High-resolution transmission electron microscopy

High-resolution transmission electron microscopy

High Resolution Transmission Electron Microscopy (HRTEM) is an imaging mode of the transmission electron microscope (TEM) that allows the imaging of the crystallographic structure of a sample at an atomic scale. [cite book |title=Experimental high-resolution electron microscopy |last=Spence |first=John C. H. |year=1988 |origyear=1980 |publisher=Oxford U. Press |location=New York |isbn=0195054059 ] Because of its high resolution, it is an invaluable tool to study nanoscale properties of crystalline material such as semiconductors and metals. At present, the highest resolution realised is convert|0.8|Å|nm|2|abbr=off|lk=on with microscopes such as the OAM at NCEM. Ongoing research and development such as efforts in the framework of TEAM will soon push the resolution of HRTEM to 0.5 Å. At these small scales, individual atoms and crystalline defects can be imaged.

One of the difficulties with HRTEM is that image formation relies on phase-contrast. In phase-contrast imaging, contrast is not intuitively interpretable as the image is influenced by strong aberrations of the imaging lenses in the microscope.

Image contrast and interpretation

As opposed to conventional microscopy, HRTEM does not use amplitudes, i.e. absorption by the sample, for image formation. Instead, contrast arises from the interference in the image plane of the electron wave with itself. Due to our inability to record the phase of these waves, we generally measure the amplitude resulting from this interference, however the phase of the electron wave still carries the information about the sample and generates contrast in the image, thus the name "phase-contrast imaging". This, however is true only if the sample is thin enough so that amplitude variations only slightly affect the image (the so-called "weak phase object approximation", WPOA).

The interaction of the electron wave with the crystallographic structure of the sample is not entirely understood yet, but a qualitative idea of the interaction can readily be obtained. Each imaging electron interacts independently with the sample. Above the sample, the wave of an electron can be approximated as a plane wave incident on the sample surface. As it penetrates the sample, it is attracted by the positive atomic potentials of the atom cores, and channels along the atom columns of the crystallographic lattice (s-state model). At the same time, the interaction between the electron wave in different atom columns leads to Bragg diffraction. The exact description of dynamical scattering of electrons in a sample not satisfying the WPOA (almost all real samples) still remains the holy grail of electron microscopy. However, the physics of electron scattering and electron microscope image formation are sufficiently well known to allow accurate [http://www.nature.com/nature/journal/v274/n5669/abs/274322a0.html simulation] of electron microscope images.

As a result of the interaction with the sample, the electron exit wave right below the sample "φe(x,u)" as a function of the spatial coordinate "x" is a superposition of a plane wave and a multitude of diffracted beams with different in plane spatial frequencies "u" (high spatial frequencies correspond to large distances from the optical axis). The phase change of "φe(x,u)" compared to the incident wave peaks at the location of the atom columns. The exit wave now passes through the imaging system of the microscope where it undergoes further phase change and interferes as the image wave in the imaging plane (photo plate or CCD). It is important to realize, that the recorded image is NOT a direct representation of the samples crystallographic structure. For instance, high intensity might or might not indicate the presence of an atom column in that precise location (see simulation). The relationship between the exit wave and the image wave is a highly nonlinear one and is a function of the aberrations of the microscope. It is described by the "contrast transfer function".

The phase Contrast Transfer Function

The phase Contrast Transfer Function (CTF) is a function of limiting apertures and aberrations in the imaging lenses of a microscope. It describes their effect on the phase of the exit wave "φe(x,u)" and propagates it to the image wave. Following "Williams and Carter", [cite book |title=Transmission electron microscopy: A textbook for materials science |last=Williams |first=David B. | coauthors=Carter, C. Barry |year=1996 |publisher=Plenum Press |location=New York |isbn=030645324X] if we assume the WPOA holds (thin sample) the CTF becomes


where "A(u)" is the "aperture function", "E(u)" describes the attenuation of the wave for higher spatial frequency "u", also called "envelope function". "χ(u)" is a function of the aberrations of the electron optical system.

The last, sinusoidal term of the CTF will determine the sign with which components of frequency "u" will enter contrast in the final image. If one takes into account only spherical aberration to third order and defocus, χ is rotationally symmetric about the optical axis of the microscope and thus only depends on the modulus "u" = "u", given by

chi(u)=frac{pi}{2}C_slambda^3u^4-pi Delta f lambda u^2,

where "Cs" is the spherical aberration coefficient, "λ" is the electron wavelength, and "Δf" is the defocus. In TEM, defocus can easily be controlled and measured to high precision. Thus one can easily alter the shape of the CTF by defocusing the sample. Contrary to optical applications, defocusing can actually increase the precision and interpretability of the micrographs.

The "aperture function" cuts off beams scattered above a certain critical angle (given by the objective pole piece for ex), thus effectively limiting the attainable resolution. However it is the "envelope function" "E(u)" which usually dampens the signal of beams scattered at high angles, and imposes a maximum to the transmitted spatial frequency. This maximum determines the highest resolution attainable with a microscope and is known as the information limit. "E(u)" can be described as a product of single envelopes:

E(u)=E_s(u)E_c(u)E_d(u)E_v(u)E_D(u),due to:"Es(u)": angular spread of the source:"Ec(u)": chromatic aberration:"Ed(u)": specimen drift:"Ev(u)": specimen vibration:"ED(u)": detector

Specimen drift and vibration can be minimized relatively easily by a suitable working environment. It is usually the spherical aberration "Cc" that limits spatial coherency and defines "Es(u)" and the chromatical aberration, together with current and voltage instabilities that define the temporal coherency in "Ec(u)". These two envelopes determine the information limit.

If we consider the probe to have a Gaussian distribution of electron intensity, the spatial envelope function is given by

E_s(u)=exp [-(frac{pialpha}{lambda})^2(frac{deltaChi(u)}{delta u})^2] =exp [-(frac{pialpha}{lambda})^2(C_slambda^3u^3+Delta flambda u)^2] ,

where α is the semiangle describing the Gaussian distribution. Clearly, if the spherical aberration "Cs" where zero, this envelope function would be a constant one for Gaussian focus. Else, the damping due to this envelope function can be minimized by optimizing the defocus at which the image is recorded (Lichte defocus).

The temporal envelope function can be expressed as

E_c(u)=exp [-frac{1}{2}(pilambdadelta)^2u^4] ,

here δ is the focus spread due to chromatical aberration "Cc":

delta=C_csqrt{4(frac{Delta I_{obj{I_{obj)^2 + (frac{Delta E}{V_{acc)^2 + (frac{Delta V_{acc{V_{acc})^2,

The terms Delta I_{obj}/I_{obj} and Delta V_{acc}/V_{acc} represent instabilities in of the currents in the objective lens and the high voltage supply of the electron gun. Delta E/V_{acc} is the energy spread of electrons leaving the gun.

The information limit of current (2006) microscopes lies little below 1 Å. The TEAM project aims at pushing the information limit to 0.5 Å. To do so it will be fully corrected for third and fifth order spherical aberration as well as chromatical aberration. Further, the electron beam will be highly monochromatised and current and voltage have to be stabilized.

Optimum defocus in HRTEM

Choosing the optimum defocus is crucial to fully exploit the capabilities of an electron microscope in HRTEM mode. However, there is no simple answer as to which one is the best.

In "Gaussian focus" one sets the defocus to zero, the sample is in focus. As a consequence contrast in the image plane gets its image components from the minimal area of the sample, the contrast is "localized" (no blurring and information overlap from other parts of the sample). The CTF now becomes a function that oscillates quickly with "Csu4". What this means is that for certain diffracted beams with a given spatial frequency "u" the contribution to contrast in the recorded image will be reversed, thus making interpretation of the image difficult.

cherzer defocus

In Scherzer defocus, one aims to counter the term in "u4" with the parabolic term "Δfu2" of "χ(u)". Thus by choosing the right defocus value "Δf" one flattens "χ(u)" and creates a wide band where low spatial frequencies "u" are transferred into image intensity with a similar phase. In 1949, Scherzer found that the optimum defocus depends on microscope properties like the spherical aberration "Cs" and the accelerating voltage (through "λ") in the following way:

Delta f_{Scherzer}=-1.2sqrt{C_slambda},

where the factor 1.2 defines the extended Scherzer defocus. For the CM300 at NCEM, "Cs=0.6mm" and an accelerating voltage of 300keV ("λ = 1.97 pm") ( [http://hyperphysics.phy-astr.gsu.edu/hbase/quantum/debrog2.html#c1 Wavelength calculation] ) result in "ΔfScherzer = -41.25 nm".

The point resolution of a microscope is defined as the spatial frequency "ures" where the CTF crosses the abscissa for the first time. At Scherzer defocus this value is maximized:

u_{res}(Scherzer)=0.6lambda^{3/4} C_s^{1/4},

which corresponds to 6.1 nm-1 on the CM300. Contributions with a spatial frequency higher than the point resolution can be filtered out with an appropriate aperture leading to easily interpretable images at the cost of a lot of information lost.

Gabor defocus

Gabor defocus is used in electron holography where both amplitude and phase of the image wave are recorded. One thus wants to minimize crosstalk between the two. The Gabor defocus can be expressed as a function of the Scherzer defocus as

Delta f_{Gabor}=0.56Delta f_{Scherzer}

Lichte defocus

To exploit all beams transmitted through the microscope up to the information limit, one relies on a complex method called exit wave reconstruction which consists in mathematically reversing the effect of the CTF to recover the original exit wave "φe(x,u)". To maximize the information throughput, Hannes Lichte proposed in 1991 a defocus of a fundamentally different nature than the Scherzer defocus: because the dampening of the envelope function scales with the first derivative of "χ(u)", Lichte proposed a focus minimizing the modulus of d"χ(u)/"d"u" [cite journal |last=Lichte |first=Hannes | year=1991 |month= |title=Optimum focus for taking electron holograms |journal=Ultramicroscopy |volume=38 |issue=1 |pages=13–22 |doi=10.1016/0304-3991(91)90105-F ]

Delta f_{Lichte}=-0.75 C_s(u_{max}lambda)^2,

where "umax" is the maximum transmitted spatial frequency. For the CM300 with an information limit of 0.8 Å Lichte defocus lies at -272 nm.

Exit Wave Reconstruction

To calculate back to "φe(x,u)" the wave in the image plane is back propagated numerically to the sample. If all properties of the microscope are well known, it is possible to recover the real exit wave with very high accuracy.

First however, both phase and amplitude of the electron wave in the image plane must be measured. As our instruments only record amplitudes, an alternative method to recover the phase has to be used. There are two methods in use today:
*Holography, which was developed by Gabor expressly for TEM applications, uses a prism to split the beam into a reference beam and a second one passing through the sample. Phase changes between the two are then translated in small shifts of the interference pattern, which allows recovering both phase and amplitude of the interfering wave.

* Through focal series method takes advantage of the fact that the CTF is focus dependent. A series of about 20 pictures is shot under the same imaging conditions with the exception of the focus which is incremented between each take. Together with exact knowledge of the CTF the series allows for computation of "φe(x,u)" (see figure).

Both methods extend the point resolution of the microscope the information limit, which is the highest possible resolution achievable on a given machine. The ideal defocus value for this type of imaging is known as Lichte defocus and is usually several hundred nanometers negative.

ee also

*Electron beam induced deposition
*Electron diffraction
*Electron energy loss spectroscopy (EELS)
*Electron microscope
*Energy filtered transmission electron microscopy (EFTEM)
*Scanning confocal electron microscopy
*Scanning electron microscope (SEM)
*Scanning transmission electron microscope (STEM)
*Transmission Electron Microscopy (TEM)
*Transmission Electron Aberration-corrected Microscope


*Topical review "Optics of high-performance electron Microscopes" [http://dx.doi.org/10.1088/0031-8949/9/1/014107 Sci. Technol. Adv. Mater. 9 (2008) 014107 (30pages)] "free download "
* [http://www.maxsidorov.com/ctfexplorer/index.htm CTF Explorer by Max V. Sidorov, freeware program to calculate the CTF]
* [http://www.tf.uni-kiel.de/matwis/amat/def_en/kap_6/backbone/r6_3_4.html High Resolution Transmission Electron Microscopy Overview]


Wikimedia Foundation. 2010.

Игры ⚽ Поможем написать реферат

Look at other dictionaries:

  • High Resolution Transmission Electron Microscopy — Hochauflösende Transmissionselektronenmikroskopie (engl.: high resolution transmission electron microscopy, HRTEM) ist ein TEM Abbildungsmodus, der es erlaubt, die kristallographische Struktur einer Probe mit atomarer Auflösung abzubilden. Wegen… …   Deutsch Wikipedia

  • Transmission electron microscopy — A TEM image of the polio virus. The polio virus is 30 nm in size.[1] Transmission electron microscopy (TEM) is a microscopy technique whereby a beam of electrons is transmitted through an ultra thin specimen, interacting with the specimen as it… …   Wikipedia

  • Scanning transmission electron microscopy — A scanning transmission electron microscope (STEM) is a type of transmission electron microscope. With it, the electrons pass through the specimen, but, as in scanning electron microscopy, the electron optics focus the beam into a narrow spot… …   Wikipedia

  • Photoemission electron microscopy — (PEEM, also called photoelectron microscopy, PEM) is a widely used type of emission microscopy. PEEM utilizes local variations in electron emission to generate image contrast. The excitation is usually produced by UV light, synchrotron radiation… …   Wikipedia

  • Cryo-electron microscopy — CryoEM image of GroEL suspended in vitreous ice at 50,000X magnification. Cryo electron microscopy (cryo EM), or electron cryomicroscopy, is a form of transmission electron microscopy (EM) where the sample is studied at cryogenic temperatures… …   Wikipedia

  • Conventional transmission electron microscope — (CTEM) is a rarely used abbreviation referring to transmission electron microscope (TEM) and high resolution transmission electron microscope (HRTEM). It is used to distinguish those parallel illumination techniques from convergent beam scanning… …   Wikipedia

  • Electron microscope — Diagram of a transmission electron microscope A 197 …   Wikipedia

  • Electron crystallography — is a method to determine the arrangement of atoms in solids using a transmission electron microscope (TEM). Contents 1 Comparison with X ray crystallography 2 Radiation damage 3 Protein structures determined by electron crystallography …   Wikipedia

  • Scanning confocal electron microscopy — (SCEM) is an electron analogue of scanning confocal optical microscopy (SCOM) where electrons and electron lenses are used instead of light and optical lenses. Advantages of SCEM High energies of incident particles (200 keV electrons vs. 2 eV… …   Wikipedia

  • Microscopy — is the technical field of using microscopes to view samples and objects that cannot be seen with the unaided eye (objects that are not within the resolution range of the normal eye). There are three well known branches of microscopy, optical,… …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”