Provided are an inorganic fluorescent nanoparticle composite that can suppress the degradation of inorganic fluorescent nanoparticles when sealed in glass and a wavelength conversion member using the inorganic fluorescent nanoparticle composite. An inorganic fluorescent nanoparticle composite 1 is made up by including: an inorganic fluorescent nanoparticle 2; and an inorganic fine particle 3 deposited on a surface of the inorganic fluorescent nanoparticle 2.

Provided are an inorganic fluorescent nanoparticle composite that can suppress the degradation of inorganic fluorescent nanoparticles when sealed in glass and a wavelength conversion member using the inorganic fluorescent nanoparticle composite. An inorganic fluorescent nanoparticle composite 1 is made up by including: an inorganic fluorescent nanoparticle 2; and an inorganic fine particle 3 deposited on a surface of the inorganic fluorescent nanoparticle 2.

The present disclosure provides a ratiometric fluorescent probe, a preparation method thereof, and an application in detection of hydrogen peroxide. In the present disclosure, MoO.sub.x QDs (nanoenzymes) and Co/Zn-MOFs both have catalytic activity, and the large specific surface area and porous structure of Co/Zn-MOFs can provide more binding sites for the contact between nanoenzymes and substrates. Moreover, Co/Zn-MOFs have high catalytic activity similar to natural enzymes. When nanoenzymes with fluorescent properties encounter Co/Zn-MOFs with similar catalytic activity, they will collide with a spark of “synergy catalysis”, and the fusion of the two plays a role of synergy catalysis; in addition, the uniform cavity of Co/Zn-MOFs can provide “hosts” for nanoenzymes, and Co/Zn-MOFs provide “anchors” for MoO.sub.x QDs, avoiding the aggregation of MoO.sub.x QDs and enhancing the stability of the probe.

A quantum dot organic light-emitting diode according to an embodiment of the present disclosure may include a blue organic light-emitting diode (OLED) layer, a quantum dot color conversion layer which is provided on the blue OLED layer and has different scattering particle structures according to R, G and B colors, a color filter layer which is provided on the quantum dot color conversion layer and filters color other than the color that the color filter layer passes from the colors emitted by the quantum dot color conversion layer, and a coating layer provided on the color filter layer.

A quantum dot organic light-emitting diode according to an embodiment of the present disclosure may include a blue organic light-emitting diode (OLED) layer, a quantum dot color conversion layer which is provided on the blue OLED layer and has different scattering particle structures according to R, G and B colors, a color filter layer which is provided on the quantum dot color conversion layer and filters color other than the color that the color filter layer passes from the colors emitted by the quantum dot color conversion layer, and a coating layer provided on the color filter layer.

The invention relates to a luminophore mixture which comprises at least one quantum dot luminophore and at least one functional material, the functional material is formed such that it scatters electromagnetic radiation and/or has a high density.

A semiconductor nanoparticle complex in which two or more ligands including an aliphatic ligand and a polar ligand are coordinated to a surface of a semiconductor nanoparticle, wherein: the ligands are composed of an organic group and a coordinating group; in the aliphatic ligand, the organic group is an aliphatic hydrocarbon group; the polar ligand includes a hydrophilic functional group in the organic group; a mass ratio of the aliphatic ligand to the polar ligand (aliphatic ligand/polar ligand) is 0.05 to 1.00; a ratio ({(X.sub.H)/L}×100) of a mass reduction rate of the semiconductor nanoparticle complex in a range of 350° C. or higher and 550° C. or lower in a thermogravimetric analysis (X.sub.H) to a mass fraction of all ligands in the semiconductor nanoparticle complex at room temperature (L) is 10 or more and 55 or less.

A semiconductor nanoparticle complex in which two or more ligands including an aliphatic ligand and a polar ligand are coordinated to a surface of a semiconductor nanoparticle, wherein: the ligands are composed of an organic group and a coordinating group; in the aliphatic ligand, the organic group is an aliphatic hydrocarbon group; the polar ligand includes a hydrophilic functional group in the organic group; a mass ratio of the aliphatic ligand to the polar ligand (aliphatic ligand/polar ligand) is 0.05 to 1.00; a ratio ({(X.sub.H)/L}×100) of a mass reduction rate of the semiconductor nanoparticle complex in a range of 350° C. or higher and 550° C. or lower in a thermogravimetric analysis (X.sub.H) to a mass fraction of all ligands in the semiconductor nanoparticle complex at room temperature (L) is 10 or more and 55 or less.

A CuInS.sub.2@ZnS nanomaterial synthesized with thiosalicylic acid and sodium citrate as dual-stabilizers is taken as a chemiluminescent luminophore, and Tris buffer containing both N.sub.2H.sub.4.H.sub.2O and H.sub.2O.sub.2 is taken as the triggering solution; introducing the H.sub.2O.sub.2 into the triggering solution can bring out greatly enhanced CL emission and obviously shortened CL process, enable the CuInS.sub.2@ZnS nanomaterial with strong flash-type and near-infrared CL; the luminophore of CuInS.sub.2@ZnS nanomaterial is synthesized by a one-pot method; compared with acridinium ester (a classical flash-type chemiluminescent substance), the CuInS.sub.2@ZnS nanomaterial is simple in synthesis method, mild in conditions and short in the required time, the synthesized CuInS.sub.2@ZnS nanomaterial is not easy to decompose under light, and the CL waveband is in the near-infrared region.

A CuInS.sub.2@ZnS nanomaterial synthesized with thiosalicylic acid and sodium citrate as dual-stabilizers is taken as a chemiluminescent luminophore, and Tris buffer containing both N.sub.2H.sub.4.H.sub.2O and H.sub.2O.sub.2 is taken as the triggering solution; introducing the H.sub.2O.sub.2 into the triggering solution can bring out greatly enhanced CL emission and obviously shortened CL process, enable the CuInS.sub.2@ZnS nanomaterial with strong flash-type and near-infrared CL; the luminophore of CuInS.sub.2@ZnS nanomaterial is synthesized by a one-pot method; compared with acridinium ester (a classical flash-type chemiluminescent substance), the CuInS.sub.2@ZnS nanomaterial is simple in synthesis method, mild in conditions and short in the required time, the synthesized CuInS.sub.2@ZnS nanomaterial is not easy to decompose under light, and the CL waveband is in the near-infrared region.