TECHNICAL FIELD
[0001] The present invention relates generally to the fabrication of semiconductor structures
or devices, such as photovoltaic devices, including quantum dot structures, and more
particularly, to intermediate structures including a plurality of absorption structures
having distinct effective band-gaps.
BACKGROUND
[0002] Solar energy is an abundant resource that may provide an alternative electrical energy
source. However, solar energy can present problems to economically collect, store,
and transport. One of the ways to collect and utilize solar energy is through photovoltaic
(PV) cells, which convert solar energy directly into electrical energy. This conversion
of energy can be provided utilizing i-type (intrinsic), n-type and p-type conductivity
regions in semiconductor materials thereby producing a photo-voltage potential and
a photo-current generated when electron-hole pairs are formed in the semiconductor
material. These electron-hole pairs are formed as a response to impinging photons
in the photovoltaic cell.
[0003] The energy absorbed by a semiconductor is dependent on its characteristic band-gap.
A semiconductor material's "band-gap energy" is defined as the amount of energy required
to free an outer shell electron from its orbit about the nucleus to a free state.
In semiconductors, the required energy for an electron to be excited from the valence
band to the semiconductor conduction band differs based on the separation between
the two bands (i.e. the band-gap). Different material may have different characteristic
band-gap energies. Band-gap engineering is the process of controlling or altering
the band-gap of a material. Conventional silicon based semiconductor materials used
in photovoltaic cells (PVs) have a band-gap energy of about 1.1 eV, i.e. only covering
a small portion of the broad range of solar radiation spectrum, which has a useable
energy in the photon range of approximately 0.4 eV to 4.0 eV.
[0004] Light with energy below the bandgap of the semiconductor will not be absorbed and
converted to electrical power. Light with energy above the bandgap will be absorbed,
but electron-hole pairs that are created quickly lose their excess energy above the
bandgap in the form of heat. Thus, this energy is not available for conversion to
electrical power.
[0005] Therefore, in order to maximize the absorption and conversion of energy in a photovoltaic
cell, multi-layered, multi-junction, or multi-subcell, photovoltaic devices have been
developed. These multi-subcell devices utilize various materials having different
characteristic band-gap energies so that a wider spectrum of solar energy may be absorbed.
[0006] A multi-subcell photovoltaic device conventionally includes multiple layers (i.e.,
subcells) of semiconductor material in a vertically stacked orientation. Each subcell
is designed to absorb and convert a different solar energy or wavelength range than
that of another subcell of different material. The subcell first exposed to radiant
energy, generally has highest band-gap energy while subcells positioned below it have
correspondingly smaller band-gap energies. As a result of this arrangement, energy
that is not absorbed at one subcell (i.e., level) may be transmitted and converted
in another subcell of the device enabling a broad spectrum of solar energy to be converted
into electrical energy.
[0007] However, this type of multi-junction photovoltaic device is limited by the ability
to lattice match a number of dissimilar materials by heteroepitaxial growth. Lattice
mismatching between adjacent subcells results in strain and dislocations to form which
reduce the overall efficiency of the photovoltaic device. Typically, materials which
may be used in a photovoltaic device are severely limited due to the lattice mismatch
problem. Attempts to overcome this problem and increase photovoltaic cell efficiency
are described, for example,
U.S. Patent 6,372,980 to Freundlich and
U.S. Patent 5,851,310 to Freundlich et al., which disclose photovoltaic cells including one or more quantum wells. In addition,
U.S. Patent 6,252,287 to Kurtz et al. discloses multi-junction solar cells including an indium gallium arsenide nitride
(InGaAsN)/gallium arsenide (GaAs) semiconductor p-n heterojunction to improve energy
conversion.
[0008] Another area of interest in increasing the efficiency of PV cells relates to the
use of quantum dots (QD). The band-gap energy of a quantum dot may be affected not
only by its composition but also by varying its dimensions. Quantum dots have been
incorporated into photovoltaic devices. For example,
U.S. Patent Application 111/038,230, which was filed January 21, 2005 by Fafard (
U.S. Publication 2005/0155641 A1, published July 21, 2005), discloses a photovoltaic solar cell including a plurality of subcells, at least
one of which includes an epitaxially grown self-assembled quantum dot material. A
germanium (Ge) bottom subcell is grown on a germanium substrate with a gallium arsenide
middle subcell and a gallium indium phosphor (GaInP) or aluminum gallium arsenic (AIGaAs)
top subcell connected in series. The efficiency of the photovoltaic solar cell is
improved by using the self-assembled quantum dot material in the middle subcell instead
of bulk gallium arsenide material. Document
US 2002/162995 A discloses solar cells and related method to manufacture them.
[0009] Photovoltaic devices utilize dissimilar materials to obtain the capability to absorb
a broad spectrum of solar energies. However, the dissimilar materials create problems
of lattice mismatch which leads to poor crystal quality and limited solar cell efficiency.
Accordingly, it would be an improvement in the art to provide a method of forming
a photovoltaic device having a number of subcell elements capable of producing a photovoltage
at multiple wavelengths of absorbed energy while maintaining a high quality crystal.
DISCLOSURE
[0010] In some embodiments, the present invention includes methods of forming semiconductor
structures or devices, as recited in claim 1. The methods include depositing a layer
of semiconductor material over a substrate, forming a subcell including at least one
structure on the layer of semiconductor material and forming at least another subcell
on the barrier material. The at least one structure includes a plurality of quantum
dots at least partially surrounded by a barrier material. The at least another subcell
includes another plurality of quantum dot structures surrounded with another barrier
material. The another barrier material has a substantially lower effective band gap
than the barrier material of the underlying subcell.
[0011] The present invention includes additional embodiments of methods of fabricating semiconductor
structures or devices. Such methods include depositing at least one layer of semiconductor
material over a base substrate, fabricating at least one absorption structure on the
at least one layer of semiconductor material to form a subcell and forming at least
another absorption structure over the at least one absorption structure to form another
subcell. The subcell is formed by growing a plurality of quantum dots comprising indium
gallium nitride on the at least one layer of semiconductor material and depositing
a barrier material comprising indium gallium nitride over and at least partially surrounding
the plurality of quantum dots at a first temperature while the another subcell is
formed by growing a plurality of quantum dots comprising indium gallium nitride on
the barrier material of the at least one absorbance structure and depositing another
barrier material comprising indium gallium nitride over and at least partially surrounding
the plurality of quantum dots at a second temperature, the second temperature being
different from the first temperature.
[0012] In yet further embodiments, the present invention includes a photovoltaic structure
as recited in Claim 8 that includes a plurality of subcells in a stacked arrangement
overlying a first layer of semiconductor material on a substrate. Each of the plurality
of subcells has a lower effective band-gap than an adjacent subcell and includes at
least one absorption structure. A second layer of semiconductor material is disposed
over an upper surface of the plurality of subcells and comprise a material different
from the first semiconductor material.
BRIEF DESCRIPTION OF THE DRAWINGS
[0013] While the specification concludes with claims particularly pointing out and distinctly
claiming that which is regarded as the present invention, the advantages of this invention
may be more readily ascertained from the description of the invention when read in
conjunction with the accompanying drawings, in which:
FIG. 1 is a simplified cross-sectional view of a partially formed structure that may
be formed during embodiments of methods of the present invention and that includes
at least one layer of semiconductor material overlying a growth substrate;
FIG. 2 is a simplified cross-sectional view of another partially formed structure
that may be formed during embodiments of methods of the present invention and that
includes a plurality of quantum dot structures on a layer of semiconductor material
overlying a growth substrate;
FIG. 3 is a simplified cross-sectional view of another partially formed structure
that may be formed during embodiments of methods of the present invention and that
includes an absorption structure comprising a barrier material encapsulating the plurality
of quantum dot structures, as shown in FIG. 2;
FIG. 4 is a simplified cross-sectional view of another partially formed structure
that may be formed during embodiments of methods of the present invention and that
includes a plurality of vertically stacked absorption structures forming a subcell
overlying a growth substrate;
FIG. 5 is a simplified cross-sectional view of another partially formed structure
that may be formed during embodiments of methods of the present invention and that
includes a plurality of subcells overlying a growth substrate;
FIG. 6 is a simplified cross-sectional view of another partially formed structure
that may be produced during embodiments of methods of the present invention and that
includes another layer of semiconductor material overlying another plurality of subcells;
FIG. 7 is a simplified cross-sectional view of a partially formed structure that may
be formed during embodiments of methods of the present invention and that includes
at least a layer of semiconductor material overlying a growth substrate;
FIG. 8 is a simplified cross-sectional view of a partially formed structure that may
be produced during embodiments of methods of the present invention and that includes
a subcell including a plurality of absorption structures;
FIG. 9 is a simplified cross-sectional view of a partially formed structure that may
be produced during embodiments of methods of the present invention and that includes
a plurality of subcells, the subcell proximate the base substrate having the highest
effective band-gap;
FIG. 10 is a simplified cross sectional view of a partially formed structure that
may be produced during embodiments of methods of the present invention that includes
a plurality of subcells overlying a layer of semiconductor material on a substrate
and disposed below a second semiconductor material;
FIG. 11 illustrates attachment of a bonding substrate to the partially formed structure
of FIG. 10, the bonding substrate is attached to the second semiconductor material
on an inverted structure; and
FIG. 12 is a simplified cross sectional view of a photovoltaic device, formed as illustrated
in FIGS. 8-11, following delamination of the base substrate from the first semiconductor
material.
MODE(S) FOR CARRYING OUT THE INVENTION
[0014] The illustrations presented herein are not meant to be actual views of any particular
material, apparatus, system, or method, but are merely idealized representations which
are employed to describe the present invention. Additionally, elements common between
figures may retain the same numerical designation.
[0015] As used herein, the terms "upper" and "lower" refer to a location relative to a base
or growth substrate. The term "upper" refers to a location that is distal to the substrate,
while the term "lower" indicates proximity to the substrate.
[0016] As used herein, the term "effective band-gap," means and includes the lowest energy
transitions at which photons may be absorbed by a material and is selected by the
quantized energy levels of the heterostructure (i.e. the quantum dot structures and
the barrier material).
[0017] As used herein, the term "absorption edge" means and includes a wavelength value
at which the absorption shows a sudden decrease in value.
[0018] As used herein, the term "III type semiconductor material" means and includes any
material predominantly comprised of one or more elements from group IIIA of the periodic
table (B, Al, Ga, In, and Ti).
[0019] As used herein, the term "III-nitride material" means and includes any material substantially
comprised of nitrogen and one or more elements from group III of the periodic table
such as, for example, usually aluminum (Al), gallium (Ga) and/or indium (In).
[0020] As used herein, the term "III-V type semiconductor material" means and includes any
material predominantly comprised of one or more elements from group IIIA of the periodic
table (B, Al, Ga, In, and Tl) and one or more elements from group VA of the periodic
table (N, P, As, Sb, and Bi).
[0021] As used herein, the term "dopant" or "doping agent" means and includes atoms added
into a semiconductor lattice in order to increase the number of free charge carriers.
Further, "n-type" dopants mean agents that act as electron donors and include atoms
such as Ge, Si, O etc., while "p-type" dopants mean agents that act as electron acceptors
and include atoms such as Mg, Ca, Be, C etc.
[0022] As used herein, the term "engineered substrate," in its broadest sense, means and
includes any substrate comprising two or more layers of material and that is intended
to be used as a substrate for the fabrication of one or more semiconductor device
thereon. Engineered substrates include, for example, semiconductor-on-insulator type
substrates.
[0023] As used herein, the term "epitaxial layer of material," means a layer of material
that is at least substantially a single crystal of the material and that has been
formed such that the single crystal exhibits a known crystallographic orientation.
[0024] As used herein, the term "lattice strain," when used with respect to a layer of material,
means strain of the crystal lattice in directions at least substantially parallel
to the plane of the layer of material.
[0025] It should be understood a layer referred to as being "on" or "over" another layer
or substrate may be disposed in direct contact with the layer or substrate, or alternatively,
may be disposed on an intervening layer overlying the layer or substrate. It should
also be understood that when a layer is referred to as being "on" or "over" another
layer or substrate, it may cover the entire layer or substrate, or a portion of the
layer or substrate.
[0026] Embodiments of the present invention include methods and structures that facilitate
the fabrication of a solar cell or photovoltaic device that have selected degrees
of effective band-gap energies such that a broad spectrum of solar energy may be absorbed
and converted to electrical energy. Example embodiments of methods of fabricating
photovoltaic devices that include such effective band-gap characteristics are described
below with reference to FIGS. 1 through 12.
[0027] Embodiments of the invention may comprise non-inverted and inverted photovoltaic
structures wherein FIGs. 1-6 are directed towards embodiments related to non-inverted
photovoltaic structures and FIGs. 6-12 are directed towards embodiments related to
inverted photovoltaic structures. Heading are used herein for clarity only and without
any intended limitation. A number of references are cited herein. Further, none of
the cited references, regardless of how characterized above, is admitted as prior
art relative to the invention of the subject matter claim herein
NON-INVERTED PHOTOVOLTIAC STRUCTURES
[0028] Referring to FIG. 1, a partially formed photovoltaic device structure 110 may be
fabricated that includes a layer of semiconductor material 114 overlying a growth
substrate 112. The layer of semiconductor material 114 comprises a seed layer for
forming one or more additional layers of semiconductor material thereon as part of
the fabrication of a photovoltaic device. In some embodiments, the layer of semiconductor
material 114 may comprise a single epitaxial layer, or multiple epitaxial layers of
a semiconductor material. Furthermore, in some embodiments, the layer of semiconductor
material 114 may comprise a doped epitaxial layer of III-V type semiconductor material.
By way of non-limiting example, the layer of semiconductor material 114 may comprise
at least one of an epitaxial layer of gallium nitride (GaN) and an epitaxial layer
of indium gallium nitride (In
xGa
1-xN). In some embodiments, the layer of semiconductor material 114 comprises an n-type
material or a p-type material, such as silicon n-type doped gallium nitride or indium
gallium nitride. As a non-limiting example, the layer of semiconductor material may
have an indium concentration greater than about twelve and one-half percent (12.5
%).
[0029] The growth substrate 112 may comprise homogenous or heterogeneous substrates suitable
for growing III-nitride materials. As particular non-limiting examples, the growth
substrate 112 may comprise aluminum oxide (Al
2O
3), which is often referred to as "sapphire", silicon carbide (SiC), gallium nitride
(GaN), GaN on sapphire, indium gallium nitride (InGaN), InGaN on sapphire, quartz
(SiO
2), gallium arsenide (GaAs), fused silica (SiO
2) glass, a glass-ceramic composite material (such as, for example, that sold by Schott
North America, Inc. of Duryea, Pennsylvania under the trademark ZERODUR®), or a fused
silica glass composite material (such as, for example, SiO
2-TiO
2 or Cu
2-Al
2O
3-SiO
2).
[0030] With continuing reference to FIG. 1, the growth substrate 112 includes a base material
113 and, optionally, one or more intermediate layers of semiconductor material 115,
depicted using a shadow line, that are ultimately disposed between the layer of semiconductor
material 114 and the growth substrate 112. Such intermediate layers of material 115
may be used, for example, as a seed layer to reduce the level of compressive or tensile
strain when it is difficult or impossible to form the layer of semiconductor material
114 directly on the base material 113 of the growth substrate 112. The figures are
not shown to scale, and, in actuality, the intermediate layer of semiconductor material
115 and the layer of semiconductor material 114 may be relatively thin in relation
to a thickness of the base material 113 of the growth substrate 112.
[0031] By way of example and not limitation, the partially formed structure 110 may comprise
a single intermediate layer of semiconductor material 115 formed on the base material
113 of the growth substrate 112, and the layer of semiconductor material 114 may be
formed on the single intermediate layer of semiconductor material 115. The intermediate
layer of semiconductor material 115 may include one or more layers of semiconductor
material such as, for example, a III-V type semiconductor material and may be formed
to have a thickness sufficient for epitaxial growth of additional layers of semiconductor
material thereon. In some embodiments, the layer of semiconductor material 114 may
comprise an n-type or p-type doped semiconductor material. As a non-limiting example,
the intermediate layer of semiconductor material 115 may comprise a tunnel junction
structure, such as stacked layers of doped semiconductor material. Additionally, the
intermediate layer of semiconductor material 115 may include a layer of an isolation
material or a layer of a conductive material, examples of which are known in the art
and are not described in detail herein. The intermediate layer of semiconductor material
115 may be grown using various methods known in the art such as, for example, hydride
vapor phase epitaxy (HVPE), metal organic vapor phase epitaxy (MOVPE), and molecular
beam epitaxy (MBE). Additionally, various methods may be used in forming the intermediate
layer of semiconductor material 115 to reduce the density of dislocations therein,
such as, for example, epitaxial lateral over-growth (ELO), facet-initiated epitaxial
lateral over-growth (FIELO),
in-situ masking, and wafer bonding.
[0032] To form the partially formed photovoltaic device structure 110 shown in FIG. 1, one
or more intermediate layers of semiconductor material 115 may be epitaxially grown
or otherwise formed on a major surface of the base material 113, after which the layer
of semiconductor material 114 may be epitaxially grown or otherwise formed on the
one or more intermediate layers of semiconductor material 115. In other embodiments,
the layer of semiconductor material 114 may be epitaxially grown or otherwise formed
directly on the base material 113 without including any intermediate layers of semiconductor
material 115.
[0033] Referring to FIG. 2, a plurality of quantum dot structures 118 may be formed on the
doped semiconductor material 114 to form the partially formed photovoltaic device
structure 116. The plurality of quantum dot structures 118 may comprise a III-nitride
material such as, for example, indium gallium nitride (In
xGa
1-xN) or aluminum gallium nitride (Al
xG
1-xN). Various methods known in the art may be used in forming the quantum dot structures
118. As a particular non-limiting example, the quantum dot structures 118 may be formed
using a Stranski-Krastanow (S-K) growth mode, often referred to as "layer-plus-island
growth," such as those described in detail in Adelmann et al., "Growth and Optical
Characterization of InGaN QDs Resulting from 2D-3D Transition," Phys. Stat. Sol. (a),
(176):639-642. Such a Stranski-Krastanow (S-K) growth mode may include forming a strained
layer of GaN using, for example, a plasma-assisted molecule beam epitaxy (PA-MBE)
process or a MBE process, or a MOCVD process, followed by reorganization (i.e., strain
relaxation) in which three-dimensional structures are formed.
[0034] In additional embodiments, the quantum dot structures 118 may be formed using surfactants
and anti-surfactants utilizing methods such as those described in detail in
Tanaka et al., "Fabrication of Self-Assembling GaN Quantum Dots on AlxGa1-xN Surfaces
Using a Surfactant," App. Phys. Lett., 69:4096 (1996). Specifically, quantum dot structures 118 may be fabricated on a surface of first
layer of a III-nitride material, such as an indium gallium nitride (In
xGa
1-xN) layer, using a metal organic vapor phase epitaxy (MOVPE) process. To form self-assembling
quantum dot structures 118, a second layer of a III-nitride material, such as a gallium
nitride layer or indium gallium nitride (In
xGa
1-xN) with a dissimilar indium composition to the first layer, may be formed on the surface
of the first layer of the III-nitride material and may be modified into a three-dimensional
mode by using a "surfactant." Without wishing to be bound by any particular theory,
it is believed that the surfactant inhibits the second layer of III-nitride material
from wetting the surface of the first layer of III-nitride material due to the change
in surface free energy.
[0035] In further embodiments, the quantum dot structures 118 may be formed using deposition
of nanodroplets of type III-metals followed by nitridation of the nanodroplets, and
selective growth methods. Additionally, the quantum dot structures 118 may be formed
by annealing thin epitaxial layers of a III-nitride material, such as indium gallium
nitride, in molecular nitrogen at a temperature of between about 400°C to about 1000°C.
The quantum dot structures 118 may also be formed using an interrupted growth mode,
such as that disclosed in, for example,
Choi et al., "Fabrication of InGaN Quantum Dots by Periodically Interrupted Growth
in MOCVD," Proceedings of the SPIE, v. 6831, pp. 683119 (2008). The quantum dot structures 118 may be formed by a metal organic chemical vapor
deposition (MOCVD) process using trimethyl-gallium (TMG), trimethyl-indium (TMI),
and ammonia (NH
3) as precursors and N
2 and H
2 as carrier gases.
[0036] As is known in the art, the quantization energies and the effective band-gap energies
of the quantum dot structures 118 may be controlled by varying the composition, dimensions,
and configuration thereof. In some embodiments, the effective band-gap energy may
be controlled by growing the quantum dot structures 118 to have an average diameter
of less than 100 nm and an average height of less than 25 nm. As a non-limiting example,
the initial growth temperature of the quantum dot structures 118 may be adjusted to
control the shape and composition of the quantum dot structures 118. For example,
the initial growth temperature of quantum dot structures 118 may be adjusted between
about 400°C to about 1000°C. In addition the size and composition of quantum dot structures
118 may be controlled via the duration of the growth of quantum dot structures 118,
for example a growth duration of between about 15 seconds to about 120 seconds maybe
utilized. Additionally, the size and composition of the quantum dot structures 118
may be controlled by altering the partial pressure of precursor gases during formation.
The quantum dot structures 118 formed on a surface of the layer of semiconductor material
114 or, if present, a surface of the intermediate layer of semiconductor material
115, may comprise substantially the same or similar dimensions. In other embodiments
the effective band-gap energy is controlled by altering, for example, the percent
indium content of the dots 118. The quantum dot structures 118 may have band-gap energies
ranging from about 0.7 eV to about 3.4 eV. As a non-limiting example, the quantum
dot structures 118 may have an effective band-gap energy of about 1.0 eV.
[0037] Referring to FIG. 3, a barrier material 122 may be formed over the quantum dot structures
118 to form the partially formed photovoltaic device structure 120 including an absorption
structure 124. As a non-limiting example, the barrier material 122 may be deposited
to surround or encapsulate exposed surfaces of the quantum dot structures 118. The
barrier material 122 may have a thickness sufficient to substantially cover a surface
of each of the quantum dot structures 118 opposing a major surface of the layer of
semiconductor material 114 or, if present, the intermediate layer of semiconductor
material 115. As one particular non-liming example, the barrier material 122 may have
a thickness of less than about 50 nm and, more particularly, of between about 20 nm
and about 40 nm.
[0038] The barrier material 122 may comprise a material having a substantially increased
effective band-gap in comparison to the quantum dot structures 118. By way of example
and not limitation, the barrier material 122 may comprise a III-nitride material such
as, for example, aluminum gallium nitride Al
xGa
1-xN), gallium nitride (GaN), indium gallium nitride (In
xGa
1-xN), and other binary and ternary III-nitrides. In some embodiments, the barrier material
122 may comprise a substantially decreased indium content in comparison to the quantum
dot structures 118 so that the effective band-gap of the barrier material 122 is greater
than the effective band-gap of the quantum dot structures 118 it surrounds. Further,
since the incorporation of indium into ternary indium gallium nitride is, at least
in part, dependent upon the deposition temperature, a difference between a deposition
temperature of the quantum dot structures 118 and a deposition temperature of the
barrier material 122 may be less than about 200°C. The difference in deposition temperatures
may be maintained to substantially prevent desorption of elements from the quantum
dot structures 118, For example, it is known in the art that increasing the temperature
of an indium gallium nitride material above a deposition temperature thereof may result
in desorption therefrom. Further, desorption of indium from indium gallium nitride
quantum dot structures may result in a change in the composition of the quantum dot
structures and hence may change the effective band-gap of the quantum dot structures.
[0039] In other embodiments, the temperature during formation of the barrier material 122
can be varied during overgrowth of the quantum dot structures 118 to further control
the size and composition of the quantum dot structures 118. For example, the variation
of growth temperature during formation of barrier material 122 can result in, decreased
desorption from quantum dot structure 118, controlled quantum dot structure dimensions
and increased crystalline quality of barrier material 122.
[0040] As a non-limiting example, the variation of growth temperature during barrier material
122 formation may comprise an initial growth temperature for formation of a portion
of the barrier material proximate to the quantum dot structures and a subsequent growth
temperature for a remaining portion of the barrier material more distal from quantum
dot structures 118. For example, an initial growth temperature for formation of a
portion of the barrier material proximate to quantum dot structures 118 can be substantially
equal to that utilized for the growth of the quantum dot structures. As the growth
of the barrier material continues the temperature of the growth can be increased,
such an increase in growth temperature as the thickness of barrier material 122 increases
can assist in improving the crystalline quality of barrier material 122.
[0041] In further embodiments of the invention, a portion of the barrier material may be
grown at an initial growth temperature substantially equal to that used to form quantum
dot structures 118, growth can then continue at the initial growth temperature until
such time as the quantum dot structures are enclosed by barrier material 122. Upon
enclosure of quantum dot structure 118 with barrier material 122 the growth temperature
of the barrier layer may be increased to improve the crystalline quality of the barrier
material or growth can be paused upon enclosure of the quantum dot structures and
the temperature of the reactor increased, in a gas ambient suitable for maintaining
crystalline quality, for example ammonia (NH
3) can be introduced to maintain the quality of III-nitride materials. Upon reaching
the desired subsequent growth temperature the remaining portion of barrier material
122 can be grown.
[0042] In still further embodiments, the characteristics of the quantum dot structures 118
may be modified by altering, for example, the partial pressure of precursor gases,
the choice of substrate, and the growth rate. In this manner, the effective band-gap
energy of the absorption structure 124 may be controlled.
[0043] Referring to FIG. 4, a partially formed photovoltaic device structure 126 may be
fabricated that includes a growth substrate 112 having a semiconductor material 114,
optionally doped with p-type or n-type atoms, and having a first subcell 128 formed
thereon. The first subcell 128 may comprise multiple absorption structures 124A, 124B,
124C disposed over one another in a stacked configuration over the semiconductor material
114. Within the first subcell 128, each absorption structure 124A, 124B, 124C maybe
fabricated using methods similar or identical to those described with respect to FIGs.
2 and 3. For example, the first absorption structure 124A may be formed by growing
a layer of quantum dot structures 118 at an initial temperature, followed by deposition
of a barrier material 122 around the quantum dots 118 at a different temperature,
as described with respect to FIG. 3.
[0044] Following formation of the first absorption structure 124A, a plurality of absorption
structures 124B, 124C may be fabricated on an upper surface of the barrier material
122 of the first absorption structure 124A to form a first subcell 128. The number
of absorption structures within a subcell may be selected based on the electromagnetic
radiation to be absorbed. For example, by increasing the thickness of each of the
absorption structures 124A, 124B, 124C within the photovoltaic structure 126 and increasing
the number of absorption structures 124A, 124B, 124C, the probability of absorbing
electromagnetic radiation may be increased. Therefore, the number of absorption structures
124A, 124B, 124C may be selected based on an absorption depth of incoming electromagnetic
radiation. In some embodiments the absorption structures 124A, 124B, 124C within a
given subcell may have substantially the same configuration. As one non-limiting example,
each of the quantum dot structures 118 of absorption structure 124A may have a general
size and composition substantially identical to each of the quantum dot structures
118 of absorption structures 124B and 124C. Alternatively, each of the quantum dot
structures 118 of the absorption structure 124A may have a substantially different
size and composition in comparison to each of the quantum dot structures 118 of the
absorption structures 124B, 124C.
[0045] With continued reference to FIG. 4, in some embodiments, the quantum dot structures
118 of the absorption structures 124A, 124B, 124C in the first subcell 128 may be
in substantially alignment with one another. The alignment of the quantum dot structures
118 may be produced by the strain in the underlying absorption structure 124, which
is present as a result of lattice mismatch between materials of the quantum dot structures
118 and the barrier material 122 using fabrication methods known in the art. Thus,
by selectively tailoring the lattice parameter of the barrier material 122, lattice
mismatch between the barrier material 122 and the quantum dot structures 118 forming
part of the overlying absorption structures 124B, 124C may be utilized to promote
alignment of subsequent quantum dot structures 118 in subsequent absorption structures
124B, 124C. As a result, embodiments of the present invention may allow the fabrication
of quantum dot structures 118 in substantial alignment in each of the absorption structures
124A, 124B, 124C that may substantially increase the efficiency of the photovoltaic
device structure 126.
[0046] The average dimensions of each of the quantum dot structures 118 may be selected
to have a desired effective band-gap. The effective band-gap of each of the quantum
dot structures 118 may be substantially increased by decreasing the average diameter
thereof. For example, the average dimensions of the quantum dot structures 118 within
the subcell 128 may be formed to have an absorption energy (i.e., an effective band-gap)
of between about 0.7 eV and about 6.2 eV, and more particularly, from about 0.7 eV
to about 4 eV. The effective band-gap of each of the quantum dot structures 118 may
further be selected based on the number of subcells to be incorporated into the photovoltaic
device, the ideal absorption energy and therefore the effective band gap energy of
the individual subcells may vary according to Table 1 below, which provides calculated
efficiencies for photovoltaic structure comprising one or more subcells determined
under idealized conditions. Such conditions are described in detail in, for example,
United States Patent Application Publication No.
2007/0137698 to Wanlass et al.
TABLE 1
| Optimum Band-gap Energy and Efficiencies for PVs |
| Number of Subcells |
Efficiency (%) |
Effective Band-gap Energy (eV) |
| 1 |
32.4 |
1.4 |
|
|
|
|
|
| 2 |
44.3 |
1.0 |
1.8 |
|
|
|
|
| 3 |
50.3 |
1.0 |
1.6 |
2.2 |
|
|
|
| 4 |
53.9 |
0.8 |
1.4 |
1.8 |
2.2 |
|
|
| 5 |
56.3 |
0.6 |
1.0 |
1.4 |
1.8 |
2.2 |
|
| 6 |
58.5 |
0.6 |
1.0 |
1.4 |
1.8 |
2.0 |
2.2 |
[0047] With reference to FIG. 5, another partially formed photovoltaic structure 130 is
shown having a second subcell 136 formed over the barrier material 122 of the first
subcell 128. The subcell 136 may include, for example, a plurality of absorption structures
134A, 134B, and 134C, each of which includes a barrier material 122 overlying a plurality
of quantum dots structures 118' and may be formed using methods similar or identical
to those described with respect to FIGs. 2 and 3. In some embodiments, the quantum
dot structures 118' in each of the absorption structures 134A, 134B, and 134C, may
be formed having substantially the same average dimensions, to form the partially
formed photovoltaic structure 130 shown in FIG. 5. In other embodiments, the quantum
dot structures 118' in each of the absorption structures 134A, 134B, and 134C, may
be formed having various average dimensions. The average dimensions of the quantum
dot structures 118' may be selected to have a desired effective band-gap as described
with respect to FIG. 4. As a non-limiting example, the quantum dot structures 118'
may be formed such that an effective band-gap thereof is between about 0.7 eV and
about 4 eV, or in certain embodiments an effective band-gap of approximately 1.6 eV.
The barrier material 122' may comprise a III-nitride material such as, for example,
aluminum gallium nitride (Al
xGa
1-xN), gallium nitride (GaN), indium gallium nitride (InxGa
1-xN), and other binary and ternary III-nitrides and may be formed using methods similar
or identical to those described with respect to FIG. 3. The barrier material 122'
may have an indium content substantially less than that of the barrier material 122
of the first subcell 128 and thus, an effective band-gap substantially greater than
that of the barrier material 122. To form such a barrier material 122', the barrier
material 122' of the second subcell 136 may be deposited at temperature greater than
a deposition temperature of the barrier material 122 of the first subcell 128. As
previously discussed, the deposition temperature of the barrier material 122'the second
subcell 136 may be maintained at about no greater than 200°C above a deposition temperature
of the barrier material 122 of the first subcell 128 to prevent desorption of indium
from the quantum dot structures 118 and 118'.
[0048] Referring to FIG. 6, a third subcell 144 may be formed over the second subcell 136
to form a partially formed photovoltaic device structure 138 having a plurality of
subcells 128, 136, 144 overlying the growth substrate 112. The third subcell 144 may
include a plurality of quantum dot structures 118" and a barrier material 122" formed
over and at least partially surrounding each of the quantum dot structures 118 The
quantum dot structures 118" of the third subcell 144 may be formed having average
dimensions of substantially less than the average dimensions of the quantum dot structures
118' of the underlying subcell 136. The barrier material 122" may comprise a III-nitride
material such as, for example, aluminum gallium nitride Al
xGa
1-xN), gallium nitride (GaN), indium gallium nitride (in
xGa
1-xN), and other binary and ternary III-nitrides. The barrier material 122" of the third
subcell 40 may be deposited at temperature greater than a deposition temperature of
the barrier material 122' of the second subcell 136 so that the barrier material 122"
of the third subcell 144 has an indium content of substantially less than the indium
content of the barrier material 122' of the second subcell 136.
[0049] In some embodiments, the average dimensions of each of the quantum dot structures
118 within each of the subcells 128, 136, 144 may be substantially identical or similar
such that each of the quantum dot structures 118 within one of the subcells 128, 136,
144 includes a substantially similar or identical effective bandgap. The average dimensions
of each of the quantum dot structures 118 in subsequent subcells 136, 144 may be varied
within each of the subcells 128, 136, 144. The effective bandgap energy of each of
the quantum dots 118 within a selected one of the subcells 128, 136, 144 may be controlled
by altering the average dimensions thereof such that an absorption edge of the selected
one of the subcells 128, 136, 144 corresponds to a desired portion of the electromagnetic
spectrum. As a non-limiting example, the quantum dot structures 118 of the first subcell
128 may have an effective band-gap of about 1.0 eV, while the quantum dot structures
118' of the second subcell 136 may have a band-gap of about 1.6 eV, and the quantum
dot structures 118" of the third subcell 144 may have a band-gap of about 2.2 eV.
[0050] Additionally, a composition of the barrier material 122 may be selected to maintain
the effective band-gap between the quantum dot structures 118 while providing a barrier
between subcells 128, 136, 144. By way of non-limiting example, if the barrier material
122 includes indium gallium nitride, an effective band-gap thereof may be substantially
increased by decreasing an atomic percentage of indium therein. The incorporation
of indium into the indium gallium nitride barrier material 122 may be substantially
reduced by depositing the indium gallium nitride barrier material 122 at a substantially
increased temperature, using methods known in the art. As each of the subcells 128,
136, 144 is formed, a deposition temperature thereof may be substantially increased
in comparison to that of the previously formed subcells such that the indium concentration
decreases and, thus, the absorption edge of adjacent subcells 128, 136, 144 sequentially
increases.
[0051] As one such example, shown in FIG. 6, the dimensions of the quantum dot structures
118 in each subcell 128, 136, 144 may sequentially decrease in relation to an electromagnetic
radiation source and thus, the effective band-gap of the subcell increases in relation
to an electromagnetic radiation source. The corresponding barrier layers 122, 122',
122" of each of the subcells 128, 136, 144 may comprise indium gallium nitride and
the effective band-gap thereof may be substantially sequentially increased by increasing
the deposition temperatures as previously described. After forming a desired number
of subcells 128, 136, 144, each having a different absorption edge, another layer
of semiconductor material 140 may be deposited over an upper surface 131 of an uppermost
subcell (e.g., subcell 144). The semiconductor material 140 may include, for example,
a III-nitride material. In some embodiments, the layer of semiconductor material 140
may comprise an n-type or p-type doped III-nitridematerial. As a non-limiting example,
the layer of semiconductor material 140 may include magnesium (Mg) doped gallium nitride
or magnesium doped indium gallium nitride. By way of example and not limitation, the
layer of semiconductor material 114 may comprise an n-type doped III-nitride material
and the another layer of semiconductor material 140 may comprises a p-type doped III-nitride
material, thereby producing a PIN photovoltaic diode device 138.
[0052] With continued reference to FIG. 6, in other embodiments, the band-gap energy of
the subcells 128, 136, 144 may be controlled, while the average dimensions of the
quantum dot structures 118, 118', 118" between subcells remain substantially similar
or identical, by altering the composition of the quantum dot structures 118, 118',
118 In some embodiments, the indium content of the quantum dot structures 118 in each
of the subcells 128, 136, 144 may substantially decrease as the subcell is located
farther from the growth substrate 112 and closer to an incident electromagnetic source.
By way of example and not limitation, the percentage indium content in the quantum
dot structures 118, 118', 118" and the barrier material 122, 122', 122" may decrease
toward the upper surface 132 of the photovoltaic device. Alternatively, the indium
content in the barrier material 122 may remain constant, while the indium content
in the quantum dot structures 118, 118', 118" decreases farther from the growth substrate
112 and closer to an incident electromagnetic source. By increasing deposition temperatures
of the quantum dots structures 118, 118', 118" and the barrier layers 122, 122', 122"
within each of the subcells 128, 136, 144, the indium content of each of the subcells
128, 136, 144 may be substantially less than that of the underlying subcell and, thus,
the effective band gap of each of the subcells 128, 136, 144 may be substantially
greater than that of the underlying subcell.
INVERTED PHOTOVOLTIAC STRUCTURES
[0053] The following embodiments comprise structure and methods for producing inverted photovoltaic
structures. By way of explanation and by no means limitation, in a photovoltaic device
structure it is common for the absorption structure, i.e. the subcell, with the largest
effective absorption energy (i.e. the largest effective band-gap) to be proximate
to the impinging radiation source (e.g., solar radiation). In such a configuration,
radiation which is not absorbed in the uppermost absorption structure may be transmitted
through said structure and absorbed in an underlying absorption structure with a lower
effective absorption energy (i.e. a lower effective band-gap). In such a configuration
a higher percentage of impinging radiation may be usefully converted to electrical
energy. In an opposing configuration, i.e., when the smallest effective absorption
energy is proximate to the impinging radiation, a higher percentage of impinging radiation
may be wasted due to losses within the photovoltaic device structure, e.g. in form
of heat.
[0054] In order to more efficiently produce the desired absorption configuration in the
completed photovoltaic device structure it may be necessary to grow the crystalline
absorption structures in a reverse manner, i.e., with the absorption structure with
the smallest effective absorption energy most distal from the base substrate and the
absorption structure with the highest effective absorption energy most proximal to
the base substrate. Such a reversed growth configuration may be effective due to reasons
of growth parameters or lattice matching the various absorption structures to each
other and also to the base substrate.
[0055] Upon completion of the reversed crystal structure an inversion of the structure may
be required to produce a final device configuration favoring a more efficient conversion
of incoming radiation to electrical energy. The inversion of the photovoltaic device
structure can involve the attachment of the upper surface of the photovoltaic device
structure to a carrier substrate. Following attachment to a suitable carrier substrate
the initial base substrate can be removed thereby enabling the exposure of the photovoltaic
device structure to impinging solar radiation.
[0056] Referring to FIG. 7, a partially formed photovoltaic device structure 110 may be
fabricated that includes a layer of semiconductor material 114 overlying a growth
substrate 112 using methods similar or identical to those described with respect to
FIG. 1. As a non-limiting example, the layer of semiconductor material 114 may comprise
a p-type doped III-nitride material.
[0057] Referring to FIG. 8, another embodiment of a partially formed photovoltaic device
structure 146 may be fabricated that includes a layer of semiconductor material 114
attached to a growth substrate 112 using methods substantially similar or identical
to those described with respect to FIG. 1. The growth substrate 112 may comprise homogenous
or heterogeneous substrates suitable for the growth of type III-nitrides and the layer
of semiconductor material 114 may comprise a single epitaxial layer, or multiple epitaxial
layers of a semiconductor material, as previously described with respect to FIG. 1.
[0058] The growth substrate 112 may include a base material 113 (FIG. 1) and, optionally,
one or more intermediate layers of semiconductor material 115 (FIG. 1), depicted using
a shadow line, that are ultimately disposed between the layer of semiconductor material
114 and the base substrate 113.
[0059] Referring still to FIG. 8, partially formed photovoltaic device structure 146 may
include a first subcell 150 comprising a plurality of absorption structures 148A,
148B, 148C having quantum dot structures 118" surrounded by barrier material 122"
is illustrated. The subcell 150 may be fabricated using method substantially similar
or identical to those described with respect to FIGS. 2-4 above. By way of non-limiting
example, the quantum dot structures 118" may comprise indium gallium nitride (In
xGa
1-xN). Subsequently, a barrier material 122" including a III-nitride material may be
deposited, at a deposition temperature, over the quantum dot structures 118". The
quantum dot structures 118" within each of the plurality of absorption structures
148A, 148B, 148C may comprise the same dimensions. Additionally, each of the absorption
structures 148A, 148B, 148C may be formed having a desired effective band-gap by controlling
the average dimensions and composition of the quantum dot structures 118" and barrier
material 122" as discussed with respect to FIG. 4. For example, the quantum dots structures
118" may be formed to have an effective band-gap of 2.2 eV.
[0060] With reference to FIG. 9, partially formed photovoltaic structure 152 including a
plurality of subcells 150, 156 on the base substrate 112 is shown. The second subcell
156 may be formed over the first subcell 150 using a method substantially similar
or identical to those described with respect to FIGS. 2-4 above. The second subcell
156 may include a plurality of absorption structures 154A, 154B, 154C, each having
an absorption edge corresponding to a different portion of the electromagnetic spectrum
than an absorption edge of the absorption structures 148A, 148B, 148C of the first
subcell. By way of example and not limitation, the dimensions of the quantum dot structures
118" of a first subcell 150 may be substantially less than the dimensions of the quantum
dot structures 118' of a second subcell 156. As a consequence of the increased size,
the effective band-gap of the quantum dot structures 118' is substantially decreased.
To form the quantum dot structures 118' having increased dimensions, the quantum dot
structures 118' of the second subcell 156 may be formed at a lower temperature than
a temperature at which the quantum dot structures 118" of the first subcell 150 are
formed.
[0061] In additional embodiments, the effective band-gap of the subcells 150, 156 may be
controlled, while maintaining the dimensions of the quantum dot structures 118", 118'
between subcells, by altering a composition of the quantum dot structures 118'. As
a non-limiting example, the quantum dot structures 118", 118' may have substantially
similar or identical dimensions and may comprise indium gallium nitride throughout
the subcells of the photovoltaic structure. The composition such as, for example,
the indium content, of each of the quantum dot structures 118", 118' may be varied
to provide a desired effective band gap for each subcell.
[0062] The barrier material 122", 122' deposited over each of the plurality of quantum dot
structures may be selected to maintain a desired difference between the effective
band-gap of the quantum dot structures 118", 118' and the barrier material 122", 122'.
Since the effective band-gap of the quantum dots structures 118", 118' has been substantially
reduced by increasing the average dimensions of the quantum dots structures 118",
118', the effective band-gap of the barrier material 122", 122' may be decreased by
increasing an indium content thereof. Therefore, the difference between the effective
band-gap of the quantum dot structures 118", 118' and the barrier material 122", 122'
may be maintained by depositing the barrier material 122", 122' at a substantially
reduced temperature in comparison to a deposition temperature of underlying structures,
such as the first subcell 150. By forming the barrier material 122' of the second
subcell 156 at a reduced temperature, desorption of indium from the barrier material
122" of the first subcell 150 into the barrier material 122' of the second subcell
156 is substantially reduced or eliminated.
[0063] As shown in FIG. 10, a third subcell 162 may be formed over the second subcell 156
to form a partially formed photovoltaic structure 158. The third subcell 162 may include
a plurality of absorption structures 160A, 160B, 160C, each of which includes a plurality
of quantum dot structures 118 surrounded by a barrier material 122. The quantum dot
structures 118 of the third subcell 162 may have substantially similar or identical
average dimensions and may be formed to have an effective band-gap of less than that
of the quantum dot structures 118", 118'of the first subcell 150 and the second subcell
156. For example, the quantum dot structures 118 of the third subcell 162 may have
an effective band-gap of about 1.0 eV. As previously described, the dimensions of
the quantum dot structures 118 may be selected such that each of the absorption structures
160A, 160B, 160C, includes an absorption edge corresponding to another portion of
the electromagnetic spectrum. By way of non-limiting example, the absorption edge
of the absorption structures 160A, 160B, 160C, of the third subcell may correspond
to a different portion of the electromagnetic spectrum that those of the first subcell
150 and the second subcell 156. The barrier material 122 may be deposited over the
quantum dot structures 118 of each absorption structure 156 using methods similar
or identical to those described with respect to FIG. 3. An effective band-gap of the
barrier material 122 of the third subcell 162 is substantially reduced by reducing
a deposition temperature thereof to substantially increase incorporation of indium
therein and to substantially reduce or eliminate desorption of indium from overlying
materials (i.e., the barrier material 122" of the first subcell 150 and the barrier
material 122' of the second subcell 156 and quantum dot structures 118" and 118').
[0064] The subcells 150, 156, 162 of the partially formed photovoltaic structure 158 have
each been formed such that a deposition temperature used to form the individual subcells
150, 156, 162 is substantially decreased from subcell to subcell so each subcell includes
an increased indium content in comparison to an underlying subcell. As a result the
effective band-gap energy for each subcell 150, 156, 162, as shown in FIG. 10, is
highest in the lower subcell 150, nearest the base substrate 112, and is lowest in
upper subcell 162, or farthest from the base substrate 112. In contrast the indium
content for each subcell 150, 156, 162, as shown in FIG. 10, is lowest in the lower
subcell 150, nearest the base substrate 112, and is highest in upper subcell 162,
or farthest from the base substrate 112.
[0065] The decreasing deposition temperature during subcell formation aids in the prevention
of desorption of underlying subcells thereby improving the stability of the composition
of the underlying material and hence the effective band-gap of the underlying absorption
structures. The partially formed photovoltaic structure 158 may be inverted to operate
as an effective solar device.
[0066] Referring still to FIG. 10, another layer of semiconductor material 140 may be deposited
on the upper subcell (i.e., the third subcell 162) of the partially formed photovoltaic
structure 158. By way of example and not limitation, the layer of semiconductor material
114 may comprise a p-type doped semiconductor material and the another layer of semiconductor
material 140 may comprises an n-type doped semiconductor material.
[0067] Each subeell 150, 156, 162, and associated absorption structures 148A-C, 154A-C,
160A-C, may be formed to absorb a specific portion of the electromagnetic spectrum
depending on the number of subcells to be incorporated into the photovoltaic device.
Accordingly, an ideal absorption energy, and therefore an effective band-gap, of the
individual subcells may vary. As one non-limiting example, the effective band-gap
of each of the subcells 150, 156, 162 may be controlled by altering the dimensions
of the quantum dots structures 118 118', 118 in each subcell. In some embodiments,
the dimensions of the quantum dot structures 118", 118', 118 are varied from subcell-to-subcell
while the dimensions are maintained within individual subcells 150, 156, 162. As one
such example, shown in FIG. 10, the size of the quantum dot structures 118", 118',
118 in each of the subcells 150, 156, 162 may sequentially increase in relation to
the subcell's proximity to an electromagnetic radiation source. In other embodiments,
the physical size of the quantum dot structures 118", 118', 118 in each of the plurality
of subcells 150, 156, 162 may remain constant and a composition of the quantum dot
structures 118", 118', 118 may be varied to render a desired effective band-gap. For
simplicity, the partially formed photovoltaic structure 158 is shown including three
subcells, each including three absorption structures. However, the partially formed
photovoltaic structure 158 may be formed to include any number of subcells, each including
any number of absorption structures, using the methods described herein.
[0068] With reference to FIG. 11, the partially formed photovoltaic structure 164 is shown
including a bonding substrate 166 attached to semiconductor material 140 of the structure
depicted in FIG. 10. To fabricate the intermediate photovoltaic device 164, the structure
of FIG. 10 is inverted and attached to bonding substrate 166 using methods known in
the art. As a result, the band-gap energies are also inverted, placing the highest
effective band-gap energy subcell proximate to the incoming electromagnetic radiation.
However, the base substrate 112 may prevent absorption of incoming solar radiation
by the subcells. In some embodiments, the base substrate 112 is removed from the intermediate
structure 164 thereby forming a photovoltaic device 168, as shown in FIG. 12, capable
of transferring solar radiation into electrical energy. The base substrate 112 may
be removed by known methods such as ion implantation, etching, lift off, grinding,
and laser lift off. As one such non-limiting example the base substrate 112 may be
separated according to the Smart-Cut process described in detail in, for example,
U.S. Patent No. RE39,484 to Bruel,
U.S. Patent No. 6,303,468 to Aspar et al.,
U.S. Patent No. 6,335,258 to Aspar et al.,
6,756,286 to Moriceau et al.,
6,809,044 to Aspar et al., and
6,946,365 to Aspar et al.
[0069] For example, using embodiments of methods of the present invention described above,
an absorption structure may be formed to include a plurality of indium nitride quantum
dots structures surrounded by a gallium nitride barrier material. A gallium nitride
(GaN) material may be formed on a sapphire substrate by exposing the sapphire substrate
to, for example, ammonia and trimethylgallium, at a temperature of about 1170°C using
a metal organic chemical vapor deposition (MOCVD) process. Following growth of the
GaN material, indium nitride (InN) quantum dot structures thereon. The quantum dot
structures may be grown by exposing the gallium nitride to trimethylindium and ammonia
at a temperature of about 520°C for about 10 seconds to 60 seconds. The quantum dots
may have a density of about 1X10
12 cm
-2, a mean height of about 10 nm and a mean width of about 10 nm.
[0070] After formation of the InN quantum dots a barrier material of GaN may be deposited
over the quantum dots. The GaN in this example may be deposited at the same temperature
as the quantum dots using a trimethylgallium precursor. Alternatively, triethylgallium
may also be used as a precursor to the barrier material. As described herein, multiple
subcells may be fabricated according to the principles above.
[0071] Although embodiments of the present invention have been primarily described herein
with reference to layers of semiconductor material 114, 140 comprising indium gallium
nitride, the present invention is not so limited, and embodiments of the present invention
may be used to provide layers of semiconductor material comprising other III-nitride
materials, layers of other III-V type semiconductor materials, or layers of other
semiconductor materials (such as, for example, layer of II-VI type semiconductor materials,
layers of silicon, and layers of germanium). Additionally, although the embodiments
of the present invention have been primarily depicted herein with three subcells,
the present invention is not so limited and embodiments of the present invention may
include more or less subcells.
1. Verfahren zum Ausbilden einer Halbleiterstruktur oder Halbleitervorrichtung, Folgendes
umfassend:
Aufbringen wenigstens einer Schicht aus Halbleitermaterial (114) über einem Basissubstrat
(112),
Ausbilden einer Unterzelle (128), die eine oder mehrere Absorptionsstrukturen (124A,
124B, 124C) umfasst, wobei das Ausbilden jeder der einen oder mehreren Absorptionsstrukturen
Folgendes umfasst:
Anordnen mehrerer Quantenpunkte (118), die Indium-Gallium-Nitrid umfassen, und dies
derart, dass sie wenigstens einen Teil der wenigstens einen Schicht aus Halbleitermaterial
überlagern; und
Aufbringen eines Sperrschichtmaterials (122), das Indium-Gallium-Nitrid umfasst, bei
einer ersten Temperatur, wobei das Sperrschichtmaterial wenigstens einen Teil der
mehreren Quantenpunkte überlagert und wenigstens teilweise umgibt; und
Ausbilden wenigstens einer weiteren Unterzelle (136), die eine oder mehrere Absorptionsstrukturen
(134A, 134B, 134C) umfasst, wobei das Ausbilden jeder der einen oder mehreren Absorptionsstrukturen
Folgendes umfasst:
Anordnen mehrerer Quantenpunkte (118), die Indium-Gallium-Nitrid umfassen, und dies
derart, dass sie wenigstens einen Teil des Sperrschichtmaterials überlagern; und
Aufbringen eines weiteren Sperrschichtmaterials (122'), das Indium-Gallium-Nitrid
umfasst, bei einer zweiten Temperatur, wobei die zweite Temperatur niedriger ist als
die erste Temperatur, die zum Aufbringen des Sperrschichtmaterials verwendet wurde,
um eine weitere Unterzelle zu realisieren, die einen erheblich kleineren Indiumanteil
als die darunter liegende Unterzelle hat, wobei das weitere Sperrschichtmaterial wenigstens
einen Teil der mehreren Quantenpunkte überlagert und wenigstens teilweise umgibt.
2. Verfahren nach Anspruch 1, außerdem Folgendes umfassend:
Umdrehen der Halbleiterstruktur oder Halbleitervorrichtung;
Bonden eines Trägersubstrats an die Halbleiterstruktur oder Halbleitervorrichtung,
wobei das Trägersubstrat an eine Oberfläche der Halbleiterstruktur oder Halbleitervorrichtung
gebondet wird, die benachbart zur weiteren Unterzelle liegt; und
Entfernen des Basissubstrats.
3. Verfahren nach Anspruch 1, wobei das Aufbringen eines Sperrschichtmaterials, das Indium-Gallium-Nitrid
umfasst, auf den mehreren Quantenpunkten und diese wenigstens teilweise umgebend das
Aufbringen eines Sperrschichtmaterials umfasst, das einen erheblich kleineren Indiumanteil
hat als ein Indiumanteil der mehreren Quantenpunkte.
4. Verfahren nach Anspruch 3, wobei das Aufbringen eines Sperrschichtmaterials, das einen
erheblich kleineren Indiumanteil hat als ein Indiumanteil der mehreren Quantenpunkte,
das Aufbringen des Sperrschichtmaterials bei einer Temperatur umfasst, die größer
ist als eine Wachstumstemperatur der mehreren Quantenpunkte.
5. Verfahren nach Anspruch 1, wobei das Ausbilden der wenigstens einen weiteren Unterzelle,
die eine oder mehrere Absorptionsstrukturen umfasst, das Ausbilden wenigstens einer
weiteren Absorptionsstruktur umfasst, die eine erheblich niedrigere effektive Bandlücke
als die darunter liegende Unterzelle aufweist.
6. Verfahren nach Anspruch 1, wobei das Anordnen mehrerer Quantenpunkte, die Indium-Gallium-Nitrid
umfassen, und dies derart, dass sie wenigstens einen Teil des Sperrschichtmaterials
überlagern, das Aufwachsen der mehreren Quantenpunkte auf einer Zwischenschicht umfasst,
die auf dem Sperrschichtmaterial angeordnet ist.
7. Verfahren nach Anspruch 1, wobei das Anordnen mehrerer Quantenpunkte, die Indium-Gallium-Nitrid
umfassen, und dies derart, dass sie wenigstens einen Teil des Sperrschichtmaterials
überlagern, das Aufwachsen der mehreren Quantenpunkte direkt auf dem Sperrschichtmaterial
umfasst.
8. Photovoltaik-Struktur, Folgendes umfassend:
mehrere Unterzellen (124A, 124B, 124C, 134A, 134B, 134C) in einer gestapelten Anordnung,
die eine erste Schicht aus Halbleitermaterial (114) auf einem Substrat (112) überlagert,
wobei eine Bandlücke einer zum Substrat benachbarten Unterzelle erheblich kleiner
ist als diejenige wenigstens einer darüber liegenden Unterzelle und wobei jede der
mehreren Unterzellen folgendes umfasst:
mehrere Quantenpunkte (118), von denen jeder wenigstens eines der folgenden Elemente
umfasst: Indium, Gallium, Aluminium;
ein III-Nitrid-Material, das die mehreren Quantenpunkte einkapselt; und eine zweite
Schicht aus Halbleitermaterial, die eine obere Oberfläche der mehreren Unterzellen
überlagert, wobei die zweite Schicht aus Halbleitermaterial verschieden vom ersten
Halbleitermaterial ist,
dadurch gekennzeichnet, dass die zum Substrat benachbarte Unterzelle Indium-Gallium-Nitrid umfasst, das, verglichen
mit Unterzellen der weiter entfernt vom Substrat liegenden Anzahl, einen erheblich
verringerten Indiumanteil aufweist, und wobei ein mittlerer Durchmesser der Quantenpunktstrukturen
der benachbart zum Substrat liegenden Unterzelle erheblich kleiner ist als ein mittlerer
Durchmesser der Quantenpunktstrukturen von Unterzellen der weiter entfernt vom Substrat
liegenden Anzahl.
9. Struktur nach Anspruch 8, wobei eine effektive Bandlücke des wenigstens einen Sperrschichtmaterials
verschieden von einer effektiven Bandlücke der mehreren Quantenpunkte ist.
10. Struktur nach Anspruch 8, wobei jede Unterzelle der Anzahl Quantenpunkte umfasst,
die im Wesentlichen dieselben mittleren Abmessungen haben.
11. Struktur nach Anspruch 8, wobei die Quantenpunktstrukturen jeder Unterzelle eine effektive
Bandlücke haben, die kleiner ist als eine effektive Bandlücke des III-Nitrid-Materials.