CN106926781A - The electrochromism air locking that a kind of high pressure resistant water vapour corrodes - Google Patents

The electrochromism air locking that a kind of high pressure resistant water vapour corrodes Download PDF

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Publication number
CN106926781A
CN106926781A CN201511022989.7A CN201511022989A CN106926781A CN 106926781 A CN106926781 A CN 106926781A CN 201511022989 A CN201511022989 A CN 201511022989A CN 106926781 A CN106926781 A CN 106926781A
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CN
China
Prior art keywords
substrate
rearview mirror
electrochromic
solution type
adhesive
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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.)
Pending
Application number
CN201511022989.7A
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Chinese (zh)
Inventor
曹贞虎
胡珊珊
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NINGBO MIRROR ELECTRONIC TECHNOLOGY Co Ltd
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NINGBO MIRROR ELECTRONIC TECHNOLOGY Co Ltd
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Priority to CN201511022989.7A priority Critical patent/CN106926781A/en
Publication of CN106926781A publication Critical patent/CN106926781A/en
Pending legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60RVEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
    • B60R1/00Optical viewing arrangements; Real-time viewing arrangements for drivers or passengers using optical image capturing systems, e.g. cameras or video systems specially adapted for use in or on vehicles
    • B60R1/02Rear-view mirror arrangements
    • B60R1/08Rear-view mirror arrangements involving special optical features, e.g. avoiding blind spots, e.g. convex mirrors; Side-by-side associations of rear-view and other mirrors
    • B60R1/083Anti-glare mirrors, e.g. "day-night" mirrors
    • B60R1/088Anti-glare mirrors, e.g. "day-night" mirrors using a cell of electrically changeable optical characteristic, e.g. liquid-crystal or electrochromic mirrors
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/15Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on an electrochromic effect
    • G02F1/153Constructional details
    • G02F1/1533Constructional details structural features not otherwise provided for
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/15Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on an electrochromic effect
    • G02F1/153Constructional details
    • G02F1/155Electrodes
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/15Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on an electrochromic effect
    • G02F1/153Constructional details
    • G02F1/157Structural association of cells with optical devices, e.g. reflectors or illuminating devices

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  • Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Multimedia (AREA)
  • Mechanical Engineering (AREA)
  • Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
  • Optical Elements Other Than Lenses (AREA)

Abstract

The electrochromism air locking that a kind of high pressure resistant water vapour corrodes.The invention discloses a kind of solution type electrochromic rearview mirror of good airproof performance, the adhesive used in the solution type electrochromic rearview mirror of the good airproof performance is cyanate adhesive, cyanate adhesive is not bonding with metallic reflector but bonding with transparent metal conductive oxide layer, so as to improve sealing effectiveness, stability and the service life of solution electrochromic rearview.

Description

The electrochromism air locking that a kind of high pressure resistant water vapour corrodes
Technical field
The present invention relates to electrochromic device, more particularly to solution type electrochromic rearview mirror, but it is not limited only to the electroluminescent change of solution-type Color rearview mirror, also comprising solid-state and semisolid type electrochromic rearview.
Technical background
Electrochromism refers to the reversible change of the color that material occurs under extra electric field and transparency, and this change is due to material Expect the optical properties (transmissivity, reflectivity or absorptivity) in ultraviolet, visible ray or near infrared region under DC Electric Field Generate the reversible change of stabilization and cause.
Electrochromic device is that one kind can be by changing self color and then changing overall transmissivity or reflectivity under extra electric field Device, it is the device for being aided with other relevant layers or material and constituting based on electrochromic material.Electrochromic device Can be divided into 3 classes according to structure.One class is solution type electrochromic device;Wherein, electrochromic material is dissolved in electrolysis all the time In liquid, electrochromic material is typically organic molecule.Equations of The Second Kind is half solution-type electrochromic device;Device in coloured state and Along with the transmission and the change of materials chemistry property of electronics during being changed between clear state.When device is in pellucidity, Electrochromic material is dissolved in electrolyte;When device is in colored state, electrochromic material can be in electrode surface enrichment simultaneously It is covered in electrode surface and forms thin film.Usual this kind of electrochromic material is aromatics viologen compound, contains methoxyl group Compound of fluorene class etc..3rd class is full-solid electrochromic device;During the entire process of device discoloration, electrochromic material begins Solid state is in eventually.Usual this kind of electrochromic material is metal oxide, purpurine Prussian blue, containing organic acid group And conducting polymer etc..Wherein, solution type electrochromic device has simple structure, preparation technology simplicity and response time short The features such as, so the always focus of electrochromic device research.
The mode of operation of electrochromic device has transmission mode and reflective-mode.The main application fields of transmission mode are electrochromism Smart window.The smart window that spectral characteristic according to electrochromic material makes is selectively passed through and absorbed by solar radiation, Can efficiently control by the spectrum and energy of window, reach the purpose for making soft indoor light, amenity and reducing energy consumption; The main application fields of reflective-mode are automobile automatic dazzling-proof mesh rearview mirror.Automobile automatic dazzling-proof mesh rearview mirror is running into the feelings of dazzle Under condition, automobile rearview mirror can be reduced to partial reflectance mode from the emission mode that is all-trans automatically, so that the security of driver is improved, Current automatic dazzling-proof mesh rearview mirror has become the standard fitting of numerous famous automakers.
The construction of early stage solution type electrochromic rearview mirror as shown in figure 1, transparency conducting layer 2 is placed on the rear surface of preceding substrate 1, And another transparency conducting layer 4 is placed on the preceding surface of rear substrate 5.8) reflector (6,7 and generally comprises protection copper metal layer The silver metal layer 6 of 7 coverings, and one or more layers protective paint 8, they are arranged on the rear surface of rear substrate 5.Using adhesive 3 separate keeping parallelism and space between preceding substrate and rear substrate, and so as to set up cavity, electrochromic solutions 9 are included in cavity It is interior.Electrochromic solutions 9 and the directly contact of transparency conducting layer 2 and 4.Transparency conducting layer is connected with extraneous driving power supply, with Just current potential can be applied across electrochromic solutions.But in order to simplify preparation technology and reduce the reflection between different interfaces and thus (refer to specially on the ghost image for causing, the preceding surface that the reflecting layer of electrochromic rearview gradually goes to rear substrate from the rear surface of rear substrate Sharp US700975, US7417781, CN104496888).And, by changing the reflectivity in reflecting layer so that electrochromism Rearview mirror possesses the performance of fractional transmission, such that it is able to install the display with information display function on rear side of electrochromic rearview Device.
Automatic color-changing rearview mirror is widely used in various environment, including:The temperature of scope from about -40 DEG C to about 85 DEG C, Yi Jicong The humidity of about 0% to about 100% scope, further, it is necessary to undergo under these temperature and humidities up to 100000 times colour fading Circulation.Used as the part in solution type electrochromic device, it plays the conductive layer, anti-separated in front and rear substrate to adhesive The only effect such as electrochromic solutions leakage, the influence of blocking oxygen, vapor and other dangerous vapors to electrochromism liquid.Therefore, The quality of the sealing effectiveness of adhesive plays the effect of key to the service life of electrochromic device, security and performance etc..Mesh Before, the method for comparing the sealing effectiveness of extreme detection adhesive is, at 121 DEG C, to be surveyed under the saturation high-pressure steam of 14~16psi Examination 168 hours, whether detection electrochromic device is intact after having tested.
In Organic adhesive, epoxy resin adhesive occupies topmost status.US6714334 is disclosed by asphalt mixtures modified by epoxy resin Fat (including bisphenol A epoxide resin, bisphenol F epoxy resin and novolac epoxy resin) and curing agent (including double (aminocyclohexyls Base) methane, aliphatic cyclic amine and double (alicyclic ring) amine) composition for electrochromic device sealing adhesive.But epoxy resin Hydrothermal stability it is poor, particularly under the high temperature conditions easily by electrochromic material erosion make adhesive property fail lead Cause electrolyte leakage, the requirement therefore, it is difficult to meet the long-term use under severe rugged environment.
Additionally, in automatic color-changing rearview mirror, reflecting layer be usually white gold, silver or silver and other metals (such as gold, chromium, Ruthenium, platinum, rhodium and palladium) formed alloy.But, in actual applications, there is adhesive and above-mentioned metal adhesion difference asked Topic.It is probably that the above-mentioned metal or alloy of reason is difficult to form stronger chemical bond with adhesive.
The content of the invention
For the above-mentioned state of the art, the present invention provides a kind of solution type electrochromic rearview mirror of good sealing effect.
In order to realize the purpose of the present invention, there is provided a kind of solution type electrochromic rearview mirror, its composition includes:
Preceding substrate, the preceding substrate has two relative and parallel surfaces;
Substrate afterwards, the rear substrate has two relative and parallel surfaces;
With the relation for separating parallel to each other be bonded together for described preceding substrate and rear substrate by adhesive, the adhesive, and described Cavity is formed between the rear surface of preceding substrate and the preceding surface of rear substrate;
Electrochromic solutions, the electrochromic solutions are located at by the rear surface of described preceding substrate, the preceding surface of rear substrate and gluing dosage form Into cavity in;
Transparency conducting layer, the transparency conducting layer is covered in the rear surface and the preceding surface of rear substrate of described preceding substrate;And reflecting layer, should Reflecting layer is covered on the transparency conducting layer in described rear substrate, and the region of reflecting layer covering is less than transparency conducting layer covering Region, is not covered on the transparency conducting layer contacted with adhesive especially.
The substrate can be by it is any be enough to make the solution type electrochromic rearview mirror use in exposed environment it is strong Degree and the material manufacture that predetermined shape can be processed into, wherein, preceding substrate need to possess transparent nature, can be selected from visible-range Interior transparent glass or high-molecular organic material (for example polymethyl methacrylate, polyester, polyvinyl chloride, Vingon, Polypropylene, polyethylene, makrolon etc.).Preceding substrate is preferably glass.Substrate must also is fulfilled for above-mentioned condition of work afterwards, no With it need not be transparent in all applications.A greater variety of high-molecular organic materials, glass thus can be included Glass, ceramics etc., and preferably glass.
The adhesive is selected from cyanate adhesive.Cyanate typically refers to contain 2 or more than 2 phenol of-OCN functional groups Analog derivative, under heating or catalyst action, can form tripolymer, and then form cross-linked network structure.The catalyst for using Including transition metal carboxylate, acetylacetone metallic compound and lewis acid etc..In order to increase above-mentioned catalyst dissolubility and Accelerate solidification, it is also possible to add alkylphenol as co-catalyst.Cyanate adhesive has excellent resistance to elevated temperatures (work Temperature is up to 230 DEG C or more), low hydroscopicity (hydroscopicity be less than 1.5%), toughness (elongation at break is 3-4%) higher, Shrinkage factor is small, adhesion strength temperature influence is small and is easy to and metal when low-k is with dielectric loss, easy processing, solidification Oxide forms coordinate bond, therefore it can meet requirement of the device used under severe rugged environment to adhesive.
Cyanate is typically to react generation in the presence of tertiary amine with cyaniding halogen with dihydric phenol or polyhydric phenols, therefore uses different binary Phenol or polyhydric phenols, can synthesize the cyanate of different structure, such as tetramethyl bisphenol-f type cyanate, bisphenol A cyanate ester, Novolac Cyanate Eater Resin, bisphenol E-type cyanate, dicyclopentadiene type ethylene rhodanate, resorcinol cyanate.Cyanate also usually leads to Cross mode of heating and be partly polymerized to form the polymer of low-molecular-weight and use, because the polymer of low-molecular-weight can be in broad range Interior regulation viscosity and cure shrinkage is smaller, thus use as adhesive more convenient more preferable with effect.It must be noted that The polymer and their mixture of cyanate, the low-molecular-weight formed by cyanate, all can rising as cyanate adhesive Beginning raw material is used.
The electrochromic solutions comprise at least anode electroactive material, cathodic electroactive materials and solvent.Wherein, with patent CN102165032A is consistent, and this paper terms " electroactive " are defined as when under specific electrical potential difference, experiencing its oxidation The change of state.Cathodic electroactive materials are reduced under electric field action by receiving electronics from negative electrode;Anode electroactive material is in electricity It is oxidized by supplying electronics to anode under field action.Cathodic electroactive materials and anode electroactive material are used cooperatively and can played The effect of balancing charge.Wherein, at least one in the anode electroactive material and cathodic electroactive materials is electrochromism material Material, that is, possess electrochromic property.
The anode electroactive material that the suitable present invention is used can be selected from multiple material, including triphenylamine, triphenylamine, two of substitution Luxuriant iron, substitution ferrocene, ferrocene salt, substitution ferrocene salt, phenthazine, substitution phenthazine, thianthrene, substitution Thianthrene, azophenlyene and substituted azophenlyene.
The cathodic electroactive materials that the suitable present invention is used can be selected from multiple material, including purpurine, substitution purpurine, green onion quinone and Substituted anthraquinone.
In electrochromic solutions, can also add other functional materials, such as UV light stabilizing agent, heat stabilizer, antioxidant, Thickener, viscosity modifier and redox-stable agent.
Transparency conducting layer on the rear surface of the preceding substrate and the preceding surface of rear substrate is selected from tin oxide, zinc oxide, tin oxide One or more in indium, indium gallium zinc complexes, fluorine doped tin oxide, Al-Doped ZnO and fluorine doped zinc oxide.
Reflecting layer in the rear substrate is selected from the alloy that white gold, silver or silver are formed with gold, chromium, ruthenium, platinum, rhodium, lawrencium or palladium.
The reflectivity in reflecting layer can be regulated and controled by controlling the thickness in reflecting layer, so as to obtain the solution-type electricity with certain transmissivity Cause electrochromic rearview.Active display is placed at the rear portion of the solution type electrochromic rearview mirror with certain transmissivity, can Relevant information is understood with convenient use person or driver in real time.Wherein, selectable active display includes GPS device, navigation Equipment, compass, time marker, temperature indicator, humidity indicator, convergence warning device, lane departur warning device, Rear-view mirror device, signal for turn indicator lamp, tire pressure display and illuminating lamp etc..
In order that solution type electrochromic rearview mirror is provided simultaneously with transmission and reflection function, the transmissivity in reflecting layer between 10% to 60%, more preferably between 20% to 50%.
Compared with prior art, beneficial effects of the present invention are:
By encapsulant is used as using adhesion strength is high, wet and heat ageing resistant is good cyanate adhesive and avoid adhesive with The metallic reflector directly contact of bond effect difference realizes the lifting of the sealing effectiveness to solution type electrochromic rearview mirror, so that Improve the stability and service life of solution electrochromic rearview.
Brief description of the drawings
Fig. 1 is the profile of early stage solution type electrochromic rearview mirror;
Fig. 2 is the profile of solution type electrochromic rearview mirror in the present invention, wherein, 21 is preceding substrate, and 26 is rear substrate, 22 Hes 25 is transparency conducting layer, and 23 is adhesive, and 24 is reflecting layer and 27 is electrochromic solutions.
Fig. 3 is the profile of the solution type electrochromic rearview mirror in comparative example 4, wherein, 31 is preceding substrate, and 36 is rear substrate, 32 and 35 is transparency conducting layer, and 33 is adhesive, and 34 is reflecting layer and 37 is electrochromic solutions.
Specific embodiment
The present invention is described in further detail below in conjunction with specific embodiment, it is necessary to be pointed out that the present embodiment is served only for this Invention is further detailed, it is impossible to be interpreted as limiting the scope of the invention.
Embodiment 1:
By 1,1 '-dioctyl -4,4'-Bipyridine double (tetrafluoroborate) and 5,10- dihydro -5,10- dimethylphenazines are all according to 30 The concentration of mmol/L is dissolved in butyrolactone, is made into electrochromic solutions, is poured into electrochromic device as shown in Figure 2. Wherein, adhesive is the polymer that the mean molecule quantity that bisphenol A cyanate ester is formed in a heated condition is 1500 or so, Gu To be heating and curing, solidification temperature is 170 DEG C to change mode.The solution type electrochromic rearview mirror is placed in 121 DEG C, 14~18psi Saturation high-pressure steam under.After 168 hours, its still intact and electrochromic solutions is without leakage.Circulation experiment is done in energization, electricity The change color depth of electrochromic solution is caused not changed with color change.
Comparative example 1:
By 1,1 '-dioctyl -4,4'-Bipyridine double (tetrafluoroborate) and 5,10- dihydro -5,10- dimethylphenazines are all according to 30 The concentration of mmol/L is dissolved in butyrolactone, is made into electrochromic solutions, is poured into electrochromic device as shown in Figure 2, Wherein, adhesive is N, N, glycidyl -4 of N ', N '-four, and 4 '-MDA, curing agent is diaminodiphenyl-methane. The solution type electrochromic rearview mirror is placed in 121 DEG C, is tested under the saturation high-pressure steam of 14~18psi.Observed after 6 hours, Ftractureed at adhesive sealing.
Embodiment 2:
By 1,1 '-dihexyl -4,4'-Bipyridine double (fluoroform sulphonate) with 4,4 ', 4 "-trimethyl triphenylamine is all according to 50mmol/L Concentration be dissolved in acetonitrile, be made into electrochromic solutions, be poured into electrochromic device as shown in Figure 2, wherein, glue Glutinous agent is the polymer that the mean molecule quantity that dicyclopentadiene type ethylene rhodanate is formed in a heated condition is 1700 or so, using hexamethylene Alkane copper butyrate (II) salt and nonyl phenol catalytic curing.The solution type electrochromic rearview mirror is placed in 121 DEG C, 14~18psi's is full Under high-pressure steam.After 168 hours, the solution type electrochromic rearview mirror is intact and electrochromic solutions are without leakage.It is powered Circulation experiment is done, change color depth and the color change of electrochromic solutions do not change.
Comparative example 2:
By 1,1 '-dihexyl -4,4'-Bipyridine double (fluoroform sulphonate) with 4,4 ', 4 "-trimethyl triphenylamine is all according to 50mmol/L Concentration be dissolved in acetonitrile, be made into electrochromic solutions, be poured into electrochromic device as shown in Figure 2, wherein, glue Glutinous agent is bisphenol F epoxy resin, and curing agent is bis(p-aminocyclohexyl)methane.The solution type electrochromic rearview mirror is placed in 121 DEG C, under the saturation high-pressure steam of 14~18psi.Observed after 2 hours, ftractureed at adhesive sealing.
Embodiment 3:
By 1,1 '-di neo-pentyl -4,4'-Bipyridine double (hexafluoro borate) and 5,10- diisopropyl -5,10- dimethylphenazines all according to The concentration of 20mmol/L is dissolved in propene carbonate, is made into electrochromic solutions, is poured into electrochromism as shown in Figure 2 In device, wherein, adhesive is the polymerization that the mean molecule quantity that resorcinol cyanate is formed in a heated condition is 1400 or so Thing, using ferric acetyl acetonade and nonyl phenol catalytic curing.The solution type electrochromic rearview mirror is placed in 121 DEG C, 14~18psi Saturation high-pressure steam under.After 168 hours, the solution type electrochromic rearview mirror is intact and electrochromic solutions are without leakage. Circulation experiment is done in energization, and change color depth and the color change of electrochromic solutions do not change.
Comparative example 3:
By 1,1 '-di neo-pentyl -4,4'-Bipyridine double (hexafluoro borate) and 5,10- diisopropyl -5,10- dimethylphenazines all according to The concentration of 20mmol/L is dissolved in propene carbonate, is made into electrochromic solutions, is poured into electrochromism as shown in Figure 2 In device, wherein, adhesive be by PPG, methyl diphenylene diisocyanate and hydroxypropyl acrylate be Material synthesis Urethane acrylate, using ultraviolet light polymerization, light trigger is benzoin ethyl ether.By the solution type electrochromic rearview mirror It is placed in 121 DEG C, under the saturation high-pressure steam of 14~18psi.Observed after 2 hours, ftractureed at adhesive sealing.
Comparative example 4:
By 1,1 '-di neo-pentyl -4,4'-Bipyridine double (hexafluoro borate) and 5,10- diisopropyl -5,10- dimethylphenazines all according to The concentration of 20mmol/L is dissolved in propene carbonate, is made into electrochromic solutions, is poured into electrochromism as shown in Figure 3 In device, wherein, adhesive is the polymerization that the mean molecule quantity that resorcinol cyanate is formed in a heated condition is 1400 or so Thing, using ferric acetyl acetonade and nonyl phenol catalytic curing.The solution type electrochromic rearview mirror is placed in 121 DEG C, 14~18psi Saturation high-pressure steam under.After 168 hours, the solution type electrochromic rearview mirror is intact and electrochromic solutions are without leakage. Circulation experiment is done in energization, and change color depth and the color change of electrochromic solutions do not change.
From above-described embodiment as can be seen that by use cyanate adhesive be used as encapsulant and cyanate adhesive with it is transparent The bonding sealing effectiveness to solution type electrochromic rearview mirror of conductive layer improves significantly, so as to significantly improve solution The stability and service life of property electrochromic rearview.

Claims (10)

1. a kind of solution type electrochromic rearview mirror, it is characterised in that it includes:
Preceding substrate, the preceding substrate has two relative and parallel preceding surfaces and rear surface;
Substrate afterwards, the rear substrate has two relative and parallel preceding surfaces and rear surface;
With the relation for separating parallel to each other be bonded together for described preceding substrate and rear substrate by adhesive, the adhesive, and Cavity is formed between the rear surface of described preceding substrate and the preceding surface of rear substrate, the adhesive is cyanate adhesive;
Electrochromic solutions, the electrochromic solutions be located at by the rear surface of described preceding substrate, the preceding surface of rear substrate and In the cavity that adhesive is formed;
Transparency conducting layer, the transparency conducting layer is covered in the rear surface and the preceding surface of described rear substrate of described preceding substrate;
With
Reflecting layer, the reflecting layer is covered on the transparency conducting layer in substrate in the rear, but does not include transparency conducting layer and glue The part of glutinous agent contact.
2. solution type electrochromic rearview mirror according to claim 1, first substrate and the second substrate are separately Selected from glass or high-molecular organic material.
3. solution type electrochromic rearview mirror according to claim 1, the cyanate adhesive is solidified using mode of heating Or solidify under transition metal carboxylate, acetylacetone metallic compound or Louis acid catalysis.
4. solution type electrochromic rearview mirror according to claim 1, the electrochromic solutions at least include that anode electricity is living Property material, cathodic electroactive materials and solvent, and the one kind at least in anode electroactive material and cathodic electroactive materials Possesses electrochromism property.
5. solution type electrochromic rearview mirror according to claim 1, the transparency conducting layer be selected from tin oxide, zinc oxide, One kind or many in indium tin oxide target, indium gallium zinc complexes, fluorine doped tin oxide, Al-Doped ZnO and fluorine doped zinc oxide Kind.
6. solution type electrochromic rearview mirror according to claim 1, the reflecting layer be selected from silver, platinum or silver and gold, The alloy that chromium, ruthenium, platinum, rhodium, lawrencium or palladium are formed.
7. electrochromic solutions according to claim 4, the anode electroactive material is selected from triphenylamine, the triphen of substitution Amine, ferrocene, substitution ferrocene, ferrocene salt, substitution ferrocene salt, phenthazine, substitution phenthazine, One or more in thianthrene, the thianthrene of substitution, azophenlyene and substituted azophenlyene.
8. electrochromic solutions according to claim 4, the cathodic electroactive materials be selected from purpurine, the purpurine of substitution, One or more in green onion quinone and the anthraquinone of substitution.
9. a kind of vehicle rearview mirror assembly, it is characterised in that it includes:
Solution type electrochromic rearview mirror as claimed in claim 1;
Active display, the active display is placed in the rear surface of the rear substrate of described solution type electrochromic rearview mirror;With It is coupled to the control circuit of the solution type electrochromic rearview mirror and active display.
10. a kind of vehicle rearview mirror assembly according to claim 8, the active display includes that GPS device, navigation set Standby, compass, time marker, temperature indicator, humidity indicator, convergence warning device, lane departur warning One or more in device, rear-view mirror device, signal for turn indicator lamp, tire pressure display and illuminating lamp.
CN201511022989.7A 2015-12-29 2015-12-29 The electrochromism air locking that a kind of high pressure resistant water vapour corrodes Pending CN106926781A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111500247A (en) * 2019-01-30 2020-08-07 宁波祢若电子科技有限公司 Adhesive and application thereof in electrochromic field
CN112394583A (en) * 2020-09-07 2021-02-23 深圳市光羿科技有限公司 Electrochromic device and preparation method thereof
CN113715436A (en) * 2021-08-18 2021-11-30 东风柳州汽车有限公司 A interactive composite board of environment, sunroof and car for car
WO2022048122A1 (en) * 2020-09-01 2022-03-10 深圳市光羿科技有限公司 Electrochromic device and manufacturing methods therefor

Citations (3)

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Publication number Priority date Publication date Assignee Title
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Application publication date: 20170707