US2015225838A1PendingUtilityA1

Directed surface functionalization on selected surface areas of topographical features with nanometer resolution

Assignee: IBMPriority: Oct 15, 2013Filed: Apr 24, 2015Published: Aug 13, 2015
Est. expiryOct 15, 2033(~7.2 yrs left)· nominal 20-yr term from priority
C23C 14/221C23C 14/225B82Y 5/00G01N 33/551G01N 33/48721G01N 33/54373C23C 14/22B82Y 15/00C23C 14/34G01N 33/553C23C 14/12C23C 14/046G01N 33/533
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Claims

Abstract

A method for making a single molecule receptor in a nanopore structure includes depositing a material by a physical vapor deposition (PVD) technique onto a selected interior surface of a nanochannel and functionalizing a surface of the material with a chemical compound having at least two functional groups. The material forms a patch having a diameter of about 3 to about 10,000 nanometers (nm). Also disclosed are embodiments of a nanopore structure including a single molecule receptor.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for making a single molecule receptor in a nanopore structure, the method comprising:
 tilting the nanopore structure at an angle with respect to a beam to position the beam onto a selected interior surface of a nanochannel in the nanopore structure, the beam being operative to deposit a material by a PVD technique;   operating the beam to deposit the material onto a selected interior surface of the nanochannel, the material forming a patch having a surface area of about 3 to about 10,000 nm 2 ; and   functionalizing a surface of the patch to form the single molecule receptor.   
     
     
         2 . The method of  claim 1 , wherein functionalizing is depositing a chemical compound onto a surface of the patch, and the chemical compound comprises a first functional group that forms a contact product with the material, a second functional group that forms a contact product with an analyte, and a linker connecting the first functional group to the second functional group. 
     
     
         3 . The method of  claim 2 , wherein the linker is a hydrocarbon, a peptide, a synthetic polymer, or any combination thereof. 
     
     
         4 . The method of  claim 2 , wherein the first functional group is a an acyl halide group, an amine group, an amide group, an alcohol group, a carboxylate thiol group, a nitrile group, a phosphate group, a phosphine group, silane group, a sulfate group, a sulfide group, a sulfite group, thiol group, a thiolate group, or any combination thereof. 
     
     
         5 . The method of  claim 1 , wherein the beam is an electron beam, an ion beam, or a combination thereof. 
     
     
         6 . The method of  claim 1 , wherein the angle is between about 1° and about 52°. 
     
     
         7 . The method of  claim 1 , wherein the nanochannel diameter is about 30 to about 100 nm. 
     
     
         8 . The method of  claim 1 , further comprising forming a self-assembled monolayer on at least a portion of an interior surface of the nanochannel. 
     
     
         9 . The method of  claim 8 , wherein the self-assembled monolayer comprises silane groups.

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