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What is the working principle of a TEM? 


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Transmission electron microscopy (TEM) works by irradiating a sample with an electron beam and using the transmitted electrons to form an image on a screen. The objective lens can be defocused to create a phase difference between scattered and un-scattered electron waves, resulting in contrast on the screen . The contrast in TEM images arises from differences in electron density of the specimen's elements . TEM can be used for imaging supermolecules and provides information on the periodic ordered structure of the specimen through electron diffraction . TEM tomography allows for the visualization of the specimen's three-dimensional structure . In the field of cell biology, TEM is used to observe cells and tissue ultrastructure, but proper sample preparation is crucial for obtaining good results . TEM also has applications in cloud computing, where it provides strong safety guarantees to high-assurance Java applications .

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The provided paper is about the working principle and control algorithm of an analog microgrid control system. It does not provide information about the working principle of a TEM (Transmission Electron Microscope).
The working principle of a TEM is to transmit a beam of electrons through an ultrathin section of a biological specimen, allowing for the observation of cells and tissue ultrastructure.
Reference EntryDOI
Jun-ichi Kikuchi, Kazuma Yasuhara 
15 Mar 2012
16 Citations
The working principle of a TEM is based on illuminating the specimen with electron beams in high-vacuum conditions and using the differences in electron density of the elements constituting the specimen to create contrast in the image.
The working principle of a TEM involves irradiating the sample with electrons and using the transmitted electrons to form an image on a screen, utilizing phase contrast for necessary contrast.

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Whats the detection limit of TEM10 answersThe detection limit of Transmission Electron Microscopy (TEM) is a multifaceted concept that depends on various factors including the electron dosage, the efficiency of electron detectors, and the specific analytical techniques employed. High-resolution TEM studies are often constrained by the electron dosage, with sensitive samples such as catalysts and macromolecules only preserving their structures below a threshold of 100 ē/Å^2 due to the detrimental effects of high radiation doses. The efficiency of electron detectors plays a crucial role, as advancements in electron sources and optics have highlighted the limitations of current detection systems, pushing the need for novel sensor technologies that offer improved Modulation Transfer Function (MTF) and Detective Quantum Efficiency (DQE). Analytical techniques within TEM, such as Energy Dispersive X-ray Spectroscopy (EDS) and Electron Energy Loss Spectroscopy (EELS), have their own detection limits. EELS is more sensitive for light elements, while EDS is better suited for heavy elements, with the detection efficiency of EDS significantly improved by new detector technology. Diagnostic negative staining electron microscopy, a technique used for pathogen detection, has shown detection limits of 10^6 particles per ml using direct adsorption and can be improved to 10^5 particles per ml for spores and 5 × 10^4 particles per ml for poxviruses with airfuge ultracentrifugation. Furthermore, the detection limit is also influenced by the method of sample preparation and analysis, with arbitrary detection limits potentially misstating the "true" detection limits. The concept of randomly exposing areas of the specimen to the electron beam to mitigate damage introduces challenges in immediate qualitative analysis due to the difficulty in interpreting subsampled images. Lastly, the effect of chromatic aberrations and the choice of using energy-filtered electrons can impact the detection limit, especially in the context of dark field microscopy of unstained specimens. In summary, the detection limit of TEM is not a fixed value but varies with the specific conditions of the experiment, including the type of sample, the analytical technique used, and the efficiency of the detection system.
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