TECHNICAL FIELD
[0001] The present invention relates to a substrate provided with a transparent conductive
film for a photoelectric conversion device, a method for manufacturing the substrate,
and a photoelectric conversion device using the substrate.
BACKGROUND ART
[0002] In recent years, in order to make reduction of costs and attainment of higher efficiency
be compatible with each other in a solar cell which is one of the photoelectric conversion
devices, a thin film solar cell, which can be produced with a small amount of raw
materials, is attracting people's attention, and the development is eagerly carried
out. In particular, a method of forming a good-quality semiconductor layer on an inexpensive
substrate such as glass plate by using a low-temperature process is expected as a
method that can realize low costs.
[0003] Generally, a thin film solar cell includes a transparent electrode, at least one
semiconductor thin film photoelectric conversion unit, and a back electrode that are
sequentially superimposed on a transparent substrate. Further, one photoelectric conversion
unit includes an i-type layer (which is also referred to as a photoelectric conversion
layer) that is sandwiched between a p-type layer and an n-type layer which are conductivity
type layers.
[0004] Meanwhile, a thin film solar cell can reduce the thickness of the photoelectric conversion
layer as compared with a conventional solar cell that uses a bulk single crystal or
polycrystal silicon. On the negative side thereof, however, there is a problem in
that the light absorption by the total thin film may be restricted due to its small
thickness. Therefore, in order to utilize the light that is incident into the photoelectric
conversion unit including the photoelectric conversion layer, a devise is carried
out in which the surface of the transparent conductive film or the metal layer that
is in contact with the photoelectric conversion unit is made uneven (made into a texture)
and, after light is scattered at the interface thereof, the light is made incident
into the photoelectric conversion unit so as to extend the optical path length and
to increase the amount of light absorption within the photoelectric conversion layer.
This technique is referred to as "light confinement", and is an important element
technique in putting a thin film solar cell having a high photoelectric conversion
efficiency into practical use.
[0005] An amorphous silicon solar cell which is one example of a thin film solar cell is
formed on a substrate such as glass plate and often uses a tin oxide (SnO
2) film having a surface unevenness as a transparent electrode layer. This surface
unevenness of the transparent electrode layer effectively contributes to the light
confinement into the photoelectric conversion layer. However, a glass substrate on
which an SnO
2 film is formed by the thermal chemical vacuum deposition method (thermal CVD method)
as a transparent electrode layer having a surface unevenness effective for light confinement
necessitates a high-temperature process of about 550 to 650°C for forming the transparent
electrode layer thereof, thereby raising a problem of high production costs. Also,
since the film forming temperature is high, there is a problem in that an inexpensive
substrate such as a plastic film cannot be used. In addition, when a tempered glass
is subjected to a high-temperature process, the reinforcement is removed, so that
the tempered glass cannot be used as a substrate. In application to a large-area solar
cell, in order to ensure the strength of the glass substrate, a thickness of the glass
plate have to be increased and this raises a problem in that the whole solar cell
will be heavy, as a result.
[0006] In addition, the SnO
2 film has a low plasma resistance, so that the SnO
2 film will be reduced under a photoelectric conversion layer deposition environment
at a large plasma density using hydrogen. When the SnO
2 film is deoxidized, it will be blackened, and the blackened transparent electrode
layer part absorbs incident light, whereby the amount of light transmitted into the
photoelectric conversion layer will decrease, giving cause for inviting decrease in
the conversion efficiency.
[0007] Furthermore, compared with a single crystal silicon or polycrystal silicon solar
cell, an amorphous silicon solar cell has a problem of having a lower initial photoelectric
conversion efficiency, and moreover the conversion efficiency decreases by a photodegradation
phenomenon. Therefore, a crystalline silicon thin film solar cell using crystalline
silicon such as a thin film polycrystal silicon or microcrystalline silicon as a photoelectric
conversion layer is expected and studied as one capable of making reduction of costs
and attainment of higher efficiency be compatible. This is because a crystalline silicon
thin film solar cell can be formed at a low temperature by the plasma enhanced CVD
method in the same manner as the forming of amorphous silicon, and further, little
photodegradation phenomenon occurs. Also, while an amorphous silicon photoelectric
conversion layer can perform photoelectric conversion of light having a wavelength
of about 800 nm on the longer wavelength side, a crystalline silicon photoelectric
conversion layer can perform photoelectric conversion of light up to having a wavelength
of about 1200 nm which is longer than that. However, compared with a deposition condition
for forming amorphous silicon, higher plasma density is required for depositing a
crystalline silicon photoelectric conversion layer, so that when an SnO
2 film is used in a transparent electrode, a great improvement in the conversion efficiency
has been difficult.
[0008] Here, the terms of "crystalline" and "microcrystalline" in the specification of the
present application are assumed to include partially amorphous material.
[0009] On the other hand, zinc oxide (ZnO) is less expensive than SnO
2 or indium tin oxide (ITO) that is widely used as a material of a transparent electrode
layer, and also has an advantage of having a high plasma resistance. Therefore, zinc
oxide is suitable as a transparent electrode layer material for a thin film solar
cell.
(Precedent Example 1)
[0010] A substrate for a thin film solar cell provided with a ZnO film disclosed in Patent
Document 1 for example. According to Patent Document 1, a substrate for a thin film
solar cell having a surface unevenness can be provided by forming an underlying layer
having a small particle size on a transparent insulating substrate such as glass plate
and forming a ZnO film thereon by the low-pressure CVD method (or also referred to
as the MOCVD method) under a low-temperature condition of 150°C or higher and 200°C
or lower. Cost reduction can be achieved when this low-pressure CVD method is employed,
because it is a lower temperature process such as 200°C or lower as compared with
the high-pressure thermal CVD method. Also, an inexpensive substrate such as a plastic
film can be used. Further, since a tempered glass can be used, the thickness of the
glass substrate of a large-area solar cell can be reduced to about 2/3 thereof, thereby
reducing the weight. Also, by the low-pressure CVD method, a film can be formed at
a larger forming speed by one digit as compared with the sputtering method, and also
the efficiency of using a raw material is high, so that it is preferable for a thin
film solar cell in view of the production cost.
(Precedent Example 2)
[0011] On the other hand, Patent Document 2 shows the following example as a method for
forming unevenness on the surface of a transparent electrode of a substrate for a
thin film solar cell. The transparent electrode is made to have a double layer structure
in which first and second transparent conductive films are deposited from the substrate
side and, even in the case in which the surface unevenness of the first transparent
conductive film is too rough, the second transparent conductive film is made to have
a smooth surface unevenness. This is a technique such that, by doing so, the spike-shaped
protruding parts can be eliminated, and the short circuit between the junctions in
the photoelectric conversion unit can be reduced, whereby the variation in the performance
of the photoelectric conversion device can be reduced.
Patent Document 1: Japanese Patent Application Laid-Open No. 2005-311292
Patent Document 2: Japanese Patent Application Laid-Open No. 2000-252500
DISCLOSURE OF THE INVENTION
PROBLEMS TO BE SOLVED BY THE INVENTION
[0012] An object of the present invention is to increase the light confinement effects by
effectively increasing the surface unevenness of a substrate for a photoelectric conversion
device used in a thin film solar cell or the like, thereby to provide a substrate
for a photoelectric conversion device that improves the performance of a photoelectric
conversion device with use of an inexpensive production method. Further, an object
thereof is to improve the performance of a photoelectric conversion device by using
the substrate.
[0013] First, according to the method disclosed in the Examples of Patent Document 1, in
order to make a substrate for a thin film solar cell, the transparent electrode layer
mainly using a ZnO film must be made to be about 1.5 to 1.6 µm, and a film thickness
of about the double has been needed even when compared with an SnO
2 film formed by the thermal CVD method of high temperature. This seems to be caused
by the fact that the grain size of the ZnO film is small because it is mainly formed
at a low temperature and the mobility as a transparent conductive film is small. Also,
when the film thickness of the transparent electrode layer is large, the film exfoliation
from the transparent insulating substrate generated by the internal stress within
the transparent electrode layer will be a problem in an integration processing step
of a large area.
[0014] Further, in the Examples of Patent Document 2, the first transparent electrode film
having a large surface unevenness is shown only for the case of SnO
2 formed by the thermal CVD method under a high temperature. Therefore, the present
inventors have confirmed using a ZnO film formed by the low-pressure CVD method that,
in order to obtain one having an average height difference of the surface unevenness
of the first transparent conductive film of 100 to 1000 nm, a film thickness of 2
µm or more is needed, and it has been found out that a problem in the processing step
will be generated in the same manner as in the case of Patent Document 1.
MEANS FOR SOLVING THE PROBLEMS
[0015] In view of the above problems, as a result of eager studies on a method of forming
a sufficient surface unevenness in a region where the film thickness of the transparent
electrode layer itself is small, the present inventors have unexpectedly found out
that, by forming a thin ZnO film which will be a nucleus of growth before depositing
a main ZnO film, there are cases such that the surface unevenness of the transparent
electrode layer made of the main ZnO film deposited thereon can be formed to be large,
thereby the present invention have been completed.
[0016] In order to solve the above problems, a substrate provided with a transparent conductive
film for a photoelectric conversion device of the present invention includes a transparent
insulating substrate and a transparent electrode layer containing at least zinc oxide
(ZnO) deposited thereon. The transparent electrode layer is composed of a double layer
structure wherein first and second transparent conductive films are deposited from
a substrate side. The first transparent conductive film has an average film thickness
of 10 to 500 nm, and the second transparent conductive film has an average film thickness
of 300 to 1500 nm. An average height difference of an unevenness on a surface of the
second transparent conductive film is 10 to 300 nm, and the average height difference
of the unevenness on the surface thereof is larger than that of the first transparent
conductive film.
[0017] In particular, it is characterized in that the average film thickness of the second
transparent conductive film is larger than the average film thickness of the first
transparent conductive film.
[0018] Since, in the present invention, the substrate provided with a transparent conductive
film for the photoelectric conversion device has such a construction of the transparent
electrode layer as described above, the substrate having haze ratio of 20% or more
can be obtained readily. Thereby, it will be able to generate the light confinement
effectively, so that the performance of the photoelectric conversion device can be
improved. The haze ratio is a ratio of a diffusion light transmittance to a total
light transmittance as measured by using a C light source or a D65 light source, which
is one index of the unevenness of the substrate.
[0019] The substrate provided with the transparent conductive film for the photoelectric
conversion device of the present invention as described above can be produced by deposition
using a step of forming a first transparent conductive film by the sputtering method
and a step of forming a second transparent conductive film by the low-pressure CVD
method, successively on a transparent insulating substrate.
[0020] Also, a photoelectric conversion device according to the present invention includes
at least one crystalline photoelectric conversion unit deposited on the substrate
provided with the transparent conductive film for the photoelectric conversion device,
and a back electrode layer. These layers are further separated by a plurality of separation
grooves so as to form a plurality of photoelectric conversion cells, and the plurality
of these photoelectric conversion cells are electrically connected with each other
in series via a plurality of connection grooves.
EFFECTS OF THE INVENTION
[0021] According to the present invention, a substrate provided with a transparent conductive
film for a photoelectric conversion device producing large light confinement effects
can be provided by effectively increasing the unevenness of the substrate provided
with a transparent electrode layer using an inexpensive production method. Also, by
applying this substrate provided with a transparent conductive film for a photoelectric
conversion device to a photoelectric conversion device, the performance of the photoelectric
conversion device can be improved by increasing the generated electric current owing
to the light confinement effects. Further, a substrate provided with a transparent
conductive film for a photoelectric conversion device having a large surface unevenness
can be fabricated with a thickness of the transparent conductive film of about 1 µm,
whereby the process damage to the transparent electrode layer at the time of fabricating
an integrated structure can be restrained, making the light confinement effects and
the low resistance be compatible with each other. This is effective in improving the
performance and the reliability of the photoelectric conversion device.
BRIEF DESCRIPTION OF THE DRAWINGS
[0022]
Fig. 1 is a haze ratio of a substrate provided with a transparent conductive film
for a photoelectric conversion device relative to an average film thickness of a first
transparent conductive film.
Fig. 2 is a cross-sectional view of a substrate provided with a transparent conductive
film for a photoelectric conversion device, which is one embodiment of the present
invention.
Fig. 3 is a cross-sectional view of a photoelectric conversion device, which is one
embodiment of the present invention.
Fig. 4 is a schematic plan view showing an element surface of one typical example
of an integrated-type photoelectric conversion device.
Fig. 5 is a schematic cross-sectional view showing, in a further enlargement, a more
detailed integration structure of a region surrounded by an ellipse 5A within Fig.
4.
DESCRIPTION OF THE SYMBOLS
[0023] In the drawings, 1 represents a substrate provided with a transparent conductive
film for a photoelectric conversion device, 11 a transparent insulating substrate,
12 a transparent electrode layer, 121 a first transparent conductive film, 122 a second
transparent conductive film, 2 a photoelectric conversion unit, 21 one-conductivity
type layer, 22 an intrinsic photoelectric conversion layer, 23 an opposite-conductivity
type layer, 3 a back electrode layer, 31 a conductive oxide layer, 32 a metal layer,
4 a photoelectric conversion device, 6 an integrated-type photoelectric conversion
device, 61a photoelectric conversion device cell, 62 a transparent electrode layer
separation groove, 63 a connection groove, and 64 a back electrode layer separation
groove.
BEST MODE FOR CARRYING OUT THE INVENTION
[0024] The present inventors have made eager studies on the fabrication of a substrate provided
with a transparent conductive film for a photoelectric conversion device mainly concentrating
on a transparent electrode layer by the low-pressure CVD method. As a result thereof,
the present inventors have found out that, with the transparent electrode layer using
the low-pressure CVD method, the size of the unevenness of the substrate provided
with a transparent conductive film for a photoelectric conversion device will differ
depending on the presence or absence of the first transparent conductive film and,
in particular, that the film thickness dependency of the unevenness of the substrate
provided with a transparent conductive film for a photoelectric conversion device
will differ depending on the presence or absence of the first transparent conductive
film.
[0025] Here, in the present invention, the haze ratio is mainly used as an evaluation index
of the unevenness of a substrate provided with a transparent conductive film for a
photoelectric conversion device. The haze ratio is represented by (diffusion light
transmittance / total light transmittance) × 100 [%] (JIS K7136). With regard to the
measurement of the haze ratio, a haze meter is commercially available which makes
automatic measurement of the haze ratio, whereby the measurement can be carried out
easily. As a light source for the measurement, a C light source or a D65 light source
are generally used.
[0026] Also, as a method for evaluating the average film thickness of the first transparent
conductive film and the average film thickness of the second transparent conductive
film in the present invention, it is possible to carry out by a method of using a
probe step difference meter or an ellipsometry every time after each film is formed
or by an electron microscope (TEM, SEM, STEM, or the like) observation. Here, when
the measurement is carried out by TEM observation, it is possible to distinguish between
the transparent conductive film formed by the sputtering method and the transparent
conductive film formed by the low-pressure CVD method. Therefore, the evaluation of
the average film thickness of the transparent conductive film in the present invention
is most preferably carried out by the TEM observation.
[0027] Fig. 1 shows the haze ratio of a substrate provided with a transparent conductive
film for a photoelectric conversion device relative to the average film thickness
of the first transparent conductive film in the first embodiment of the present invention.
In the first embodiment, the first transparent conductive film is formed by the sputtering
method and the second transparent conductive film is formed by the low-pressure CVD
method in a structure such that the first transparent conductive film and the second
transparent conductive film mainly made of zinc oxide (ZnO) are superimposed as a
transparent electrode layer. Glass was used as a substrate, and ZnO containing Al
as a dopant was used as the first transparent conductive film. The second transparent
conductive film was formed with ZnO by the low-pressure CVD method using a mixture
gas of diethyl zinc (DEZ), water, diborane (B
2H
6), hydrogen, and argon as a source gas. The film thickness of the second transparent
conductive film of Fig. 1 is about 1.1 µm, and is constant. Also, the haze ratio of
a glass substrate on which only the first transparent conductive film had been formed
was 1.0% or less, and there was little optical scattering effect.
[0028] As will be understood from Fig. 1, when the first transparent conductive film is
absent, the haze ratio is about 10% when the average film thickness of the second
transparent conductive film is about 1.1 µm. When the first transparent conductive
film was absent, in order to obtain a haze ratio of 20% or more, an average film thickness
of about 1.5 to 2 µm was needed. In contrast, when the first transparent conductive
film is present, a haze ratio of 20% or more can be obtained even when the average
film thickness of the second transparent conductive film is about 1.1 µm, though it
depends on the film thickness of the first transparent conductive film. From this,
it can be said that, regarding ZnO by the low-pressure CVD method, the situation of
film growth differs depending on the presence or absence of the first transparent
conductive film. It is conjectured that, when the average film thickness of the first
transparent conductive film is 30 nm or more, the growth of the ZnO film is promoted
more on the surface of the first transparent conductive film, thereby increasing the
haze ratio.
[0029] Accordingly, it has been found out that, even when the film thickness of the second
transparent conductive film is kept constant, the haze ratio can be greatly increased.
Also, even when the film thickness of ZnO is comparatively small to be 1.0 µm, a high
haze ratio of 20% or more can be obtained which is not obtainable in the case where
the first transparent conductive film is absent. In this manner, a transparent conductive
film having a large unevenness of a substrate for a photoelectric conversion device
can be fabricated with a thickness of about 1 µm; the internal stress generated within
the transparent conductive film can be reduced; and the process damage to the transparent
electrode layer at the time of fabricating an integrated structure can be restrained,
making the light confinement effects and the low resistance be compatible with each
other. This is effective in improving the performance and the reliability of the photoelectric
conversion device.
[0030] Fig. 2 is a schematic cross-sectional view of a substrate 1 provided with a transparent
conductive film for a photoelectric conversion device of the present invention. The
substrate 1 provided with the transparent conductive film for the photoelectric conversion
device of the present invention is formed by depositing a transparent electrode layer
12 on a transparent insulating substrate 11.
[0031] Here, since the transparent insulating substrate 11 is positioned on the light incidence
side when the photoelectric conversion device is constructed, so that the transparent
insulating substrate 11 is preferably as transparent as possible in order to allow
more solar light to be transmitted and to be absorbed into an amorphous or crystalline
photoelectric conversion unit. As a material thereof, a glass plate, a transparent
plastic film, or the like is used. Under a similar intention, it is preferable to
carry out non-reflection coating on the light incidence surface of the transparent
insulating substrate 11 in order to reduce the light reflection loss at the light
incidence surface of the solar light.
[0032] Regarding the transparent electrode side of the transparent insulating substrate
11, a fine surface unevenness may be imparted to the surface of the transparent insulating
substrate 11 in order to improve the adhesion force of the transparent electrode layer
12.
[0033] The transparent electrode layer 12 is constructed to have a double-layer structure
in which first and second transparent conductive films are deposited. The first transparent
conductive film 121 plays a role of controlling the growth of the second transparent
conductive film 122 that will be deposited next. When the second transparent conductive
film 122 grows, the nucleus generation of the second transparent conductive film 122
occurs effectively on the surface of the first transparent conductive film 121. For
this reason, it seems that, even when the thickness of the second transparent conductive
film 122 is comparatively small, a large surface unevenness can be formed, thereby
improving the haze ratio. Therefore, it is preferable that the major components of
the first and second transparent conductive films are the same, and are preferably
made mainly of ZnO. When the thickness of the first transparent conductive film 121
is too small, it does not contribute to the nucleus generation control of the second
transparent conductive film 122, whereas when the thickness of the first transparent
conductive film 121 is too large, the film-forming costs thereof will increase due
to increase in the film-forming time. Therefore, the average film thickness of the
first transparent conductive film 121 is preferably 10 to 500 nm, more preferably
10 to 300 nm.
[0034] For the first transparent conductive film 121, the sputtering method, the vacuum
deposition method, or the low-pressure CVD method, which is more convenient than the
high-pressure thermal CVD method that requires large equipment can be used. In particular,
the first transparent conductive film 121 is preferably formed by the sputtering method.
This is because, by forming it using the sputtering method, the first transparent
conductive film 121 can be formed to be dense, whereby the adhesion force of the first
transparent conductive film 121 onto the transparent insulating substrate 11 can be
improved.
[0035] The second transparent conductive film 122 plays a role of controlling the light
confinement of the substrate 1 provided with the transparent conductive film for the
photoelectric conversion device. For this reason, the average height difference of
the surface unevenness of the second transparent conductive film 122 is preferably
10 to 300 nm. When the surface unevenness of the second transparent conductive film
122 is too small, sufficient light confinement effects cannot be obtained, whereas
when it is too large, it will be a cause of generating an electric and mechanical
short circuit in the photoelectric conversion device using the substrate 1 provided
with the transparent conductive film for the photoelectric conversion device, thereby
provoking decrease in the characteristics of the photoelectric conversion device.
Also, since the second transparent conductive film 122 plays a role of controlling
the light confinement of the substrate 1 provided with the transparent conductive
film for the photoelectric conversion device, the average height difference of the
surface unevenness thereof is preferably larger than that of the first transparent
conductive film.
[0036] As a material for the second transparent conductive film 122, it is preferable to
use a transparent conductive oxide film at least containing ZnO formed by the low-pressure
CVD method. This is because ZnO can form a texture having light confinement effects
even at a low temperature of 200°C or less, and also is a material having a high plasma
resistance, so that it is suitable for a photoelectric conversion device having a
crystalline photoelectric conversion unit. For example, the second transparent conductive
film 122 made of ZnO of the substrate 1 provided with the transparent conductive film
for the photoelectric conversion device of the present invention is formed at a substrate
temperature of 150°C or higher under a pressure of 5 to 1000 Pa, and using diethyl
zinc (DEZ), water, doping gas, and a diluting gas as a source gas. Besides this, as
a source gas of zinc, dimethyl zinc can be used. As a source gas of oxygen, oxygen,
carbon dioxide, carbon monoxide, dinitrogen oxide, nitrogen dioxide, sulfur dioxide,
dinitrogen pentoxide, alcohols (R(OH)), ketones (R(CO)R'), ethers (ROR'), aldehydes
(R(COH)), amides ((RCO)
x(NH
3-x), x = 1, 2, 3), or sulfoxides (R(SO)R') (here, R and R' are alkyl groups) can also
be used. As the diluting gas, a rare gas (He, Ar, Xe, Kr and Rn), nitrogen, hydrogen,
or the like can be used. As the doping gas, diborane (B
2H
6), trimethyl boron, alkyl aluminum, alkyl gallium, or the like can be used. The flow
rate ratio of DEZ and water is preferably 1:1 to 1:5, and the flow rate ratio of B
2H
6 to DEZ is preferably 0.05% or more. Since DEZ and water are liquid at an ordinary
temperature under an ordinary pressure, they are supplied after being gasified by
a method such as the heated evaporation, bubbling, or spraying. When the film thickness
of ZnO is made to be 0.5 to 3 µm, a thin film having a grain size of approximately
50 to 500 nm and a surface unevenness with the height of the unevenness being approximately
20 to 200 nm can be obtained, so that it is preferable in view of obtaining the light
confinement effects of the photoelectric conversion device. Here, the substrate temperature
as referred to herein refers to the temperature of the surface at which the substrate
is in contact with the heating part of the film forming apparatus.
[0037] In the event that the second transparent conductive film 122 is constructed with
a thin film mainly made of ZnO, the average film thickness of the ZnO film is preferably
300 to 1500 nm, more preferably 500 to 1200 nm. This is because, when the ZnO film
is too thin, sufficient impartation itself of the unevenness that effectively contributes
to the light confinement effects will be difficult, and it will be difficult to obtain
electric conductivity that is needed as a transparent electrode, whereas when it is
too thick, the amount of light that is transmitted through ZnO to reach the photoelectric
conversion unit will decrease due to light absorption by the ZnO film itself, thereby
leading to decrease in the efficiency. Further, when it is too thick, the film production
cost will increase due to the increase in the film production time.
[0038] The transparent electrode layer 12 of the present invention is preferably constructed
in such a manner that the average film thickness of the second transparent conductive
film 122 is larger than the average film thickness of the first transparent conductive
film 121 because each of the first and second transparent conductive films plays a
role. By having such a construction of the transparent electrode, it will be easy
for the substrate 1 provided with the transparent conductive film for the photoelectric
conversion device of the present invention to make the haze ratio be 20% or more and
it will be able to generate the light confinement effectively, so that the performance
of the photoelectric conversion device can be improved. The haze ratio is a ratio
of a diffusion light transmittance to a total light transmittance as measured by using
a C light source or a D65 light source, which is one index of the unevenness of the
substrate.
[0039] In Fig. 3, a photoelectric conversion device 4 according to an embodiment of the
present invention is shown in a schematic cross-sectional view. This photoelectric
conversion device 4 includes a first transparent conductive film 121, a second transparent
conductive film 122, a crystalline photoelectric conversion unit 2, and a back electrode
layer 3 that are successively deposited on a transparent insulating substrate 11.
Then, the crystalline photoelectric conversion unit 2 includes a one-conductivity
type layer 21, a crystalline photoelectric conversion layer 22 of substantially intrinsic
semiconductor, and an opposite-conductivity type layer 23 that are sequentially deposited.
To this photoelectric conversion device 4, the solar light (hv) to be subjected to
photoelectric conversion is made to be incident from the transparent insulating substrate
11 side. The photoelectric conversion unit 2 may be made as one photoelectric conversion
unit as illustrated; however, a plurality of photoelectric conversion units may be
superimposed. As the crystalline photoelectric conversion unit 2, those having an
absorption at the principal wavelength range (400 to 1200 nm) of solar light are preferable.
For example, a crystalline silicon based photoelectric conversion unit can be raised
in which a crystalline silicon based thin film is made to be the intrinsic crystalline
semiconductor layer 22. Also, in addition to silicon, the material of "silicon based"
includes a silicon alloy semiconductor material containing silicon such as silicon
carbide or silicon germanium.
[0040] The crystalline silicon based photoelectric conversion unit is formed, for example,
by superimposing each semiconductor layer in the order of pin type by the plasma enhanced
CVD method. Specifically, for example, a p-type microcrystalline silicon based layer
doped with boron which is a conductivity type determining impurity atom at 0.01 atom
% or higher, an intrinsic crystalline silicon layer which will be a photoelectric
conversion layer, and an n-type microcrystalline silicon based layer doped with phosphorus
which is a conductivity type determining impurity atom at 0.01 atom % or higher may
be deposited in this order. However, each of these layers is not limited to the above,
so that, for example, an amorphous silicon based film can be used as the p-type layer.
Also, as the p-type layer, an alloy material such as amorphous or microcrystalline
silicon carbide or silicon germanium may be used. Here, the film thickness of the
conductivity type (p-type, n-type) microcrystalline silicon based layer is preferably
3 nm or more and 100 nm or less, more preferably 5 nm or more and 50 nm or less.
[0041] The intrinsic crystalline silicon layer which is the intrinsic crystalline photoelectric
conversion layer 22 is preferably formed at a substrate temperature of 300°C or less
by the plasma enhanced CVD method. By forming it at a low temperature, it is preferable
to allow a lot of hydrogen atoms, which allow the defects at the crystal grain boundary
or in the grains to be terminated and inactivated, to be contained. Specifically,
the hydrogen content of the photoelectric conversion layer is preferably within a
range of 1 to 30 atom %. This layer is preferably formed as a thin film which is a
substantially intrinsic semiconductor and has a density of the conductivity type determining
impurity atom of 1 × 10
18 cm
-3 or less. Further, many of the crystal grains contained in the intrinsic crystalline
silicon layer preferably grow to extend in a columnar shape from the transparent electrode
layer 12 side, and have a preferential crystal orientation surface of (110) relative
to the film surface. The film thickness of the intrinsic crystalline silicon layer
is preferably 1 µm or more in view of light absorption, and is preferably 10 µm or
less in view of restraining the exfoliation due to the internal stress of the crystalline
thin film. However, as the thin film crystalline photoelectric conversion unit, those
having absorption at the principal wavelength region (400 to 1200 nm) of solar light
are preferable, so that one may form a crystalline silicon carbide layer (for example,
a crystalline silicon carbide layer made of crystalline silicon containing carbon
of 10 atom % or less) or a crystalline silicon germanium layer (for example, a crystalline
silicon germanium layer made of crystalline silicon containing germanium of 30 atom
% or less), which are alloy materials, in place of the intrinsic crystalline silicon
layer.
[0042] The back electrode layer 3 is formed on the photoelectric conversion unit 2. As the
back electrode layer, it is preferable to form at least one layer of a metal layer
32 made of at least one material selected from Al, Ag, Au, Cu, Pt, and Cr by the sputtering
method or the vacuum deposition method. Also, it is preferable to form a conductive
oxide layer 31 such as ITO, SnO
2, or ZnO between the photoelectric conversion unit 2 and the metal layer 32. This
conductive oxide layer 31 has a function of enhancing the light reflectivity of the
back electrode layer 3 as well as enhancing the close adhesiveness between the photoelectric
conversion unit 2 and the metal layer 32, and further has a function of preventing
chemical change of the photoelectric conversion unit 2.
[0043] Although not illustrated in the drawings, as one embodiment of the present invention,
there is a tandem type photoelectric conversion device in which an amorphous photoelectric
conversion unit and a crystalline photoelectric conversion unit are sequentially superimposed
on a substrate 1 provided with a transparent conductive film for a photoelectric conversion
device. The amorphous photoelectric conversion unit includes a front one-conductivity
type layer, an intrinsic amorphous photoelectric conversion layer, and an opposite-conductivity
type layer. When an amorphous silicon based material is selected as the amorphous
photoelectric conversion unit, it will have a sensitivity to the light of about 360
to 800 nm. When a crystalline silicon based material is selected as the crystalline
photoelectric conversion unit, it will have a sensitivity to the light of up to about
1200 nm which is longer than that of amorphous silicon based. Therefore, a solar cell
in which the amorphous silicon based photoelectric conversion unit and the crystalline
silicon based photoelectric conversion unit are arranged in this order from the light
incidence side will be a photoelectric conversion unit that can effectively use the
incident light in a wider wavelength range. The crystalline photoelectric conversion
unit may be formed in the same manner as in the third embodiment.
[0044] The amorphous photoelectric conversion unit is formed, for example, by superimposing
each semiconductor layer in the order of pin type by the plasma enhanced CVD method.
Specifically, for example, a p-type amorphous silicon based layer doped with boron
which is a conductivity type determining impurity atom at 0.01 atom % or higher, an
intrinsic amorphous silicon based layer which will be a photoelectric conversion layer,
and an n-type amorphous silicon based layer doped with phosphorus which is a conductivity
type determining impurity atom at 0.01 atom % or higher may be deposited in this order.
However, each of these layers is not limited to the above, so that, for example, a
microcrystalline silicon based film can be used as the p-type layer. Also, as the
p-type layer, an alloy material such as amorphous or microcrystalline silicon carbide,
silicon nitride, silicon oxide, or silicon germanium may be used. As the intrinsic
amorphous photoelectric conversion layer, an alloy material such as silicon carbide
or silicon germanium may be used. As the intrinsic amorphous silicon based layer,
hydrogen is preferably contained at 2 to 15% within the film in order to reduce the
recombination current loss of the thin film solar cell by reducing the defect density
within the film. Also, the intrinsic amorphous silicon based layer is preferably such
that the film thickness is 50 nm or more and 500 nm or less in order to reduce the
degradation by light radiation. As the n-type layer, a microcrystalline silicon based
film may be used. Here, the film thickness of the conductivity type (p-type, n-type)
microcrystalline silicon based layer or amorphous silicon based layer is preferably
3 nm or more and 100 nm or less, more preferably 5 nm or more and 50 nm or less.
[0045] Also, a photoelectric conversion device according to the present invention may include
at least one crystalline photoelectric conversion unit deposited on a substrate 1
provided with a transparent conductive film for a photoelectric conversion device,
and a back electrode layer, and may have an integrated structure such that these layers
are further separated by a plurality of separation grooves so as to form a plurality
of photoelectric conversion cells, and the plurality of these photoelectric conversion
cells are electrically connected with each other in series via a plurality of connection
grooves.
[0046] As one example of an integrated structure of a photoelectric conversion device, Fig.
4 shows a conceptual plan view. Fig. 5 is a structural cross-sectional view of a region
surrounded by an ellipse 5A in Fig. 4. Also, Fig. 3 corresponds to a more detailed
multilayered structural cross-sectional view of a region surrounded by an ellipse
7A in Fig. 5.
[0047] In the production of an integrated type photoelectric conversion device 6 such as
shown in Figs. 3 to 5, a glass substrate is generally used as a transparent insulating
substrate 11. A transparent electrode layer 12 formed on the glass substrate is separated
into strip-shaped transparent electrodes having a width W of about 10 mm by forming
transparent electrode separation grooves 62 having a width of about 100 µm by laser
scribing. The residues after the scribing may be removed by supersonic cleaning using
water or an organic solvent. Here, as the cleaning method, a method of removing the
residues by using a sticky agent or a sprayed gas can also be used.
[0048] Further, after one or more amorphous units or crystalline photoelectric conversion
units are formed, these units are separated into a plurality of strip-shaped regions
within a plane by connection grooves 63. Here, these connection grooves 63 are used
for electrically connecting the transparent electrode layer 12 and the back electrode
layer 3 between adjacent cells, so that there will be no problem even if the residues
of the scribing remain partially, and the supersonic cleaning may be omitted. Subsequently,
when the back electrode layer 3 is formed, the back electrode layer 3 is electrically
connected to the transparent electrode layer 12 that is formed into strips as described
above, via the connection grooves 63.
[0049] The back electrode layer 3 is patterned by laser scribing similar to that of the
one or more amorphous units or crystalline photoelectric conversion units and, after
a plurality of back electrode separation grooves 64 are formed by locally blowing
the back electrode layer 3 away together with the one or more amorphous units or crystalline
photoelectric conversion units, they are subjected to supersonic cleaning. This forms
a plurality of strip-shaped photoelectric conversion device cells 61, and these cells
are electrically connected with each other in series via the connection grooves 64.
Finally, in the case of a thin film solar cell, the back surface side is protected
by attachment of a sealing resin (not illustrated).
EXAMPLES
[0050] Hereafter, the present invention will be described in detail based on Examples; however,
the present invention is not limited to the following description examples as long
as it does not go beyond the gist thereof.
(Example 1)
[0051] As Example 1, a substrate 1 provided with a transparent conductive film for a photoelectric
conversion device such as shown in Fig. 2 was fabricated.
[0052] As the transparent insulating substrate 11, a glass plate having a thickness of 0.7
mm with 125 mm square was used, and Al-doped ZnO was formed to a thickness of 10 nm
thereon as the first transparent conductive film 121 by the sputtering method. In
forming the first transparent conductive film 121, the substrate temperature was set
to be 250°C; a 3%-Al-doped ZnO with 10-inch (diameter of 254 mm) φ was used as a target;
and a condition of the RF power of 400W under an Ar gas atmosphere was used. The haze
ratio as measured by the haze meter with use of a D65 light source on the obtained
substrate provided with the first transparent conductive film made of the ZnO film
was 0.2 %. Subsequently, as the second transparent conductive film 122, B-doped ZnO
was formed to a thickness of 1.1 µm by the low-pressure CVD method. This second transparent
conductive film 122 was formed by the CVD method under a reduced pressure condition
with a substrate temperature of 160°C and supplying diethyl zinc (DEZ) and water as
source gases, and diborane gas as a dopant gas. The obtained substrate 1 provided
with the transparent conductive film for the photoelectric conversion device had a
sheet resistance of about 13 Ω/□ and a haze ratio of 18%. Also, the total light transmittance
of the obtained substrate 1 provided with the transparent conductive film for the
photoelectric conversion device was measured by allowing light to be incident from
the glass plate side with use of a spectrophotometer. It showed a light transmittance
of 80% or more within a wavelength range of 400 to 1200 nm.
[0053] In the obtained substrate 1 provided with the transparent conductive film for the
photoelectric conversion device, the average height difference of the unevenness on
the surface of the second transparent conductive film 122 was 78 nm. At this time,
the average height difference of the unevenness on the surface was 7 nm in a state
in which up to the first transparent conductive film 121 was formed, so that the average
height difference of the unevenness on the surface of the second transparent conductive
film 122 was larger. Here, as the average height difference of the unevenness on the
surface in the present invention, a value obtained by doubling the arithmetic average
roughness (Ra) obtained by measuring with an atomic force microscope (AFM) was used.
(Example 2)
[0054] In Example 2, a substrate 1 provided with a transparent conductive film for a photoelectric
conversion device was fabricated in the same manner as in Example 1. However, the
difference from Example 1 lies in that the thickness of the first transparent conductive
film 121 was set to be 20 nm. The substrate 1 provided with the transparent conductive
film for the photoelectric conversion device obtained under this condition had a sheet
resistance of about 12 Ω/□ and a haze ratio of 22%. Also, the total light transmittance
of the obtained substrate 1 provided with the transparent conductive film for the
photoelectric conversion device was measured by allowing light to be incident from
the glass plate side with use of a spectrophotometer. It showed a light transmittance
of 80% or more within a wavelength range of 400 to 1200 nm.
(Example 3)
[0055] In Example 3, a substrate 1 provided with a transparent conductive film for a photoelectric
conversion device was fabricated in the same manner as in Example 1. However, the
difference from Example 1 lies in that the thickness of the first transparent conductive
film 121 was set to be 30 nm. The substrate 1 provided with the transparent conductive
film for the photoelectric conversion device obtained under this condition had a sheet
resistance of about 10 Ω/□ and a haze ratio of 26%. Also, the total light transmittance
of the obtained substrate 1 provided with the transparent conductive film for the
photoelectric conversion device was measured by allowing light to be incident from
the glass plate side with use of a spectrophotometer. It showed a light transmittance
of 80% or more within a wavelength range of 400 to 1200 nm.
(Example 4)
[0056] In Example 4, a substrate 1 provided with a transparent conductive film for a photoelectric
conversion device was fabricated in the same manner as in Example 1. However, the
difference from Example 1 lies in that the thickness of the first transparent conductive
film 121 was set to be 50 nm. The substrate 1 provided with the transparent conductive
film for the photoelectric conversion device obtained under this condition had a sheet
resistance of about 8 Ω/□ and a haze ratio of 33%. Also, the total light transmittance
of the obtained substrate 1 provided with the transparent conductive film for the
photoelectric conversion device was measured by allowing light to be incident from
the glass plate side with use of a spectrophotometer. It showed a light transmittance
of 80% or more within a wavelength range of 400 to 1200 nm.
(Example 5)
[0057] In Example 5, a substrate 1 provided with a transparent conductive film for a photoelectric
conversion device was fabricated in the same manner as in Examples 1. However, the
difference from Example 1 lies in that the thickness of the first transparent conductive
film 121 was set to be 100 nm. The substrate 1 provided with the transparent conductive
film for the photoelectric conversion device obtained under this condition had a sheet
resistance of about 5 Ω/□ and a haze ratio of 38%. Also, the total light transmittance
of the obtained substrate 1 provided with the transparent conductive film for the
photoelectric conversion device was measured by allowing light to be incident from
the glass plate side with use of a spectrophotometer. It showed a light transmittance
of 80% or more within a wavelength range of 400 to 1200 nm.
(Comparative Example 1)
[0058] In Comparative Example 1, a substrate 1 provided with a transparent conductive film
for a photoelectric conversion device was fabricated approximately in the same manner
as in Example 1. However, the difference from Example 1 lies in that the first transparent
conductive film 121 was not formed, and the second transparent conductive film 122
made of ZnO was formed directly on the transparent insulating substrate 11. The substrate
1 provided with the transparent conductive film for the photoelectric conversion device
obtained under this condition had a sheet resistance of about 18 Ω/□ and a haze ratio
of 11%. Also, the total light transmittance of the obtained substrate 1 provided with
the transparent conductive film for the photoelectric conversion device was measured
by allowing light to be incident from the glass plate side with use of a spectrophotometer.
If showed a light transmittance of 80% or more within a wavelength range of 400 to
1200 nm.
[0059] Fig. 1 is a graph of the haze ratio of the substrate 1 provided with the transparent
conductive film for the photoelectric conversion device according to Examples 1 to
5 as described above and Comparative Example 1 and the average thickness of the first
transparent conductive film 121. From this result, it has been found out that, by
forming the first transparent conductive film 121, the haze ratio of the substrate
1 provided with the transparent conductive film for the photoelectric conversion device
will be improved and, by a combination of the thickness of the first transparent conductive
film 121 and the thickness of the second transparent conductive film 122, the characteristics
of the haze ratio of 20% or more that can expect effective light confinement effects
into the photoelectric conversion device can be realized with a comparatively small
film thickness of 1.1 µm of the second transparent conductive film 122.
(Example 6)
[0060] As Example 6, an integrated type photoelectric conversion device 6 such as shown
in Figs. 3 and 4 were fabricated.
[0061] The transparent electrode layer 12 obtained in Example 2 is separated into strip-shaped
transparent electrodes having a width W of about 10 mm and a length L of about 10
cm by forming transparent electrode layer separation grooves 62 having a width of
about 100 µm by laser scribing. The residues after the scribing were removed by supersonic
cleaning using water.
[0062] On this transparent electrode layer 12, a crystalline photoelectric conversion layer
unit 2 made of one-conductivity type layer 21 of p-type microcrystalline silicon having
a thickness of 15 nm, an intrinsic crystalline photoelectric conversion layer 22 of
intrinsic crystalline silicon having a thickness of 1.5 µm, and an opposite- conductivity
type layer 23 of n-type microcrystalline silicon having a thickness of 15 nm was formed
successively as a photoelectric conversion layer by the plasma enhanced CVD method.
Thereafter, a conductive oxide layer 31 of Al-doped ZnO having a thickness of 90 nm
and a metal layer 32 of Ag having a thickness of 300 nm were successively formed as
the back electrode layer 3 by the sputtering method.
[0063] Light of AM1.5 was radiated at a luminous energy of 100 mW/cm
2 onto the silicon based integrated type photoelectric conversion device obtained as
described above, and the output characteristics were measured with a result that the
open circuit voltage (Voc) per one step gave 0.520V, the short-circuit current density
(Jsc) was 27.6 mA/cm
2, a fill factor (F.F.) was 0.720, and a conversion efficiency was 10.3%.
(Comparative Example 2)
[0064] In Comparative Example 2, an integrated type photoelectric conversion device 6 was
fabricated approximately in the same manner as in Example 6. However, the difference
from Example 6 lies in that the one fabricated in Comparative Example 1 was used as
a substrate 1 provided with a transparent conductive film for a photoelectric conversion
device. Light of AM1.5 was radiated at a luminous energy of 100 mW/cm
2 onto the silicon based integrated type photoelectric conversion device obtained under
this condition, and the output characteristics were measured with a result that the
open circuit voltage (Voc) per one step gave 0.500V, the short-circuit current density
(Jsc) was 23.1 mA/cm
2, a fill factor (F.F.) was 0.698, and a conversion efficiency was 8.1%.
(Comparative Example 3)
[0065] In Comparative Example 3, an integrated type photoelectric conversion device 6 was
fabricated approximately in the same manner as in Example 6. However, the difference
from Example 6 lies in that the one which was fabricated with the same construction
as in Comparative Example 1 and in which B-doped ZnO was formed to a thickness of
1.6 µm was formed as the second transparent conductive film 122 by the low-pressure
CVD method, was used as a substrate 1 provided with a transparent conductive film
for a photoelectric conversion device. The substrate 1 provided with the transparent
conductive film for the photoelectric conversion device obtained under this condition
had a sheet resistance of about 10 Ω/□ and a haze ratio of 23%. Also, the total light
transmittance of the obtained substrate 1 provided with the transparent conductive
film for the photoelectric conversion device was measured by allowing light to be
incident from the glass plate side with use of a spectrophotometer. It showed a light
transmittance of 80% or more in a wavelength range of 400 to 1200 nm; however, the
light transmittance was low in the whole wavelength region as compared with the substrate
provided with the transparent conductive film for the photoelectric conversion device
used in Example 6. Light of AM1.5 was radiated at a luminous energy of 100 mW/cm
2 onto the silicon based integrated type photoelectric conversion device obtained using
this substrate provided with the transparent conductive film for the photoelectric
conversion device, and the output characteristics were measured with a result that
the open circuit voltage (Voc) per one step gave 0.511V, the short-circuit current
density (Jsc) was 25.7 mA/cm
2, a fill factor (F.F.) was 0.721, and a conversion efficiency was 9.5%.
[0066] From the result of Example 6 and Comparative Example 2, it has been found out that
the haze ratio of the substrate 1 provided with the transparent conductive film for
the photoelectric conversion device that has been improved by forming the first transparent
conductive film 121 produces effective light confinement effects into the photoelectric
conversion device. Also, from the result of Example 6 and Comparative Example 2, it
has been found out, even with the substrate 1 provided with the transparent conductive
film for the photoelectric conversion device having a similar haze ratio, the substrate
1 provided with the transparent conductive film for the photoelectric conversion device
that can reduce the thickness of the second transparent conductive film 122 by inserting
the first transparent conductive film 121 produces effective light confinement effects
into the photoelectric conversion device. This can be conjectured to be caused by
the fact that the first transparent conductive film 121 controls the nucleus generation
of the second transparent conductive film 122, and the second transparent conductive
film 122 could be formed to have a large grain size.
[0067] As described above in detail, according to the present invention, a substrate 1 provided
with a transparent conductive film for a photoelectric conversion device having large
light confinement effects can be provided by effectively increasing the unevenness
of the substrate provided with a transparent electrode layer using an inexpensive
production method. Also, by applying this substrate 1 provided with a transparent
conductive film for a photoelectric conversion device to a photoelectric conversion
device, the performance of the photoelectric conversion device can be improved by
increasing the electric current generation owing to the light confinement effects.
Further, a substrate provided with a transparent conductive film for a photoelectric
conversion device having a large unevenness can be fabricated with a thickness of
about 1 µm, whereby the process damage to the transparent electrode layer at the time
of fabricating an integrated structure can be restrained, making the light confinement
effects and the low resistance be compatible with each other. This is effective in
improving the performance and the reliability of the photoelectric conversion device.
INDUSTRIAL APPLICABILITY
[0068] As described above, the present invention can provide a photoelectric conversion
device with improved performance.