Magnetic resonance force microscopy

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Magnetic resonance force microscopy (MRFM) is an imaging technique that acquires magnetic resonance images (MRI) at nanometer scales, and possibly at atomic scales in the future. MRFM is potentially able to observe protein structures which cannot be seen using X-ray crystallography and protein nuclear magnetic resonance spectroscopy. Detection of the magnetic spin of a single electron has been demonstrated using this technique. The sensitivity of a current MRFM microscope is 10 billion times greater than a medical MRI used in hospitals.

Contents

Basic principle

The MRFM concept combines the ideas of magnetic resonance imaging (MRI) and atomic force microscopy (AFM). Conventional MRI employs an inductive coil as an antenna to sense resonant nuclear or electronic spins in a magnetic field gradient. MRFM uses a cantilever tipped with a ferromagnetic (iron cobalt) particle to directly detect a modulated spin gradient force between sample spins and the tip. The magnetic particle is characterized using the technique of cantilever magnetometry. As the ferromagnetic tip moves close to the sample, the atoms' nuclear spins become attracted to it and generate a small force on the cantilever. The spins are then repeatedly flipped, causing the cantilever to gently sway back and forth in a synchronous motion. That displacement is measured with an interferometer (laser beam) to create a series of 2-D images of the sample, which are combined to generate a 3-D image. The interferometer measures resonant frequency of the cantilever. Smaller ferromagnetic particles and softer cantilevers increase the signal-to-noise ratio. Unlike the inductive coil approach, MRFM sensitivity scales favorably as device and sample dimensions are reduced.

Because the signal-to-noise ratio is inversely proportional to the sample size, Brownian motion is the primary source of noise at the scale in which MRFM is useful. Accordingly, MRFM devices are cryogenically cooled. MRFM was specifically devised to determine the structure of proteins in situ.

Milestones

The basic principles of MRFM imaging and the theoretical possibility of this technology were first described in 1991. [1] The first MRFM image was obtained in 1993 at the IBM Almaden Research Center with 1-μm vertical resolution and 5-μm lateral resolution using a bulk sample of the paramagnetic substance diphenylpicrylhydrazyl. [2] The spatial resolution reached nanometer-scale in 2003. [3] Detection of the magnetic spin of a single electron was achieved in 2004. [4] In 2009 researchers at IBM and Stanford announced that they had achieved resolution of better than 10 nanometers, imaging tobacco mosaic virus particles on a nanometer-thick layer of adsorbed hydrocarbons. [5]

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Scanning probe microscopy (SPM) is a branch of microscopy that forms images of surfaces using a physical probe that scans the specimen. SPM was founded in 1981, with the invention of the scanning tunneling microscope, an instrument for imaging surfaces at the atomic level. The first successful scanning tunneling microscope experiment was done by Gerd Binnig and Heinrich Rohrer. The key to their success was using a feedback loop to regulate gap distance between the sample and the probe.

<span class="mw-page-title-main">Scanning transmission electron microscopy</span> Instrument that produces images by scanning electrons across a sample

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<span class="mw-page-title-main">Magnetic force microscope</span>

Magnetic force microscopy (MFM) is a variety of atomic force microscopy, in which a sharp magnetized tip scans a magnetic sample; the tip-sample magnetic interactions are detected and used to reconstruct the magnetic structure of the sample surface. Many kinds of magnetic interactions are measured by MFM, including magnetic dipole–dipole interaction. MFM scanning often uses non-contact AFM (NC-AFM) mode.

<span class="mw-page-title-main">Focused ion beam</span> Device

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<span class="mw-page-title-main">Magnetic resonance microscopy</span>

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Magnetic resonance can mean:

<span class="mw-page-title-main">Scanning thermal microscopy</span>

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<span class="mw-page-title-main">Piezoresponse force microscopy</span> Microscopy technique for piezoelectric materials

Piezoresponse force microscopy (PFM) is a variant of atomic force microscopy (AFM) that allows imaging and manipulation of piezoelectric/ferroelectric materials domains. This is achieved by bringing a sharp conductive probe into contact with a ferroelectric surface and applying an alternating current (AC) bias to the probe tip in order to excite deformation of the sample through the converse piezoelectric effect (CPE). The resulting deflection of the probe cantilever is detected through standard split photodiode detector methods and then demodulated by use of a lock-in amplifier (LiA). In this way topography and ferroelectric domains can be imaged simultaneously with high resolution.

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<span class="mw-page-title-main">Thermal scanning probe lithography</span>

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<span class="mw-page-title-main">Light sheet fluorescence microscopy</span> Fluorescence microscopy technique

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<span class="mw-page-title-main">Non-contact atomic force microscopy</span>

Non-contact atomic force microscopy (nc-AFM), also known as dynamic force microscopy (DFM), is a mode of atomic force microscopy, which itself is a type of scanning probe microscopy. In nc-AFM a sharp probe is moved close to the surface under study, the probe is then raster scanned across the surface, the image is then constructed from the force interactions during the scan. The probe is connected to a resonator, usually a silicon cantilever or a quartz crystal resonator. During measurements the sensor is driven so that it oscillates. The force interactions are measured either by measuring the change in amplitude of the oscillation at a constant frequency just off resonance or by measuring the change in resonant frequency directly using a feedback circuit to always drive the sensor on resonance.

<span class="mw-page-title-main">Infrared Nanospectroscopy (AFM-IR)</span> Infrared microscopy technique

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Quantum microscopy allows microscopic properties of matter and quantum particles to be measured and imaged. Various types of microscopy use quantum principles. The first microscope to do so was the scanning tunneling microscope, which paved the way for development of the photoionization microscope and the quantum entanglement microscope.

References

  1. J. A. Sidles (1991). "Noninductive detection of single-proton magnetic resonance". Applied Physics Letters. 58 (24): 2854–6. Bibcode:1991ApPhL..58.2854S. doi:10.1063/1.104757.
  2. O. Zuger & D. Rugar (1993). "First images from a magnetic resonance force microscope". Applied Physics Letters. 63 (18): 2496–8. Bibcode:1993ApPhL..63.2496Z. doi:10.1063/1.110460.
  3. S. Chao; W. Dougherty; J. Garbini; J. Sidles (2003). "Nanometer-scale magnetic resonance imaging". Review of Scientific Instruments. 75 (5): 1175–81. Bibcode:2004RScI...75.1175C. doi:10.1063/1.1666983.
  4. D. Rugar; R. Budakian; H. Mamin; B. Chui (2004). "Single spin detection by magnetic resonance force microscopy". Nature. 430 (6997): 329–32. Bibcode:2004Natur.430..329R. doi:10.1038/nature02658. PMID   15254532. S2CID   4346337.
  5. C. L. Degen; M. Poggio; H. J. Mamin; C. T. Rettner & D. Rugar (2009). "Nanoscale magnetic resonance imaging". PNAS. 106 (5): 1313–7. Bibcode:2009PNAS..106.1313D. doi: 10.1073/pnas.0812068106 . PMC   2628306 . PMID   19139397.