Microscopy
Additional Information
EMSL hosts a wide variety of sophisticated microscopy instruments, including electron microscopes, optical microscopes, scanning probe microscopes, and computer-controlled microscopes for automated particle analysis. These tools are used to image a range of sample types with nanoscale—and even atomic—resolution with applications to surface, environmental, biogeochemical, atmospheric, and biological science. Each of the state-of-the-art instruments and customized capabilities is equipped with features for specific applications.
- Nanoscale imaging – Many tools offer nanoscale and sub-nanoscale resolution for a wide variety of sample types, allowing users to study nanoscale chemical processes, such as interfacial electron transfer, organic thin film devices, and cell membrane proteins.
- Atomic-level imaging – EMSL users can obtain topographical information on a variety of materials, imaging down to individual atoms on a surface; this technique has been applied to nanostructures; geological samples; and biological samples, such as protein and biomolecule structures on a surface.
- Tomography – An electron microscope equipped for tomography allows users to obtain image series for three-dimensional reconstruction; complete with cryostage, this capability is primarily devoted to biological samples for morphological and immunocytochemistry studies and supports imaging of samples such as soft materials and polymers.
- Particle Analysis – A scanning electron microscope equipped with hardware and software for computer-controlled SEM/EDX analysis allows users to obtain detailed knowledge about the particle-type composition of non-volatile samples of atmospheric particles. Environmental scanning electron microscopy allows users to study hydration properties of environmental particles.
- Sample preservation – Techniques are available in environmental mode, which does not require extensive preparation procedures that can introduce imaging artifacts; live-cell and in situ imaging in liquids can be achieved with high resolution.
- Dynamic processes in real time – Tools are available to study femtosecond dynamical processes with unprecedented spatial resolution; complex reaction dynamics such as enzymatic reactions, protein-protein interactions, and interfacial electron transfer processes; protein-protein interactions, such as those involving cell signaling; and molecular interactions, such that they can be quantified at the level of a single molecule.
- NMR imaging – A 500-MHz nuclear magnetic resonance (NMR) imaging spectrometer can be used alone and integrated with confocal fluorescence microscopy; methods include mapping of biological systems with spectroscopy and diffusion.
- Complementary information – Many EMSL microscopes offer complementary probes to study different facets of samples simultaneously.
Capability Detail
Refer to the table below for a full listing, which leads to complete information about each of EMSL's microscopy instruments. Brief details about the primary microscopy tools available to EMSL users immediately follow.
- Electron microscopes with tomography, cryo, scanning, photoemission, and high-resolution (sub-nanometer) capabilities; different microscopes are dedicated to samples types, such as biological or atmospheric particles
- NMR microscopy (10-40 µm) to study the anatomy, metabolism, and transport processes of live cell cultures, biofilms, and tissue samples
- Dual Raman confocal microscope for radiological samples
- Optical microscopes to study reaction dynamics
- Single-molecule fluorescence tools to study molecular interactions in real time
- Spectroscopy tools with visible, near-, mid-, and far-infrared capabilities
- Atomic force microscopy capabilities to study nanoscale chemical processes
- Scanning probe microscopes to obtain high-resolution topographical information for a wide variety of sample types
All Related Publications Related Publications
- Bioreduction of hematite nanoparticles by the dissimilatory iron reducing bacterium Shewanella oneidensis MR-1.
- Fluorescent Dye Encapsulated ZnO Particles with Cell-specific Toxicity for Potential use in Biomedical Applications.
- Electron donor-dependent radionuclide reduction and nanoparticle formation by Anaeromyxobacter dehalogenans strain 2CP-C.
- Interparticle Chiral Recognition of Enantiomers: A Nanoparticle-Based Regulation Strategy.
- Changes in the quaternary structure of amelogenin when adsorbed onto surfaces.
All Related Research Highlights Related Research Highlights
- Submicrometer and Nanoscale Inorganic Particles Exploit the Actin Machinery to be Propelled Along Microvilli into Alveolar Cells (Tiny Particle, Big Problem?)
- Microstructures of ZnO Films Deposited on (0001) and r-cut α-Al2O3 Using Metal Organic Chemical Vapor Deposition (Sapphires & Sunscreen)
- Laser and Electrical Current-Induced Phase Transformation of In2Se3 Semiconductor Thin Film on Si(111) (Quick Change Artist)
- Experimental Studies of Heterogeneous Gas-to-Particle Reactions Using Novel Particle-on-Substrate Stagnation Flow Reactor Approach (What Are the Chances?)
- The Synergy Between Molecular Theory and Solid-State NMR Spectroscopy (Model System for NMR)
Microscopy Capabilities Available at EMSL
To help with proposal planning, icons in the table below indicate instrument availability:
- 10 hours a day, 5 days a week
- 24 hours a day, 7 days a week
| Instrument | Contact |
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Laskin, Alexander |
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Wang, Chongmin |
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Arey, Bruce Saraf, Lax |
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Dohnalkova, Alice |
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Orr, Galya |
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Zelenyuk,Alla N |
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Hu, Dehong |
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Orr, Galya |
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Beck, Kenneth M. |
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Hess, Nancy J. |
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Hu, Dehong |
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Rosso, Kevin M. |
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Lea, Scott |
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Rosso, Kevin M. |
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Rosso, Kevin M. |
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Lyubinetsky, Igor |
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Dohnalek, Zdenek |
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Ford,Joseph J |
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Wang, Zheming |
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Johnson, Tim |
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Wang, Zheming |
Microscopy Capability Steward (Optical and Scanning Probe): Nancy Hess | Nancy.Hess@pnl.gov, 509-371-6385
Microscopy Capability Steward (NMR/Imaging): Dave Hoyt | David.Hoyt@pnl.gov, 509-371-6545

