Methods for preparation of nanocrystals using a weak electron transfer agent and mismatched shell precursors

Patent metadata

Field	Value
Publication number	US-9937560-B2
Application number	US-200913122117-A
Country	US
Kind code	B2
Filing date	Oct 2, 2009
Priority date	Oct 3, 2008
Publication date	Apr 10, 2018
Grant date	Apr 10, 2018

Abstract

Methods for preparing core/shell nanocrystals are provided, using mismatched shell precursors and an electron transfer agent to control the nucleation and growth phases of particle formation. One method includes forming a reaction mixture comprising a plurality of nanocrystals, a first shell precursor, a second shell precursor, a weak electron transfer agent, and optionally a solvent, wherein, the first shell precursor and the second shell precursor have different oxidation states; and heating the reaction mixture to a temperature high enough to induce formation of the shell on each of the plurality of nanocrystals.

First claim

What is claimed is:

1. A method for forming shells on a population of nanocrystals, comprising:
forming a reaction mixture comprising a plurality of core nanocrystals, a first semiconductor shell precursor, a second semiconductor shell precursor, a weak reducing agent comprising an unsaturated hydrocarbon group, wherein the hydrocarbon group is linked to a carboxylate group, and optionally a coordinating solvent, wherein the first shell precursor and the second shell precursor have different oxidation states, wherein the second shell precursor is elemental sulfur, selenium or tellurium, or R 3 P=X, wherein X is S, Se or Te, and each R is independently H or a C 1 -C 24 hydrocarbon group, and the reaction mixture is substantially free of a strong reducing agent, wherein the strong reducing agent is one that induces nucleation of the shell precursors in the absence of the nanocrystal core under the conditions of the shell-forming reaction, wherein the reaction mixture is formed in the absence of heating; and
heating the reaction mixture to a temperature high enough to induce formation of a shell on each of the plurality of core nanocrystals, whereby the oxidation state of the first shell precursor or the second shell precursor are changed using the weak reducing agent such that the first shell precursor and the second shell precursor can react to form a semiconductor shell around each of the plurality of core nanocrystals, wherein the shell is different from the core, wherein the number of nanocrystals composed of just shell precursors is less than 5% of the population of nanocrystals.

2. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the shell formation reaction occurs in a batch reactor system.

3. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the shell formation reaction occurs in a continuous flow reactor system.

4. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the oxidation states of the first shell precursor or the second shell precursor is changed to a neutral state by the weak reducing agent.

5. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the oxidation states of the first shell precursor and the second shell precursor are matched by the weak reducing agent.

6. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the first shell precursor is a zinc salt or a cadmium salt.

7. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the second shell precursor is selected from S 0 , Se 0 , Te 0 , R 3 P=S, R 3 P=Se, and R 3 P=Te, wherein each R is independently H, or a C 1 -C 24 hydrocarbon group.

8. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the weak reducing agent is one that does not induce nucleation of the shell precursors in the absence of the nanocrystal under the conditions of the shell-forming reaction.

9. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the shell precursors are added as quickly as temperature control will permit, avoiding the need for slow addition of at least one precursor to reduce nucleation.

10. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the first shell precursor and the second shell precursor do not form a shell around each of the plurality of nanocrystals under the same reaction conditions when the weak electron transfer agent is omitted.

11. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein an excess of the weak reducing agent is present in the reaction mixture.

12. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein shell formation occurs at least about 50% faster in the presence of the weak reducing agent than it would in the absence of the weak reducing agent.

13. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the first shell precursor is a carboxylic acid salt or a phosphonic acid salt of Cd or Zn.

14. The method for forming shells on a population of nanocrystals, as recited in claim 13 , wherein the salt of Cd or Zn is a salt of the form M(O 2 CR)X, wherein M is Cd or Zn; X is a halide or O 2 CR; and R is a C 4 -C 24 alkyl group that is optionally unsaturated.

15. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the nanocrystal core is selected from the group consisting of CdSe, CdS, CdTe, ZnTe, ZnSe, ZnS, InP, InAs and GaP.

16. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the semiconductor shell is selected from the group consisting of ZnS, ZnSe, ZnTe, CdSe, CdTe and CdS.

17. The method for forming shells on a population of nanocrystals, as recited in claim 1 , wherein the solvent comprises an alkylamine of formula R—NH 2 , a dialkylamine of formula R 2 NH, an alkane, or an alkene, and optionally further comprises a phosphine oxide of the formula R 3 P=O, wherein each R is independently a C 4 -C 24 alkyl group that is optionally unsaturated.

18. The method of claim 1 , wherein the reaction mixture is heated to a temperature high enough to change the oxidation state of the first shell precursor or the second shell precursor such that the first shell precursor and the second shell precursor can react to form a shell around each of the plurality of nanocrystals.

Assignees

• Tulsky Eric
• Bartel Joseph
• Treadway Joseph
• Life Technologies Corp

Inventors

• Tulsky Eric
• Bartel Joseph
• Treadway Joseph

Classifications

• B22F9/24 Primary

  starting from liquid metal compounds, e.g. solutions · CPC title

• C01P2004/64

  Nanometer sized, i.e. from 1-100 nanometer · CPC title

• C01B17/20

  Methods for preparing sulfides or polysulfides, in general (ammonium sulfides or polysulfides C01C; sulfides or polysulfides of metals, other than alkali metals, magnesium, calcium, strontium and barium, see the relevant groups of subclasses C01F or C01G, according to the metal) · CPC title

• B82Y30/00

  Nanotechnology for materials or surface science, e.g. nanocomposites · CPC title

• C01P2004/84

  one phase coated with the other · CPC title