Patent Application
20240049490
The present disclosure relates to a photoelectric conversion element and an imaging device.
Studies have been actively conducted on photoelectric conversion elements in which semiconductor quantum dots are used as a photoelectric conversion material to utilize the quantum size effect. Semiconductor quantum dots are nanocrystals that are semiconductor microcrystals with a size of several nanometers. The quantum size effect is a phenomenon in which when electrons, holes, and excitons are confined within the nanocrystal, the energy state is discretized, and, consequently, a particle-size-dependent energy shift appears. As the particle size of semiconductor quantum dots, which are nanocrystals, decreases, the energy gap of the semiconductor quantum dots becomes larger than the energy gap of bulk crystals, and, accordingly, an absorption edge wavelength of the semiconductor quantum dots shifts to shorter wavelengths. That is, controlling the particle size of a semiconductor material enables the semiconductor material to have a light absorption wavelength tuned to any desired wavelength, with the upper limit thereof being the absorption edge wavelength of the bulk crystal. In the following description, the “semiconductor quantum dots” are also referred to simply as “quantum dots”. In instances where quantum dots are used as a photoelectric conversion material, it is desirable that the quantum dots have a wide sensitive wavelength range suited to the application.
Japanese Patent No. 6083813 discloses a technology that can broaden the sensitive wavelength range, and the technology involves forming a photoelectric conversion layer by mixing quantum dots of different particle sizes.
Japanese Patent No. 6255417 discloses a technology that can broaden the sensitive wavelength range, and the technology involves stacking a layer formed of quantum dots having a small particle size and a layer formed of quantum dots having a large particle size, thereby modulating a bandgap at an interface therebetween.
Japanese Patent No. 6298223 discloses a technology that improves the mobility of photo-generated carriers, and the technology involves varying thicknesses and components of ligand layers that modify a surface of quantum dots, thereby controlling the band structure and providing an energy band gradient between two quantum dot semiconductor layers.
In one general aspect, the techniques disclosed here feature a photoelectric conversion element that includes a photoelectric conversion layer, a first electrode, and a second electrode. The first electrode collects holes generated in the photoelectric conversion layer. The second electrode is positioned opposite to the first electrode with the photoelectric conversion layer being disposed between the second electrode and the first electrode and collects electrons generated in the photoelectric conversion layer. The photoelectric conversion layer includes a first quantum dot layer and a second quantum dot layer. The first quantum dot layer includes a plurality of first quantum dots, each of the plurality of first quantum dots having a surface modified with a first ligand. The second quantum dot layer is located between the first quantum dot layer and the second electrode and includes a plurality of second quantum dots, each of the plurality of second quantum dots having a surface modified with a second ligand that is different from the first ligand. The second quantum dot layer has an ionization potential greater than an ionization potential of the first quantum dot layer. A second value that represents a particle diameter distribution of the plurality of second quantum dots is less than a first value that represents a particle diameter distribution of the plurality of first quantum dots.
Additional benefits and advantages of the disclosed embodiments will become apparent from the specification and drawings. The benefits and/or advantages may be individually obtained by the various embodiments and features of the specification and drawings, which need not all be provided in order to obtain one or more of such benefits and/or advantages.
While Japanese Patent No. 6083813, Japanese Patent No. 6255417, and Japanese Patent No. 6298223 disclose the broadening of the sensitive wavelength range or an improvement in mobility associated with the use of quantum dots as a photoelectric conversion material, they do not provide disclosures about a dark current, which is important for realizing a high-performance photodiode and a high-performance imaging device. In photodiodes and imaging devices, the dark current directly affects a signal-to-noise (S/N) ratio. Accordingly, for their practical use, it is desirable that the dark current be lower than that of power generation elements such as solar cells by at least several orders of magnitude.
An object of the present disclosure is to provide photoelectric conversion elements and an imaging device that can have both an extended sensitive wavelength range and a reduced dark current.
An overview of aspects of the present disclosure is as follows.
According to an aspect of the present disclosure, a photoelectric conversion element includes a photoelectric conversion layer, a first electrode, and a second electrode. The first electrode collects holes generated in the photoelectric conversion layer. The second electrode is positioned opposite to the first electrode with the photoelectric conversion layer being disposed between the second electrode and the first electrode and collects electrons generated in the photoelectric conversion layer. The photoelectric conversion layer includes a first quantum dot layer and a second quantum dot layer. The first quantum dot layer includes a plurality of first quantum dots, each of the plurality of first quantum dots having a surface modified with a first ligand. The second quantum dot layer is located between the first quantum dot layer and the second electrode and includes a plurality of second quantum dots, each of the plurality of second quantum dots having a surface modified with a second ligand that is different from the first ligand. The second quantum dot layer has an ionization potential greater than an ionization potential of the first quantum dot layer. A second value that represents a particle diameter distribution of the plurality of second quantum dots is less than a first value that represents a particle diameter distribution of the plurality of first quantum dots.
As described, the photoelectric conversion layer includes the first quantum dots and the second quantum dots that have different respective particle diameters. As a result, a sensitive wavelength range can be extended, because an absorption wavelength of quantum dots depends on the particle diameter of the quantum dots. Furthermore, in the photoelectric conversion layer, the ionization potential of the second quantum dot layer located near the second electrode is greater than the ionization potential of the first quantum dot layer. As a result, excitons that are generated by absorption of light efficiently dissociate into electrons and holes at an interface between the first quantum dot layer and the second quantum dot layer. The holes migrate through the first quantum dot layer and are collected by the first electrode, and the electrons migrate through the second quantum dot layer and are collected by the second electrode. Thus, the electrical charges flow smoothly, which can improve photoelectric conversion efficiency. Furthermore, the second quantum dots have a particle diameter smaller than that of the first quantum dots. Consequently, the second quantum dot layer has a large bandgap, and, therefore, a difference between the ionization potential of the first quantum dot layer and an electron affinity of the second quantum dot layer is likely to increase. As a result, thermal excitation is unlikely to occur at the interface between the first quantum dot layer and the second quantum dot layer. Consequently, a dark current due to thermal excitation at the interface between the first quantum dot layer and the second quantum dot layer can be reduced. Accordingly, the photoelectric conversion element according to this aspect can have both an extended sensitive wavelength range and a reduced dark current.
Furthermore, for example, the plurality of first quantum dots and the plurality of second quantum dots may each independently include at least one of CdSe, CdS, PbS, PbSe, PbTe, ZnO, ZnS, Cu2ZnSnS4, Cu2S, Bi2S3, CuInSe2, AgInS2, AgInTe2, CdSnAs2, ZnSnAs2, ZnSnSb2, Ag2S, Ag2Te, HgTe, CdHgTe, Ge, GeSn, InAs, or InSb. In other words, the plurality of first quantum dots and the plurality of second quantum dots may each independently include at least one selected from the group consisting of CdSe, CdS, PbS, PbSe, PbTe, ZnO, ZnS, Cu2ZnSnS4, Cu2S, Bi2S3, CuInSe2, AgInS2, AgInTe2, CdSnAs2, ZnSnAs2, ZnSnSb2, Ag2S, Ag2Te, HgTe, CdHgTe, Ge, GeSn, InAs, and InSb.
Combining any of these enables the sensitive wavelength of the photoelectric conversion element to be controlled as desired over a broad wavelength range from visible to infrared.
Furthermore, for example, the first ligand may have a first dipole moment, the second ligand may have a second dipole moment, and the first dipole moment may be greater than the second dipole moment provided that the first dipole moment is positive when the first dipole moment points outside of each of the plurality of first quantum dots, and that the second dipole moment is positive when the second dipole moment points outside of each of the plurality of second quantum dots.
In this case, the ionization potential of the first quantum dot layer can be easily reduced by the first ligand, and the ionization potential of the second quantum dot layer can be easily increased by the second ligand. Accordingly, an ionization potential of the second quantum dot layer greater than the ionization potential of the first quantum dot layer can be easily achieved, and, consequently, a photoelectric conversion element having both an extended sensitive wavelength range and a reduced dark current can be realized.
Furthermore, for example, the first ligand may be 1,4-benzenedithiol, and the second ligand may be a mixture of ZnI2 and 3-mercaptopropionic acid.
In this case, an extended sensitive wavelength range and a reduced dark current can be effectively achieved.
Furthermore, for example, at least one of the particle diameter distribution of the plurality of first quantum dots and the particle diameter distribution of the plurality of second quantum dots may have at least two different local maximum values. In other words, at least one selected from the group consisting of the particle diameter distribution of the plurality of first quantum dots and the particle diameter distribution of the plurality of second quantum dots may have at least two different local maximum values.
In this case, the sensitive wavelength range of the photoelectric conversion element can be further extended.
According to another aspect of the present disclosure, an imaging device includes a plurality of pixels, and the plurality of pixels each include the photoelectric conversion element.
Since the imaging device includes the photoelectric conversion element, the imaging device can have both an extended sensitive wavelength range and a reduced dark current.
Furthermore, for example, the imaging device may further include a signal readout circuit and a voltage supply circuit. The signal readout circuit may be connected to the first electrode. The voltage supply circuit may supply a voltage to the second electrode. A potential of the second electrode may be positive with respect to a potential of the first electrode when the voltage is supplied to the second electrode.
In this case, with the use of the photoelectric conversion element, the imaging device can read out the holes collected by the first electrode, which serve as signal charges.
Alternatively, for example, the imaging device may further include a signal readout circuit and a voltage supply circuit. The signal readout circuit may be connected to the second electrode. The voltage supply circuit may supply a voltage to the first electrode. A potential of the first electrode may be negative with respect to a potential of the second electrode when the voltage is supplied to the first electrode.
In this case, with the use of the photoelectric conversion element, the imaging device can read out the electrons collected by the second electrode, which serve as signal charges.
According to another aspect of the present disclosure, a photoelectric conversion element includes a photoelectric conversion layer, a first electrode, and a second electrode. The first electrode collects holes generated in the photoelectric conversion layer. The second electrode is positioned opposite to the first electrode with the photoelectric conversion layer being disposed between the second electrode and the first electrode and collects electrons generated in the photoelectric conversion layer. The photoelectric conversion layer includes a first quantum dot layer and a second quantum dot layer. The first quantum dot layer includes a plurality of first quantum dots, each of the plurality of first quantum dots having a surface modified with a first ligand. The second quantum dot layer is located between the first quantum dot layer and the second electrode and includes a plurality of second quantum dots, each of the plurality of second quantum dots having a surface modified with a second ligand that is different from the first ligand. The second quantum dot layer has an ionization potential greater than an ionization potential of the first quantum dot layer. An absorption peak wavelength of the plurality of second quantum dots is shorter than an absorption peak wavelength of the plurality of first quantum dots. A material of the plurality of first quantum dots is different from a material of the plurality of second quantum dots.
Furthermore, for example, a second value that represents a particle diameter distribution of the plurality of second quantum dots may be equal to a first value that represents a particle diameter distribution of the plurality of first quantum dots.
Alternatively, for example, a second value that represents a particle diameter distribution of the plurality of second quantum dots may be greater than a first value that represents a particle diameter distribution of the plurality of first quantum dots.
Embodiments of the present disclosure will now be described with reference to the drawings.
Note that all the embodiments described below present a generic or specific example. The numerical values, shapes, constituent elements, placement positions and forms of connection of the constituent elements, steps, orders of the steps, and the like that are presented in the embodiments described below are merely illustrative and are not intended to limit the present disclosure. Furthermore, of the constituent elements described in the present embodiments below, constituent elements not recited in the independent claims are described as optional constituent elements. Furthermore, the drawings are not necessarily precise illustrations. Accordingly, the drawings are not necessarily to scale, for example. Furthermore, in the drawings, substantially the same components are assigned the same reference signs, and redundant descriptions may be omitted or simplified.
Furthermore, in this specification, terms indicating a relationship between elements, terms indicating a shape of an element, and numerical ranges do not necessarily have strict meanings; that is, substantially equivalent ranges that differ, for example, by approximately several percent are also encompassed.
Furthermore, in this specification, the terms “above” and “below” do not refer to an upward (vertically upper) direction or a downward (vertically lower) direction based on an absolute space recognition, and the terms define relative positional relationships based on a stacking order of a stack configuration. Note that terms such as “above” and “below” are used to specify a mutual arrangement of components and are not intended to limit an orientation of an imaging device during use. Furthermore, the terms “above” and “below” are used not only in instances in which two constituent elements are spaced from each other with a different constituent element being present between the two constituent elements but also in instances in which two constituent elements are disposed on each other, that is, the two constituent elements are in contact with each other.
Furthermore, in this specification, electromagnetic waves in general, including visible light, infrared light, and ultraviolet light, are referred to as “light” for convenience.
First, an overall configuration of a photoelectric conversion element according to the present embodiment will be described.
The photoelectric conversion element 10A may further include an electron blocking layer and a hole blocking layer.
As illustrated in
Now, details of the components of the photoelectric conversion elements of the present embodiment will be described.
The substrate 1 is a supporting substrate that supports the photoelectric conversion element 10A and the photoelectric conversion element 10B. A material of the substrate 1 is not particularly limited and may be any of a variety of materials. For example, the substrate 1 may be a p-type silicon substrate or a glass or plastic substrate coated with a conductive metal oxide, such as ITO (indium tin oxide), or with a conductive polymer, such as polyacetylene. The substrate 1 is, for example, transmissive to at least a portion of light of a wavelength that is absorbed by the photoelectric conversion layer 4.
In the illustrated examples, the substrate 1 is disposed adjacent to the first electrode 2 of the photoelectric conversion element 10A and the photoelectric conversion element 10B. Alternatively, the substrate 1 may be disposed adjacent to the second electrode 3 of the photoelectric conversion element 10A and the photoelectric conversion element 10B.
The first electrode 2 and the second electrode 3 are electrodes in the form of a film, for example. The first electrode 2 is a hole-collecting electrode that collects holes generated in the photoelectric conversion layer 4, and the second electrode 3 is an electron-collecting electrode that collects electrons generated in the photoelectric conversion layer 4. The second electrode 3 is positioned opposite to the first electrode 2 with the photoelectric conversion layer 4 being disposed between the second electrode 3 and the first electrode 2.
At least one of the first electrode 2 and the second electrode 3 is a transparent electrode that is highly transmissive to light over a desired wavelength range. A desired wavelength is, for example, a wavelength range including absorption peaks of the first quantum dots and the second quantum dots. Furthermore, in this specification, “being highly transmissive to light at a certain wavelength” means, for example, that a light transmittance at the wavelength is greater than or equal to 50% or may mean that the light transmittance is greater than or equal to 80%.
A bias voltage is applied across the first electrode 2 and the second electrode 3 via an interconnect (not illustrated), for example. A polarity of the bias voltage is determined, for example, such that the electrons of the electron-hole pairs generated in the photoelectric conversion layer 4 can move to the second electrode 3, and the holes thereof can move to the first electrode 2. Specifically, a bias voltage in which a potential of the second electrode 3 is positive with respect to a potential of the first electrode 2 is applied. Accordingly, the first electrode 2 collects the holes, and the second electrode 3 collects the electrons. It is also possible to enable the holes to be collected by the first electrode 2 and the electrons to be collected by the second electrode 3 by reducing the work function of the second electrode 3 with respect to the work function of the first electrode 2
In instances where the first electrode 2 and the second electrode 3 are highly transmissive to light over a desired wavelength range, examples of materials thereof include a transparent conducting oxide (TCO) with a low resistance value. Examples of the TCO include, but are not limited to, ITO, IZO (InZnO: indium zinc oxide), AZO (AlZnO: aluminum zinc oxide), FTO (fluorine-doped tin oxide), SnO2, TiO2, and ZnO2.
Other examples of the materials of the first electrode 2 and the second electrode 3 include Al, Cu, Ti, TiN, Ta, TaN, Mo, Ru, In, Mg, Ag, Au, and Pt.
Hole-electron pairs, which are excitons, are produced in the photoelectric conversion layer 4 when light enters the photoelectric conversion layer 4. The photoelectric conversion layer 4 includes, as photoelectric conversion materials, quantum dots having different particle sizes so that a sensitive wavelength range of the photoelectric conversion element 10A can be extended. A quantum dot is a nanocrystal having a diameter of approximately 2 nm to 10 nm and formed of approximately dozens of atoms. Examples of materials of the quantum dots include group IV semiconductors, such as Si and Ge, group IV-VI semiconductors, such as PbS, PbSe, and PbTe, group III-V semiconductors, such as InAs and InSb, and ternary mixed crystals, such as HgCdTe and PbSnTe.
Specifically, the photoelectric conversion layer 4 includes the first quantum dot layer 4a, which includes the first quantum dots, and the second quantum dot layer 4b, which includes the second quantum dots. The first quantum dot layer 4a and the second quantum dot layer 4b each generate hole-electron pairs upon absorption of light. In the photoelectric conversion layer 4, the first quantum dot layer 4a is located adjacent to the first electrode 2, which is a hole-collecting electrode, and the second quantum dot layer 4b is located adjacent to the second electrode 3, which is an electron-collecting electrode. The first quantum dots and the second quantum dots may each independently include, for example, at least one of CdSe, CdS, PbS, PbSe, PbTe, ZnO, ZnS, Cu2ZnSnS4 (CZTS), Cu2S, Bi2S3, CuInSe2, AgInS2, AgInTe2, CdSnAs2, ZnSnAs2, ZnSnSb2, Ag2S, Ag2Te, HgTe, CdHgTe, Ge, GeSn, InAs, and InSb. Using any of these enables the sensitive wavelength of the photoelectric conversion element to be freely controlled over a broad wavelength range from visible to infrared.
A second value that represents a particle diameter distribution of the plurality of second quantum dots is less than a first value that represents a particle diameter distribution of the plurality of first quantum dots. The first value and the second value are measured values of modal diameters that are local maximum values in a particle diameter distribution of the particles in an instance in which, for example, the distribution is obtained by using, for instance, a transmission electron microscope and expressed as a frequency distribution. Furthermore, for example, the second value may be a maximum value among the particle diameters exhibiting the local maximum values in the particle diameter distribution of the second quantum dots, and the first value may be a minimum value among the particle diameters exhibiting the local maximum values in the particle diameter distribution of the first quantum dots. Note that the first value and the second value may each be an average particle diameter that is an average of the particle diameters of multiple quantum dots that are randomly selected from each of the layers.
Furthermore, at least one of the particle diameter distribution of the first quantum dots and the particle diameter distribution of the second quantum dots may have at least two different local maximum values. In this case, the sensitive wavelength range of the photoelectric conversion element 10A can be further extended. In the instance where a particle diameter distribution of quantum dots has at least two different local maximum values, the particle diameter is, for example, an average of the particle diameters indicated by the at least two local maximum values.
Furthermore, since an absorption peak wavelength of quantum dots depends on the particle diameter, the particle diameter of quantum dots can be represented by the absorption peak wavelength. For example, the absorption peak wavelength of quantum dots corresponds to the modal diameter of the quantum dots. Specifically, quantum dots with longer absorption peak wavelengths have larger particle diameters, and quantum dots with shorter absorption peak wavelengths have smaller particle diameters. Accordingly, the first quantum dots have an absorption peak at a wavelength longer than the absorption peak wavelength of the second quantum dots. Furthermore, the first quantum dots may have an absorption peak at a wavelength longer than the absorption peak wavelength of the second quantum dots by 100 nm or greater.
The particle size of the quantum dots can be controlled by adjusting a reaction time and temperature in an existing method for growing quantum dots. Accordingly, quantum dots having, for example, a substantially uniform particle diameter can be obtained. Examples of the quantum dots having a uniform particle diameter include quantum dots having a single absorption peak in a near-infrared range. The first quantum dots and the second quantum dots may each be formed of one type of quantum dots having a uniform particle diameter or may be formed of multiple types of quantum dots with each type having a uniform particle diameter. In the instance where the first quantum dots and the second quantum dots are each formed of multiple types of quantum dots with each type having a uniform particle diameter, a minimum particle diameter of the particle diameters of the multiple types of quantum dots that form the first quantum dots is greater than a maximum particle diameter of the particle diameters of the multiple types of quantum dots that form the second quantum dots.
The first quantum dots and the second quantum dots may each have an absorption peak in the near-infrared range. Furthermore, at least one of the first quantum dots and the second quantum dots may have multiple absorption peaks in the near-infrared range. In the instance where at least one of the first quantum dots and the second quantum dots have multiple absorption peaks in the near-infrared range, the longest absorption peak wavelength of the second quantum dots is shorter than the shortest absorption peak wavelength of the first quantum dots, in the near-infrared range.
The first quantum dots and the second quantum dots not only have different respective particle sizes but also are coated with different respective surface-modifying ligands. Specifically, a surface of the first quantum dots is modified with a first ligand, and a surface of the second quantum dots is modified with a second ligand that is different from the first ligand.
The measurement of the ionization potential was performed with a photoelectron yield spectrometer (AC-3, manufactured by Riken Keiki Co., Ltd.) under a nitrogen atmosphere. The number of photoelectrons was measured at various levels of UV radiation energy, and the ionization potential was determined as the energy location at which photoelectrons began to be detected. The measurement of the electron affinity was performed as follows. First, an absorption spectrum of the quantum dots was measured, and then, an optical bandgap was calculated from the result of an absorption edge wavelength of the obtained absorption spectrum. Thereafter, the electron affinity was calculated from the ionization potential, which was measured in the described manner, and the calculated optical bandgap. In
As shown in
As illustrated in
Accordingly, in the present embodiment, regarding a comparison between the ionization potential and the electron affinity, the first quantum dot layer 4a, which has relatively low values thereof, is positioned nearer the first electrode 2, which collects holes, than is the second quantum dot layer 4b, and the second quantum dot layer 4b, which has relatively high values of the ionization potential and the electron affinity, is positioned nearer the second electrode 3, which collects electrons, than is the first quantum dot layer 4a. That is, a configuration is realized in which when the electron-hole pairs, which are excitons generated by the entrance of light, are dissociated, the holes are collected by the first electrode 2, and the electrons are collected by the second electrode 3, in the absence of an energy barrier under the bias voltage, which is described above. In such a configuration, an interface between the first quantum dot layer 4a and the second quantum dot layer 4b can be regarded as a heterojunction interface. An energy difference at the heterojunction interface and an electric field of a depletion layer formed at the interface enable the excitons generated by the absorption of light to be dissociated into electrons and holes, and, accordingly, photoelectric conversion efficiency, that is, quantum efficiency, is improved.
Furthermore, since the second quantum dot layer 4b, which is positioned adjacent to the second electrode 3 that collects electrons, is formed of quantum dots having a particle size smaller than that of the quantum dots of the first quantum dot layer 4a, which is positioned adjacent to the first electrode 2 that collects holes, a dark current that may be thermally induced at the interface between the first quantum dot layer 4a and the second quantum dot layer 4b can be reduced. It is presumed that the dark current that may be thermally induced is correlated with an energy difference ΔEQD at the interface between the first quantum dot layer 4a and the second quantum dot layer 4b, illustrated in
As described above, the ionization potential of quantum dots is independent of the particle size and depends on the surface-modifying ligand. On the other hand, an energy gap of quantum dots depends on the particle size. Quantum dots with smaller particle sizes, that is, larger energy gaps, tend to have lower electron affinities. Accordingly, as described above, when the ionization potential of the second quantum dot layer 4b is greater than the ionization potential of the first quantum dot layer 4a, because of the surface-modifying ligand, the smaller the particle size of the second quantum dots that are included in the second quantum dot layer 4b, the larger the energy gap of the second quantum dot layer 4b, and, consequently, the larger the energy difference ΔEQD. Thus, a stack configuration (I) can increase the energy difference ΔEQD to a greater extent than a stack configuration (II), where the stack configuration (I) is constituted by (i) the first quantum dot layer 4a made of a combination of the first ligand and the first quantum dots and (ii) the second quantum dot layer 4b made of a combination of the second ligand and the second quantum dots, and the stack configuration (II) is constituted by (i) a quantum dot layer made of a combination of the first ligand and the second quantum dots and (ii) a quantum dot layer made of a combination of the second ligand and the first quantum dots. Consequently, a photoelectric conversion element having a further reduced dark current can be realized.
As described above with reference to
In instances where two types of surface-modifying ligands in which the dipole moments of the surface-modifying ligands have the same direction are compared, the ionization potential varies depending on the magnitude relationship between the magnitudes of the dipole moments. For example, in instances where in two different types of surface-modifying ligands, the dipole moments of the surface-modifying ligands point outside of the quantum dots, one of the surface-modifying ligands that has a larger dipole moment tends to provide a lower ionization potential. That is, assuming that the dipole moment of a surface-modifying ligand adsorbed on the surface of quantum dots is positive when the dipole moment points outside of the quantum dots, larger dipole moments of a surface-modifying ligand in the positive direction tend to result in lower ionization potentials, and, on the contrary, larger dipole moments in the negative direction tend to result in higher ionization potentials. Note that in instances where the surface-modifying ligand is one in which the dipole moment cannot be defined, such as ions of elements, the dipole moment at the interface between the surface-modifying ligand and the quantum dots becomes dominant. The dipole moment of the surface-modifying ligand and the dipole moment at the interface between the surface-modifying ligand and the quantum dots can be determined by calculation based on the density functional theory.
The surface-modifying ligand may be any ligand as long as the ligand can be coordinated to quantum dots. For example, the surface-modifying ligand may be an organic compound, such as an alkyl ammonium salt or a thiol, or may be an inorganic compound, such as a halide salt. The halide salt may be used as a mixture of the halide salt and a carboxylic acid terminated thiol, such as 3-mercaptopropionic acid.
Specifically, examples of the surface-modifying ligand that has a positive charge on the side opposite to the quantum dot-side of the surface-modifying ligand and has a dipole moment pointing outside of the quantum dots include compounds having a structure in which, when a thiol group is coordinated, a localized positive charge is created on an opposite side. Examples of the compounds include 1,2-ethanedithiol (1,2-EDT) and 1,4-benzenedithiol (1,4-BDT). Other examples of the surface-modifying ligand that has a dipole moment pointing outside of the quantum dots include compounds having a carboxyl group that is coordinated to the surface of the quantum dots and having an electron-donating group on a side opposite to that of the carboxyl group, and examples of the compounds include 4-methoxycinnamic acid. Examples of the surface-modifying ligand that has a dipole moment pointing outside of the quantum dots include compounds having a backbone that enables a coordination in which an electron-donating moiety, such as a phenol or an aniline, is positioned on an outer side with respect to the quantum dots.
Examples of the surface-modifying ligand that has a negative charge on the side opposite to the quantum dot-side of the surface-modifying ligand and has a dipole moment pointing inside of the quantum dots include halogen-ion-containing compounds, such as lead halide; zinc halide; mixtures of either of these and 3-mercaptopropionic acid; and tetrabutylammonium halides. Examples of the halogen include chlorine, bromine, and iodine. Other examples of the surface-modifying ligand that has a dipole moment pointing inside of the quantum dots include compounds having a backbone that enables a coordination in which an electron-withdrawing moiety, such as a cyano group, a carbonyl group, or a nitro group, is positioned on an outer side with respect to the quantum dots.
In many cases, available quantum dots have a surface modified with a surface-modifying ligand containing a long-chain alkyl so that high dispersibility can be achieved during synthesis. Since the surface-modifying ligand containing a long-chain alkyl hinders the movement of charges, the surface-modifying ligand is displaced with the first ligand or the second ligand. Known methods for the displacement include solid-state displacement methods, in which quantum dots are formed into a film (solid phase) and subsequently exposed to a solution of a displacing surface-modifying ligand, to accomplish displacement by using a difference in a concentration and a difference in a binding energy between the ligands; and liquid-state displacement methods, in which displacement between the surface-modifying ligands is carried out in a solution (liquid phase). Any of these known methods may be used.
In the present embodiment, for example, the first ligand has a first dipole moment, and the second ligand has a second dipole moment. The first dipole moment is greater than the second dipole moment provided that the first dipole moment is positive when the first dipole moment points outside of the first quantum dots, and that the second dipole moment is positive when the second dipole moment points outside of the second quantum dots. That is, subtracting the second dipole moment from the first dipole moment gives a positive dipole moment. Consequently, the ionization potential of the second quantum dot layer 4b can be easily made to be greater than the ionization potential of the first quantum dot layer 4a. For example, the first dipole moment may be a positive dipole moment pointing outside of the first quantum dots, and the second dipole moment may be a negative dipole moment pointing inside of the second quantum dots. Specifically, the first ligand may be a thiol-group-containing compound, such as 1,4-benzenedithiol, and the second ligand may be a halogen-ion-containing compound, such as a mixture of ZnI2 and 3-mercaptopropionic acid. Combining such surface-modifying ligands facilitates improvement in photoelectric conversion efficiency while reducing the dark current.
In the present embodiment, the holes of the hole-electron pairs generated in the photoelectric conversion layer 4 are collected by the first electrode 2, and the electrons thereof are collected by the second electrode 3. In this process, there is a possibility that charges with polarities opposite to those of the respective charges collected by the first electrode 2 and the second electrode 3 may be injected into the photoelectric conversion layer 4 from the first electrode 2 and the second electrode 3. These charges injected from the electrodes are a cause of a dark current that flows regardless of whether light enters the photoelectric conversion layer 4.
Accordingly, photoelectric conversion elements of the present embodiment may include the electron blocking layer 5, which is used for suppressing the dark current, between the first electrode 2 and the first quantum dot layer 4a, as in the photoelectric conversion element 10B, illustrated in
For example, a material of the electron blocking layer 5 is a material that satisfies the relationships regarding the electron affinity and the ionization potential. The material is, for example, a p-type semiconductor. The material of the electron blocking layer 5 may be an organic material, such as [N4,N4′-di(naphthalen-1-yl)-N4,N4′-bis(4-vinylphenyl)biphenyl-4,4′-diamine] (VNPB) or poly[N,N′-bis(4-butylphenyl)-N,N′-bis(phenyl)-benzidine] (poly-TPD), or a metal oxide, such as NiO, CoO, Co3O4, Cr2O3, Cu2O, or CuO.
Likewise, photoelectric conversion elements of the present embodiment may include the hole blocking layer 6 between the second electrode 3 and the second quantum dot layer 4b, as in the photoelectric conversion element 10B, illustrated in
For example, a material of the hole blocking layer 6 is a material that satisfies the relationships regarding the electron affinity and the ionization potential. The material is, for example, an n-type semiconductor. Examples of the material of the hole blocking layer 6 include bathocuproine (BCP), bathophenanthroline (BPhen), fullerenes, zinc oxide, aluminum-doped zinc oxide, titanium oxide, and tin oxide.
The electron blocking layer 5 has hole conductivity for transporting holes. The hole blocking layer 6 has electron conductivity for transporting electrons. Accordingly, since the first quantum dot layer 4a is in contact with the electron blocking layer 5, the first quantum dot layer 4a is electrically connected to the first electrode 2 via the electron blocking layer 5. Furthermore, since the second quantum dot layer 4b is in contact with the hole blocking layer 6, the second quantum dot layer 4b is electrically connected to the second electrode 3 via the hole blocking layer 6.
Note that the photoelectric conversion element 10B need not necessarily include both of the electron blocking layer 5 and the hole blocking layer 6.
Now, a second embodiment will be described. The second embodiment describes an imaging device that uses a photoelectric conversion element of the first embodiment. In the following description of the second embodiment, differences from the first embodiment will be mainly described, and descriptions of common features will be omitted or simplified.
First, an overall configuration of the imaging device according to the present embodiment will be described.
The pixels 20 are arranged on a semiconductor substrate one-dimensionally or two-dimensionally to form a light-sensitive area, which is a so-called pixel area. In the configuration illustrated in
The plurality of pixels 20 each include a photoelectric converter 10C and a signal detection circuit 40, which detects a signal generated by the photoelectric converter 10C. The signal detection circuit 40 is an example of a signal readout circuit. The photoelectric converter 10C includes the first electrode 2, the second electrode 3, and the photoelectric conversion layer 4 disposed therebetween. For example, the photoelectric converter 10C is formed of the photoelectric conversion element 10A or the photoelectric conversion element 10B of the first embodiment. The first electrode 2 serves as a charge collector. The signal detection circuit 40 is connected to the first electrode 2. The second electrode 3 is connected to the voltage supply circuit 30 via a storage control line 22. In the operation of the imaging device 100, a predetermined bias voltage is applied to the second electrode 3 via the storage control line 22. In the present embodiment, the first electrode 2 is a pixel electrode that collects signal charges, and the second electrode 3 is a counter electrode positioned opposite to the pixel electrode.
The photoelectric converter 10C has a configuration in which the holes (i.e., positive charges) of the electron-hole pairs generated by photoelectric conversion are collected as signal charges by the first electrode 2. Controlling the potential of the second electrode 3 by using a bias voltage generated by the voltage supply circuit 30 enables the holes to be collected by the first electrode 2. The voltage supply circuit 30 provides a voltage to the second electrode 3 via the storage control line 22. The voltage is a voltage in which the potential of the second electrode 3 is positive with respect to the potential of the first electrode 2. Specifically, for example, a voltage of approximately 10 V is applied to the storage control line 22 so that the potential of the second electrode 3 can be higher than that of the first electrode 2.
In the configuration illustrated in
Note that, in this specification, the “semiconductor substrate” is not limited to a substrate formed entirely of a semiconductor and may be, for instance, an insulating substrate including a semiconductor layer provided on a surface on the side on which the light-sensitive area is to be formed. An example of the semiconductor substrate is a p-type silicon substrate.
As illustrated in
A voltage corresponding to the signal charges stored at the charge storage node 41 is applied to the gate of the amplifier transistor 42. The amplifier transistor 42 amplifies the voltage. That is, the amplifier transistor 42 amplifies a signal generated by the photoelectric converter 10C. The voltage amplified by the amplifier transistor 42 is selectively read as a signal voltage via the address transistor 44.
One of the source and the drain of the reset transistor 46 is connected to the charge storage node 41, and, therefore, the one of the source and the drain of the reset transistor 46 has an electrical connection with the first electrode 2.
The reset transistor 46 resets the signal charges stored at the charge storage node 41. In other words, the reset transistor 46 resets the potential of the gate of the amplifier transistor 42 and the potential of the first electrode 2.
As illustrated in
The peripheral circuits of the imaging device 100 include a vertical scanning circuit 52, a horizontal signal readout circuit 54, a plurality of column signal processing circuits 56, a plurality of load circuits 58, and a plurality of inverting amplifiers 59. The vertical scanning circuit 52 is also referred to as a “row scanning circuit”, the horizontal signal readout circuit 54 is also referred to as a “column scanning circuit”, and the column signal processing circuit 56 is also referred to as a “row signal storage circuit”. The column signal processing circuits 56, the load circuits 58, and the inverting amplifiers 59 are provided for the respective columns of the plurality of pixels 20, which are arranged in the row direction and the column direction. Each of the column signal processing circuits 56 is electrically connected to the pixels 20 arranged in a corresponding column, via the vertical signal line 24 provided for each of the columns of the plurality of pixels 20. The plurality of column signal processing circuits 56 are electrically connected to the horizontal signal readout circuit 54. Each of the load circuits 58 is electrically connected to a corresponding one of the vertical signal lines 24, and the load circuit 58 and the amplifier transistor 42 form a source follower circuit.
The vertical scanning circuit 52 is connected to the address signal lines 25 and the reset signal lines 26. The vertical scanning circuit 52 applies a row select signal, which is a signal for controlling the on and off of the address transistors 44, to the gates of the address transistors 44 via the address signal lines 25. The row select signal is sent on a per-address signal line 25 basis, and, accordingly, the row to be read is scanned and selected. A signal voltage is read out from the pixels 20 of the selected row to the vertical signal lines 24. Furthermore, the vertical scanning circuit 52 applies a reset signal, which is a signal for controlling the on and off of the reset transistors 46, to the gates of the reset transistors 46 via the reset signal lines 26. A row select signal is sent on a per-reset signal line 26 basis, and, accordingly, the row of the pixels 20 on which a reset operation is to be performed is selected. In this manner, the vertical scanning circuit 52 selects a plurality of pixels 20 on a row basis, to read a signal voltage and reset the potential of the first electrode 2.
The signal voltage read out from the pixel 20 selected by the vertical scanning circuit 52 is sent to the column signal processing circuit 56 via the vertical signal line 24. The column signal processing circuit 56 performs, for instance, noise suppression signal processing, representative examples of which include correlated double sampling, and analog-digital conversion (AD conversion). The horizontal signal readout circuit 54 sequentially reads out signals from the plurality of column signal processing circuits 56 to a horizontal common signal line (not illustrated).
Note that the vertical scanning circuit 52 may partially include the voltage supply circuit 30. Alternatively, the voltage supply circuit 30 may have an electrical connection with the vertical scanning circuit 52. In other words, the bias voltage may be applied to the second electrode 3 via the vertical scanning circuit 52.
In the configuration illustrated in
As illustrated in
The amplifier transistor 42, the address transistor 44, and the reset transistor 46 are formed in or on the semiconductor substrate 62.
The amplifier transistor 42 includes impurity regions 62a and 62b, which are formed in the semiconductor substrate 62, a gate insulating layer 42g, which is located on the semiconductor substrate 62, and a gate electrode 42e, which is located on the gate insulating layer 42g. The impurity regions 62a and 62b serve as a drain or a source of the amplifier transistor 42. The impurity regions 62a and 62b and impurity regions 62c, 62d, and 62e, which will be described later, are, for example, n-type impurity regions.
The address transistor 44 includes impurity regions 62a and 62c, which are formed in the semiconductor substrate 62, a gate insulating layer 44g, which is located on the semiconductor substrate 62, and a gate electrode 44e, which is located on the gate insulating layer 44g. The impurity regions 62a and 62c serve as a drain or a source of the address transistor 44. In this example, the amplifier transistor 42 and the address transistor 44 share the impurity region 62a, and, accordingly, the source (or drain) of the amplifier transistor 42 is electrically connected to the drain (or source) of the address transistor 44.
The reset transistor 46 includes impurity regions 62d and 62e, which are formed in the semiconductor substrate 62, a gate insulating layer 46g, which is located on the semiconductor substrate 62, and a gate electrode 46e, which is located on the gate insulating layer 46g. The impurity regions 62d and 62e serve as a drain or a source of the reset transistor 46.
In the semiconductor substrate 62, an isolation region 62s is provided between adjacent pixels 20 and between the amplifier transistor 42 and the reset transistor 46. The isolation region 62s electrically separates adjacent pixels 20 from each other. Furthermore, the isolation region 62s provided between adjacent pixels 20 suppresses leakage of signal charges stored at the charge storage node 41.
A contact plug 65A, a contact plug 65B, and an interconnect 66A are formed in the interlayer insulating layer 63A. The contact plug 65A is connected to the impurity region 62d of the reset transistor 46, the contact plug 65B is connected to the gate electrode 42e of the amplifier transistor 42, and the interconnect 66A connects the contact plug 65A to the contact plug 65B. Accordingly, the impurity region 62d (e.g., drain) of the reset transistor 46 is electrically connected to the gate electrode 42e of the amplifier transistor 42. The configuration illustrated in
The configuration illustrated in
In the present embodiment, the photoelectric converter 10C is an example of a photoelectric conversion element and is formed of a photoelectric conversion element of the first embodiment. For example, as illustrated in
Note that the photoelectric converter 10C may have a structure similar to that of the photoelectric conversion element 10B described above and may have a structure in which one of the electron blocking layer 5 and the hole blocking layer 6 of the photoelectric conversion element 10B described above is not included. In this instance, too, the signal detection circuit 40 is connected to the first electrode 2, and the voltage supply circuit 30 provides a voltage to the second electrode 3 via the storage control line 22.
The imaging device 100, described above, can be manufactured with a typical semiconductor manufacturing process. In particular, in instances where a silicon substrate is used as the semiconductor substrate 62, the production can be carried out by using any of a variety of silicon semiconductor processes.
A modification of the second embodiment will now be described. In the following description of the modification of the second embodiment, differences from the first embodiment and the second embodiment will be mainly described, and descriptions of common features will be omitted or simplified.
As illustrated in
In the present modification, the plurality of pixels 20A each include a photoelectric converter 10D and a signal detection circuit 40, which detects a signal generated by the photoelectric converter 10D. Similar to the photoelectric converter 10C, the photoelectric converter 10D is formed of the photoelectric conversion element 10A or the photoelectric conversion element 10B of the first embodiment; however, the stacking order for the first electrode 2, the second electrode 3, and the photoelectric conversion layer 4 is opposite to that of the photoelectric converter 10C, as illustrated in
The photoelectric converter 10D has a configuration in which the electrons (i.e., negative charges) of the electron-hole pairs generated by photoelectric conversion are collected as signal charges by the second electrode 3. Controlling the potential of the first electrode 2 by using a bias voltage generated by the voltage supply circuit 30 enables the electrons to be collected by the second electrode 3. The voltage supply circuit 30 provides a voltage to the first electrode 2 via the storage control line 22. The voltage is a voltage in which the potential of the first electrode 2 is negative with respect to the potential of the second electrode 3.
As illustrated in
In the pixel 20A, as illustrated in
In the present modification, the photoelectric converter 10D is an example of a photoelectric conversion element and is formed of a photoelectric conversion element of the first embodiment. For example, as illustrated in
Note that the photoelectric converter 10D may have a structure similar to that of the photoelectric conversion element 10B described above and may have a structure in which one of the electron blocking layer 5 and the hole blocking layer 6 of the photoelectric conversion element 10B described above is not included. In this instance, too, the signal detection circuit 40 is connected to the second electrode 3, and the voltage supply circuit 30 provides a voltage to the first electrode 2 via the storage control line 22.
The present disclosure will now be described in detail with reference to Examples. It should be noted that the present disclosure is in no way limited to the Examples described below.
First, Example 1 and Comparative Examples 1 to 4 will be described.
Photoelectric conversion elements were prepared in the following manner.
A sheet of glass coated with ITO, which served as an electrode, was prepared to be used as a substrate. Before being used, the substrate was ultrasonically cleaned with acetone and propanol and subsequently dry-cleaned with a UV-ozone treatment. Subsequently, film forming for a photoelectric conversion element was performed in a glove box under a nitrogen atmosphere.
First, a poly-TPD chlorobenzene solution with a concentration of 6 mg/mL was spin-coated onto the ITO electrode to form an electron blocking layer with a thickness of 60 nm.
Subsequently, a PbS quantum dot octane solution with a concentration of 20 mg/mL was spin-coated onto the electron blocking layer. The PbS quantum dots had an absorption peak wavelength of 1400 nm. The solvent was then evaporated, subsequently, the resultant was immersed in a 1,4-BDT acetonitrile solution with a concentration of 1.5 mg/mL for 30 seconds to exchange surface-modifying ligands, and the resultant was washed twice with acetonitrile. The ligand exchange step was repeated five times. Accordingly, a first quantum dot layer with a thickness of 60 nm was formed. The first quantum dot layer had a surface modified with 1,4-BDT and was formed of PbS quantum dots having an absorption peak wavelength of 1400 nm.
Subsequently, a PbS quantum dot octane solution with a concentration of 20 mg/mL was spin-coated onto the first quantum dot layer. The PbS quantum dots had an absorption peak wavelength of 1200 nm. The solvent was then evaporated, subsequently, the resultant was immersed in a 0.06 vol. % mercaptopropionic acid (MPA)-doped zinc iodide (ZnI2) ethanol solution with a concentration of 4.8 mg/mL for 5 seconds to exchange surface-modifying ligands, and the resultant was washed twice with ethanol. The ligand exchange step was repeated five times. Accordingly, a second quantum dot layer with a thickness of 60 nm was formed. The second quantum dot layer had a surface modified with ZnI2:MPA and was formed of PbS quantum dots having an absorption peak wavelength of 1200 nm. In this manner, a photoelectric conversion layer having a structure including a stack of the first quantum dot layer and the second quantum dot layer was formed.
Subsequently, a zinc oxide nanoparticle dispersion (trade name: Avantama N-11) was spin-coated onto the second quantum dot layer to form a hole blocking layer with a thickness of 60 nm.
Lastly, a film of aluminum with a thickness of 80 nm was formed on the hole blocking layer by thermal vacuum deposition to form an aluminum electrode, and, accordingly, a photoelectric conversion element was obtained. Table 1 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Example 1, except that the PbS quantum dots used in the first quantum dot layer were used in the second quantum dot layer, and vice versa. Table 1 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Example 1, except that the ZnI2:MPA used in the second quantum dot layer was replaced with 1,4-BDT. Table 1 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Comparative Example 2, except that the PbS quantum dots used in the first quantum dot layer were used in the second quantum dot layer, and vice versa. Table 1 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
An operation similar to that of Example 1 was performed, except for the formation of the photoelectric conversion layer. The photoelectric conversion layer was formed as follows. A PbS quantum dot mixture octane solution with a concentration of 20 mg/mL was spin-coated onto the electron blocking layer. The mixture contained PbS quantum dots having different particle diameters and respective absorption peak wavelengths of 1400 nm and 1200 nm, in a mass ratio of 1:1. The surface-modifying ligand of the PbS quantum dots was exchanged with 1,4-BDT in a manner similar to that of Example 1. Accordingly, a photoelectric conversion layer with a thickness of 120 nm was formed. The photoelectric conversion layer was formed of a mixture of PbS quantum dots having an absorption peak wavelength of 1200 nm and PbS quantum dots having an absorption peak wavelength of 1400 nm, each having a surface modified with 1,4-BDT. That is, in Comparative Example 4, the photoelectric conversion layer did not have the stack structure of the first quantum dot layer and the second quantum dot layer. Table 1 shows the absorption peak wavelengths and the surface-modifying ligand of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
Evaluations of the photoelectric conversion elements prepared as described above were performed. Specifically, a dark current and external quantum efficiency were measured by introducing the photoelectric conversion elements into a sealable measurement jig in a glove box under a nitrogen atmosphere and using a long wavelength-sensitive spectral sensitivity measuring device (CEP-25RR, manufactured by Bunkoukeiki Co., Ltd.). Table 1 shows the values of the dark current resulting from the application of a voltage of −3 V to the ITO electrode.
In the measurement of the external quantum efficiency, the external quantum efficiency was measured under the condition in which a voltage of −3 V was applied to the ITO electrode. That is, the measurement of the external quantum efficiency was performed under conditions in which holes were collected by the ITO electrode, and the electrons were collected by the aluminum electrode. Table 1 shows the results of the measurement of the external quantum efficiency performed at a wavelength of 1200 nm and a wavelength of 1400 nm.
In Table 1, in the columns labeled “First quantum dot layer” and “Second quantum dot layer”, the upper row shows the absorption peak wavelengths of the quantum dots used in the respective layers, and the lower row shows the surface-modifying ligands used in the respective layers. The same applies to Tables 2 to 5, which will be described below.
As described above with reference to
Furthermore, the photoelectric conversion elements of Comparative Example 2 and Comparative Example 3 also had a higher dark current than the photoelectric conversion element of Example 1. Although the zinc oxide layer with a thickness of 60 nm was provided as a hole blocking layer, there was a possibility that a conduction path that facilitated injection of holes into the second quantum dot layer from the aluminum electrode for collecting electrons existed. Such a case may have occurred due to a locally reduced thickness of the hole blocking layer or damage caused to the hole blocking layer during the deposition of the aluminum electrode for collecting electrons. In such an instance, a low ionization potential of the second quantum dot layer can be a factor for an increase in the dark current. In Comparative Example 2 and Comparative Example 3, the surface-modifying ligand used in the second quantum dot layer was 1,4-BDT, and, consequently, the ionization potentials of the second quantum dot layers were lower than those of Example 1 and Comparative Example 1. As a result, presumably, the injection of holes from the aluminum electrode was increased.
Furthermore, in Comparative Example 4, the photoelectric conversion layer was formed of a mixture of quantum dots having two particle sizes, and in this case, the external quantum efficiency was lower than those of the other examples. In the photoelectric conversion element of Comparative Example 4, although the dark current was low, the photoelectric conversion efficiency was also low, and thus, the sensitive wavelength was not extended. That is, presumably, the photoelectric conversion layer behaved like a large resistance, which hindered the current flow.
The results described above demonstrate that both an extended sensitive wavelength range and a reduced dark current can be achieved with high quantum efficiency in the instance in which, regarding the broadening of the sensitive wavelength by stacking the first quantum dot layer and the second quantum dot layer that include quantum dots having different respective particle sizes, the ionization potential is differentiated by using different surface-modifying ligands for the respective layers, and in addition, in the second quantum dot layer adjacent to the aluminum electrode for collecting electrons, the quantum dots having a relatively small particle size is modified with ZnI2:MPA, which relatively increases the ionization potential.
Now, Example 2 and Comparative Example 5 will be described.
Photoelectric conversion elements were prepared in the following manner.
A photoelectric conversion element was prepared in a manner similar to that of Example 1, except that the thicknesses of the first quantum dot layer and the second quantum dot layer were 180 nm. Table 2 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Comparative Example 4, except that the thickness of the photoelectric conversion layer was 360 nm. Table 2 shows the absorption peak wavelengths and the surface-modifying ligand of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
Evaluations of the photoelectric conversion elements prepared as described above were performed by measuring the dark current and the external quantum efficiency in the manners previously described. Table 2 shows the values of the dark current and the results of the measurement of the external quantum efficiency performed at a wavelength of 1200 nm and a wavelength of 1400 nm.
As shown in Table 2, in the photoelectric conversion element of Example 2, the photoelectric conversion layer had a thickness larger than that of the photoelectric conversion element of Example 1, and, consequently, the external quantum efficiency was further improved, and the dark current was reduced. In contrast, in Comparative Example 5, in which the photoelectric conversion layer was formed of a mixture of quantum dots having two particle sizes, the photoelectric conversion element had a lower quantum efficiency and a higher dark current than the photoelectric conversion element of Example 2. In particular, regarding the reduction in the dark current, the larger the thickness of the photoelectric conversion layer, the greater the effect of the configuration of the present disclosure, and thus, the photoelectric conversion element of Example 2 realized a dark current lower than that of the photoelectric conversion element of Comparative Example 5 by two orders of magnitude.
Now, Example 3 and Comparative Examples 6 and 7 will be described.
Photoelectric conversion elements were prepared in the following manner.
A photoelectric conversion element was prepared in a manner similar to that of Example 2, except that the first quantum dot layer was formed with PbS quantum dots having an absorption peak wavelength of 1450 nm, and the second quantum dot layer was formed with PbS quantum dots having an absorption peak wavelength of 1300 nm. Table 3 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Example 3, except that the PbS quantum dots used in the first quantum dot layer were used in the second quantum dot layer, and vice versa. Table 3 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Comparative Example 5, except that the photoelectric conversion layer was formed with a PbS quantum dot mixture octane solution with a concentration of 20 mg/mL, where the mixture contained PbS quantum dots having different particle diameters and respective absorption peak wavelengths of 1450 nm and 1300 nm, in a mass ratio of 1:1. Table 3 shows the absorption peak wavelengths and the surface-modifying ligand of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
Evaluations of the photoelectric conversion elements prepared as described above were performed by measuring the dark current and the external quantum efficiency in the manners previously described. Table 3 shows the values of the dark current and the results of the measurement of the external quantum efficiency performed at a wavelength of 1300 nm and a wavelength of 1480 nm.
As shown in Table 3, it was demonstrated that the photoelectric conversion element of Example 3, in which quantum dots having particle sizes different from those of the photoelectric conversion elements of Example 1 and Example 2 were used, also had a high external quantum efficiency and a low dark current. In contrast, the photoelectric conversion element of Comparative Example 6, in which the quantum dots used in the first quantum dot layer and the quantum dots used in the second quantum dot layer had a particle size combination opposite to that of Example 3, had a higher dark current than the photoelectric conversion element of Example 3. Furthermore, the photoelectric conversion element of Comparative Example 7, in which the photoelectric conversion layer was formed of a mixture of quantum dots having two particle sizes, had a lower quantum efficiency and a higher dark current than the photoelectric conversion element of Example 3.
Now, Example 4 and Comparative Example 8 will be described.
Photoelectric conversion elements were prepared in the following manner.
A photoelectric conversion element was formed in a manner similar to that of Example 2, except that the first quantum dot layer was formed with a PbS quantum dot mixture octane solution with a concentration of 20 mg/mL, where the mixture contained PbS quantum dots having different particle diameters and respective absorption peak wavelengths of 1300 nm and 1450 nm, in a mass ratio of 1:1; and the second quantum dot layer was formed with a PbS quantum dot mixture octane solution with a concentration of 20 mg/mL, where the mixture contained PbS quantum dots having different particle diameters and respective absorption peak wavelengths of 1000 nm and 1200 nm, in a mass ratio of 1:1. Table 4 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was prepared in a manner similar to that of Comparative Example 5, except that a PbS quantum dot mixture octane solution with a concentration of 20 mg/mL was used, where the mixture contained PbS quantum dots having different particle diameters and respective absorption peak wavelengths of 1000 nm, 1200 nm, 1300 nm, and 1450 nm, in a mass ratio of 1:1:1:1. Table 4 shows the absorption peak wavelengths and the surface-modifying ligand of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
Evaluations of the photoelectric conversion elements prepared as described above were performed by measuring the dark current and the external quantum efficiency in the manners previously described. Table 4 shows the values of the dark current and the results of the measurement of the external quantum efficiency performed at wavelengths of 1000 nm, 1200 nm, 1360 nm, and 1440 nm.
As shown in Table 4, the photoelectric conversion element of Example 4 had a higher quantum efficiency and a lower dark current than the photoelectric conversion element of Comparative Example 8. That is, with the effect of the configuration of the present disclosure, both an extended sensitive wavelength range and a reduced dark current can be achieved with high quantum efficiency even in the instance in which multiple sets of quantum dots with different respective particle sizes are used both in the first quantum dot layer and in the second quantum dot layer, as long as the ionization potential is differentiated by using different surface-modifying ligands for the respective layers, and in addition, in the second quantum dot layer adjacent to the aluminum electrode for collecting electrons, a surface of the quantum dots having a relatively large particle diameter is modified with ZnI2:MPA, which relatively increases the ionization potential. In Example 4, multiple sets of quantum dots with different respective particle sizes were used both in the first quantum dot layer and in the second quantum dot layer, and, therefore, the particle diameter distribution of the quantum dots of each of the layers, namely, the first quantum dot layer and the second quantum dot layer, had at least two different local maximum values.
Now, Example 5 and Comparative Example 9 will be described.
Photoelectric conversion elements were prepared in the following manner.
A photoelectric conversion element was formed in a manner similar to that of Example 4, except that the hole blocking layer was formed by depositing fullerene (C60) to a thickness of 50 nm by vacuum vapor deposition, instead of forming a film of zinc oxide, and that an ITO electrode was formed, instead of an aluminum electrode, on the hole blocking layer by depositing a film of ITO by sputtering to a thickness of 30 nm. Table 5 shows the absorption peak wavelengths and the surface-modifying ligands of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
A photoelectric conversion element was formed in a manner similar to that of Comparative Example 8, except that the hole blocking layer was formed by depositing fullerene (C60) to a thickness of 50 nm by vacuum vapor deposition, instead of forming a film of zinc oxide, and that an ITO electrode was formed, instead of an aluminum electrode, on the hole blocking layer by depositing a film of ITO by sputtering to a thickness of 30 nm. Table 5 shows the absorption peak wavelengths and the surface-modifying ligand of the quantum dots used in the photoelectric conversion layer of the prepared photoelectric conversion element and also shows the thickness of the photoelectric conversion layer.
Evaluations of the photoelectric conversion elements prepared as described above were performed by measuring the dark current and the external quantum efficiency in the manners previously described. Note that the dark current and the external quantum efficiency were measured under the condition in which a voltage of −5 V was applied to the ITO electrode on the substrate-side. Furthermore, the measurement of the external quantum efficiency was performed by causing light to enter from the side of the ITO electrode formed by sputtering, which was the side opposite to the ITO substrate-side. Table 5 shows the values of the dark current and the results of the measurement of the external quantum efficiency performed at wavelengths of 1000 nm, 1180 nm, 1340 nm, and 1480 nm.
As shown in Table 5, the photoelectric conversion element of Example 5 had a higher quantum efficiency and a lower dark current than the photoelectric conversion element of Comparative Example 9. That is, the effect of the configuration of the present disclosure was successfully produced even with the change in the material of the hole blocking layer from that of Example 4. Furthermore, the effect of the configuration of the present disclosure was successfully produced even in the instance in which light entered from the direction opposite to that of Example 4. Accordingly, both an extended sensitive wavelength range and a reduced dark current can be achieved with high quantum efficiency, regardless of the direction of the entering light, as long as the ionization potential is differentiated by using different surface-modifying ligands for the respective layers, and in addition, in the second quantum dot layer adjacent to the electrode for collecting electrons, a surface of the quantum dots having a relatively large particle diameter is modified with ZnI2:MPA, which relatively increases the ionization potential.
In the embodiments described above, the energy gap of the second quantum dot layer 4b is greater than the energy gap of the first quantum dot layer 4a because of the fact that the particle diameter of the second quantum dots included in the second quantum dot layer 4b is smaller than the particle diameter of the first quantum dots included in the first quantum dot layer 4a. However, the energy gap (i.e., absorption peak wavelength) of a quantum dot layer can be controlled with the constituent elements of the quantum dots that are to be included.
An example of a photoelectric conversion element in which quantum dots having different constituent elements are used will be described with reference to
While photoelectric conversion elements and imaging devices of the present disclosure have been described above with reference to embodiments, a modification, and examples, it should be noted that the present disclosure is not limited to the embodiments, the modification, and the examples. Any of various modifications contemplated by those skilled in the art may be applied to the embodiments, the modification, and the examples, and some of the constituent elements in the embodiments, the modification, and the examples may be combined to constitute different embodiments. These modifications are also encompassed by the scope of the present disclosure as long as they do not depart from the essence of the present disclosure.
For example, a photoelectric conversion element of the present disclosure can allow the charge generated by light to be extracted as energy and, therefore, may be used as a solar cell. Furthermore, a photoelectric conversion element of the present disclosure can allow the charge generated by light to be extracted as a signal and, therefore, may be used as an optical sensor.
Photoelectric conversion elements and imaging devices of the present disclosure can be used in photodiodes, image sensors, and the like and, in particular, can be used in high-sensitivity, low-dark-current optical sensing that utilizes infrared wavelengths.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2021-086045 | May 2021 | JP | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2022/018142 | Apr 2022 | US |
| Child | 18490823 | US |
