Complexes between block polymers and ions as contrast agents for medical imaging
US-2018318455-A1 · Nov 8, 2018 · US
US10604699B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10604699-B2 |
| Application number | US-201616068455-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 9, 2016 |
| Priority date | Jan 6, 2016 |
| Publication date | Mar 31, 2020 |
| Grant date | Mar 31, 2020 |
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Provided are an organic rare-earth solid micelle, a preparation method therefor, and a method for increasing the photoelectric conversion efficiency of a solar battery. A small organic conjugated ligand is taken as a first ligand, an amphiphilic diblock polymer is taken as a second ligand, and the first ligand and the second ligand are mixed and doped with a rare-earth chloride solution, and self-assembled to form an organic rare-earth solid micelle, whereby the fluorescence emission intensity and the fluorescence efficiency of the rare-earth element are improved. Next, the prepared organic rare-earth solid micelle is spin coated on an ITO layer of a solar battery, to prepare a solar battery with the organic rare-earth solid micelle. Therefore the sunlight absorption of a cell is increased, and the photoelectric conversion efficiency is improved. The preparation process is simple, low in cost, high in photoelectric conversion efficiency, and environmentally friendly.
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The invention claimed is: 1. A method for preparing an organic rare-earth solid micelle, comprising: taking a small organic conjugated ligand as a first ligand and an amphiphilic diblock polymer as a second ligand, mixing and doping the first ligand and the second ligand with a rare-earth chloride solution, and self-assembling to form an organic rare-earth solid micelle; wherein the amphiphilic diblock polymer is polymethyl methacrylate-b-polyacrylic acid (PMMA-b-PAA), the molar ratio of the small organic conjugated ligand:rare-earth chloride:amphiphilic diblock polymer is 3:1:1, wherein the small organic conjugated ligand:rare-earth chloride:amphiphilic diblock polymer are subjected to complexation reaction for 5-10 hrs in an oil bath at 50-70° C., to obtain a solution of an organic rare-earth solid micelle that is a complex having a size of 10-20 nm. 2. The preparation method according to claim 1 , wherein the polymethyl methacrylate-b-polyacrylic acid (PMMA-b-PAA) useful as the amphiphilic diblock polymer is prepared through a process comprising: (1) weighing an amount of a reversible addition fragmentation chain transfer (RAFT) agent and an appropriate amount of an initiator, dissolving the RAFT agent and initiator in dioxane as a solvent, adding an amount of methyl methacrylate (MMA) monomer, and reacting for 8 hrs in an oil bath at 70° C. under a nitrogen atmosphere to obtain a first reaction solution; and washing the first reaction solution with petroleum ether, filtering with suction to obtain an upper solid, and drying the upper solid to obtain a first polymer; and (2) weighing an amount of the first polymer obtained in Step (1), adding an appropriate amount of an initiator, dissolving the first polymer and initiator in dioxane as a solvent, adding an amount of acrylic acid monomer when the first polymer is completely dissolved, and reacting for 6 hrs in an oil bath at 50° C. under a nitrogen atmosphere to obtain a second reaction solution; and washing the second reaction solution with petroleum ether to remove impurities and unreacted monomers, pouring an upper liquid to obtain a solid, and drying to obtain the amphiphilic diblock polymer (PMMA-b-PAA). 3. The preparation method according to claim 1 , wherein the rare-earth chloride solution comprises europium chloride, terbium chloride, thulium chloride or gadolinium chloride. 4. The preparation method according to claim 3 , wherein the small organic conjugated ligand is 2-thenoyltrifluoroacetone. 5. The preparation method according to claim 3 , wherein the small organic conjugated ligand is one of 1,10-o-phenanthroline, acetylacetone, salicylic acid, or dibenzoyl methane.
containing organic luminescent materials · CPC title
using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title
Introducing metal atoms or metal-containing groups · CPC title
containing sulfur as the only heteroatom · CPC title
of the rare earth metals, i.e. Sc, Y or lanthanide · CPC title
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