Two-dimensional mesoporous superlattices of inorganic materials and method of making and using same

Patent metadata

Field	Value
Publication number	US-12528705-B2
Application number	US-202017765766-A
Country	US
Kind code	B2
Filing date	Oct 5, 2020
Priority date	Oct 3, 2019
Publication date	Jan 20, 2026
Grant date	Jan 20, 2026

Abstract

Porous compositions and methods of making and using same. The compositions may be one or more layer(s) of mesoporous inorganic materials. The mesoporous inorganic material(s) may be a plurality of inorganic nanocages, which may be microporous. A composition may include homostacks of layers of the same inorganic mesoporous materials. A composition may include heterostacks of layers of inorganic mesoporous materials, where at least two of the layers are different. The compositions may be surface functionalized. The compositions may be formed in a reaction mixture including one or more precursor(s), one or more surfactant(s), water, and one or more organic solvent(s). The compositions may be formed at the liquid-liquid interface between the water and the one or more organic solvent(s). A composition may be used as a catalyst, in a catalytic method, as a separation medium, in a separation method, in nanomedicine applications, or the like.

First claim

The invention claimed is:

1 . A method of making a composition comprising two or more layer(s) of an inorganic mesoporous material, wherein each individual layer of inorganic mesoporous material comprises 1 to 100 monolayers of inorganic nanocages, the method comprising:
forming a reaction mixture comprising one or more precursor(s), one or more surfactant(s), water, optionally, one or more pH modifying agent(s), and one or more organic solvent(s), holding the reaction mixture at a time (t1) and temperature (T1); and optionally, adding a terminating agent to the reaction mixture, whereby an individual layer of inorganic mesoporous material is formed; and repeating the forming, holding, and, optionally, holding for each repetition of forming and holding, a desired number of times, whereby one or more additional individual layers of inorganic mesoporous materials are formed; and stacking the individual layer and additional individual layer(s), wherein at least two of the individual layer and/or the additional layer(s) are from different reaction mixtures and wherein the composition is formed.

2 . The method of claim 1 , wherein at least a portion of a surface of at least a portion of or all of the inorganic nanocages is/are functionalized.

3 . The method of claim 1 , wherein
the one or more surfactant(s) is/are chosen from C 8 to C 18 alkyltrimethylammonium halides, sodium dodecyl sulfate, N-myristoyl-L-glutamic acid, and combinations thereof, and/or the one or more organic solvent(s) is/are chosen from trialkylated benzenes, polymer monomers, hydrophobic solvents, and combinations thereof.

4 . The method of claim 1 , wherein the one or more surfactant(s) is/are chosen from cationic surfactants, anionic surfactants, neutral surfactants, and combinations thereof.

5 . The method of claim 1 , wherein the one or more surfactant(s) is/are present in the reaction mixture at a concentration of 1 mg/mL to 50 mg/mL and/or the one or more organic solvent(s) is/are present at a concentration of from 100 mg/mL to 600 mg/mL.

6 . The method of claim 1 , wherein the molar ratio of the one or more surfactant(s) to the one or more organic solvent(s) is 1:10,000 to 10:1.

7 . The method of claim 1 , wherein the one or more precursor(s) is/are one or more non-metal oxide precursor(s) chosen from silica precursors, alkyltrialkoxysilane precursors, tetraalkoxysilane precursors, functionalized non-metal oxide precursors, and combinations thereof.

8 . The method of claim 7 , wherein at least one of non-metal oxide precursors comprises one or more functional group(s).

9 . The method of claim 1 , wherein the terminating agent is a PEG-silane conjugate.

10 . The method of claim 9 , wherein before or after the PEG-silane conjugate is added, the method further comprises
adding a PEG-silane conjugate comprising a ligand at room temperature to the reaction mixture, holding the resulting reaction mixture at a time (t2) and temperature (T2), and subsequently heating the resulting reaction mixture at a time (t3) and temperature (T3), whereby inorganic nanocages surface functionalized with PEG groups comprising a ligand are formed.

11 . The method of claim 9 , wherein at least a portion of or all of the PEG-silane comprises a reactive group on a terminus of the PEG group of the PEG-silane conjugate opposite the terminus conjugated to the silane group of the PEG-silane conjugate and after formation of inorganic nanocages surface functionalized with PEG groups having a reactive group, and, optionally, PEG groups, are reacted with a second ligand functionalized with a second reactive group thereby forming inorganic nanocages surface functionalized with PEG groups functionalized with a second ligand and, optionally, PEG groups.

12 . The method of claim 1 , wherein the pH of the reaction mixture is 6 or greater.

13 . The method of claim 1 , wherein the one or more precursor(s) is/are one or more transition metal precursor(s) chosen from transition metal salts, transition metal alkoxides, transition metal coordination complexes, organometallic compounds, and combinations thereof.

14 . The method of claim 13 , wherein the transition metal salts are chosen from gold salts, silver salts, palladium salts, platinum salts, zirconium salts, iron salts, rhodium salts, copper salts, nickel salts, tantalum salts, hafnium salts, niobium salts, and combinations thereof.

15 . The method of claim 13 , wherein the terminating agent is a reducing terminating agent.

16 . The method of claim 15 , wherein the reducing terminating agent is chosen from tetrakis(hydroxymethyl)phosphonium chloride (THPC), bis[tetrakis(hydroxymethyl)phosphonium] sulfate (THPS), and combinations thereof.

17 . The method of claim 1 , wherein the one or more precursor(s) is/are one or more transition metal oxide precursor(s) chosen from transition metal alkoxides, transition metal salts, and combinations thereof.

18 . The method of claim 17 , wherein the transition metal alkoxides are chosen from vanadium alkoxides, titanium alkoxides, niobium alkoxides, zirconium alkoxides, tantalum alkoxides, hafnium alkoxides, copper alkoxides, nickel alkoxides, iron alkoxides, and combinations thereof.

19 . The method of claim 1 , wherein the one or more organic solvent(s) is/are present at a volume ratio of organic solvent(s) to water of 0.1:1 to 1.5:1.

20 . A method of making a composition comprising one or more layer(s) of an inorganic mesoporous material, wherein each individual layer of inorganic mesoporous material comprises 1 to 100 monolayers of inorganic nanocages, the method comprising:
forming a reaction mixture comprising one or more precursor(s), one or more surfactant(s), water, optionally, one or more pH modifying agent(s), and one or more organic solvent(s), wherein the one or more surfactant(s) is/are chosen from C 8 to C 18 alkyltrimethylammonium halides, sodium dodecyl sulfate, N-myristoyl-L-glutamic acid, and combinations thereof and/or the one or more organic solvent(s) is/are chosen from trialkylated benzenes, polymer monomers, hydrophobic solvents, and combinations thereof and/or the one or more organic solvent(s) is/are present at a volume ratio of organic solvent(s) to water of 0.1:1 to 1.5:1 and/or the pH of the reaction mixture is 6 or greater, holding the reaction mixture at a time (t1) and temperature (T1); and optionally, adding a terminating agent to the reaction mixture, whereby an individual layer of inorganic mesoporous material is formed; and optionally, repeating the forming, holding, and, optionally, holding for each repetition of forming and holding, a desired number of times, whereby one or more additional 15 individual layers of inorganic mesoporous materials are formed; and optionally, stacking the individual layer and additional individual layer(s), wherein the composition is formed.

21 . A method of making a composition comprising one or more layer(s) of an inorganic mesoporous material, wherein each individual layer of inorganic mesoporous material comprises 1 to 100 monolayers of inorganic nanocages, the method comprising:
forming a reaction mixture comprising one or more precursor(s), one or more surfactant(s), water, optionally, one or more pH modifying agent(s), and one or more organic solvent(s), holding the reaction mixture at a time (t1) and temperature (T1); and adding a terminating agent to the reaction mixture, wherein the terminating agent is a PEG-silane conj

Assignees

• Univ Cornell

Inventors

• Wiesner Ulrich B
• Ma Kai
• Aubert Tangi

Classifications

• C01P2006/16

  Pore diameter · CPC title

• C01P2002/30

  Three-dimensional structures · CPC title

• C01P2002/01

  depicted by a TEM-image · CPC title

• C01B33/26

  Aluminium-containing silicates {, i.e. silico-aluminates} · CPC title

• C01B37/02

  Crystalline silica-polymorphs, e.g. silicalites {dealuminated aluminosilicate zeolites} · CPC title