U.S. patent application number 12/651136 was filed with the patent office on 2010-09-09 for electroconductive thick film composition, electrode, and solar cell formed therefrom.
This patent application is currently assigned to E. I DU PONT DE NEMOURS AND COMPANY DUPONT KABUSHIKI KAISHA. Invention is credited to TAKUYA KONNO.
Application Number | 20100227433 12/651136 |
Document ID | / |
Family ID | 36688086 |
Filed Date | 2010-09-09 |
United States Patent
Application |
20100227433 |
Kind Code |
A1 |
KONNO; TAKUYA |
September 9, 2010 |
ELECTROCONDUCTIVE THICK FILM COMPOSITION, ELECTRODE, AND SOLAR CELL
FORMED THEREFROM
Abstract
The electroconductive thick film paste of the present invention
is a silver electroconductive paste, which includes silver
particles, glass particles, and an organic vehicle, and is used in
an electrode for connecting a back face terminal on the silicon
substrate of a solar cell, and is characterized by the fact that
the average particle diameter of said silver particles is 3.0-15.0
.mu.m. The present invention is further directed to an electrode
formed from the composition as detailed above and a solar cell
comprising said electrode.
Inventors: |
KONNO; TAKUYA; (Tochigi-Ken,
JP) |
Correspondence
Address: |
E I DU PONT DE NEMOURS AND COMPANY;LEGAL PATENT RECORDS CENTER
BARLEY MILL PLAZA 25/1122B, 4417 LANCASTER PIKE
WILMINGTON
DE
19805
US
|
Assignee: |
E. I DU PONT DE NEMOURS AND COMPANY
DUPONT KABUSHIKI KAISHA
Wilmington
DE
|
Family ID: |
36688086 |
Appl. No.: |
12/651136 |
Filed: |
December 31, 2009 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12037306 |
Feb 26, 2008 |
7718093 |
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12651136 |
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11106261 |
Apr 14, 2005 |
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12037306 |
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Current U.S.
Class: |
438/98 ;
257/E21.159 |
Current CPC
Class: |
C03C 2214/08 20130101;
Y02E 10/50 20130101; C03C 8/18 20130101; C03C 14/006 20130101; H01L
31/022425 20130101; H01B 1/22 20130101; C03C 8/10 20130101; H01L
31/022408 20130101; H05K 1/092 20130101; C03C 2214/16 20130101 |
Class at
Publication: |
438/98 ;
257/E21.159 |
International
Class: |
H01L 21/283 20060101
H01L021/283 |
Claims
1. A thick film conductive composition comprising: (a) metal
particles selected from Cu, Au, Ag, Pd, Pt, alloys of Cu, Au, Ag,
Pd, Pt, and mixtures thereof; (b) glass particles; dispersed in (c)
an organic vehicle, and wherein said composition is used in an
electrode for connecting a back face terminal on a silicon
substrate of a solar cell, and wherein the average particle
diameter of said metal particles is in the range of 3.0-15.0
.mu.m.
2. The composition of claim 1 comprising, based on weight percent
total composition: 40-93 weight percent of said metal particles,
2-10 weight percent of said glass particles, and 5-50 weight
percent organic vehicle.
3. The thick film composition of any one of claim 1 or 2 wherein
said glass particles are characterized by the fact that the
softening point of said glass particles is in the range of
450-550.degree. C.
4. The composition of claim 1 further comprising aluminum.
5. An electrode formed from the composition of claim 1 wherein said
composition has been fired to remove the organic vehicle and sinter
said glass particles.
Description
FIELD OF THE INVENTION
[0001] The present invention is directed to a silicon semiconductor
device. In particular, it pertains to an electroconductive
composition used in the formation of a thick film electrode of a
solar cell. The present invention is further directed to a silver
electroconductive thick film composition (paste) for a solar
cell.
TECHNICAL BACKGROUND OF THE INVENTION
[0002] The present invention can be applied to a broad range of
semiconductor devices, although it is especially effective in
light-receiving elements such as photodiodes and solar cells. The
background of the invention is described below with reference to
solar cells as a specific example of the prior art.
[0003] A conventional solar cell structure with a p-type base has a
negative electrode that is typically on the front-side or sun side
of the cell and a positive electrode on the backside. It is
well-known that radiation of an appropriate wavelength falling on a
p-n junction of a semiconductor body serves as a source of external
energy to generate hole-electron pairs in that body. Because of the
potential difference which exists at a p-n junction, holes and
electrons move across the junction in opposite directions and
thereby give rise to flow of an electric current that is capable of
delivering power to an external circuit. Most solar cells are in
the form of a silicon wafer that has been metallized, i.e.,
provided with metal contacts that are electrically conductive.
[0004] Most electric power-generating solar cells currently used on
earth are silicon solar cells. Process flow in mass production is
generally aimed at achieving maximum simplification and minimizing
manufacturing costs. Electrodes in particular are made by using a
method such as screen printing to form a metal paste.
[0005] An example of this method of production is described below
in conjunction with FIG. 1. FIG. 1 shows a p-type silicon
substrate, 10.
[0006] In FIG. 1(b), an n-type diffusion layer, 20, of the reverse
conductivity type is formed by the thermal diffusion of phosphorus
(P) or the like. Phosphorus oxychloride (POCl.sub.3) is commonly
used as the phosphorus diffusion source. In the absence of any
particular modification, the diffusion layer, 20, is formed over
the entire surface of the silicon substrate, 10. This diffusion
layer has a sheet resistivity on the order of several tens of ohms
per square (.OMEGA./.quadrature.), and a thickness of about 0.3 to
0.5 .mu.m.
[0007] After protecting one surface of this diffusion layer with a
resist or the like, as shown in FIG. 1(c), the diffusion layer, 20,
is removed from most surfaces by etching so that it remains only on
one main surface. The resist is then removed using an organic
solvent or the like.
[0008] Next, a silicon nitride film, 30, is formed as an
anti-reflection coating on the n-type diffusion layer, 20, to a
thickness of about 700 to 900 .ANG. in the manner shown in FIG.
1(d) by a process such as plasma chemical vapor deposition
(CVD).
[0009] As shown in FIG. 1(e), a silver paste, 500, for the front
electrode is screen printed then dried over the silicon nitride
film, 30. In addition, a backside silver or silver/aluminum paste,
70, and an aluminum paste, 60, are then screen printed and
successively dried on the backside of the substrate. Firing is then
typically carried out in an infrared furnace at a temperature range
of approximately 700 to 975.degree. C. for a period of from several
minutes to several tens of minutes.
[0010] Consequently, as shown in FIG. 1(f), aluminum diffuses from
the aluminum paste into the silicon substrate, 10, as a dopant
during firing, forming a p+ layer, 40, containing a high
concentration of aluminum dopant. This layer is generally called
the back surface field (BSF) layer, and helps to improve the energy
conversion efficiency of the solar cell.
[0011] The aluminum paste is transformed by firing from a dried
state, 60, to an aluminum back electrode, 61. The backside silver
or silver/aluminum paste, 70, is fired at the same time, becoming a
silver or silver/aluminum back electrode, 71. During firing, the
boundary between the back side aluminum and the back side silver or
silver/aluminum assumes an alloy state, and is connected
electrically as well. The aluminum electrode accounts for most
areas of the back electrode, owing in part to the need to form a p+
layer, 40. Because soldering to an aluminum electrode is
impossible, a silver back electrode is formed over portions of the
back side as an electrode for interconnecting solar cells by means
of copper ribbon or the like. In addition, the front
electrode-forming silver paste, 500, sinters and penetrates through
the silicon nitride film, 30, during firing, and is thereby able to
electrically contact the n-type layer, 20. This type of process is
generally called "fire through." This fired through state is
apparent in layer 501 of FIG. 1(f).
[0012] In the formation of the backside electrodes, there are two
prior art methods which are typically used to form the Aluminum and
silver electrodes (or Ag/Al electrode). The first method is
disclosed in Japanese Kokai Patent Application Nos. 2001-127317 and
2004-146521 wherein a Ag paste is printed and dried, an Al paste is
printed and dried, and both pastes are baked (to form the silver
and Al electrodes).
[0013] The second method, as disclosed in Japanese Kokai Patent
Application Hei 11[1999]-330512, is a process in which the
formation sequence of the Al electrode and the Ag electrode of the
first method is reversed wherein the paste for the Al electrode is
printed and dried first, the Ag paste is printed and dried second,
and both pastes are baked.
[0014] In the second method, cracks were apt to be generated in the
superposed part of two electrodes due to the difference in the
thermal contraction behavior of the Al electrode and the Ag
electrode, so that the electrical characteristics (conversion
efficiency, etc.) of the solar cell were degraded.
[0015] Japanese Kokai Patent Application No. 2003-223813 considers
the thermal contraction of aluminum. In this publication, it is
presented that the thermal contraction of Al is improved by
including a material with a low thermal expansion coefficient, such
as SiO.sub.2 in the paste composition. However, in this
publication, although the decrease of the characteristics of the
solar cell is improved by the addition of SiO.sub.2, it is not
described that cracks of the superposed part of the Al electrode
and the Ag electrode do not occur by the addition of SiO.sub.2.
[0016] Additionally, when SiO.sub.2 is used, there is a possibility
that the solderability will be lowered, and the suppression of the
thermal contraction and the solderability have a trade-off
relationship. Usually, since the material of the second electrode
used as an electrode for connection requires adhesive strength, as
well as solderability, it must be designed so that glass particles
used as a binder are necessarily included in the material to
improve the adhesion with the Si substrate.
[0017] In the conventional electroconductive pastes, it was
difficult to obtain an electroconductive paste for connection that
suppresses the generation of cracks and that can form the second
electrode having both a sufficient adhesive strength and that can
maintain sufficient cell characteristics.
[0018] The present invention solves the above-mentioned problems by
providing an electroconductive paste that essentially does not
generate cracks in the superposed part, even by simultaneously
baking an aluminum electrode and a silver electrode of the back
face. This invention can form an electrode with a sufficient
adhesive strength while still maintaining sufficient solar cell
characteristics.
SUMMARY OF THE INVENTION
[0019] The electroconductive thick film paste of the present
invention is a silver electroconductive paste, which includes
silver particles, glass particles, and an organic vehicle, and is
used in an electrode for connecting a back face terminal on the
silicon substrate of a solar cell. This paste is characterized by
the fact that the average particle diameter of said silver
particles is 3.0-15.0 .mu.m. The present invention is further
directed to an electrode formed from the composition, as detailed
above, and a solar cell comprising said electrode.
BRIEF DESCRIPTION OF THE FIGURES
[0020] FIG. 1 is a process flow diagram illustrating the
fabrication of a semiconductor device.
[0021] Reference numerals shown in FIG. 1 are explained below.
[0022] 10: p-type silicon substrate [0023] 20: n-type diffusion
layer [0024] 30: silicon nitride film, titanium oxide film, or
silicon oxide film [0025] 40: p+ layer (back surface field, BSF)
[0026] 60: aluminum paste formed on backside [0027] 61: aluminum
back electrode (obtained by firing back side aluminum paste) [0028]
70: silver or silver/aluminum paste formed on backside [0029] 71:
silver or silver/aluminum back electrode (obtained by firing back
side silver paste) [0030] 500: silver paste formed on front side
[0031] 501: silver front electrode (formed by firing front side
silver paste)
[0032] FIGS. 2 (a)-(d) explain the manufacturing processes for
manufacturing a solar cell using the electroconductive paste of the
present invention. Reference numerals shown in FIG. 2 are explained
below. [0033] 102 Silicon substrate [0034] 104 Light-receiving
surface side electrode [0035] 106 Paste composition for a first
electrode [0036] 108 Electroconductive paste for a second electrode
[0037] 110 First electrode [0038] 112 Second electrode
DETAILED DESCRIPTION OF THE INVENTION
[0039] The conductive thick film composition (paste) of the present
invention provides the ability to form an electrode from said paste
wherein the electrode essentially does not generate cracks in the
overlapped part (back side Al, Ag electrodes), even when
simultaneously baking an aluminum electrode and a silver electrode
installed on the back face of a solar cell.
[0040] In order to achieve the above-mentioned objective, the
present invention is a conductive thick film composition, in
particular a silver electroconductive paste, which includes silver
particles, glass particles, and an organic vehicle, and is used in
an electrode for connecting a back face terminal on the silicon
substrate of a solar cell. It is characterized by the fact that the
average particle diameter of said silver particles is 3.0-15.0
.mu.m. In the present invention, preferably, the silver particles
are included at 40-93 wt % based on the total weight of the paste,
the glass particles are included at 2-10 wt % based on the total
weight of the paste, and the organic vehicle is included at 5-50 wt
% based on the total weight of the paste. Furthermore, it is
preferable for the glass powder included in the silver
electroconductive paste to have a softening point of
450-550.degree. C.
[0041] According to the present invention, a silver
electroconductive paste is used for a second electrode, which
suppresses the generation of cracks in the superposed part of the
first electrode and second electrode, with the second electrode
having a sufficient adhesive strength and does not degrade the
characteristics of a solar cell.
[0042] The present invention pertains to a silver electroconductive
paste that includes an electroconductive metal, especially silver
particles, a binder, especially glass particles, and an organic
vehicle, and is used in an electrode for connecting a back face
terminal on the silicon substrate of a solar cell. The
electroconductive paste of the present invention is used in the
above-mentioned second method, that is, the method that prints and
dries an electroconductive paste for the Al electrode, prints and
dries an electroconductive paste for the silver electrode, and
bakes them, in the formation of back electrodes of a solar
cell.
[0043] Next, each component of the electroconductive thick film
paste of the present invention is explained.
1. Electroconductive Metal
[0044] As the electroconductive metal usable in the
electroconductive paste of the present invention, silver (Ag)
particles can be mentioned and are most preferable. The silver
particles are preferably the flake form or powder form. In the use
as a general electroconductive paste, the particle diameter of the
silver particles is not particularly limited in terms of technical
effects; however, since the particle diameter has an influence on
the sintering characteristic of the silver (for example, the silver
particles with a large particle diameter are sintered at a speed
slower than that of the silver particles with a small particle
diameter), it is preferable to have a specific diameter for the
purpose of the present invention. Furthermore, it is also necessary
for the silver particles to have a particle diameter suitable for a
method for spreading the electroconductive paste (for example,
screen printing).
[0045] In order to satisfy the above-mentioned requirements, the
average particle diameter of the silver particles is 3.0-15.0
.mu.m, preferably 5.0-11.0 .mu.m. With the use of silver particles
with such a particle diameter, the electroconductive paste is
appropriately spread, the melting contraction behavior of the
aluminum paste for the first electrode of the back face, and the
sintering behavior of the silver electroconductive paste for the
second electrode are matched, and the generation of cracks in the
superposed part of two electrodes can be suppressed.
[0046] If the particle diameter of the silver particles is smaller
than the above-mentioned range, the silver electroconductive paste
exhibits a steep sintering behavior, and cracks are apt to be
generated between the two electrodes due to the mismatch of the
sintering speed with the aluminum paste. Also, if the particle
diameter of the silver particles is greater than the
above-mentioned range, since the sintering is not sufficiently
advanced, the electrical conductivity is lowered, and the strength
of the electrode film is decreased.
[0047] It is preferable for the silver to have a high purity
(99+%); however, a substance with a low purity can also be used in
response to the electrical demand of the electrode pattern.
[0048] In the present invention, the electroconductive metal is
most preferably the silver particles as mentioned above; however,
an electroconductive metal other than silver can also be used.
Metals such as Cu, Au, Ag, Pd, and Pd may be useful. Additionally,
alloys and mixtures of the preceding metals are also useful in the
present invention. For example, Cu, Au, Ag--Pd, Pt--Au, etc., can
be used. It is understood that the preceding discussion regarding
the use of silver particles is not limiting and applies to the use
of the other metals, alloys and mixtures detailed above.
[0049] The content of the electroconductive metal is not
particularly limited as long as it is an amount that can achieve
the objective of the present invention; however, the silver
particles are preferably present at 40-93 wt % based on the weight
of the electroconductive paste. Furthermore, aluminum may be added
to the composition to enhance desired properties.
2. Inorganic Binder
[0050] It is preferable for the electroconductive paste of the
present invention to include an inorganic binder. The inorganic
binder usable in the present invention is a glass frit with a
softening point of 450-550.degree. C. so that the electroconductive
paste can be baked at 600-800.degree. C., appropriately sintered
and moistened, and appropriately adhered to a silicon substrate. If
the softening point is lower than 450.degree. C., the sintering is
excessive, and the effects of the present invention sometimes
cannot be sufficiently obtained. On the other hand, if the
softening point is higher than 550.degree. C., since a sufficient
melt flow is not caused during the baking, a sufficient adhesive
strength is not exerted, and the liquid-phase sintering of the
silver sometimes cannot be promoted.
[0051] Here, the "softening point" is that obtained by the fiber
elongation method of ASTM C338-57.
[0052] Since the chemical composition of the glass frit is not
important in the present invention, any glass frit used in
electroconductive pastes for electronic material can be applied.
For example, lead borosilicate glass, etc., can be appropriately
used. Lead silicate glass and lead borosilicate glass are excellent
materials in the present invention in terms of both the softening
point range and the glass fusibility. A leadless glass such as zinc
borosilicate can also be used.
[0053] The content of the glass frit as the inorganic binder is not
particularly limited as long as it is an amount that can achieve
the objective of the present invention; however, the content is
2.0-10.0 wt %, preferably 3.0-6.0 wt %, based on the total weight
of the electroconductive paste.
[0054] If the amount of the inorganic binder is smaller than 2.0 wt
%, the adhesive strength is sometimes insufficient, and if the
amount of the inorganic binder is more than 10.0 wt %, soldering as
a postprocess is sometimes hindered by glass floating, etc.
3. Organic Vehicle
[0055] The electroconductive paste of the present invention
includes an organic vehicle. In the present invention, an optional
inactive liquid can be used as the organic vehicle. As usable
organic liquids, for example, alcohols; esters of alcohols (such as
an acetate or propionate); starch (such as pine oil and terpineol);
various solutions such as a pine oil solution or ethylene glycol
monobutyl ether monoacetate solution of a resin (polymethacrylate,
etc.) or ethylcellulose, or a terpineol solution of ethylcellulose
can be mentioned. In the present invention, the terpineol solution
of ethylcellulose (ethyl cellulose content=5-50 wt %) is preferably
used.
[0056] The content of the organic vehicle is 5-50 wt % based on the
total weight of the electroconductive paste.
4. Additives
[0057] In the electroconductive paste of the present invention, a
thickener and/or a stabilizer and/or other general additives may or
may not be used. When additives are used, a tackifier (thickener),
stabilizer, etc., can be added, or as other general additives, a
dispersant, viscosity adjustor, etc., can also be used. The amount
of additives is used determined in accordance with the
characteristics of the electroconductive paste that is finally
obtained. The amount of additives can be appropriately determined
by the manufacturer concerned. Also, several kinds of additives may
be used.
[0058] As will be explained below, it is preferable for the
electroconductive paste of the present invention to have a
viscosity in a prescribed range. In order to give an appropriate
viscosity to the electroconductive paste, if necessary, a tackifier
(thickener) can be added. As an example of the tackifier, for
example, the above-mentioned substances can be mentioned. The
amount of tackifier, etc., being added varies in accordance with
the viscosity of the final electroconductive paste; however, it can
be appropriately determined by the manufacturer concerned.
[0059] The electroconductive paste of the present invention is
conveniently manufactured by mixing each of the above-mentioned
components by a three-roll kneader. The electroconductive paste of
the present invention is preferably spread on the desired part of
the back face of a solar cell by screen printing; in spreading by
such a method, it is preferable to have a viscosity in a prescribed
range. The viscosity of the electroconductive paste of the present
invention is preferably 50-300 PaS when it is measured at 10 rpm
and 25.degree. C. by a utility cup using a Brookfield HBT
viscometer and #14 spindle.
[0060] The electroconductive paste of the present invention is used
for the second electrode formed in a partially superposed state
with the first electrode formed from an electroconductive paste
mainly composed of aluminum. In other words, the electroconductive
paste of the present invention is formed by printing and drying an
electroconductive paste for the Al electrode, printing and drying
an electroconductive paste for the silver electrode, and
simultaneously baking them, and is used for an electrode to connect
an electrode on the back face. Next, an example in which a solar
cell is prepared using the electroconductive paste (silver
electroconductive paste) of the present invention is explained,
referring to the figure (FIG. 2).
[0061] First, a Si substrate 102 is prepared. On the
light-receiving side face (surface) of the Si substrate, electrodes
(for example, electrodes mainly composed of Ag) 104 are installed
(FIG. 2(a)). On the back face of the substrate, aluminum pastes
used as a back face electrode for a solar cell (although it is not
particularly limited as long as it is used for a solar cell, for
example, PV333, PV322 (commercially available from E. I. du Pont de
Nemours and Company)) 106 are spread by screen printing, etc., then
dried (FIG. 2(b)). The electroconductive paste of the present
invention is then spread in a partially overlapped state with the
aluminum paste, printed and dried in advance, and dried (FIG.
2(c)). The drying temperature of each paste is preferably
180.degree. C. or lower. Also, as the film thickness of each
electrode of the backface, the aluminum paste preferably has a
dried film thickness of 40-60 .mu.m, and the thickness of the
silver electroconductive paste of the present invention is
preferably 20-30 .mu.m. Also, the overlapped part of the aluminum
paste and the silver electroconductive paste is preferably about
0.5-2.5 mm.
[0062] Next, the substrate obtained is baked at a temperature of
600-900.degree. C. for about 2-15, for instance, so that the
desired solar cell is obtained (FIG. 2(d)).
[0063] The solar cell obtained using the electroconductive paste of
the present invention, as shown in FIG. 2(d), has electrodes 104 on
the light-receiving face (surface) of the substrate (for example,
Si substrate) 102, Al electrodes (first electrodes) 110 mainly
composed of Al and silver electrodes (second electrodes) 112 mainly
composed of Ag, on the back face.
EXAMPLES
[0064] Next, the present invention is explained in further detail
by an application example. In the following application example, a
manufacturing example of the silver electroconductive paste of the
present invention and an example in which the silver
electroconductive paste is used as an electrode material for the
back face of a Si substrate in manufacturing a solar cell are
explained.
Application Example 1
[0065] Application Example 1 is detailed below.
Manufacture of Electroconductive Paste
[0066] 1.7 wt % of a viscosity adjustor and 22.5 wt % of an organic
vehicle (terpineol solution of ethylcellulose (containing 20 parts
ethylcellulose)) were added to a mixture of 4.8 wt % glass frit
(Si--B--Pb--O system) and 71.0 wt % silver powder with an average
particle diameter of 8.5 .mu.m. This mixture was premixed by a
universal mixer and kneaded by a three-roll kneader, so that a
silver electroconductive paste was obtained. The particle diameter,
content, and characteristics of the materials used are shown in
FIG. 2.
Manufacture of Solar Cell
[0067] Using the silver electroconductive paste obtained, a solar
cell was formed in the following sequence.
[0068] (1) On the back face of a Si substrate having a silver
electrode on the surface, an aluminum paste PV333 for the back face
electrode of a solar cell (commercially available from E. I. du
Pont de Nemours and Company) was screen-printed at a dried film
thickness of 40-60 .mu.m and dried at a temperature of 180.degree.
C. or lower. After drying the silver electroconductive paste of the
present invention, a film thickness of 20-30 .mu.m was obtained;
the silver paste was screen-printed so that it overlapped the
above-mentioned aluminum paste by a width of 1 mm, and dried.
[0069] (2) The aluminum paste and the silver electroconductive
paste were simultaneously baked at a heater temperature of
800.degree. C. for a baking time of 10 min in an infrared baking
furnace.
Evaluation
[0070] The overlapped part of the back face electrode of the baked
product obtained was enlarged at a magnification of 100 times and
observed by a microscope (digital microscope); the existence of
cracks was observed with the naked eye.
[0071] In addition to the observation of cracks, the adhesive
strength of the second electrode was measured. As its measuring
method, the adhesive strength was measured at a tensile speed of 2
inches (5.08 cm) per min using an "Instron" tensile tester with a
peeling-off angle of 90.degree..
[0072] Furthermore, the other characteristics required of the solar
cell, including the conversion coefficient, were decided.
[0073] These results were shown in Table II.
Comparative Examples 1-3
[0074] Electroconductive pastes with mixture compositions and
characteristics as shown in Table I were used instead of the
electroconductive paste of the present invention explained in
Application Example 1; and solar cells were manufactured by a
sequence similar to that shown in Application Example 1. Also,
Comparative Example 1 corresponds to a conventional
electroconductive paste.
[0075] The solar cells obtained were evaluated similarly to
Application Example 1. The results are shown in Table II.
TABLE-US-00001 TABLE I Comparative Example 1 Application
(conventional Comparative Comparative Example 1 example) Example 2
Example 3 Silver Average .mu.m 8.5 2.5 8.5 8.5 particles particle
diameter Content wt % 71.0 71.0 71.0 71.0 Glass frit Softening
.degree. C. 500.0 500.0 500.0 600.0 point Content wt % 4.8 2.5 1.0
4.8 Organic vehicle wt % 22.5 25.0 26.5 22.5 Viscosity adjustor wt
% 1.7 1.5 1.5 1.7
TABLE-US-00002 TABLE II Comparative Example 1 Application
(Conventional Comparative Comparative Example 1 example) Example 2
Example 3 Generation of cracks.sup.1) OK NG OK OK Adhesive strength
(N) 2.2 2.7 0.7 0.3 Characteristics of OK NG OK OK solar
cell.sup.2) .sup.1)As for the generation of cracks, when cracks
were essentially not generated (no cracks were generated, or even
if few cracks were generated, they had no influence on the
characteristics), it was decided as OK; when cracks were generated,
it was decided as NG. .sup.2)The characteristics required for solar
cells including the conversion coefficient were decided. When
sufficient practical characteristics were obtained, it was decided
as OK, and when impractical characteristics were obtained, it was
decided as NG.
[0076] According to Application Example 1, in the solar cell using
the silver electroconductive paste of the present invention, there
was essentially no generation of cracks, and the adhesive
characteristic and the characteristics of the solar cell were
maintained (sufficiently practical). On the contrary, in
Comparative Example 1 (conventional example), since the particle
diameter of the silver particles was smaller than that of the
silver electroconductive paste of the present invention, cracks
were generated, and the characteristics of the solar cell were
insufficient. Also, in Comparative Example 2, since the content of
the glass frit was low, a sufficient adhesive strength could not be
obtained. Furthermore, in Comparative Example 3, since the glass
softening point was higher than that of the electroconductive paste
of the present invention, a sufficient adhesive strength could not
be obtained.
INDUSTRIAL APPLICABILITY
[0077] The electroconductive paste of the present invention can be
utilized in the manufacture of a solar cell.
* * * * *