Microwave assisted synthesis of metal oxyhydroxides

Patent metadata

Field	Value
Publication number	US-2017314142-A1
Application number	US-201715581387-A
Country	US
Kind code	A1
Filing date	Apr 28, 2017
Priority date	Apr 29, 2016
Publication date	Nov 2, 2017
Grant date	—

Abstract

A method for making a metal oxyhydroxide electrocatalytic material comprises titrating a precursor solution with a (bi)carbonate salt, the precursor solution comprising a first metal salt and a solvent, wherein the titration induces reactions between the (bi)carbonate salt and the first metal salt to provide first metal carbonate species in the titrated precursor solution; and exposing the titrated precursor solution to microwave radiation to decompose the first metal carbonate species to form the metal oxyhydroxide electrocatalytic material and carbon dioxide. Mixed metal oxyhydroxide electrocatalytic materials such as nickel-iron oxyhydroxide may be formed. Also provided are the materials themselves, electrocatalytic systems comprising the materials, and methods of using the materials and systems.

First claim

What is claimed is:

1 . A method for making a metal oxyhydroxide electrocatalytic material, the method comprising:
(a) titrating a precursor solution with a (bi)carbonate salt, the precursor solution comprising a first metal salt and a solvent, wherein the titration induces reactions between the (bi)carbonate salt and the first metal salt to provide first metal carbonate species in the titrated precursor solution; and (b) exposing the titrated precursor solution to microwave radiation to decompose the first metal carbonate species to form the metal oxyhydroxide electrocatalytic material and carbon dioxide.

2 . The method of claim 1 , wherein the solvent is water.

3 . The method of claim 1 , wherein the titration is carried out at about room temperature and atmospheric pressure.

4 . The method of claim 1 , wherein the titration is carried out by adding the (bi)carbonate salt to the precursor solution at a rate of from about 0.5 mL/min to about 10 mL/min per 100 mL of the precursor solution for a period of time in the range of from about 15 min to about 120 min.

5 . The method of claim 1 , further comprising forming the precursor solution.

6 . The method of claim 1 , further comprising depositing the microwaved, titrated precursor solution onto a substrate to form a film of the metal oxyhydroxide electrocatalytic material on the substrate.

7 . The method of claim 1 , wherein the precursor solution further comprises a second metal salt wherein the titration also induces reactions between the (bi)carbonate salt and the second metal salt to provide second metal carbonate species in the titrated precursor solution and further wherein the microwave exposure also decomposes the second metal carbonate species to form a mixed metal oxyhydroxide electrocatalytic material.

8 . The method of claim 7 , wherein the metals of the mixed metal oxyhydroxide electrocatalytic material are selected from transition metals, post-transition metals and metalloids.

9 . The method of claim 8 , wherein the metals of the mixed metal oxyhydroxide electrocatalytic materials are selected from Fe, Co, Ni, W, In, Sb, Pb, and Bi.

10 . The method of claim 7 , wherein the mixed metal oxyhydroxide electrocatalytic material is a nickel-iron oxyhydroxide electrocatalytic material.

11 . The method of claim 10 , wherein the nickel-iron oxyhydroxide electrocatalytic material is Ni 0.8 :Fe 0.2 oxyhydroxide.

12 . The method of claim 1 , wherein the metal oxyhydroxide electrocatalytic material has a morphology characterized as a substantially continuous matrix having irregularly shaped pores distributed throughout the matrix as determined by scanning electron microscopy.

13 . The method of claim 1 , wherein the metal oxyhydroxide electrocatalytic material is nanoamorphous as determined by high resolution transmission electron microscopy electron diffraction patterns exhibiting a lack of selected area electron diffraction spots at about a 5 nm spatial resolution.

14 . The method of claim 1 , wherein the metal oxyhydroxide electrocatalytic material is characterized by a homogeneous distribution of metal atoms throughout the material as exhibited by oxygen (O) 1s X-ray photoelectron spectroscopy spectra having no more than a single peak.

15 . The method of claim 1 , wherein the metal oxyhydroxide electrocatalytic material has a morphology characterized as a substantially continuous matrix having irregularly shaped pores distributed throughout the matrix as determined by scanning electron microscopy;
wherein the metal oxyhydroxide electrocatalytic material is nanoamorphous as determined by high resolution transmission electron microscopy electron diffraction patterns exhibiting a lack of selected area electron diffraction spots at about a 5 nm spatial resolution; and further wherein the metal oxyhydroxide electrocatalytic material is characterized by a homogeneous distribution of metal atoms throughout the material as exhibited by oxygen (O) 1s X-ray photoelectron spectroscopy spectra having no more than a single peak.

16 . The method of claim 15 , wherein the metal oxyhydroxide electrocatalytic material is a nickel-iron oxyhydroxide electrocatalytic material.

17 . A metal oxyhydroxide electrocatalytic material having a morphology characterized as a substantially continuous matrix having irregularly shaped pores distributed throughout the matrix as determined by scanning electron microscopy;
wherein the metal oxyhydroxide electrocatalytic material is nanoamorphous as determined by high resolution transmission electron microscopy electron diffraction patterns exhibiting a lack of selected area electron diffraction spots at about a 5 nm spatial resolution; and further wherein the metal oxyhydroxide electrocatalytic material is characterized by a homogeneous distribution of metal atoms throughout the material as exhibited by oxygen (O) 1s X-ray photoelectron spectroscopy spectra having no more than a single peak.

18 . The material of claim 17 , wherein the metal oxyhydroxide electrocatalytic material is a mixed metal oxyhydroxide electrocatalytic material.

19 . The material of claim 18 , wherein metals of the mixed metal oxyhydroxide electrocatalytic material are selected from transition metals, post-transition metals and metalloids.

20 . The material of claim 18 , wherein the mixed metal oxyhydroxide electrocatalytic material is a nickel-iron oxyhydroxide electrocatalytic material.

Assignees

• Univ Kansas

Inventors

• Leonard Kevin C
• Barforoush Joseph M
• Seuferling Tess E
• Song Kelly R

Classifications

• C25B11/04 Primary

  characterised by the material · CPC title

• C25B1/003 Primary

  Chemistry & Metallurgy · mapped topic

• C25B11/077

  the compound being a non-noble metal oxide · CPC title

• C25B11/055

  characterised by the substrate or carrier material · CPC title

• C25B11/075

  consisting of a single catalytic element or catalytic compound · CPC title