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CryO-TEM

What Is Cryo-TEM?

Cryo-TEM is a form of transmission electron microscopy in which samples are rapidly vitrified (frozen so fast that water forms amorphous ice rather than crystals) and imaged at cryogenic temperatures.

This approach preserves:

  • native morphology

  • internal structure

  • dispersion state

  • interfaces and assemblies

Cryo-TEM allows direct visualization of structures as they exist in real environments, rather than after drying or chemical treatment.

Why Use Cryo-TEM?

Cryo-TEM is chosen when traditional TEM introduces artifacts such as:

  • collapse of soft structures

  • aggregation after drying

  • phase separation

  • redistribution of components

  • beam-induced damage

Cryo-TEM helps answer questions such as:

  • What is the true morphology of nanoparticles or soft materials?

  • Are particles dispersed, aggregated, or self-assembled?

  • How are internal structures organized in hydrated systems?

  • Do interfaces or shells exist around particles?

  • How does processing affect nanoscale structure?

What Cryo-TEM Can Reveal

Cryo-TEM provides high-resolution insight into:

  • nanoparticle size, shape, and dispersion

  • soft matter morphology (micelles, vesicles, emulsions)

  • polymer and polymer-blend nanostructure

  • internal structure of gels and colloids

  • core–shell and multilayer nanostructures

  • early-stage aggregation or phase separation

Because imaging is performed under cryogenic conditions, observed features are closer to real functional states.

Typical Application Scenarios

Nanoparticles & Colloidal Systems

  • Particle size and shape evaluation

  • Dispersion vs. aggregation analysis

  • Stability assessment in liquid or hydrated environments

Polymers & Soft Materials

  • Nanostructure of polymer assemblies

  • Phase separation in blends or composites

  • Morphology of gels, elastomers, and soft matrices

Pharmaceuticals & Drug Delivery

  • Liposomes, micelles, nanoparticles

  • Encapsulation structure and uniformity

  • Aggregation or instability investigation

Biological & Bio-Inspired Materials

  • Hydrated biological structures

  • Biomimetic materials and interfaces

  • Structural integrity without staining artifacts

R&D & Failure Investigation

  • Comparison of “good vs. failed” samples

  • Evaluation of processing-induced structural changes

  • Root-cause analysis for nanoscale defects

Sample Types

Cryo-TEM is commonly applied to:

  • aqueous or solvent-based dispersions

  • nanoparticles and colloids

  • soft polymers and polymer assemblies

  • gels, emulsions, and suspensions

  • biological or bio-related materials (case-dependent)

Xinbodi evaluates sample suitability based on composition, sensitivity, and analytical objectives before testing.

What You Will Receive

Each Cryo-TEM project is delivered with a clear, structured report designed for technical decision-making. A typical deliverable includes:

  • project objective and sample description

  • cryogenic preparation and imaging conditions

  • high-resolution Cryo-TEM images

  • particle size or structural observations (when applicable)

  • comparison summaries (batch vs. batch, treated vs. untreated)

  • interpretation focused on structure–performance relationships

  • recommendations for optimization or complementary analysis

Why Choose Xinbodi for Cryo-TEM?

  • Experience with soft, hydrated, and beam-sensitive materials

  • Careful cryogenic preparation to preserve native structure

  • Application-driven interpretation, not just images

  • Support for R&D, troubleshooting, and formulation optimization

  • Ability to combine Cryo-TEM with other analytical techniques when needed

  • Strict confidentiality for proprietary samples and data

FAQs

Cryo-TEM images frozen, hydrated samples without drying or staining, reducing artifacts and preserving native morphology.

Yes. Electron beam exposure and sample preparation are destructive to the analyzed region, but they allow accurate visualization of otherwise unstable structures.

Yes. Particle size and distribution can be evaluated from images when appropriate statistical sampling is performed.

No. Cryo-TEM is recommended only when room-temperature TEM preparation risks altering the true structure.

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