Illustrated Physics
physics, drawn
Concept

Coherence length — where it appears

The distance over which a light wave keeps a fixed phase relation with itself, roughly the square of its wavelength divided by its spectral width. It sets how far two paths may differ and still interfere, and in coherence tomography it is the depth resolution.

Named by 2 essays across one field — each of them below, with the objects they name alongside it.

Fringe contrast against baseline, for four stellar diameters. The visibility of the fringes an interferometer would obtain at 575 nm, against the separation of its two apertures, for uniform discs of angular diameter 10, 20, 47, 100 milliarcseconds. Each curve is 2J₁(πθB/λ)/(πθB/λ), the transform of a uniform disc, and each first reaches zero at 14.47 m for 10 mas, 7.23 m for 20 mas, 3.08 m for 47 mas, 1.45 m for 100 mas. Dividing each of those by λ/θ returns the same number, 1.2197, which is the 1.22 in every textbook and is the first zero of J₁ divided by π — recovered here from the four curves rather than written into them. The practical content is that a smaller star needs a longer baseline, in exact inverse proportion, and that the measurement is of a contrast rather than of a picture. Michelson and Pease found the fringes from Betelgeuse vanishing at a 3.07 m separation in 1920 at a wavelength of 575 nm, which by the same arithmetic is a disc 47.1 milliarcseconds across — and no telescope resolved that star for another seventy years.

The fringe that measures a star

Set two apertures 3.07 metres apart in 1920 and the fringes from Betelgeuse vanish. That single fact gives the star's angular diameter to two significant figures, without ever forming an image of it — because the contrast of a fringe pattern is a Fourier component of the source's own shape.

optics · Coherence A scan into a layered sample, with a broad source and a narrower one. The envelope of the interference signal against depth in a sample with five reflecting boundaries (marked), at 60, 72, 150, 158 and 260 µm, scanned with a 50 nm source (solid) and a 10 nm source (dashed), both centred at 840 nm. The broad source, with a 6.2 µm resolution, separates every boundary, including the two that are only 8 µm apart. The narrow one, with 31 µm, merges the pairs into single blurred echoes. Every boundary in a real eye or skin sample is a small change of refractive index that reflects a tiny fraction of the light; the scan is a map of where those changes are.

The depth a broad spectrum can see

Interference is usually spoiled by a broad spectrum: many colours drift out of step, and fringes wash out a few wavelengths from where two paths are equal. Turned round, that failure is a ruler. Light whose colours stay in step only when two paths match to within a few micrometres can report the depth of every reflecting layer inside something translucent — a retina, a skin, a coat of paint — to that precision, without cutting it open. Optical coherence tomography reads depth off the width of a spectrum, and it has become one of the most used imaging methods in medicine; its resolution is set by how many colours the light contains, and the finest instruments use sources whose spectra span hundreds of nanometres.

optics · Coherence

Named alongside it

The objects these essays reach for when they reach for this one.

CoherenceFourier transformAngular diameterAperture synthesisBandwidthInterferometryOptical coherence tomographyResolutionSpatial coherenceSpectrumVan cittert zernikeVisibility

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