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Atlas / Physics / The Light Thread

Field · Emerged 1801 – 1893

Wave Optics

If light is a wave, what is its wavelength, what is waving, and what limits does being a wave impose on what can be seen?

4 chapters6 min read6 turning points1 open problem

Branched from
Classical Optics + Electromagnetism
Branched into
Nonlinear and Nano-Optics + Quantum Optics
Figures
Thomas Young, Augustin Fresnel, Siméon Poisson, François Arago, Hippolyte Fizeau, Léon Foucault, Ernst Abbe, Albert Michelson

In brief

In 1801 Thomas Young sent light through two narrow openings and found bands of dark where two beams overlapped. Darkness produced by adding light is something a stream of particles cannot do, and Young used the spacing of the bands to measure the wavelength of red light to within a few per cent of the modern value — in a quantity, inches, that gives the answer as about one thirty-seven-thousandth of one.

It took twenty years and a hostile prize competition for the wave theory to win. Augustin Fresnel's mathematics predicted a bright spot in the middle of a circular shadow, which the judge Poisson produced as a reductio and Arago then observed. Fresnel also showed that light must be a transverse wave, which made the supposed medium carrying it increasingly absurd and set up the problem Maxwell solved by removing the medium's job: light is an electromagnetic wave. The practical legacy is a hard limit. Because light diffracts, no lens can resolve detail much finer than half a wavelength, and that number — about 200 nanometres for visible light — bounded what biology could see for 120 years.

Key ideas

InterferenceEnters 1801 – 1803

Two waves arriving at the same place add. Where crests coincide the result is brighter than either; where a crest meets a trough they cancel. The dark bands between bright fringes are the signature no particle theory can imitate.

Fringe spacingEnters 1801 – 1803

For two slits a distance dd apart and a screen a distance LL away, bright fringes are spaced Δx=λL/d\Delta x = \lambda L / d. Measuring Δx\Delta x, dd and LL gives the wavelength, which is how a quantity smaller than a thousandth of a millimetre was measured with a card and a candle.

DiffractionEnters 1818 – 1819

Light spreads when it passes an edge or an aperture, by an angle of roughly λ/a\lambda / a for an opening of width aa. It is why shadows have fringed edges and why a small aperture makes a blurrier image, not a sharper one.

Transverse polarisationEnters 1817 – 1821

The oscillation is perpendicular to the direction of travel, and it has an orientation. Two beams polarised at right angles cannot interfere, which is how the transverse character was established.

Numerical aperture and the resolution limitEnters 1873

A lens collecting light over a half-angle α\alpha in a medium of index nn has numerical aperture NA=nsin⁡α\mathrm{NA} = n \sin\alpha, and cannot separate two points closer than about λ/2 NA\lambda / 2\,\mathrm{NA}. The limit is set by the wave, not by the quality of the glass.

Coherence lengthEnters 1892 – 1893

The distance over which a wave keeps a predictable phase. Interference fringes are only visible when the two paths differ by less than this, so a source's spectral purity sets how long an interferometer can be.

Draws on other domains

Chapter I

Darkness Made of Light

Thomas Young was a physician who read Greek at six and later did decisive work on hieroglyphs, elasticity and insurance. In 1801 he addressed the Royal Society on a thought that would have struck most of his audience as perverse: if light is a wave, then two beams should sometimes cancel.

The demonstration is simple to describe and was delicate to perform with sunlight and a pinhole. Send light through two narrow openings close together and let the two emerging beams overlap on a screen. They do not merely brighten each other. They produce a regular series of bright and dark bands. Where the two paths differ by a whole number of wavelengths the crests coincide and the light is doubled; where they differ by half a wavelength, crest meets trough and the screen is dark. There is no way to arrange two streams of particles so that adding one to the other produces nothing.

Young's reward was a review in the Edinburgh Review so contemptuous that he published a pamphlet in reply, of which one copy is said to have sold. Contradicting Newton in Britain in 1803 was a professional error.

Chapter II

The Spot That Should Not Be There

The decisive episode happened in France, and it is the best-known example in physics of a prediction intended as a refutation. The Academy of Sciences set diffraction as the subject of its 1819 prize, expecting the particle theory to be vindicated. Augustin Fresnel, a road engineer, submitted a wave theory in which the field at any point is obtained by adding contributions from every element of the wavefront, each with its own phase — an integral, in modern terms.

Siméon Poisson, on the jury and a convinced Newtonian, examined Fresnel's integrals and extracted an absurdity: behind an opaque circular disc, at the exact centre of the shadow, all the contributions from the rim arrive in phase, so there must be a bright spot. François Arago set up the experiment. The spot was there, and it is there in every undergraduate laboratory now. Fresnel won.

Fresnel and Arago then found something less convenient. Two beams polarised at right angles produce no fringes at all, at any path difference. Young supplied the interpretation and Fresnel made it quantitative: light's oscillation is perpendicular to its travel, and perpendicular polarisations have no common component to add. This was a problem, because a transverse wave requires a medium that resists shear — a solid — and the planets move through it without resistance. The ether grew steadily more preposterous until Maxwell's equations showed in 1865 that the oscillating quantities are the electric and magnetic fields themselves, which is the subject of electromagnetism.

Chapter III

A Closer Look: Measuring a Wavelength with a Card, and the Limit It Sets

The fringe geometry is the whole of Young's measurement. With slits separated by dd, a screen at distance L≫dL \gg d, and wavelength λ\lambda, the mmth bright fringe sits where the path difference is mλm\lambda, which puts it at xm=mλL/dx_m = m \lambda L / d. So the spacing between neighbouring fringes is

Δx=λLd.\Delta x = \frac{\lambda L}{d}.

Everything on the right except λ\lambda is measurable with a ruler. Take a modern demonstration: d=0.25d = 0.25 mm, L=1L = 1 m, and fringes measured 2.4 mm apart. Then

λ=Δx dL=(2.4×10−3)(2.5×10−4)1=6.0×10−7 m=600 nm.\lambda = \frac{\Delta x \, d}{L} = \frac{(2.4 \times 10^{-3})(2.5 \times 10^{-4})}{1} = 6.0 \times 10^{-7} \text{ m} = 600 \text{ nm}.

Young's own numbers, in his units, were 0.0000266 inch for the extreme red and 0.0000167 inch for the violet. Converting at 25.4 mm to the inch:

0.0000266 in×25.4=6.76×10−4 mm=676 nm,0.0000167 in→424 nm.0.0000266 \text{ in} \times 25.4 = 6.76 \times 10^{-4} \text{ mm} = 676 \text{ nm}, \qquad 0.0000167 \text{ in} \to 424 \text{ nm}.

The accepted range for visible light is about 400 to 700 nm. In 1803, with sunlight, a slit and a screen, he was within a few per cent at both ends of the spectrum — and he had measured a length ten thousand times smaller than anything he could see, by counting something he could.

The same wave behaviour that makes this measurement possible imposes a ceiling. Ernst Abbe showed in 1873 that a microscope forms an image by collecting the light a specimen diffracts, so it can only reconstruct detail whose diffracted orders fall inside the objective's cone. The smallest resolvable separation is about

dmin⁡≈λ2 NA,d_{\min} \approx \frac{\lambda}{2\,\mathrm{NA}},

where NA=nsin⁡α\mathrm{NA} = n\sin\alpha is the numerical aperture. The best oil-immersion objectives reach NA≈1.4\mathrm{NA} \approx 1.4, so at λ=550\lambda = 550 nm,

dmin⁡≈5502×1.4=196 nm.d_{\min} \approx \frac{550}{2 \times 1.4} = 196 \text{ nm}.

Two hundred nanometres is a hard line drawn across biology. A mitochondrion, at 0.5 to 1 µm, is resolvable; a ribosome at 25 nm, a virus at 100 nm, the 20-nm gap at a synapse are not, and no improvement in glass or grinding changes that. Everything below the line had to be inferred, or stained, or killed and examined with electrons — a constraint that shaped cell biology until fluorescence tricks found a way round it in the 1990s.

The same formula pointed the other way gives the telescope version, the Rayleigh criterion θ≈1.22λ/D\theta \approx 1.22\lambda/D. For the Hubble Space Telescope's 2.4-m mirror at 550 nm,

θ=1.22×550×10−92.4=2.8×10−7 rad=0.058 arcsec.\theta = \frac{1.22 \times 550 \times 10^{-9}}{2.4} = 2.8 \times 10^{-7} \text{ rad} = 0.058 \text{ arcsec}.

Which is why large telescopes are large: resolution is bought by aperture, and nothing else.

Chapter IV

What the Limit Was For

By 1893 the wave theory was complete enough to be used as a ruler. Albert Michelson compared the prototype metre with the red line of cadmium and found it to be 1,553,163.5 wavelengths long, tying a unit of length to a property of an atom instead of a bar of platinum-iridium. The idea became the SI definition, first through krypton and now through the fixed speed of light, and the instrument became the standard way to measure small distances: count fringes, each worth half a wavelength.

Classical wave optics was, by then, apparently finished. It had a complete theory of propagation, a quantitative limit on imaging, and an instrument that measured length to a fraction of a wavelength. What it did not have was any account of how light is emitted or absorbed, and that is where it broke. A blackbody's spectrum, the photoelectric effect and the sharp lines of atoms all involve light arriving in lumps, and the wave description says nothing about them — the opening of old quantum theory. Re-describing the interference of this chapter in terms of individual quanta, and asking what it means for one photon to interfere with itself, is the business of quantum optics.

Applications

Where it is used

  • Microscopy↗ Biology · Cell Biology

    The limit that bounded cell biology

    Abbe's formula says what a light microscope can and cannot show. At 200 nm, a mitochondrion is resolvable and a ribosome, a virus or the gap at a synapse is not. That boundary defined the agenda of cell biology for over a century: structures below it had to be inferred, stained into visibility, or examined by electron microscopy on dead material, until fluorescence techniques in the 1990s found ways around the limit without breaking it.

    › Sources (2)
    • Abbe, E. (1873). Beiträge zur Theorie des Mikroskops. Archiv für Mikroskopische Anatomie 9: 413–468.
    • Lichtman, J. W. & Conchello, J.-A. (2005). Fluorescence microscopy. Nature Methods 2: 910–919.
  • Metrology

    Measuring by counting fringes

    An interferometer converts a displacement into a count of light and dark cycles, each worth half a wavelength. That makes nanometre measurement routine: machine-tool positioning, optical flats, semiconductor wafer alignment, and the kilometre-scale instruments that measure a gravitational wave as a path difference a thousandth the width of a proton.

    › Sources (1)
    • Hariharan, P. (2007). Basics of Interferometry, 2nd edition. Academic Press.
  • Coatings

    Thin films that cancel reflections

    A quarter-wavelength layer of the right index makes the reflection from its top surface cancel the reflection from its bottom one. Stacks of such layers give lenses that transmit 99.9%, mirrors that reflect 99.999%, and the colour filters in every camera and display. The design problem is interference arithmetic, done over dozens of layers.

    › Sources (1)
    • Macleod, H. A. (2010). Thin-Film Optical Filters, 4th edition. CRC Press.

Open problems

Where the map runs out

Open

Whether light localises in three dimensions

Open as of 2026; the clearest experimental claims were later attributed to fluorescence rather than localisation.

In a sufficiently disordered medium, a wave is predicted to stop diffusing and become trapped in a finite region — Anderson localisation. It has been demonstrated for light in one and two dimensions and for matter waves and microwaves in three. For light in three dimensions it has not been convincingly shown, and theoretical arguments suggest the vector nature of light may prevent it for point scatterers.

Why it is hard

Strong localisation needs scattering so strong that the mean free path approaches the wavelength, which in practice means dense high-index powders that also absorb and fluoresce. Absorption mimics the signature of localisation in transmission measurements, and disentangling them has defeated several claimed demonstrations.

What resolving it unlocks

Whether a random medium can trap light as a cavity does, which would supply disordered lasers and sensors; and a cleaner understanding of transport in strongly scattering media generally.

› Sources (2)
  • Skipetrov, S. E. & Page, J. H. (2016). Red light for Anderson localization. New Journal of Physics 18: 021001.
  • Sperling, T. et al. (2016). Can 3D light localization be reached in 'white paint'? New Journal of Physics 18: 013039.

Further reading

  1. Buchwald, J. Z. (1989). The Rise of the Wave Theory of Light. University of Chicago Press.

    How the wave theory won, including how much of the fight was about mathematics rather than evidence.

  2. Born, M. & Wolf, E. (1999). Principles of Optics, 7th edition. Cambridge University Press.

    The authoritative treatment of classical wave optics; dense but complete.

  3. Robinson, A. (2006). The Last Man Who Knew Everything. Pi Press.

    A biography of Young, who also worked on Egyptian hieroglyphs and insurance mathematics.