阅读说明：本技术 包含引达省-4-酮衍生物的共轭聚合物、其制备方法和包括其的光伏装置 (Conjugated polymer comprising indacen-4-one derivative, method for preparing same, and photovoltaic device comprising same ) 是由 加布里尔·比安奇 于 2019-09-18 设计创作，主要内容包括：一种具有通式(I)的包含引达省-4-酮的衍生物的共轭聚合物：其中,-R-1和R-2彼此相同或不同,优选彼此相同,选自直链或支链的C-1-C-(30),优选C-2-C-(20)烷基；任选取代的环烷基；任选取代的芳基；任选取代的杂芳基；直链或支链的C-1-C-(30),优选C-2-C-(20)烷氧基；R-4-O-[CH-2-CH-2-O]-m-聚氧乙烯基,其中R-4选自直链或支链的C-1-C-(30),优选C-2-C-(20)烷基,并且m是1至4范围内的整数；-R-5-OR-6基团,其中R-5选自直链或支链的C-1-C-(30),优选C-2-C-(20)亚烷基,并且R-6表示氢原子或者选自直链或支链的C-1-C-(30),优选C-2-C-(20)烷基,或者选自R-4-[-OCH-2-CH-2-]-p-聚氧乙烯基,其中R-4具有如上所报告的相同含义并且p是1至4范围内的整数；-COR-7基团,其中R-7选自直链或支链的C-1-C-(30),优选C-2-C-(20)烷基；-COOR-8基团,其中R-8选自直链或支链的C-1-C-(30),优选C-2-C-(20)烷基；或者它们表示-CHO基团,或者氰基(-CN)基团；-R-3选自直链或支链的C-1-C-(30),优选C-2-C-(20)烷基；任选取代的环烷基；任选取代的芳基；直链或支链的C-1-C-(30),优选C-2-C-(20)烷氧基；-n是10至500范围内,优选20至300范围内的整数。所述包含引达省-4-酮的衍生物的共轭聚合物可以有利地用于构建在刚性支撑件上或在柔性支撑件上的光伏装置(或太阳能装置),诸如例如光伏电池(或太阳能电池)、光伏模块(或太阳能模块)。(A conjugated polymer comprising derivatives of indacen-4-one having the general formula (I): wherein, -R 1 And R 2 Identical or different from each other, preferably identical to each other, selected from linear or branched C 1 ‑C 30 Preferably C 2 ‑C 20 An alkyl group; optionally substituted cycloalkyl; optionally substituted aryl; optionally substituted heteroaryl; straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 An alkoxy group; r 4 ‑O‑[CH 2 ‑CH 2 ‑O] m -polyoxyethylene group, wherein R 4 Selected from straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 Alkyl, and m is an integer ranging from 1 to 4; -R 5 ‑OR 6 Group, wherein R 5 Selected from straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 Alkylene, and R 6 Represents a hydrogen atom or is selected from linear or branched C 1 ‑C 30 Preferably C 2 ‑C 20 Alkyl, or selected from R 4 ‑[‑OCH 2 ‑CH 2 ‑] p -polyoxyethylene group, wherein R 4 Have the same meaning as reported above and p is an integer ranging from 1 to 4; -COR 7 Group, wherein R 7 Selected from straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 An alkyl group; -COOR 8 Group, wherein R 8 Selected from straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 An alkyl group; or they represent a-CHO group, or a cyano (-CN) group; -R 3 Selected from straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 An alkyl group; optionally substituted cycloalkyl; optionally substituted aryl; straight or branched C 1 ‑C 30 Preferably C 2 ‑C 20 An alkoxy group; -n is an integer ranging from 10 to 500, preferably ranging from 20 to 300. The conjugated polymers comprising derivatives of indacen-4-one can be advantageously used in photovoltaic devices (or solar devices) built on rigid supports or on flexible supports, such as, for example, photovoltaic cells (or solar cells), photovoltaic modules (or solar modules).)

1. A conjugated polymer comprising derivatives of indacen-4-one having the general formula (I):

wherein:

-R₁and R₂Identical or different from each other, preferably identical to each other, selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; optionally substituted cycloalkyl; optionally substituted aryl; optionally substituted heteroaryl; straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkoxy group; r₄-O-[CH₂-CH₂-O]_n-polyoxyethylene group, wherein R₄Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀Alkyl, and n is an integer ranging from 1 to 4; -R₅-OR₆Group, wherein R₅Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀Alkylene, and R₆Represents a hydrogen atom or is selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀Alkyl, or selected from R₄-[-OCH₂-CH₂-]_pA polyoxyethylene group, whereinR₄Have the same meaning as reported above and p is an integer ranging from 1 to 4; -COR₇Group, wherein R₇Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; -COOR₈Group, wherein R₈Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; or they represent a-CHO group, or a cyano (-CN) group;

-R₃selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; optionally substituted cycloalkyl; optionally substituted aryl; straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkoxy group;

-n is an integer ranging from 10 to 500, preferably ranging from 20 to 300.

2. The conjugated polymer comprising derivatives of indacen-4-one of claim 1, having the general formula (I) wherein in said general formula (I):

-R₁and R₂Are identical to each other and are selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; preferably they are 3, 7-dimethyloctyl, or dodecyl;

-R₃selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; preferably it is 2-octyldodecyl;

-n is an integer ranging from 20 to 300.

3. A photovoltaic device (or solar device), such as a photovoltaic cell (or solar cell), a photovoltaic module (or solar module), on a rigid support or on a flexible support, comprising at least one conjugated polymer comprising derivatives of indacen-4-one according to claim 1 or 2, of general formula (I).

Technical Field

The present invention relates to a conjugated polymer comprising a derivative of indacen-4-one.

More particularly, the present invention relates to a conjugated polymer comprising a derivative of indacen-4-one containing sulfur.

The conjugated polymers comprising derivatives of indacen-4-one can be advantageously used in photovoltaic devices (or solar devices) built on rigid supports or on flexible supports, such as, for example, photovoltaic cells (or solar cells), photovoltaic modules (or solar modules).

The invention therefore also relates to a photovoltaic device (or solar device), such as, for example, a photovoltaic cell (or solar cell), a photovoltaic module (or solar module), on a rigid support or on a flexible support, comprising said conjugated polymer comprising a derivative of indacen-4-one.

Background

Photovoltaic devices (or solar devices) are devices that are capable of converting the energy of light radiation into electrical energy. Currently, most photovoltaic devices (or solar devices) that can be used for practical applications exploit the chemical-physical properties of photoactive materials of inorganic type, in particular high-purity crystalline silicon. However, due to the high production costs of silicon, scientific research has been devoted for some time to the development of alternative materials of organic type with conjugated structure (oligomers or polymers) to obtain organic photovoltaic devices (or solar devices), such as, for example, organic photovoltaic cells (or solar cells). Indeed, unlike high purity crystalline silicon, the organic material is characterized by relatively easy synthesis and low production costs, a reduced weight of the respective organic photovoltaic device (or solar device), and allows the organic material to be recovered at the end of the life cycle of the photovoltaic device (or solar device) in which it is used.

The above advantages make the use of said organic type of materials attractive in terms of energy and economy, although any efficiency (η) of the organic photovoltaic devices (or solar devices) thus obtained is lower compared to inorganic photovoltaic devices (or solar devices).

The operation of organic photovoltaic devices (or solar devices), such as for example organic photovoltaic cells (or solar cells), is based on the combined use of an electron-acceptor compound and an electron-donor compound. Among the electron-acceptor compounds most commonly used in organic photovoltaic devices (or solar devices) in the prior art are fullerene derivatives, in particular PC61BM (6, 6-phenyl-C)₆₁-methyl butyrate) or PC71BM (f)6, 6-phenyl-C₇₁-methyl butyrate) with a polymer chosen from pi-conjugated polymers such as, for example, polythiophenes (η [ ])>5%), polycarbazole (. eta.))>6%), poly (thienothiophene) benzodithiophene (PTB) (. eta.) (η)>8%) of the electron-donor compounds in the derivatives give the highest efficiencies when mixed.

The basic process of converting light into electrical current in organic photovoltaic cells (or solar cells) is known to occur through the following stages:

1. absorption of photons by the electron-donor compound, accompanied by the formation of excitons, i.e., a pair of "electron-electron gap (or hole)" charge carriers;

2. the excitons diffuse into the region of the electron-donor compound up to the interface with the electron-acceptor compound;

3. the exciton dissociates into two charge carriers: electron (-) in the acceptor phase (i.e., in the electron-acceptor compound) and the electron gap [ (or hole) (+) ] in the donor phase (i.e., in the electron-donor compound);

4. the charge thus formed is transferred to the cathode (by means of electrons of the electron-acceptor compound) and to the anode (by means of electron gaps (or holes) of the electron-donor compound), wherein an electric current is generated in the organic photovoltaic cell (or solar cell).

The process of light absorption accompanied by exciton formation and subsequent electron transfer to the electron-acceptor compound involves the excitation of electrons from the HOMO ("highest occupied molecular orbital") to the LUMO ("lowest unoccupied molecular orbital") of the electron-donor compound, and the subsequent transport therefrom to the LUMO of the electron-acceptor compound.

Since the efficiency of an organic photovoltaic cell (or solar cell) depends on the number of free electrons generated by dissociation of excitons, which in turn may be directly related to the number of photons absorbed, one of the structural characteristics of the electron-donor compound that most affects this efficiency is the energy difference between the HOMO and LUMO orbitals of the electron-donor compound, or the so-called bandgap. In particular, the maximum value of the wavelength at which the electron-donor compound is able to collect and efficiently convert photons into electrical energy (or the so-called "photo-trapping" or "photon-trapping" process) depends on this difference. In order to obtain an acceptable current, the bandgap (i.e. the energy difference between the HOMO and LUMO of the donor compound) on the one hand needs to be not too high to allow absorption of the maximum number of photons, and on the other hand must not be too low, since this may reduce the voltage at the electrode of the device.

In the simplest operating mode, an organic photovoltaic cell (or solar cell) is manufactured by introducing a thin layer (about 100 nm) of a mixture of electron-acceptor and electron-donor compounds (a structure known as "bulk heterojunction") between two electrodes (usually consisting of Indium Tin Oxide (ITO) (anode) and aluminum (Al) (cathode)). Typically, to make this type of layer, a solution of the two compounds is prepared and subsequently, using a suitable deposition technique such as, for example, spin coating, spray coating, ink jet printing, etc., the solution forms a photoactive film on the anode [ Indium Tin Oxide (ITO) ]. Finally, a counter electrode (i.e., an aluminum cathode (Al)) was deposited on the dried film. Optionally, between the electrode and the photoactive film, further additional layers (often called buffer layers) can be introduced, which are capable of performing specific functions of electrical, optical or mechanical nature.

Generally, in order to facilitate the arrival of electron gaps (or holes) at the anode [ Indium Tin Oxide (ITO) ] and at the same time block the transport of electrons, thereby improving the trapping of charges by the electrode and suppressing the recombination phenomenon, the film is deposited from an aqueous suspension of PEDOT: PSS [ poly (3, 4-ethylenedioxythiophene) polystyrene sulfonate ] using a suitable deposition technique such as, for example, spin coating, spray coating, inkjet printing, etc., before forming a photoactive film from a mixture of acceptor and donor compounds as described above.

The most commonly used electron-donor compound in the manufacture of organic photovoltaic cells (or solar cells) is regioregular poly (3-hexylthiophene) (P3 HT). Such polymers have optimal electronic and optical properties (good HOMO and LUMO orbital values, good molar absorption coefficient), good solubility in solvents used for manufacturing photovoltaic cells (or solar cells) and discrete mobility of electron holes.

Other examples of polymers which can be advantageously used as electron-donor compounds are: polymer PCDTBT { poly [ N-9 ' -heptadecyl-2, 7-carbazole-alt-5, 5- (4',7' -di-2-thienyl-2 ',1',3' -benzothiadiazole ] }, polymer PCPDTBT { poly [2,6- (4, 4-bis- (2-ethylhexyl) -4H-cyclopenta [2, 1-b; 3,4-b ' ] -dithiophene) -alt-4, 7- (2,1, 3-benzothiadiazole) ] }.

Electron-donor compounds containing benzodithiophene units are also known, which have a structure similar to poly (3-hexylthiophene) (P3HT), in which the thiophene units are however planarized by means of a benzene ring. This characteristic, together with the reduction of the oxidation potential of the electron-donor compounds, improves their stability in air and ensures their rapid filling during the production of photoactive films and therefore the high molecular order: this translates into excellent transport properties for charges [ electrons or electron gaps (holes) ]. Thus, the use of electron-donor compounds containing benzodithiophene units may allow the realization of photovoltaic devices with improved properties.

For example, Huo L. et al describe electron-donor compounds containing benzodithiophene units in the following articles: "Synthesis of a polythieno [3,4-b ] thiophene derivative with a low-melting HOMO level and its application in polymer solar cells", Chemical Communication (2011), Vol.47, p.8850-8852. The article describes the preparation of polythieno [3,4-b ] thiophene derivatives for the copolymerization between planar benzodithiophene and thieno [3,4-b ] thiophene units having low HOMO values.

It is known that benzodithiophene and/or its isomers [ e.g., benzo [1,2-b:4,5-b '] dithiophene or (BDT) and benzo [2,1-b:3,4-b' ] dithiophene or (BDP) ] are very interesting compounds, the synthesis of which has been the subject of many research projects.

Generally, the electron-donor materials used in high-efficiency photovoltaic cells are almost entirely represented by polymers, in which electron-rich units alternate with electron-poor units. More details about the polymers can be found, for example, in the following articles: yu L. et al, "How to design low band-gap polymers for high-efficiency organic solar cells", Materials Today (2014), Vol.17, No. 11, pp.11-15; you w. et al: "Structure-Performance optimization in Donor Polymers via electrons, Substituents and Side Chains of Donor Polymers towards High Efficiency Solar Cells-Performance optimization", Macromolecular Rapid Communications (2012), Vol.33, p.1162-; havinga e.e. et al: "A new class of small band-gap organic Polymer conductors", Polymer Bulletin (1992), Vol.29, p.119-126.

However, the electron-donor polymers are not always optimal. In fact, since the photon flow of solar radiation reaching the earth's surface is greatest for energy values of about 1.8eV (corresponding to radiation having a wavelength of about 700 nm), the so-called "light-trapping" or "photon-trapping" process is not very efficient because of the high band gap values (generally greater than 2eV-3eV) characteristic of many of the above-mentioned electron-donor polymers, and only a fraction of the total solar radiation is converted into electrical energy.

In order to improve the yield of the so-called "light-trapping" or "photon-trapping" process, and thus the efficiency of organic photovoltaic (or solar) devices, it is therefore necessary to identify new electron-donor polymers capable of capturing and converting solar radiation wavelengths with lower energy, i.e. electron-donor polymers characterized by a lower band gap value than the ones typically used as electron-donors.

For this purpose, efforts have therefore been made in the art to identify electron-donor polymers having low band gap values (i.e. band gap values less than 2 eV).

For example, one of the most common strategies for obtaining electron-donor polymers with low band gap values is the synthesis of alternating conjugated polymers comprising electron rich units (donors) and electron poor units (acceptors). Such a synthesis is described, for example, by Chen j. et al in the following article: "Development of Novel Conjugated Donor Polymers for High-Efficiency Bulk-Heterojunction Photovoltaic Devices", Account of Chemical Research (2009), Vol. 42(11), p. 1709-1718.

International patent application WO 2016/180988 in the name of the applicant relates to a derivative of indacen-4-one that can be advantageously used as a monomer unit in the synthesis of electron-donor polymers with low band gap values (i.e. band gap values less than 2eV), which in turn can be used in the construction of photovoltaic (or solar) devices.

Disclosure of Invention

The applicant has therefore posed the problem of finding electron-donor polymers with low band gap values, i.e. band gap values less than 2eV, capable of providing higher performances, in particular energy conversion efficiencies (PCEs) calculated as described below, of the photovoltaic devices (or solar devices) in which they are used_av) In respect of both, with respect to the known electron-donor polymers and with respect to the electron-donor polymers described in detail in the above-reported international patent application WO 2016/180988.

The applicant has now found that some electron-donor polymers not specifically described in the above-reported international patent application WO 2016/180988, in particular the conjugated polymers comprising derivatives of indacen-4-one containing sulphur, reported below, having the specific general formula (I), are able to provide the above-mentioned properties. The conjugated polymers comprising derivatives of indacen-4-one containing sulfur can be advantageously used in photovoltaic devices (or solar devices) built on rigid supports or on flexible supports, such as, for example, photovoltaic cells (or solar cells), photovoltaic modules (or solar modules). More particularly, the conjugated polymers comprising derivatives of indacen-4-one containing sulfur have low band gap values (i.e. band gap values of less than 2eV) and are able to provide higher performance, in particular energy conversion efficiency (PCE) calculated as described below, of the photovoltaic devices (or solar devices) in which they are used_av) Both with respect to the known electron-donor polymers and with respect to the international patent application reported abovePlease see WO 2016/180988 for a specific description of electron-donor polymers.

The subject of the present invention is therefore a conjugated polymer comprising derivatives of indacen-4-one having general formula (I):

wherein:

-R₁and R₂Identical or different from each other, preferably identical to each other, selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; optionally substituted cycloalkyl; optionally substituted aryl; optionally substituted heteroaryl; straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkoxy group; r₄-O-[CH₂-CH₂-O]_n-polyoxyethylene group, wherein R₄Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀Alkyl, and n is an integer ranging from 1 to 4; -R₅-OR₆Group, wherein R₅Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀Alkylene, and R₆Represents a hydrogen atom or is selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀Alkyl, or selected from R₄-[-OCH₂-CH₂-]_p-polyoxyethylene group, wherein R₄Have the same meaning as described above and p is an integer ranging from 1 to 4; -COR₇Group, wherein R₇Selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; -COOR₈Group, wherein R₈Selected from straight or branched C₁-C₃₀Preferably C₂-C₃₀An alkyl group; or they represent a-CHO group, or a cyano (-CN) group;

-R₃selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; optionally substituted cycloalkyl; renAn optionally substituted aryl group; straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkoxy group;

-n is an integer ranging from 10 to 500, preferably ranging from 20 to 300.

For the purposes of this specification and the appended claims, the definition of numerical ranges always includes the limits, unless otherwise specified.

For the purposes of this specification and the appended claims, the term "comprising" also includes the term "it consists essentially of … …" or "it consists of … …".

The term "C₁-C₃₀Alkyl "is understood to mean a linear or branched, saturated or unsaturated alkyl radical having from 1 to 30 carbon atoms. C₁-C₃₀Specific examples of alkyl groups are: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl, ethylhexyl, hexyl, heptyl, n-octyl, nonyl, decyl, dodecyl, 3, 7-dimethyloctyl, 2-ethylhexyl, 2-butyloctyl, 2-hexyldecyl, 2-octyldecyl, 2-octyldodecyl, 2-decyltetradecyl.

The term "cycloalkyl" is understood to mean a cycloalkyl group having 3 to 30 carbon atoms. Said cycloalkyl groups may be optionally substituted by one or more groups, equal to or different from each other, selected from: halogen atoms such as, for example, fluorine, chlorine, bromine, preferably fluorine; a hydroxyl group; c₁-C₁₂An alkyl group; c₁-C₁₂An alkoxy group; c₁-C₁₂A thioalkoxy group; c₃-C₂₄A tri-alkylsilyl group; a polyoxyethylene group; a cyano group; an amino group; c₁-C₁₂Mono-or di-alkylamino; a nitro group. Specific examples of cycloalkyl groups are: cyclopropyl, 2-difluorocyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, methylcyclohexyl, methoxycyclohexyl, fluorocyclohexyl, phenylcyclohexyl, decalin, abietyl (abieth).

The term "aryl" is understood to mean an aromatic carbocyclic group containing from 6 to 60 carbon atoms. The aryl group may be optionally substituted with one or more groups, which may be the same or different from each otherSelected from: halogen atoms such as, for example, fluorine, chlorine, bromine, preferably fluorine; a hydroxyl group; c₁-C₁₂An alkyl group; c₁-C₁₂An alkoxy group; c₁-C₁₂A thioalkoxy group; c₃-C₂₄A tri-alkylsilyl group; a polyoxyethylene group; a cyano group; an amino group; c₁-C₁₂Mono-or di-alkylamino; a nitro group. Specific examples of aryl groups are: phenyl, methylphenyl, trimethylphenyl, methoxyphenyl, hydroxyphenyl, phenoxyphenyl, fluorophenyl, pentafluorophenyl, chlorophenyl, bromophenyl, nitrophenyl, dimethylaminophenyl, naphthyl, phenylnaphthyl, phenanthrene, anthracene.

The term "heteroaryl" is understood to mean an aromatic heterocyclic, five-or six-atom group containing from 4 to 60 carbon atoms and from 1 to 4 heteroatoms selected from nitrogen, oxygen, sulfur, silicon, selenium, phosphorus, and benzo-fused or heterobicyclic groups. The heteroaryl group may be optionally substituted by one or more groups, equal to or different from each other, selected from: halogen atoms such as, for example, fluorine, chlorine, bromine, preferably fluorine; a hydroxyl group; c₁-C₁₂An alkyl group; c₁-C₁₂An alkoxy group; c₁-C₁₂A thioalkoxy group; c₃-C₂₄A tri-alkylsilyl group; a polyoxyethylene group; a cyano group; an amino group; c₁-C₁₂Mono-or di-alkylamino; a nitro group. Specific examples of heteroaryl groups are: pyridine, picoline, methoxypyridine, phenylpyridine, fluoropyridine, pyrimidine, pyridazine, pyrazine, triazine, tetrazine, quinoline, quinoxaline, quinazoline, furan, thiophene, hexylthiophene, bromothiophene, dibromothiophene, pyrrole, oxazole, thiazole, isoxazole, isothiazole, oxadiazole, thiadiazole, pyrazole, imidazole, triazole, tetrazole, indole, benzofuran, benzothiophene, benzoxazole, benzothiazole, benzooxadiazole, benzothiadiazole, benzopyrazole, benzimidazole, benzotriazole, triazolopyridine, triazolopyrimidine, coumarin.

The term "C₁-C₃₀Alkoxy "is understood to mean a radical comprising a saturated or unsaturated C bound to a linear or branched chain₁-C₃₀The oxygen atom of the alkyl group. C₁-C₃₀Specific examples of alkoxy groups are: methoxy, ethoxy, n-propoxy, isopropoxy, n-butyl, isobutyl, tert-butyl, pentyloxy, hexyloxy, 2-ethylhexyloxy, heptyloxy, octyloxy, nonyloxy, decyloxy, dodecyloxy, 2-butyloctyloxy, 2-hexyldecyloctyloxy, 2-octyldecyloxy, 2-decyltetradecyloxy.

The term "C₁-C₃₀The alkylene group "means a linear or branched alkylene group having 1 to 30 carbon atoms. C₁-C₃₀Specific examples of alkylene groups are: methylene, ethylene, n-propylene, isopropylene, n-butylene, isobutylene, t-butylene, pentylene, ethylhexylene, hexylene, heptylene, octylene, nonylene, decylene, dodecylene.

The term "polyoxyethylene" is understood to mean a group having oxyethylene units in the molecule. Specific examples of polyoxyethylene groups are: methoxy-vinyloxy, methoxy-divinyloxy, 3-oxabutoxy (3-oxaetrraoxy), 3, 6-dioxaheptyloxy, 3,6, 9-trioxadecyloxy, 3,6,9, 12-tetraoxahexadecyloxy.

According to a preferred embodiment of the invention, in said general formula (I):

-R₁and R₂Are identical to each other and are selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; preferably they are 3, 7-dimethyloctyl, or dodecyl;

-R₃selected from straight or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group; preferably it is 2-octyldodecyl;

-n is an integer ranging from 20 to 300.

The conjugated polymers comprising derivatives of indacen-4-one of general formula (I) which are the subject of the present invention can be obtained by means of methods known in the art.

For example, conjugated polymers containing derivatives of indacen-4-one having general formula (I) which are the subject of the present invention can be obtained by a process comprising reacting at least one halogenated indacen-4-one derivative having general formula (II):

wherein R is₁And R₂Having the same meaning as described above, and X represents a halogen atom, such as for example chlorine, bromine, iodine, preferably bromine, with at least one benzotriazole disubstituted with thienyl groups having the general formula (III):

wherein R is₂Have the same meanings as described above and Q represents Sn (R)₃Wherein R, equal to or different from each other, are selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀Alkyl OR represents B (OR')₃Wherein R' are the same or different from each other and represent a hydrogen atom, or are selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀The alkyl, OR OR' groups together with the other atoms to which they are bound, may form a heterocyclic ring having one of the following formulae:

wherein R' are the same or different from each other and represent a hydrogen atom, or are selected from linear or branched C₁-C₃₀Preferably C₂-C₂₀An alkyl group.

The above-mentioned process can be carried out according to techniques known in the art, such as, for example, the techniques described by Xu J. et al in the article "Effect of fluorine performance of the electrochromic properties of benzothiadiazole-based donor-acceptor copolymers", Journal of Materials Chemistry (2015), volume 3, page 5589-.

Further details regarding the use of conjugated polymers comprising derivatives of indacen-4-one of the general formula (I) as subject of the present invention can be found, for example, in the above-mentioned international patent application 2016/180988 in the name of the applicant and incorporated herein by reference, and in the examples below.

As mentioned above, the conjugated polymer comprising a derivative of indacen-4-one can be advantageously used in photovoltaic devices (or solar devices) built on rigid supports or on flexible supports, such as, for example, photovoltaic cells (or solar cells), photovoltaic modules (or solar modules).

The invention therefore also relates to a photovoltaic device (or solar device), such as for example a photovoltaic cell (or solar cell), a photovoltaic module (or solar module), on a rigid support or on a flexible support, comprising at least one conjugated polymer comprising derivatives of indacen-4-one of general formula (I).

Detailed Description

Fig. 5, reported below, represents a cross-sectional view of an inverted polymer photovoltaic cell (or solar cell) used in examples 4-7, reported below.

Referring to fig. 5, the inverted polymer photovoltaic cell (or solar cell (1)) comprises:

-a transparent glass support (7);

-an Indium Tin Oxide (ITO) cathode (2);

-a cathode buffer layer (3) comprising zinc oxide (ZnO);

-comprises regioregular poly (3-hexylthiophene) (P3HT) and [6,6]]-phenyl-C₆₁-butyric acid methyl ester (PC)₆₁BM) of a layer of photoactive material (4);

-an anode buffer layer (5) comprising PEDOT: PSS [ poly (3, 4-ethylenedioxythiophene): polystyrene sulfonate ];

-an anode (6) of silver (Ag).

For a better understanding of the present invention and to put it into practice, the following are some illustrative and non-limiting examples of the invention.

Examples

Determination of molecular weight

The molecular weight of the conjugated polymers as subject of the invention obtained by operating according to the examples reported below was determined by Gel Permeation Chromatography (GPC) using a HT5432 column with trichlorobenzene eluent at 80 ℃ on a WATERS 150C instrument.

Weight average molecular weight (M) is reported_w) Number average molecular weight (M)_n) And corresponds to M_w/M_nPolydispersity index (PDI) of the ratio.

Determination of optical band gap

The conjugated polymers as subject of the invention obtained by operating according to the following examples have been characterized by UV-Vis-NIR spectroscopy according to the following procedure, to determine the energy entity of the optical bandgap in solution or on a film.

In the case where the optical band gap is measured in solution, the polymer is dissolved in toluene, chloroform, chlorobenzene, dichlorobenzene, trichlorobenzene or another suitable solvent. The solution thus obtained was placed in a quartz cuvette and analyzed in transmission mode with the aid of a Perkin Elmer λ 950 dual-beam, double monochromator UV-Vis-NIR spectrophotometer in the range 200nm to 850nm, with a bandwidth of 2.0nm, a scanning speed of 220nm/min and a step size of 1nm, using as reference the same quartz cuvette containing only the solvent used as reference.

In the case where the optical band gap is measured on a thin film, the monomer or polymer is dissolved in toluene, chloroform, chlorobenzene, dichlorobenzene, trichlorobenzene or another suitable solvent to give a solution with a concentration of about 10mg/ml, which is deposited (for spin coating) on a Suprasil quartz slide. The resulting films were analyzed in transmission mode using a Perkin Elmer λ 950 dual beam, double monochromator, UV-Vis-NIR spectrophotometer in the range 200nm to 850nm with a bandwidth of 2.0nm, a scanning speed of 220nm/min and a step size of 1nm, using the same Superasil quartz slide as used as such as a reference.

The optical band gap is estimated from the transmission spectrum by measuring the absorption edge corresponding to the transition from the Valence Band (VB) to the Conduction Band (CB). For the determination of the edges, the intersection of the line tangent to the absorption band at the inflection point with the X-axis is used.

Inflection point (lambda)_F，y_F) Determined from the minimum coordinates of the first derivative spectrum, in'_minAnd y'_minAnd (4) showing.

At the inflection point (lambda)_F，y_F) The equation at the line tangent to the UV-Vis spectrum is as follows:

y＝y’_min+λy_F–y’_minλ’_min

finally, according to the condition of intersection with the X axis ψ 0, the following results are obtained:

λ_EDGE＝(y’_minλ’_min-y_F)/y’_min

thus, by measuring the minimum coordinate of the first derivative spectrum and the corresponding absorbance value y from the UV-Vis spectrum_FObtaining λ directly by substitution_EDGE。

The corresponding energy is:

E_EDGE＝hv_EDGE＝h c/λ_EDGE

wherein:

-h＝6.626 10-34J s；

-c＝2.998 108m s^-1；

that is to say:

E_EDGE＝1.988 10-16J/λ_EDGE(nm)。

finally, bearing in mind that 1J — 6.241018eV, we get:

E_EDGE＝1240eV/λ_EDGE(nm)。

HOMO and LUMO determination

The determination of the HOMO and LUMO values of the conjugated polymers which are the subject of the invention obtained by operating according to the following examples was carried out using the Cyclic Voltammetry (CV) technique. With this technique, the values of the formation potentials of radical cations and radical anions of the sample to be examined can be measured. Inserting these values into the appropriate equations allows to obtain the HOMO and LUMO values of the polymer in question. The difference between HOMO and LUMO gives the value of the electrochemical bandgap.

The value of the electrochemical band gap is generally higher than that of the optical band gap, since during the execution of Cyclic Voltammetry (CV) neutral compounds are added and undergo conformational reorganization, wherein the energy gap increases, without optical measurements leading to the formation of the added species.

In a three-electrode cell, Cyclic Voltammetry (CV) measurements were performed using an Autolab PGSTAT12 potentiostat (using the GPES ecohemie software). In the measurements carried out, an Ag/AgCl electrode was used as reference electrode, a platinum wire as counter electrode and a glassy graphite electrode as working electrode. The sample to be analyzed is dissolved in a suitable solvent and then placed on the working electrode using a calibrated capillary to form a film. These electrodes were immersed in a 0.1M electrolyte solution of 95% tetrabutylammonium tetrafluoroborate in acetonitrile. The sample is then subjected to a cyclic potential having a triangular waveform. At the same time, the current is monitored according to the difference in applied potential, which signals that an oxidation or reduction of the species present has taken place.

The oxidation process corresponds to the removal of electrons from the HOMO, while the reduction cycle corresponds to the introduction of electrons into the LUMO. The potential for radical cation and radical anion formation originates from the peak initial value (E)_onset) As determined by molecules and/or segments having HOMO-LUMO energy levels closer to the band limits. If both involve vacuum, then the electrochemical potentials at those related to the electron levels may be correlated. For this purpose, the potential of ferrocene in vacuum, known in the literature and equal to-4.8 eV, was used as reference. Selection of the Intersolvent Redox couple ferrocene/ferrocenium (Fc/Fc)⁺) Because it has an oxidation-reduction potential independent of the working solvent.

Therefore, the general formula for calculating the energy of the HOMO-LUMO energy level is given by the following equation:

E(eV)＝-4,8+[E_1/2Ag/AgCl(Fc/Fc⁺)-E_{onset Ag/AgCl}(Polymer)]

Wherein:

-E ═ HOMO or LUMO, depending on the E fed in_onsetA value;

-E_1/2Ag/AgClhalf-wave potential of the peak corresponding to the ferrocene/ferrocenium redox pair measured under the same sample analysis conditions and with the same three electrode settings used for the sample;

-E_{onset Ag/AgCl}the starting potential measured for the polymer in the anode region when the HOMO is to be calculated and in the cathode region when the LUMO is to be calculated.

Example 1

Preparation of 4, 7-bis [5- (tributylstannyl) thiophen-2-yl having the general formula (IIIa)]-5, 6-difluoro-2- (2-) Octyl dodecyl) -2H-benzotriazole

To a 250-ml flask equipped with magnetic stirring, the following were added in the following order under argon flow: 5, 6-difluoro-2- (2-octyldodecyl) -4, 7-di (thiophen-2-yl) -2H-benzotriazole (Sunatech) (1,2 g; 2mmol) and 60ml of anhydrous Tetrahydrofuran (THF) (Aldrich) the reaction mixture was left at-78 ℃ for about 10 minutes. Subsequently, 4.4ml of a solution of lithium di-isopropylamide (LDA) (Aldrich) was added dropwise to a mixture of Tetrahydrofuran (THF) (Aldrich)/hexane (Aldrich) (1:1, v/v)1.0M (0.471 g; 4.4mmol) and the reaction mixture was held at-78 ℃ for 3 hours. Then 0.678ml of tributyltin chloride (Aldrich) (1.627 g; 5mmol) was added dropwise: the resulting reaction mixture was held at-78 ℃ for 30 minutes and at ambient temperature for 16 hours. The reaction mixture was then placed into a 500ml separatory funnel: the reaction mixture was diluted with a 0.1M solution of sodium bicarbonate (Aldrich) (200ml) and extracted with diethyl ether (Aldrich) (3X 100ml) to give an acidic aqueous phase and an organic phase. The entire organic phase (obtained by combining the organic phases obtained from the three extractions) was washed in neutral water (3 × 50ml), then dried over sodium sulfate (Aldrich) and evaporated. The residue obtained was purified by elution on a column of basic alumina (Aldrich) [ (eluent: n-heptane/ethyl acetate 99/1v/v) (Carlo Erba) ] to yield 5.595g of 4, 7-bis [5- (tributylstannyl) thiophen-2-yl ] -5, 6-difluoro-2- (2-octyldodecyl) -2H-benzotriazole of formula (IIIa) as a rice yellow oil (yield 95%).

Example 2

Preparation of conjugated polymers having formula (Ia)

To a 250ml flask equipped with magnetic stirring, thermometer and refrigerant, under an inert atmosphere, the following were added in the following order: 2, 7-dibromo-5, 5-bis (3, 7-dimethyloctyl) -5H-1, 8-dithia-asymmetric-indacen-4-one of formula (XIIb) (1.483 g; 2.3mmol), 60ml of toluene (Aldrich) obtained as described in example 13 of International patent application WO 2016/180988 reported above, 4, 7-bis [5- (tributylstannyl) thiophen-2-yl of formula (IIIa) obtained as described in example 1]-5, 6-difluoro-2- (2-octyldodecyl) -2H-benzotriazole (2.709 g; 2.3mmol), tris (dibenzylidene-acetone) dipalladium (0) [ Pd₂(dba)₃](Aldrich) (0.042 g; 0.046mmol) and tri (o-tolyl) phosphine [ P (o-tol)₃](Aldrich) (0.140 g; 0.46 mmol). Subsequently, the reaction mixture obtained was heated under reflux and kept under stirring for 48 hours: the color of the reaction mixture turned purple after 3 hours and turned dark purple at the end of the reaction (i.e. after 24 hours). After cooling to room temperature (25 ℃), the resulting reaction mixture was then placed in methanol (Aldrich) (300ml) and the precipitate obtained was extracted successively in a Soxhlet apparatus with methanol (Aldrich), acetone (Aldrich), n-heptane (Aldrich) and finally chloroform (Aldrich). The residue remaining in the extractor was dissolved in chlorobenzene (50ml) (Aldrich) at 80 ℃. The hot solution was precipitated in methanol (300ml) (Aldrich). The obtained precipitate was collected and dried under vacuum at 50 ℃ for 16 hours to yield 2.167g of a dark purple solid product (yield 80%) corresponding to the conjugated polymer of formula (Ia).

The solid product was subjected to molecular weight determination by Gel Permeation Chromatography (GPC) as described above, obtaining the following data:

-(M_w) 65424 daltons;

-(PDI)＝2.0128。

in addition, the measurement is in solutionAnd on the filmAnd the value of HOMO, operating as described above:

-(λ_EDGEsolution) 636 nm;

-(λ_EDGEfilm) 644 nm;

-E_{g.opt. solution}＝1.95eV；

-E_{g.opt. film}＝1.93eV；

-(HOMO)＝-5.39eV。

Example 3

Preparation of 4, 5-dodecyl-4, 5-dihydro-1, 8-dithio-asymmetric-indacene-4, 5- Diols

To a 250ml two-neck Pyrex glass flask equipped with magnetic stirring, a thermometer and a refrigerant, under an inert atmosphere, the following were added in the following order: 100ml of anhydrous Tetrahydrofuran (THF) (Aldrich), n-dodecyl-magnesium bromide (Aldrich) (19.656 g; 72.0mmol), benzo [1,2-b:6, 5-b' ] dithiophene-4, 5-dione (2.643 g; 12.0mmol) of formula (VIa) obtained as described in example 3 of the above-reported International patent application WO 2016/180988: the reaction mixture was cooled to 0 ℃ and kept at this temperature for 1 hour while stirring. Subsequently, the reaction mixture was heated to ambient temperature (25 ℃) and kept at this temperature for 3 hours while stirring. The reaction mixture was then placed in a 500ml separatory funnel, diluted with saturated aqueous ammonium chloride (Aldrich) (50ml), concentrated, diluted again with saturated aqueous ammonium chloride (Aldrich) (100ml) and extracted with ethyl acetate (Aldrich) (3X 100ml) to give an acidic aqueous phase and an organic phase. The entire organic phase (obtained by combining the organic phases obtained from the three extractions) was washed in neutral water (3 × 50ml), then dried over sodium sulfate (Aldrich) and evaporated. The residue obtained was purified by elution on a silica gel chromatography column [ (eluent: n-heptane/ethyl acetate 9/1) (Carlo Erba) ] to yield 3.029g of 4, 5-didodecyl-4, 5-dihydro-1, 8-di-dithia-asymmetric-indacene-4, 5-diol of formula (IIa) as a light yellow oil (yield 45%).

Example 4

Preparation of 5, 5-didodecyl-5H-1, 8-dithia-asymmetric-indacen-4-one of formula (IIb)

To a 100ml flask equipped with magnetic stirring, thermometer and refrigerant, under an inert atmosphere, the following were added in the following order: 4, 5-Didodecyl-4, 5-dihydro-1, 8-dithia-asymmetric-indacene-4, 5-diol of formula (IIa) obtained as described in example 3 (2.715 g; 5.00mmol), 50ml of toluene (Aldrich), p-toluenesulfonic acid (Aldrich) (0.162 g; 0.85 mmol): the reaction mixture was heated under reflux and kept under reflux for 1.5 hours while stirring. Subsequently, after cooling to (25 ℃), the reaction mixture was placed in a 500ml separatory funnel, diluted with saturated aqueous sodium chloride (Aldrich) (100ml) and extracted with ethyl acetate (Aldrich) (3 × 50ml) to give an acidic aqueous phase and an organic phase. The entire organic phase (obtained by combining the organic phases obtained from the three extractions) was washed in neutral water (3 × 50ml), then dried over sodium sulfate (Aldrich) and evaporated. The residue obtained was purified by elution on a silica gel chromatography column [ (eluent: n-heptane/ethyl acetate 99/1) (Carlo Erba) ] to yield 2.660g of 5, 5-didodecyl-5H-1.8-dithio-asymmetric-indacen-4-one of formula (IIb) as a light yellow oil (yield 98%).

Example 5

Preparation of 2, 7-dibromo-5, 5-didodecyl-5H-1, 8-dithia-asymmetric-indacene- 4-ketones

To a 100ml flask equipped with magnetic stirring, thermometer and refrigerant, under an inert atmosphere, the following were added in the following order: 5, 5-Didodecyl-5H-1, 8-dithio-asymmetric-indacen-4-one of formula (IIb) obtained as described in example 4 (2.714 g; 5.00mmol), 40ml of N, N-dimethylformamide (Aldrich), N-bromosuccinimide (Aldrich) (1.781 g; 10.01 mmol): the reaction mixture was protected from light and kept at ambient temperature (25 ℃) for 16 hours while stirring. Subsequently, the reaction mixture was placed in a 500ml separatory funnel: the reaction mixture was diluted with a 0.1M solution of sodium thiosulfate (Aldrich) (100ml) and extracted with diethyl ether (Aldrich) (3X 50ml) to give an acidic aqueous phase and an organic phase. The entire organic phase (obtained by combining the organic phases obtained from the three extractions) was washed in neutral water (3 × 50ml), then dried over sodium sulfate (Aldrich) and evaporated. The residue obtained was purified by elution on a silica gel chromatography column [ (eluent: n-heptane/ethyl acetate 99/1) (Carlo Erba) ] to yield 3.328g of 2, 7-dibromo-5, 5-didodecyl-5H-1, 8-dithio-asymmetric-indacen-4-one of formula (IIc) as a yellow-green solid (yield 95%).

Example 6

Preparation ofConjugated polymers having the formula (Ib)

To a 500-ml flask equipped with magnetic stirring, a thermometer and a refrigerant, under an inert atmosphere, the following were added in the following order: 2, 7-dibromo-5, 5-didodecyl-5H-1, 8-dithia-asymmetric-indacen-4-one of formula (IIc) obtained as described in example 5 (6.152 g; 8.78mmol), 230ml of toluene (Aldrich), 4, 7-bis [5- (tributylstannyl) thiophen-2-yl of formula (IIIa) obtained as described in example 1]-5, 6-difluoro-2- (2-octyldodecyl) -2H-benzotriazole (10.343 g; 8.78mmol), tris (dibenzylideneacetone) dipalladium (0) [ Pd [)₂(dba)₃](Aldrich) (0.161 g; 0.175mmol) and tri (o-tolyl) phosphine [ P (o-tol)₃](Aldrich) (0.053 g; 0.175 mmol). Subsequently, the reaction mixture obtained was heated under reflux and kept for 24 hours while stirring: the color of the reaction mixture turned purple after 3 hours and turned dark purple at the end of the reaction (i.e. after 24 hours). Then, after cooling to ambient temperature (25 ℃), the resulting reaction mixture was placed in methanol (Aldrich) (300ml) and the obtained precipitate was extracted in a Soxhlet apparatus successively with methanol (Aldrich), acetone (Aldrich), n-heptane (Aldrich) and finally chloroform (Aldrich). The residue remaining in the extractor was dissolved in chlorobenzene (50ml) (Aldrich) at 80 ℃. The hot solution was precipitated in methanol (300ml) (Aldrich). The precipitate obtained was collected and dried in vacuo at 50 ℃ for 16 hours to give 7.5g of a dark purple solid product (75% yield), corresponding to the conjugated polymer of formula (Ib).

The solid product was subjected to molecular weight determination by Gel Permeation Chromatography (GPC), operating as described above, to obtain the following data:

-(M_w) 41941 daltons;

-(PDI)＝1.7558。

in addition, the measurement is in solutionAnd on the filmAnd the value of HOMO, operating as described above:

-(λ_EDGEsolution) 636 nm;

-(λ_EDGEfilm) ═ 656 nm;

-E_{g.opt. solution}＝1.95eV；

-E_{g.opt. film}＝1.89eV；

-(HOMO)＝-5.41eV。

Example 7 (comparative)

Solar cell comprising regioregular poly (3) -hexylthiophene- (P3HT)

For this purpose an inverted polymer solar cell as schematically shown in fig. 5 is used.

For this purpose, polymer-based devices were prepared on ITO (indium tin oxide) coated glass substrates (Kintec Company-Hong Kong) previously subjected to a cleaning procedure consisting of manual cleaning, wiping with a lint-free cloth soaked in a detergent diluted with tap water. The substrate was then rinsed with tap water. Subsequently, the substrate was thoroughly cleaned using the following methods in sequence: sequentially (i) adding a detergent to distilled water (followed by manual drying with lint-free cloth); (ii) distilled water [ followed by hand drying with lint-free cloth ]; (iii) (iii) ultrasonic baths in acetone (Aldrich) and (iv) isopropanol (Aldrich). Specifically, the substrate was placed in a beaker containing a solvent, and placed in an ultrasonic bath maintained at 40 ℃ for treatment for 10 minutes. After treatments (iii) and (iv), the substrate was dried with a stream of compressed nitrogen.

Subsequently, the glass/ITO was further cleaned in an air plasma device (Tucano type-Gambetti) immediately before proceeding to the next step.

The substrate thus treated is ready for deposition of a cathode buffer layer. For this purpose, from [ Zn ]²⁺]-ethanolamine (Aldrich) complex inZinc oxide (ZnO) buffer layers were obtained in 0.162M solution in butanol (Aldrich). The solution was deposited by spinning on the substrate by operating at a spin speed of 600rpm (acceleration of 300 rpm/s) for 2 minutes 30 seconds, then at a spin speed of 1500rpm for 5 seconds. Immediately after deposition of the cathode buffer layer, zinc oxide formation was achieved by heat treating the device at 140 ℃ for 5 minutes on a hot plate in ambient air. The resulting cathode buffer layer had a thickness of 30nm and was partially removed from the surface with acetic acid 0.1m (aldrich), leaving the layer only on the desired surface.

On top of the cathode buffer layer, a solution containing regioregular poly (3) hexylthiophene (P3HT) (Plexcore OS) and [6,6] was deposited by spin coating a solution in ortho-dichlorobenzene (Aldrich) 1:0.8(v: v) with a concentration of P3HT of 10mg/ml, operating at a spin speed of 300rpm (acceleration of 255rpm/s) for 90 seconds while stirring]-phenyl-C₆₁-an active layer of methyl butyrate (PCBM) (Aldrich). The thickness of the active layer was found to be 250 nm.

On top of the active layer thus obtained, an anodic buffer layer is deposited, which is a molybdenum oxide (MoO) deposited by a thermal process₃) (Aldrich) to yield: the thickness of the anode buffer layer is equal to 10 nm. By evaporation under vacuum, the area of the device is suitably masked in order to obtain 25mm²On top of the anode buffer layer, a silver anode (Ag) was deposited to a thickness of 100 nm.

The deposition of the anode buffer layer and the anode was carried out in a standard vacuum evaporation chamber containing a substrate and two molybdenum oxide (MoO) chambers equipped with heating elements, each containing 10mg of molybdenum oxide (MoO)₃) Powder and 10 evaporation vessels of silver (Ag) (1 mm-3mm diameter) (Aldrich). The evaporation process is carried out under vacuum (at about 1X 10)^-6Bar pressure). After evaporation, molybdenum oxide (MoO3) and silver (Ag) were condensed in the unshielded portions of the device.

The thickness was measured using a Dektak 150 profilometer (Veeco Instruments Inc.).

The electrical characterization of the device obtained was carried out at ambient temperature (25 ℃) in a glove box under a controlled atmosphere (nitrogen). Electric currentVoltage (I-V) curve using a connection to a personal computer for data collection2600A multimeter acquisition. By exposing the device to ABET2000-4 solar simulator light to measure photocurrent, which light can provide intensity (using Ophir coupled with 3A-P thermal sensors)II Power meter measurement) of 100mW/cm²(1 solar intensity (sun)) of 1.5G AM radiation. In particular, the device is masked before said electrical characterization, so as to obtain a value equal to 16mm²Effective active area of (2): table 1 shows the four characteristic parameters as mean values.

Example 8 (invention)

Solar cell comprising conjugated polymer having formula (Ia)

Polymer-based devices were prepared on ITO (indium tin oxide) coated glass substrates (Kintec Company-Hong Kong) that had previously been subjected to a cleaning procedure as described in example 7.

The deposition of the cathode buffer layer and the deposition of the anode buffer layer were performed as described in example 7; the composition of the cathode buffer layer and the composition of the anode buffer layer were the same as those reported in example 7; the thickness of the cathode buffer layer and the thickness of the anode buffer layer were the same as those reported in example 7.

On top of the thus obtained cathode buffer layer, a solution comprising the conjugated polymer having formula (Ia) obtained as described in example 2 and [6,6] was deposited by spin-coating a 1:2(v: v) solution in ortho-dichlorobenzene (Aldrich) with a concentration of the conjugated polymer having formula (Ia) of 18mg/ml, operating at a rotation speed of 5000rpm (acceleration of 2500rpm/s) for 30 seconds, kept overnight while stirring]-phenyl-C₆₁Of methyl butyrate (PCBM) (Aldrich)And an active layer. The thickness of the active layer was found to be 60 nm.

The deposition of silver anodes (Ag) was carried out as described in example 7: the thickness of the silver anode (Ag) was the same as reported in example 7.

The thickness was measured using a Dektak 150 profilometer (Veeco Instruments Inc.).

The electrical characterization of the obtained device was performed as described in example 7: in table 1, four characteristic parameters are given as average values.

Fig. 1 shows the current-voltage (I-V) curve obtained [ X-axis gives the voltage in volts (V); the Y-axis shows the milliampere/cm²(mA/cm²) Short-circuit current density in units (Jsc)]。

Fig. 3 shows the External Quantum Efficiency (EQE) curves recorded under monochromatic light in an instrument from Bentham Instruments Ltd (obtained with TMc300F-U (I/C) monochromator-three grating monochromator-and a dual light source with xenon and quartz halogen lamps) [ X-axis gives the wavelength in nanometers (nm); the Y-axis gives the External Quantitative Efficiency (EQE) in percent (%).

Example 9 (invention)

Solar cell comprising conjugated polymer having formula (Ib)

Polymer-based devices were prepared on ITO (indium tin oxide) coated glass substrates (Kintec Company-Hong Kong) that had previously been subjected to a cleaning procedure as described in example 7.

The deposition of the cathode buffer layer and the deposition of the anode buffer layer were performed as described in example 7; the composition of the cathode buffer layer and the composition of the anode buffer layer were the same as those reported in example 7; the thickness of the cathode buffer layer and the thickness of the anode buffer layer were the same as those reported in example 7.

On top of the thus obtained cathode buffer layer, an active layer comprising the conjugated polymer of formula (Ib) obtained as described in example 6 and [6,6] -phenyl-C61-methyl butyrate (PCBM) (Aldrich) was deposited by spin-coating a 1:2(v: v) solution in o-dichlorobenzene (Aldrich) with a concentration of the conjugated polymer of formula (Ib) of 18mg/ml, operating at a spin speed of 5000rpm (acceleration of 2500rpm/s) for 30 seconds, kept overnight while stirring. The thickness of the active layer was found to be 60 nm.

The deposition of silver anodes (Ag) was carried out as described in example 7: the thickness of the silver anode (Ag) was the same as reported in example 7.

The thickness was measured using a Dektak 150 profilometer (Veeco Instruments Inc.).

The electrical characterization of the obtained device was performed as described in example 7: in table 1, four characteristic parameters are given as average values.

Fig. 2 shows the current-voltage (I-V) curve obtained [ X-axis gives the voltage in volts (V); the Y-axis shows the milliampere/cm²(mA/cm²) Short-circuit current density in units (Jsc)]。

Fig. 4 shows the External Quantum Efficiency (EQE) curves recorded under monochromatic light in an instrument from Bentham Instruments Ltd (obtained with TMc300F-U (I/C) monochromator-three grating monochromator-and a dual light source with xenon and quartz halogen lamps) [ X-axis gives the wavelength in nanometers (nm); the Y-axis gives the External Quantitative Efficiency (EQE) in percent (%).

TABLE 1

⁽¹⁾: FF (fill factor) is calculated according to the following formula:

wherein V_MPPAnd J_MPPRespectively, the voltage and current density, V, corresponding to the maximum power point_OCIs an open circuit voltage and J_SCIs the short circuit current density;

⁽²⁾：V_OCis the open circuit voltage;

⁽³⁾：J_SCis the short circuit current density;

⁽⁴⁾: PCEav is the efficiency of the device calculated according to the following formula:

wherein V_OC、J_SCAnd FF have the same meaning as reported above, and P_inIs the intensity of the incident light on the device.