist coating.The SiO that adopts photoresist spinner cleaning up
2/ sapphire/SiO
2The upper surface SiO of sample
2Resist coating on the film; The process conditions of resist coating are: at room temperature, drip the JHF-30 photoresist of 3ml at SiO
2On the film, the rotary speed of glue spreader is 3400r/min, and rotational time is 47s, obtains scribbling the SiO of photoresist
2/ sapphire/SiO
2Sample, i.e. photoresist/SiO
2/ sapphire/SiO
2Sample.
Step 3, front baking.With photoresist/SiO
2/ sapphire/SiO
2Sample is put into baking oven and is carried out front baking; The process conditions of front baking are: pre-bake temperature is 105 ℃, and the front baking temperature retention time is 120s, then with photoresist/SiO
2/ sapphire/SiO
2Sample takes out air cooling to room temperature, obtains the photoresist/SiO through front baking
2/ sapphire/SiO
2Sample.
Step 4, exposure.Adopt mask aligner to the photoresist/SiO through front baking
2/ sapphire/SiO
2Sample exposes; The process conditions of exposure are: will have the cycle is 700 μ m, and live width is that the mask of 2.0 μ m is pressed in photoresist/SiO
2/ sapphire/SiO
2The photoresist surface of sample, the time for exposure is 38s, obtains the photoresist/SiO through overexposure
2/ sapphire/SiO
2Sample.
Step 5 is developed.To the photoresist/SiO through overexposure
2/ sapphire/SiO
2Sample develops; The process conditions of developing are: at room temperature, get concentration and be 3% FX-C type developing solution 20ml, and will be through the photoresist/SiO of overexposure
2/ sapphire/SiO
2Sample is put into developing solution and is developed, and developing time is 90s, obtains the photoresist/SiO through developing
2/ sapphire/SiO
2Sample.
Step 6, rear baking.Will be through the photoresist/SiO that develops
2/ sapphire/SiO
2Sample is put into baking oven and is carried out rear baking; The process conditions of rear baking are: the temperature of rear baking is 108 ℃, and the temperature retention time of rear baking is 126s, then with photoresist/SiO
2/ sapphire/SiO
2Sample takes out air cooling to room temperature, obtains the photoresist/SiO that dries by the fire through later
2/ sapphire/SiO
2Sample.
Step 7, deposition Au film.Adopt radio frequency magnetron sputtering method at the photoresist/SiO through drying by the fire later
2/ sapphire/SiO
2Deposition Au film on the sample; The process conditions of rf magnetron sputtering are: sputtering power is 86W, and the Ar throughput is 13.0SCCM, and underlayer temperature is room temperature, and target-substrate distance is 6.2cm, and sputtering pressure is 0.3Pa, and sedimentation time 5min obtains being coated with the photoresist/SiO of Au net grid film
2/ sapphire/SiO
2Sample.
Step 8 is removed photoresist.To being coated with the photoresist/SiO of Au net grid film
2/ sapphire/SiO
2Sample removes photoresist; Go the process conditions of photoresist to be: the photoresist/SiO that will be coated with Au net grid film
2/ sapphire/SiO
2Sample is put into SN-01 type glue-dispenser Ultrasonic Cleaning, and hyperacoustic power is 300W, and hyperacoustic frequency is 24kHz, and scavenging period is 4 minutes, obtains removing the SiO that photoresist is coated with Au net grid film
2/ sapphire/SiO
2Sample, i.e. Au net grid/SiO
2/ sapphire/SiO
2Sample.
Step 9 is cleaned.To Au net grid/SiO
2/ sapphire/SiO
2Sample cleans; The process conditions of cleaning are: with Au net grid/SiO
2/ sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the deionized water, and hyperacoustic power is 300W, and hyperacoustic frequency is 24kHz, and scavenging period is 6 minutes, then with Au net grid/SiO
2/ sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, and hyperacoustic power is 300W, and hyperacoustic frequency is 24kHz, and scavenging period is 6 minutes, obtains infrared transparent conductive film.
Embodiment two
Present embodiment is a kind ofly to be coated with SiO at single face
2The SiO of the sapphire sample of anti-reflection film
2Cover again layer of Au net grid film on the film, form infrared transparent conductive film.Desired Au net grid and the SiO of being coated with
2It is 7.21dB that the sapphire of anti-reflection film has electromagnetic shielding efficiency, and the average infrared transmittivity in 3~4.5 mum wavelength scopes is 90.4%.
Upper surface in Sapphire Substrate plates SiO
2Anti-reflection film forms the sapphire sample.In the present embodiment, be the upper surface SiO at the sapphire sample
2Cover again layer of Au net grid film on the anti-reflection film.Be plated in the SiO on the Sapphire Substrate
2The thickness of film is 640nm, and refractive index is 1.38; The thickness of Au net grid film is 25nm, and the cycle of Au net grid film is 600 μ m, and the live width of Au net grid film is 3.0 μ m.
The concrete preparation process of present embodiment is:
Step 1 is cleaned the sapphire sample.Upper surface is coated with SiO
2The sapphire sample of anti-reflection film, i.e. SiO
2/ sapphire sample cleans.The process conditions of cleaning are: first with SiO
2/ sapphire sample is placed on and uses Ultrasonic Cleaning in the deionized water, and hyperacoustic power is 150W, and hyperacoustic frequency is 22kHz, and scavenging period is 3 minutes, then with SiO
2/ sapphire sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, and hyperacoustic power is 150W, and hyperacoustic frequency is 22kHz, and scavenging period is 4 minutes, the SiO that obtains cleaning up
2/ sapphire sample.
Step 2, resist coating.The SiO that adopts photoresist spinner cleaning up
2The upper surface SiO of/sapphire sample
2Resist coating on the film; The process conditions of resist coating are: at room temperature, drip the NR9-1000PY photoresist of 4ml at SiO
2On the film, the rotary speed of glue spreader is 3450r/min, and rotational time is 50s, obtains scribbling the SiO of photoresist
2/ sapphire sample, i.e. photoresist/SiO
2/ sapphire sample.
Step 3, front baking.With photoresist/SiO
2/ sapphire sample is put into baking oven and is carried out front baking; The process conditions of front baking are: pre-bake temperature is 107 ℃, and the front baking temperature retention time is 118s, then with photoresist/SiO
2/ sapphire sample takes out air cooling to room temperature, obtains the photoresist/SiO through front baking
2/ sapphire sample.
Step 4, exposure.Adopt mask aligner to the photoresist/SiO through front baking
2/ sapphire sample exposes; The process conditions of exposure are: will have the cycle is 600 μ m, and live width is that the mask of 3.0 μ m is pressed in photoresist/SiO
2The photoresist surface of/sapphire sample, the time for exposure is 40s, obtains the photoresist/SiO through overexposure
2/ sapphire sample.
Step 5 is developed.To the photoresist/SiO through overexposure
2/ sapphire sample develops; The process conditions of developing are: at room temperature, get concentration and be 3.5% RD6 type developing solution 25ml, and will be through the photoresist/SiO of overexposure
2/ sapphire sample is put into developing solution and is developed, and developing time is 93s, obtains the photoresist/SiO through developing
2/ sapphire sample.
Step 6, rear baking.Will be through the photoresist/SiO that develops
2/ sapphire sample is put into baking oven and is carried out rear baking; The process conditions of rear baking are: the temperature of rear baking is 110 ℃, and the temperature retention time of rear baking is 124s, then with photoresist/SiO
2/ sapphire sample takes out air cooling to room temperature, obtains the photoresist/SiO that dries by the fire through later
2/ sapphire sample.
Step 7, deposition Au film.Adopt radio frequency magnetron sputtering method at the photoresist/SiO through drying by the fire later
2Deposition Au film on the/sapphire sample; The process conditions of rf magnetron sputtering are: sputtering power is 88W, and the Ar throughput is 14.0SCCM, and underlayer temperature is room temperature, and target-substrate distance is 6.1cm, and sputtering pressure is 0.25Pa, and sedimentation time 6min obtains being coated with the photoresist/SiO of Au net grid film
2/ sapphire sample.
Step 8 is removed photoresist.To being coated with the photoresist/SiO of Au net grid film
2/ sapphire sample removes photoresist; Go the process conditions of photoresist to be: the photoresist/SiO that will be coated with Au net grid film
2/ sapphire sample is put into RR4 type glue-dispenser Ultrasonic Cleaning, and hyperacoustic power is 250W, and hyperacoustic frequency is 22kHz, and scavenging period is 5 minutes, obtains removing the SiO that photoresist is coated with Au net grid film
2/ sapphire sample, i.e. Au net grid/SiO
2/ sapphire sample.
Step 9 is cleaned.To Au net grid/SiO
2/ sapphire sample cleans; The process conditions of cleaning are: with Au net grid/SiO
2/ sapphire sample is placed on and uses Ultrasonic Cleaning in the deionized water, and hyperacoustic power is 250W, and hyperacoustic frequency is 22kHz, and scavenging period is 7 minutes, then with Au net grid/SiO
2/ sapphire sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, and hyperacoustic power is 250W, and hyperacoustic frequency is 22kHz, and scavenging period is 7 minutes, obtains infrared transparent conductive film.
Embodiment three
Present embodiment is a kind of at sapphire specimen surface covering layer of Au net grid film, forms infrared transparent conductive film.A surface of described sapphire sample is coated with SiO
2Anti-reflection film; Au net grid film directly overlays sapphire surface.Desired Au net grid and the SiO of being coated with
2It is 7.45dB that the sapphire of anti-reflection film has electromagnetic shielding efficiency, and the average infrared transmittivity in 3~4.5 mum wavelength scopes is 90.1%.
Be plated in the SiO on the Sapphire Substrate
2The thickness of film is 660nm, and refractive index is 1.40; The thickness of Au net grid film is 30nm, and the cycle of Au net grid film is 500 μ m, and the live width of Au net grid film is 4.0 μ m.
The concrete preparation process of present embodiment is:
Step 1 is cleaned the sapphire sample.Lower surface is coated with SiO
2The sapphire sample of anti-reflection film, i.e. sapphire/SiO
2Sample cleans.The process conditions of cleaning are: first with sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the deionized water, and hyperacoustic power is 100W, and hyperacoustic frequency is 20kHz, and scavenging period is 4 minutes, then with sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, and hyperacoustic power is 100W, and hyperacoustic frequency is 20kHz, and scavenging period is 5 minutes, the sapphire/SiO that obtains cleaning up
2Sample.
Step 2, resist coating.Sapphire/the SiO that adopts photoresist spinner cleaning up
2Resist coating on the upper surface sapphire of sample; The process conditions of resist coating are: at room temperature, drip the RFJ-220 photoresist of 5ml at SiO
2On the film, the rotary speed of glue spreader is 3500r/min, and rotational time is 53s, obtains scribbling the sapphire/SiO of photoresist
2Sample, i.e. photoresist/sapphire/SiO
2Sample.
Step 3, front baking.With photoresist/sapphire/SiO
2Sample is put into baking oven and is carried out front baking; The process conditions of front baking are: pre-bake temperature is 110 ℃, and the front baking temperature retention time is 116s, then with photoresist/sapphire/SiO
2Sample takes out air cooling to room temperature, obtains the photoresist/sapphire/SiO through front baking
2Sample.
Step 4, exposure.Adopt mask aligner to through the photoresist/sapphire of front baking/SiO
2Sample exposes; The process conditions of exposure are: will have the cycle is 500 μ m, and live width is that the mask of 4.0 μ m is pressed in photoresist/sapphire/SiO
2The photoresist of sample surface, the time for exposure is 42s, obtains the photoresist/sapphire/SiO through overexposure
2Sample.
Step 5 is developed.To through the photoresist/sapphire of overexposure/SiO
2Sample develops; The process conditions of developing are: at room temperature, get concentration and be 4% RFX type developing solution 30ml, and will be through the photoresist/sapphire of overexposure/SiO
2Sample is put into developing solution and is developed, and developing time is 96s, obtains through photoresist/sapphire of developing/SiO
2Sample.
Step 6, rear baking.Will be through photoresist/sapphire of developing/SiO
2Sample is put into baking oven and is carried out rear baking; The process conditions of rear baking are: the temperature of rear baking is 112 ℃, and the temperature retention time of rear baking is 120s, then with photoresist/sapphire/SiO
2Sample takes out air cooling to room temperature, obtains the photoresist/sapphire/SiO through later baking
2Sample.
Step 7, deposition Au film.Adopt radio frequency magnetron sputtering method at the photoresist/sapphire through drying by the fire later/SiO
2Deposition Au film on the sample; The process conditions of rf magnetron sputtering are: sputtering power is 90W, and the Ar throughput is 15.0SCCM, and underlayer temperature is room temperature, and target-substrate distance is 6.0cm, and sputtering pressure is 0.2Pa, and sedimentation time 7min obtains being coated with the photoresist/sapphire of Au net grid film/SiO
2Sample.
Step 8 is removed photoresist.To photoresist/sapphire of being coated with Au net grid film/SiO
2Sample removes photoresist; Go the process conditions of photoresist to be: will be coated with the photoresist/sapphire of Au net grid film/SiO
2Sample is put into SN-01 type glue-dispenser Ultrasonic Cleaning, and hyperacoustic power is 200W, and hyperacoustic frequency is 20kHz, and scavenging period is 6 minutes, obtains removing sapphire/SiO that photoresist is coated with Au net grid film
2Sample, i.e. Au net grid/sapphire/SiO
2Sample.
Step 9 is cleaned.To Au net grid/sapphire/SiO
2Sample cleans; The process conditions of cleaning are: with Au net grid/sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the deionized water, and hyperacoustic power is 200W, and hyperacoustic frequency is 20kHz, and scavenging period is 8 minutes, then with Au net grid/sapphire/SiO
2Sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, and hyperacoustic power is 200W, and hyperacoustic frequency is 20kHz, and scavenging period is 8 minutes, obtains infrared transparent conductive film.
Claims (2)
1. an infrared transparent conductive film is characterized in that: be coated with one deck SiO at the Sapphire Substrate single face
2Anti-reflection film forms the sapphire sample, at the SiO of sapphire sample
2Cover again layer of Au net grid film on the anti-reflection film or on the Sapphire Substrate surface, form infrared transparent conductive film; Perhaps at the two-sided one deck SiO that is coated with of Sapphire Substrate
2Anti-reflection film forms the sapphire sample, at one of them SiO of sapphire sample
2Cover again layer of Au net grid film on the anti-reflection film, form infrared transparent conductive film; The thickness of Au net grid film is 20~30nm, and the cycle of Au net grid film is 500~700 μ m, and the live width of Au net grid film is 2.0~4.0 μ m.
2. a method for preparing the described infrared transparent conductive film of claim 1 is characterized in that, comprises the steps:
Step 1 is cleaned the sapphire sample: to being coated with SiO
2The sapphire sample of anti-reflection film cleans; The process conditions of cleaning are: the sapphire sample is placed on uses Ultrasonic Cleaning in the deionized water first, hyperacoustic power is 100~200W, and hyperacoustic frequency is 20~24kHz, and scavenging period is 2~4 minutes; Then the sapphire sample is placed on and uses Ultrasonic Cleaning in the absolute ethyl alcohol, hyperacoustic power is 100~200W, and hyperacoustic frequency is 20~24kHz, and scavenging period is 3~5 minutes, the sapphire sample that obtains cleaning up;
Step 2, resist coating: adopt photoresist spinner at the SiO of the sapphire sample that cleans up
2Resist coating on the anti-reflection film; The process conditions of resist coating are: at room temperature, drip the photoresist of 3~5ml at SiO
2On the anti-reflection film, the rotary speed of glue spreader is 3400~3500r/min, and rotational time is 47~53s, obtains scribbling the sapphire sample of photoresist;
Step 3, front baking: the sapphire sample that will scribble photoresist is put into baking oven and is carried out front baking; The process conditions of front baking are: pre-bake temperature is 105~110 ℃, and the front baking temperature retention time is 116~120s; Described sapphire sample is taken out air cooling to room temperature, obtain the sapphire sample that scribbles photoresist through front baking;
Step 4, exposure: adopt mask aligner that the sapphire sample that scribbles photoresist through front baking is exposed; The process conditions of exposure are: will have the cycle is 500~700 μ m, and live width is the photoresist surface that the mask of 2.0~4.0 μ m is pressed in described sapphire sample, and the time for exposure is 38~42s, obtains the sapphire sample that scribbles photoresist through overexposure;
Step 5 is developed: the sapphire sample that scribbles photoresist through overexposure is developed; The process conditions of developing are: at room temperature, get concentration and be developing solution 20~30ml of 3~4%, described sapphire sample is put into developing solution develop, developing time is 90~96s, obtains the sapphire sample that scribbles photoresist through developing;
Step 6, rear baking: baking after will putting into baking oven and carry out through the sapphire sample that scribbles photoresist that develops; The process conditions of rear baking are: the temperature of rear baking is 108~112 ℃, and the temperature retention time of rear baking is 120~126s, then described sapphire sample is taken out air cooling to room temperature, obtains the sapphire sample that scribbles photoresist that dries by the fire through later;
Step 7, deposition Au film: adopt radio frequency magnetron sputtering method at the sapphire sample deposition Au film that scribbles photoresist through later baking; The process conditions of rf magnetron sputtering are: sputtering power is 86~90W, the Ar throughput is 13.0~15.0SCCM, underlayer temperature is room temperature, target-substrate distance is 6.0~6.2cm, sputtering pressure is 0.2~0.3Pa, sedimentation time 5~7min obtains being coated with the sapphire sample that scribbles photoresist of Au net grid film;
Step 8 is removed photoresist: the sapphire sample that scribbles photoresist that is coated with Au net grid film is removed photoresist; Go the process conditions of photoresist to be: the sapphire sample that scribbles photoresist that will be coated with Au net grid film is put into the glue-dispenser Ultrasonic Cleaning, hyperacoustic power is 200~300W, hyperacoustic frequency is 20~24kHz, scavenging period is 4~6 minutes, obtains removing the sapphire sample that photoresist is coated with Au net grid film;
Step 9 is cleaned: the sapphire sample that is coated with Au net grid film is cleaned; The process conditions of cleaning are: the sapphire sample that will be coated with Au net grid film is placed on uses Ultrasonic Cleaning in the deionized water, hyperacoustic power is 200~300W, hyperacoustic frequency is 20~24kHz, scavenging period is 6~8 minutes, the sapphire sample that then will be coated with Au net grid film is placed on uses Ultrasonic Cleaning in the absolute ethyl alcohol, hyperacoustic power is 200~300W, and hyperacoustic frequency is 20~24kHz, scavenging period is 6~8 minutes, obtains infrared transparent conductive film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 201110133106 CN102280163B (en) | 2011-05-20 | 2011-05-20 | Infrared transparent conductive film and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 201110133106 CN102280163B (en) | 2011-05-20 | 2011-05-20 | Infrared transparent conductive film and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN102280163A CN102280163A (en) | 2011-12-14 |
CN102280163B true CN102280163B (en) | 2013-01-16 |
Family
ID=45105561
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 201110133106 Expired - Fee Related CN102280163B (en) | 2011-05-20 | 2011-05-20 | Infrared transparent conductive film and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN102280163B (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103985478B (en) * | 2014-04-28 | 2016-07-06 | 华南师范大学 | A kind of preparation method of spider reticulation transparency conductive electrode |
CN105845772A (en) * | 2015-01-13 | 2016-08-10 | 北京仿真中心 | Infrared/radio-frequency radiation frequency selecting device based on infrared mesh |
CN105887032A (en) * | 2016-05-10 | 2016-08-24 | 中国建筑材料科学研究总院 | Shielding optical window and preparation method thereof |
CN106061218A (en) * | 2016-06-14 | 2016-10-26 | 苏州大学 | Electromagnetic shielding film and manufacturing method of electromagnetic shielding window |
CN107144899B (en) * | 2017-06-29 | 2023-04-18 | 中国建筑材料科学研究总院 | Chalcogenide optical element with electromagnetic shielding performance and preparation method thereof |
CN110838390B (en) * | 2019-11-21 | 2021-08-24 | 武汉大学 | Method for preparing patterned transparent conductive film by laser |
CN111025446B (en) * | 2019-12-10 | 2022-03-15 | 西安应用光学研究所 | Infrared binary optical device and electromagnetic shielding mesh grid preparation method |
CN111276277B (en) * | 2020-02-12 | 2021-06-29 | 哈尔滨工业大学 | Window with infrared transparent conductive function |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101055881A (en) * | 2007-04-30 | 2007-10-17 | 西安交通大学 | Back shining type ZnO base ultraviolet imaging solid state focal plane detection array and its preparation |
CN101752026A (en) * | 2010-01-21 | 2010-06-23 | 西北工业大学 | Infrared transparent conductive film and preparation method thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030077600A1 (en) * | 2001-10-23 | 2003-04-24 | Chi-Chan Chen | Photovoltaic device to accelerate the interaction among biomolecules |
-
2011
- 2011-05-20 CN CN 201110133106 patent/CN102280163B/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101055881A (en) * | 2007-04-30 | 2007-10-17 | 西安交通大学 | Back shining type ZnO base ultraviolet imaging solid state focal plane detection array and its preparation |
CN101752026A (en) * | 2010-01-21 | 2010-06-23 | 西北工业大学 | Infrared transparent conductive film and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN102280163A (en) | 2011-12-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102280163B (en) | Infrared transparent conductive film and preparation method thereof | |
CN108627889B (en) | Germanium substrate wide-spectrum infrared anti-reflection optical window | |
KR20190092260A (en) | Infrared cut filter and its manufacturing method | |
CN109182972A (en) | Multispectral hard anti-reflection film of large-size sapphire substrate and preparation method thereof | |
CN107502865B (en) | A kind of production method of wide-angle imaging mould group optical filter | |
CN107678081A (en) | A kind of low haze cutoff filter and its film plating process | |
CN103018797B (en) | Film system structure for laser and infrared two-waveband high-reflection film and preparation method of film system structure | |
CN107300783B (en) | A kind of visible light, laser and middle infrared band recombination dichroic elements and design method | |
CN201383012Y (en) | Optical lens with infrared multi-layered antireflection coating | |
CN110160659A (en) | A kind of the uncooled ir narrowband detector and preparation method of sensitive first etching type | |
CN102914807A (en) | Multi-spectral permeability-increasing protection film for zinc sulfide substrate | |
CN106094241A (en) | Crystal cloth of coating-type optical low-pass filter and manufacture method | |
CN110095022A (en) | A kind of economic benefits and social benefits answer infrared stealth structure | |
CN107144899B (en) | Chalcogenide optical element with electromagnetic shielding performance and preparation method thereof | |
CN104950354A (en) | Infrared stealth thin film with selective low emissivity in waveband of 3-5 mu m and preparation method of infrared stealth thin film | |
CN207232419U (en) | A kind of low haze cutoff filter | |
CN112363262B (en) | Infrared stealth film for radar antenna and preparation method thereof | |
CN102912293A (en) | Multi-spectrum protective film and preparation method thereof | |
JP2005181990A (en) | Thin-film structure and method for producing the same | |
CN113825377A (en) | Method for preparing electromagnetic shielding metal mesh grid with limited space of inner concave surface | |
CN110275233B (en) | Narrow-period long-wave infrared multilayer grating structure | |
JP2003344651A (en) | Thin-film structure and thin-film polarizer using the same | |
Zhu et al. | Research on ITO transparent electromagnetic shielding coatings for EO system | |
CN110530206B (en) | Preparation process of high-damage-threshold protective film for optical code disc of laser information field | |
WO2024067055A1 (en) | Optical assembly, preparation method for optical assembly, and electronic device |
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: 20130116 Termination date: 20180520 |