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Definitions

• the invention relates to a method for obtaining salts, organic iodides, with a general formula (R X NI) featuring high purity of the obtained products, a perovskite- forming composition, suitable to be used in obtaining a perovskite photoactive coating, containing at least one iodide obtained using this method, and a photovoltaic cell with a perovskite photoactive layer formed using this composition.
• R X NI general formula
• Photoactive coatings are used to produce photovoltaic cells, i.e. semiconductor elements used to convert solar radiation into electricity.
• the photoactive layer acts as a sunlight (photon) absorber, so it is usually applied as a visible surface of the cell, coated with a suitable sunlight permeable (translucent/ transparent) electrode material.
• photoactive inks One of the known types of photoactive coatings are photoactive inks.
• One of the advantages of a photoactive ink is easy and inexpensive method of application of the ink onto the substrate: the ink is printed, wherein the choice of the printing technique depends on the production scale, the type of substrate and the physical properties of the ink, such as its viscosity and adhesive properties.
• organic photoactive inks containing organic film-forming substance in a form of doped polymers or monomers capable of polymerisation after its application onto the target substrate There are known organic photoactive inks containing organic film-forming substance in a form of doped polymers or monomers capable of polymerisation after its application onto the target substrate.
• a US patent application US20130087744 describes a composition of a photovoltaic ink consisting of polymeric precursors with a formula M B (ER) 3 , where M B is a metal selected from the group of: In, Ga or Al; E is S or Se, and R represents an alkyl, aryl, heteroaryl, alkenyl, amide or silyl moiety.
• M B is a metal selected from the group of: In, Ga or Al
• E is S or Se
• R represents an alkyl, aryl, heteroaryl, alkenyl, amide or silyl moiety.
• Organic substances such as aliphatic and aromatic hydrocarbons as well as siloxanes, cyclosiloxanes, silicone fluids, acetonitrile, esters and ethers are used as ink solvents.
• the ink is admixed with compounds with the molecular formula: M a3 ⁇ 4 M B (ER) 4 or with the formula: M aft (ER) where M alk is: Li, Na or K, and R is an alkyl or aryl moiety.
• Other ink ingredients are surfactants, dispersants and emulsifiers, anti-foaming agents, viscosity modifiers, antioxidants and pro-adhesive agents.
• the ink is in a l form of a suspension or solution, prepared by mixing all the ingredients.
• the ink acts as a photovoltaic layer and is applied onto the substrate by printing. In order to solidify the coating applied, the ink is dried by evaporation of the solvent.
• perovskites are known materials used to obtain photovoltaic cells.
• Perovskites are hybrid organic-inorganic compounds with a general formula ABX 3 , wherein, typically in solar cells, A is an organic methylammonium cation (CH 3 NH 3 + ) whose presence enhances the solubility of the material, so that perovskite is suitable for thin layer application, B is an inorganic cation such as lead cation (Pb 2+ ), and the anion X is selected from the halogen group, typically being an anion of iodide (G), bromide (Bf) or chloride (Cl ).
• Perovskites are produced in a form of films, i.e.
• the perovskite layer is located between a layer of p-type conductive material and a layer of n-type conductive material, which are typically covered with suitable electrodes, including one electrode allowing the transmission of sunlight photons.
• Perovskite thin films intended for photoactive layers of photovoltaic cells are prepared from perovskite-forming compositions, which are colloidal solutions containing perovskite precursors, i.e. substrates for the synthesis of a particular perovskite, constituting the dispersed phase, wherein the colloid contains a suitable liquid as the dispersion medium , usually an organic solvent.
• perovskite-forming compositions which are colloidal solutions containing perovskite precursors, i.e. substrates for the synthesis of a particular perovskite, constituting the dispersed phase, wherein the colloid contains a suitable liquid as the dispersion medium , usually an organic solvent.
• Two-component perovskite-forming compositions are also known that contain two physically separated components, which, after mixing, react to produce perovskite.
• the colloidal particles take a form of coordination complexes, typically represented by the structure of lead polyhalides between organic and inorganic components, which structure may be adjusted by changing the degree of coordination of the complex, which allows a formation of a perovskite layer, in a form of a thin film with predetermined film coverage parameters and morphology of the perovskite structure obtained.
• perovskite-forming compositions in a form of inks, containing at least one perovskite precursor, in which the mechanism of curing, i.e. of forming a photoactive coating, comprises the synthesis of perovskite from the perovskite precursors contained in the composition.
• This composition may take a form of a powder or ink and may contain as a solvent, dimethylformamide (DMF) or isopropanol (IPA) as well as additives including thickening agents such as glycerol or d-sorbitol, and crystallisation retardants such as dimethylsulphoxide (DMSO).
• DMF dimethylformamide
• IPA isopropanol
• thickening agents such as glycerol or d-sorbitol
• crystallisation retardants such as dimethylsulphoxide (DMSO).
• the method for curing this composition, on a selected substrate, in order to form a photoactive layer consists in applying a layer of said composition having an appropriate thickness onto the substrate and curing the composition consisting in synthesising suitable perovskites from their precursors, evaporating the solvent, if present in the composition.
• the film-forming composition may be applied onto the substrate using the spin-coating technique, printing and heating of the applied layer or applying a coating from the gaseous phase, including dual source evaporation, or using the ablation technique, or printing, including in particular ink-jet printing, as well as spraying, blade-coating, meniscus-coating, slot die coating, or dip coating.
• the resulting photoactive layer features good absorption of photons, whereas the prepared photovoltaic cells comprising the perovskite film obtained by curing the film-forming composition exhibit good efficiency.
• phosphoric acid (I) also referred to as phosphinic acid: H 3 P0 2 in stabilising hydrogen iodide: HI is necessary for the synthesis of the perovskite precursor from the OPT group - methylammonium iodide (MAI - MethylAmmonium Iodide).
• phosphoric acid (I): H 3 P0 2 as the stabiliser of hydrogen iodide HI during the MAI synthesis effects the contamination of the reaction product with methylammonium hypophosphite: MAH 2 P0 2 , which is due to H 3 P0 2 reacting with methylamine (MA).
• perovskite precursors i.e. raw materials for the synthesis of perovskites
• the methods for obtaining perovskite precursors are continuously modified so as to obtain compounds with an appropriate degree of purity in order to use these compounds for preparing perovskite- forming compositions for fine perovskite coatings exhibiting appropriate morphology and quality of crystals, and, consequently, increasingly superior properties of photovoltaic cells produced using such coatings as photosensitive elements.
• R X N is an organic cation (R X N + )
• R represents substituents (R-) independently selected from a group consisting of organic substituents: R 1 -, R 2 -, R 3 - and hydrogen (H-)
• x is a number of the substituents R- directly linked with the nitrogen (N) atom in the organic cation R X N + , wherein x is 3 or 4
• I is an iodide anion (G).
• the method comprises: preparing a reaction mixture comprising the steps of: synthesizing hydrogen iodide (HI) in situ by mixing molecular iodine (l 2 ) with formic acid (COOH) in a molar ratio of molecular iodine (l 2 ) : formic acid (COOH) of no less than 1.01 :1 , in a solvent medium, introducing into the solvent medium a compound being a donor of organic cation R X N + in an amount providing the molar ratio of the donor of organic cation R X N + : molecular iodine (l 2 ) of no less than 1.01 :1 , and maintaining the reaction mixture at a temperature of not less than 20 °C for the time necessary to obtain the reaction product being the salt with the general formula R X NI.
• the donor of organic cation R X N + contains as the organic substituents: R 1 -, R 2 - and optionally R 3 - moieties independently selected from the group consisting of: straight chain or branched chain alkyl substituents containing 1 to 8 carbon atoms in the substituent molecule, optionally containing at least one heteroatom substituting the carbon atom or hydrogen atom in the substituent molecule, wherein the heteroatom is selected from the group consisting of: silicon, oxygen, nitrogen, sulphur, iodine, chlorine and bromine.
• molecular iodine (l 2 ) is mixed with formic acid (HCOOH) at the molar ratio: molecular iodine (l 2 ) : formic acid (COOH) of 1.01 :1 to 1.1 :1 , and the donor of organic cation R X N + is introduced to the solvent medium in the amount providing the molar ratio of the donor of organic cation R X N + : molecular iodine (l 2 ) of 1.01 :1 to 1.50:1.
• molecular iodine (l 2 ) is mixed with formic acid (HCOOH) at the molar ratio of iodine (l 2 ) : formic acid (COOH) of 1.01 : 1.
• the reaction mixture is heated to a temperature in the range from 20 to 80 °C.
• the donor of organic cation R X N + is introduced to the solvent medium following the synthesis in situ of hydrogen iodide (HI).
• amine is used as the donor of organic cation R X N +
• the obtained salt (R X NI) contains the organic cation (R X N + ) selected from the group consisting of: alkylammonium cations (R(H 3 )N + ), dialkylammonium cations R 2 (H 2 )N + , and trialkylammonium cations (R 3 (H)N + ).
• alkyl ammonium iodide has the general formula of R(H 3 )NI, where the substituent R represents an alkyl moiety containing 1 to 8 carbon atoms.
• methylamine is used as the donor of organic cation R X N + , and methylammonium iodide (MAI) is obtained as the salt.
• MAI methylammonium iodide
• octylamine is used as the donor of organic cation R X N + , and octylammonium iodide (OAI) is obtained as the salt.
• OAI octylammonium iodide
• the solvent medium comprises at least one compound selected from the group consisting of: methanol, ethanol, absolute ethanol, isopropanol, dioxane, tetrahydrofuran (THF) and dimethylformamide (DMF).
• the solvent medium is water.
• preparing the reaction mixture further comprises the step of introducing, into the solvent medium, a catalyst being a salt with the general formula R x NI.
• the catalyst is a compound identical to the salt R X NI being the reaction product.
• the catalyst is obtained by the method according to the present disclosure.
• the catalyst is introduced at a molar ratio of catalyst: molecular iodine (l 2 ) ranging from 0.01 :1 to 0.03 :1.
• perovskite-forming composition which comprises the salt with the general formula: R X NI obtained using the method according to the present disclosure.
• the composition comprises the salt with the general formula: R X NI selected from the group consisting of: methylammonium iodide (MAI), ethylammonium iodide, propylammonium iodide, butylammonium iodide, pentylammonium iodide, hexylammonium iodide, heptylammonium iodide, octylammonium iodide (OAI) and formamidinium iodide (FAI).
• MAI methylammonium iodide
• OAI octylammonium iodide
• FAI formamidinium iodide
• the composition further comprises at least one lead salt and at least one solvent.
• the composition further comprises methylammonium dihydrogen phosphate (I) CH3NH3H2PO2.
• the composition comprises the following compounds: methyl ammonium iodide (MAI), anhydrous lead (II) acetate (CFhCOO ⁇ Pb and lead (II) chloride PbCh in the amounts effective for the synthesis of perovskite from said compounds, as well as dimethylformamide (DMF) as a solvent and methyl ammonium dihydrogen phosphate (I) CFI3NFI3FI2PO2 in the amount of 0.3% by weight with respect to the weight of methylammonium iodide (MAI) contained in the composition.
• MAI methyl ammonium iodide
• II anhydrous lead
• II lead
• chloride PbCh in the amounts effective for the synthesis of perovskite from said compounds
• DMF dimethylformamide
• I methyl ammonium dihydrogen phosphate
• CFI3NFI3FI2PO2 methyl ammonium dihydrogen phosphate
• the composition comprises formamidinium iodide (FAI), methylammonium bromide CFIsNFIsBr, lead (II) iodide Pbl 2 and caesium iodide (Csl), in the amounts effective for the synthesis of perovskite from said compounds.
• FI formamidinium iodide
• CFIsNFIsBr methylammonium bromide
• lead (II) iodide Pbl 2 lead
• Caesium iodide Csl
• the cell comprises a perovskite layer obtained from the perovskite- forming composition comprising ingredients as described above.
• Fig. 1 is a schematic representation of the synthesis reactions of organic iodide (R X NI) using the method according to the disclosure;
• Fig. 3 is a schematic representation of the synthesis reactions of octylammonium iodide (OAI) using the method according to the disclosure;
• OAI octylammonium iodide
• Fig. 11A shows a SEM image of a perovskite coating prepared with
• Composition I, Example VIII, and Fig. 11 B shows a SEM image of a perovskite coating prepared with Composition II, Example VIII;
• Fig. 14A shows images of colloids containing MAI obtained using the method according to the invention
• Fig. 14D shows photographs of colloids of identical composition containing MAI obtained using a prior art method, and recrystallized trice.
• the developed method for preparing R X NI compounds ensures improved purity of the obtained products, which in turn enable for using them as perovskite precursors in various perovskite-forming compositions, including colloidal solutions, such as inks, for producing perovskite coatings with improved morphology and quality of perovskite crystals.
• the developed method of the iodide synthesis differs from the prior art methods in that the method according to the present disclosure involves the step of obtaining hydrogen iodide (HI) in situ in the reaction medium.
• hydrogen iodide (HI) is not used as a direct substrate for the synthesis of the respective iodides.
• the developed method comprises the step of supplying, into the reaction medium, the substrates that are suitable for in situ hydrogen iodide (HI) synthesis.
• the substituents R-, R 1 -, R 2 -, R 3 - may be the same or different moieties selected from a group consisting of: hydrogen (H-), straight chain and/or branched aliphatic hydrocarbons (C y H z -), alicyclic hydrocarbons, including saturated hydrocarbons and/or containing an unsaturated bond or bonds, and aromatic hydrocarbons.
• every substituent: R- R 1 -, R 2 -, R 3 - of organic cation (R X N + ), other than (H-) may contain 1 to 8 carbon atoms in the molecule, i.e.
• R- R 1 -, R 2 -, R 3 - with the general formula CyH z -, y may be: 1 ⁇ 8.
• at least one substituent: R 1 -, R 2 -, R 3 - of the organic cation may have at least one atom of carbon or hydrogen substituted with another atom, for example: silicon, oxygen, nitrogen, sulphur, iodine, chlorine or bromine.
• the developed method may be used to obtain iodide salts (R X NI), wherein the organic cation (R X N + ),
• MAI methylammonium iodide
• OAI octylammonium iodide
• FAI formamidinium iodide
• iodide salts R 4 NI (Fig. 5, formula I), such as: methylammonium iodide (MAI), dimethylammonium iodide, propylammonium iodide, methylethylammonium iodide, butylammonium iodide, pentylammonium iodide, hexylammonium iodide, heptylammonium iodide, octylammonium iodide (OAI), as well as iodide salts with the general formula R 3 NI (Fig. 5, formula II), such as formamidinium iodide (FAI) or guanidinium iodide (GAI).
• MAI methylammonium iodide
• FAI formamidinium iodide
• GAI guanidinium iodide
• Figs. 1 - 4 are schematic representation of the reactions occurring during the synthesis according to the developed method, with Fig. 1A, 2A, 3A and 4A showing the synthesis without the use of a catalyst, while Fig. 1 B, 2B, 3B, and 4B show synthesis with the use of catalyst, being an option.
• the developed method for preparing iodide salts comprises steps in which, - molecular iodine l 2 is supplied to a reaction medium in excess with respect to formic acid (HCOOH), and in deficit with respect to a donor of organic cation ( xN + ),
• HCOOH hydrogen iodine
• organic compounds may be used as the donors of organic cation R X N + i.e. the compounds that are capable of dissociation in the reaction medium to form a respective organic cation: R X N + , i.e. a cation selected from the group: R 4 N + and R 3 N + .
• compounds whose dissociation does not involve introducing additional, and difficult to remove, contaminations to the reaction medium are used as the donors of organic cation R X N + .
• the respective amines will therefore dissociate, yielding the respective organic cation R 4 N + being the substrate for salt synthesis.
• a compound serving as the donor of organic cation provides high purity of synthesis product, i.e. a salt containing an iodide anion and an organic cation, so that the quality of perovskite coatings made with the salt R x NI prepared using the developed method is improved.
• the reaction may be carried out in polar or apolar medium, with various solvents providing good solubility of molecular iodine (l 2 ) (reactions presented in Figs: 1A, 2A, 3A and 4A) or iodine in ionised form: l 3 (reactions presented in Figs: 1 B, 2B, 3B and 4B) as well as providing good solubility of the donor of organic cation R X N + used.
• molecular iodine l 2
• iodine in ionised form: l 3 reactions presented in Figs: 1 B, 2B, 3B and 4B
• the solvent should preferably allow the reaction to be carried out at a temperature above 50 °C, so that for example the solvent should have a boiling point of over 50 °C, and, more preferably, a boiling point between 50 and 150 °C.
• a solvent with a boiling point above 150 °C could be difficult to remove when cleaning the reaction product, thus, such the solvent may constitute an undesired contamination, and therefore is less preferred for use.
• the reaction can be carried out in a solvent such as water, methanol, ethanol, absolute ethanol (at a concentration of 99.8%, for example, obtained by distillation with added benzene; the contamination of the solvent with a small amount of benzene does not adversely affect the final purity of the product, since it may be removed in the course of purification), isopropanol, a mixture of suitable alcohol with water, dioxane, tetrahydrofuran (THF), wherein the reaction is preferably carried out using absolute ethanol as the solvent, since absolute ethanol provides relatively high solubility of substrates including molecular iodine and the donors of organic cation, including methylamine. Furthermore ethanol has a boiling point of 78 °C, thus allowing the reaction to be carried out at preferred temperature of over 50 °C.
• a solvent such as water, methanol, ethanol, absolute ethanol (at a concentration of 99.8%, for example, obtained by distillation with added benzene; the contamination of
• absolute ethanol is easily removable in the course of the purification of the reaction product.
• the polar character of the molecule weakens in favor of non-polar character of the molecule. This imposes using, instead of water, solvents such as methanol, ethanol, isopropanol, absolute ethanol, dioxane, tetrahydrofuran (THF).
• ethanol may be used as the solvent.
• Introduction of the donor of organic cation in the course of preparation of the reaction mixture is preferably accomplished at the temperature from the range of 0 to 30 °C
• the addition of the donor of organic cation may be accomplished at room temperature, since the reaction triggered by such the addition is exothermic by nature.
• the reaction mixture is heated preferably to the temperature exceeding 50 °C. This ensures an increase in the reaction rate. In such temperature conditions the reaction can be carried out within a relatively short period of time, e.g., less than 2 hours, with satisfactory product yield.
• Fig. 1A, 2A, 3A, 4A schematically represent the respective reaction stages of iodides salts synthesis, according to the developed method, in a form of stoichiometric equations, wherein Fig. 1A is a general representation of the reaction of R X NI iodide synthesis, while Fig. 2A presents synthesis of methylammonium iodide (MAI), Fig. 3A presents synthesis of octylammonium iodide (OAI), while Fig. 4A presents synthesis of formamidinium iodide (FAI).
• reactions marked with reference numbers 1 and 2 represent the individual synthesis steps, including intermediate products, while the reaction marked with reference number 3 is a summary of reactions 1 and 2.
• reaction 1 formic acid (FICOOFI) reacts with molecular iodine (l 2 ) to form hydrogen iodide (FTl ) in situ and by-product carbon dioxide (C0 2 ) which is released.
• FICOOFI formic acid
• l 2 molecular iodine
• C0 2 by-product carbon dioxide
• the formed hydrogen iodide constitutes the source of iodide anions.
• the iodide ions (G) then react (reaction 2) with the compound being the donor of organic cations, yielding the reaction product: iodide of the respective organic cation R X NI.
• the reaction is carried out with an excess of iodine (l 2 ) with respect to formic acid (HCOOH), wherein, preferably, in the reaction there is used an excess of iodine at a molar ratio from 1 .01 (l 2 ) : 1 .0 (HCOOH) to 2.0 (l 2 ) : 1 .0 (HCOOH) and more preferably, molecular iodine (ll 2 ) is used in excess at a molar ratio with respect to formic acid of 1 .01 (l 2 ): 1 .0 (HCOOH) to 1 .10 (l 2 ) : 1 (HCOOH), and most preferably at a molar ratio of 1.05 (l 2 ) : 1 (HCOOH).
• HCOOH formic acid
• the product needs to be purified, and if an excess of iodine used is higher than indicated, the purification procedure may need to be repeated (recrystallization), which generates additional costs due to the use of additional solvents, which is also time-consuming.
• reaction is carried out in an excess of the donor of organic cation (R x N +) (examples of which are indicated above) with respect to molecular iodine (l 2 ), wherein the most preferred excess of the donor of organic cation with respect to molecular iodine is in the range of 1.01 to 1.50 mole of the donor of organic cation for each 1 mole of molecular iodine (l 2 ).
• R x N + examples of which are indicated above
• the excess of organic cation (R X N + ) with respect to molecular iodine ensures complete reaction of the hydrogen iodide (HI), obtained in-situ, with the organic cation. If the obtained HI remained in the reaction environment, resulting from a molar deficit of the donor of organic cation, at the end of the reaction, this remained acid HI might undergo oxidation to iodine oxoacids such as: HIO, HI0 2 , HIO 3 and HIO 4 , so that by-products (in a form of respective salts) might be formed through anion-exchange reactions between the iodine oxoacids and the reaction product.
• iodine oxoacids such as: HIO, HI0 2 , HIO 3 and HIO 4
• An additional advantage of providing an excess of the donor of organic cation (R X N + ), at the preparation of the reaction mixture, is a relatively low price of the mentioned compounds (such as methylamine) comparing to the price of molecular iodine (l 2 ), which means a reduction in the cost of preparing respective iodides using the developed method.
• a small (catalytic) amount of MAI is mixed with iodine (l 2 ) in the first step, as shown in Fig. 2B (reaction 1 ).
• reaction 1 to 3 show the individual steps of the synthesis of the product with the catalyst, indicating the transition states and intermediate products, while reaction 4 is a summary of reactions 1 - 3: substrates and products.
• the catalyst being a respective iodide salt (preferably the same as the one to be obtained) reacts with iodine (l 2 ), yielding a transition state: a three-atom iodine anion: l 3 , which then (reaction 2) reacts with formic acid, yielding: a respective iodide salt, hydrogen iodide (HI) in situ and carbon dioxide.
• reaction 3 the resulting iodide anions react with the organic cation donor compound R X N + to yield the respective R X NI, iodide salt, which is the reaction product.
• I 3 ions formed with the catalyst added to the reaction, feature greatly improved solubility, in polar solvents, and they react more readily with formic acid FICOOFI, yielding hydrogen iodide (HI) in situ, when compared to that of molecular iodine (l 2 ), which is slightly less prone to react with formic acid with obtaining hydrogen iodide (HI) in situ.
• a catalyst Fig. 1 B - 4B, respectively
• the addition of the catalyst reduces the reaction time by approximately 60 to 180 minutes.
• the average reaction time is 20 to 120 minutes, while without catalyst, the average reaction time is 120 to 300 minutes.
• An additional advantage of using the catalyst being the same compound as the product of the reaction is improved purity of the resulting product as the catalyst and the reaction product are the same compounds, thereby the catalyst does not constitute contamination of the product.
• a iodide salt, preferably R X NI which is not the same compound as the synthesised product, will also increase the reaction rate.
• the catalyst is added to the system in an amount of 0.01 to 0.03 mole per each mole of molecular iodine (ll 2 ), i.e. in the molar ratio of 0.01 (mole of the catalyst ) : 1 (mole of l 2 ) to 0.03 (mole of the catalyst): 1 (mole of l 2 ).
• the reaction with the presence of catalyst is carried out at a temperature ranging from 0 to 80 °C.
• MAI may be preferably used as the catalyst
• OAI may be preferably used as the catalyst
• FAI may be preferably used as the catalyst
• R X NI iodides salts obtained using the developed method feature improved product purity and are suitable e.g. to be used as one of the precursor components of the respective perovskite, in perovskite-forming compositions, for example, such as perovskite inks for printing on various substrates, such as: ITO, to prepare perovskite photoactive layers in photovoltaic cells.
• R X NI iodides obtained using the inventive method in perovskite- forming compositions especially those used in photovoltaics in photoactive layers, is particularly advantageous. This is because the R X NI iodides obtained, used as one of the substrates in the synthesis of perovskites, ensure the formation of a perovskite layer exhibiting improved morphology, resulting in improved photoactive properties of the resulting perovskite layer.
• Fig. 6 shows exemplary reactions of perovskites synthesis from the iodides R X NI prepared using the method according to the present disclosure.
• the obtained perovskites are suitable for use in photovoltaic cells, as photoactive layers.
• the reactions: 1 , 2, 3, 5 and 6 present syntheses in which one of the precursors of perovskite is methylammonium iodide (MAI) prepared using the developed method, while another precursor is iodide, bromide or lead (II) chloride or tin (II) iodide, respectively.
• MAI methylammonium iodide
• Reaction 4 represents a synthesis wherein one of the perovskite precursors is formamidinium iodide (FAI) prepared using the method according to the present disclosure, and another perovskite precursor is lead (II) iodide.
• FAI formamidinium iodide
• II lead
• iodides prepared using the developed method can be used to obtain various perovskites, including in particular those used in photovoltaics, for photoactive layers.
• the iodides obtained using the developed method are suitable to be used in perovskite-forming compositions as precursor components of perovskites (for example, in accordance with the reactions in Fig. 6) including those in a form of colloidal solutions containing, as the other perovskite precursor, the respective lead salt: lead halide: lead (II) iodide, lead (II) chloride or lead (II) bromide.
• a particularly advantageous perovskite-forming composition in a form of a colloidal solution is the composition containing iodide salt obtained using the developed method and added methylammonium dihydrogen phosphate (I) CFI 3 NFI 3 FI 2 P0 2 is especially suitable, since the perovskite-forming layers obtained with this composition provide improved parameters of the photovoltaic cell obtained therewith.
• Bubble formation was observed only after adding methylamine, which can be explained by the fact that the use of hydrogen iodide (HI) produced in situ significantly accelerates the reaction.
• the brown mixture was heated for 1 hour while maintaining the temperature of the mixture at 80 °C, after which the reaction was terminated. After 1 hour of heating, the mixture turned pale brown from brown; however, the colour of the mixture was not considered to be an indicator of the termination of the reaction, due to the excess of iodine used with respect to formic acid, preventing the conversion of the whole content of iodine (l 2 ) into hydrogen iodide (HI).
• the excess iodine used added to the reaction prevented the formation of methylammonium formate as a by-product of the reaction.
• the obtained product was isolated by evaporation of the solvent from the post-reaction mixture to obtain a yellow and brown powder, which was completely dissolved in boiling absolute ethyl alcohol (100%) for recrystallization. After cooling to room temperature, diethyl ether was added to the mixture to precipitate more product. The precipitate was filtered and washed with diethyl ether until the precipitate turned white. The resulting precipitate being the product of the reaction, i.e. MAI, was vacuum dried for 5 hours (pressure below 0.2 mbar), after which the product was weighed. A product (MAI) yield of 88% was obtained, comparing to the theoretical yield as per the stoichiometry of the reaction. The composition of the resulting product was subjected to analysis which confirmed the absence of even trace amounts of phosphorus salts since no phosphorus donors were used at any step of the synthesis.
• iodine (l 2 ) was dissolved in ethanol in a round-bottomed flask in a single step to obtain a non-translucent dark brown solution demonstrating the presence of molecular iodine (l 2 ). After 15 minutes, the iodine dissolved in ethanol with the solution remaining dark brown and non-translucent. Formic acid was then added to the flask, in the molar ratio HCOOH:l 2 of 0.97:1.0 with no changes observed in the flask. 2.6 moles of octylamine per each mole of l 2 iodine were then slowly added dropwise to the solution.
• iodine (l 2 ) A portion of iodine (l 2 ) was dissolved in ethanol in a round-bottomed flask in a single step to obtain a non-translucent dark brown solution demonstrating the presence of molecular iodine (l 2 ). After 15 minutes, the iodine dissolved in ethanol with the solution remaining dark brown and non-translucent. 1.0 Eq (equivalent) of formic acid HCOOH (with respect to iodine (l 2 )) was then added to the flask with no changes observed in the flask.
• Formamidine acetate (solid at room temperature) was then added to the solution in a single step in a total amount of 2.1 Eq (equivalents) of formamidine acetate (with respect to iodine (l 2 )). After adding formamidine acetate (the reaction mixture remained brown), the flask was heated for 12 hours, maintaining the reaction mixture temperature at 50 °C. The reaction was then terminated, and the resulting mixture had a lighter brown colour.
• the mixture was evaporated on a rotary evaporator under reduced pressure of 30 mbar, keeping the flask with the solution being evaporated in a 50 °C water bath to obtain as a result of the evaporation a yellow and brown powder which was then dissolved in boiling absolute ethanol for recrystallization in 1 ml_ of absolute ethanol per 1 g of the expected product (the assumed yield was 1 ml_/1 g).
• the solution was then cooled to room temperature and diethyl ether was added to the cooled mixture to increase the precipitation efficiency. This was filtered to obtain a white precipitate, which was washed with diethyl ether until the precipitate turned white.
• reaction product (FAI) The resulting precipitate constituting the reaction product (FAI) was vacuum dried (pressure below 0.2 mbar) for 5 hours, after which the product was weighed. A product (FAI) yield of 82% was obtained, comparing to the theoretical yield as per the stoichiometry of the reaction.
• Example IV preparation of a perovskite-forminq composition in a form of ink. using MAI as the perovskite precursor:
• the perovskite-forming composition was prepared by dissolving the following compounds in 954 pL of dimethylformamide (DMF):
• MAI methylammonium iodide
• the ingredients were mixed for 12 hours, after which the resulting colloidal solution was filtered using a 0.45 mM filter to obtain a colloid with a suitable particle size of the dispersed phase.
• the resulting composition had the form of a stable colloid, suitable for printing (ink). No changes in colloidal particle sizes and no agglomeration tendency have been observed. During several weeks of observation the composition remained in form of a clear (translucent) colloidal solution.
• the obtained colloid (containing single-crystallized MAI) is shown in the images:
• Fig. 14A - the images show the same sample of the colloid, wherein image I shows a sample of the colloid on the day of its preparation, image II shows the colloid 24 hours after its preparation, image III shows the colloid 96 hours after its preparation, and image IV shows said colloid 168 hours after its preparation, which confirms that the clarity of the colloid has not changed over time.
• Fig. 14B, 14C and 14D show images of the colloid with the identical composition, with Fig. 14B showing images of a colloid containing conventionally prepared, commercially available MAI (using no FI I produced in situ); Fig.
• FIG. 14C shows a colloid with MAI prepared using a method known in the art - a colloid containing single-recrystallized MAI
• Fig. 14D shows a colloid with MAI obtained by a method known in the art - a colloid containing triple-recrystallized MAI
• Fig. 14B shows, like Fig 14A, the following photographs: I, II, III and IV of the same colloid sample, taken respectively: I - on the day of its preparation, II - 24 hours, III - 96 hours and IV - 168 hours after its preparation
• Fig. 14C I shows a image of the colloid taken on the day of its preparation
• Fig. 14C, II - 72 hours after the preparation of said colloid and, likewise: Fig.
• the perovskite-forming composition prepared in the form of a colloidal solution contains the inventive MAI as one of the perovskite-forming ingredients.
• composition I containing ingredients the same as the perovskite-forming composition of example IV above, using MAI obtained by a method known in the art
• composition II containing ingredients the same as the perovskite-forming composition of example IV above, but without the addition of CH 3 NH 3 H 2 PO 2 ,
• composition III containing ingredients the same as the perovskite-forming composition of example IV above , wherein used MAI is the MAI obtained by the method according to the present disclosure and with the addition of CH3NH3H2PO2).
• a substrate was prepared for the application of the composition of: I, II and III accordingly, as follows: plates were cut out of the PET/ITO (ethylene terephthalate / indium tin oxide) board by means of a laboratory punch and then, by immersion, etched in a 15 % hydrochloric acid (HCI) solution to obtain the desired pattern in the ITO conductive layer. The etched plates were cleaned in an ultrasonic bath (cleaning solutions used: deionized water, isopropyl alcohol).
• HCI hydrochloric acid
• the substrates thus prepared were air-dried for 1 hour at 95°C, and then PEDOT:PSS (poly(3,4-ethylene- 1 ,4-dioxyethiophene : styrene polysulphonate) was applied on cleaned and dried substrates using the method of spin-coating in air. Substrates were then heated for 45 minutes at 95 °C in air. Respective perovskite-forming compositions: composition I, composition II, composition III were then applied on the respective plates using the spin-coating technique under nitrogen atmosphere (inside the glove chamber). In order to crystallize the perovskite material, the substrate coated with films of respective perovskite-forming compositions: composition I, composition II, composition III, were heated at 96 °C for 15 minutes.
• PEDOT:PSS poly(3,4-ethylene- 1 ,4-dioxyethiophene : styrene polysulphonate
• Fig. 7A is a SEM image of a perovskite coating prepared with composition I, containing in its composition MAI prepared using a method known in the art
• Fig. 7B is a SEM image of a perovskite coating prepared with composition II, containing in its composition MAI prepared using the method according to the present disclosure, but without added CFI 3 NFI 3 FI 7 PO 7, while Fig.
• FIG. 7C is a SEM photograph of a perovskite coating prepared with composition III, containing in its composition MAI prepared using the method according to the present disclosure, and with added CFI 3 NFI 3 FI 7 PO 7 .
• the results of the SEM analysis of perovskite coatings prepared with compositions I, II and III confirmed the improved morphology of perovskite coatings prepared with MAI obtained using the method according to the present disclosure.
• the perovskite layer (with prior art MAI) is compact, i.e. it does not contain any pinholes and it features small grains of perovskite material
• the perovskite layer of Fig. 7B prepared using MAI obtained using the method according to the present disclosure features larger grains and improved crystallinity, which is more advantageous for the operation of the cell; also, pinholes are visible in the layer.
• the layer of Fig. 7C prepared using the MAI obtained by the method according to the present disclosure with added CFI 3 NFI 3 FI 2 PO 2 , also features larger grains and, additionally, reduced quantity of pinholes. This may be achieved by the addition of CFI 3 NFI 3 FI 2 PO 2 in the amount of 0.3% CFI 3 NFI 3 FI 2 PO 2 by weight with respect to the weight of MAI, which allows for adjusting the chemical parameters of the perovskite-forming composition being a colloidal solution to obtain an optimised morphology of the perovskite layer.
• Fig. 8A shows diffractions of CFl 3 NFl 3 Pbl 3 perovskite network
• Fig. 8B shows an enlarged peak corresponding to the reflection (110) in the tetragonal plane of the perovskite phase
• Fig. 8C shows an enlarged (control) peak corresponding to the PET material - differences between samples are negligible.
• the thickness measured using an optical profilometer was the same for all the coatings obtained with the compositions: I, II and III, so the differences in intensity of peaks in diffractograms were not due to the amounts of perovskite material varying between samples.
• the obtained X-ray diffractograms demonstrated, for the samples with the MAI prepared according to the present disclosure (composition II and III), a higher intensity of peaks corresponding to perovskite reflections positions, especially the peak at 14° corresponding to the reflection (110) in the tetragonal symmetry of the perovskite material (Fig. 8B).
• This may be due to the formation of a higher share of crystalline phase and/or a higher level of orientation of perovskite grains, which is particularly advantageous for photosensitive perovskite coatings for optoelectronic applications, and may provide improved functionality when said coatings are used in solar cells.
• perovskite compositions were prepared with the composition as in example V above, namely:
• composition I containing ingredients as the perovskite-forming composition of example IV above, using MAI obtained using a method known in the art,
• composition II containing ingredients as the perovskite-forming composition of example IV above, containing the MAI according to the present disclosure (with HI produced in situ) but with no CH3NH3H2PO2 added,
• composition III containing ingredients as the perovskite-forming composition of example IV above, wherein used MAI is the MAI obtained by the method according to the present disclosure, and with the addition of CH 3 NH 3 H 2 PO 2 ).
• compositions were used to prepare photovoltaic cells with a simple sandwich architecture containing the following layers: PET / ITO / PEDOT:PSS / perovskite: CH 3 NH 3 Pbl 3 / PCBM / BCP / Ag.
• PEDOT:PSS / perovskite : CH 3 NH 3 Pbl3 were prepared for each cell separately from the above perovskite-forming compositions: I, II and III.
• PCBM phenyl-C61 -butyric acid methyl ester
• Fig. 9B is a summary of the results of tests presenting dependence: current density-voltage, which also confirmed improved parameters of the cells with the perovskite layer made of the composition: II and III containing the MAI obtained according to the method of the present disclosure.
• the average efficiency of cells with the perovskite layer is composition II is 8.2%, while the efficiency of cells with the perovskite layer of prior art composition I ranges from 7.2 to 8.0%, which indicates an improvement in cell efficiency at the level of 2.5 to 14%.
• Cells with the perovskite layer made of composition III (containing the MAI according to the disclosure and CFI3NFI3FI2PO2) showed an additional increase in efficiency, both for the cells of composition I and those of composition II.
• the efficiency of cells of composition III ranged from 9.0 to 9.2%.
• the cells with the perovskite layer made of compositions II and III exhibit improved reproducibility and long-term stability of operation compared to the cells with the perovskite layer made of composition I containing prior art MAI, which is due to the difference in the density of defects of the perovskite layer made of the respective composition: I, II, III.
• ageing tests were carried out for selected cells: ageing at the maximum power point with continuous sunlight of 800 W/m 2 in an inert atmosphere and at a temperature of 32 °C.
• the results of these tests, summarized in Fig. 10 have shown that cells containing the perovskite layer with the inventive MAI show good performance for an extended period of time.
• the use of the MAI obtained according to the present disclosure enables greater control over the quality of the layer of the perovskite obtained, including, in particular, greater crystallinity of the perovskite layer, which may result in improved stability of the cell produced with such perovskite.
• the ingredients were mixed for 12 hours, after which the resulting colloidal solution was filtered using a 0.45 mM filter to obtain a colloid with a suitable particle size of the dispersed phase.
• the resulting composition had the form of a stable colloid. No changes in colloidal particle sizes and no agglomeration tendency have been observed (which is the case for colloids containing prior art FAI). During several weeks of observation, the composition had the form of a clear (translucent) colloidal solution.
• the perovskite-forming composition prepared in the form of a colloidal solution contains the inventive FAI as one of the perovskite-forming ingredients (perovskite precursors).
• composition I containing ingredients the same as the perovskite-forming composition of Example VII above, but using FAI obtained by a method known in the art
• - composition II containing ingredients the same as the perovskite-forming composition of Example VII above , but containing the FAI prepared by the method according to the present disclosure.
• compositions I and II were then prepared for depositing compositions I and II as described in Example V above.
• a layer of PTAA (poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine]) in toluene was then applied onto the plates by spin-coating a PTAA solution in toluene (concentration of 2 mg/mL, solution filtered using a 0.2 mhp filter).
• Composition I (control) and composition II, respectively, were then applied on the substrates using the spin-coating technique, under nitrogen, with the following predetermined parameters: spinning time: 30 seconds, acceleration: 2500 rpm, rotational speed: 2500 rpm.
• Fig. 11A is a SEM image of a perovskite coating prepared with composition I, containing in its composition FAI prepared using a method known in the art
• Fig. 11 B is a SEM image of a perovskite coating prepared with composition II, containing in its composition FAI prepared using the method according to the present disclosure.
• Fig. 12A shows the diffraction of the network of the perovskite obtained: CS 0,I (FA 0, 83MA 0, 17)0, 9Pb(lo , 84Br 0, 16)3, where MA is the methylammonium moiety, and FA is the formamidinium moiety;
• Fig. 12B shows an enlarged peak corresponding to the reflection (100) for the cubic perovskite phase.
• composition II a higher intensity of peaks corresponding to perovskite reflections positions, especially (100) in the cubic perovskite phase (Fig. 9B). This may be due to the formation of a higher share of crystalline phase and/or a higher level of orientation of perovskite grains, which is particularly advantageous for photosensitive perovskite coatings for optoelectronic applications.
• perovskite compositions were prepared with the ingredients as in example VIII above, containing the FAI according to the present disclosure (composition II - with HI prepared in situ).
• composition as above was used to prepare a photovoltaic cell with a simple sandwich architecture containing the following layers: PET / ITO / PTAA / perovskite: Cso ,i (FAO ,83 MAO ,I 7 )o ,9 Pb( lo ,84 Bro ,i 6 )3 / PCBM / BCP / Ag.
• a substrate containing respective layers of PET / ITO / PTAA / perovskite were prepared: CS 0,I (FA 0,83 MA 0, 17 )0, 9Pb(l 0,84 Br 0, 10 )3.

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