Band excitation method applicable to scanning probe microscopy

US9535087B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9535087-B2
Application numberUS-201514752387-A
CountryUS
Kind codeB2
Filing dateJun 26, 2015
Priority dateSep 1, 2006
Publication dateJan 3, 2017
Grant dateJan 3, 2017

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  2. Abstract

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Abstract

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Scanning probe microscopy may include a method for generating a band excitation (BE) signal and simultaneously exciting a probe at a plurality of frequencies within a predetermined frequency band based on the excitation signal. A response of the probe is measured across a subset of frequencies of the predetermined frequency band and the excitation signal is adjusted based on the measured response.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method, comprising: generating a band excitation signal; simultaneously exciting a probe at a plurality of frequencies within a predetermined frequency band based on the band excitation signal; scanning a sample held in an apparatus to measure a response of the probe across a subset of frequencies of the predetermined frequency band; separately extracting, by a processor of a relevant dynamic parameter extractor, resonant frequency, maximum amplitude, and Q factor parameters associated with each position crossed during the scan; and adjusting the band excitation signal based on the extracting. 2. The method of claim 1 , further comprising performing a mathematical transform on the measured response of the probe and outputting an amplitude-frequency data and phase-frequency data at each scanned position of the sample. 3. The method of claim 2 , wherein the mathematical transform is selected from the group consisting of an integral transform and a discrete transform. 4. The method of claim 2 , wherein the relevant dynamic parameter extractor extracts the resonant frequency, the maximum amplitude, and the Q factor parameters for each position of the sample based on an analysis of the amplitude frequency data and the phase-frequency data. 5. The method of claim 1 , wherein the relevant dynamic parameter extractor extracts the resonant frequency, the maximum amplitude, and the Q factor parameters independently for each position. 6. The method of claim 1 , wherein the subset of frequencies of the predetermined frequency band includes a selected frequency and associated resonance frequencies. 7. The method of claim 1 , wherein the subset of frequencies is substantially the same as the predetermined frequency band. 8. The method of claim 1 , wherein the band excitation signal includes a controlled amplitude and phase density within the predetermined frequency band. 9. The method of claim 1 , wherein the adjusting the band excitation signal is based on the extracted resonant frequency, maximum amplitude, and Q factor parameters.

Assignees

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Classifications

  • AC mode · CPC title

  • Methods or apparatus for measurement or analysis of nanostructures · CPC title

  • G01Q10/06Primary

    Circuits or algorithms therefor · CPC title

  • G01Q20/00Primary

    Monitoring the movement or position of the probe · CPC title

  • Display or data processing devices · CPC title

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What does patent US9535087B2 cover?
Scanning probe microscopy may include a method for generating a band excitation (BE) signal and simultaneously exciting a probe at a plurality of frequencies within a predetermined frequency band based on the excitation signal. A response of the probe is measured across a subset of frequencies of the predetermined frequency band and the excitation signal is adjusted based on the measured response.
Who is the assignee on this patent?
Ut Battelle Llc
What technology area does this patent fall under?
Primary CPC classification G01Q10/06. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Jan 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).