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Sandbox Physics

E24 · Low-voltage transmission

STEM-in-SEM: Through a Thin Specimen

How thin must a specimen be for a useful SEM transmission image? Thin enough that a good share of the electrons gets through at the low beam energy you have chosen. A thicker foil lets fewer through and blurs the image more. The detector collection angles then decide which transmitted electrons form the contrast.

Choose the beam energy, foil thickness and collection angles. Learn to tell weak transmission, probe blur and counting noise apart.

Interactive modelSTEM-in-SEM: Through a Thin Specimen
Selected virtual detector counts—\text{—}
Selected-point transmitted fraction—\text{—}
Signed contrast in separate audit regions—\text{—}
Pooled ROI difference SNR—\text{—}
More measurements and target
Selected sampled primary outcome total—\text{—}
Simulated counts beyond 250 mrad—\text{—}
Simulated removed-electron counts—\text{—}
Assumed probe FWHM—\text{—}
ROI 2 / ROI 1 mean count ratio—\text{—}
Expected incident dose per scan pixel—\text{—}
Experiment target—\text{—}

Physics tutorial

STEM-in-SEM: Through a Thin Specimen

BackgroundTo make a transmission image in an SEM, you choose the beam energy, the foil thickness and the collection angles. When the image is poor, you then work out whether weak transmission, probe blur or counting noise is to blame.

Why it mattersThe task is to see the inclusion in transmission. Collect from zero angle. Reach a dark inclusion contrast of at least 0.1, a pooled region difference SNR of at least 10 and a transmitted fraction of at least 30 percent at the selected point, with an assumed probe FWHM of at most 5 nm.

Start with the essentials

Focus question
How thin must a specimen be for a useful SEM transmission image?
One-sentence intuition
The angle range you choose decides which of the stored electrons make up the image.

Core mathematical model

Counts in angular bins

μj=Iτe pjNann=∑j∈ANj\begin{aligned}\mu_j&=\frac{I\tau}{e}\,p_j\\N_{\rm ann}&=\sum_{j\in\mathcal A}N_j\end{aligned}

Each virtual image adds up the stored radial counts in its chosen angular interval. The interval includes its lower edge but not its upper edge.

Assumed angular spread of scattered electrons

f(θ)=θs2 e−θ2/(2s2)r=Ltan⁡θ\begin{aligned}f(\theta)&=\frac{\theta}{s^2}\,e^{-\theta^2/(2s^2)}\\r&=L\tan\theta\end{aligned}

The isotropic Gaussian radial law stands in for a real transport calculation. The radius on the collector follows from the angle through the collector geometry shown on screen.

Contrast and noise in two known regions

C=N‾2−N‾1N‾2+N‾1σΔ2=∑1Nn12+∑2Nn22S=∣N‾2−N‾1∣σΔ\begin{aligned}C&=\frac{\overline N_2-\overline N_1}{\overline N_2+\overline N_1}\\\sigma_\Delta^2&=\frac{\sum_1N}{n_1^2}+\frac{\sum_2N}{n_2^2}\\S&=\frac{|\overline N_2-\overline N_1|}{\sigma_\Delta}\end{aligned}

This pooled difference uses the count statistics of two regions fixed in advance. It is not a per-pixel SNR, and it does not recover composition.

Common difficulties

A bright pixel is not a chemical analysis

Typical misconceptionAny annular image tells me directly which atoms are there.

Better mental modelThickness, the range of collected angles and probe overlap also change contrast. Phase effects at low angles need a coherent wave model, which this Lab does not include.

Run the experiment

  1. 01

    Predict the contrast

    Compare the separate specimen input with the bright-field image and the image from your selected angles.

    What to observe: The known regions are there to check contrast. They are not a recovered chemical map.
  2. 02

    Change the collection angles without re-acquiring

    Change the inner and outer angles while watching the native histogram and the outcome totals.

    What to observe: The virtual images change, but the native radial counts stay the same.
  3. 03

    Try a setting that works

    Use the Resolve the thin specimen preset and check the target. Compare the row profiles built from the counts.

    What to observe: Read the signed contrast and the pooled difference SNR together.
  4. 04

    Find the limits

    Try low exposure, a broad probe and reversed bounds. Then increase the specimen thickness.

    What to observe: Gain changes how the image looks. It cannot put back counts that were never collected or sharpen a blurred probe.
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