Stable inp quantum dots with thick shell coating and method of producing the same

a quantum dots and thick shell technology, applied in the field of high-luminescent quantum dots, can solve the problems of cadmium, mercury, or lead posing serious threats to human health and the environment, prone to degradation mechanisms, and most quantum dots do not retain their original high quantum yield

Inactive Publication Date: 2018-05-03
NANOSYS INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The invention relates to making plastic products with improved light-emitting properties that have better energy conversion rates compared to traditional methods like incandescent lamps or fluorescence tubing used for analysis purposes. This can lead to more efficient use of electricity during production processes by reducing waste heat generation while also improving productivity.

Problems solved by technology

Technologies described in this patents involve creating small shell compositions containing quantum dyes called quantum diketones, specifically lanthanoquantum dithransistants (LDQ), where the presence of certain atoms affects the performance of the final product. Thermally induced changes occur upon removal of guest metal centres through interactions with other metallic surfaces. These technical problem addressed include controllability of particle sizes, reproducibility of shell dimensions, stabilization of dopant concentration, and minimizing impurities associated with the shell components themselves.

Method used

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  • Stable inp quantum dots with thick shell coating and method of producing the same
  • Stable inp quantum dots with thick shell coating and method of producing the same
  • Stable inp quantum dots with thick shell coating and method of producing the same

Examples

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example 1

[0286]The deposition of a thick ZnSe / ZnS multi-layered shell on a green InP core using zinc oleate, tri-n-butylphosphine selenide, and octanethiol as precursors at temperatures exceeding 280° C. is described. Synthesis of a green InP core is disclosed in U.S. Patent Appl. Publication No. 2014 / 0001405.

[0287]The stoichiometry was calculated for InP cores with an absorption peak at 470 nm, a concentration in hexane of 66.32 mg / mL, and a shell thickness of 3.5 monolayers of ZnSe and 4.5 monolayers of ZnS. Zinc oleate was prepared from zinc acetate and oleic acid as a solid. TBPSe was prepared from selenium pellets and tri(n-butyl)phosphine.

[0288]To a 250 mL 3 neck round-bottom flask was added 3.48 g (5.54 mmol, 13.38 equivalents) of zinc oleate and 33.54 mL of 1-octadecene at room temperature in air. The flask was equipped with a stir bar, a rubber septum, a Schlenk adaptor, and a thermocouple. The flask was connected to a Schlenk line via a rubber hose. Inert conditions were establi

example 2

[0295]The deposition of a thick ZnSe / ZnS multi-layered shell on a green InP core using zinc oleate, tri-n-butylphosphine selenide, and octanethiol as precursors at temperatures exceeding 280° C. is described. The resultant nanostructure had a target shell thickness of 1.5 monolayers of ZnSe and 2.5 monolayers of ZnS.

[0296]To a 100 mL 4 neck round-bottom flask was added 0.409 g (0.651 mmol, 3.1 equivalents) of zinc oleate and 2 mL of 1-octadecene at room temperature in air. The flask was equipped with a glass stopper, a rubber septum, a Schlenk adaptor, and a thermocouple. The flask was connected to a Schlenk line via a rubber hose. Inert conditions were established by at least three cycles of vacuum (<50 mtorr) and nitrogen flushing. The mixture was heated to 80° C. under nitrogen flow to afford a clear solution. The temperature was maintained and the flask was put under vacuum once again and pumped until no further gas evolution (<50 mtorr) was observed. The heating mantle was remov

example 3

[0303]Nanostructures with green InP cores with a target shell thickness of 1.5 monolayers of ZnSe and (A) 4.5 monolayers of ZnS; and (B) 7.5 monolayers of ZnS were prepared using the synthetic method of Example 2 and varying the amount of zinc oleate and octanethiol added to the reaction mixture. The following amounts of zinc oleate and octanethiol precursors were used to prepare the ZnS shell:

(A) for the 4.5 monolayers of ZnS:

[0304]4.47 g of zinc oleate; and

[0305]1.13 mL of octanethiol.

(B) for the 7.5 monolayers of ZnS:

[0306]11.44 g of zinc oleate; and

[0307]2.88 mL of octanethiol.

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Abstract

Highly luminescent nanostructures, particularly highly luminescent quantum dots, comprising a nanocrystal core and thick shells of ZnSe and ZnS, are provided. The nanostructures may have one or more gradient ZnSexS1-x monolayers between the ZnSe and ZnS shells, wherein the value of x decreases gradually from the interior to the exterior of the nanostructure. Also provided are methods of preparing the nanostructures comprising a high temperature synthesis method. The thick shell nanostructures of the present invention display increased stability and are able to maintain high levels of photoluminescent intensity over long periods of time. Also provided are nanostructures with increased blue light absorption.

Description

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Claims

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Application Information

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Owner NANOSYS INC
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