CN110114441A

CN110114441A - Composition, film, laminate structure, light emitting device and display

Info

Publication number: CN110114441A
Application number: CN201780078433.0A
Authority: CN
Inventors: 内藤翔太; 酒谷能彰
Original assignee: Sumitomo Chemical Co Ltd
Current assignee: Sumitomo Chemical Co Ltd
Priority date: 2016-12-22
Filing date: 2017-12-20
Publication date: 2019-08-09
Anticipated expiration: 2037-12-20
Also published as: JP6830967B2; WO2018117141A1; TWI750284B; CN110114441B; JPWO2018117141A1; TW201842156A

Abstract

The present invention relates to one kind to have luminiferous composition, and it includes (1) and (2), and also includes at least one of (3) or (4).(1) semiconductive particles；(2) halogenated hydrocarbon compound；(3) solvent；(4) at least one kind of in polymerizable compound and polymer.Above-mentioned (1) is preferably the particle of the perovskite compound using A, B and X as constituent.A is the ingredient for being located at hexahedral each vertex centered on B in perovskite type crystal structure, is 1 valence cation.X indicates the ingredient for being located at octahedral each vertex centered on B in perovskite type crystal structure, is selected from one or more of halide ion and thiocyanate ion anion.B is metal ion.

Description

Composition, film, laminate structure, light emitting device and display

Technical field

The present invention relates to composition, film, laminate structure, light emitting device and displays.

The application is required excellent based on Japanese Patent Application 2016-250171 to file an application on December 22nd, 2016 to Japan It first weighs, and its content is incorporated herein.

Background technique

In recent years, constantly surging to the care of the characteristics of luminescence of semiconductor material.

Reporting for example has strong luminous intensity from ultraviolet to the range of red SPECTRAL REGION at room temperature Composition (non-patent literature 1).

Existing technical literature

Non-patent literature

Non-patent literature 1:M.Era, A.Shimizu and M.Nagano, Rep.Prog.Polym.Phys.Jpn., 42, 473-474(1999)

Summary of the invention

Subject to be solved by the invention

However, in the case where stating the composition of the record of non-patent literature 1 in use as luminescent material, it is desirable that further Improve quantum yield.

The present invention is the invention completed in view of the above subject, and its purpose is to provide the quantum receipts comprising semiconductive particles The high composition of rate, film, laminate structure, light emitting device and display.

Means for solving the problems

In order to solve the above problems, the inventors of the present invention have made intensive studies, and as a result complete the present invention below.

That is, the present invention includes the invention of following [1]~[9].

[1] a kind of to have luminiferous composition, it includes (1) and (2), and also comprising at least one in (3) and (4) Person.

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(3) solvent

(4) at least one kind of in polymerizable compound and polymer

[2] composition according to above-mentioned [1], wherein above-mentioned (1) is the perovskite using A, B and X as constituent The particle of compound.

A is the ingredient for being located at hexahedral each vertex centered on B in perovskite type crystal structure, is 1 valence sun Ion.

X indicates the ingredient for being located at octahedral each vertex centered on B in perovskite type crystal structure, is to be selected from One or more of halide ion and thiocyanate ion anion.

B is to be located at that A is configured at the hexahedron on vertex and X is configured to the octahedral on vertex in perovskite type crystal structure The ingredient at the center of body is metal ion.

[3] composition according to above-mentioned [1] or [2] also includes that (5) are selected from ammonia, amine, carboxylic acid and their salt Or it is at least one kind of in ion.

[4] a kind of composition is the composition comprising (1), (2) and (4 '), wherein (1), (2) and (4 ') it is total Content is 90 mass % or more relative to the gross mass of above-mentioned composition.

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(4 ') polymer

[5] composition according to above-mentioned [4], also include (5) be selected from ammonia, amine, carboxylic acid and their salt or from It is at least one kind of in son.

[6] a kind of film, it includes compositions described in above-mentioned [4] or [5].

[7] a kind of laminate structure, with multiple layers, and at least one layer of is to include combination described in above-mentioned [4] or [5] The layer of object.

[8] a kind of light emitting device has laminate structure described in above-mentioned [7].

[9] a kind of display has laminate structure described in above-mentioned [7].

The effect of invention

In accordance with the invention it is possible to provide the high composition of the quantum yield comprising semiconductive particles, film, laminate structure, Light emitting device and display.

Detailed description of the invention

Fig. 1 is the cross-sectional view for indicating an embodiment of laminate structure of the present invention.

Fig. 2 is the cross-sectional view for indicating an embodiment of display of the present invention.

Fig. 3 is the figure for indicating the result of quantum yield of the composition of the present invention obtained in embodiment.

Specific embodiment

Hereinafter, showing embodiment, the present invention is described in detail.

< composition >

Composition of the invention has photism." photism " refers to the property for issuing light.Photism is preferably by electricity The excitation of son and luminous property, more preferably property luminous and the electron excitation based on exciting light.The wave of exciting light Length can be such as 200nm~800nm, or 250nm~700nm can also be 300nm~600nm.

Composition of the invention includes (1) and (2), and also includes at least one of (3) and (4).

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(3) solvent

(4) at least one kind of in polymerizable compound and polymer

Above-mentioned composition can also include that (5) are at least one kind of in ammonia, amine, carboxylic acid and their salt or ion.

In addition, above-mentioned composition can have other ingredients other than above-mentioned (1)~(5).

As other ingredients, it can be mentioned, for example several impurity and with the element comprising constituting semiconductive particles at Compound, the polymerization initiator of the amorphous structure divided.

The content of other ingredients is preferably 10 mass % hereinafter, more preferably 5 mass % relative to the gross mass of composition Hereinafter, further preferably 1 mass % or less.

The inventors of the present invention have made intensive studies, as a result, it has been found that:

Polymerizable compound and polymerization are selected from (1) semiconductive particles, (2) halogenated hydrocarbon compound, (3) solvent and (4) Among one or more of object substance, the composition comprising (1) and (2) and also comprising at least one of (3) or (4) can Improve quantum yield.

It is thought that due to: (2) organic compound is utilized, is prevented by the defect capture on the surface of (1) semiconductive particles Electronic deactivation, electronics are excited, to improve quantum yield.

In the composition of present embodiment, (1) and (2) and contain selected from the total of at least one of (3) and (4) Measuring relative to the gross mass of above-mentioned composition can be 90 mass % or more, or 95 mass % or more can also be 99 Quality % or more can also be 100 mass %.

Composition of the invention can be comprising (1), (2) and (4 '), and total content of (1), (2) and (4 ') is opposite The composition for being 90 mass % or more in the gross mass of above-mentioned composition.

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(4 ') polymer

In the composition of present embodiment, total matter of the total content of (1), (2) and (4 ') relative to above-mentioned composition Amount can be 95 mass % or more, or 99 mass % or more can also be 100 mass %.

This composition can also include that (5) are at least one kind of in ammonia, amine, carboxylic acid and their salt or ion.As Ingredient other than (1), (2), (4 ') and (5) can enumerate ingredient same as above-mentioned other ingredients.

In the composition comprising (1), (2) and the present embodiment selected from any one of (3) and (4) or both, (1) content relative to composition gross mass is not particularly limited, and from the viewpoint for being not easy to condense semiconductive particles and is prevented From the perspective of concentration quenching, preferably 50 mass % hereinafter, more preferably 1 mass % hereinafter, further preferably 0.1 matter % is measured hereinafter, in addition, from the viewpoint of obtaining good quantum yield, preferably 0.0001 mass % or more, more preferably 0.0005 mass % or more, further preferably 0.001 mass % or more.

Above-mentioned upper limit value and lower limit value can be combined arbitrarily.

(1) content relative to composition gross mass is usually 0.0001~50 mass %.

(1) content relative to composition gross mass is preferably 0.0001~1 mass %, more preferably 0.0005~1 matter Measure %, further preferably 0.001~0.1 mass %.

(1) cooperation range is not susceptible to the cohesion of (1) semiconductive particles for the composition in above range, moreover it is possible to good Ground plays photism, is preferred in this regard.

In the present specification, the content relative to (1) semiconductive particles of composition gross mass for example can use inductance ICP mass spectroscopy (below be also referred to as ICP-MS) and ion chromatograph measure.

In the composition comprising (1), (2) and the present embodiment selected from any one of (3) and (4) or both, (1) and (2) are not particularly limited relative to total content of composition gross mass, from the viewpoint for being not easy to condense semiconductive particles And from the perspective of preventing concentration quenching, preferably 60 mass % hereinafter, more preferably 10 mass % hereinafter, further preferably 2 mass % hereinafter, particularly preferably 0.2 mass % hereinafter, in addition, from the viewpoint of obtaining good quantum yield, preferably For 0.0002 mass % or more, more preferably 0.002 mass % or more, further preferably 0.005 mass % or more.

(1) and (2) relative to total content of composition gross mass are usually 0.0002~60 mass %.

(1) and (2) relative to total content of composition gross mass are preferably 0.001~10 mass %, more preferably 0.002~2 mass %, further preferably 0.005~0.2 mass %.

(1) and the range of the match ratio of (2) is that composition in above range is not susceptible to the solidifying of (1) semiconductive particles It is poly-, moreover it is possible to play photism well, be preferred in this regard.

In the composition of the present embodiment comprising (1), (2) and (4 '), the content of (1) relative to composition total measurement (volume) It is not particularly limited, from the viewpoint of the viewpoint for being not easy to condense semiconductive particles and preventing concentration quenching, preferably 100g/ L hereinafter, more preferably 10g/L hereinafter, further preferably 5g/L hereinafter, in addition, from the viewpoint of good quantum yield is obtained It sets out, preferably 0.01g/L or more, more preferably 0.1g/L or more, further preferably 0.5g/L or more.

(1) content relative to composition total measurement (volume) is preferably 0.01~100g/L, more preferably 0.1~10g/L, into one Step is preferably 0.5~5g/L.

(1) cooperation range is that the composition in above range can play photism well, is preferred in this regard 's.

In the present specification, (1) for example can use ICP-MS and ion chromatography relative to the content of composition total measurement (volume) Instrument measures.

In the case where composition is film shape, the total measurement (volume) of composition can by by above-mentioned film be cut into vertical 1cm × Horizontal 1cm, it is calculated again with the measurement thickness such as micrometer.

In the case where composition is liquid, graduated cylinder is can be used to measure in the total measurement (volume) of composition.

In the case where composition is powder, the total measurement (volume) of composition can be by according to JIS R 93-1-2-3:1999 The weight of measurement refitting bulk specific gravity and the composition used in measurement is calculated divided by above-mentioned refitting bulk specific gravity.

In the composition of the present embodiment comprising (1), (2) and (4 '), (1) and (2) is relative to composition total measurement (volume) Total content be not particularly limited, from the viewpoint of the viewpoint for being not easy to make semiconductive particles to condense and preventing concentration quenching, Preferably 1000g/L hereinafter, more preferably 500g/L hereinafter, further preferably 300g/L hereinafter, in addition, good from obtaining From the perspective of quantum yield, preferably 0.02g/L or more, more preferably 0.2g/L or more, further preferably 0.6g/L with On.

(1) and (2) relative to total content of composition total measurement (volume) are preferably 0.02~1000g/L, more preferably 0.2~ 500g/L, further preferably 0.6~300g/L.

(1) and the range of the match ratio of (2) be above range in composition can play photism well, in this point On be preferred.

Composition of the invention is illustrated hereinafter, showing embodiment.

(1) semiconductive particles

Composition of the present invention includes (1) semiconductive particles, and preferably (1) semiconductive particles are dispersed.As Decentralized medium can enumerate at least one kind of and (the 4 ') polymer of (3) solvent, (4) in polymerizable compound and polymer.

In the present specification, " dispersed " state for referring to that semiconductive particles are swum or are suspended in decentralized medium.

As semiconductive particles, it can be mentioned, for example the particles of the crystal of II race-VI compound semiconductor ,-V race, II race Close the particle of the crystal of object semiconductor, particle, the III group-IV compounds of group of the crystal of III group-V compound semiconductor are partly led The particle of the crystal of body, the particle of the crystal of III group-VI compound semiconductor, IV race-VI compound semiconductor crystal Particle, the area transition metal-p compound semiconductor crystal particle and the particle of perovskite compound etc..

From the viewpoint of obtaining good quantum yield, semiconductive particles preferably comprise the micro- of the crystal of the semiconductor of cadmium Grain, semiconductor comprising indium crystal particle and perovskite compound particle, from less strictly requiring size controlling And set out in terms of being easy to get the narrow glow peak of half breadth, the particle of more preferable perovskite compound.

At least part of these semiconductive particles can be covered by (2) halogenated hydrocarbon compound.

The average grain diameter of semiconductive particles contained in composition is not particularly limited, from being well maintained crystal structure Viewpoint is set out, and average grain diameter is preferably 1nm or more, more preferably 2nm or more, further preferably 3nm or more, in addition, never From the perspective of easily settling semiconductive particles of the present invention, average grain diameter be preferably 10 μm hereinafter, more preferably 1 μm with Under, further preferably 500nm or less.

The average grain diameter of semiconductive particles contained in composition is not particularly limited, from being not easy to settle semiconductive particles Viewpoint and be well maintained from the perspective of crystal structure, average grain diameter be preferably 1nm or more and 10 μm hereinafter, more preferably 2mm or more and 1 μm hereinafter, further preferably 3nm or more and 500nm or less.

In the present specification, the average grain diameter of semiconductive particles contained in composition for example can use transmission electron Microscope (below be also referred to as TEM), scanning electron microscope (being also referred to as SEM below) measure.Specifically, utilizing TEM Or SEM, the maximum Feret's diameter (Feret ' s diameter) of 20 semiconductive particles contained in above-mentioned composition is observed, The i.e. average maximum Feret's diameter of average value for calculating them, it is possible thereby to acquire above-mentioned average grain diameter.In the present specification, " maximum Feret's diameter " refers to the maximum distance that 2 parallel lines of semiconductive particles are clamped on TEM or SEM image.

The size distribution of semiconductive particles contained in composition is not particularly limited, from being well maintained crystal structure Viewpoint is set out, and median particle diameter (D50) is preferably 3nm or more, more preferably 4nm or more, further preferably 5nm or more, in addition, From the viewpoint of being not easy to settle semiconductive particles of the present invention, median particle diameter (D50) is preferably 5 μm hereinafter, more excellent 500nm is selected as hereinafter, further preferably 100nm or less.

As another side of present embodiment, in the composition in the size distribution of contained semiconductive particles, in Value partial size (D50) is preferably 3nm~5 μm, more preferably 4nm~500nm, further preferably 5nm~100nm.

In the present specification, the size distribution of semiconductive particles contained in composition for example can use TEM, SEM Measurement.Specifically, can use the maximum expense thunder of 20 semiconductive particles contained in TEM or SEM observation above-mentioned composition Special diameter, and above-mentioned median particle diameter (D50) is acquired by their distribution.

(particle of the crystal of II race-VI compound semiconductor)

II race-VI compound semiconductor includes 2 races of the periodic table of elements or the element of 12 races and the element of 16 races.

It is explained, in the present specification, " periodic table of elements " refers to the long period type periodic table of elements.

In the II race-VI compound semiconductor of binary system, can enumerate CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, HgS, HgSe or HgTe etc..

As comprising in the element (the first element) in 2 races selected from the periodic table of elements and 16 races selected from the periodic table of elements Element (second element) binary system II race-VI compound semiconductor, it can be mentioned, for example MgS, MgSe, MgTe, CaS, CaSe, CaTe, SrS, SrSe, SrTe, BaS, BaSe or BaTe.

Include the member in the element (the first element) in 2 races selected from the periodic table of elements and 16 races selected from the periodic table of elements II race-VI the compound semiconductor of plain (second element) can be the element in 2 races comprising a kind selected from the periodic table of elements - VI race, the II race chemical combination of the ternary system of (the first element) and the element (second element) in 2 kinds of 16 races selected from the periodic table of elements Object semiconductor, be also possible to comprising in 2 kinds of 2 races selected from the periodic table of elements element (the first element) and a kind it is all selected from element II race-VI the compound semiconductor of the ternary system of element (second element) in 16 races of phase table can also be and select comprising 2 kinds (second yuan of element from the element (the first element) and 2 kinds of 16 races selected from the periodic table of elements in 2 races of the periodic table of elements Element) quaternary system II race-VI compound semiconductor.

As including the element (the first element) in 12 races selected from the periodic table of elements and 16 races selected from the periodic table of elements In element (second element) binary system II race-VI compound semiconductor, it can be mentioned, for example ZnS, ZnSe, ZnTe, CdS, CdSe, CdTe, HgS, HgSe or HgTe.

Comprising in the element (the first element) in 12 races selected from the periodic table of elements and 16 races selected from the periodic table of elements II race-VI the compound semiconductor of element (second element) can be the member in 12 races comprising a kind selected from the periodic table of elements - VI the race, II race of the ternary system of plain (the first element) and the element (second element) in 2 kinds of 16 races selected from the periodic table of elements Close object semiconductor, be also possible to comprising in 2 kinds of 12 races selected from the periodic table of elements element (the first element) and a kind be selected from element II race-VI the compound semiconductor of the ternary system of element (second element) in 16 races of periodic table, can also be comprising 2 kinds The element (second in element (the first element) and 2 kinds of 16 races selected from the periodic table of elements in 12 races selected from the periodic table of elements Element) quaternary system II race-VI compound semiconductor.

II race-VI compound semiconductor may include the element other than 2 races of the periodic table of elements, 12 races and 16 races As doped chemical.

(particle of the crystal of II race-V compound semiconductor)

II race-V compound semiconductor includes the element of 12 races of the periodic table of elements and the element of 15 races.

As including the element (the first element) in 12 races selected from the periodic table of elements and 15 races selected from the periodic table of elements In element (second element) binary system II race-V compound semiconductor, it can be mentioned, for example Zn₃P₂、Zn₃As₂、Cd₃P₂、 Cd₃As₂、Cd₃N₂Or Zn₃N₂。

Comprising in the element (the first element) in 12 races selected from the periodic table of elements and 15 races selected from the periodic table of elements II race-V the compound semiconductor of element (second element) can be the element in 12 races comprising a kind selected from the periodic table of elements II race-V the compounds of group of the ternary system of (the first element) and the element (second element) in 2 kinds of 15 races selected from the periodic table of elements Semiconductor, be also possible to comprising in 2 kinds of 12 races selected from the periodic table of elements element (the first element) and a kind be selected from period of element II race-V the compound semiconductor of the ternary system of element (second element) in 15 races of table, can also be and be selected from comprising 2 kinds The element (second element) in element (the first element) and 2 kinds of 15 races selected from the periodic table of elements in 12 races of the periodic table of elements Quaternary system II race-V compound semiconductor.

II race-V compound semiconductor may include the element conduct other than 12 races of the periodic table of elements and 15 races Doped chemical.

(particle of the crystal of III group-V compound semiconductor)

III group-V compound semiconductor includes the element in 13 races selected from the periodic table of elements and the member in 15 races Element.As including the member in the element (the first element) in 13 races selected from the periodic table of elements and 15 races selected from the periodic table of elements III group-V the compound semiconductor of the binary system of plain (second element), it can be mentioned, for example BP, AlP, AlAs, A1Sb, GaN, GaP, GaAs, GaSb, InN, InP, InAs, InSb, A1N or BN.

Comprising in the element (the first element) in 13 races selected from the periodic table of elements and 15 races selected from the periodic table of elements III group-V the compound semiconductor of element (second element) can be the member in 13 races comprising a kind selected from the periodic table of elements III group-V the race of the ternary system of plain (the first element) and the element (second element) in 2 kinds of 15 races selected from the periodic table of elements Close object semiconductor, be also possible to comprising in 2 kinds of 13 races selected from the periodic table of elements element (the first element) and a kind be selected from element III group-V the compound semiconductor of the ternary system of element (second element) in 15 races of periodic table, can also be comprising 2 kinds The element (second in element (the first element) and 2 kinds of 15 races selected from the periodic table of elements in 13 races selected from the periodic table of elements Element) quaternary system III group-V compound semiconductor.

III group-V compound semiconductor may include the element conduct other than 13 races of the periodic table of elements and 15 races Doped chemical.

(particle of the crystal of III group-IV compound semiconductor)

III group-IV compound semiconductor is comprising the element in 13 races selected from the periodic table of elements and in 14 races Element.As comprising in the element (the first element) in 13 races selected from the periodic table of elements and 14 races selected from the periodic table of elements III group-IV the compound semiconductor of the binary system of element (second element), it can be mentioned, for example B₄C₃、Al₄C₃、Ga₄C₃。

Comprising in the element (the first element) in 13 races selected from the periodic table of elements and 14 races selected from the periodic table of elements III group-IV the compound semiconductor of element (second element) can be the member in 13 races comprising a kind selected from the periodic table of elements III group-IV the race of the ternary system of plain (the first element) and the element (second element) in 2 kinds of 14 races selected from the periodic table of elements Close object semiconductor, be also possible to comprising in 2 kinds of 13 races selected from the periodic table of elements element (the first element) and a kind be selected from element III group-IV the compound semiconductor of the ternary system of element (second element) in 14 races of periodic table, can also be comprising 2 Element (the in element (the first element) and 2 kinds of 14 races selected from the periodic table of elements in kind of 13 races selected from the periodic table of elements Was Used) quaternary system III group-IV compound semiconductor.

III group-IV compound semiconductor may include the work of the element other than 13 races of the periodic table of elements and 14 races For doped chemical.

(particle of the crystal of III group-VI compound semiconductor)

III group-VI compound semiconductor is comprising the element in 13 races selected from the periodic table of elements and in 16 races Element.

As including the element (the first element) in 13 races selected from the periodic table of elements and 16 races selected from the periodic table of elements In element (second element) binary system III group-VI compound semiconductor, it can be mentioned, for example Al₂S₃、Al₂Se₃、 Al₂Te₃、Ga₂S₃、Ga₂Se₃、Ga₂Te₃、GaTe、In₂S₃、In₂Se₃、In₂Te₃Or InTe.

Comprising in the element (the first element) in 13 races selected from the periodic table of elements and 16 races selected from the periodic table of elements III group-VI the compound semiconductor of element (second element) can be the member in 13 races comprising a kind selected from the periodic table of elements III group-VI the race of the ternary system of plain (the first element) and the element (second element) in 2 kinds of 16 races selected from the periodic table of elements Close object semiconductor, be also possible to comprising in 2 kinds of 13 races selected from the periodic table of elements element (the first element) and a kind be selected from element III group-VI the compound semiconductor of the ternary system of element (second element) in 16 races of periodic table, can also be comprising 2 Element (the in element (the first element) and 2 kinds of 16 races selected from the periodic table of elements in kind of 13 races selected from the periodic table of elements Was Used) quaternary system III group-VI compound semiconductor.

III group-VI compound semiconductor may include the work of the element other than 13 races of the periodic table of elements and 16 races For doped chemical.

(particle of the crystal of IV race-VI compound semiconductor)

IV race-VI compound semiconductor includes the element in 14 races selected from the periodic table of elements and the member in 16 races Element.As including the member in the element (the first element) in 14 races selected from the periodic table of elements and 16 races selected from the periodic table of elements IV race-VI the compound semiconductor of the binary system of plain (second element), it can be mentioned, for example PbS, PbSe, PbTe, SnS, SnSe Or SnTe.

Comprising in the element (the first element) in 14 races selected from the periodic table of elements and 16 races selected from the periodic table of elements IV race-VI the compound semiconductor of element (second element) can be the member in 14 races comprising a kind selected from the periodic table of elements - VI the race, IV race of the ternary system of plain (the first element) and the element (second element) in 2 kinds of 16 races selected from the periodic table of elements Close object semiconductor, be also possible to comprising in 2 kinds of 14 races selected from the periodic table of elements element (the first element) and a kind be selected from element IV race-VI the compound semiconductor of the ternary system of element (second element) in 16 races of periodic table, can also be comprising 2 kinds The element (second in element (the first element) and 2 kinds of 16 races selected from the periodic table of elements in 14 races selected from the periodic table of elements Element) quaternary system IV race-VI compound semiconductor.

IV race-VI compound semiconductor may include the element conduct other than 14 races of the periodic table of elements and 16 races Doped chemical.

(particle of the crystal of the area transition metal-p compound semiconductor)

Transition metal-p area's compound semiconductor is comprising the element in transition metal element and in p p-block element p Element.

As comprising the element (the first element) in the transition metal element of the periodic table of elements and selected from period of element The area the transition metal-p compound semiconductor of the binary system of element (second element) in the p p-block element p of table, it can be mentioned, for example NiS、CrS。

Include the element (the first element) in the transition metal element of the periodic table of elements and the p selected from the periodic table of elements The area the transition metal-p compound semiconductor of element (second element) in p-block element p can be comprising a kind selected from the periodic table of elements Transition metal element in element (the first element) and 2 kinds of elements (second element) in p p-block element p ternary system The area transition metal-p compound semiconductor is also possible to comprising the element in 2 kinds of transition metal elements selected from the periodic table of elements Transition metal-the p of the ternary system of (the first element) and the element (second element) in a kind of p p-block element p selected from the periodic table of elements Area's compound semiconductor can also be comprising the element (the first element) in 2 kinds of transition metal elements selected from the periodic table of elements With the area the transition metal-p compound half of the quaternary system of the element (second element) in 2 kinds of p p-block element ps selected from the periodic table of elements Conductor.

The area transition metal-p compound semiconductor may include the transition metal element and p p-block element p in addition to the periodic table of elements Element in addition is as doped chemical.

The concrete example of semiconductor as above-mentioned ternary system or quaternary system, can enumerate ZnCdS, CdSeS, CdSeTe, CdSTe、ZnSeS、ZnSeTe、ZnSTe、HgSeS、HgSeTe、HgSTe、CdZnS、CdZnSe、CdZnTe、CdHgS、CdHgSe、 CdHgTe、HgZnS、HgZnSe、HgZnTe、ZnCdSSe、CdZnSeS、CdZnSeTe、CdZnSTe、CdHgSeS、CdHgSeTe、 CdHgSTe、HgZnSeS、HgZnSeTe、HgZnSTe、GaNP、GaNAs、GaPAs、AlNP、AlNAs、AlPAs、InNP、 InNAs、InPAs、GaAlNP、GaAlNAs、GaAlPAs、GaInNP、GaInNAs、GaInPAs、InAlNP、InAlNAs、 CuInS₂Or InAlPAs etc..

(perovskite compound)

As an example of semiconductive particles, the particle of perovskite compound can be enumerated.

Perovskite compound is compound using A, B and X as constituent, with perovskite type crystal structure.

In the present invention, A is the hexahedral each vertex being located at centered on B in above-mentioned perovskite type crystal structure Ingredient is 1 valence cation.

X indicates the ingredient for being located at octahedral each vertex centered on B in above-mentioned perovskite type crystal structure, is Selected from one or more of halide ion and thiocyanate ion anion.

B is to be located at that A is configured at the hexahedron on vertex and X is configured at vertex in above-mentioned perovskite type crystal structure The ingredient at octahedral center is metal ion.

As the perovskite compound using A, B and X as constituent, it is not particularly limited, it can be for three-dimensional knot Structure, two-dimensional structure, any structure in quasi- two-dimensional structure compound.

In the case where three-dimensional structure, the composition formula of perovskite compound is with AB_x(3+δ)To indicate.

In the case where two-dimensional structure, the composition formula of perovskite compound is with A₂BX_(4+δ)To indicate.

Here, above-mentioned δ be can corresponding to B charge balance and the numerical value that suitably changes, be -0.7 or more and 0.7 with Under.

For example, in the case where A is 1 valence cation, B is divalent cation, X is 1 valence anion, it can be above-mentioned according to making The mode of compound neutral (charge 0) selects δ.

In the case where above-mentioned three-dimensional structure, have centered on B, vertex is set as the BX of X₆Shown in altogether vertex it is octahedra Three-dimensional network.

In the case where above-mentioned two-dimensional structure, by centered on B, vertex be set as the BX of X₆Shown in octahedron it is shared same The X on 4 vertex of one plane, be consequently formed be alternately laminated that two dimension is connected comprising BX₆Layer and the layer comprising A knot Structure.

In the present specification, perovskite type crystal structure can use X-ray diffraction pattern to confirm.

In the case where the compound of the perovskite type crystal structure with above-mentioned three-dimensional structure, in X-ray diffraction pattern In, usually 2 θ=12~18 ° location confirmation to from (hkl)=(001) peak or in the position of 2 θ=18~25 ° Confirm the peak from (hkl)=(100).More preferably 2 θ=13~16 ° location confirmation to from (hkl)=(001) Peak or 2 θ=20~23 ° location confirmation to come from (hkl)=(100) peak.

In the case where the compound of the perovskite type crystal structure with above-mentioned two-dimensional structure, in X-ray diffraction pattern In, usually 2 θ=1~10 ° location confirmation to come from (hkl)=(002) peak, it is more preferably true in the position of 2 θ=2~8 ° Recognize the peak from (hkl)=(002).

Perovskite compound is preferably perovskite compound shown in the following general formula (1).

ABX_(3+δ)(-0.7≤δ≤0.7)…(1)

[in general formula (1), A is 1 valence cation, and B is metal ion, and X is in halide ion and thiocyanate ion 1 kind or more anion.]

〔A〕

In perovskite compound of the present invention, A is located at centered on B in above-mentioned perovskite type crystal structure The ingredient on hexahedral each vertex is 1 valence cation.As 1 valence cation, cesium ion, organoammonium ions or amidine can be enumerated (amidinium) ion.In perovskite compound, A be cesium ion, carbon atom number be 3 organoammonium ions below or Carbon atom number be 3 amidine ions below in the case where, it is however generally that, perovskite compound have ABX (_{30 δ}) shown in three-dimensional Structure.In compound, the preferred cesium ion of A or organoammonium ions.

As the organoammonium ions of A, specifically, cation shown in the following general formula (A3) can be enumerated.

[changing 1]

In general formula (A3), R⁶~R⁹It separately indicates hydrogen atom, can have amino as the alkyl of substituent group or can Using the naphthenic base with amino as substituent group.But R⁶~R⁹Not all hydrogen atoms.

R⁶~R⁹Shown in alkyl can be straight-chain, or branched can also have amino as substituent group.

R⁶~R⁹Shown in the carbon atom number of alkyl be usually 1~20, preferably 1~4, more preferably 1~3.

R⁶~R⁹Shown in naphthenic base can have alkyl as substituent group, it is possible to have amino is as substituent group.

R⁶~R⁹Shown in the carbon atom number of naphthenic base be usually 3~30, preferably 3~11, more preferably 3~8.Carbon is former Subnumber includes the carbon atom number of substituent group.

As R⁶~R⁹Shown in group, separately preferably hydrogen atom or alkyl.

Pass through and reduces the quantity of the alkyl that can contain and naphthenic base in general formula (A3) and reduce alkyl and naphthenic base Carbon atom number, so as to obtain the compound of the high perovskite type crystal structure with three-dimensional structure of luminous intensity.

In the case where the carbon atom number of alkyl or cycloalkyl is 4 or more, available part or it is all have two peacekeepings/ Or the compound of the perovskite type crystal structure of quasi- two-dimentional (quasi-2D).If two-dimensional perovskite type crystal structure is infinitely greatly Stacking, then become with three-dimensional perovskite type crystal structure it is same (bibliography: P.P.Boix et al., J.Phys.Chem.Lett.2015,6,898-907 etc.).

R⁶~R⁹Shown in the total number of carbon atom number contained in alkyl and naphthenic base be preferably 1~4, it is even more preferred that R⁶~R⁹In 1 be carbon atom number 1~3 alkyl, R⁶~R⁹In 3 be hydrogen atom.

As R⁶~R⁹Alkyl, methyl, ethyl, n-propyl, isopropyl, normal-butyl, isobutyl group, sec-butyl, uncle can be illustrated Butyl, n-pentyl, isopentyl, neopentyl, tertiary pentyl, 1- methyl butyl, n-hexyl, 2- methyl amyl, 3- methyl amyl, 2,2- Dimethylbutyl, 2,3- dimethylbutyl, n-heptyl, 2- methylhexyl, 3- methylhexyl, 2,2- dimethyl amyl group, 2,3- bis- Methyl amyl, 2,4- dimethyl amyl group, 3,3- dimethyl amyl group, 3- ethylpentyl, 2, it is 2,3- trimethyl butyls, n-octyl, different Octyl, 2- ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, myristyl, pentadecyl, hexadecane Base, heptadecyl, octadecyl, nonadecyl, eicosyl.

As R⁶~R⁹Naphthenic base, can enumerate in R⁶~R⁹Alkyl in illustrated by 3 or more carbon atom number alkyl shape Group after cyclization, as an example, can illustrate cyclopropyl, cyclobutyl, cyclopenta, cyclohexyl, suberyl, cyclooctyl, cyclononyl, Cyclodecyl, norborny, isobornyl, 1- adamantyl, 2- adamantyl, tricyclodecyl etc..

As organoammonium ions shown in A, preferably CH₃NH₃ ⁺(also referred to as ammonium ion), C₂H₅NH₃ ⁺(also referred to as second Base ammonium ion) or C₃H₇NH₃ ⁺(also referred to as propyl ammonium ion), more preferably CH₃NH₃ ⁺Or C₂H₅NH₃ ⁺, further preferably CH₃NH₃ ⁺。

As amidine ion shown in A, it can be mentioned, for example amidine ions shown in the following general formula (A4).

(R¹⁰R¹¹N=CH-NR¹²R¹³)⁺···(A4)

In general formula (A4), R¹⁰~R¹³Separately indicate hydrogen atom, can have amino as the alkyl of substituent group or It can have naphthenic base of the amino as substituent group.

R¹⁰~R¹³Shown in alkyl can be straight-chain, or branched, can also have amino as replace Base.

R¹⁰~R¹³Shown in the carbon atom number of alkyl be usually 1~20, preferably 1~4, more preferably 1~3.

R¹⁰~R¹³Shown in naphthenic base can have alkyl as substituent group, it is possible to have amino is as substituent group.

R¹⁰~R¹³Shown in the carbon atom number of naphthenic base be usually 3~30, preferably 3~11, more preferably 3~8.Carbon Atomicity includes the carbon atom number of substituent group.

As R¹⁰~R¹³Alkyl concrete example, can enumerate in R⁶~R⁹In illustrated by alkyl.

As R¹⁰~R¹³Naphthenic base concrete example, can enumerate in R⁶~R⁹In illustrated by naphthenic base.

As R¹⁰~R¹³Shown in group, preferably hydrogen atom or alkyl.

By reducing the quantity of alkyl contained in general formula (A4) and naphthenic base, and the carbon for reducing alkyl and naphthenic base is former Subnumber, so as to obtain the perovskite compound of the high three-dimensional structure of luminous intensity.

In the case where the carbon atom number of alkyl or cycloalkyl is 4 or more, available part or it is all have two peacekeepings/ Or the compound of the perovskite type crystal structure of quasi- two-dimentional (quasi-2D).In addition, R¹⁰~R¹³Shown in alkyl and naphthenic base The total number of contained carbon atom number is preferably 1~4, it is even more preferred that R¹⁰For the alkyl of carbon atom number 1~3, R¹¹~R¹³For Hydrogen atom.

〔B〕

In perovskite compound, B is to be located at that A is configured at the hexahedron on vertex and is incited somebody to action in perovskite type crystal structure X is configured at the ingredient at octahedral center on vertex, indicates metal ion.As B component metal ion can for comprising Ion selected from one or more of 1 valence metal ion, divalent metal ion and trivalent metal ion.B preferably comprise divalent metal from Son, more preferably comprising being selected from one or more of lead or tin metal ion.

〔X〕

X indicates to be selected from one or more of halide ion and thiocyanate ion anion.X can be for selected from chloride One or more of ion, bromide ion, fluoride ion, iodide ion and thiocyanate ion anion.

As expected X emission wavelength can be selected suitably, for example, X may include bromide ion.

In the case where X is halide ion of more than two kinds, the containing ratio of above-mentioned halide ion can be according to luminous Wavelength is suitably selected, for example, can be the combination of bromide ion and chloride ion or bromide ion and iodate The combination of object ion.

It as perovskite compound and is ABX_(3+δ)Shown in three-dimensional structure perovskite type crystal structure chemical combination The concrete example of object can enumerate CH₃NH₃PbBr₃、CH₃NH₃PbCl₃、CH₃NH₃PbI₃、CH₃NH₃PbBr_(3-y)I_y(0 < y < 3), CH₃NH₃PbBr_(3-y)Cl_y(0 < y < 3), (H₂N=CH-NH₂)PbBr₃、(H₂N=CH-NH₂)PbCl₃、(H₂N=CH-NH₂) PbI₃、CH₃NH₃Pb_(1-a)Ca_aBr_(3+δ)(0 < a≤0.7,0≤δ≤0.7), CH₃NH₃Pb_(1-a)Sr_aBr(_3+δ)(0 < a≤0.7,0 ≤δ≤0.7)、CH₃NH₃Pb_(1-a)La_aBr_(3+δ)(0 < a≤0.7,0≤δ≤0.7), CH₃NH₃Pb_(1-a)Ba_aBr_(3+δ)(0 < a≤ 0.7,0≤δ≤0.7), CH₃NH₃Pb_(1-a)Dy_aBr_(3+δ)(0 < a≤0.7,0≤δ≤0.7), CH₃NH₃Pb_(1-a)Na_aBr_(3+δx(0 A≤0.7 <, -0.7≤δ≤0), CH₃NH₃Pb_(1-a)Li_aBr_(3+δ)(0 a≤0.7 <, -0.7≤δ≤0), CsPb_(1-a) Na_aBr_(3+δ)(0 a≤0.7 <, -0.7≤δ≤0), CsPb_(1-a)Li_aBr_(3+δ) (0 a≤0.7 <, -0.7≤δ≤0), CH₃NH₃Pb_(1-a)Na_aBr_(3+δ-y)I_y(0 a≤0.7 <, -0.7≤δ≤0,0 < y < 3), CH₃NH₃Pb_(1-a)Li_aBr_(3+δ-y)I_y(0 A≤0.7 <, -0.7≤δ≤0,0 < y < 3), CH₃NH₃Pb_(1-a)Na_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, -0.7≤δ≤0,0 < Y < 3), CH₃NH₃Pb_(1-a)Li_aBr_(3+δ-y)C1_y(0 a≤0.7 <, -0.7≤δ≤0,0 < y < 3), (H₂N=CH-NH₂)Pb_(1-a) Na_aBr_(3+δ)(0 a≤0.7 <, -0.7≤δ≤0), (H₂N=CH-NH₂)Pb_(1-a)Li_aBr_(3+δ)(0 a≤0.7 <, -0.7≤δ≤ 0)、(H₂N=CH-NH₂)Pb_(1-a)Na_aBr_(3+δ-y)I_y(0 a≤0.7 <, -0.7≤δ≤0,0 < y < 3), (H₂N=CH-NH₂) Pb_(1-a)Na_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, -0.7≤δ≤0,0 < y < 3), CsPbBr₃、CsPbCl₃、CsPbI₃、 CsPbBr_(3-y)I_y(0 < y < 3), CsPbBr_(3-y)Cl_y(0 < y < 3), CH₃NH₃PbBr_(3-y)Cl_y(0 < y < 3), CH₃NH₃Pb_(1-a)Zn_aBr_(3+δ)(0 < a≤0.7,0≤δ≤0.7), CH₃NH₃Pb_(1-a)Al_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤ 0.7)、CH₃NH₃Pb_(1-a)Co_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7), CH₃NH₃Pb_(1-a)Mn_aBr_(3+δ)(0 a≤0.7 <, 0 ≤δ≤0.7)、CH₃NH₃Pb_(1-a)Mg_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7), CsPb_(1-a)Zn_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7)、CsPb_(1-a)Al_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7), CsPb_(1-a)Co_aBr_(3+δ)(0 < a≤0.7,0 ≤δ≤0.7)、CsPb_(1-a)Mn_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7), CsPb_(1-a)Mg_aBr_(3+δ)(0 a≤0.7 <, 0≤ δ≤0.7)、CH₃NH₃Pb_(1-a)Zn_aBr_(3+δ-y)I_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a) Al_aBr_(3+δ-y)I_y(the 0 < < y of a≤0.7,0≤δ≤0.7,0 < 3), CH₃NH₃Pb_(1-a)Co_aBr_(3+δ-y)I_y(0 a≤0.7 <, 0≤ δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a)Mn_aBr_(3+δ-y)I_y(the 0 < < y of a≤0.7,0≤δ≤0.7,0 < 3), CH₃NH₃Pb_(1-a)Mg_aBr_(3+δ-y)I_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a)Zn_aBr_(3+δ-y)Cl_y(0 A≤0.7 <, 0≤δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a)Al_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a)Co_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a) Mn_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 3), CH₃NH₃Pb_(1-a)Mg_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, 0 ≤ δ≤0.7,0 < y < 3), (H₂N=CH-NH₂)Zn_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7), (H₂N=CH-NH₂) Mg_aBr_(3+δ)(0 a≤0.7 <, 0≤δ≤0.7), (H₂N=CH-NH₂)Pb_(1-a)Zn_aBr_(3+δ-y)I_y(0 a≤0.7 <, 0≤δ≤ 0.7,0 < y < 3), (H₂N=CH-NH₂)Pb_(1-a)Zn_aBr_(3+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 3) etc. makees For preferred example.

It as perovskite compound and is A₂BX_(4+δ)Shown in two-dimensional structure perovskite type crystal structure change The concrete example for closing object, can enumerate (C₄H₉NH₃)₂PbBr₄、(C₄H₉NH₃)₂PbCl₄、(C₄H₉NH₃)₂PbI₄、(C₇H₁₅NH₃)₂PbBr₄、 (C₇H₁₅NH₃)₂PbCl₄、(C₇H₁₅NH₃)₂PbI₄、(C₄H₉NH₃)₂Pb_(1-a)Li_aBr₄(0 a≤0.7 <), (C₄H₉NH₃)₂Pb_(1-a) Na_aBr₄(0 a≤0.7 <), (C₄H₉NH₃)₂Pb_(1-a)Rb_aBr₄(0 a≤0.7 <), (C₇H₁₅NH₃)₂Pb_(1-a)Na_aBr₄(0 < a≤ 0.7)、(C₇H₁₅NH₃)₂Pb_(1-a)Li_aBr₄(0 a≤0.7 <), (C₇H₁₅NH₃)₂Pb_(1-a)Rb_aBr₄(0 a≤0.7 <), (C₄H₉NH₃)₂Pb_(1-a)Na_aBr_(4-y)I_y(0 a≤0.7 <, 0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Li_aBr_(4-y)I_y(0 < a≤ 0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Rb_aBr_(4-y)I_y(0 a≤0.7 <, 0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a) Na_aBr_(4-y)Cl_y(0 a≤0.7 <, 0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Li_aBr_(4-y)Cl_y(0 a≤0.7 <, 0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Rb_aBr_(4-y)Cl_y(0 a≤0.7 <, 0 < y < 4), (C₄H₉NH₃)₂PbBr₄、(C₇H₁₅NH₃)₂PbBr₄、 (C₄H₉NH₃)₂PbBr_(4-y)Cl_y(0 < y < 4), (C₄H₉NH₃)₂PbBr_(4-y)I_y(0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a) Zn_aBr_(4+δ)(0 a≤0.7 <), (C₄H₉NH₃)₂Pb_(1-a)Mg_aBr_(4+δ)(0 a≤0.7 <, 0≤δ≤0.7) (C₄H₉NH₃)₂Pb_(1-a) Co_aBr_(4+δ)(0 a≤0.7 <, 0≤δ≤0.7), (C₄H₉NH₃)₂Pb_(1-a)Mn_aBr_(4+δ)(0 a≤0.7 <, 0≤δ≤0.7), (C₇H₁₅NH₃)₂Pb_(1-a)Zn_aBr_(4+δ)(0 a≤0.7 <, 0≤δ≤0.7), (C₇H₁₅NH₃)₂Pb(_1-a)Mg_aBr_(4+δ)(0 < a≤ 0.7、0≤δ≤0.7)、(C₇H₁₅NH₃)₂Pb_(1-a)Co_aBr_(4+δ)(0 a≤0.7 <, 0≤δ≤0.7), (C₇H₁₅NH₃)₂Pb_(1-a) Mn_aBr_(4+δ)(0 a≤0.7 <, 0≤δ≤0.7), (C₄H₉NH₃)₂Pb_(1-a)Zn_aBr_(4+δ-y)I_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Mg_aBr_(4+δ-y)I_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a) Co_aBr_(4+δ-y)I_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Mn_aBr_(4+δ-y)I_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Zn_aBr_(4+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Mg_aBr_(4+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Co_aBr_(4+δ-y)Cl_y(0 a≤0.7 <, 0≤δ≤0.7,0 < y < 4), (C₄H₉NH₃)₂Pb_(1-a)Mn_aBr_(4+δ-y)Cl_y(0 A≤0.7 <, 0≤δ≤0.7,0 < y < 4) etc. be used as preferred example.

" luminescent spectrum "

Perovskite compound is that can issue the illuminator of fluorescence in visible wavelength region, is bromide ion in X In the case of, can be emitted in usual 480nm or more, preferably 500nm or more, more preferable 520nm or more and usually 700nm or less, It is preferred that with the fluorescence at intensity maximum peak in the range of 600nm or less, more preferable 580nm wave-length coverage below.

As another side of the invention, in the case that the X in perovskite compound is bromide ion, issued The peak of fluorescence be usually 480~700nm, preferably 500~600nm, more preferably 520~580nm.

X be iodide ion in the case where, can be emitted in usual 520nm or more, preferably 530nm or more, more preferably Have in the range of 540nm or more and usually 800nm or less, preferably 750nm or less, more preferable 730nm wave-length coverage below The fluorescence at intensity maximum peak.

As another side of the invention, in the case that the X in perovskite compound is iodide ion, issued The peak of fluorescence be usually 520~800nm, preferably 530~750nm, more preferably 540~730nm.

X be chloride ion in the case where, can be emitted in usual 300nm or more, preferably 310nm or more, more preferably Have in the range of 330nm or more and usually 600nm or less, preferably 580nm or less, more preferable 550nm wave-length coverage below The fluorescence at intensity maximum peak.

As another side of the invention, in the case that the X in perovskite compound is chloride ion, issued The peak of fluorescence be usually 300~600nm, preferably 310~580nm, more preferably 330~550nm.

(2) halogenated hydrocarbon compound

Halogenated hydrocarbon compound can be shown in any one in the following general formula (A5-1)~(A5-3) with halohydrocarbyl Compound.

[changing 2]

R¹⁴-C≡C-Y···(A5-3)

In general formula (A5-1)~(A5-3), C-Y indicates that halohydrocarbyl, C indicate carbon atom, R¹⁴~R¹⁶Independently earth's surface Show hydrogen atom or monovalent organic group.As organic group, it preferably can have the alkyl of substituent group or can have substituent group The alkyl such as naphthenic base.

In R¹⁴~R¹⁶It can be straight-chain, or branched can have as substituent group in the case where for alkyl There is alkoxysilyl, it is possible to have halogeno-group.The carbon atom number of alkyl is usually 1~20, and preferably 5~20, it is more excellent It is selected as 8~20.Above-mentioned carbon atom number includes the carbon atom number of substituent group.

In R¹⁴~R¹⁶In the case where naphthenic base, naphthenic base can have alkoxysilyl as substituent group, can also , as substituent group, can also have alkyl as substituent group with halogeno-group.The carbon atom number of naphthenic base is usually 3~30, Preferably 3~20, more preferably 3~11.Above-mentioned carbon atom number includes the carbon atom number of substituent group.

Abovementioned alkyl and naphthenic base preferably do not have substituent group.

Wherein, R¹⁴~R¹⁶Preferably hydrogen atom or alkyl, more preferably make R¹⁴~R¹⁶In at least one be abovementioned alkyl.Into One step is preferably: in (A5-1), R¹⁴~R¹⁶In 1 be carbon atom number 1~20 alkyl, R¹⁴~R¹⁶In 2 be hydrogen Atom.

As R¹⁴~R¹⁶Alkyl concrete example, can enumerate in R⁶~R⁹In illustrated by alkyl.

As R¹⁴~R¹⁶Naphthenic base concrete example, can enumerate in R⁶~R⁹In illustrated by naphthenic base.

In general formula (A5-1)~(A5-3), Y indicates halogens.As halogens shown in Y, it can be mentioned, for example fluorine originals Son, chlorine atom, bromine atom, iodine atom, preferably bromine atom.

Part or all of halogenated hydrocarbon compound shown in general formula (A5-1)~(A5-3) can be adsorbed in the present invention and relate to And semiconductive particles surface, can also be distributed in composition.

Shown in general formula (A5-1)~(A5-3) with halogenated alkyl organic compound can enumerate fluothane, chlorine alkane, bromine alkane, Iodine alkane etc., preferably 1- bromo-octadecane, pe-ntadecyl bromide, 1- bromo-tetradecane, 1- bromo-n-11,1- bromine hexadecane, 1- chlorine hexadecane, 1- chlorine octadecane, 1- pentamethylene, the 1- chlorine tetradecane, 1- fluorine octadecane, 1- fluorine pentadecane, the 1- fluorine tetradecane, 1- fluorine hendecane, 1- Fluorine hexadecane, 1- iodine octadecane, 1- iodine pentadecane, the 1- iodine tetradecane, 1- iodine hendecane, Cetyl Iodide, more preferable 1- bromine ten Six alkane, 1- fluorine hexadecane, Cetyl Iodide, 1- chlorine hexadecane.

Another side of the invention is (2) halogenated hydrocarbon compound, and is had in addition to-NH₃ ⁺Shown in group and-COO- Shown in the organic compound of ionic group other than group, the compound with sulfydryl or have amino, alkoxy and The organic compound of silicon atom can be except.

(3) solvent

As long as the medium that solvent can be such that semiconductive particles disperse, then be not particularly limited, preferably not readily dissolve and partly lead The solvent of body particle.

In the present specification, " solvent " refers to that the substance that liquid condition is presented at 1 atmospheric pressure, 25 DEG C (still, polymerize Except property compound and polymer).

As solvent, it can be mentioned, for example: methyl formate, Ethyl formate, propyl formate, amyl formate, methyl acetate, acetic acid The esters such as ethyl ester, pentyl acetate；Gamma-butyrolacton, acetone, dimethyl ketone, diisobutyl ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone Equal ketone；Anaesthetie Ether, methyl tertiary butyl ether(MTBE), Di Iso Propyl Ether, dimethoxymethane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1, The ethers such as 3- dioxolanes, 4- methyl dioxolane, tetrahydrofuran, methyltetrahydrofuran, methyl phenyl ethers anisole, phenetole；Methanol, ethyl alcohol, 1- propyl alcohol, 2- propyl alcohol, n-butyl alcohol, 2- butanol, the tert-butyl alcohol, 1- amylalcohol, 2- methyl -2- butanol, methoxypropanol, diacetone alcohol, Cyclohexanol, 2- fluoroethanol, 2,2,2- trifluoroethanols, 2, the alcohol such as 2,3,3- tetra- fluoro- 1- propyl alcohol；Ethylene glycol single methyl ether, ethylene glycol The glycol ethers such as single ethylether, ethylene glycol monobutyl ether, ethylene glycol monomethyl ether acetate, triethylene glycol dimethyl ether；N- methyl -2- Pyrrolidones, n,N-Dimethylformamide, acetamide, n,N-dimethylacetamide etc. have the organic solvent of amide groups；Acetonitrile, Isobutyronitrile, propionitrile, methoxyacetonitrile etc. have the organic solvent of itrile group；Ethylene carbonate, propylene carbonate etc. have alkyl Organic solvent；Methylene chloride, chloroform etc. have the organic solvent of halohydrocarbyl；Pentane, hexamethylene, n-hexane, benzene, toluene, Dimethylbenzene etc. has the organic solvent of alkyl；Dimethyl sulfoxide etc..

Wherein, it is contemplated that polarity is low, not readily dissolve semiconductive particles and it is preferred that: methyl formate, Ethyl formate, formic acid third The esters such as ester, amyl formate, methyl acetate, ethyl acetate, pentyl acetate；Gamma-butyrolacton, acetone, dimethyl ketone, diisobutyl The ketone such as ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone；Anaesthetie Ether, methyl tertiary butyl ether(MTBE), Di Iso Propyl Ether, dimethoxy first Alkane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1,3-dioxolane, 4- methyl dioxolane, tetrahydrofuran, methyltetrahydrofuran, The ethers such as methyl phenyl ethers anisole, phenetole；Acetonitrile, isobutyronitrile, propionitrile, methoxyacetonitrile etc. have the organic solvent of itrile group；Ethylene carbonate, Propylene carbonate etc. has the organic solvent of carbonate group；Methylene chloride, chloroform etc. have the organic solvent of halohydrocarbyl；Positive penta Alkane, hexamethylene, n-hexane, benzene,toluene,xylene etc. have the organic solvent of alkyl.It is more preferable: the tool such as methylene chloride, chloroform There is the organic solvent of halohydrocarbyl；The hydrocarbon systems organic solvent such as pentane, hexamethylene, n-hexane, benzene,toluene,xylene.

(4) at least one kind of in polymerizable compound and polymer

Polymerizable compound contained in composition of the present invention is not particularly limited, but preferably in above-mentioned group of manufacture The semiconductive particles polymerizable compound low relative to the solubility of polymerizable compound at a temperature of conjunction object.

In the present specification, " polymerizable compound " refers to the compound of the monomer with polymerizable group.

For example, as above-mentioned polymerizable compound, there is no particular restriction in the case where being manufactured at room temperature and normal pressure, It can be mentioned, for example polymerizable compounds well known to styrene, methyl methacrylate etc..Wherein, excellent as polymerizable compound It is elected to be any one of acrylate and methacrylate of the monomer component for acrylic resin or both.

Polymer contained in composition of the present invention is not particularly limited, but preferably in manufacture above-mentioned composition At a temperature of the above-mentioned semiconductive particles polymer low relative to the solubility of polymer.

For example, as above-mentioned polymer, there is no particular restriction in the case where being manufactured at room temperature and normal pressure, can enumerate Such as polymer well known to polystyrene, methacrylic resin etc..Wherein, as polymer, preferably acrylic resin. Acrylic resin includes the structural unit from any one of acrylate and methacrylate or both.

(4) in the structural unit of polymerizable compound and polymer, acrylate and/or methacrylate and come It can be 10% or more relative to entire infrastructure unit in the case where being indicated with a mole % from their structural unit, it can also be with It is 30% or more, can also is 50% or more, can also be 80% or more, can also is 100%.

(5) at least one kind of in ammonia, amine, carboxylic acid and their salt or ion

Composition of the present invention may include selected from ammonia, amine, carboxylic acid and can take as above compound It is at least one kind of in their salt or ion of form.

That is, composition of the present invention may include selected from ammonia, amine, carboxylic acid, the salt of ammonia, the salt of amine, the salt of carboxylic acid, ammonia Ion, at least one kind of in the ion of amine and the ion of carboxylic acid.

Ammonia, amine, carboxylic acid and their salt or ion play a role usually as capping ligands.Capping ligands refer to It is adsorbed in the surface of semiconducting compound and has the function of the chemical combination for being distributed to semiconducting compound steadily in composition Object.As the ion or salt (ammonium salt etc.) of ammonia or amine, ammonium cation shown in aftermentioned general formula (A1) and the ammonium comprising it can be enumerated Salt.As the ion or salt (carboxylate etc.) of carboxylic acid, carboxylate anion shown in aftermentioned general formula (A2) can be enumerated and comprising it Carboxylate.Both composition of the present invention may include any one of ammonium salt etc. and carboxylate etc., also may include.

As ammonium salt, the ammonium salt comprising ammonium cation shown in general formula (A1) can be enumerated.

[changing 3]

In general formula (A1), R¹~R⁴Separately indicate hydrogen atom, organic group.For organic group, R¹ ~R⁴It is separately preferably the alkyl such as alkyl, naphthenic base, unsaturated alkyl.

R¹~R⁴Shown in alkyl can be straight-chain, or branched.

R¹~R⁴Shown in the carbon atom number of alkyl be usually 1~20, preferably 5~20, more preferably 8~20.

R¹~R⁴Shown in naphthenic base can have alkyl as substituent group.Carbon atom number is usually 3~30, preferably 3~ 20, more preferably 3~11.Carbon atom number includes the carbon atom number of substituent group.

R¹~R⁴Unsaturated alkyl can be straight-chain, or branched.

R¹~R⁴The carbon atom number of unsaturated alkyl be usually 2~20, preferably 5~20, more preferably 8~20.

R¹~R⁴Preferably hydrogen atom, alkyl or unsaturated alkyl.As unsaturated alkyl, preferably alkenyl.More preferably It is: R¹~R⁴In 1 be carbon atom number 8~20 alkenyl, R¹~R⁴In 3 be hydrogen atom.

As R¹~R⁴Alkyl concrete example, can enumerate in R⁶~R⁹In illustrated by alkyl.

As R¹~R⁴Naphthenic base concrete example, can enumerate in R⁶~R⁹In illustrated by naphthenic base.

As R¹~R⁴Alkenyl, R can be illustrated in⁶~R⁹In illustrated by above-mentioned straight-chain or branched alkyl in appoint Singly-bound (C-C) between one carbon atom is replaced into alkenyl obtained by double bond (C=C), and the position of double bond is simultaneously not limited.

As the preference of such alkenyl, it can be mentioned, for example vinyl, acrylic, 3- cyclobutenyl, 2- cyclobutenyl, 2- penta Alkenyl, 2- hexenyl, 2- nonenyl, 2- dodecenyl succinic, 9- octadecene base.

As counter anion, there is no particular restriction, can enumerate Br^-、Cl^-、I^-、F^-Halide ion or carboxylate radical from Son etc. is used as preferred example.

As the ammonium salt with ammonium cation and counter anion shown in general formula (A1), n-octyl ammonium salt, oil can be enumerated Base ammonium salt is as preferred example.

As carboxylate, the carboxylate comprising carboxylate anion shown in the following general formula (A2) can be enumerated.

R⁵-CO₂ ^-···(A2)

In general formula (A2), R⁵Indicate monovalent organic group.As organic group, preferably alkyl, wherein can enumerate alkyl, Naphthenic base, unsaturated alkyl are as preferred example.

R⁵Shown in alkyl can be straight-chain, or branched.R⁵Shown in the carbon atom number of alkyl be usually 1 ~20, preferably 5~20, more preferably 8~20.

R⁵Shown in naphthenic base can have alkyl as substituent group.Carbon atom number is usually 3~30, and preferably 3~20, More preferably 3~11.Carbon atom number includes the carbon atom number of substituent group.

The unsaturated alkyl of Rw can be straight-chain, or branched.

The carbon atom number of the unsaturated alkyl of Rw is usually 2~20, and preferably 5~20, more preferably 8~20.

R⁵Preferably alkyl or unsaturated alkyl.As unsaturated alkyl, preferably alkenyl.

As R⁵Alkyl concrete example, can enumerate in R⁶~R⁹In illustrated by alkyl.

As R⁵Naphthenic base concrete example, can enumerate in R⁶~R⁹In illustrated by naphthenic base.

As R⁵Alkenyl concrete example, can enumerate in R¹~R⁴In illustrated by alkenyl.

Carboxylate anion shown in general formula (A2) is preferably oily acid radical anion.As carboxylate radical shown in general formula (A2) The counter cation of anion, there is no particular restriction, can enumerate proton, alkali metal cation, alkaline earth metal cation, ammonium sun from Son etc. is used as preferred example.

The composition of present embodiment includes (1) and (2), and also includes at least one of (3) and (4).

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(3) solvent

(4) at least one kind of in polymerizable compound and polymer

The composition of present embodiment includes (1), (2) and (4 ').

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(4 ') polymer

In the composition of present embodiment, (1) with (2) if match ratio be that can play organising based on (2) This degree of the effect of raising quantum yield of object is closed, can be appropriately configured according to (1) and the type of (2) etc..

In the composition of present embodiment, in the case where (1) semiconductive particles are the particle of perovskite compound, calcium The molar ratio [(2)/B] of the metal ion of the B of titanium ore compound and the organic compound of (2) can be 0.001~1000, can also Think 0.01~700, can also be 0.1~500.

In the composition of present embodiment, (1) semiconductive particles be the particle of perovskite compound, (2) it is organic Compound is shown in general formula (A5-1)~(A5-3) in the case where halogenated hydrocarbon compound, the metal of the B of perovskite compound from The molar ratio [(A5)/B] of son and the organic compound of (A5-1)~(A5-3) can be 1~1000, or 10~700, It can also be 100~500.

(1) having based on (2) can particularly good be played for the composition in above range with the range of the match ratio of (2) The effect of the raising quantum yield of machine compound, is preferred in this regard.

In the composition of present embodiment, (1) be selected from (3) and (4) if any one of or both match ratio It is the degree that can play the luminous function based on (1) semiconductive particles well, it can be according to the type of (1)~(4) Etc. being appropriately configured.

In the composition comprising (1), (2) and the present embodiment selected from any one of (3) and (4) or both, It (1) can with the mass ratio [(1)/selected from any one of (3) and (4) or both] selected from any one of (3) and (4) or both Think 0.00001~10, or 0.0001~1, it can also be 0.0005~0.1.

(1) with the range of the match ratio selected from any one of (3) and (4) or both for the composition in above range not The cohesion of (1) semiconductive particles easily occurs, photism can also be played well, is preferred in this regard.

In the composition of the present embodiment comprising (1), (2) and (4 '), (1) with (4 ') as long as match ratio can be good The degree for playing the luminous function based on (1) semiconductive particles well, can be fitted according to (1) and the type of (4 ') etc. Work as setting.

In the composition of present embodiment, the mass ratio [(1)/(4 ')] of (1) and (4 ') can be 0.00001~10, It may be 0.0001~1, can also be 0.0005~0.1.

(1) photism can be played well for the composition in above range with the range of the match ratio of (4 '), at this It is preferred on point.

Hereinafter, the manufacturing method about composition of the invention, shows embodiment and is illustrated.According to the present embodiment Composition manufacturing method, the composition of embodiment of the present invention can be manufactured.It is explained, combination of the invention Object is not limited to the composition of the manufacturing method manufacture using the composition of the following embodiments and the accompanying drawings.

(particle of the crystal of II race-VI compound semiconductor, the crystal of II race-V compound semiconductor particle, The particle of the crystal of III group-V compound semiconductor, the particle of the crystal of III group-IV compound semiconductor, III group-VI The particle of the crystal of compound semiconductor, the particle of the crystal of IV race-VI compound semiconductor and the area transition metal-p Close the manufacturing method of the particle of the crystal of object semiconductor)

As the manufacturing method of semiconductive particles, the simple substance or its chemical combination to the element that will constitute semiconductive particles can be enumerated The method that the mixed liquor that object and fat-soluble solvent mix is heated.

As the simple substance for the element for constituting semiconductive particles or the example of its compound, there is no particular restriction, can enumerate gold Category, oxide, acetate, organo-metallic compound, halide, nitrate etc..

As fat-soluble solvent, it can be mentioned, for example the nitrogenous compound of the alkyl with carbon atom number 4~20, have carbon former The oxygenatedchemicals etc. of the alkyl of subnumber 4~20.It as the alkyl of carbon atom number 4~20, can enumerate: normal-butyl, isobutyl group, just The saturated aliphatic hydrocarbons such as amyl, octyl, decyl, dodecyl, cetyl, octadecyl；The unsaturated aliphatics such as oil base Alkyl；The alicyclic type hydrocarbons such as cyclopenta, cyclohexyl；Aromatic hydrocarbyls such as phenyl, benzyl, naphthalene, naphthyl methyl etc., wherein excellent Select saturated aliphatic hydrocarbons or unsaturated fatty hydrocarbons base.As nitrogenous compound, amine, amides can be enumerated, as oxygen-containing Compound can enumerate fatty acid etc..In such fat-soluble solvent, preferably there is containing for the alkyl of carbon atom number 4~20 Nitrogen compound, preferably for example n-butylamine, isobutyl amine, n-amylamine, n-hexylamine, octylame, decyl amine, lauryl amine, hexadecylamine, The alkylamines such as octadecylamine；The alkenyl amines such as oleyl amine.Such fat-soluble solvent can be bonded with particle surface, bonding pattern It can be mentioned, for example the chemical bonds such as covalent bond, ionic bond, coordinate bond, hydrogen bond, Van der Waals key.

As long as the heating temperature of mixed liquor is appropriately configured according to the type of used simple substance or compound, example It is such as preferably set to 130~300 DEG C of range, is more preferably set as 240~300 DEG C of range.Under if heating temperature is above-mentioned It is more than limit value, then the easy unification of crystal structure, therefore it is preferred that.As long as in addition, heating time be also according to used simple substance or Type, the heating temperature of compound are appropriately configured, it is usually preferred to be set as several seconds~a few hours range, more preferably It is set as 1~60 minute range.

In the preparation method of semiconductive particles of the invention, can will the mixed liquor after heating it is cooling after be separated into supernatant and Organic solvent (such as chloroform, toluene, hexane, n-butanol is added in the above-mentioned semiconductive particles (sediment) isolated by precipitating Deng) in, the solution comprising semiconductive particles is made.Alternatively, supernatant can also will be separated into after the cooling of the mixed liquor after heating And precipitating, addition keeps nanoparticle insoluble or the solvent of indissoluble (such as methanol, ethyl alcohol, third in the above-mentioned supernatant isolated Ketone, acetonitrile etc.), so that it is generated sediment, collects above-mentioned sediment, be added in above-mentioned organic solvent, be made comprising semiconductor The solution of particle.

(manufacturing method of the particle of the crystal of perovskite compound)

The semiconductive particles of perovskite compound of the present invention can with reference to known references (Nano Lett.2015, 15,3692-3696, ACSNano, 2015,9,4533-4542), and manufactured using method described below.

For example, the manufacturing method of the semiconductive particles as perovskite compound of the present invention, can enumerate including such as The manufacturing method of lower process: B component, X ingredient and A ingredient is made to be dissolved in solvent, the process for obtaining solution；And it will be resulting molten Liquid and semiconductive particles relative to solvent solubility than obtaining what the low solvent of solvent used in the process of solution mixed Process.

More specifically, the manufacturing method comprised the following steps can be enumerated: make the compound comprising B component and X ingredient with And the compound comprising A ingredient or A ingredient and X ingredient is dissolved in solvent, the process for obtaining solution；And by resulting solution with Semiconductive particles relative to solvent solubility than obtain solvent used in the process of solution it is low solvent mixing process.

In addition, can also enumerate the manufacturing method comprised the following steps: by compound and packet comprising B component and X ingredient The compound of ingredient containing A or A ingredient and X ingredient is added in the solvent of high temperature, makes it dissolve, the process for obtaining solution；And By the cooling process of resulting solution.

Hereinafter, being illustrated to the manufacturing method comprised the following steps, that is, make the compound comprising B component and X ingredient with And the compound comprising A ingredient or A ingredient and X ingredient is dissolved in solvent, the process for obtaining solution；And by resulting solution with Semiconductive particles relative to solvent solubility than obtain solvent used in the process of solution it is low solvent mixing process.

Be explained, solubility refer to carry out mixed processes at a temperature of solubility.

From the viewpoint of can be steadily discrete nucleation particle, above-mentioned manufacturing method preferably includes addition capping ligands The process of body.Capping ligands are preferably added before above-mentioned mixed processes, can dissolved with A ingredient, B component and Capping ligands are added in the solution of X ingredient, solution can also obtained relative to the solubility ratio of solvent in semiconductive particles Process used in be added in the low solvent of solvent, can also dissolved with A ingredient, B component and X ingredient solution, And semiconductive particles relative to solvent solubility than in both solvents that obtain solvent used in the process of solution low In be added.

Above-mentioned manufacturing method is preferably included in after above-mentioned mixed processes and removes coarse grain using the methods of centrifuge separation, filtering The process of son.10 μm or more, more preferably 1 μm or more are preferably dimensioned to be using the oversize grain that above-mentioned removal step removes, Further preferably 500nm or more.

It is above-mentioned by solution and semiconductive particles relative to solvent solubility than obtaining used in the process of solution Solvent it is low solvent mixing process can be (I) by solution be added drop-wise to semiconductive particles relative to solvent solubility ratio Process in the low solvent of solvent used in process to solution is also possible to (II) and semiconductive particles phase is added dropwise into solution For solvent solubility than the process in the solvent that obtain solvent used in the process of solution low, from the sight for improving dispersibility Point sets out, preferably (I).

From the viewpoint of improving dispersibility, preferably it is stirred when being added dropwise.

By solution and semiconductive particles relative to solvent solubility than obtaining solvent used in the process of solution In the process of low solvent mixing, for temperature, there is no particular restriction, from the compound for ensuring to have perovskite type crystal structure Precipitation easiness from the perspective of, preferably -20~40 DEG C of range, more preferably -5~30 DEG C of range.

2 kinds of solvents as the semiconductive particles used in above-mentioned manufacturing method relative to the different solubility of solvent, It is not particularly limited, it can be mentioned, for example 2 kinds of solvents in following solvent: methanol, ethyl alcohol, 1- propyl alcohol, 2- propyl alcohol, 1- fourth Alcohol, 2- butanol, the tert-butyl alcohol, 1- amylalcohol, 2- methyl -2- butanol, methoxypropanol, diacetone alcohol, cyclohexanol, 2- fluoroethanol, 2, 2,2- trifluoroethanols, 2, the alcohols such as 2,3,3- tetra- fluoro- 1- propyl alcohol；Ethylene glycol single methyl ether, ethylene glycol monomethyl ether, ethylene glycol list The glycol ethers such as butyl ether, ethylene glycol monomethyl ether acetate, triethylene glycol dimethyl ether；N,N-Dimethylformamide, acetamide, N, N- dimethyl acetamide etc. has the organic solvent of amide groups；Dimethyl sulfoxide, methyl formate, Ethyl formate, propyl formate, first The esters such as sour pentyl ester, methyl acetate, ethyl acetate, pentyl acetate；Gamma-butyrolacton, n-methyl-2-pyrrolidone, acetone, dimethyl The ketone such as ketone, diisobutyl ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone；Anaesthetie Ether, methyl tertiary butyl ether(MTBE), Di Iso Propyl Ether, Dimethoxymethane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1,3-dioxolane, 4- methyl dioxolane, tetrahydrofuran, first The ethers such as base tetrahydrofuran, methyl phenyl ethers anisole, phenetole；Acetonitrile, isobutyronitrile, propionitrile, methoxyacetonitrile etc. have the organic solvent of itrile group； Ethylene carbonate, propylene carbonate etc. have the organic solvent of carbonate group；Methylene chloride, chloroform etc. have having for halohydrocarbyl Solvent；Pentane, hexamethylene, n-hexane, benzene,toluene,xylene etc. have the organic solvent of alkyl.

As contained in above-mentioned manufacturing method, obtaining solvent used in the process of solution, preferred semiconductor particle The high solvent of solubility relative to solvent, for example, in the case where carrying out above-mentioned operation under room temperature (10 DEG C~30 DEG C), it can It enumerates: methanol, ethyl alcohol, 1- propyl alcohol, 2- propyl alcohol, n-butyl alcohol, 2- butanol, the tert-butyl alcohol, 1- amylalcohol, 2- methyl -2- butanol, methoxyl group Propyl alcohol, diacetone alcohol, cyclohexanol, 2- fluoroethanol, 2,2,2- trifluoroethanols, 2, the alcohols such as 2,3,3- tetra- fluoro- 1- propyl alcohol；Ethylene glycol Monomethyl ether, ethylene glycol monomethyl ether, ethylene glycol monobutyl ether, ethylene glycol monomethyl ether acetate, triethylene glycol dimethyl ether etc. Glycol ethers；N,N-Dimethylformamide, acetamide, n,N-dimethylacetamide etc. have the organic solvent of amide groups；Dimethyl Sulfoxide.

As contained in above-mentioned manufacturing method, the solvent used in mixed processes, preferred semiconductor particle phase for The low solvent of the solubility of solvent, for example, can be enumerated in the case where carrying out above-mentioned operation under room temperature (10 DEG C~30 DEG C): The esters such as methyl formate, Ethyl formate, propyl formate, amyl formate, methyl acetate, ethyl acetate, pentyl acetate；Gamma-butyrolacton, The ketone such as n-methyl-2-pyrrolidone, acetone, dimethyl ketone, diisobutyl ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone；Diethyl Base ether, methyl tertiary butyl ether(MTBE), Di Iso Propyl Ether, dimethoxymethane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1,3- dioxy penta The ethers such as ring, 4- methyl dioxolane, tetrahydrofuran, methyltetrahydrofuran, methyl phenyl ethers anisole, phenetole；Acetonitrile, isobutyronitrile, propionitrile, first Oxygroup acetonitrile etc. has the organic solvent of itrile group；Ethylene carbonate, propylene carbonate etc. have the organic solvent of carbonate group；Two Chloromethanes, chloroform etc. have the organic solvent of halohydrocarbyl；Pentane, hexamethylene, n-hexane, benzene,toluene,xylene etc. have The organic solvent of alkyl.

In 2 kinds of solvents of different solubility, the difference of solubility is preferably 100 μ g/ solvent 100g~90g/ solvent 100g, More preferably 1mg/ solvent 100g~90g/ solvent 100g.From the 100 μ g/ solvent 100g~90g/ solvent of difference for making solubility From the perspective of 100g, for example, in the case where carrying out mixed processes under room temperature (10 DEG C~30 DEG C), it is preferred that Solvent used in process to solution is organic solvent, the dimethyl sulfoxide with amide groups such as n,N-dimethylacetamide, The solvent used in mixed processes is the organic solvent with halohydrocarbyl such as methylene chloride, chloroform；Pentane, hexamethylene, N-hexane, benzene,toluene,xylene etc. have the organic solvent of alkyl.

In the case where taking out semiconductive particles from the dispersion liquid comprising semiconductive particles, by being separated by solid-liquid separation, So as to only recycle semiconductive particles.

Above-mentioned solid-liquid separating method can enumerate the methods of filtering, method that solvent evaporation is utilized etc..

Hereinafter, being illustrated to the manufacturing method comprised the following steps, that is, B component, X ingredient and A ingredient are added to height In the solvent of temperature, make it dissolve, the process for obtaining solution；And the process that resulting solution is cooling.

More specifically, the manufacturing method comprised the following steps can be enumerated: by the compound comprising B component and X ingredient with And the compound comprising A ingredient or A ingredient and X ingredient is added in the solvent of high temperature, makes it dissolve, the process for obtaining solution； And the process that resulting solution is cooling.

In above-mentioned manufacturing method, semiconductor microactuator of the present invention is made using the difference based on the solubility of temperature difference Size separation goes out, and can manufacture semiconductive particles of the present invention.

From the viewpoint of can be steadily discrete nucleation particle, above-mentioned manufacturing method preferably includes addition capping ligands The process of body.

Above-mentioned manufacturing method is preferably included in after cooling process and removes oversize grain using the methods of centrifuge separation, filtering Process.10 μm or more, more preferably 1 μm or more are preferably dimensioned to be using the oversize grain that above-mentioned removal step removes, into one Step is preferably 500nm or more.

As long as here, compound of the solvent of high temperature comprising B component and X ingredient and including A ingredient or A ingredient and X The solvent for the temperature that the compound of ingredient dissolves, for example, it is preferable to for 60~600 DEG C of solvent, more preferably 80~ 400 DEG C of solvent.

As cooling temperature, preferably -20~50 DEG C, more preferably -10~30 DEG C.

As cooling velocity, preferably 0.1~1500 DEG C/min, more preferably 10 DEG C/min~150 DEG C/min.

As solvent used in above-mentioned manufacturing method, as long as can dissolve the compound comprising B component and X ingredient with And the solvent of the compound comprising A ingredient or A ingredient and X ingredient, then it is not particularly limited, it can be mentioned, for example: methyl formate, first The esters such as acetoacetic ester, propyl formate, amyl formate, methyl acetate, ethyl acetate, pentyl acetate；Gamma-butyrolacton, N- methyl -2- pyrrole The ketone such as pyrrolidone, acetone, dimethyl ketone, diisobutyl ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone；Anaesthetie Ether, methyl- tert Butyl ether, Di Iso Propyl Ether, dimethoxymethane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1,3-dioxolane, 4- methyl two The ethers such as butyl oxide link, tetrahydrofuran, methyltetrahydrofuran, methyl phenyl ethers anisole, phenetole；Methanol, ethyl alcohol, 1- propyl alcohol, 2- propyl alcohol, 1- fourth Alcohol, 2- butanol, the tert-butyl alcohol, 1- amylalcohol, 2- methyl -2- butanol, methoxypropanol, diacetone alcohol, cyclohexanol, 2- fluoroethanol, 2, 2,2- trifluoroethanols, 2, the alcohol such as 2,3,3- tetra- fluoro- 1- propyl alcohol；Ethylene glycol single methyl ether, ethylene glycol monomethyl ether, ethylene glycol only son The glycol ethers such as base ether, ethylene glycol monomethyl ether acetate, triethylene glycol dimethyl ether；N,N-Dimethylformamide, acetamide, N, N- Dimethyl acetamide etc. has the organic solvent of amide groups；Acetonitrile, isobutyronitrile, propionitrile, methoxyacetonitrile etc. have having for itrile group Solvent；Ethylene carbonate, propylene carbonate etc. have the organic solvent of carbonate group；Methylene chloride, chloroform etc. have halogenated The organic solvent of alkyl；Pentane, hexamethylene, n-hexane, benzene,toluene,xylene etc. have the organic solvent of alkyl；Dimethyl Sulfoxide, 1- octadecene.

As the method for taking out semiconductive particles from the dispersion liquid comprising semiconductive particles, can enumerate by carrying out solid-liquid The method for separating and only recycling semiconductive particles.

For example, the manufacturer as the composition comprising (1) semiconductive particles, (2) halogenated hydrocarbon compound and (3) solvent Method can enumerate the manufacturing method comprised the following steps:

(a) process for mixing (1) semiconductive particles, (2) halogenated hydrocarbon compound and (3) solvent.

Above-mentioned operation (a) can be such as following process:

(a1) after mixing (1) semiconductive particles with (3) solvent, the process that remixes (2) halogenated hydrocarbon compound；

(a2) after mixing (1) semiconductive particles with (2) halogenated hydrocarbon compound, the process that remixes (3) solvent.

From the viewpoint of the dispersibility for improving semiconductive particles, process (a) is preferably process (a1).

From the viewpoint of improving dispersibility, preferably it is stirred in mixing.

In the process for mixing (1) semiconductive particles, (2) halogenated hydrocarbon compound, (3) solvent, spy is had no for temperature It does not limit, from the point of view of even mixing, preferably 0~100 DEG C of range, more preferably 10~80 DEG C of range.

The manufacturing method of composition of the < comprising (1), (2), (3) and (5) >

For example, being selected from ammonia, amine, carboxylic acid as comprising (1) semiconductive particles, (2) halogenated hydrocarbon compound, (3) solvent and (5) And the manufacturing method of at least one kind of composition in their salt or ion, the manufacturing method comprised the following steps can be enumerated:

(a ') by (1) semiconductive particles, (2) halogenated hydrocarbon compound, (3) solvent and (5) be selected from ammonia, amine, carboxylic acid and At least one kind of mixed process in their salt or ion.

Above-mentioned operation (a ') can be such as following process:

(a ' 1) remixes (2) halogenated hydrocarbon compound and (5) is selected from after mixing (1) semiconductive particles with (3) solvent It is at least one kind of in ammonia, amine, carboxylic acid and their salt or ion；

(a ' 2) will include that at least one kind of (1) of (5) in ammonia, amine, carboxylic acid and their salt or ion is partly led After body particle is mixed with (3) solvent, then mix with (2) halogenated hydrocarbon compound.

From the viewpoint of the dispersibility for improving semiconductive particles, process (a ') is preferably (a ' 2).

In (a ' 2), partly led comprising at least one kind of (1) of (5) in ammonia, amine, carboxylic acid and their salt or ion Body particle above-mentioned can partly be led by the way that (5) at least one kind of in ammonia, amine, carboxylic acid and their salt or ion to be added to Manufactured in included any process in the manufacturing method of body particle, can also by by resulting (1) semiconductive particles and (5) at least one kind of mixing in ammonia, amine, carboxylic acid and their salt or ion manufactures.From point for improving semiconductive particles From the perspective of dissipating property, preferably manufactured by being added in any process included in the manufacturing method of semiconductive particles. Thus, it is possible to at least one kind of (1) semiconductor for example comprising (5) in ammonia, amine, carboxylic acid and their salt or ion Particle is scattered in the dispersion of (3) solvent and the form of the mixture of (2) halogenated hydrocarbon compound obtains combination of the present invention Object.

By (1) semiconductive particles, (2) halogenated hydrocarbon compound, (3) solvent and (5) be selected from ammonia, amine, carboxylic acid and they Salt or ion at least one kind of mixed process in, for temperature, there is no particular restriction, from the point of view of even mixing, Preferably 0~100 DEG C of range, more preferably 10~80 DEG C of range.

As the manufacturing method of the composition comprising (1), (2) and (4), can enumerate (1) semiconductive particles, (2) are halogenated At least one kind of mixed method of hydrocarbon compound and (4) in polymerizable compound and polymer.

From the viewpoint of the dispersibility of raising (1) semiconductive particles, by (1) semiconductive particles, (2) halogenated hydrocarbon compound And at least one kind of mixed process of (4) in polymerizable compound and polymer preferably carries out while stirring.

By (1) semiconductive particles, (2) halogenated hydrocarbon compound and (4) in polymerizable compound and polymer In at least one kind of mixed process, for temperature, there is no particular restriction, from the point of view of even mixing, preferably 0~100 DEG C Range, more preferably 10~80 DEG C of range.

Comprising (1) semiconductive particles, (2) halogenated hydrocarbon compound and (4) in polymerizable compound and polymer The manufacturing method of at least one kind of composition can be for for example:

(b) manufacturing method comprised the following steps, that is, make (1) semiconductive particles be distributed to (4) and be selected from polymerizable compound And at least one kind of in polymer and the process that obtains dispersion；And resulting dispersion is mixed with (2) halogenated hydrocarbon compound Process；

(c) manufacturing method comprised the following steps, that is, make (2) halogenated hydrocarbon compound be distributed to (4) and be selected from polymerism chemical combination At least one kind of in object and polymer and the process for obtaining dispersion；And resulting dispersion is mixed with (1) semiconductive particles Process,

(d) manufacturing method comprised the following steps, that is, make the mixture of (1) semiconductive particles and (2) halogenated hydrocarbon compound It is distributed at least one kind of process of (4) in polymerizable compound and polymer.

In the manufacturing method of (b)~(d), from the viewpoint of the dispersibility for improving semiconductive particles, preferably (b) Manufacturing method.Using the above method, (4) can be distributed in polymerizable compound and polymer with (1) semiconductive particles It is at least one kind of in dispersion and the form of mixture of (2) halogenated hydrocarbon compound obtain composition of the present invention.

It is included in the manufacturing method of (b)~(d) to obtain in the process of each dispersion, (4) can be added drop-wise to (1) And/or in (2), (1) and/or (2) can also be added drop-wise in (4).

From the viewpoint of improving dispersibility, preferably (1) and/or (2) is added drop-wise in (4).

In the manufacturing method of (b)~(d) in included each mixed processes, (1) or (2) can be added drop-wise to dispersion In, dispersion can also be added drop-wise in (1) or (2).

From the viewpoint of improving dispersibility, preferably (1) or (2) is added drop-wise in dispersion.

In the case where the organic compound using polymer as (4), polymer can be the polymerization for being dissolved in solvent Object.

As long as the solvent dissolved with above-mentioned polymer can then have no special limit with the solvent of dissolving resin (polymer) It is fixed, the preferred solvent of semiconductive particles that is related to of indissoluble solution aforementioned present invention.

As the solvent for being dissolved with above-mentioned resin, it can be mentioned, for example methyl formate, Ethyl formate, propyl formate, formic acid penta The esters such as ester, methyl acetate, ethyl acetate, pentyl acetate；Gamma-butyrolacton, n-methyl-2-pyrrolidone, acetone, dimethyl ketone, The ketone such as diisobutyl ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone；Anaesthetie Ether, methyl tertiary butyl ether(MTBE), Di Iso Propyl Ether, diformazan Oxygroup methane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1,3-dioxolane, 4- methyl dioxolane, tetrahydrofuran, methyl four The ethers such as hydrogen furans, methyl phenyl ethers anisole, phenetole；Methanol, ethyl alcohol, 1- propyl alcohol, 2- propyl alcohol, n-butyl alcohol, 2- butanol, the tert-butyl alcohol, 1- amylalcohol, 2- methyl -2- butanol, methoxypropanol, diacetone alcohol, cyclohexanol, 2- fluoroethanol, 2,2,2- trifluoroethanols, 2,2,3,3- tetra- The alcohol such as fluoro- 1- propyl alcohol；Ethylene glycol single methyl ether, ethylene glycol monomethyl ether, ethylene glycol monobutyl ether, ethylene glycol monomethyl ether acetic acid The glycol ethers such as ester, triethylene glycol dimethyl ether；N,N-Dimethylformamide, acetamide, n,N-dimethylacetamide etc. have amide The organic solvent of base；Acetonitrile, isobutyronitrile, propionitrile, methoxyacetonitrile etc. have the organic solvent of itrile group；Ethylene carbonate, carbonic acid Sub- propyl ester etc. has the organic solvent of carbonate group；Methylene chloride, chloroform etc. have the organic solvent of halohydrocarbyl；Pentane, Hexamethylene, n-hexane, benzene,toluene,xylene etc. have the organic solvent of alkyl；Dimethyl sulfoxide.

Wherein, it is contemplated that polarity is low, not readily dissolve perovskite compound of the present invention and it is preferred that: methyl formate, first The esters such as acetoacetic ester, propyl formate, amyl formate, methyl acetate, ethyl acetate, pentyl acetate；Gamma-butyrolacton, acetone, diformazan The ketone such as base ketone, diisobutyl ketone, cyclopentanone, cyclohexanone, methyl cyclohexanone；Anaesthetie Ether, methyl tertiary butyl ether(MTBE), diisopropyl Ether, dimethoxymethane, dimethoxy-ethane, Isosorbide-5-Nitrae-dioxanes, 1,3-dioxolane, 4- methyl dioxolane, tetrahydrofuran, The ethers such as methyltetrahydrofuran, methyl phenyl ethers anisole, phenetole；Acetonitrile, isobutyronitrile, propionitrile, methoxyacetonitrile etc. have the organic molten of itrile group Agent；The carbonic esters such as ethylene carbonate, propylene carbonate system organic solvent；Methylene chloride, chloroform etc. have the organic of halohydrocarbyl Solvent；Pentane, hexamethylene, n-hexane, benzene,toluene,xylene etc. have the organic solvent of alkyl, more preferably: methylene chloride, Chloroform etc. has the organic solvent of halohydrocarbyl；Pentane, hexamethylene, n-hexane, benzene,toluene,xylene etc. have alkyl Organic solvent.

The manufacturing method of composition of the < comprising (1), (2), (4) and (5) >

Comprising (1) semiconductive particles, (2) halogenated hydrocarbon compound, (4) in polymerizable compound and polymer at least In the manufacturing method of at least one kind of composition of a kind and (5) in ammonia, amine, carboxylic acid and their salt or ion, remove Other than at least one kind of in ammonia, amine, carboxylic acid and their salt or ion of addition (5), can for it is above-mentioned include (1) And (2) and also comprising (4) composition the same method of manufacturing method.

(5) at least one kind of in ammonia, amine, carboxylic acid and their salt or ion can be in above-mentioned (1) semiconductive particles Manufacturing method in include any process in be added, can also be above-mentioned comprising (1) and (2) and also comprising (4) It is added in included any process in the manufacturing method of composition.

From the viewpoint of improve semiconductive particles dispersibility, (5) be selected from ammonia, amine, carboxylic acid and their salt or from It is added at least one kind of included any process preferably in the manufacturing method of (1) semiconductive particles in son.As a result, It can be at least one kind of (1) semiconductive particles for example comprising (5) in ammonia, amine, carboxylic acid and their salt or ion point The mixture of the dispersion and (2) halogenated hydrocarbon compound that are scattered in (4) at least one kind of in polymerizable compound and polymer Form obtain composition of the present invention.

The manufacture of < the composition for adding up to 90 mass % or more comprising (1), (2) and (4 ') and (1), (2) and (4 ') Method >

As the composition for adding up to 90 mass % or more comprising (1), (2) and (4 ') and (1), (2) and (4 ') Manufacturing method, it can be mentioned, for example:

The manufacturing method comprised the following steps, that is, by (1) semiconductive particles, (2) halogenated hydrocarbon compound and polymerism chemical combination The process of object mixing；With the process for polymerizeing polymerizable compound；And

The manufacturing method comprised the following steps, that is, by (1) semiconductive particles, (2) halogenated hydrocarbon compound and be dissolved in solvent Mixed with polymers process；With the process for removing solvent.

In above-mentioned manufacturing method in included mixed processes can using with it is already explained, include (1), (2) And the same mixed method of manufacturing method of the composition of (4).

Above-mentioned manufacturing method can be for for example:

(b1) manufacturing method comprised the following steps, that is, (1) semiconductive particles is made to be distributed in polymerizable compound and obtain To the process of dispersion；The process that resulting dispersion is mixed with (2) halogenated hydrocarbon compound；And keep polymerizable compound poly- The process of conjunction；

(b2) manufacturing method comprised the following steps, that is, (1) semiconductive particles is made to be distributed to the polymer for being dissolved in solvent In and the process that obtains dispersion；The process that resulting dispersion is mixed with (2) halogenated hydrocarbon compound；And remove solvent Process；

(c1) manufacturing method comprised the following steps, that is, make (2) halogenated hydrocarbon compound be distributed in polymerizable compound and The process for obtaining dispersion；The process that resulting dispersion is mixed with (1) semiconductive particles；And keep polymerizable compound poly- The process of conjunction；

(c2) manufacturing method comprised the following steps, that is, (2) halogenated hydrocarbon compound is made to be distributed to the polymerization for being dissolved in solvent The process of dispersion is obtained in object；The process that resulting dispersion is mixed with (1) semiconductive particles；And remove solvent Process；

(d1) manufacturing method comprised the following steps, that is, make the mixing of (1) semiconductive particles and (2) halogenated hydrocarbon compound Object is distributed to the process in polymerizable compound；And the process for polymerizeing polymerizable compound,

(d2) manufacturing method comprised the following steps, that is, make the mixing of (1) semiconductive particles and (2) halogenated hydrocarbon compound Object is distributed to the process in the polymer for being dissolved in solvent；And the process for removing solvent.

The process of included removing solvent can be to stand at room temperature, make its natural drying again in above-mentioned manufacturing method Process, be also possible to by using being dried under reduced pressure or heating for vacuum drier and the process that evaporates solvent.

For example, by making its drying 1 minute~7 day at 0~300 DEG C, so as to remove solvent.

The included process for polymerizeing polymerizable compound can be properly used free radical polymerization in above-mentioned manufacturing method It is carried out Deng well known polymerization reaction.

It, can be by (1) semiconductive particles, (2) halogenated hydrocarbon compound and poly- for example, in the case where free radical polymerization Radical polymerization initiator is added in the mixture of conjunction property compound and generates free radicals it to carry out polymerization reaction.

Radical polymerization initiator is not particularly limited, and can enumerate optical free radical polymerization initiator.

As above-mentioned optical free radical polymerization initiator, it can be mentioned, for example the oxidations of bis- (2,4,6- trimethylbenzoyl) phenyl Phosphine etc..

< the combination for adding up to 90 mass % or more comprising (1), (2), (5) and (4 ') and (1), (2), (4 ') and (5) The manufacturing method of object >

The combination for adding up to 90 mass % or more comprising (1), (2), (5) and (4 ') and (1), (2), (4 ') and (5) In the manufacturing method of object, in addition to addition such as (5) in ammonia, amine, carboxylic acid and their salt or ion it is at least one kind of with It outside, can be to add up to 90 mass % or more comprising (1), (2) and (4 ') and (1), (2) and (4 ') with already explained Composition the same method of manufacturing method.

(5) at least one kind of in ammonia, amine, carboxylic acid and their salt or ion can be in above-mentioned (1) semiconductive particles Manufacturing method in be added in included any process, can also be by above-mentioned (1) semiconductive particles, (2) halogenated hydrocarbons It is added in compound and the process of polymerizable compound mixing, it can also be halogenated by above-mentioned (1) semiconductive particles, (2) It is added in the process of hydrocarbon compound and the mixed with polymers for being dissolved in solvent.

From the viewpoint of improve semiconductive particles dispersibility, (5) be selected from ammonia, amine, carboxylic acid and their salt or from It is added at least one kind of included any process preferably in the manufacturing method of (1) semiconductive particles in son.

" measurements of semiconductive particles "

The amount of semiconductive particles contained in composition of the present invention using ICP-MS (such as ELAN DRCII, Perkin Elmer corporation) and ion chromatograph measure.

It is measured after being dissolved semiconductive particles using good solvents such as n,N-Dimethylformamide.

" measurement of quantum yield "

The quantum yield of composition of the present invention comprising semiconductive particles uses absolute PL quantum yield measurement dress (such as creek pine photoelectricity corporation, trade name C9920-02) is set, is measured under exciting light 450nm, room temperature, atmosphere.

In the composition comprising (1) semiconductive particles and (2) halogenated hydrocarbon compound and also comprising (3) solvent, according to So that the mode of the concentration 200ppm (μ g/g) of semiconductive particles contained in composition is adjusted mixing ratio, is measured.

Comprising (1) semiconductive particles and (2) halogenated hydrocarbon compound and also comprising (4) be selected from polymerizable compound and In at least one kind of composition in polymer, according to the 1000 μ g/mL's of concentration for making semiconductive particles contained in composition Mode adjusts mixing ratio, is measured.The case where (4) are replaced with (4 ') is also the same.

The composition of present embodiment can be 32% or more using the quantum yield of said determination method measurement, can also be with It is 40% or more, can also is 50% or more.

The composition of present embodiment can be for 100% hereinafter, can also using the quantum yield of said determination method measurement Think 95% or less, or 90% or less, or 80% or less, or 70% hereinafter, can also be 65% Below.

As a side of the invention, the composition of present embodiment utilizes the quantum yield of said determination method measurement Preferably 32% or more and 100% hereinafter, more preferably 40% or more and 100% hereinafter, further preferably 50% or more and 100% or less.

As another side of the invention, the composition of present embodiment is received using the quantum of said determination method measurement Rate be preferably 32% or more and 95% hereinafter, more preferably 40% or more and 90% hereinafter, further preferably 40% or more and 80% or less.In addition, above-mentioned quantum yield can be 50% or more and 70% or less, or 50% or more and 65% with Under.

<film>

Film of the present invention is opposite comprising total content containing (1), (2) and (4 ') and (1), (2) and (4 ') In the film for the composition that the gross mass of composition is 90 mass % or more.

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(4 ') polymer

Film shape is not particularly limited, and can be the shapes such as sheet, rodlike.In the present specification, " rodlike shape " is Refer to for example with anisotropic shape.The plate different as the length that each side with anisotropic shape, can be illustrated Shape.

The thickness of film can be 0.01 μm~1000mm, or 0.1 μm~10mm, can also be 1 μm~1mm.

In the present specification, the thickness of above-mentioned film can be by being measured and calculating at arbitrary 3 points using micrometer Its average value obtains.

Film can be single layer, or multilayer.In the case of multiple layers, the embodiment party of identical type can be used in each layer The composition of the embodiment of type different from each other also can be used in the composition of formula.

As the manufacturing method of film, such as can use (i)~(iV) of the manufacturing method of aftermentioned laminate structure Manufacturing method and obtain being formed in the film on substrate.

Laminate structure of the present invention be there are multiple layers and at least one layer be comprising containing (1), (2) and The layer for the composition that total content of (4 ') and (1), (2) and (4 ') is 90 mass % or more relative to the gross mass of composition Laminate structure.

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(4 ') polymer

Composition comprising (1), (2) and (4 ') can also include (5) be selected from ammonia, amine, carboxylic acid and their salt or from It is at least one kind of in son.

In multiple layers possessed by laminate structure, as in addition to comprising containing (1), (2) and (4 ') and (1), (2) And total content of (4 ') is the layer other than the layer of the composition of 90 mass % or more relative to the gross mass of composition, can be enumerated The arbitrary layer such as substrate, barrier layer, light scattering layer.

The shape for the composition being laminated is not particularly limited, and can be the arbitrary shape such as sheet, rodlike.It is laminated Composition can be the film of present embodiment.

(substrate)

As the layer that laminate structure of the present invention can have, there is no particular restriction, can enumerate substrate.

Substrate is not particularly limited, and can be film, taking out light when luminous, the substrate of preferably clear. As substrate, material well known to the plastics such as polyethylene terephthalate, glass etc. can be used.

For example, including total content containing (1), (2) and (4 ') and (1), (2) and (4 ') in laminate structure The layer for the composition that gross mass relative to composition is 90 mass % or more can be set on substrate.Above-mentioned layer can be this The film of embodiment.

Fig. 1 is the cross-sectional view for schematically showing the composition of laminate structure of present embodiment.First cascade structural body 1a The film 10 of present embodiment is equipped between first substrate 20 and the second substrate 21.Film 10 is sealed by sealant 22.

A side of the invention is a kind of laminate structure 1a, which is characterized in that it is with first substrate 20, second The stacking knot of substrate 21, film of the present embodiment 10 and sealant 22 between first substrate 20 and the second substrate 21 Structure body, above-mentioned sealant configuration is on the face of above-mentioned film 10 not contacted with above-mentioned first substrate 20 and the second substrate 21.

(barrier layer)

As the layer that laminate structure of the present invention can have, there is no particular restriction, can enumerate barrier layer.In order to It protects above-mentioned composition from the influence of the air in the vapor and atmosphere of ambient atmos, may include barrier layer.

There is no particular restriction on barrier layer, and from taking out issued this viewpoint of light, the barrier layer of preferably clear can be with Using barrier layer well known to the polymer such as such as polyethylene terephthalate, glass-film etc..

(light scattering layer)

As the layer that laminate structure of the present invention can have, there is no particular restriction, can enumerate light scattering layer.From From the perspective of effectively absorbing incident light, light scattering layer may include.

There is no particular restriction for light scattering layer, from taking out issued this viewpoint of light, the light scattering layer of preferably clear, It can be using light scattering layer well known to the light diffusing particles such as silicon dioxide granule, enhanced diffustion film etc..

As the manufacturing method of laminate structure, it can be mentioned, for example:

(i) manufacturing method of the laminate structure comprised the following steps, that is, by (1) semiconductive particles, (2) halogenated hydrocarbonylation The process for closing object and the mixing of (3) solvent；The process that resulting composition is coated on substrate；And the process for removing solvent,

(ii) manufacturing method of the laminate structure comprised the following steps, that is, by (1) semiconductive particles, (2) halogenated hydrocarbonylation The process closed object and be dissolved in the mixed with polymers of solvent；By resulting composition coated on the process on substrate；And it removes The process of solvent,

(iii) manufacturing method of the laminate structure comprised the following steps, that is, will comprising (1), (2) and (4 ') and (1), the process that the composition for adding up to 90 mass % or more of (2) and (4 ') is pasted on substrate,

(1) semiconductive particles

(2) halogenated hydrocarbon compound

(4 ') polymer

(iv) manufacturing method comprised the following steps, that is, by (1) semiconductive particles, (2) halogenated hydrocarbon compound and polymerism The process that compound and (4 ') polymer are mixed；By resulting composition coated on the process on substrate；And make to polymerize Property compound polymerization process.

(i) it included mixed processes and removes the process of solvent in manufacturing method, wrapped in the manufacturing method of (ii) It the mixed processes that include and removes the process of solvent, included mixed processes and make polymerizable compound in the manufacturing method of (iv) The process of polymerization can be respectively and already explained add up to comprising (1), (2) and (4 ') and (1), (2) and (4 ') The included same process of process in the manufacturing method of the composition of 90 mass % or more.

(i), included in the manufacturing method of (ii) and (iv) coated on the process on substrate, there is no particular restriction, can be with Use coating method well known to gravure coating process, stick rubbing method, print process, spray coating method, spin-coating method, infusion process, die coating method etc..

In the manufacturing method of (iii) in the included process for being pasted on substrate, arbitrary bonding agent can be used.

As long as bonding agent does not dissolve the substance of (1) semiconductive particles, then there is no particular restriction, can be used well known viscous Connect agent.

The manufacturing method of laminate structure can be include to utilize on the obtained laminate structure of (i)~(iv) further Paste the manufacturing method of the process of any film.

As the film pasted, it can be mentioned, for example reflectance coatings, diffusion barrier.

In the process of adhesive film, arbitrary bonding agent can be used.

As long as above-mentioned bonding agent does not dissolve the substance of (1) semiconductive particles, then there is no particular restriction, can be used known Bonding agent.

Light emitting device of the present invention can by by above-mentioned composition or above-mentioned laminate structure and light source cooperate come It obtains.Light emitting device of the present invention is made by irradiating the above-mentioned composition for being set to back segment from the light that light source issues Above-mentioned composition shines and takes out the device of light.Laminate structure in above-mentioned light emitting device may include reflectance coating, diffusion The layers such as the layer of dielectric material between film, brightness strengthening section, prismatic lens, light guide plate, component.

A side of the invention be sequentially laminated with prismatic lens 50, light guide plate 60, above-mentioned first cascade structural body 1a and The light emitting device 2 of light source 30.

(light source)

Constituting the light source of light emitting device of the present invention, there is no particular restriction, from making above-mentioned composition or laminate structure In semiconductive particles shine from the perspective of, preferably with the light source of 600nm emission wavelength below, can be used for example blue Light source well known to the light emitting diodes such as color light emitting diode (LED), laser, EL etc..

(reflectance coating)

There is no particular restriction for light emitting device of the present invention, may include for above-mentioned composition or above-mentioned stacking knot The light reflecting member of the light of structure body radiation source.

There is no particular restriction for reflectance coating, may include reflecting mirror, the film of reflective particle, reflecting metallic film or reflector etc. and appoints The suitable well known materials of meaning.

(diffusion barrier)

There is no particular restriction for light emitting device of the present invention, may include light for making light source or from above-mentioned composition The light of the light diffusion of sending scatters component.Diffusion barrier may include known any expansion in the above-mentioned technical field such as enhanced diffustion film Dissipate film.

(brightness strengthening section)

There is no particular restriction for light emitting device of the present invention, may include the direction of a part direction transmission light of light The brightness strengthening section of reflection and return.

(prismatic lens)

Representative prismatic lens have base part and prism portion.Be explained, base part can according to adjacent component come It omits.Prismatic lens can be bonded by any suitable adhesive layer (such as adhesive layer, adhesive phase) with adjacent component.Rib Eyeglass is made up of multiple unit prisms of oriented side (back side) protrusion opposite with observation side arranged side by side.By by prism The protrusion of piece is configured towards back side, to be easy to will transmit through the light optically focused of prismatic lens.In addition, if by the protrusion court of prismatic lens Surface side configuration of supporting or opposing is not incident to prismatic lens and the light that reflects then compared with the case where configuring protrusion towards observation side It is less, display of high brightness can be obtained.

(light guide plate)

As light guide plate, any suitable light guide plate can be used.It can be used for example according to can make from lateral Mode light guide plate, overleaf side and/or the observation side that overleaf side is formed with lens pattern that light deflects to thickness direction are formed There is the light guide plate of prism shape etc..

(layer of dielectric material between component)

There is no particular restriction for light emitting device of the present invention, can include in the optical path between adjacent component (layer) Layer containing a kind or more dielectric material.1 kind or more of medium includes vacuum, air, gas, optical material, bonding agent, optics Bonding agent, glass, polymer, solid, liquid, gel, curing materials, optical bond material, index matching or refractive index are lost With material, index gradient materials, cladding (cladding) or anti-covering material, spacer, silica gel, brightness strengthening material, dissipate Penetrate or diffusion material, reflection or antireflection material, wavelength selectivity material, wavelength selectivity antireflection material, colour filter or on Known other suitable medium in technical field is stated, but it's not limited to that, can also include any suitable material.

As the concrete example of light emitting device of the present invention, it can be mentioned, for example with EL display or liquid crystal display use Wavelength conversion material light emitting device.

Specifically, can enumerate:

(1) composition of the invention is added in glass tube etc. and is sealed, by it according to the end face (side along light guide plate Face) mode configure between the blue LED and light guide plate as light source, blue light is converted into green light or red The backlight (backlight for opening edge (on edge) mode) of coloured light；

(2) sheet material is made in composition of the present invention, it is clamped with 2 barrier films and seals and forms film, it will Resulting film is set on light guide plate, will pass through light guide plate from the blue LED for the end face (side) for being placed in light guide plate The backlight (backlight of surface mount manner) of green light or red light is converted to the blue light of above sheet irradiation；

(3) semiconductive particles are distributed in resin etc., and are arranged near the illumination region of blue LED, by institute The blue light of irradiation is converted to the backlight (backlight of chip package (on-chip) mode) of green light or red light；And

(4) semiconductive particles are distributed in resist, and be arranged in colorized optical filtering on piece, the blue that will be irradiated from light source Light is converted to the backlight of green light or red light.

In addition, the concrete example as light emitting device of the present invention, can enumerate: by composition molding of the invention, and The back segment in the blue LED as light source is configured, blue light is converted into green light or red light and issues white light Illumination.

It can be mentioned, for example include that above-mentioned light source is arranged and above-mentioned composition or stacking are arranged in the optical path of the back segment of light source The manufacturing method of the process of structural body.

As shown in Fig. 2, the display 3 of present embodiment successively has liquid crystal display panel 40 and above-mentioned luminous dress from observation side Set 2.Light emitting device 2 has the second laminate structure 1b and light source 30.Second laminate structure 1b is above-mentioned first cascade structure Body 1a is also equipped with the laminate structure of prismatic lens 50 and light guide plate 60.Representative liquid crystal display panel has liquid crystal cells, is configured at The back side polarization plates of the observation side polarization plates of the observation side of above-mentioned liquid crystal cells and the back side for being configured at above-mentioned liquid crystal cells. Display can be also equipped with any suitable other components.

A side of the invention is to be sequentially laminated with liquid crystal display panel 40, prismatic lens 50, light guide plate 60, above-mentioned first cascade The liquid crystal display 3 of structural body 1a and light source 30.

Representative above-mentioned liquid crystal display panel has the observation lateral deviation of liquid crystal cells, the observation side for being configured at above-mentioned liquid crystal cells The back side polarization plates of vibration plate and the back side for being configured at above-mentioned liquid crystal cells.Observation side polarization plates and back side polarization plates can be with It is configured according to the mode for keeping respective absorption axiss substantially orthogonal or parallel.

(liquid crystal cells)

The liquid crystal layer as display medium that liquid crystal cells have a pair of of substrate and are held between aforesaid substrate.General In composition, it is provided with colored filter and black matrix" on one substrate, control liquid crystal is provided on another substrate The switch element of electrical optical characteristics, the scan line that grid signal is assigned to the switch element and the signal for assigning source signal Line and pixel electrode and opposite electrode.The interval (cell gap) of aforesaid substrate can use spacer etc. to control.Upper The side contacted with liquid crystal layer for stating substrate can be set such as the alignment films comprising polyimides.

(polarization plates)

Representative polarization plates have polarizing film and are set to the protective layer of polarizing film two sides.Representative polarizing film is to inhale Receipts type polarizing film.

As above-mentioned polarizing film, any suitable polarizing film can be used.It can be mentioned, for example: make polyvinyl alcohol mesentery, part The hydrophilic macromolecule films such as formalizing polyvinyl alcohol mesentery, the partly-hydrolysed film of vinyl-vinyl acetate copolymer system adsorb iodine Or the dichroic substances such as dichroic dye and polarizing film made of being uniaxially stretched；The dehydration treatment or polychlorostyrene of polyvinyl alcohol The polyenoid such as dehydrochlorinated products of ethylene system alignment films etc..Wherein, the dichroic substances such as polyvinyl alcohol mesentery absorption iodine is made to go forward side by side The polarization dichroic ratio of polarizing film made of row is uniaxially stretched is high, therefore particularly preferably.

As the purposes of composition of the present invention, it can be mentioned, for example the wavelength conversion material of laser diode.

<LED>

The material that composition of the present invention can be used as the luminescent layer of such as LED come using.

As the LED comprising composition of the present invention, it can be mentioned, for example: by composition of the present invention and ZnS Equal electroconductive particles mix and are laminated film-like, are formed in single side stacking N-shaped transportation level and transport layer stackup another side with p-type Structure, recirculation electric current, the electronics in the hole and n-type semiconductor that thus make p-type semiconductor is contained by the composition on joint surface Charge is offset in semiconductive particles and carries out luminous mode.

Composition of the present invention can be used as the transportability material of electronics contained in the active layer of solar battery It utilizes.

As above-mentioned solar battery, composition is not particularly limited, and it can be mentioned, for example the oxidations successively with doping fluorine Tin (FTO) substrate, titanium oxide compacted zone, porous alumina layer, the active layer comprising composition of the present invention, 2,2 ', 7, 7 '-four (N, N '-di-p-methoxy phenyl amines) -9, the hole transport layers such as 9 '-spiral shell, two fluorenes (Spiro-OMeTAD) and silver (Ag) The solar battery of electrode.

Titanium oxide compacted zone has the function of that electronics transport, the effect for the roughness for inhibiting FTO and inhibition inversion electron move The function of shifting.

Porous alumina layer has the function of improving efficiency of light absorption.

Composition of the present invention contained in active layer plays the effect of separation of charge and electronics transport.

It is explained, technical scope of the invention is not limited to the above embodiment, and can not depart from master of the present invention It is subject to various changes in the range of purport.

Embodiment

Hereinafter, being further illustrated based on Examples and Comparative Examples to the present invention, but the present invention is not by below The restriction of embodiment.

(synthesis of composition)

[embodiment 1]

The solvent 40mL of cesium carbonate 0.814g, 1- octadecene and oleic acid 2.5mL is mixed.It is stirred with magnetic stirring apparatus It mixes, flows into nitrogen on one side, heated 1 hour at 150 DEG C on one side, prepare cesium carbonate solution.

By lead bromide (PbBr₂) 0.276g mixes with the solvent 20mL of 1- octadecene.It is stirred with magnetic stirring apparatus, Flow into nitrogen on one side, on one side 120 DEG C at a temperature of heat 1 hour, later, add oleic acid 2mL, oleyl amine 2mL.It is warming up to 160 DEG C temperature after, add the above-mentioned cesium carbonate solution of 1.6mL.After addition, reaction vessel is impregnated in ice water, is thus cooled to room Temperature.

Then, by dispersion liquid with the centrifuge separation of 10000rpm progress 5 minutes precipitation and separation, half thus precipitated Conductor particles.

It is measured with X-ray diffraction measure device (XRD, Cu K alpha ray, X ' pert PRO MPD, SPECTRIS corporation) As a result the X-ray diffraction pattern of above-mentioned semiconductive particles has the peak from (hkl)=(001) in the position of 2 θ=14 °, It confirms with three-dimensional perovskite type crystal structure.

With the average expense thunder of TEM (the Jeol Ltd.'s system, JEM-2200FS) perovskite compound observed Special diameter is 11nm.

After so that semiconductive particles is scattered in toluene 5mL, divides and take 50 μ L of dispersion liquid, it is made to be redispersed in toluene 5mL, thus To the dispersion liquid comprising semiconductive particles and solvent.Utilize the concentration for the perovskite compound that ICP-MS and ion chromatograph measure For 200ppm (μ g/g).

Then, in the dispersion liquid for being dispersed with above-mentioned semiconductive particles, according to making molar ratio 1- bromine hexadecane/Pb= 147 mode is mixed, and composition is obtained.

[embodiment 2]

Other than being set as 1- bromine hexadecane/Pb=245, composition is obtained using the method being the same as in example 1 above.

[embodiment 3]

Other than being set as 1- bromine hexadecane/Pb=489, composition is obtained using the method being the same as in example 1 above.

[comparative example 1]

The solvent 40mL of cesium carbonate 0.814g, 1- octadecene and oleic acid 2.5mL is mixed.It is stirred with magnetic stirring apparatus It mixes, flows into nitrogen on one side, heated 1 hour at 150 DEG C on one side, be prepared into cesium carbonate solution.

By lead bromide (PbBr₂) 0.276g mixes with the solvent 20mL of 1- octadecene.It is stirred with magnetic stirring apparatus, Flow into nitrogen on one side, on one side 120 DEG C at a temperature of heat 1 hour, later, add oleic acid 2mL, oleyl amine 2mL.It is warming up to 160 DEG C temperature after, add the above-mentioned cesium carbonate solution of 1.6mL.After addition, reaction vessel is impregnated in ice water, is cooled to room temperature.

(measurements of semiconductive particles)

The concentration of semiconductive particles in the composition obtained in Examples and Comparative Examples makes its redisperse respectively Obtained by add n,N-Dimethylformamide in the dispersion liquid comprising semiconductive particles and solvent, thus dissolve semiconductive particles Afterwards, it is determined using ICP-MS (ELAN DRCII, PerkinElmer corporation) and ion chromatograph.

(quantum yield measurement)

Using absolute PL quantum yield measurement device (creek pine photoelectricity corporation, trade name C9920-02, exciting light 450nm, Under room temperature, atmosphere) determine the quantum yield of composition obtained in Examples 1 to 3 and comparative example 1.

In table 1 below record Examples 1 to 3, comparative example 1 composition composition and quantum yield (%).Table 1 In, " halogenated hydrocarbon compound/Pb " indicates the amount of halogenated hydrocarbon compound divided by the resulting molar ratio of amount of Pb.

The result of Examples 1 to 3 is shown in FIG. 3.

[table 1]

	Halogenated hydrocarbon compound	Halogenated hydrocarbon compound/Pb	Quantum yield (%)
				Embodiment 1	1- bromine hexadecane	147	51
Embodiment 2	1- bromine hexadecane	245	49
				Embodiment 3	1- bromine hexadecane	489	48
Comparative example 1	-		30

It may validate that compared with the not composition of application comparative example 1 of the invention, apply of the invention by the above results The composition that Examples 1 to 3 is related to has superior quantum yield.

(composition)

[embodiment 4]

After so that semiconductive particles is scattered in toluene 5mL, divides and take 500 μ L of dispersion liquid, it is made to be redispersed in toluene 4.5mL, by This obtains the dispersion liquid comprising semiconductive particles and solvent.The perovskite compound measured using ICP-MS and ion chromatograph Concentration is 1500ppm (μ g/g).Then, according to making methacrylic resin (PMMA, sumitomo chemical company system, SUMIPEX Methacrylic resin, MH, molecular weight about 120,000, specific gravity 1.2g/ml) it is mixed with toluene for the mode of 16.5 mass % Afterwards, it is heated 3 hours at 60 DEG C, obtains the solution dissolved with polymer.By the dispersion comprising above-mentioned semiconductive particles and solvent After liquid 0.15g and solution 0.913g mixing dissolved with polymer, according to making the side molar ratio 1- bromine hexadecane/Pb=48.9 Formula is mixed in the cup (4.5 φ cm) of aluminum.

Evaporate toluene using natural drying, the concentration for thus obtaining perovskite compound is the composition of 1000 μ g/mL. Composition is cut into the size of 1cm × 1cm.

[embodiment 5]

Other than being set as 1- bromine hexadecane/Pb=97.9, combined using with the same method of above-described embodiment 4 Object.

[comparative example 2]

By lead bromide (PbBr₂) 0.276g mixes with the solvent 20mL of 1- octadecene.It is stirred with magnetic stirring apparatus, Flow into nitrogen on one side, on one side 120 DEG C at a temperature of heating 1 hour after, add oleic acid 2mL, oleyl amine 2mL.It is warming up to 160 DEG C After temperature, the above-mentioned cesium carbonate solution of 1.6mL is added.After addition, reaction vessel is impregnated in ice water, is thus cooled to room temperature.

After so that semiconductive particles is scattered in toluene 5mL, divides and take 500 μ L of dispersion liquid, it is made to be redispersed in toluene 4.5mL, by This obtains the dispersion liquid comprising semiconductive particles and solvent.The perovskite compound measured using ICP-MS and ion chromatograph Concentration is 1000 μ g/mL.

Then, according to making methacrylic resin (PMMA, sumitomo chemical company system, SUMIPEX methacrylic Resin, MH, molecular weight about 120,000, specific gravity 1.2g/m1) be 16.5 mass % mode it is mixed with toluene after, at 60 DEG C Heating 3 hours obtains the solution dissolved with polymer.

By the above-mentioned dispersion liquid 0.15g comprising semiconductive particles and solvent and the solution 0.913g dissolved with polymer in aluminium It is mixed in the cup (4.5 φ cm) of system.

Evaporate toluene using natural drying, the concentration for obtaining perovskite compound is the composition of 1000 μ g/mL.Combination Object is cut into the size of 1cm × 1cm.

(measurements of semiconductive particles)

The concentration of semiconductive particles in the composition obtained in Examples and Comparative Examples makes its redisperse respectively Obtained from add n,N-Dimethylformamide in the dispersion liquid comprising semiconductive particles and solvent, thus make semiconductive particles molten Xie Hou is determined using ICP-MS (ELAN DRCII, PerkinElmer corporation) and ion chromatograph.

(quantum yield measurement)

Using absolute PL quantum yield measurement device (creek pine photoelectricity corporation, trade name C9920-02, exciting light 450nm, Under room temperature, atmosphere) determine the quantum yield of composition obtained in embodiment 3,4 and comparative example 2.

Embodiment 3,4, the composition and quantum yield (%) of the composition of comparative example 2 are recorded in table 2 below.In table 2, Organic compound with halogenated alkyl/Pb indicates the amount of halogenated hydrocarbon compound divided by the resulting molar ratio of amount of Pb.

[table 2]

	Halogenated hydrocarbon compound	Halogenated hydrocarbon compound/Pb	Quantum yield (%)
				Embodiment 4	1- bromine hexadecane	48.9	35
Embodiment 5	1- bromine hexadecane	97.9	37
				Comparative example 2	-	-	27

It may validate that compared with the not composition of application comparative example 2 of the invention, apply of the invention by the above results The composition of embodiment 4,5 has superior quantum yield.

[reference example 1]

The composition recorded in Examples 1 to 5 is added in glass tube etc., after being sealed, is configured as light Between the blue LED and light guide plate in source, thus the blue light of blue LED can be converted to green by manufacture The backlight of light or red light.

[reference example 2]

By the way that sheet material is made in the composition recorded in Examples 1 to 5, so as to obtain resin combination, by it with 2 Piece barrier film clamps and seals and form film, and resulting film is set on light guide plate, and thus manufacture can will be led from being placed in The blue LED of the end face (side) of tabula rasa is converted to green light by the blue light that light guide plate irradiates above sheet Or the backlight of red light.

[reference example 3]

By the way that the composition recorded in Examples 1 to 5 to be set near the illumination region of blue LED, to make Make the backlight that the blue light irradiated can be converted to green light or red light.

[reference example 4]

After mixing the composition recorded in Examples 1 to 5 and resist, solvent is removed, so as to obtain wave Long transition material.By by resulting wavelength conversion material configuration as light source blue LED and light guide plate it Between or OLED as light source back segment, so that the blue light of light source can be converted to green light or red light by manufacture Backlight.

[reference example 5]

The composition recorded in Examples 1 to 5 is mixed and formed a film with electroconductive particles such as ZnS, in single side stacking N-shaped fortune Defeated layer, and layer stackup another side is transported with p-type, thus obtain LED.It can make the sky of p-type semiconductor by flowing into electric current The electronics of cave and n-type semiconductor offsets charge in the semiconductive particles on joint surface, to carry out luminous.

[reference example 6]

Titanium oxide compacted zone is laminated on the surface of tin oxide (FTO) substrate of doping fluorine, porous oxygen is laminated from the upper side Change aluminium layer, the composition recorded in stacking embodiment 1~5 on it is laminated 2,2 ', 7,7 '-four after removing solvent from the upper side (N, N '-di-p-methoxy phenyl amine) -9, the hole transport layers such as 9 '-spiral shell, two fluorenes (Spiro-OMeTAD), stacking is silver-colored on it (Ag) layer makes solar battery.

[reference example 7]

After mixing the composition recorded in Examples 1 to 5 and resin, solvent is removed, is formed, so as to The resin combination comprising composition of the present invention is obtained, by being disposed at the back segment of blue LED, from And green light or red light will be converted to the blue light that above-mentioned resin-formed body irradiates from blue LED and sends out by manufacturing The laser diode illumination of white light out.

Industrial availability

According to the present invention it is possible to provide the high composition of quantum yield, the film comprising above-mentioned composition, comprising said combination The laminate structure of object and the display for having used above-mentioned composition.

Therefore, composition of the invention, the film comprising above-mentioned composition, the laminate structure comprising above-mentioned composition and make With the display of above-mentioned composition can compatibly use illuminating on the way.

Description of symbols

1a ... first cascade structural body, the second laminate structure of 1b ..., 10 ... films, 20 ... first substrates, 21 ... second bases Plate, 22 ... sealants, 2 ... light emitting devices, 3 ... displays, 30 ... light sources, 40 ... liquid crystal display panels, 50 ... prismatic lens, 60 ... leaded lights Plate

Claims

1. one kind have luminiferous composition, it includes (1) and (2), and also include at least one of (3) and (4),

(1) semiconductive particles；

(2) halogenated hydrocarbon compound；

(3) solvent；

(4) at least one kind of in polymerizable compound and polymer.

2. composition according to claim 1, wherein described (1) is the perovskite using A, B and X as constituent The particle of object is closed,

A is the ingredient for being located at hexahedral each vertex centered on B in perovskite type crystal structure, is 1 valence cation,

X indicates the ingredient for being located at octahedral each vertex centered on B in perovskite type crystal structure, is selected from halogenation One or more of object ion and thiocyanate ion anion,

B is to be located at that A is configured at the hexahedron on vertex and X is configured at the octahedral of vertex in perovskite type crystal structure The ingredient at center is metal ion.

3. composition according to claim 1 or 2, also include (5) be selected from ammonia, amine, carboxylic acid and their salt or from It is at least one kind of in son.

It, total content phase of (2) and (4 ') is the composition comprising (1), (2) and (4 ') 4. a kind of composition, wherein (1) Gross mass for the composition is 90 mass % or more,

(1) semiconductive particles；

(2) halogenated hydrocarbon compound；

(4 ') polymer.

5. composition according to claim 4 also includes (5) in ammonia, amine, carboxylic acid and their salt or ion It is at least one kind of.

6. a kind of film, it includes compositions described in claim 4 or 5.

7. a kind of laminate structure, with multiple layers, and at least one layer of is to include composition described in claim 4 or 5 Layer.

8. a kind of light emitting device has laminate structure as claimed in claim 7.

9. a kind of display has laminate structure as claimed in claim 7.