Coatings for relatively movable surfaces
US-9150410-B2 · Oct 6, 2015 · US
US9487397B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9487397-B2 |
| Application number | US-201514844779-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 3, 2015 |
| Priority date | Dec 18, 2012 |
| Publication date | Nov 8, 2016 |
| Grant date | Nov 8, 2016 |
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 device has a microelectromechanical system (MEMS) component with at least one surface and a coating disposed on at least a portion of the surface. The coating has a compound of the formula M(CnF2n+1Or), wherein M is a polar head group and wherein n≧2r. The value of n may range from 2 to about 20, and the value of r may range from 1 to about 10. The value of n plus r may range from 3 to about 30, and a ratio of n:r may have a value of about 2:1 to about 20:1.
Opening claim text (preview).
The invention claimed is: 1. A method of fabricating a microelectromechanical system (MEMS) device comprising: forming a MEMS component having a surface; and coating at least a portion of the surface with a compound of the formula M(C n F 2n+1 O r ), wherein M comprises a polar head group, and wherein n≧2r. 2. The method of claim 1 , wherein the polar head group comprises a central atom having a coordination number of 3, 4, or 5. 3. The method of claim 2 , wherein the polar head group comprises an oxygen atom bound to the central atom. 4. The method of claim 3 , wherein the polar head group comprises a hydroxyl functional group bound to the central atom. 5. The method of claim 1 , wherein the polar head group comprises at least one functional group selected from the group consisting of: a carboxylic acid functional group; a sulfonic acid functional group, a phosphonic acid functional group, an amide functional group, and a hydroxamide functional group. 6. The method of claim 1 , wherein n has a value ranging from 2 to about 20. 7. The method of claim 1 , wherein r has a value ranging from 1 to about 10. 8. The method of claim 1 , wherein n+r ranges from 3 to about 30. 9. The method of claim 1 , wherein a ratio of n:r has a value of about 2:1 to about 20:1. 10. The method of claim 1 , wherein the MEMS component comprises a digital micromirror device. 11. The method of claim 1 , wherein the MEMS component comprises at least one of an actuator, a motor, an RF switch, a sensor, a variable capacitor, an optical modulator, a microgear, an accelerometer, a transducer, a fluid nozzle, a gyroscope, or any combination thereof. 12. The method of claim 1 , wherein the compound is coated on the at least the portion of the surface as a self-assembling monolayer. 13. The method of claim 1 , wherein a polydispersity of the compound is less than about 2.0. 14. The method of claim 1 , wherein the compound comprises at least one material selected from the group consisting of: a perfluoropoly(alkylene) monoether carboxylic acid, a perfluoro(alkylene) monoether sulfonic acid, a perfluoro(alkylene) monoether phosphonic acid, a perfluoro(alkylene) monoether carboxamide, and a perfluoro(alkylene) monoether hydroxamide, a perfluoropoly(alkylene) polyether carboxylic acid, a perfluoro(alkylene)polyether sulfonic acid, a perfluoro(alkylene)polyether phosphonic acid, a perfluoro(alkylene)polyether carboxamide, and a perfluoro(alkylene)polyether hydroxamide. 15. The method of claim 1 , wherein the compound comprises at least one material selected from the group consisting of: perfluoro-3-oxadecanoic acid, perfluoro-2-oxaoctane-sulfonic acid, perfluoro-2-oxaoctane-phosphonic acid, N-hydroxy-perfluoro-2-oxaoctanamide, perfluoro-4-oxaheptanoic acid, perfluoro-4-oxaoctanoic acid, perfluoro-4-oxanonanoic acid, perfluoro-4-oxadecanoic acid, perfluoro-3-oxaundecanoic acid, perfluoro-3,6-dioxadodecanoic acid, perfluoro-3,6,9-trioxatridecanoic acid, and perfluoro-3,6,9,12-tetraoxatetrdecanoic acid.
Organic materials, e.g. photoresists · CPC title
Packages or encapsulation (processes for packaging MEMS B81C1/00261; packaging of smart-MEMS B81C1/0023) · CPC title
Cross-Sectional Technologies · mapped topic
Anti-stiction coatings · CPC title
For avoiding stiction when the device is in use, i.e. after manufacture has been completed · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.