Highly active, robust and versatile multifunctional, fully non-noble metals based electro-catalyst compositions and methods of making for energy conversion and storage
US-2021184226-A1 · Jun 17, 2021 · US
US12491499B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12491499-B2 |
| Application number | US-202318185106-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 16, 2023 |
| Priority date | Mar 16, 2023 |
| Publication date | Dec 9, 2025 |
| Grant date | Dec 9, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method of degrading a dye in an aqueous solution including contacting nanoparticles with the dye in the aqueous solution and irradiating the aqueous solution. The nanoparticles have a formula of Zn 1-2x Ce x Yb x O, x=0.01-0.1, and where at least 90 wt. % of the dye is degraded during the irradiating of the aqueous solution.
Opening claim text (preview).
The invention claimed is: 1 . A method of degrading a dye in an aqueous solution, comprising: contacting nanoparticles with the dye in the aqueous solution; and irradiating the aqueous solution, wherein the nanoparticles have a formula of Zn 1-2x Ce x Yb x O, x=0.01-0.1, and wherein at least 90 wt. % of the dye is degraded during the irradiating. 2 . The method of claim 1 , wherein the nanoparticles have an average crystallite size of less than 40 nm. 3 . The method of claim 1 , wherein the nanoparticles have an average crystallite size of 51-53 nm. 4 . The method of claim 1 , wherein the nanoparticles have a unit cell volume of 47.62-47.75 Å 3 . 5 . The method of claim 1 , wherein the ZnO of the nanoparticles have a hexagonal crystal system, and wherein at least a portion of the Zn is replaced with Ce and Yb. 6 . The method of claim 1 , wherein the nanoparticles have a nanorod shape. 7 . The method of claim 6 , wherein the nanorod shape has a length of 150-250 nm. 8 . The method of claim 6 , wherein the nanorod shape has a width of 50-70 nm. 9 . The method of claim 1 , wherein the nanoparticles have a zeta potential of 10-20 mV. 10 . The method of claim 1 , wherein the nanoparticles have a bandgap of 3.21 to 3.25 eV. 11 . The method of claim 1 , wherein the nanoparticles further comprise 0.1-1 wt. % Yb 0.3 Ce 0.4 O 1.85 , based on the total weight of the nanoparticles. 12 . The method of claim 1 , wherein the dye is selected from the group consisting of methylene orange, methylene blue, methyl red, phenolphthalein, bromothymol blue, and congo red. 13 . The method of claim 1 , wherein the irradiating comprises light with a wavelength of 300-700 nm. 14 . A method of claim 1 , wherein the degrading of the dye has a rate constant of at least 0.02 min −1 . 15 . The method of claim 1 , wherein 0.1 to 10 mg/mL of the nanoparticles are present in the aqueous solution. 16 . A method of claim 1 , wherein the aqueous solution has a temperature of 50 to 70° C. 17 . The method of claim 1 , wherein the aqueous solution further comprises at least one ionic species selected from the group consisting of ions of alkali metals, alkaline earth metals, halides, carbonates, phosphates, and sulfates. 18 . The method of claim 1 , wherein the nanoparticles are made by a method comprising: mixing separately three solutions of a zinc salt, an ytterbium salt, and a cerium salt each in water; mixing together the three solutions at a temperature of 70-90° C. for 30-120 mins to form a reaction mixture; adjusting the pH of the reaction mixture to 7 with a base to form a second reaction mixture; evaporating the water from the second reaction mixture to form a gel; combusting the gel to form a powder; and calcining the powder at a temperature of 400 to 600° C. 19 . The method of claim 1 , wherein the irradiating is for less than 120 minutes.
Metal or metal oxide crystallite size · CPC title
Photocatalytic properties · CPC title
Electric or magnetic properties · CPC title
in a colloidal state · CPC title
to form a gel or a cogel · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.