Method for synthesis of blue-emitting ZnSe1-xTEx alloy nanocrystals
The invention relates to highly luminescent nanostructures, particularly highly luminescent nanostructures comprising a ZnSe 1-x Te x core and ZnS and/or ZnSe shell layers. The invention also relates to methods of producing such nanostructures.
1. A method of producing a ZnSe 1-x Te x nanocrystal comprising:
(a) admixing a selenium source and at least one ligand to produce a reaction mixture; and
(b) contacting the reaction mixture obtained in (a) with a zinc source and a solution comprising a tellurium source, a reducing agent, and a zinc carboxylate;
to provide a ZnSe 1-x Te x nanocrystal.
2. The method of claim 1 , wherein the selenium source in (a) is selected from the group consisting of trioctylphosphine selenide, tri(n-butyl)phosphine selenide, tri(secbutyl) phosphine selenide, tri(tert-butyl)phosphine selenide, trimethylphosphine selenide, triphenylphosphine selenide, diphenylphosphine selenide, phenylphosphine selenide, cyclohexylphosphine selenide, octaselenol, dodecaselenol, selenophenol, elemental selenium, hydrogen selenide, bis(trimethylsilyl) selenide, and mixtures thereof.
3. The method of claim 1 , wherein the zinc source in (b) is selected from the group consisting of diethylzinc, dimethylzinc, diphenylzinc, zinc acetate, zinc acetylacetonate, zinc iodide, zinc bromide, zinc chloride, zinc fluoride, zinc carbonate, zinc cyanide, zinc nitrate, zinc oxide, zinc peroxide, zinc perchlorate, and zinc sulfate.
4. The method of claim 1 , wherein the tellurium source in (b) is selected from the group consisting of trioctylphosphine telluride, tri(n-butyl)phosphine telluride, trimethylphosphine telluride, triphenylphosphine telluride, tricyclohexylphosphine telluride, elemental tellurium, hydrogen telluride, bis(trimethylsilyl) telluride, and mixtures thereof.
5. The method of claim 1 , wherein the reducing agent in (b) is selected from the group consisting of diborane, sodium hydride, sodium borohydride, lithium borohydride, sodium cyanoborohydride, calcium hydride, lithium hydride, lithium aluminum hydride, diisobutylaluminum hydride, sodium triethylborohydride, and lithium triethylborohydride.
6. The method of claim 1 , wherein the zinc carboxylate in (b) is selected from the group consisting of zinc oleate, zinc hexanoate, zinc octanoate, zinc laurate, zinc myristate, zinc palmitate, zinc stearate, zinc dithiocarbamate, or mixtures thereof.
7. The method of claim 1 , further comprising:
(c) contacting the reaction mixture in (b) with a zinc source and a selenium source.
8. The method of claim 7 , wherein the zinc source in (c) is selected from the group consisting of diethylzinc, dimethylzinc, diphenylzinc, zinc acetate, zinc acetylacetonate, zinc iodide, zinc bromide, zinc chloride, zinc fluoride, zinc carbonate, zinc cyanide, zinc nitrate, zinc oxide, zinc peroxide, zinc perchlorate, and zinc sulfate.
9. The method of claim 7 , wherein the selenium source in (c) is selected from the group consisting of trioctylphosphine selenide, tri(n-butyl)phosphine selenide, tri(secbutyl) phosphine selenide, tri(tert-butyl)phosphine selenide, trimethylphosphine selenide, triphenylphosphine selenide, diphenylphosphine selenide, phenylphosphine selenide, cyclohexylphosphine selenide, octaselenol, dodecaselenol, selenophenol, elemental selenium, hydrogen selenide, bis(trimethylsilyl) selenide, and mixtures thereof.
10. The method of claim 1 , wherein the selenium source in (a) is trioctylphosphine selenide, the zinc source in (b) is diethylzinc, the tellurium source in (b) is trioctylphosphine telluride, the reducing agent in (b) is lithium triethylborohydride, and the zinc carboxylate in (b) is zinc oleate.
11. The method of claim 7 , wherein the selenium source in (a) and (c) is trioctylphosphine selenide, the zinc source in (b) and (c) is diethylzinc, the tellurium source in (b) is trioctylphosphine telluride, the reducing agent in (b) is lithium triethylborohydride, and the zinc carboxylate in (b) is zinc oleate.