Organic species that facilitate charge transfer to or from nanostructures
View Patent ↗The present invention provides compositions (small molecules, oligomers and polymers) that can be used to modify charge transport across a nanocrystal surface or within a nanocrystal-containing matrix, as well as methods for making and using the novel compositions.
1. A conductive ligand for modification of charge transport across a nanostructure-containing matrix, the ligand comprising:
a monomeric body structure comprising a conjugated organic moiety;
a head group coupled to the body structure at a first position on the conjugated organic moiety, wherein the head group comprises a functionalized head group capable of binding to a nanostructure surface or a head group bound to a nanostructure surface wherein the nanostructure is a nanocrystal; and
a tail group coupled to the body structure at a second position on the conjugated organic moiety;
wherein the body structure further comprises one or more O-linked or N-linked sidechain coupled to the conjugated organic moiety, the sidechain comprising a conducting chemical structure, whereby the one or more sidechain extends the conjugation of the body structure, and
wherein one or more elements of the conductive ligand are capable of removing or adding charges to a nanostructure upon attachment to a surface of the nanostructure, thereby modifying charge transport across a nanostructure-containing matrix.
2. The ligand of claim 1 , wherein the nanostructure is an inorganic nanocrystal.
3. The ligand of claim 1 , wherein the functionalized head group comprises one or more phosphonic acid, carboxylic acid, amine, phosphine, or thiol moieties.
4. The ligand of claim 1 , wherein the functionalized head group or bound head group comprises a monodentate structure.
5. The ligand of claim 1 , wherein the functionalized head group or bound head group comprises a multidentate structure.
6. The ligand of claim 1 , wherein the body structure comprises a conjugated alkyl moiety or a conjugated aryl moiety.
7. The ligand of claim 6 , wherein the body structure comprises a phenylene, thiophene, ethene, ethyne, aniline, fluorene, pyridine, perylene, phenanthralene, anthracene, alkenyl or polynuclear aromatic moiety.
8. The ligand of claim 1 , wherein the sidechain comprises an electron donating group.
9. The ligand of claim 1 , wherein the sidechain comprises an electron withdrawing group.
10. The ligand of claim 1 , wherein the sidechain comprises a polymerizable element.
11. The ligand of claim 10 , wherein the polymerizable element comprises an acrylate moiety, a methacrylate moiety, or a vinyl moiety.
12. The ligand of claim 1 , wherein a first sidechain is coupled to the body structure at a first sidechain position, and wherein a second sidechain is coupled to the body structure at a second sidechain position.
13. The ligand of claim 12 , wherein the first and second sidechains are different chemical moieties.
14. The ligand of claim 12 , wherein the first and second sidechains are identical chemical moieties.
15. The ligand of claim 1 , wherein the sidechain alters a solubility of the ligand.
16. The ligand of claim 1 , wherein the sidechain is matched functionally and/or electronically to a matrix ligand of the nanostructure-containing matrix.
17. The ligand of claim 1 , wherein the sidechain comprises an O-linked hexane moiety, an O-linked 2-ethylhexyl moiety, an O-linked octyl moiety, an O-linked decyl moiety, or an O-linked alkyl moiety comprising between 5 and 22 carbons.
18. The ligand of claim 1 , wherein the sidechain comprises an N-linked hexane moiety, an N-linked 2-ethylhexyl moiety, an N-linked octyl moiety, an N-linked decyl moiety, or an N-linked alkyl moiety comprising between 5 and 22 carbons.
19. The ligand of claim 1 , wherein the sidechain comprises a chemical substituent having greater than 22 carbons.
20. The ligand of claim 1 , wherein the one or more sidechain and the tail group comprise identical chemical ligands.
21. The ligand of claim 1 , wherein the tail group comprises a conducting chemical structure.
22. The ligand of claim 1 , wherein the tail group comprises a nonconducting chemical structure.
23. The ligand of claim 1 , wherein the tail group comprises an alkene or an alkyne moiety.
24. The ligand of claim 1 , wherein the tail group comprises 1-propyne, 1-butyne, 1-pentyne, 1-hexyne, 1-heptyne, 1-octyne, 1-nonyne, 1-decyne, or an alkyne comprising between 3 and 22 carbons.
25. The ligand of claim 1 , wherein the tail group comprises a chemical functionality capable of binding to the nanostructure surface or an additional nanostructure surface.
26. The ligand of claim 1 , wherein the tail group comprises a monodentate structure.
27. The ligand of claim 1 , wherein the tail group comprises a multidentate structure.
28. The ligand of claim 1 , wherein the tail group comprises a polymerizable element.
29. A conductive ligand for modification of charge transport across a nanostructure-containing matrix, the ligand comprising:
a monomeric body structure comprising a conjugated organic moiety;
a head group coupled to the body structure at a first position on the conjugated organic moiety, wherein the head group comprises a functionalized head group capable of binding to a nanostructure surface or a head group bound to a nanostructure surface wherein the nanostructure is a nanocrystal; and
a tail group coupled to the body structure at a second position on the conjugated organic moiety;
wherein the tail group comprises an alkyne comprising more than 22 carbons,
wherein the tail group further comprises a thiophene moiety positioned between the body structure and an alkyne moiety; and
wherein one or more elements of the conductive ligand are capable of removing or adding charges to a nanostructure upon attachment to a surface of the nanostructure, thereby modifying charge transport across a nanostructure-containing matrix.