KR20120028789A - Paste for forming electrode of solar cell and solar cell using the same - Google Patents

Abstract

PURPOSE: A paste for a solar battery electrode and a solar battery manufactured using the same are provided to manufacture the paste by mixing metal oxide particles of nano/micro size, thereby improving printing properties and conversion efficiency of the paste. CONSTITUTION: A wafer(100) comprises a p layer(101) and an n layer(102). A rear surface electrode(210) and a front surface electrode(230) are formed by printing paste on the wafer. The paste for electrodes comprises conductive powder, glass frit, an organic vehicle, and metal oxide particles. The metal oxide particles includes a first particle which has an average grain diameter of 15 to 50nm and a second particle which has an average grain diameter of 0.1 to 2μm. The weight percentage of the first particles among the total metal oxide particles is 5 to 50 percent.

Description

Paste for solar cell electrode and solar cell manufactured using same {Paste for forming electrode of solar cell and solar cell using the same}

The present invention relates to a solar cell electrode paste and a solar cell manufactured using the same. More specifically, the present invention includes two or more kinds of metal oxide particles having different sizes, and provides an electrode paste for a solar cell having excellent printability and conversion efficiency.

As the energy resources of fossil fuels such as petroleum and coal are depleted, solar cells using solar as a new alternative energy source are attracting attention.

Solar cells are configured to generate electrical energy using the photoelectric effect of p-n junctions that convert photons of sunlight into electricity. The solar cell forms front and rear electrodes on and under the semiconductor wafer or substrate on which the pn junction is formed, so that the photoelectric effect of the pn junction is induced by sunlight incident on the wafer. The electrons generated by the effect provide an electric current flowing through the electrode to the outside. The electrode of such a solar cell is formed on the wafer surface by application, patterning, and firing of an electrode paste.

One measure of the quality of solar cells is the conversion efficiency. The conversion efficiency of the solar cell is a number indicating how much of the incident light energy is converted into electrical energy, and is expressed as a ratio of the maximum output and the incident energy. In order to improve the conversion efficiency of such a solar cell, the characteristics of the electrode are important. The front electrode paste facing the direction in which sunlight is incident usually includes conductive particles, glass frit powder, and a vehicle that is a liquid carrier. It is configured by.

Recently, a method for improving the conversion efficiency of solar cells by deforming or adjusting the components has been studied.

For example, Korean Patent Publication No. 2008-0099406 discloses a technique for selecting a tap density range of Ag powder, and Korean Patent Publication No. 2007-0084100 discloses a method of improving the conversion efficiency by changing the composition of glass frit. Korean Patent Laid-Open No. 2007-0067636 proposes a method of changing the crystallite diameter of Ag powder. In addition, Korean Patent Publication No. 2007-0066938 discloses a method of improving conversion efficiency using a sintering inhibitor, and Korean Patent Publication No. 2006-0034001 uses zinc oxide powder of 7-100 nm as an additive to improve electrical performance. Improvement measures are suggested.

 However, in the prior art, the solar cell paste is printed on the front and back, and after drying, the Ag ions penetrate into the silicon wafer and the distribution of Ag ions on the electrode is reduced, resulting in a large series resistance and parallel resistance. Could not significantly improve the conversion efficiency.

In addition, when the zinc oxide powder of 7 ~ 100 nm is used, the viscosity of the paste is high, the printability is poor, the pattern drop out is increased, the conversion efficiency is reduced.

An object of the present invention is to provide an electrode paste composition for solar cells that is excellent in printability improvement and conversion efficiency of a paste.

Technical problems to be achieved by the present invention are not limited to the technical problems mentioned above, and other technical problems not mentioned will be clearly understood by those skilled in the art from the following description.

In order to achieve the above object,

According to one aspect of the invention,

A paste for a solar cell electrode comprising (a) conductive powder, (b) glass frit, (c) organic vehicle, and (d) metal oxide particles, wherein the metal oxide particles have an average particle diameter (D50) of 15-50. It is possible to provide a paste for a solar cell electrode including first particles of nm and second particles having an average particle diameter (D50) of 0.1 to 2 μm.

The conductive powder is silver (Ag), gold (Au), palladium (Pd), platinum (Pt), copper (Cu), chromium (Cr), cobalt (Co), aluminum (Al), tin (Sn), lead (Pb), zinc (Zn), iron (Fe), iridium (Ir), osmium (Os), rhodium (Rh), tungsten (W), molybdenum (Mo), nickel (Nickel) and ITO (indium tin oxide) It may include at least one conductive powder selected from the group consisting of.

The glass frit may be any of a lead glass frit, a lead-free glass frit, or a mixture thereof, and may be any of crystallized and amorphous glass frits, and a mixture thereof may be used.

The organic vehicle may comprise an organic binder and a solvent.

The metal oxide particles may include at least one of metal oxide particles such as zinc oxide (ZnO), lead oxide (PbO), copper oxide (CuO), silicon oxide (SiO 2), and titanium oxide (TiO 2).

In a specific embodiment, the paste for solar cell electrodes of the present invention comprises (a) 60 to 90 weight percent conductive powder, (b) 1 to 10 weight percent glass frit, (c) 5 to 20 weight percent organic vehicle, and (d) metal. It may include 1 to 10% by weight of oxide particles.

The paste for a solar cell electrode of the present invention may further include additives such as a plasticizer, a dispersant, a thixotropic agent, a viscosity stabilizer, an antifoaming agent, a pigment, an ultraviolet stabilizer, an antioxidant, and a coupling agent.

In addition, according to another aspect of the present invention, it is possible to present an electrode formed from the solar cell electrode paste.

In addition, according to another aspect of the present invention, it is possible to provide a solar cell including an electrode formed from the paste for the solar cell electrode.

According to the present invention, a paste for forming a solar cell electrode having excellent printability and conversion efficiency can be manufactured by mixing and using nano and micro size metal oxide particles.

1 is a schematic diagram schematically showing a structure of a solar cell manufactured using a paste according to an embodiment of the present invention.

The paste for solar cell electrodes of the present invention

(a) conductive powder, (b) glass frit, (c) organic vehicle, and (d) metal oxide with first particles having an average particle diameter (D50) of 15-50 nm and an average particle diameter (D50) of 0.1-2 μm. Characterized in that it comprises a second particle of, each component will be described in more detail below.

(a) conductive powder

As the conductive powder used in the present invention, both conductive organic and inorganic materials may be used. Specifically, silver (Ag), gold (Au), palladium (Pd), platinum (Pt), copper (Cu), chromium (Cr), cobalt (Co), aluminum (Al), tin (Sn), lead ( Pb), zinc (Zn), iron (Fe), iridium (Ir), osmium (Os), rhodium (Rh), tungsten (W), molybdenum (Mo), nickel (Nickel) or ITO (indium tin oxide) Can be used 1 type or in mixture of 2 or more types.

Preferably, the conductive powder includes silver (Ag) particles, and nickel (Ni), cobalt (Co), iron (Fe), zinc (Zn) or copper (Cu) particles may be further added in addition to the silver particles. .

The conductive powder may have a spherical shape, a plate shape, an amorphous form, or a combination thereof. In a specific embodiment, the conductive particles may be spherical to further improve filling rate, sintered density, and ultraviolet transmittance.

The conductive powder may be one having an average particle diameter (D50) of 0.1 to 10㎛, preferably an average particle diameter (D50) of 0.2 to 7㎛, more preferably 0.5 to 5㎛ may be used. The average particle diameter was measured using a 1064LD model manufactured by CILAS after dispersing the conductive powder in isopropyl alcohol (IPA) at room temperature by ultrasonic wave for 3 minutes.

The conductive powder may be included in 60 to 90% by weight, preferably 70 to 88% by weight of the total composition of the paste for a solar cell electrode of the present invention. It is possible to prevent the conversion efficiency from being lowered due to the increase of the resistance within the above range, and to prevent the pasting from becoming difficult due to the relative decrease of the amount of the organic vehicle.

(b) glass frit

The glass frit etches the anti-reflection film during the firing process of the electrode paste, generates silver crystal grains in the emitter region so that the resistance can be lowered by melting the silver particles, and improves the adhesion between the conductive powder and the wafer and sinters the glass frit. Softening at time can lead to an effect of lowering the firing temperature.

The glass frit is a crystallized glass frit or an amorphous glass frit, and any of a leaded glass frit, a lead free glass frit, or a mixture thereof can be used.

For example, zinc oxide-silicon oxide (ZnO-SiO2), zinc oxide-boron oxide-silicon oxide (ZnO-B2O3-SiO2), zinc oxide-boron oxide-silicon oxide-aluminum oxide (ZnO-B2O3- SiO2-Al2O3), bismuth oxide-silicon oxide based (Bi2O3-SiO2), bismuth oxide-boron oxide-silicon oxide based (Bi2O3-B2O3-SiO2), bismuth oxide-boron oxide-silicon oxide-aluminum oxide-based (Bi2O3-B2O3) -SiO2-Al2O3), bismuth oxide-zinc oxide-boron oxide-silicon oxide system (Bi2O3-ZnO-B2O3-SiO2) and bismuth oxide-zinc oxide-boron oxide-silicon oxide-aluminum oxide system (Bi2O3-ZnO-B2O3- SiO 2 -Al 2 O 3) may include any one or more glass frit.

The glass frit may have an average particle diameter (D50) of 0.1 to 5 μm, preferably 0.5 to 3 μm. It does not interfere with the deep curing of the UV wavelength within the above range, and does not cause pinhole defects in the developing process during electrode formation. The average particle diameter is measured using a 1064LD model manufactured by CILAS after dispersing the glass frit at room temperature with ultrasonic waves in isopropyl alcohol (IPA) for 3 minutes.

In one embodiment the glass frit may have a softening point of 300 to 600 ℃, preferably 400 to 550 ℃.

In the present invention, the glass frit may include 1 to 10% by weight, preferably 1 to 7% by weight of the total paste composition. Within this range, the sinterability, adhesion and resistance of the conductive powder may be increased to prevent the conversion efficiency from being lowered, and the amount of glass frit remaining after firing may be excessively distributed to increase the resistance and lower the solderability. You can stop it.

(c) organic vehicle

The organic vehicle may include an organic binder that imparts liquid properties to the paste.

The organic binder may be an acrylic polymer copolymerized with an acrylic monomer having a hydrophilic property such as a carboxyl group, a carboxyl group, ethyl cellulose, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose or hydroxy. Cellulose-based polymers such as ethyl hydroxypropyl cellulose (Hydroxyethylhydroxypropyl) may be used alone or in combination of two or more, respectively, but is not limited thereto.

The organic vehicle may further comprise a solvent. In this case, the organic vehicle may include 5 to 40 wt% of the organic binder and 60 to 95 wt% of the solvent. Preferably it is 7 to 30% by weight of the organic binder and 70 to 93% by weight of the solvent.

The solvent may be an organic solvent having a boiling point of 120 ℃ or more. Specific examples include methyl cellosolve, ethyl cellosolve, butyl cellosolve, aliphatic alcohol, α-terpineol, β-terpineol, dihydro Terpineol (Dihydro-terpineol), ethylene glycol (Ethylene Grycol), ethylene glycol mono butyl ether (Ethylene glycol mono butyl ether), butyl cellosolve acetate, Texanol, etc. alone or 2 Although it may mix and use species, it is not limited to these.

The organic vehicle may be included in 5 to 20% by weight, preferably 10 to 15% by weight of the total paste composition. Within this range, the dispersion may not be smooth or the viscosity may be too high after the paste is manufactured to prevent the printing from being impossible, and the resistance may be increased and the problems that may occur during the firing process may be prevented.

(d) metal oxide particles

Metal oxide particles in the present invention serves to improve the contact resistance of the electrode and to promote crystallization.

The metal oxide particles may include one or more metal oxides such as zinc oxide (ZnO), lead oxide (PbO), copper oxide (CuO), silicon oxide (SiO 2), titanium oxide (TiO 2), but are not limited thereto. It is not. Preferably zinc oxide (ZnO) is used.

In the present invention, the metal oxide particles are characterized by mixing the first particles having an average particle diameter (D50) of 15 to 50 nm and the second particles having an average particle diameter (D50) of 0.1 to 2 μm.

In a preferred embodiment, the metal oxide particles are mixed with a first particle having an average particle diameter of 20 to 40 nm and a second particle having an average particle diameter (D50) of 0.1 to 2㎛.

The average particle diameter was measured using a 1064LD model manufactured by CILAS after dispersing metal oxide particles in isopropyl alcohol (IPA) at room temperature for 3 minutes with ultrasonic waves. It can have an excellent fill factor and conversion efficiency in the above range.

The metal oxide particles may be added 1 to 10% by weight of the total paste, preferably 1 to 8% by weight may be included. Within this range, the sintering property during the firing process may be lowered to prevent the resistance and the change efficiency from being poor, and the resistance may be increased and the viscosity of the paste may be increased to prevent the possibility of poor printing.

In addition, the first particles having an average particle diameter (D50) of 15 to 50 nm are included in 5 to 50% by weight, preferably 25 to 50% by weight, more preferably 25 to 40% by weight of the total metal oxide particles. . Within this range, the specific surface area and volume of the metal oxide particles are increased to increase the space capable of reacting with the glass frit, thereby achieving the expected effect.

The paste for a solar cell electrode of the present invention may further include a conventional additive as necessary to improve the flow characteristics, process characteristics and stability in addition to the above components. The additives may be used alone or in combination of two or more plasticizers, dispersants, thixotropic agents, viscosity stabilizers, defoamers, pigments, ultraviolet stabilizers, antioxidants, coupling agents and the like. These are added in an amount of 0.1 to 5% by weight in the total composition, but can be changed as necessary.

Another aspect of the present invention relates to an electrode formed from the solar cell electrode paste and a solar cell including the same. 1 illustrates a structure of a solar cell according to an embodiment of the present invention.

Referring to FIG. 1, the pastes are printed and fired on a wafer 100 or a substrate including a p layer 101 and an n layer 102 as an emitter to form a back electrode 210 and a front electrode. 230 may be formed. For example, the paste may be printed on the back side of the wafer 100 and then dried at a temperature of about 200 to 400 ° C. for about 10 to 60 seconds to perform a preliminary preparation step for the back electrode 210. In addition, the paste may be printed on the entire surface of the wafer 100 and then dried to perform a preliminary preparation step for the front electrode 230. Thereafter, the front electrode 230 and the rear electrode 210 may be formed by performing a sintering process at about 30 to 50 seconds at 400 to 900 ° C.

Hereinafter, the configuration and operation of the present invention through the preferred embodiment of the present invention will be described in more detail. However, this is presented as a preferred example of the present invention and in no sense can be construed as limiting the present invention.

Details that are not described herein will be omitted since those skilled in the art can sufficiently infer technically.

Example

The specifications of each component used in the following Examples and Comparative Examples are as follows:

(a) Conductive Particles: A spherical AG-4-8 (Ag powder) having an average particle diameter (D50) of Dowa Hightech of 2.0 µm was used.

(b) glass frit

(b1) A low melting point flexible glass frit (flexible glass, Particle, PSL1004C) having an average particle diameter (D50) of 1.0 µm and a transition point of 451 ° C was used.

(b2) A low melting lead-free glass frit (Phoenix PDE, CSF-6) having an average particle diameter (D50) of 1.7 µm and a transition point of 371 ° C was used.

(c) Organic vehicle: A thing obtained by dissolving ethyl cellulose (Dow chemical company, STD4) in terpineol (Nippon Terpine) at 60 ° C.

(d) metal oxide particles

(d1) First particle: ZnO powder (SB chemical Co., Inc.) whose average particle diameter (D50) is 30 nm was used.

(d2) Second particle: An average particle diameter (D50) of 1.2 μm ZnO powder (Kanto chemical co. inc.) was used.

Examples 1-4

The components were added in the amounts shown in Table 1 below, 0.3 parts by weight of dispersant BYK111 (BYK-chemie), 0.3 parts by weight of thixotropic agent BYK430 (BYK-chemie), and 0.1 parts by weight of antifoaming agent BYK053 (BYK-chemie). After input and mixing, the mixture was mixed and dispersed in a three-roll kneader (roll milling) to prepare a paste for forming a solar cell electrode.

Comparative Example 1

The same procedure as in Example 1 was conducted except that no first particles were used.

Comparative Example 2

The same procedure as in Example 1 was conducted except that no second particles were used.

Example 1 Example 2 Example 3 Example 4 Comparative Example 1 Comparative Example 2 (a) Ag particles 80 80 80 80 80 80 (b)
(b1) 3 3 3 - 3 3 (b2) - - - 3 - - (c)
Ethyl cellulose One One One One One One Terpineol 11.3 11.3 13.3 11.3 11.3 11.3 (d)
(d1) One 2 0.5 One - 4 (d2) 3 2 1.5 3 4 - additive

Dispersant 0.3 0.3 0.3 0.3 0.3 0.3 Thixotropic 0.3 0.3 0.3 0.3 0.3 0.3 Antifoam 0.1 0.1 0.1 0.1 0.1 0.1 total 100 100 100 100 100 100

The solar cell electrode forming pastes prepared in Examples 1 to 4 and Comparative Examples 1 and 2 were printed by screen printing on a front surface of a wafer in a predetermined pattern, and dried using an infrared drying furnace. Thereafter, the aluminum paste was completely printed on the rear surface of the wafer and dried in the same manner. The cell formed by the above process was calcined for 30 seconds to 50 seconds between 400 to 900 ° C. using a belt type kiln, and the cell thus manufactured was manufactured using a solar cell efficiency measuring equipment (Pasan, CT-801). The Fill Factor (FF,%) and the conversion efficiency (Eff.,%) Were measured and shown in Table 2 below.

Example 1 Example 2 Example 3 Example 4 Comparative Example 1 Comparative Example 2 FF (%) 74.1 71.5 72.2 73.15 60.8 51.3 Eff. (%) 17.1 16.675 16.625 17.005 13.3 11.21

As shown in the above results, when the flexible or lead-free glass frit was mixed with the first particles and the second particles to be used in the paste preparation, the results were excellent in the Fill Factor and the conversion efficiency.

This is because the glass promotes crystallization together with zinc oxide powder in the cooling process when the electrode forming paste of the present invention is printed on the solar cell before and after the drying and firing, and then changes from the silicon wafer layer (or emitter layer) to crystalline. It appears that silver (Ag) ions prevent further penetration into the silicon wafer and increase the distribution of silver ions, thereby improving the fill factor and conversion efficiency.

Although the present invention has been described with reference to the embodiments, these are merely exemplary, and those skilled in the art will appreciate that various modifications and equivalent other embodiments are possible therefrom.

100 wafer 101 p layer
102: n layer 210: rear electrode
230: front electrode

Claims (10)

A paste for a solar cell electrode comprising (a) conductive powder, (b) glass frit, (c) organic vehicle, and (d) metal oxide particles, wherein the metal oxide particles have an average particle diameter (D50) of 15-50. A solar cell electrode paste comprising nm first particles and second particles having an average particle diameter (D50) of 0.1 to 2 µm.

The method of claim 1, wherein the metal oxide particles are at least one selected from the group consisting of zinc oxide (ZnO), lead oxide (PbO) and copper oxide (CuO), silicon oxide (SiO 2), and titanium oxide (TiO 2). Paste for solar cell electrode containing particles.
The paste for solar cell electrodes of claim 1, wherein the first particles are contained in an amount of 5 to 50 wt% in total metal oxide particles.
The method of claim 1, wherein the conductive powder is silver (Ag), gold (Au), palladium (Pd), platinum (Pt), copper (Cu), chromium (Cr), cobalt (Co), aluminum (Al), Tin (Sn), lead (Pb), zinc (Zn), iron (Fe), iridium (Ir), osmium (Os), rhodium (Rh), tungsten (W), molybdenum (Mo), nickel (Nickel) and A paste for a solar cell electrode comprising at least one selected from the group consisting of ITO (indium tin oxide).
The paste for solar cell electrodes of claim 1, wherein the glass frit comprises a flexible glass frit, a lead-free glass frit, or a mixture thereof.
The paste of claim 1, wherein the organic vehicle comprises an organic binder and a solvent.
The method of claim 1, wherein the paste comprises (a) 60 to 90% by weight of conductive powder, (b) 1 to 10% by weight of glass frit, (c) 5 to 20% by weight of organic vehicle, and (d) 1 to 1 metal oxide particles. Solar cell electrode paste containing 10% by weight.
The method of claim 1, wherein the paste further comprises at least one additive selected from the group consisting of plasticizers, dispersants, thixotropic agents, viscosity stabilizers, defoamers, pigments, UV stabilizers, antioxidants and coupling agents. Paste.
An electrode formed from the paste for solar cell electrodes according to claim 1.
The solar cell comprising the electrode of claim 9.

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