Reducing dimension. Crystalline structures

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Reducing dimension 2D surfaces, interfaces and quantum wells 1D carbon nanotubes, quantum wires and conducting polymers 0D nanocrystals, nanoparticles, lithographically patterned quantum dots Crystalline structures

Creation of nanostructures Top-down lithographic patterning Bottom-up growth and self-assembly Boundary at 50nm?

Top-down nanofabrication

Bottom-up Nanofabrication

Surface to bulk ratio N / N 3a / surf R For R = 6a ~1nm, more than ½ of the atoms are on the surface. Gas storage Catalysis Stability melting Quantized electronic and vibrational excitation important in the 1-100nm ragan

Carbon Nanotubes and electrodes

IMAGING TECHNIQUES FOR NANOSTRUCTURES Need new methods to image and probe nanostructures Limitation in X-ray diffraction for nanostructures Real-space probes Focal and Scanning probes

Focal Microscopy resolution limitations Wavelike nature of the particles Heisenberg Uncertainty Principles Resolution: d λ / 2β

Optical Microscopy Resolution limited Live specimen Low damage Rich spectroscopy content Confocal microscopy Fluorescence microscopy

Lifetime (ps) 1 2208 2 2213 3 2162 4 2157 5 2208 6 2042 Average 2165

Core protein (of Dengue Virus) egfp single exponential fit lifetime (ps) 1 2270 2 2228 3 2057 4 1971 average 2131 ps

egfp egfp & dsred2 Laser wavelength 800nm Laser power 19mW Objective 40x/1 Scanning rate 10kHz Collection time 30 sec sample HeLa Cell Fluorophores egfp egfp & dsred (FRET) lifetime 2057 ps 1700 ps

Scanning Probe Microscopy AFM, atomic force microscopy contact AFM non-contact AFM dynamic contact AFM EFM, electrostatic force microscope ESTM electrochemical scanning tunneling microscope FMM, force modulation microscopy KPFM, kelvin probe force microscopy MFM, magnetic force microscopy MRFM, magnetic resonance force microscopy NSOM, near-field scanning optical microscopy (or SNOM, scanning nearfield optical microscopy) PSTM, photon scanning tunneling microscopy SECM, scanning electrochemical microscopy SCM, scanning capacitance microscopy SGM, scanning gate microscopy SICM, scanning ion-conductance microscopy SPSM spin polarized scanning tunneling microscopy SThM, scanning thermal microscopy STM, scanning tunneling microscopy SVM, scanning voltage microscopy

Atomic Force Microscopy

Advantages of scanning probe microscopy The resolution of the microscopes is not limited by diffraction, but only by the size of the probe-sample interaction volume (i.e., point spread function), which can be as small as a few picometres. The interaction can be used to modify the sample to create small structures (nanolithography).

Disadvantages of scanning probe microscopy The scanning techniques are generally slower in acquiring images, due to the scanning process. As a result, efforts are being made to greatly improve the scanning rate. The maximum image size is generally smaller.

Density of States imaging As long as measured in STM current is determined by the tunneling processes through tip-sample surface gap its value depends not only on the barrier height but on the electron density of states also. Accordingly obtained in STM images are not simply images of sample surface relief (topography), these images can be hardly affected by the density of electronic states distribution over the sample surface. Good example of Local Density of States (LDOS) influence on the STM image is well-known image of highly oriented pyrolitic graphite (HOPG) atomic lattice. Only half atoms are visible in STM. Similar case is image of GaAs atomic lattice. LDOS determining can also help to distinguish chemical nature of the surface atoms. LDOS acquisition is provided simultaneously with the STM images obtaining. During scanning the Bias Voltage is modulated on the value du, the modulation period is chosen to be much shorter than the time constant of the feedback loop in the STM. Suitable modulation of tunnel current di is measured, divided by du and presented as LDOS image. On Example the topography and LDOS image of HOPG sample are presented.

Local Density of States imaging HOPG sample. Upper picture - topography image, lower picture - simultaneously obtained LDOS image. Scan size: 1 x 1 um http://www.ntmdt.ru/spm- Techniques/Principles/

Magnetic domains of cobalt monocrystal Topography (left) and magnetic force distribution for same area (right) of cobalt monocrystal with strong perpendicular magnetocrystalline anisotropy. Right image corresponds to deflection of the nonvibrating cantilever. Domains of closure in the form of flowers are seen on magnetic image.

Magnetic phase transition in cobalt Topography (left column) and corresponding MFM images (right) of the cobalt monocrystal. Magnetic images show changes of the domain structure at heating (from top row to lower: 220C, 250C, 290C).

Magnetic structures of permalloy Left image is topography of the thin film permalloy rectangles, and right image shows corresponding domain structure.

Lattice of magnetic dipoles Topography (left) and magnetic force microscopy image (right) of ferromagnetic islands in paramagnetic film. Magnetic image looks like a sub-micron dipole array. Dark and light areas on right image correspond to different poles. This is perspective data storage medium. Both images were obtained simultaneously by two-pass method.

Force Modulation mode

Transmission Electron Microscopy http://www.matter.org.uk/tem/default.htm

Atomic Resolution

Core-Loss Spectroscopy

Low-Loss Spectroscopy

Phase Retrieval Devices X-rays Zernike Phase plate Interferometer phase grating holography Electrons Zernike Phase plate holography

Nanofabrication: 45nm/300nm Outmost zones

Test pattern 20 nm line width 400 nm thick photoresist

Zernike Type Electrostatic Phase plate manufactured by MEMS process LPCVD low stress Si nitride

Phase enhanced TEM images of biology specimens CT26 Cell Drosophila brain

Phase Contrast Imaging SiO 2-x N x SiO 2 Si f = 0nm Electro-static phase Plate f = 15360nm de-localization of image f = 120nm Carbon Film Phase Plate f = 4050nm

X-ray Fluorescence image of a single cell with 150 nm x-ray microbeam APS, Argonne National Laborator

Ca and Os distribution in a single cell Ca Os

Os distribution viewed from different angle 3D structure information can be obtained In collaboration with B. Lai, APS, Argonne

Human HaLa Cell radiograph of 60nm resolution FOV: 30x30µm

Vimentin of the Cervix Tumor (HeLa) Cells Immunolabelled with DAB Chromogen with Ni Enhancement

GFP-tagged Yeast Sup35-GFP-yeast DAB-nickel

2 m 1 m

20 nm 200 nm 4 1.7 m

3 83 nm 2 1.7 m 1 1 m

Wehnelt cap 200keV Laser Al mirror

Synchrontron or Laser source

1 2 3 4 5 Project supported by IOP, AS 6 Recording 7

objective upper pole piece sample sample holder -30keV TEM/PEEM 40mm 1) Larger Cs =40mm. It can be corrected by Cs corrector, but it takes long time to re-design the objective lens and Cs corrector 2) Larger Cc =30mm~40mm it can not be corrected, until Cc corrector is available x-ray or laser objective lower pole piece 2000FX Cs=5mm 2010FEG Cs=1 mm

LPCVD low stress Si nitride Process Flow by MEMS

Installation of Phase Plate sample holder phase plate holder

Electron Gun for Ultrafast TEM Cathode Anode

Wehnelt Cap

gun chamber anode

Anode gun chamber anode base