Nanoparticles wtih grafted organic molecules
Abstract
An apparatus for producing grafted Group IV nanoparticles is provided and includes a source of Group IV nanoparticles. A chamber is configured to carry the nanoparticles in a gas phase and has an inlet and an exit. The inlet configured to couple to an organic molecule source which is configured to provide organic molecules to the chamber. A plasma source is arranged to generate a plasma. The plasma causes the organic molecules to break down and/or activate in the chamber and bond to the nanoparticles. A method of producing grafted Group IV nanoparticles is also provided and includes receiving Group IV nanoparticles in a gas phase, creating a plasma with the nanoparticles, and allowing the organic molecules to break down and/or become activated in the plasma and bond with the nanoparticles.
Claims
exact text as granted — not AI-modified1 . An apparatus for producing grafted Group IV nanoparticles, comprising:
a source of Group IV nanoparticles; a chamber configured to carry the nanoparticles in a gas phase having an inlet and an exit; an organic molecule source coupled to the inlet configured to provide organic molecules to the chamber; a plasma source arranged to generate a plasma; and wherein the plasma causes the organic molecules to break down and/or become activated in the chamber and bond to the particles.
2 . The apparatus of claim 1 including at least one electrode coupled to the chamber and a radio frequency (RF) signal source coupled to the electrode configured to create a plasma to break down and/or activate organic molecules in the chamber whereby organic molecules in the chamber bond to the nanoparticles.
3 . The apparatus of claim 2 including a second electrode coupled to the chamber and driven by the radio frequency (RF) signal source.
4 . The apparatus of claim 1 including a filter coupled to the exit from the chamber arranged to receive particles from in the chamber.
5 . The apparatus of claim 4 wherein the filter comprises a wire mesh.
6 . The apparatus of claim 1 wherein the organic molecule source includes a gas source.
7 . The apparatus of claim 1 wherein the organic molecule source includes a liquid precursor.
8 . The apparatus of claim 1 wherein organic molecules are selected from the group of organic molecules consisting of 1-dodecene; Dodecane; Octyl-alcohol; 1-hexene; 1-hexyne; Hexane; Hexyl-alcohol; Hexyl-amine; 1-pentene; Acrylic acid; Allylamine; Ethylene-Diamine; Decyl-aldehyde (Decanal); Ethylene-glycol; compounds with saturated carbon bonds; compounds with one or more aromatic rings; compounds with unsaturated terminal functional group; alcohols (—OH), thiols (—SH), amines (—NH 2 ), aldehydes)-CH═O), carboxylic acids (—COOH); compounds with one or more aromatic rings or unsaturated terminal functional group and with more than one of the same functional group present in the same molecule; compounds with one or more aromatic rings or unsaturated terminal functional group and with different functional groups present in the same molecule.
9 . The apparatus of claim 1 wherein the organic molecule source includes a solid precursor or a gaseous precursor.
10 . The apparatus of claim 1 wherein the inlet for the organic molecule source is positioned in an afterglow of a plasma of the nanoparticles.
11 . The apparatus of claim 1 wherein the nanoparticles are generated from the nanoparticles sources consisting of plasmas, thermal methods, laser pyrolysis, laser photolysis, laser ablation, liquid phase reactions, combustion processes and flame processes.
12 . The apparatus of claim 1 wherein the Group IV nanoparticles comprise doped nanoparticles.
13 . The apparatus of claim 1 wherein the Group IV nanoparticles comprise silicon or germanium.
14 . The apparatus of claim 1 wherein the plasma also provides electromagnetic radiation (such as visible or ultraviolet radiation) to assist bonding of the organic molecules to the nanoparticles.
15 . The apparatus of claim 1 including a second source of nanoparticles.
16 . The apparatus of claim 1 including a second organic molecule source.
17 . A method of producing grafted Group IV nanoparticles, comprising:
receiving Group IV nanoparticles in a gas phase; creating a plasma to immerse the nanoparticles in; providing organic molecules to the nanoparticles; and allowing the organic molecules to break down and/or become activated in the plasma and bond with the nanoparticles.
18 . The method of claim 18 including collecting nanoparticles in a filter from the exit of the chamber.
19 . The method of claim 18 including applying an RF signal to an electrode to form the plasma.
20 . The method of claim 18 wherein providing organic molecules comprises providing a liquid, solid or gaseous precursor.
21 . The method of claim 21 including injecting a gas into the liquid precursor to thereby bubble the liquid precursor and provide the organic molecules.
22 . The method of claim 18 wherein the organic molecules are acetylene or methane.
23 . The method of claim 18 including injecting a gas into a liquid precursor.
24 . The method of claim 18 wherein the organic molecules are provided in an afterglow of a plasma of the nanoparticles.
25 . The method of claim 18 wherein the Group IV nanoparticles comprises silicon or germanium.
26 . The method of claim 18 including using the plasma to also provide a source of radiation to assist bonding of the organic molecules to the nanoparticles.
27 . The method of claim 17 wherein receiving nanoparticles comprises receiving doped nanoparticles.Cited by (0)
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