CN105655416A - Electrode slurry for silicon solar cell - Google Patents
Electrode slurry for silicon solar cell Download PDFInfo
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- CN105655416A CN105655416A CN201610163798.0A CN201610163798A CN105655416A CN 105655416 A CN105655416 A CN 105655416A CN 201610163798 A CN201610163798 A CN 201610163798A CN 105655416 A CN105655416 A CN 105655416A
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- 239000011267 electrode slurry Substances 0.000 title claims abstract description 47
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims abstract description 26
- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 26
- 239000010703 silicon Substances 0.000 title claims abstract description 26
- 239000000843 powder Substances 0.000 claims abstract description 70
- 239000002041 carbon nanotube Substances 0.000 claims abstract description 59
- 229910021393 carbon nanotube Inorganic materials 0.000 claims abstract description 59
- 239000011521 glass Substances 0.000 claims abstract description 42
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 39
- GELKBWJHTRAYNV-UHFFFAOYSA-K lithium iron phosphate Chemical compound [Li+].[Fe+2].[O-]P([O-])([O-])=O GELKBWJHTRAYNV-UHFFFAOYSA-K 0.000 claims abstract description 35
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 32
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000000034 method Methods 0.000 claims abstract description 15
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 14
- 239000002002 slurry Substances 0.000 claims description 41
- 239000000463 material Substances 0.000 claims description 35
- -1 carbon nano tube compound Chemical class 0.000 claims description 31
- 229910045601 alloy Inorganic materials 0.000 claims description 21
- 239000000956 alloy Substances 0.000 claims description 21
- MOFOBJHOKRNACT-UHFFFAOYSA-N nickel silver Chemical compound [Ni].[Ag] MOFOBJHOKRNACT-UHFFFAOYSA-N 0.000 claims description 19
- 239000006185 dispersion Substances 0.000 claims description 16
- 239000007788 liquid Substances 0.000 claims description 16
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 claims description 14
- 229920000742 Cotton Polymers 0.000 claims description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 14
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Inorganic materials [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 claims description 12
- 229910052681 coesite Inorganic materials 0.000 claims description 12
- 229910052906 cristobalite Inorganic materials 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 12
- 239000000377 silicon dioxide Substances 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052682 stishovite Inorganic materials 0.000 claims description 12
- 229910052905 tridymite Inorganic materials 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 239000011159 matrix material Substances 0.000 claims description 9
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 7
- 229930006000 Sucrose Natural products 0.000 claims description 7
- 238000000889 atomisation Methods 0.000 claims description 7
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(III) oxide Inorganic materials O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 claims description 7
- 238000000227 grinding Methods 0.000 claims description 7
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical class [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 claims description 7
- 239000012046 mixed solvent Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 239000005720 sucrose Substances 0.000 claims description 7
- 238000001291 vacuum drying Methods 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 229910052725 zinc Inorganic materials 0.000 claims description 7
- 239000011701 zinc Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000007772 electrode material Substances 0.000 abstract description 3
- 238000005516 engineering process Methods 0.000 abstract description 2
- NTKBNCABAMQDIG-UHFFFAOYSA-N 3-butoxypropan-1-ol Chemical compound CCCCOCCCO NTKBNCABAMQDIG-UHFFFAOYSA-N 0.000 abstract 1
- 239000001293 FEMA 3089 Substances 0.000 abstract 1
- 229910000990 Ni alloy Inorganic materials 0.000 abstract 1
- 239000000020 Nitrocellulose Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 239000002131 composite material Substances 0.000 abstract 1
- 229920001220 nitrocellulos Polymers 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 description 27
- 230000000694 effects Effects 0.000 description 5
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910000676 Si alloy Inorganic materials 0.000 description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 206010013786 Dry skin Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229910021419 crystalline silicon Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022408—Electrodes for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/022425—Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/02—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/04—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of carbon-silicon compounds, carbon or silicon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Abstract
The invention belongs to photovoltaic-cell electrode materials, and discloses an electrode slurry for a silicon solar cell. The electrode slurry comprises, by weight, 40-60 parts of silver powder, 5-10 parts of zinc powder, 10-20 parts of silver coated nickel alloy powder, 1-5 parts of a lithium iron phosphate and carbon nanotube composite material, 1-8 parts of glass powder, 0.5-2 parts of silane coupling agent, 8-10 parts of propylene glycol mono-n-butyl ether, 1-5 parts of turpentine oil, 1-3 parts of zinc naphthenate, 0.1-0.5 part of nitrocellulose and 0.25-1 part of organobentonite. The invention further discloses a preparing method of the electrode slurry. The obtained electrode slurry is free of lead, completely meets the environment-friendly requirement, and is applied to production of a solar cell, and high adhesive force and photoelectric conversion efficiency can be formed on the surface of the solar cell; meanwhile, the electrode slurry is simple in technology and low in cost, and therefore has the broad application prospect.
Description
Technical field
The present invention relates to photocell electrode materials, particularly relate to a kind of silicon solar cell electrode slurry.
Background technology
Light energy conversion can be directly electric energy by solar cell, is a kind of mode that can effectively utilize sun power, is also important renewable and clean energy resource. Nearly ten years, in the photovoltaic industry of fast development, high-level efficiency and low cost are two main competition spots always, and crystalline silicon is as current topmost solar cell material, and the efficient stable by means of its battery occupies most of share in light volt market always.
Silicon solar cell is the device directly light energy conversion being become electric energy by photovoltaic effect or Photochemical effects. When sunlight is on crystal silicon semiconductor p-n junction, form new hole-electronics pair, under the effect of p-n junction electric field, hole flows to p district by n district, electronics flows to n district by p district, just forms electric current after connecting circuit, and this is exactly the principle of work of photovoltaic effect solar cell. Silicon solar cell electrode slurry makes the important base mateiral of photovoltaic solar cells.
CN101651155A discloses composition and the preparation method of a kind of silicon solar cell electrode slurry, the Al-back-surface-field (BSF) paste of the silicon solar cell of the ohmic contact that this patent formulation is formed with a kind of silicon-containing alloy powder, its composition is aluminium powder 40-70 quality %, simple substance element indium powder 0.01-5 quality %, organic bond 20-30 quality %, inorganic binder 0.1-15 quality %, silicon alloy powder 0.1-40 quality %, total amount is 100 quality %. Adopt this slurry can increase alloy layer thickness, improve ohmic contact, but in this slurry, it is only simple mechanically mixing between silicon alloy powder and functional conductive powder (i.e. aluminium powder), the melt temperature of aluminium powder can't be reduced during sintering, also may introduce impurity element in back surface field, reduce the transformation efficiency of battery. In addition, this slurry adopts rare metal indium powder so that the cost of slurry increases greatly.
Summary of the invention
The goal of the invention of the present invention is: for above-mentioned Problems existing, it is provided that a kind of silicon solar cell electrode slurry. The electrode slurry of the present invention has in the excellent feature of solar cell surface strong adhesion, cell photoelectric efficiency of conversion and conductive capability; The electrode slurry of the present invention has in the excellent feature of solar cell surface strong adhesion, cell photoelectric efficiency of conversion and conductive capability; Technique of the present invention is simple, and cost is low, has broad application prospects.
The technical solution used in the present invention is as follows:
A kind of silicon solar cell electrode slurry, according to weight parts, described slurry feedstock consists of: 40 ~ 60 parts, silver powder, zinc powder 5 ~ 10 parts, silver nickel coat alloy powder 10 ~ 20 parts, iron lithium phosphate/carbon nano tube compound material 1 ~ 5 part, 1 ~ 8 part, glass powder, silane coupling agent 0.5 ~ 2 part, propylene glycol monobutyl ether 8-10 part, turps 1-5 part, the pungent 1-3 part of alkanoic acid, soluble cotton 0.1-0.5 part, organobentonite 0.25-1 part.
Further, described silver powder is length is 3 ~ 7 ��m, and diameter is the nano silver wire of 50 ~ 100nm; Described zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m.
Further, described silver nickel coat alloy powder is diameter is the spheroidal particle of 5 ~ 8 ��m.
Further, the preparation method of described iron lithium phosphate/carbon nano tube compound material is:
(1) by 5 ~ 10 parts of carbon nanotube ultrasonic disperse in the volume ratio of 400 ~ 500 parts of ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, add 20 ~ 25 parts of Quilonum Retards, 5 ~ 10 parts of iron nitrates, 5 ~ 10 parts of monometallics and 10 ~ 15 portions of sucrose more respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 10 ~ 20min after room temperature, move into and vacuum drying oven is placed 15 ~ 20h, then vacuumize and it is heated to 50 ~ 70 DEG C, until the solvent volatilization in slurries is completely;
(3) matrix material 300 ~ 400 DEG C of pre-burning 5 ~ 7h in retort furnace that will process through step (2), then at 700 ~ 800 DEG C roasting 5 ~ 7h, obtain described iron lithium phosphate/carbon nano tube compound material.
Further, the component of described glass powder is SiO215 ~ 30 parts, Bi2O310 ~ 20 parts, B2O310 ~ 20 parts, BaO/BaCO35 ~ 10 parts, ��-AL2O315 ~ 25 parts, ZnO5 ~ 10 part.
Further, the glass powder I and glass powder II of described glass powder to be mass ratio be 1:1, the particle diameter of glass powder I is 5 ~ 15 ��m, and the particle diameter of glass powder II is 1 ~ 5 ��m.
Further, described silane coupling agent is KH550, KH560 or KH602.
Further, present invention also offers the preparation method of described silicon solar cell electrode slurry, described preparation method is: is first dissolved in propylene glycol monobutyl ether by pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite, obtains sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
In sum, owing to have employed technique scheme, the invention has the beneficial effects as follows:
(1) the present invention has selected the silver powder of different-grain diameter and zinc powder and silver nickel coat alloy powder simultaneously, increases interparticle contact area, thus improves the conductive capability of slurry; Compared with prior art, adopt existing stable preparation process and the cost nano silver wire more cheap relative to nano-Ag particles due to silver powder major part, effectively reduce the material cost of electrode slurry;And silver powder gap can be filled mutually due to nano silver wire and micron zinc powder and silver nickel coat alloy powder, thus add conductive path to form conductive network, the volume specific resistance that electrode slurry burns till electrode materials can be reduced further;
(2) the present invention with the addition of zinc powder and silver nickel coat alloy powder in electrode slurry, can contribute to reducing slurry production cost, save a large amount of noble silvers, improve the conductivity of slurry simultaneously, thus reach the object reducing solar cell manufacturing cost, achieve good economic benefit;
(3) the present invention with the addition of iron lithium phosphate/carbon nano tube compound material in electrode slurry, the contact between particle and particle is improved by carbon nanotube, form the conductive network that volume specific resistance is very little, enhance conductive network, thus improve the conductive capability of slurry, present invention also offers the preparation method of iron lithium phosphate/carbon nano tube compound material, carbon nanotube (carbon nano tube dispersion liquid) is just introduced in the stage (preparations of slurries) preparing presoma, and then presintering, roasting obtains iron lithium phosphate/carbon nano tube compound material, the carbon nanotube introduced like this can be scattered between a particle of iron lithium phosphate, easily between a particle, form conductive network, improve the electroconductibility of material greatly, and be not in ready-made iron lithium phosphate slurries, add carbon nano tube dispersion liquid as prior art, the carbon nanotube introduced like this can only be scattered between the second particle of iron lithium phosphate, electroconductibility is limited. therefore, the present invention prepares the matrix material and has good electroconductibility, add electrode slurry prepared by this matrix material and there is good chemical property,
(4) the present invention with the addition of silane coupling agent in electrode slurry, silane coupling agent has the avidity effect strengthened between organism and mineral compound, the physical and chemical performance improving electrode slurry can be strengthened, improve the bonding Combination between functional conductive powder, thus improve the sticking power of slurry in solar cell surface;
(5) electrode slurry of gained of the present invention is not containing plumbous, meets environmental requirement completely, is applied to the production of solar cell, strong adhesion, cell photoelectric efficiency of conversion height can be formed in solar cell surface, technique of the present invention is simple simultaneously, and cost is low, thus has broad application prospects.
Embodiment
All features disclosed in this specification sheets, or the step in disclosed all methods or process, except mutually exclusive feature and/or step, all can combine by any way.
Any feature disclosed in this specification sheets (comprise any appended claims require, summary), unless specifically stated otherwise, all can be replaced by other equivalences or the alternative features with similar object. Unless specifically stated otherwise, that is, each feature is an example in a series of equivalence or similar characteristics.
Embodiment 1
First prepare iron lithium phosphate/carbon nano tube compound material:
(1) by 8g carbon nanotube ultrasonic disperse in the volume ratio of 450g ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, 20g Quilonum Retard, 10g iron nitrate, 8g monometallic and 15g sucrose is added again respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 15min after room temperature, move in vacuum drying oven and place 15h, then vacuumize and it is heated to 60 DEG C, until the solvent volatilization in slurries is completely;
(3) the matrix material 350 DEG C of pre-burning 6h in retort furnace that will process through step (2), then at 750 DEG C roasting 6h, obtain described iron lithium phosphate/carbon nano tube compound material.
Formulate glass powder and organic carrier again, wherein the component of glass powder I is 5 ~ 15 ��m of SiO220g, 5 ~ 15 ��m of Bi2O315g, 5 ~ 15 ��m of B2O315g, 5 ~ 15 ��m of BaO/BaCO38g, 5 ~ 15 ��m of ��-AL2O320g, 5 ~ 15 ��m of ZnO8g; Wherein the component of glass powder II is 1 ~ 5 ��m of SiO220g��1~5��mBi2O315g, 1 ~ 5 ��m of B2O315g, 1 ~ 5 ��m of BaO/BaCO38g, 1 ~ 5 ��m of ��-AL2O320g, 1 ~ 5 ��m of ZnO8g;
Prepare the silicon solar cell electrode slurry of the present invention again, first take silver powder 50g respectively, zinc powder 8g, silver nickel coat alloy powder 15g, iron lithium phosphate/carbon nano tube compound material 3g, above-mentioned the glass powder 7g prepared, KH5501g, propylene glycol monobutyl ether 8g, turps 4g, the pungent 2g of alkanoic acid, soluble cotton 0.25g, organobentonite 0.5g; Wherein silver powder is diameter is the nanometer ball of 50 ~ 80nm, zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m; Then pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite are dissolved in propylene glycol monobutyl ether, obtain sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
Embodiment 2
First prepare iron lithium phosphate/carbon nano tube compound material:
(1) by 5g carbon nanotube ultrasonic disperse in the volume ratio of 400g ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, 25g Quilonum Retard, 5g iron nitrate, 5g monometallic and 10g sucrose is added again respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 10min after room temperature, move in vacuum drying oven and place 20h, then vacuumize and it is heated to 50 DEG C, until the solvent volatilization in slurries is completely;
(3) the matrix material 300 DEG C of pre-burning 7h in retort furnace that will process through step (2), then at 700 DEG C roasting 5h, obtain described iron lithium phosphate/carbon nano tube compound material.
Formulate glass powder and organic carrier again, wherein the component of glass powder I is 5 ~ 15 ��m of SiO215g, 5 ~ 15 ��m of Bi2O320g, 5 ~ 15 ��m of B2O310g, 5 ~ 15 ��m of BaO/BaCO35g, 5 ~ 15 ��m of ��-AL2O315g, 5 ~ 15 ��m of ZnO5g; Wherein the component of glass powder II is 1 ~ 5 ��m of SiO210g��1~5��mBi2O320g, 1 ~ 5 ��m of B2O310g, 1 ~ 5 ��m of BaO/BaCO35g, 1 ~ 5 ��m of ��-AL2O315g, 1 ~ 5 ��m of ZnO5g;
Prepare the silicon solar cell electrode slurry of the present invention again, first take silver powder 50g respectively, zinc powder 8g, silver nickel coat alloy powder 15g, iron lithium phosphate/carbon nano tube compound material 3g, above-mentioned the glass powder 7g prepared, KH5501g, propylene glycol monobutyl ether 10g, turps 1g, the pungent 1g of alkanoic acid, soluble cotton 0.5g, organobentonite 0.25g; Wherein silver powder is diameter is the nanometer ball of 50 ~ 80nm, zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m; Then pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite are dissolved in propylene glycol monobutyl ether, obtain sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
Embodiment 3
First prepare iron lithium phosphate/carbon nano tube compound material:
(1) by 10g carbon nanotube ultrasonic disperse in the volume ratio of 500g ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, 20g Quilonum Retard, 10g iron nitrate, 10g monometallic and 15g sucrose is added again respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 10min after room temperature, move in vacuum drying oven and place 20h, then vacuumize and it is heated to 50 DEG C, until the solvent volatilization in slurries is completely;
(3) the matrix material 300 DEG C of pre-burning 7h in retort furnace that will process through step (2), then at 700 DEG C roasting 5h, obtain described iron lithium phosphate/carbon nano tube compound material.
Formulate glass powder and organic carrier again, wherein the component of glass powder I is 5 ~ 15 ��m of SiO230g, 5 ~ 15 ��m of Bi2O310g, 5 ~ 15 ��m of B2O320g, 5 ~ 15 ��m of BaO/BaCO310g, 5 ~ 15 ��m of ��-AL2O325g, 5 ~ 15 ��m of ZnO10g; Wherein the component of glass powder II is 1 ~ 5 ��m of SiO230g��1~5��mBi2O310g, 1 ~ 5 ��m of B2O320g, 1 ~ 5 ��m of BaO/BaCO310g, 1 ~ 5 ��m of ��-AL2O325g, 1 ~ 5 ��m of ZnO10g;
Prepare the silicon solar cell electrode slurry of the present invention again, first take silver powder 50g respectively, zinc powder 8g, silver nickel coat alloy powder 15g, iron lithium phosphate/carbon nano tube compound material 3g, above-mentioned the glass powder 7g prepared, KH5501g, propylene glycol monobutyl ether 9g, turps 5g, the pungent 3g of alkanoic acid, soluble cotton 0.5g, organobentonite 1g; Wherein silver powder is diameter is the nanometer ball of 50 ~ 80nm, zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m; Then pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite are dissolved in propylene glycol monobutyl ether, obtain sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
Embodiment 4
First prepare iron lithium phosphate/carbon nano tube compound material:
(1) by 8g carbon nanotube ultrasonic disperse in the volume ratio of 450g ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, 20g Quilonum Retard, 10g iron nitrate, 8g monometallic and 15g sucrose is added again respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 15min after room temperature, move in vacuum drying oven and place 15h, then vacuumize and it is heated to 60 DEG C, until the solvent volatilization in slurries is completely;
(3) the matrix material 350 DEG C of pre-burning 6h in retort furnace that will process through step (2), then at 750 DEG C roasting 6h, obtain described iron lithium phosphate/carbon nano tube compound material.
Formulate glass powder and organic carrier again, wherein the component of glass powder I is 5 ~ 15 ��m of SiO220g, 5 ~ 15 ��m of Bi2O315g, 5 ~ 15 ��m of B2O315g, 5 ~ 15 ��m of BaO/BaCO38g, 5 ~ 15 ��m of ��-AL2O320g, 5 ~ 15 ��m of ZnO8g; Wherein the component of glass powder II is 1 ~ 5 ��m of SiO220g��1~5��mBi2O315g, 1 ~ 5 ��m of B2O315g, 1 ~ 5 ��m of BaO/BaCO38g, 1 ~ 5 ��m of ��-AL2O320g, 1 ~ 5 ��m of ZnO8g;
Prepare the silicon solar cell electrode slurry of the present invention again, first take silver powder 40g respectively, zinc powder 10g, silver nickel coat alloy powder 20g, iron lithium phosphate/carbon nano tube compound material 1g, above-mentioned the glass powder 2g prepared, KH5601g, propylene glycol monobutyl ether 8g, turps 4g, the pungent 2g of alkanoic acid, soluble cotton 0.25g, organobentonite 0.5g; Wherein silver powder is length is 3 ~ 7 ��m, and diameter is the nano silver wire of 50 ~ 100nm, zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m;Then pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite are dissolved in propylene glycol monobutyl ether, obtain sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
Embodiment 5
First prepare iron lithium phosphate/carbon nano tube compound material:
(1) by 8g carbon nanotube ultrasonic disperse in the volume ratio of 450g ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, 20g Quilonum Retard, 10g iron nitrate, 8g monometallic and 15g sucrose is added again respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 15min after room temperature, move in vacuum drying oven and place 15h, then vacuumize and it is heated to 60 DEG C, until the solvent volatilization in slurries is completely;
(3) the matrix material 350 DEG C of pre-burning 6h in retort furnace that will process through step (2), then at 750 DEG C roasting 6h, obtain described iron lithium phosphate/carbon nano tube compound material.
Formulate glass powder and organic carrier again, wherein the component of glass powder I is 5 ~ 15 ��m of SiO220g, 5 ~ 15 ��m of Bi2O315g, 5 ~ 15 ��m of B2O315g, 5 ~ 15 ��m of BaO/BaCO38g, 5 ~ 15 ��m of ��-AL2O320g, 5 ~ 15 ��m of ZnO8g; Wherein the component of glass powder II is 1 ~ 5 ��m of SiO220g��1~5��mBi2O315g, 1 ~ 5 ��m of B2O315g, 1 ~ 5 ��m of BaO/BaCO38g, 1 ~ 5 ��m of ��-AL2O320g, 1 ~ 5 ��m of ZnO8g;
Prepare the silicon solar cell electrode slurry of the present invention again, first take silver powder 60g respectively, zinc powder 5g, silver nickel coat alloy powder 10g, iron lithium phosphate/carbon nano tube compound material 5g, above-mentioned the glass powder 8g prepared, KH6021g, propylene glycol monobutyl ether 8g, turps 4g, the pungent 2g of alkanoic acid, soluble cotton 0.25g, organobentonite 0.5g; Wherein silver powder is length is 3 ~ 7 ��m, and diameter is the nano silver wire of 50 ~ 100nm, zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m; Then pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite are dissolved in propylene glycol monobutyl ether, obtain sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
The electrode slurry embodiment of the present invention 1 ~ 5 prepared respectively adopts screen printer print on 125mm �� 125mmSi substrate, then 180 DEG C of dryings, quick fired electrodes lead-in wire is carried out again, the contact conductor made after high temperature sintering surface silvery white, smooth zero defect at 880 DEG C; Again the electrode slurry of embodiment and the performance of respective electrode are tested, refer to following table 1.
Table 1
As can be seen from Table 1, the electrode of solar battery that the solar battery electrode slurry of employing the present invention and preparation method obtain, the electrode of hinge structure all effectively reduces silverskin surface resistivity, further increases interface sticking power and photoelectric transformation efficiency.
To sum up, the solar battery electrode slurry that the embodiment of the present invention provides and preparation method, greatly reduce material cost, and battery performance have also been obtained and promotes to a certain extent simultaneously.
The present invention is not limited to aforesaid embodiment. The present invention expands to any new feature of disclosing in this manual or any combination newly, and the step of the arbitrary new method disclosed or process or any combination newly.
Claims (8)
1. a silicon solar cell electrode slurry, it is characterised in that, according to weight parts, described slurry feedstock consists of: 40 ~ 60 parts, silver powder, zinc powder 5 ~ 10 parts, silver nickel coat alloy powder 10 ~ 20 parts, iron lithium phosphate/carbon nano tube compound material 1 ~ 5 part, 1 ~ 8 part, glass powder, silane coupling agent 0.5 ~ 2 part, propylene glycol monobutyl ether 8-10 part, turps 1-5 part, the pungent 1-3 part of alkanoic acid, soluble cotton 0.1-0.5 part, organobentonite 0.25-1 part.
2. silicon solar cell electrode slurry according to claim 1, it is characterised in that, described silver powder is length is 3 ~ 7 ��m, and diameter is the nano silver wire of 50 ~ 100nm; Described zinc powder be active zinc content more than 98%, diameter is the spherical zinc powder of atomization of 1 ~ 3 ��m.
3. silicon solar cell electrode slurry according to claim 1, it is characterised in that, described silver nickel coat alloy powder is diameter is the spheroidal particle of 5 ~ 8 ��m.
4. silicon solar cell electrode slurry according to claim 1, it is characterised in that, the preparation method of described iron lithium phosphate/carbon nano tube compound material is:
(1) by 5 ~ 10 parts of carbon nanotube ultrasonic disperse in the volume ratio of 400 ~ 500 parts of ethanol and water be first 1:1 mixed solvent in, formed carbon nano tube dispersion liquid;
(2) in carbon nano tube dispersion liquid, add 20 ~ 25 parts of Quilonum Retards, 5 ~ 10 parts of iron nitrates, 5 ~ 10 parts of monometallics and 10 ~ 15 portions of sucrose more respectively, heated and stirred forms slurries, it is cooled to ultrasonic disperse 10 ~ 20min after room temperature, move into and vacuum drying oven is placed 15 ~ 20h, then vacuumize and it is heated to 50 ~ 70 DEG C, until the solvent volatilization in slurries is completely;
(3) matrix material 300 ~ 400 DEG C of pre-burning 5 ~ 7h in retort furnace that will process through step (2), then at 700 ~ 800 DEG C roasting 5 ~ 7h, obtain described iron lithium phosphate/carbon nano tube compound material.
5. silicon solar cell electrode slurry according to claim 1, it is characterised in that, the component of described glass powder is SiO215 ~ 30 parts, Bi2O310 ~ 20 parts, B2O310 ~ 20 parts, BaO/BaCO35 ~ 10 parts, ��-AL2O315 ~ 25 parts, ZnO5 ~ 10 part.
6. silicon solar cell electrode slurry according to claim 5, it is characterised in that, the glass powder I and glass powder II of described glass powder to be mass ratio be 1:1, the particle diameter of glass powder I is 5 ~ 15 ��m, and the particle diameter of glass powder II is 1 ~ 5 ��m.
7. silicon solar cell electrode slurry according to claim 1, it is characterised in that, described silane coupling agent is KH550, KH560 or KH602.
8. the preparation method of silicon solar cell electrode slurry according to claim 1 to 7 arbitrary claim, it is characterized in that, described preparation method is: is first dissolved in propylene glycol monobutyl ether by pungent to iron lithium phosphate/carbon nano tube compound material, silane coupling agent, turps, alkanoic acid, soluble cotton and organobentonite, obtains sticky thick slurry; Again silver powder, zinc powder, silver nickel coat alloy powder and glass powder are added in sticky thick slurry, mix, then with three-roll grinder grinding, obtain described electrode slurry.
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Application publication date: 20160608 |