Core-shell quantum dot, preparation method, device and composition thereof
A technology of core-shell quantum dots and quantum dots, applied in the field of core-shell quantum dots, devices and compositions, and their preparation methods, can solve problems such as poor stability, difficult to control the etching process, and wide half-peak luminescence, and achieve stability Good, narrow half-width, high quantum efficiency effect
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[0058] The invention also provides a method for preparing the core-shell quantum dot, including the preparation of the quantum dot core and the preparation of the shell layer.
[0059] The preparation step of the quantum dot core is: mixing and heating the group III element precursor, the first ligand, the first solvent, and the optional Y element precursor to obtain a group III element mixture, wherein the Y element is selected from the following elements: One or several kinds: Zn, Mg, Ca, Sr, Ba, Ti, Zr, Cr, Mo, Mn, Fe, Co, Ni, Al, Ga, Si, group V element precursor, optional second The mixture of the ligand and the second solvent is added to the group III element mixture, and a solution containing quantum dot nuclei is obtained after heating and reacting. It is worth mentioning that the meaning of "optional Y element precursor" is: the Y element precursor can be added or not, and the meaning of "optional second ligand" is: the second ligand can Choose to add or not to add. ...
Embodiment 1
[0091] Weigh 0.2mmol In(Ac) 3 (indium acetate), 0.6mmol MA (myristic acid), 5.0g ODE (octadecene), were added to a 100mL three-necked flask, N 2 Heated to 200°C in the exhaust state to keep it warm. A mixture of 0.1 mmol TMS-P (tris(trimethylsilyl)phosphine) and 0.5 ml ODE (octadecene) was quickly injected, and the InP core solution was obtained after 10 min of reaction. Lower the reaction temperature to 150 °C, add 1.5 mmol ZnAC 2 (zinc acetate), exhaust for 30min, heat up to 260°C, add 1ml Se-TOP (0.1mmol / ml) (selenium-trioctylphosphine) to react for 10min, then add 0.8ml S-TOP (1mmol / ml) (sulfur -trioctylphosphine), reacted 30min, then added the AlMA of 0.5mmol 3 (aluminum myristate), and finally add 0.5 mmol of dodecanol to react for 20 min. After the reaction was completed, it was lowered to room temperature, extracted three times with methanol, and centrifuged with acetone precipitation, and the precipitate was dissolved in toluene to obtain an InP / ZnSe / ZnS / ZnAlO qua...
Embodiment 2
[0093] Weigh 0.2mmol In(Ac) 3 (indium acetate), 0.6mmol MA (myristic acid), 5.0g ODE (octadecene), were added to a 100mL three-necked flask, N 2 Heated to 200°C in the exhaust state to keep it warm. A mixture of 0.1 mmol TMS-P (tris(trimethylsilyl)phosphine) and 0.5 ml ODE (octadecene) was quickly injected, and the InP core solution was obtained after 10 min of reaction. Lower the reaction temperature to 150 °C, add 1.5 mmol ZnAC 2 (zinc acetate), exhaust for 30min, heat up to 260°C, add 1ml Se-TOP (0.1mmol / ml) (selenium-trioctylphosphine) and 0.8ml S-TOP (1mmol / ml) (sulfur-trioctyl Phosphine), reacted for 30min, then added 0.5mmol of AlMA 3 (aluminum myristate), and finally add 0.5 mmol of dodecanol to react for 20 min. After the reaction was completed, it was lowered to room temperature, extracted three times with methanol, and centrifuged with acetone precipitation, and the precipitate was dissolved in toluene to obtain an InP / ZnSeS / ZnAlO quantum dot solution. Its agin...
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