Aryl, heteroaryl, and heterocyclic compounds for treatment of immune and inflammatory disorders
US-2024199583-A1 · Jun 20, 2024 · US
US9073937B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9073937-B2 |
| Application number | US-201213525559-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 18, 2012 |
| Priority date | Jun 16, 2011 |
| Publication date | Jul 7, 2015 |
| Grant date | Jul 7, 2015 |
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Photoactive layers for use in a photovoltaic cell are described. The photoactive layers comprise at least one photoactive ion paired with another ion. This photoactive ion pair can be in the form of an ionic liquid, hydrogen bonded ion pair, cocrystal, or complex to allow for greater flexibility and portability. Also described are photovoltaic cells that contain the described photoactive layers sandwiched between two electrodes.
Opening claim text (preview).
What is claimed is: 1. A photoactive composition comprising a cation and an anion, wherein the cation is Janus Green B, Astrazon Orange G, Crystal Violet, Rhodamine B, or Basic Yellow, wherein the anion is a dye-substituted fullerene or graphene, aliphatic sulfate, aliphatic carboxylate, aliphatic phosphonate, oleic acid, linoleic acid, oleate, linoleate, graphene, or protoporphyrin IX or a salt thereof, and wherein the cation and anion form an ion pair, an ionic liquid, are hydrogen bonded, form a complex, or form a cocrystal. 2. The composition of claim 1 , wherein the cation is photoactive. 3. The composition of claim 1 , wherein the cation absorbs light in a range of from about 400 to about 900 nm and has a HOMO from about 0.1 eV to about 1 eV of the HOMO of the cathode. 4. The composition of claim 3 , wherein the cation has a HOMO from about 0.1 eV to about 0.6 eV of the HOMO of the cathode. 5. The composition of claim 1 , wherein the anion is photoactive ion. 6. The composition of claim 1 , wherein the anion absorbs light in a range of from about 400 to about 900 nm and has a LUMO from about 0.1 eV to about 1 eV of the LUMO of the anode. 7. The composition of claim 6 , wherein the anion has a LUMO from about 0.1 eV to about 0.6 eV of the LUMO of the anode. 8. The composition of claim 1 , wherein both the cation and the anion are photoactive. 9. The composition of claim 1 , wherein the cation and the anion form an ionic liquid that has a melting point below 100° C. 10. The composition of claim 1 , wherein both the cation's and the anion's molecular orbitals are within 1 eV of the molecular orbitals of the corresponding electrodes. 11. The composition of claim 1 , wherein the cation and the anion form the ion pair. 12. The composition of claim 1 , wherein the composition absorbs light in a range of from about 250 nm to about 900 nm. 13. The composition of claim 1 , wherein the cation and the anion form an ionic liquid and the ionic liquid is synthesized by metathesis of salt forms of the cation and the anions or by an acid base reaction. 14. The composition of claim 1 , wherein the anion contains at least one conjugated bond. 15. The composition of claim 1 , wherein the anion contains all conjugated bonds. 16. The composition of claim 1 , wherein the anion is protoporphyrin IX disodium salt, perylene tetracarboxylic acid, Copper(II) phthalocyanine-tetrasulfonic acid, carboxylic derivative of [6,6]-phenyl C61 butyric acid methyl ester, or a fullerene anion. 17. The composition of claim 16 , wherein the cation is a protonated aliphatic amine. 18. The composition of claim 1 , wherein the cation and anion are selected from the following combinations: Astrazon Orange G protoporphyrin IX, Astrazon orange—phenyl C61 butyrate, Astrazon orange perylene tetracarboxylate, Janus Green B dodecyl sulfonate, Janus Green B oleate, Janus Green B—phenyl C61 butyrate, Janus Green B—perylene tetracarboxylate, Janus Green B—protoporphyrin IX, Janus Green B—protoporphyrin IX—Cu(II)-oleate, Janus Green B—protoporphyrin IX—Zn(II)-oleate, Janus Green B—protoporphyrin IX—Co(II)-oleate, Janus Green B—protoporphyrin IX—Ag(I)-oleate, Crystal Violet dodecyl sulfonate, Crystal Violet oleate, Crystal violet—phenyl C61 butyrate, Crystal violet—perylene tetracarboxylate, Crystal Violet—protoporphyrin IX, Crystal Violet—protoporphyrin IX—Cu(II)-oleate, Crystal Violet—protoporphyrin IX—Co(II)-oleate, Crystal Violet—protoporphyrin IX—Zn(II)—oleate, Crystal Violet—protoporphyrin IX—Ag(I)-oleate, Astrazon Orange dodecyl sulfonate, Astrazon Orange oleate, Astrazon Orange—protoporphyrin IX—Cu(II)-oleate, Astrazon Orange—protoporphyrin IX—Co(II)-oleate, Astrazon Orange—protoporphyrin IX—Zn(II)-oleate, Astrazon Orange—protoporphyrin IX—Ag(I)-oleate, Basic Yellow 11—dodecyl sulfonate, Basic Yellow 11—oleate, Basic Yellow 11—protoporphyrin IX, Basic Yellow 11—phenyl C61 butyrate, Basic Yellow 11—perylene tetracarboxylate, Basic Yellow 11—protoporphyrin IX—Cu(II)-oleate, Basic Yellow 11—protoporphyrin IX—Co(II)-oleate, Basic Yellow 11—protoporphyrin IX—Zn(II)-oleate, Basic Yellow 11—protoporphyrin IX—Ag(I)-oleate, Rhodamine B—dodecyl sulfonate, Rhodamine B—oleate, Rhodamine B—protoporphyrin IX, Rhodamine B—phenyl C61 butyrate, Rhodamine B—perylene tetracarboxylate, Rhodamine B—protoporphyrin IX—Cu(II)—oleate, Rhodamine B—protoporphyrin IX—Co(II)-oleate, Rhodamine B—protoporphyrin IX—Zn(II)-oleate, and Rhodamine B—protoporphyrin IX—Ag(I)-oleate.
Photovoltaic [PV] devices · CPC title
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Electricity · mapped topic
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