Patent Application
20230139873
The present disclosure relates to (manufacturing of) inks with colloidal nanoparticles, such as quantum dots, in particular inks and compositions suitable in the deposition, e.g., printing, of active layers, e.g. for use in optoelectronic devices.
Colloidal suspensions of nanoparticles, nanocrystals and/or quantum dots are used in a broad range of applications including for fabrication of electronic devices such as field-effect transistors (FETs), solar cells, light emitting FETs, light emitting diodes, photodetectors for visible, IR, X-ray or gamma irradiation, phototransistors, thermoelectrics, bolometers and others. Also, water-based dispersions of quantum dots can be used as a platform for bioapplications. Linkers, e.g. ligands on the quantum dot surface allow manufacturing of conjugates of various biological molecules, e.g., using quantum dots as fluorescent markers.
Colloidal quantum dots typically comprise nanocrystals of inorganic material that have discrete energy levels due to quantum confinement of electrons within the volume of the nanoparticles. Quantum dots can be synthesized in a form of a colloidal solution of quantum dots, and after purification can be dispersed in a nonpolar organic solvent such as hexane. In the colloidal solution individual quantum dots are capped with long aliphatic molecules, called ligands. For example, these ligands may include oleic acid (OA) or oleylamine (OAm), which bind to the surface of quantum dots via carboxyl or amine group. The aliphatic tails of the ligands ensure the colloidal stability of such quantum dot solutions, creating repulsive forces between quantum dots counterbalancing the attractive component of van der Waals forces acting on a particle approaching another particle. This way of stabilization is referred to as steric stabilization of colloids. However, such quantum dot solutions are generally less suitable for direct application. For example, the nonpolar solvent may be incompatible with an envisioned biological application. Further, a film deposited from such quantum dot solution typically shows very poor electronic performance. One approach to overcome this problem comprises use of a phase-transfer ligand exchange, which is a method wherein the ligands on the surface of the quantum dots are substituted by different entities, e.g., ligands. Typically, this process is performed in solution.
As background, U.S. Pat. No. 6,251,303B1 discloses a method for manufacturing of water-soluble fluorescent nanocrystals. In the method fluorescent nanocrystals bearing a cap of nonpolar ligands are separated from suspension. The nonpolar ligands are exchanged for a different precursor ligand by exposing the separated fluorescent nanocrystals to a new solution comprising a 30-fold excess of said precursor ligands at elevated temperatures. The nanocrystals can be rendered water soluble in separate step by protonating the precursor ligands. Besides the extensive elaborate manufacturing process disadvantages of the disclosed method include: the presence of a nonpolar ligands and/or the presence of a large excess of unbound precursor ligand in the formed composition; and/or possible nanocrystal degradation or agglomeration due to their length exposure to elevated temperatures.
As further background, Hak Soo Choi et al (Nature biotechnology 25; 1165-1170 (2007) disclose a ligand exchange process that can provide CdSe/ZnS core-shell quantum dots that are capped with cysteamine for bio applications. The process uses a water/chloroform-based ligand exchange process in which the water phase is provided with a phosphate-buffered saline buffer to dissolve the quantum dots. Formed quantum dot suspensions thus comprise a lot of salt and/or a large excess of unbound ligand rendering them less suitable for fabrication of electronic devices.
As further background, Byung-Ryool Hyun eat al (J. Phys. Chem. B 2007, 111, 20, 5726-5730) disclose a multi-step method of manufacturing water-soluble lead salt quantum dots for near-infrared fluorescence imaging. The method uses a large excess of ligand and includes precipitation of QDs followed by a subsequent reaction to render the quantum dots water soluble.
As further background, Noipa T et al (Spectrochim Acta A Mol Biomol Spectrosc. 2014 Jan. 24; 118:17-23) disclose a method of manufacturing cysteamine CdS quantum dots decorated with Fe3+ as a fluorescence sensor for the detection of pyrophosphate. The CdS quantum dots were directly synthesized with cysteamine ligands using a one-pot synthesis. During synthesis the dots do not benefit from the stabilizing effect of long aliphatic ligands. Formed dots were found to be of lower quality and thus less suitable for electronic grade quantum dot inks.
As further background, US2007174939A1 discloses methods of making quantum dot films for use in optical and optoelectronic devices. The method comprises pre-fabricate quantum dots and ligand exchange. Similar to U.S. Pat. No. 6,251,303B1 the ligand exchange includes precipitating the as-synthesized quantum dots from their original solution and dispersing the separated particles in a liquid comprising the exchange ligands. Accordingly, the method of US2007174939A1 shares one or more of the disadvantages described in relation to U.S. Pat. No. 6,251,303B1.
The method of manufacturing of an ink composition comprising the biphasic ligand exchange process according to the present invention aims to mitigate one or more of the disadvantages described above and/or offering one or more further advantages in the manufacturing of electronic devices from the ink compositions.
Aspects of the present disclosure relate to a method of manufacturing of an ink composition. A first phase liquid comprises a nonpolar solvent with a suspension (a colloidal suspension) of nanoparticles dispersed in the nonpolar solvent. The nanoparticles, e.g. quantum dots, can be capped with a shell of first ligands comprising a surface binding head group and an alkyl or alkenyl tail for at least initially keeping the nanoparticles (quantum dots) in a colloidal suspension in the nonpolar solvent. A second phase liquid comprises a polar solvent with second ligands dissolved therein. The second ligand has a molecular architecture preferably including at least one surface binding head group that has an affinity for binding to a surface site of said nanoparticle. Furthermore, the architecture preferably includes at least an ionically charged tail group and a counter ion associated therewith. A biphasic ligand exchange process can be used wherein the second ligand displace the first ligands that are bound to the nanoparticles. This may cause releasing the first ligands to the first phase liquid. Typically, the biphasic ligand exchange process involves contacting the first and second phase liquid. This can form a dispersion of the nanoparticles, e.g., the quantum dots, that are capped with a shell of the second ligands in the second phase liquid. The nanoparticles that are capped with a shell of the second ligands can be separated from the second phase liquid. The separated nanoparticles (quantum dots) that are capped with a shell of the second ligands can be (re)dispersed in a printable liquid medium. In this way an ink can be formed of which the printing properties may be further tuned, e.g. by addition of other or further additives.
Further aspects of the present disclosure relate to a dry composition, comprising the nanoparticles, preferably quantum dots, that are capped with a shell of second ligand obtainable by any of the methods as described herein, wherein the method further comprises drying the separated quantum dots that are capped with a shell of the second ligands.
Yet, further aspects of the present disclosure relate to an ink composition comprising nanoparticles that are capped with a shell of polar organic ligands. The ink composition comprising a colloidal suspension of quantum dots in a polar printable liquid medium, wherein the quantum dots are capped with a shell of second ligands and wherein the second ligand has a molecular architecture including: at least one surface binding head group that has an affinity for binding to a surface site of said quantum dot; and an ionically charged tail group and a counter ion associated therewith.
Even further aspects relate to the use of a dry composition obtainable according to the disclosed method in the manufacturing of a printable ink composition, and to the use of the ink as described herein, preferably quantum dot based inks, for the manufacturing of optoelectronic devices. Accordingly, aspects of the present disclosure also relate to a method of manufacturing an imaging device comprising a stack of photoactive layers including at least a p-type photoactive layer and/or an n-type photoactive layer. The method comprising depositing one or more layers of the ink composition comprising a p-type dopant as described herein or of the ink obtainable by the method as described herein; and depositing one or more layers of the ink composition comprising a n-type dopant as described herein or of the ink obtainable by the method as described herein, to from a stack of photoactive layers including at least a p-type photoactive layer and/or an n-type photoactive layer, and wherein the photoactive layers are amorphous, comprising a disordered structure of nanoparticles resulting from deposition of the respective ink composition.
As will become clarified herein below the disclosed method, ink, and intermediary products offer certain advantages. These include provision of a facile and/or versatile ligand exchange process allowing manufacturing of quantum dots that are capped with a broad variety of second ligands. Advantageously, nanoparticle degradation can be mitigated as manufacturing of the ink can be performed at room temperature and/or without the presence of harsh conditions, e.g. without exposure to high concentration of strong acids or bases. Further, separating the nanoparticle that are capped with a shell of the second ligands from the second phase comprising a first polar solvent and re-dispersing the quantum dots in a different polar liquid, e.g. a liquid printing medium, allows optimizing properties of the ink, e.g. the type of solvent comprised therein, independent from selection criteria governed by the ligand exchange process.
Further, the optical and electronic properties of obtained nanoparticle can remain stable, e.g., over prolonged periods of time, as dry compositions of obtained nanoparticle that are capped with a shell of the second ligands can be stored without losing essential functionality. Advantageously stored compositions can be (re)dispersed in a suitable printable liquid medium before usage.
The two phase ligand exchange process according to the present invention can be understood to yield capped nanoparticles that were found to be particularly beneficial for use in the manufacturing of a photoactive layer of an optoelectronic device by providing a combination of advantageous properties. Advantages include that the particles manufactured according to the disclosed process were found to be essentially free of hydrophobic ligand moieties and/or oily or waxy impurities that were associated with the nanoparticles as synthesized. As such the biphasic ligand process according to the present invention can be understood as a purification or cleaning procedure allowing to essentially replace the an initial hydrophobic capping layer, including possible contaminants, by a replacement capping layer of different functional moieties as disclosed herein. As will be clarified herein the replacement capping layer offers improved optoelectronic properties. In addition the replacement capping layer was found to effectively stabilize the nanoparticles in dry form while allowing (re)solubilization of dried particles in polar solvents including ink compositions for use in the manufacturing of a photoactive layer for optoelectronic devices.
These and other features, aspects, and advantages of the apparatus, systems and methods of the present disclosure will become better understood from the following description with examples, appended claims, and accompanying drawing wherein:
Terminology used for describing particular embodiments is not intended to be limiting of the invention. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. The term “and/or” includes any and all combinations of one or more of the associated listed items. It will be understood that the terms “comprises” and/or “comprising” specify the presence of stated features but do not preclude the presence or addition of one or more other features. It will be further understood that when a particular step of a method is referred to as subsequent to another step, it can directly follow said other step or one or more intermediate steps may be carried out before carrying out the particular step, unless specified otherwise. Likewise it will be understood that when a connection between structures or components is described, this connection may be established directly or through intermediate structures or components unless specified otherwise.
Unless specified otherwise, properties of compounds of mixtures, e.g., solubility, referred to herein are specified at room temperature and standard pressure, e.g. twenty degrees Celsius and one atmosphere.
(Colloidal) Nanoparticles comprise a dense core of inorganic material that has at least one dimension lower than one thousand nanometer, e.g. in a range between one, or ten, Angstrom and one hundred nm, preferably in a range between about one nanometer and about fifty nanometer, e.g. a about two to ten nanometer, e.g. three nanometer. Colloidal nanocrystals (NCs) of semiconducting materials with distinctive electronic properties determined by their size are often referred as quantum dots (QDs) or colloidal quantum dots (QCDs) due to quantum confinement effect. Advantages of QDs include: size-tunable band gap, high light absorption coefficient and solution processability.
Quantum dots synthesized from solution are typically referred to as colloidal quantum dots or colloidal nanocrystals. As synthesized, colloidal quantum dots are generally capped with long aliphatic ligands (such as oleic acid or oleylamine), ensuring homogeneous growth of the nanoparticles and the colloidal stability of the solution. For certain nanoparticles other ligands including and not limited to various phosphines and phosphine oxides (such as trioctylphosphine and trioctylphosphine oxide) can be employed. Quantum dots can be manufactured using other methods including plasma synthesis. Quantum dots synthesized by plasma are usually in the form of powder, for which surface modification, e.g. passivation with aliphatic ligands may be carried out.
Nanoparticles have been reported for a broad range of compositions. Examples include mono-elemental nanoparticles (Ag, Au, Ni, Ru, Rh, Pd, Pt, Sn, Si, Ge, Ga, In, Fe, Mn, Co, Cu, Be, C, B, Al, Sb, Li, Na, K, Y, lanthanide, etc.), carbonaceous-based nanoparticles, metal and/or lanthanide oxide nanoparticles (Fe2O3, Fe3O4, MnO, Mn2O3, Mn3O4, MgO, CaO, BaO, ZnO, TiO2, NiO, Ni2O3, In2O3, Ga2O3, Be2O3, Y2O3, SiO2, V2O3, V2O5, CeO2, Al2O3, GeO2, ZrO2, HfO2, CuO, Cu2O, SnO2, WO3, Au2O3, BaFe12O19, As2O3, Bi2O3, Bi2O5, CoO, CdO, PbO, HgO, Au2O3, Li2O, Na2O, K2O, Rb2O, Cs2O, SrO, Ln2O3 where Ln represents a lanthanide element etc), chalcogenide nanoparticles (e.g., ZnX, CdX, PbX, HgX, BiX, Cu2X, CuX, Bi2X3, Bi2X5, In2X3, Al2X3, GaX, Ga2X3, SnX, SnX2, FeX, FeX2, NiX, Ni2X3, CoX, Co2X3, GeX2, MnX, Mn2X3, Ag2X, MoX2, WX2, Cr2X3, where X represents S, Se, or Te), pnictogenide nanoparticles (BX, AlX, GaX, InX, Si3X4, wherein X represents N, P, As, or Sb), carbide nanoparticles (SiC, TiC, WC, MoC2, HfC, ZrC), and mixtures of thereof. It will be understood that particles suitable for use with the invention are not to be construed as to be limited to the listed exemplary compositions. Particles comprising a mixture or combination of the abovementioned materials can be equally used to advantage, including for example, core/shell structures or segmented particles, and also alloys, such as AgInS2, and/or doped particles.
The shape of the nanoparticles can be understood to include, but not limited to, spheres, cylinders, discs, toroids, wires, rods, needles, cubes, cuboctahedrons, parallelepipeds (bar), tetrahedral, octahedral, icosahedra, dodecahedra, prisms, nanoplates, nanofoil, nanotubes, of various shape (quadratic, triangular, rectangular, hexagonal etc), stars, tetrapods, hyperbranched and branched. Abovementioned nanoparticles can be provided in a core/shell configuration or core/shell/shell structures having layers of different composition, wherein the interface between layers of different composition may be a sharp interface or gradual interface. The nanoparticlescan be hollowed or porous or could combine two or more shapes of one or more materials.
It will be understood that the biphasic ligand exchange process as described herein can be used to advantage for a broad variety of nanoparticles, including nanocrystals and quantum dots. A process or step as described herein below that is explained relation to a specific type of nanoparticle, e.g. a quantum dots, is not to be inferred as to be limited to that specific type of nanoparticle. Rather, a selection of nanoparticles type can be understood to be governed by a target application, e.g. based on a requirement of an active component in an optoelectronic device.
Unless specified otherwise, non polar solvents used herein may be understood to include, linear-, branched-, cyclic-, or halogenated alkanes, alkenes, and alkynes, as well as aromatic compounds. Nonpolar solvents include but are not limited to pentanes, like n-pentane and 2,2,4-trimethylpentane, hexanes, like n-hexane, heptanes, octanes, nonane, decane, dodecane, hexadecane, 1-octadecene, petroleum ether, poly(α-olefin)s and oligo(α-olefin)s, squalane, cyclopentane, cyclohexane, benzene, toluene, ethylbenzene, xylenes, like p-xylene, trimethylbenzenes, cumene, chlorobenzene, dichlorobenzenes, 1,2,4-trichlorobenzene, fluorobenzene, difluorobenzenes, hexafluorobenzene, biphenyl, diphenyl oxide, cresols, terphenyls, mesitylene, nitrobenzenen, tetralin, decalin, dichloromethane, trichloromethane, tetrachloromethane, carbon disulfide, trichloroethylene, 1,1,1-trichloroethane, tetrachloroethylene, ethyl acetate, diisopropyl ether, diethyl ether and mixtures thereof.
Unless specified otherwise, polar solvents used herein may be understood to include, but not limited to, methanol, ethanol, propanol, isopropanol, butanol, ethylene glycol, glycerol, 1,3-butanediol, ammonia, hydrazine, acetone, acetonitrile, benzonitrile, formamide, N-methylformamide, dimethylformamide, dimethylacetamide, dimethylsulfoxide, hexamethylphosphoramide, propylene carbonate, N-methyl-2-pyrrolidone, nitromethane, methylamine, dimethylamine, ethylamine, propylamine, butylamine, triethylamine, trimethylamine, ethanolamine, methoxyethanol, ethylenediamine, dimethylethylenediamine, tetramethylethylenediamine, tetrakis(dimethylamino)ethylene, pyridine, 2,6-difluoropyridine, water and mixtures thereof.
The invention is described more fully hereinafter with reference to the accompanying drawings, in which embodiments of the invention are shown. In the drawings, the absolute and relative sizes of systems, components, layers, and regions may be exaggerated for clarity.
Embodiments may be described with reference to schematic and/or cross-section illustrations of possibly idealized embodiments and intermediate structures of the invention. In the description and drawings, like numbers refer to like elements throughout. Relative terms as well as derivatives thereof should be construed to refer to the orientation as then described or as shown in the drawing under discussion. These relative terms are for convenience of description and do not require that the system be constructed or operated in a particular orientation unless stated otherwise.
Added to the container 50 is a first phase liquid 10. The first phase liquid 10 comprises or is essentially formed of a nonpolar solvent 11 or a mixture of nonpolar solvents. Dispersed in the solvent is a suspension (a colloidal suspension) of quantum dots 1. The quantum dots 1 are capped with a shell 2s of first ligands 2. The ligands comprise a surface binding head group 2h that binds to a surface site on the quantum dot. The ligands further comprise a nonpolar alkyl or alkenyl tail 2t for at least initially keeping the quantum dots 1 in a colloidal suspension in the nonpolar solvent 11. The shell 2s of first ligands (indicated by a dashed circle) is sometimes referred to as a corona, may be understood to included a volume around the quantum dot that is occupied by the second ligands. Quantum dots synthesized from solution are typically referred to as colloidal quantum dots or colloidal nanocrystals. As synthesized, colloidal quantum dots are generally capped with long aliphatic ligands (such as oleic acid or oleylamine) which are believed to ensure homogeneous growth of the nanoparticles and the colloidal stability of the solution. Quantum dots can be manufactured using other methods including plasma synthesis. For quantum dots not already comprising a shell of first of ligands the method, e.g., a powder of quantum dots synthesized by plasma, the method includes a step of capping the quantum dots with a shell 2s of first ligands 2.
Typically, the type and/or composition of the quantum dots can depend on its desired application. The method as disclosed herein is not to be construed to be limited to a certain type and/or composition of quantum dots per se. The disclosed method of forming an ink was found to work for a broad range of quantum dots that are capped with a shell of aliphatic ligands which are sufficiently labile to be replaced by second ligands. Suitable quantum dots include but are not limited to Au, PbS, PbSe, and CdSe quantum dots as well as multi-layer dots comprising such outer coating.
Added to the container 50 is a second phase liquid 20. The second phase liquid comprises or is essentially formed of a polar solvent 21 or mixture of polar solvents in which an amount of second ligand 3 is dissolved.
Optionally, a third solvent (co-solvent) can be added to the biphasic mixture. The third solvent being miscible with the liquids that make up the first and second phase liquids. Addition of a co-solvent was found to promote, speed up, ligand exchange. Miscibility of the third solvent being defined as forming a single phase fluid with an equal volume of the nonpolar solvent, respectively with an equal volume of the first polar solvent.
The second ligand has a multi-block molecular architecture that includes at least one surface binding head group 3h that has an affinity for binding to a surface site of the quantum dots 1, and an ionically charged tail group 3t and a counter ion 3c associated therewith. Typically, the second ligand comprises an organic spacer 3s separating the head group and the tail group. Details regarding the second ligand will be described later. It was found that further additives, such as pH-buffers, are not required to drive the ligand exchange reaction to completion. As additives, such as pH-buffers or ionic strength modifiers, can be particularly difficult to remove, and/or can negatively affect optoelectronic properties of the quantum dots, the second phase liquid is preferably free of such additives, i.e. consist of a solution of one or more second ligands in a polar solvent or mixture of solvents.
The first and second phase liquid may be understood to be mutually essentially immiscible. Mutually essentially immiscible liquids, e.g. the first and second phase liquid, can spontaneously form a biphasic liquid system. Providing mutually essentially immiscible phases can advantageously be separated form each other relative ease, e.g. by decanting or pouring. The exact composition of the first and second phase liquid can depend on the type of quantum dot and/or of the type of the first ligands capping said quantum dot. Preferably, the first phase liquid can disperse the quantum dots that are capped with a shell of first ligands in a concentration of at least 10 mg/mL. Likewise, the first phase liquid can preferably dissolve the first ligands in a concentration of at least 10 mM.
The second phase liquid is a poor dispersing medium for the first ligands and for the quantum dots that are capped with a shell of first ligands. Preferably, the solubility of the first ligands in the second phase liquid is below 0.1 mM. Preferably, the solubility of the quantum dots that are capped with the first ligands in the second phase liquid is below 0.1 mg/mL, or lower, e.g. below 0.01 mg/mL, preferably practicable negligible. The second phase liquid is a good solvent for the second ligands. The higher the solubility of the second ligands the better dispersing medium the second phase liquid can be for quantum dots that are capped with a shell of the second ligands. The solubility of the second ligands is preferably at least 10 mM, preferably higher e.g. at least 20 mM or more, e.g. at least 30 mM. The higher the concentration of the second ligands the faster the ligand exchange reaction can be.
The first and second phase liquid may each individually comprise a single solvent or a mixture of solvents. In some embodiments, the first phase liquid comprises a nonpolar solvent or mixture of nonpolar solvents. A nonpolar solvent sometimes referred to as an apolar solvent, may be understood to include solvents having a low net dipole moment. Preferably the nonpolar solvent has a dipole moment below 1.5 D (Debye units/1×10−18 statcoulomb-centimeters). The lower the dipole moment of a solvent the lower the solubility of polar compounds in that solvent. More preferably, the nonpolar solvent has a dipole moment below 1.0 D or lower, e.g., below 0.5 D, e.g., in a range between 0.35 and 0 D. Choice of the first phase liquid, including the one or more polar solvents may be limited by an availability, e.g. a commercial availability, of quantum dots that are capped with a shell of first ligands. For quantum dots that are capped with a shell of ligands comprising a surface binding head group and an alkyl or alkenyl having a number of carbon atoms n in a range between 12 and 20, e.g. oleic acid, oleylamine, ocdadecylamine and hexdecanoic acid) inventors found that first phase liquids comprising or essentially consisting of one or more aliphatic solvents, including but not limited to hexanes and octane to be suitable. The polar solvent 21, may be understood to include solvents having a high net dipole moment. Preferably, the polar solvent has a dipole moment above 1.5 D (Debye units/1×10−18 statcoulomb-centimeters). The higher the dipole moment of a solvent the lower the solubility of nonpolar compounds in the solvent. More preferably, the nonpolar solvent has a dipole moment above 1.6 D or higher, e.g., above 2, e.g., in a range between 1.5 and 5.
The difference in dipole moment and/or log P (n-octanol/water) were found to provide further selection criteria. The difference in dipole moment between the first and second phase liquids was found to be preferably at least 0.5D. The higher the difference the lower the mutual solubility between the liquid phases. Preferably, the difference in dipole moment between the first and second phase liquids is higher, e.g. at least 0.7 D or at least 1.0 D or more. Suitable polar solvents were typically found to have a negative log P value. Solvents with a negative log P value were generally found to be good solvents for the second ligands. Preferably, the polar solvents has a log P below about negative 0.2. Solvents with a lower log P value were generally found to be less miscible in the first phase liquid and/or less good solvents for the first ligands.
By adding the first and second phase liquids including their respective constituents to a common container a two phase system is formed in which the respective liquids are separated across a common interface. Across the interphase a ligand exchange process, a biphasic ligand exchange process, can start wherein the second ligand displaces the first ligands that are bound to the quantum dots 1.
At the interface ligands (first ligands 2), initially bound to the surface of the quantum dots 1, are displaced by the second ligand 3. It is believed that the exchange reaction proceeds on account of the higher surface affinity of the head group 3h of the second ligand 3 towards the quantum dot compared to the affinity of the head group 2h of the first ligand 2. Displaced first ligand moieties are thereby released ligands to the first phase liquid 10.
In some embodiments the method comprises washing the second phase liquid 20 which contains quantum dots capped with a shell of the second ligands 3s with one or more portions of a solvent for the first ligand. Washing the quantum dots that are capped with a shell of the second ligands 3s in second phase liquid 20 with one or more portions of a solvent for the first ligand can reduce an amount of free (unbound) first ligand in the product, which can be dissolved in liquid 20 in a minor concentration. Contaminations, e.g. an excess of ligand, can form a non-conductive or interfering domains in printed layers of quantum dots. As such the excess ligands which can negatively impart properties, e.g., electrical conductance, of a sensing material layer.
In some embodiments, the dispersion of quantum dots 1 that are capped with a shell 3s of the second ligands 3 in the second phase liquid may be considered to be an ink 100 composition. As will become clear below, the quantum dots 1 that are capped with a shell 3s of the second ligands 3 are preferably separated from the second phase liquid.
The quantum dots 1 that are capped with a shell 3s of the second ligands 3 are preferably essentially free of contaminants, i.e. highly pure. Contaminants, e.g. unbound ligands, salts, grease and/or wax, were found to negatively affect photoelectrical properties of the particles, e.g. of a film formed from an ink comprising said particles and impurities. Mitigating introduction and/or reducing a level of impurities is preferred over subsequent removal or purification procedures, as such subsequent cleaning or purification procedures, e.g. washing steps, can impact particle stability. Purity can be understood to be defined as the mass fraction of the quantum dots with a shell of the second ligands in the final dry powder. Preferably, the purity of the quantum dots is 90%, more preferably above 99%.
Separation of the quantum dots that are capped with a shell of the second ligands from the second phase liquid may be attained by any suitable method known in the field. Preferably, separation may be attained by centrifuging, to sediment the second ligand capped quantum dots from the polar phase. Centrifuging was found to be a reliable and fast method to separate particles from suspension forming a pellet of quantum dots 1 that are capped with a shell 3s of the second ligands 3. The separates quantum dots, e.g. in the form of a pellet, may be retrieved and stored easily. Quantum dots that are capped with a shell of the polar ligands when provided in a dry form, e.g. essentially in a solid form, were found to display improved stability compared to quantum dots that are stored in a fluid. Storage in dry form may mitigate quantum dot degradation, e.g. due to Oswald ripening. Storage under inert atmosphere, e.g., N2, may further mitigate quantum dot degradation, e.g. due to oxidation. In some embodiments, separating comprises adding of an anti-solvent to precipitate the quantum dots. The supernatant comprising a possible excess of free unbound second ligands can be discarded. Preferably, separation further includes a drying step, e.g. a vacuum drying step, to evaporate remaining solvent.
The second ligands comprise at least one surface binding head group that has an affinity for binding to a surface site of the quantum dots; and an ionically charged tail group and a counter ion associated therewith. The head group of the second ligand binds to the surface of the quantum dots, i.e. surface atoms of the quantum dots, via a hetero atom. The nature of the quantum dots, i.e. the type of binding sites available on an outer surface of the quantum dot, can determine selection of the type of surface binding head group of the second ligands. The surface binding head group comprises one or more hetero atoms selected from a group consisting of: O, S, Se, Te, N, P, As. Moieties comprising sulfur-based functional groups, e.g. thiols, thioesters and disulfides, are known to readily bind to a broad variety of surfaces by formation of a covalent metal-sulfur bond. Suitable surfaces including metal surfaces like Au and Ag, and semi-conductor surfaces including but not limited to chalcogenic materials such as CdS, CdSe, PbS, PbSe. Accordingly, for quantum dots of which the outer surface comprises such materials, the surface binding head of the second ligands preferably is thio-based.
The charged tail group of the second ligand provides the quantum dots with a shell that includes electrically charged groups. The charge functionality can be provided by a permanent ionic charge or a functional group which can become charged, e.g. a conjugate acid of a weak base or a conjugate base of a weak acid. Suitable charged tail groups group include, but are not limited to, carboxylates, sulphonic acids, phosphites, phosphonates, hydroxyls, sulphonates, amines, quaternary ammonium salts, carbocations, carboanions, etc. In some embodiments, the charged tail group includes acid adducts of a weak organic base, e.g., a hydrochloride adduct of a primary-, secondary or ternary amine. In other or further embodiments, the charged tail group includes a water soluble salt of an organic acid, e.g. sodium carboxylates or sulfonates.
The organic spacer separating the head group and the tail group can in principle be formed by any organic group that links, covalently links, the head group to the tail group. Depending on a desired application of the quantum dots the nature of the linker may play a more or less important role. For example, in applications wherein the quantum dots are comprised in a dense functional layer, e.g., an electrically conductive sensing layer, the size or length of the length of the spacer influences the interdistance between adjacent quantum dots within a dense layer of quantum dots. Preferably the organic spacer is a short spacer. The shorter the spacer the closer the quantum dots, i.e. the lower the particle-particle interdistance, can be in sensing layers formed from an ink comprising the quantum dots that are capped with second ligands. The shorter the particle-particle interdistance the better the optoelectronic properties can be. Preferably, the spacer is an aliphatic spacer, e.g. —CnH2n—, wherein the number of carbon atoms (n) equals 1, 2 or 3.
Exemplary second ligands 3 as described herein include cysteamine hydrochloride (
Inventors found that for the class of second ligands 3 as described herein (e.g., as described in relation to
Inks comprising quantum dots capped with a layer of cysteamine hydrochloride, cysteamine hydrobromide, sodium 2-sulfanylethanesulfonate, potassium 2-sulfanylethanesulfonate, or 2-(dimethylamino)ethanethiol hydrochloride were found to be stable for at least 24 hours. Quantum dots capped with a layer of cysteamine hydrochloride, cysteamine hydrobromide, sodium 2-sulfanylethanesulfonate, potassium 2-sulfanylethanesulfonate, or 2-(dimethylamino)ethanethiol hydrochloride were found to be particularly suitable in the manufacturing of a photoactive layer for optoelectronic devices such as solar cells, near-infrared photodetectors and X-ray detectors.
Contact time may be determined by process conditions, including but not limited to the concentration of the quantum dots in the first phase liquid and/or the concentration of second ligands in the second phase liquid, process temperature, and agitation conditions. To reduce contact time, the method preferably includes agitating the contacted first and second phase liquids, e.g. shaking or stirring, to increase the contact area between the phases. Preferably, contact between the first and second phase liquids is stopped after completion of the reaction, preferably within one hour of completion of the ligand exchange, or faster. Stopping the reaction preferably also includes separating the formed quantum dots that are capper with a shell of second ligands from the second phase liquid (the polar solvent). Stopping the reaction faster reduces a likelihood of contamination and/or of quantum dot degradation, e.g. by Oswald ripening. Typically the contact time is in the order of seconds or minutes, up to hours, e.g. about 30 seconds, about 1-5 minutes, about 15 minutes to one hour, or more. Progress of the ligand exchange can be determined experimentally, e.g. by chemical analysis and/or optically, to minimize contact time.
The amount (concentration times volume) of second ligands in the second phase is in excess with respect to the number of available binding sites on the quantum dots. The amount of second ligands in the second phase is at least sufficient to displace the aliphatic ligands, preferably all aliphatic ligands, from the quantum dots. The required amount can be determined experimentally. Progress of the ligand exchange reaction can for example be followed visually. Inventors find that the speed and completeness of ligand exchange correlates with the concentration of second ligands. Inventors found that the exchange reaction can proceed faster with higher concentrations of second ligands. The concentration of second ligands in the second phase is at least one hundred micro molar (μM). Preferably higher, e.g. at least one milli molar (mM) or at least ten mM or more, e.g. about thirty mM. A maximum solubility of the second ligands in the second phase can determine an upper concentration limit. Typically the concentration is below ninety percent of a maximum solubility
In a preferred embodiment, the amount of the second ligand that is dissolved in the polar solvent 21 does not exceed about 1.5 times, preferably below 1.05 times, a pre-determined required amount of the second ligand relative to an amount needed to completely cap the quantum dots 1 with a shell 3s of the second ligands. The exact amount of second ligand to be added can be determined experimentally. A too low amount may result in an incomplete or partial transfer of quantum dots from the first to the second phase liquid which can be observed visually. Presence of an excess of ligand can e.g., be determined by analysis of the solvent, e.g. the supernatant obtained after centrifuging. Alternatively, thermogravimetric analysis (TGA) can be used to measure an amount of second ligand that is to be added. This amount can be related to a mass fraction of first ligands bound to the colloidal nanoparticle. Typically, the ligand fraction in a colloidal PbS sample capped with oleic acid ranges from 10 to 50 wt % of the total weight (the weight of QD core and the capping layer of first ligands). Assuming a TGA analysis of a given QD composition shows 30 wt % mass fraction of oleic acid, and taking into account the molar mass of the ligand (282.45 g/mol), it can be calculated that a 1 mL sample comprising 20 mg/mL of such QD composition is to be contacted with an amount of second ligands that is at least 21.2 micromoles.
In some embodiments, the concentration of QDs in the first phase liquid is between about 0.5 and 100 mg/mL, e.g., 50, 30, 20, 10, 5 or 1 mg/ml. To enhance mixing, the relative volumes of the first and the second phase liquid are preferably in a range between about three to one to about one to three, more preferably the volumes of the first and the second phase liquid are about equal. Typically, for 1 mL of a first phase liquid comprising about 20 mg/mL PbS QDs about 1 mL of second phase ligand comprising about 30 mM of second ligands 3 is used. Preferably the excess of free ligand is smaller. Preferably the amount of second ligand 3 is in a range between about one and 1.01 times the pre-determined required amount. By providing the second ligands in an amount which is close to the pre-determined required the quantum dots may be capped with a shell of second ligands while at the same time an amount (concentration) of free (unbound) ligands in the polar solvent is minimized. In other words, the ligand moieties are preferably added in an amount such that, following the ligand exchange reaction, the resulting suspension of quantum dots that are capped with a shell of the second ligands has a close to zero concentration of free, unbound, ligand moieties in solution. By minimizing the amount of free ligand moieties in the ink, the particle interdistance in dense layers formed from such ink can be further reduced, e.g. further mitigate increase in particle-particle interdistance due to a presence of free ligands. Accordingly, in some embodiments, the method comprises the step of determining the required amount of the second ligand that is to be dissolved in the polar solvent 21 relative to an amount needed to cap the quantum dots 1 with a shell 3s of the second ligands.
In some embodiments, the step of determining the pre-determined required amount may be performed in a separate experiment. The step of determining the pre-determined required amount need not be included in each manufacturing cycle. The amount of second ligand added to the polar solvent 21 can be calculated (e.g. in dependence of a type and/or mass of quantum dots) from data obtained from a separate earlier experiment.
Inventors further found that it was possible to disperse (e.g. re-disperse) dry compositions of quantum dots that are capped with a shell of the second ligands in a polar solvent composition, e.g. a second polar solvent different from the first polar solvent in the ligand exchange process. Inventors find that the presence of charges in the shell helps dispersing and stabilizing the quantum dots 1.
The polar solvent composition in the ink (the second polar solvent) may or may not be of the same composition as the solvent comprised in the second phase liquid 20. Separating the quantum dots that are capped with a shell of the second ligands from the second phase comprising a first polar solvent and re-dispersing the quantum dots in a different polar liquid, e.g. a liquid printing medium, allows optimizing properties of the ink independent from selection criteria governed by the ligand exchange process.
The step of dispersing the separated quantum dots need not be directly follow the separating step. Inventors found that the separated quantum dots that are capped with a shell of the second ligands can advantageously be stored for prolonged periods without essentially losing functionality. Inventors found that the separated quantum dots can be stored for a period in excess of four weeks, before being used to formulate the printable ink. The separated quantum dots that are capped with a shell of the second ligands, e.g. pellets of the precipitated or sedimented quantum dots 1, are preferably dried, e.g. under vacuum, preferably right after separation, and before further usage.
The printable ink composition may be understood to relate to any medium that allows convenient and reliable deposition of a film of quantum dots on a target substrate. Suitable deposition methods include but are not limited to inkjet printing, blade coating, doctor blading, spin coating, slot-die coating, spray coating or any other known application method for depositing a liquid. Upon drying of the film substrates may be coated with films, or dense (dry) layers, of quantum dots that are capped with a shell of the second ligands. As such the printable ink composition can be used in the manufacturing of a variety of electronic devices, e.g. in the manufacturing of dense layers, e.g. photo-active sensing layers, for sensing applications such as near-infrared photodetectors or X-ray detectors. Such dense active layers can be manufactured by deposition and drying a layer of the ink composition on a target substrate, e.g. covering a set of electrodes.
For inks that are intended for use in the manufacturing of photo-electric sensing layers of electronic devices such as X-ray detectors, the quantum dots are preferably based on heavy metal compounds. Preferably, is such embodiment, the quantum dots comprise heavy atoms, e.g. PbS, PbSe. Typically, in a large crystal the band gap of PbS and PbSe is very small and not suitable for electronic applications. Advantageously, in the form of quantum dots the band gap increases and the film of PbS quantum dots can be used as a photosensitive semiconductor with variable band gap (in the range of 0.8-1.4 eV, more or less). Heavy metal-based quantum dots are particularly suitable as constituents of photo-active layers in devices for X-ray detection.
In some embodiments, e.g. as shown in
The printable liquid medium comprises a polar solvent (second polar solvent) or mixture of polar solvents 30 to disperse the quantum dots 1 that are capped with the shell 3s of second ligands 3. In some embodiments, the second polar solvent essentially consists of pure water, i.e. water without co-solvents. The pH of the printable liquid medium is preferably such that the tail group essentially remains charged, such that the capping layer does not lose its stabilizing character by protonation, respectively deprotonation, of the charged tail group of the second ligands. For water-based inks in which the second ligand comprises a conjugate base of an acid, the concentration of protons in the ink is preferably at least order of magnitude below the equilibrium pH of a pure solution of the corresponding weak acid (pH<pKa−1). For water-based inks in which in which the second ligand comprises a conjugate acid of a base the concentration of protons in the ink is preferably at least order of magnitude higher the equilibrium pH of a pure solution of the corresponding base (pH >pKa+1). The other pH limit of the ink (i.e. the maximum pH, or minimum pH respectively) can be governed by a known, or separately determined, stability of the quantum dot, e.g., towards etching. For quantum dots capped with cysteamine hydrochloride satisfactory colloidal stability of the ink was observed for a printable liquid medium with a pH that is in a range between about 1 to about 9. For quantum dots capped with sodium 2-sulfanylethanesulfonate or potassium 2-sulfanylethanesulfonate satisfactory colloidal stability of the ink was observed for a printable liquid medium that has a pH in a range about 7 to about 13.
The concentration of the quantum dots that are capped with a shell of the second ligands can vary on a broad range. A preferred quantum dot concentration depends on the application and the film deposition method. The quantum dot concentration in the inks the can be in a broad range from about 0.1 or 1 mg/mL up to about 300 mg/ml. High concentrations can advantageously allow deposition of thick dry films in a single deposition run. Excessively high concentrations can compromise long term ink stability. Inks with a concentration of quantum dots that is in a range between about 1 mg/ml up to about 100 mg/ml, preferably between about 3 and about 50 mg/ml, were found to yield a good balance between ink stability and quality of deposited films.
A shown in
In some embodiments, the ink comprises stabilizers. Stabilizers, e.g. antioxidants, can stabilize ligands which may degrade, e.g. oxidize. For example, if the ligand comprises a thiol or disulfide group, which can be easily oxidized (for example by oxygen) stabilizers may be added to the liquid medium. Examples of such stabilizers include but are not limited to dithiothreitol, glutathione, β-mercaptoethanol, sodium borohydride, tris(2-carboxyethyl)phosphine, ascorbic acid, N-acetylcysteine, γ-glutamylcysteine, and bacillithiol.
In some embodiments, the ink comprises a humectant. After depositing a layer of the ink on a target surface, and after evaporation of the lower boiling solvents the humectant is believed to remain in the dense film of quantum dots where it is found to improve the properties, e.g. the morphology, of the formed film. Improvement of film properties can be observed experimentally, e.g., by an improved optoelectronic properties of the film, e.g. in sensing layers for X-ray detectors. In some embodiments the humectant is a pyrrolidone. Pyrrolidone, e.g. 2-pyrrolidinone, can further improve wettability and/or reduce surface tension of the ink enabling deposition of more homogeneous quantum dot films compared to inks not comprising pyrrolidone. The concentration of pyrrolidone in the ink can be found experimentally by monitoring the morpholoy and/or electrical response of a deposited film. Similar to a presence of excess ligands an excess of pyrrolidone can increase the interdistance between adjacent quantum dots in a deposited dense film. Accordingly, in practice, and in particular for inks targeted to the deposition of dense quantum dot layers for optoelectronic applications (e.g. X-ray detectors), the amount (mass) of added pyrrolidone is below ten percent of the mass of second ligands comprised in the ink, preferably less, e.g. below five percent, e.g. in a range between 0.1 and one weight percent.
In other or further embodiments, the ink comprises one or more polymeric additive 33.
The concentration of the polymeric additives can be determined experimentally. For branched PEI with a Mw of about 25 kDa a suitable additive concentration in a range between 0.5 and 2.5 mg/mL was experimentally determined for inks with a quantum dot concentration of 20 mg/mL. For inks with other concentrations additive levels may be adjusted accordingly.
In some preferred embodiments, wherein the polar solvent in the printable liquid medium consists of a mixture of water and ethylene glycol, wherein the volume fraction of ethylene glycol in the mixture is in a range between five and fifty percent. Inks wherein liquid medium is essentially formed of water were found to display poor wetting behavior, e.g. break-up of deposited liquid film, which is believed to be a result of the high surface tension of water. Addition of ethylene glycol was found to improve wetting behavior and/or improve film formation. High fractions of water can be preferred from a cost and/or environmental perspective. Inventors found that part of the ethylene glycol can initially stay incorporated in the film upon deposition because of high boiling point. Inventors found that, upon complete drying, evaporation of this remainder can lead to significant undesirable volume shrinking of the film. Accordingly, the volume fraction of ethylene glycol in the mixture is preferably in a range between ten and thirty percent.
In other preferred embodiments, the polar solvent printable liquid medium 30 is an at least partially fluorinated lower alcohol. Lower alcohols may be understood to include alcohols having a total number of carbon atoms n of six or less. Compared to water and/or mixtures of water and ethylene glycol at least partially fluorinated lower alcohols or mixtures thereof, advantageously have a comparatively low surface tension. Inks having a comparatively low surface tension were found to display improved wetting behavior when deposited on a substrate. Compared to water and/or ethylene glycol, at least partially fluorinated lower alcohols advantageously have a high vapor pressure compared to water. Inks comprising solvents having a comparatively high vapor pressure were found to advantageously display improved, e.g. faster and/or more complete, drying when deposited on a substrate. Quantum dots capped with dimethyl(amino)ethanethiol hydrochloirde were found to display excellent colloidal stability in at least partially fluorinated lower alcohols such as 2,2,2,-trifluoroethanol and hexafluoroisopropanol. Furthermore, ternary solvent blends, including fluorinated alcohol, water and ethylene glycol can be advantageous. Fluorinated alcohol (FA) can reduce the surface tension effectively, thus the fraction of ethylene glycol can decrease. Therefore, less ethylene glycol will remain in the film. In some preferred embodiments, the blend comprises FA in a range between 20-50 vol %, water in a range between 40 and 80 vol %, and ethylene glycol in a range between 3 and 10%.
As shown and described in relation to
As shown and described in relation to
In a preferred embodiment, the amount of free unbound ligand moieties in the ink is below 10 μM, preferably lower, e.g. <1 μM. Most preferably, the ink composition is essentially without unbound (free) ligand moieties.
In some embodiments, the solvent comprised in the ink consists of a mixture of water and ethylene glycol, wherein the volume fraction of ethylene glycol in the mixture is in a range between ten and fifty percent.
In other embodiments, the solvent comprised in the ink consists of an at least partially fluorinated lower alcohol.
In other or further embodiments, the liquid printable liquid medium further comprises a p-type dopant or a n-type dopant.
As described herein the ink 100 as described herein and the method of manufacturing thereof are particularly suited for the manufacturing of dense layers comprising the quantum dots that are capped with a shell 3s of second ligands 3. These dense layers are suitable as sensing layers in a number of optoelectronic applications, including solar cells, photodetectors and X-rays sensors or even imaging devices having improved photo-electric properties. The invention provides a solution of scalable fabrication of high quality thick (>1 micron) semiconducting PbS QD films in ambient conditions, capable to detect X-ray radiation with a 10-fold sensitivity in comparison to a-Se detectors. Accordingly, the present invention relates to the use of the inks, e.g. in a manufacturing method of manufacturing an imaging device. The ink can also be used to advantage in other electronic devices such as field-effect transistors (FETs), solar cells, light emitting FETs (LEFETs), photodetectors for visible, IR or gamma irradiation and phototransistors.
to from a stack of photoactive layers 110 including at least a p-type photoactive layer 110p and an n-type photoactive layer 110n, wherein the photoactive layers are amorphous, comprising a disordered structure of quantum dots resulting from deposition by applying respective ink compositions.
In one embodiment, as shown in
Typically, n-type or p-type semiconductors are created by doping an intrinsic semiconductor with donor impurities. Alternatively or in addition the type of layer may be determined by appropriate selection of ligands. In a preferred embodiment, one or more, preferably all, of the photoactive layers comprise quantum dots (QD) formed by semiconductor quantum dots capped by ligand as described herein.
The photoactive layers are amorphous, e.g. comprising a disordered structure of quantum dots. Advantageously the ink as described herein advantageously yields photoactive layers that are amorphous, comprising a disordered structure of quantum dots resulting from deposition by applying respective solutions comprising colloidal quantum dots (CQD). The formation of amorphous photoactive layers, comprising a disordered structure of quantum dots, is believed to relate to the presence of the charged capping layer that surround the quantum dots. Preferably, each type of photoactive layer is deposited in a single (fluid) processing step, e.g. by spray coating, as opposed to a layer-by-layer deposition. Advantageously the ink as described herein advantageously can have a concentration of 1 mg/mL up to 300 mg/mL of quantum dots 1 that are capped with a shell 3s of second ligands 3 in a range photoactive which allows deposition, e.g. by spray coating of a photoactive layer in a single fluid processing step. By setting the quantum dot concentration layers that have a thickness in the order of micrometers can be obtained, e.g. layers between hundred and five hundred nanometer or layers with a thickness between one and thousand micrometer.
In some embodiments, the quantum dots are essentially separated by the ligands, e.g. without inorganic matrix there between. In some embodiments, the type of the photoactive layer is at least partially determined by inorganic dopants added to the layer. In other or further embodiments, the type of the photoactive layer is exclusively, essentially, or predominantly determined by inorganic dopants added to the layer. In one embodiment, the layers exclusively differ by the type of inorganic dopants. Alternatively, or additionally, it can be envisaged to use organic molecules/polymers as matrix.
The imaging device 1000 comprises readout electronics comprising electrodes 13t,13b sandwiching the photoactive layers 110 (with possibly other layers there between). Typically, at least one of the electrodes 13b is divided in respective pixels 100p for collecting photo-generated charges from respective parts of the photoactive layers. In a preferred embodiment, each pixel 100p comprises an amplification circuit to amplify the photo-generated charge which will be described in further detail below.
In a preferred embodiment, as shown, the stack of photoactive layers 110 comprises at least three different types of photoactive layers including an intermediate photoactive layer 110i between the p-type photoactive layer 110p and the n-type photoactive layer 110n.
Suitable materials for the semiconductor quantum dots 1 may depend on the application. For instance, PbS and PbSe quantum dots are well suited for visible and near- to mid-infrared light absorption, CdSe—for visible light, and PbS, PbSe, CdTe—for X- and gamma-ray absorption.
Optionally, as shown, further layers can be added to the stack. In the embodiment shown, an electron transport layer 120e is provided between one of the electrodes 130t and the n-type photoactive layer 110n. In the embodiment shown, a hole transport layer 120h is provided between the other electrodes 130b and the p-type photoactive layer 110n. Typically, the top electrode 130t is transparent at least to the wavelength λ of light to be measured by the detector. Alternatively, the stack can be reversed, e.g. using a transparent substrate and bottom electrode (not shown).
In some embodiments, as shown e.g. in
As described herein, relatively small quantum dots may have an average or median diameter of less than four nanometer. This may allow e.g. visible light absorption. Conversely, relatively large quantum dots may have an average or median diameter of more than four and half nanometer. This may allow e.g. infrared light absorption.
In some embodiments the intermediate photoactive layer 110i comprises relatively large quantum dots compared to quantum dots in the p-type photoactive layer 110p and the n-type photoactive layer 110n. For example, the relatively larger quantum dots in the intermediate photoactive layer 110i may be larger by at least a factor 1.1, 1.2, 1.5, or more. For example, the quantum dots in the intermediate photoactive layer 110i may be >4.5 nm. This may provide a relatively small band gap to absorb (near)infrared light. So in this way a near infrared detector may be provided.
In some embodiments e.g. as shown in
In some embodiments, the intermediate layer thickness can be on the order of micrometers, e.g. between one and thousand micrometer, preferably between ten and hundred micrometer. For example, the quantum dots in a relatively thick intermediate layer may provide a direct conversion radiation sensor where the quantum dots absorb ionizing radiation. Preferably, is such embodiment, the quantum dots comprise relatively heavy atoms and have large band gap, e.g. PbS or other material with diameter less than four nanometer.
Aspects of the invention will now be illustrated by the following non-limiting examples.
In a first example a dispersion of oleate-capped PbS quantum dots in 1 ml of hexane with 20 mg/ml of quantum dots is transferred in a vial containing 1 ml of a 30 mM solution of cysteamine hydrochloride in DMF (or 30 mM solution of MESNA in NMF). The vial is shaken at room temperature until all the QDs are transferred into the polar phase. This takes about 30s. Progress of the reaction was followed by monitoring the color of the phases. At the start of the ligand exchange process the colored quantum dots are comprised in the nonpolar phase. Transfer of the color to the polar phase is an indication that the colloidal suspension of the quantum dots 1 that are capped with a shell of second ligand is formed in the polar phase.
After completion of the ligand exchange the nonpolar phase was discarded and the polar phase was washed 3 times with 1 ml of hexane. The QDs are then precipitated by centrifugation. After the centrifugation the supernatant was discarded, and the pellet was dried in vacuum until the remaining solvent evaporates. Further, the pellet can stay in nitrogen environment until the device fabrication moment. The pellet was dispersed in a 80/20 volume/volume mixture of water/ethylene glycol shortly before device fabrication.
It was found that the ligand exchange processes according to the invention can be scaled up to the multigram scale without essentially affecting the properties of the formed QDs. The photo a 1L separation funnel comprising the biphasic mixture after the complete ligand exchange as shown in
In the second example, the procedure of example 1 was repeated successfully for CdSe quantum dots capped with oleic acid.
In the third example the procedure of example 1 was repeated for Au quantum dots 1 capped with oleylamine in heptane.
In the fourth, fifth and sixth example, the experiments of examples 1-3 were repeated using sodium 2-sulfanylethanesulfonate as second ligand. in these examples 1 mL of acetone (anti-solvent) was added to the second phase to precipitate the quantum dots. For systems using cysteamine hydrochloride DMF addition of an anti-solvent is possible but not needed. Otherwise results are comparable.
In a seventh example the ligand exchange process was repeated for PbS quantum dots capped with oleic acid using disulfide of cysteamine hydrochloride as second ligand. The disulfide of cysteamine hydrochloride was found to be poorly soluble in DMF, but was soluble in DMSO. Therefore the otherwise similar process was conducted using DMSO as solvent. Complete ligand exchange was observed and a pellet of PbS quantum dots that are capped with a shell of cysteamine hydrochloride ligands was obtained after centrifugation.
The QDs and ink composition as described herein can be of particular benefit for optoelectronic devices. Under reference to
For the external quantum efficiency (EQE) measurements, the current response was measured under short-circuit conditions (photocurrent operation mode, V=0 V), while illuminating the area of the device (4×4 mm2) through 3 mm-diameter opening.
Based on the responsivity curve, the EQE values were calculated (
To calculate the specific detectivity D*, the device was measured under reverse voltage bias in dark and under monochromatic illumination.
where R is the responsivity and Jdark is the dark current density.
This brings the values of the specific detectivity of 1.3E12 Jones for 0.1V, 9.6E11 Jones for 0.5V and 7.2E11 Jones for 1V bias.
As comparative examples inventors attempted to prepare cysteamine hydrochloride capped quantum dots according to the method disclosed by Hak Soo Choi et al (Nature biotechnology 25; 1165-1170 (2007). To this end equal volumes of a chloroform solution of oleate-capped PbS QDs were mixed with 30 mM solutions of cysteamine hydrochloride dissolved in watery PBS buffer. However, even after prolonged stirring (>12h), no ligand exchange (LE) was observed. In contrast, the method of ligand exchange according to the invention was complete after about 30 seconds.
In addition, it was attempted perform ligand exchange in a hexane/water mixture (oleate-capped PbS QDs in hexane; of cysteamine hydrochloride in water). Inventors surprisingly found that ligand exchange can be promoted by addition of a third solvent to the biphasic mixture. The third solvent being miscible with both hexane and water.
For the purpose of clarity and a concise description, features are described herein as part of the same or separate embodiments, however, it will be appreciated that the scope of the invention may include embodiments having combinations of all or some of the features described. For example, while embodiments were shown for certain quantum dots and ligands, also alternative ways may be envisaged by those skilled in the art having the benefit of the present disclosure for achieving a similar function and result. The various elements of the embodiments as discussed and shown offer certain advantages, such as a versatile method for exchanging a non polar ligand shell, e.g., a native ligand shell, of a quantum dots for a tailor made shell of ligands that can be selected according to a desired property, e.g. solubility, colloidal stability, and/or optoelectronic properties. Of course, it is to be appreciated that any one of the above embodiments or processes may be combined with one or more other embodiments or processes to provide even further improvements in finding and matching designs and advantages. It is appreciated that this disclosure offers particular advantages to inks for the manufacturing of optoelectronic devices, and in general can be applied for any application benefitting from quantum dots that are capped with a specific shell of second ligands.
In interpreting the appended claims, it should be understood that the word “comprising” does not exclude the presence of other elements or acts than those listed in a given claim; the word “a” or “an” preceding an element does not exclude the presence of a plurality of such elements; any reference signs in the claims do not limit their scope; several “means” may be represented by the same or different item(s) or implemented structure or function; any of the disclosed devices or portions thereof may be combined together or separated into further portions unless specifically stated otherwise.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20159348.0 | Feb 2020 | WO | international |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/NL2021/050124 | 2/24/2021 | WO |
