The present invention relates to novel metal-ligand coordination compounds of the general formula T1-(A-T2)i, where T1 and T2 represent metal-ligand coordination compounds, to the use thereof in a device, and to a formulation and a device which comprise the novel compounds.

Visibly transparent photovoltaic devices are disclosed, such as those are transparent to visible light but absorb near-infrared light and/or ultraviolet light. The photovoltaic devices make use of transparent electrodes and near-infrared absorbing visibly transparent photoactive compounds, optical materials, and/or buffer materials.

A polymeric dielectric may include a coordination complex of a modified elastic polymer and a metal cation. The modified elastic polymer may include an organic ligand moiety that coordinates the metal cation in a main chain of the elastic polymer. Provided are a method of manufacturing the same, and an electronic device and a thin film transistor including the same.

An ionic phosphorescent metal complex has a formula of formula (I). R.sub.1 and R.sub.2 are the same or different, and are independently selected from alkyl, aryl and heteroaryl, wherein the alkyl, aryl and heteroaryl are optionally substituted with 1-5 of the following groups: halogen, alkyl, alkoxy, alkylthio, amino, alkylamino, dialkylamino, arylamino, diarylamino, haloalkyl, cyano, nitro, alkenyl, aryl and heteroaryl optionally substituted with 1-3 aryl groups; R.sub.3 is independently selected from halogen, alkyl, haloalkyl, alkoxy, alkylthio, amino, alkylamino, dialkylamino, cyano, nitro or alkenyl; M is Cu(I), Ag(I) or Au(I). The organic light-emitting diode prepared by using the phosphorescent metal complex of formula (I) as a dopant for an emissive layer is capable of achieving high-performance organic electroluminescence and is applicable to the fields of lighting and flat-panel display.

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Electrodes useful in dye sensitized photoelectrosynthesis cells provide a coreshell nanoparticle having a chromophore and a catalyst, or a chromophore-catalyst assembly, linked to the shell material. Optionally, an overlayer stabilizes the chromophore or chromophore-catalyst assembly on the shell material. In some embodiments, the core material comprises tin oxide; the shell material comprises titanium dioxide; the chromophore-catalyst assembly includes [(PO.sub.3H.sub.2).sub.2bpy).sub.2Ru(4-Mebpy-4′-bimpy)Ru(tpy) (OH.sub.2)].sup.4+, and the overlayer comprises aluminum oxide or titanium dioxide.

An organic electronic component and a method for making an organic electronic component with a p-dopant are disclosed. In an embodiment, the component includes a matrix containing a zinc complex as a p-dopant, the zinc complex containing at least one ligand L of the following structure: formula (I) wherein R.sup.1 and R.sup.2 can be oxygen, sulphur, selenium, NH or NR.sup.4 independently selected from one another, wherein R.sup.3 may comprise alkyl, long-chain alkyl, cycloalkyl, halogen-alkyl, aryl, arylene, halogen-aryl, heteroaryl, heteroarylene, heterocyclic-alkylene, heterocycloalkyl, halogen-heteroaryl, alkenyl, halogen-alkenyl, alkynyl, halogen-alkynyl, ketoaryl, halogen-ketoaryl, ketoheteroaryl, ketoalkyl, halogen-ketoalkyl, ketoalkenyl, halogen-ketoalkenyl, halogen-alkyl-aryl or halogen-alkyl-heteroaryl, and wherein R.sup.4 is selected from the group consisting of alkyl and aryl which can be bonded to R.sup.3.

It is an object of the present invention to provide an organometallic complex that can emit phosphorescence. In the following general formula (G1), X represents —O— or —N(R.sup.10)—. R.sup.1 to R.sup.9 each represent any of hydrogen, an alkyl group or a cycloalkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkoxycarbonyl group having 1 to 6 carbon atoms, an acyl group having 1 to 6 carbon atoms, an acyloxy group having 1 to 6 carbon atoms, a halogen group, a haloalkyl group, and an aryl group having 6 to 12 carbon atoms. In addition, R.sup.10 represents any of an alkyl group or a cycloalkyl group having 1 to 6 carbon atoms, an acyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, and a heteroaryl group having 4 to 10 carbon atoms. Moreover, M represents an element belonging to Group 9 or 10. ##STR00001##

The present invention relates to a light-emitting layer B comprising a first emitter compound (a) having a non-exited state S0(a), a first excited singlet state S1(a) and a first excited triplet state T1(a); a second emitter compound (b) having a non-exited state S0(b), a first excited singlet state S1(b) and a first excited triplet state T1(b), wherein the energy level of S1(a) is higher than that of S1(b), the energy level of S1(b) is higher than that of T1(b) and wherein the rate of reverse intersystem crossing from T1(a) to S1(a) is higher than the rate of excition energy transfer from S1(a) to S1(b) and/or the rate of excition energy transfer from T1(a) to T1(b), and/or wherein the energy level of T1(b) is higher than that of T1(a). Further, the present invention also refers to an opto-electronic device comprising such light-emitting layer B and use thereof.

The present invention relates to binuclear metal complexes and electronic devices, in particular organic electroluminescent devices containing said metal complexes. ##STR00001##

Transmission of low energy light is one of the primary loss mechanisms of a single junction solar cell. Molecular photon upconversion via triplet-triplet annihilation (TTA-UC)—combining two or more low energy photons to generate a higher energy excited state—is an intriguing strategy to surpass this limit. The present disclosure is directed to self-assembled multilayers, e.g., bi- or trilayers, on metal oxide surfaces as a strategy to facilitate TTA-UC emission and demonstrate direct charge separation of the upconverted state. A three-fold enhancement in transient photocurrent is achieved at light intensities as low as two equivalent suns. The multilayer structure comprises a substrate comprising a metal oxide surface and a bulk region, and a self-assembled bilayer film, the bilayer film comprising: (a) an acceptor molecule covalently bonded to the metal oxide surface; (b) a linking metal ion bonded to the acceptor molecule; and (c) one or more sensitizer molecule(s) bonded to the linking co-ordinating metal ion.