1D Spectroscopy#

Navigate a map of per-pixel spectra and watch the spectrum change live under the crosshair — the basic EELS/EDS spectrum-imaging workflow.

Follow along in the app

Every step below is also a live walkthrough inside SpyDE: Help → 1D Spectroscopy → Guided tour. The tour loads the same small tutorial dataset for you (no download), highlights each control as you go, and closes the example data again when you exit.

Steps#

1. What you’ll do#

Spectroscopy data (EELS, EDS) pairs a spectrum — intensity per energy channel — with every position in a scan. SpyDE shows the same navigator + linked-signal layout as imaging data, except the signal window is a 1D spectrum plot instead of a 2D pattern.

Tip

A small tutorial map (Tutorial Data → Spectroscopy, two Gaussian peaks whose position/width vary per pixel) is loaded for you — no download needed.

3. Move the crosshair, watch the spectrum change#

Drag the crosshair across the navigator — the two peaks in the spectrum window shift and change height as you cross the map, since each pixel carries its own peak position and width.

4. The plot toolbar#

Hover the spectrum window to reveal its floating toolbar — Zoom, Reset, and Add Selector (to place an integration region) work the same way here as on any 2D plot.

5. Reading the axes#

The Plot Control dock shows the spectrum’s channel axis and intensity scale for the active window — the same dock used for every plot in SpyDE.

More information#

A spectrum image stores a full spectrum — EELS or EDS — at every position of a scan. The data has the same navigator/signal shape as 4D-STEM, only the signal is one-dimensional: navigating the map plays the spectrum back position by position, and integrating a real-space region averages spectra to trade spatial resolution for signal-to-noise.

The usual analysis is quantitative rather than visual: subtract a background (a power law before an EELS edge, a bremsstrahlung model under EDS lines), fit a model of components to the remaining signal, and map a fitted parameter — an edge intensity, a peak position, a composition — back over the scan.

Tip

SpyDE reads and displays this data through HyperSpy; the quantitative EELS/EDS methods live in eXSpy, HyperSpy’s spectroscopy extension.

Further reading#

SpyDE wraps pyxem, HyperSpy, eXSpy, kikuchipy and orix; those projects document the underlying methods in far more depth than a walkthrough can.