Zinc chalcogenides, doped zinc chalcogenides, and methods of making
View Patent ↗A process of preparing a zinc chalcogenide includes providing a solution of 8-hydroxyquinoline; a zinc precursor; and a reaction solvent; isolating a precipitate from the solution; and calcining the precipitate to form the zinc chalcogenide. Additionally, a polymer composite may include a polymer, bis(8-hydroxyquinolinato)zinc, and elemental sulfur or bis(8-hydroxyquinolinato) z M, wherein M is a metal ion and the value of z is equivalent to the oxidation state of the metal ion.
1. A process of preparing a doped zinc chalcogenide, the process comprising:
providing a solution comprising 8-hydroxyquinoline; a zinc precursor; a dopant precursor; and a reaction solvent;
isolating a precipitate from the solution; and
calcining the precipitate to form the doped zinc chalcogenide.
2. The process of claim 1 , wherein the zinc precursor is a zinc salt.
3. The process of claim 1 , wherein the zinc precursor is zinc chloride, zinc bromide, zinc nitrate, or zinc acetate.
4. The process of claim 1 , wherein the reaction solvent is an alcohol or an ether.
5. The process of claim 1 , further comprising heating the solution at a temperature, and for a time period, sufficient to produce the precipitate, prior to the isolating step.
6. The process of claim 5 , wherein the temperature is the refluxing temperature of the reaction solvent.
7. The process of claim 5 , wherein the time period is about 10 minutes to about 10 hours, about 30 minutes to about 10 hours, about 10 minutes to about 8 hours, about 30 minutes to about 8 hours, about 1 hour to about 8 hours, about 3 hours to about 8 hours, about 4 hours to about 6 hours, or is about 5 hours.
8. The process of claim 1 , further comprising washing the precipitate with a wash solvent before the calcining step and after the isolating step.
9. The process of claim 8 , wherein the wash solvent is an alcohol or an ether.
10. The process of claim 1 , wherein the doped zinc chalcogenide is a doped zinc oxide.
11. The process of claim 10 , wherein the doped zinc chalcogenide is Cd:ZnO or Mn:ZnO.
12. The process of claim 1 , wherein the dopant precursor comprises a metal salt or metal alkoxide.
13. The process of claim 1 , wherein the dopant precursor comprises manganese(II) chloride, manganese(II) bromide, cadmium(II) chloride, cadmium(II) bromide, manganese(II) Acetate, cadmium(II) Acetate.
14. The process of claim 1 , wherein the solution further comprises a sulfur reagent.
15. The doped zinc chalcogenide prepared by the process of claim 14 .
16. The process of claim 14 , wherein the sulfur reagent is elemental sulfur, a thiourea, an alkali sulfide, an alkali polysulfide, an alkali hydrosulfide, a quaternary ammonium sulfide, a quaternary ammonium polysulfide, a quaternary ammonium hydrosulfide, an organic polysulfide, or a thiol of the formula R—SH, wherein R is a C 1 -C 10 alkyl, C 1 -C 10 alkenyl, C 1 -C 10 alkynyl, C 3 -C 6 aryl, or a substituted analog thereof.
17. The process of claim 1 , wherein the doped zinc chalcogenide is a doped zinc sulfide.
18. The process of claim 1 further comprising combining the precipitate with a polymer before the calcining step and after the isolating step to form a polymer composite.
19. The doped zinc chalcogenide prepared by the process of claim 1 .