H01B1/127

PEROVSKITE LIGHT EMITTING DEVICE CONTAINING EXCITON BUFFER LAYER AND METHOD FOR MANUFACTURING SAME
20170346031 · 2017-11-30 ·

Provided are a perovskite light emitting device containing an exciton buffer layer, and a method for manufacturing the same. The light emitting device of the present invention comprises: an exciton buffer layer in which a first electrode, a conductive layer disposed on the first electrode and comprising a conductive material, and a surface buffer layer containing fluorine-based material having lower surface energy than the conductive material are sequentially deposited; a light-emitting layer disposed on the exciton buffer layer and containing an organic-inorganic hybrid perovskite light emitting body; and a second electrode disposed on the light-emitting layer. Accordingly, an organic-inorganic hybrid perovskite is formed with a combined FCC and BSS crystal structure in a nanoparticle light-emitting body; the present invention forms a lamellar structure in which an organic plane and an inorganic plane are alternatively deposited; and an exciton is bound by the inorganic plane, thereby being capable of expressing high color purity.

LADDER POLYBENZODIFURANS
20170342203 · 2017-11-30 ·

A polybenzodifuran ladder polymer is disclosed.

Thieno-indeno-monomers and polymers

Polymers comprising at least one unit of formulae ##STR00001## and compounds of the formulae ##STR00002## wherein, in formulae 1, 1′, 2 and 2′ n is 0, 1, 2, 3 or 4 m is 0, 1, 2, 3 or 4 M1 and M2 are independently of each other an aromatic or heteroaromatic monocyclic or bicyclic ring system; X is at each occurrence selected from the group consisting of O, S, Se or Te, Q is at each occurrence selected from the group consisting of C, Si or Ge R is at each occurrence selected from the group consisting of hydrogen, C.sub.1-100-alkyl, C.sub.2-100-alkenyl, C.sub.2-100-alkynyl, C.sub.5-12-cycloalkyl, C.sub.6-18-aryl, a 5 to 20 membered heteroaryl, C(O)—C.sub.1-100-alkyl, C(O)—C.sub.5-12-cycloalkyl and C(O)—OC.sub.1-100-alkyl. R.sup.2, R.sup.2′, R.sup.2″, R* are at each occurrence independently selected from the group consisting of hydrogen, C.sub.1-30-alkyl, C.sub.2-30-alkenyl, C.sub.2-30-alkynyl, C.sub.5-12-cycloalkyl, C.sub.6-18-aryl, 5 to 20 membered heteroaryl, OR.sup.21, OC(O)—R.sup.21, C(O)—OR.sup.21, C(O)—R.sup.21, NR.sup.21R.sup.22, NR.sup.21—C(O)R.sup.22, C(O)—NR.sup.21R.sup.22, N[C(O)R.sup.21][C(O)R.sup.22], SR.sup.21, halogen, CN, SiR.sup.SisR.sup.SitR.sup.Siu and OH, L.sup.1 and L.sup.2 are independently from each other and at each occurrence selected from the group consisting of C.sub.6-30-arylene, 5 to 30 membered heteroarylene, ##STR00003##

CONDUCTOR MATERIAL

Provided is a conductor material having high conductivity. The conductor material according to an embodiment of the present disclosure has a configuration in which a conjugated polymeric compound having an electron donating group containing a heteroatom in a side chain is doped with a dopant containing an anion selected from a nitrogen anion, a boron anion, a phosphorus anion and an antimony anion, and a counter cation. The anion is preferably an anion represented by Formula (1) below: where R.sup.1 and R.sup.2 are identical or different, and each represent an electron withdrawing group; and R.sup.1 and R.sup.2 may be bonded to each other to form a ring with an adjacent nitrogen atom.

##STR00001##

Conductive inks and conductive polymeric coatings

A conductive ink and a conductive coating are provided. The conductive ink includes a conductive polymer solution comprising conductive polymer dissolved in an aqueous-based media and a mixture of carbon nanotubes and graphene oxide sheets dispersed in the conductive polymer solution, wherein a weight ratio of the carbon nanotubes to the graphene oxide sheets is in a range from 0.25 to 2.5. The conductive coating includes a conductive polymer and a mixture of graphene oxide sheets and carbon nanotubes dispersed in the conductive polymer, wherein a weight ratio of the carbon nanotubes to the graphene oxide sheets is in a range from 0.25 to 2.5, and wherein the conductive coating has an optical transmittance value at 550 nm of at least 75%.

ELECTROCONDUCTIVE FILM AND METHOD FOR MANUFACTURING ELECTROCONDUCTIVE PATTERN

A method for manufacturing an electroconductive pattern 40, provided with: a lamination step for laminating an acid generation film 10 containing an acid proliferation agent and a photoacid generator on a polymer film 20 containing an electroconductive polymer formed on a substrate 21; a masking step for masking the top of the acid generation film 10; a light irradiation step for irradiating the laminate from the acid-generation-film 10 side; a doping step for doping the electroconductive polymer with an acid generated and proliferated in the acid generation film 10 by the light irradiation; and a releasing step for releasing the acid generation film 10 from the polymer film 20. This method makes it possible to provide an electroconductive film and a method for manufacturing an electroconductive pattern in which photoacid generation and acid proliferation effects are utilized.

Integrated conductive polymer binder composition, method for preparing the binder composition, and applications comprising the binder composition

The present invention relates to a polymer binder composition, and more specifically, to an integrated conductive polymer binder composition simultaneously having adhesion and conductivity, a method for preparing the binder composition, an energy storage device comprising the binder composition, a sensor comprising a sensing portion formed from the binder composition, and an anticorrosive coating composition comprising the binder composition as an active component.

Difluorobithiophene-Based Donor-Acceptor Polymers for Electronic and Photonic Applications
20170301862 · 2017-10-19 ·

An organic compound, a donor-acceptor conjugated polymer, a formulation and a thin film, wherein a solution of the donor-acceptor conjugated polymer exhibits a peak optical absorption spectrum red shift of at least 100 nm when the donor-acceptor conjugated polymer solution is cooled from 140° C. to room temperature.

Method for forming conjugated heteroaromatic homopolymer and copolymer, and products thereof

A method for forming a conjugated heteroaromatic polymer is described, wherein at least one compound of formula (1) is polymerized using an acid as a catalyst, ##STR00001##
wherein X is selected from S, O, Se, Te, PR.sup.2 and NR.sup.2, Y is hydrogen (H) or a precursor of a good leaving group Y.sup.− whose conjugate acid (HY) has a pK.sub.a of less than 30, Z is hydrogen (H), silyl, or a good leaving group whose conjugate acid (HZ) has a pK.sub.a of less than 30, b is 0, 1 or 2, each R.sup.1 is a substituent, and the at least one compound of formula (1) being polymerized includes at least one compound of formula (1) with Z=H and Y≠H.

Method for preparing dioxyheterocycle-based electrochromic polymers

A method for preparing a conjugated polymer involves a DHAP polymerization of a 3,4-dioxythiophene, 3,4-dioxyfuran, or 3,4-dioxypyrrole and, optionally, at least one second conjugated monomer in the presence of a Pd or Ni comprising catalyst, an aprotic solvent, a carboxylic acid at a temperature in excess of 120° C. At least one of the monomers is substituted with hydrogen reactive functionalities and at least one of the monomers is substituted with a Cl, Br, and/or I. The polymerization can be carried out at temperature of 140° C. or more, and the DHAP polymerization can be carried out without a phosphine ligand or a phase transfer agent. The resulting polymer can display dispersity less than 2 and have a degree of polymerization in excess of 10.