In short

In 1927 Clinton Davisson and Lester Germer fired a beam of low-energy electrons at a polished single crystal of nickel and measured the intensity of the scattered beam as a function of angle. At an accelerating voltage of 54 V and a detector angle of 50° they found a sharp peak — not the smooth angular distribution a classical particle picture predicts, but the kind of angular peak you get from a wave diffracting off a regularly spaced grating.

The predicted de Broglie wavelength of a 54 eV electron is

\lambda = \frac{h}{\sqrt{2 m_e e V}} = \frac{12.27\ \text{Å}}{\sqrt{V/\text{volt}}} = \frac{12.27}{\sqrt{54}}\ \text{Å} = 1.67\ \text{Å}.

The nickel crystal's surface-atom spacing is d = 2.15 Å. Treating the surface as a reflection grating (the Bragg condition for surface atoms at grazing geometry becomes d\sin\phi = n\lambda, where \phi is the scattering angle measured from the normal),

\lambda_\text{measured} = d \sin 50° = 2.15 \times 0.766 = 1.65\ \text{Å}.

The two numbers agree to better than 1%. Matter waves are real. Electrons diffract the way X-rays and light do, with wavelength set by the same Planck constant that governs photons — h/p.

The experiment also gives a quantitative, reproducible way to measure h/p for an electron: vary the accelerating voltage and watch the peak move. Higher V gives smaller \lambda (shorter de Broglie wavelength) and therefore smaller scattering angle. The peak position tracks \lambda \propto 1/\sqrt{V} exactly.

Davisson-Germer is to matter what Young's double slit is to light — the experiment that decides the question by forcing waves to show themselves where classical intuition would have none.

A low-voltage electron gun in a vacuum chamber fires electrons at about one-tenth of one percent of the speed of light onto a chunk of polished metal. A detector sweeps an arc, counting how many electrons bounce back at each angle. If electrons are tiny particles, you would expect a broad, structureless blur — roughly isotropic at small angles, falling off smoothly as the angle grows. You would not expect sharp peaks. You would certainly not expect the peaks to line up exactly with the prediction of a formula for a wave that is supposed to describe the electron.

But when Davisson and Germer ran this experiment in 1927 — partly by accident, following a vacuum failure that accidentally annealed their nickel target into a neat crystalline surface — that is exactly what they found. A sharp peak. At an angle that matched, to within the precision of their measurements, the prediction of the de Broglie formula \lambda = h/p. The experiment was one of the first direct, quantitative confirmations of the wave nature of matter. The article on the de Broglie hypothesis shows where the prediction came from. This article shows where the experiment found it.

The setup — what was actually in the chamber

A simple kinematic setup, but everything about the geometry matters.

The experiment measures the scattered intensity I(\phi) as a function of angle, with the accelerating voltage V held fixed. Then V is changed, and the curve I(\phi) is remeasured.

Davisson-Germer apparatus, schematicAn electron gun on the left fires a horizontal beam at a nickel crystal at the centre. The crystal surface is shown as a horizontal line with regularly spaced surface atoms. A detector arm sweeps through an arc above the crystal, shown at a scattering angle phi measured from the normal to the crystal surface. A voltage source V is shown connected between the filament and the anode.electron gunVincident electronsNi crystal surface (d = 2.15 Å between atoms)normalscatteredφdetector
Davisson-Germer schematic. Electrons accelerated through a potential $V$ hit a nickel crystal at normal incidence. A detector measures the scattered intensity as a function of angle $\phi$ from the normal.

At V = 54 V the scattered intensity curve shows a clear peak at \phi = 50°. At lower or higher voltages the peak sits at different angles. At still other voltages — notably those where \lambda does not match an integer multiple of the surface spacing — the peak disappears entirely. This is diffraction behaviour.

De Broglie's prediction — a one-line recap

From the de Broglie hypothesis, every particle has an associated wavelength

\lambda = \frac{h}{p}.

For a non-relativistic electron accelerated through potential V, kinetic energy is K = eV and momentum is p = \sqrt{2 m_e K} = \sqrt{2 m_e e V}. Substituting:

\lambda = \frac{h}{\sqrt{2 m_e e V}}.

Plug in h = 6.626\times 10^{-34} J·s, m_e = 9.109\times10^{-31} kg, e = 1.602\times10^{-19} C:

\lambda = \frac{6.626\times10^{-34}}{\sqrt{2 \cdot 9.109\times10^{-31} \cdot 1.602\times10^{-19} \cdot V}}\ \text{m} = \frac{1.226\times10^{-9}}{\sqrt{V}}\ \text{m}.

Converting to ångströms (1 Å = 10^{-10} m):

\boxed{\;\lambda = \frac{12.27}{\sqrt{V}}\ \text{Å} \qquad\text{(for non-relativistic electrons, } V \text{ in volts)}\;}

Why: this is the operational form of de Broglie's formula, adapted to the lab. Every electron diffraction experiment uses it, and every value comes out comparable to inter-atomic spacings in solids. That is the miracle — atoms are about 10^{-10} m apart, and accessible lab voltages give electron wavelengths of about 10^{-10} m. The two numbers were built to match by nature.

For V = 54 V: \lambda = 12.27/\sqrt{54} = 12.27/7.35 = 1.669 Å.

Why the nickel surface acts as a grating — the Bragg-like condition

A crystal is a regular three-dimensional lattice of atoms. When a wave hits it, the wave scatters off every atom, and the scattered wavelets interfere. For most directions the wavelets are out of phase and cancel; for special directions they add in phase, producing a peak in the scattered intensity. This is identical to the picture you built in young's double slit experiment and diffraction grating, except with atoms as the slits.

For the Davisson-Germer geometry, the relevant atoms are the ones on the nickel surface — slow electrons do not penetrate deep into the metal. The surface atoms form a periodic array with spacing d = 2.15 Å (the nickel (111) face). The incident electrons come in at normal incidence. The detector sits at an angle \phi from the normal.

Surface diffraction geometryA horizontal crystal surface line with two highlighted atoms separated by distance d. An incident ray comes straight down onto each atom. Two scattered rays leave the atoms at the same angle phi from the normal and travel parallel to the detector. The path-difference triangle is marked: from the second atom a segment of length d-sin-phi is the extra path the right-hand scattered ray must travel.surface atoms, spacing dincident (both in phase)to detector at angle φφd sin φ
Two adjacent surface atoms, separated by $d = 2.15$ Å. The incident electrons arrive in phase (same wavefront). When they scatter into the detector direction at angle $\phi$, the ray from the right atom travels an extra distance $d\sin\phi$ compared with the ray from the left. For constructive interference, this extra path must equal an integer number of de Broglie wavelengths.

The two rays leaving the surface from neighbouring atoms are parallel (they both head toward the distant detector). The rightmost ray has to travel an extra distance equal to d \sin\phi before reaching the detector, relative to the leftmost ray.

Derivation of the diffraction condition

Step 1. Both incident rays arrive with the same phase (they are wavefronts of the same de Broglie wave coming down normally).

Why: the electron source is a long way away, so the incoming wave has plane wavefronts parallel to the surface. Two points on the surface are hit at the same instant.

Step 2. After scattering, the rays head to the detector in parallel directions. The ray from the right atom reaches the detector after travelling an extra path length.

\Delta = d\sin\phi.

Why: drop a perpendicular from the left atom onto the outgoing ray from the right atom. The right-triangle you get has hypotenuse d and one side d\sin\phi — that is the path difference.

Step 3. Constructive interference occurs when the path difference is a whole number of wavelengths.

d\sin\phi = n\lambda, \qquad n = 1, 2, 3, \ldots

Why: two rays meeting in phase must differ by an integer multiple of \lambda. n = 0 would be the forward direction (trivial); n = 1 is the first-order peak; higher n gives peaks at larger angles.

Step 4. The observed Davisson-Germer peak at V = 54 V is first-order, so n = 1:

\lambda = d \sin\phi.

With d = 2.15 Å and \phi = 50°:

\lambda = 2.15 \times \sin 50° = 2.15 \times 0.766 = 1.647\ \text{Å}.

Why: this is the wavelength the experiment says the electrons have, read off from the diffraction peak — with no reference to de Broglie's formula. It is a direct measurement of \lambda.

Step 5. Compare with de Broglie's prediction.

\lambda_\text{dB} = \frac{12.27}{\sqrt{54}}\ \text{Å} = 1.669\ \text{Å}.

The two numbers agree to 1.3%.

Why: this is the moment the experiment clinches it. Two independent computations — one from the diffraction angle, one from the acceleration voltage and the de Broglie formula — agree to better than 2 percent. No classical particle picture predicts a peak at any angle, let alone at the angle de Broglie's wave formula demands. Electrons are waves.

Watch the peak move — an interactive tour of \lambda \propto 1/\sqrt{V}

The cleanest way to internalise Davisson-Germer is to watch the peak angle change as you dial the voltage. Higher V means higher momentum means shorter \lambda. Shorter \lambda means \sin\phi = \lambda/d is smaller. So the peak sits at a smaller angle.

Interactive: Davisson-Germer peak angle vs accelerating voltageA plot of the predicted first-order diffraction angle phi (in degrees) as a function of accelerating voltage V (in volts). The curve sweeps from large phi (shallow, near 90 degrees) at low V down to small phi (steep, near 10 degrees) at high V. A draggable red point on the voltage axis lets the user set V between 10 and 150 volts. A readout shows V, the de Broglie wavelength in angstroms, and the predicted peak angle phi.accelerating voltage $V$ (volts)scattering angle $\phi$ (degrees)0408012016022°45°68°90°$\sin\phi = \lambda/d = 12.27/(d\sqrt{V})$drag the red point
Drag the red point along the voltage axis. The curve is $\phi(V) = \arcsin\!\big(\lambda/d\big) = \arcsin\!\big(12.27/(d\sqrt V)\big)$. At $V = 54$ V the readout shows $\phi \approx 50°$ and $\lambda \approx 1.67$ Å — the original Davisson-Germer observation. Raise $V$ and both $\lambda$ and $\phi$ shrink together. Drop $V$ below about 32 V and $\sin\phi$ exceeds 1 — no first-order peak exists for that wavelength; the curve ends.

Every point on that curve is a prediction. Davisson and Germer verified several of them — enough to rule out any interpretation except the wave one. Their paper reported peaks at multiple voltages, all sitting on this curve to within experimental error.

Comparison with X-ray diffraction

Long before matter waves were a thing, X-ray crystallography had been doing the same geometric trick with X-rays. Von Laue in 1912 and the Braggs in 1913 showed that shining X-rays on a crystal produced sharp diffraction peaks obeying

2 d \sin\theta = n\lambda \qquad\text{(Bragg condition for crystal planes)}

where \theta is the angle between the incoming ray and the crystal plane (not the normal), and d is the interplanar spacing. The difference in geometry — planes vs surfaces, angle from plane vs from normal — changes the factor of 2 and swaps the sine of an angle with the sine of the complementary angle, but the underlying physics is the same: waves scattering off a regular lattice produce sharp angular peaks.

The significance of Davisson-Germer is that the same crystal gives the same kind of peak whether you aim it with an X-ray of wavelength \sim 1 Å or an electron of wavelength \sim 1 Å. The target does not care what kind of wave you send at it; it only cares about the wavelength. That is the cleanest possible demonstration that the electron, when it is propagating, is a wave in every sense that X-rays are.

This equivalence is what makes electron microscopes possible. In an electron microscope the de Broglie wavelength of a 100 keV electron is about 0.04 Å — a hundred times smaller than visible light's wavelength and small enough to resolve individual atoms. The Transmission Electron Microscopes (TEMs) at AIIMS and at major IIT materials-science labs work by shining a monochromatic electron wave through a sample and collecting its diffracted image. The physics under the hood is direct descendant of Davisson-Germer.

Worked examples

Example 1: Predicting the peak angle for a 100 V electron beam on nickel

A beam of electrons is accelerated through V = 100 V and then directed at a nickel (111) surface with atomic spacing d = 2.15 Å. Predict the angle of the first-order diffraction peak.

Step 1. Compute the de Broglie wavelength.

\lambda = \frac{12.27}{\sqrt{V}}\ \text{Å} = \frac{12.27}{\sqrt{100}} = \frac{12.27}{10} = 1.227\ \text{Å}.

Why: this is the non-relativistic de Broglie formula with voltage in volts and wavelength in ångströms.

Step 2. Apply the first-order diffraction condition d \sin \phi = \lambda.

\sin\phi = \frac{\lambda}{d} = \frac{1.227}{2.15} = 0.5707.

Why: set n = 1 because that is the peak closest to the forward direction and therefore the easiest to observe. Higher-order peaks (if they exist) sit at larger angles.

Step 3. Solve for \phi.

\phi = \arcsin(0.5707) = 34.8°.

Step 4. Sanity check against the 54 V benchmark. At 54 V the angle was 50°; at 100 V the wavelength is shorter by a factor of \sqrt{100/54} = 1.36, so \sin\phi is smaller by the same factor: \sin\phi \approx \sin 50°/1.36 = 0.766/1.36 = 0.564, giving \phi \approx 34.3°. Matches the direct calculation.

Result. \phi \approx 34.8° at V = 100 V.

Peak angles at two voltagesA nickel surface with an incident beam coming down and two outgoing scattered rays drawn: the 54-volt ray at 50 degrees from the normal and the 100-volt ray at 35 degrees from the normal. Labels mark the two angles.normalincident54 V → 50°100 V → 35°
The peak angle shrinks as the voltage rises: higher energy electrons have shorter wavelengths, so constructive interference happens closer to the incident direction.

What this shows. The experiment is a predictive tool. Pick a voltage, compute \lambda, compute \sin\phi = \lambda/d, and you know exactly where to park the detector. Any disagreement between prediction and observation — and there was none, across dozens of measurements — would have been evidence against the wave picture. There was none.

Example 2: Reverse direction — reading Planck's constant out of the peak

A hypothetical graduate student measures a first-order diffraction peak for electrons accelerated through V = 80.0 V, scattering off a crystal with d = 2.20 Å. They measure the peak at \phi = 38.5°. From this data alone, compute Planck's constant.

Step 1. Read off the electron wavelength from the diffraction angle.

\lambda = d \sin\phi = 2.20 \times \sin 38.5° = 2.20 \times 0.6225 = 1.370\ \text{Å} = 1.370 \times 10^{-10}\ \text{m}.

Why: the Bragg-like condition gives \lambda directly from the angle and the known crystal spacing, with no reference to h yet.

Step 2. Compute the electron momentum from the acceleration voltage, using classical mechanics (valid because eV \ll m_e c^2).

p = \sqrt{2 m_e e V} = \sqrt{2 \cdot 9.109\times10^{-31} \cdot 1.602\times10^{-19} \cdot 80.0} = \sqrt{2.334 \times 10^{-47}}\ \text{kg·m/s}.
p = 4.832 \times 10^{-24}\ \text{kg·m/s}.

Why: energy conservation in the gun gives eV = p^2/2m_e, from which p follows. No h involved.

Step 3. Combine de Broglie's hypothesis to extract h.

\lambda = \frac{h}{p} \quad\Rightarrow\quad h = \lambda \cdot p.
h = 1.370 \times 10^{-10} \cdot 4.832 \times 10^{-24} = 6.620 \times 10^{-34}\ \text{J·s}.

Why: this is the measurement. You have \lambda (from the crystal geometry), and p (from the gun voltage), and the de Broglie hypothesis gives you h. Compare with the accepted value h = 6.626\times 10^{-34} J·s — the student's result agrees to one part in a thousand.

Result. h_\text{measured} = 6.62 \times 10^{-34} J·s, consistent with the accepted value.

Reading Planck's constant from Davisson-Germer dataA horizontal flow diagram with three boxes. Box 1 on the left: measured angle phi equals 38.5 degrees and known crystal spacing d equals 2.20 angstrom, leading to lambda equals 1.37 angstrom. Box 2 in the middle: voltage V equals 80 volts, leading to momentum p equals 4.83 times ten to the minus 24 kilogram metre per second. Box 3 on the right: h equals lambda times p equals 6.62 times ten to the minus 34 joule second.measured φ = 38.5°known d = 2.20 Å→ λ = d sin φλ = 1.37 ÅV = 80 Vp = √(2 m_e e V)p = 4.83×10⁻²⁴kg·m/sh = λ · p= 6.62×10⁻³⁴J·s
The reverse path from Davisson-Germer to Planck's constant. The experiment takes two quantities you know from macroscopic measurements (a crystal spacing from X-ray crystallography, a voltmeter reading on the gun) and delivers the fundamental constant that governs all of quantum mechanics.

What this shows. The experiment is not just a confirmation of the de Broglie formula — it is a measurement of h. Run the experiment carefully enough and you get an independent determination of Planck's constant, to whatever precision your angle readout and voltmeter support. This is how modern precision metrology works: the ampere, the kilogram, and the second are now defined (since 2019) in terms of fixed values of h, c, and other constants, and electron diffraction is among the experiments that can directly check h.

Common confusions

Why this mattered for quantum mechanics

The de Broglie hypothesis was, at the start, a bold guess in a PhD thesis. It had beautiful symmetry with the photon case — if light of wavelength \lambda has momentum h/\lambda, why shouldn't matter of momentum p have wavelength h/p? — but symmetry is not evidence. Several physicists at the time, including de Broglie's thesis committee, were unsure what to make of it.

Davisson-Germer made matter waves experimentally undeniable. The very same electron that had been treated, for twenty-five years since J.J. Thomson's experiments, as a classical charged particle — a tiny billiard ball with mass, charge, and velocity — turned out to obey a wave equation when you asked it to scatter off a crystal. Three months after Davisson-Germer, George Thomson (J.J.'s son!) published a complementary experiment: he fired higher-energy electrons through a thin gold foil and saw a full set of Debye-Scherrer rings — the same ring pattern X-rays give when they pass through a polycrystalline sample. Thomson the elder had proved the electron was a particle (1897); Thomson the younger proved it was a wave (1927). Both father and son received Nobel prizes. The physics was right both times.

This was the experimental foundation on which Schrödinger's wave equation (1926) could be trusted. Before Davisson-Germer, Schrödinger's equation was a brilliant mathematical guess whose physical meaning was disputed. After Davisson-Germer, the wave function of an electron was an object the experiments measured directly.

Going deeper

If what you came for was the core experiment — the geometry, the derivation, and the agreement with de Broglie — you have it. What follows is the rigorous layer: why the peak has finite width, how the Bragg condition emerges from a full 3D crystal analysis, relativistic corrections, and why the modern version of this experiment still goes on in materials-science labs.

The full 3D crystal — von Laue conditions

The Bragg-like surface formula d\sin\phi = n\lambda gives the right answer for the first-order peak on a single surface row, but real crystals are 3D. The condition for constructive scattering of a wave with incoming wave vector \vec k_i and outgoing wave vector \vec k_f off a 3D lattice is

\vec k_f - \vec k_i = \vec G,

where \vec G is any reciprocal lattice vector — a vector in the Fourier-transform dual of the direct lattice. This is the Laue condition, and it reduces to 2d\sin\theta = n\lambda (Bragg) when applied to a specific family of parallel planes. For the Davisson-Germer geometry, the surface reduces the 3D lattice to a 2D surface mesh with a different set of reciprocal vectors; the condition d\sin\phi = n\lambda is the result for one particular scattering plane. The appearance of secondary peaks at other voltages in Davisson-Germer's data corresponds to other reciprocal-lattice vectors; they all sit on the same \lambda = h/p relation.

Finite peak width — why the peaks are not infinitely sharp

An ideal infinite grating would give a delta-function peak. Real crystals have finite size (so the interference sum terminates), finite temperature (so atoms vibrate around their lattice sites with amplitude roughly 0.1 Å at room temperature — the Debye-Waller factor), and finite monochromaticity in the electron beam (the thermal energy spread of the electron gun gives \Delta V/V \sim 10^{-3} for a hot cathode). Each of these broadens the peak. The Davisson-Germer peaks are about a few degrees wide, consistent with these contributions summed in quadrature. The peak position, however, is well-defined to within the experimental precision — which is why the agreement with de Broglie could be claimed to better than 2%.

Relativistic correction to the de Broglie formula

For high-energy electrons — say, the 100 keV electrons in a transmission electron microscope — the non-relativistic formula underestimates the momentum. The relativistic relation is E^2 = (pc)^2 + (m_e c^2)^2 with E = m_e c^2 + eV, giving

p = \frac{1}{c}\sqrt{(eV)^2 + 2 m_e c^2 \cdot eV} = \sqrt{2 m_e e V}\sqrt{1 + \frac{eV}{2 m_e c^2}}.

For V = 100 kV, eV/2m_e c^2 = 10^5 / 10^6 \approx 0.1, so the correction is about 5%. For the 54 V electrons of the original Davisson-Germer paper, the correction is 54/10^6 \approx 5 \times 10^{-5} — negligible. The non-relativistic formula is precisely what the experiment required.

Low-Energy Electron Diffraction (LEED) — the modern Davisson-Germer

Davisson and Germer's experiment matured into a routine surface-science tool called LEED (Low-Energy Electron Diffraction). Point a 20–200 eV electron beam at any clean crystalline surface; the back-scattered electrons produce a two-dimensional diffraction pattern on a phosphor screen behind the source. The bright spots on the LEED pattern are a direct image of the reciprocal lattice of the surface, and from them the surface structure — reconstructions, adsorbed layers, step densities — can be read. Every serious surface-science lab runs LEED. The underlying physics is still the Davisson-Germer derivation. The surface-physics group at the Tata Institute of Fundamental Research in Mumbai and the Institute of Physics in Bhubaneswar have LEED systems that were built and maintained locally.

Electron microscopy — wavelength as resolution

The resolving power of any imaging system is set, ultimately, by the wavelength of the radiation used (diffraction limit \approx \lambda/(2 \text{NA}), where NA is the numerical aperture). Optical microscopes, limited to \lambda \geq 400 nm, cannot resolve features smaller than about 200 nm. Electron microscopes, using \lambda \sim 0.04 Å for 100 keV electrons, can resolve features down to about 1 Å — the size of an atom. Every atomic-resolution image of graphene, every cryo-EM structure of a protein, every nanowire measurement in an Indian materials-science lab is an application of the wavelength the Davisson-Germer experiment measured for the first time.

Matter-wave interferometry — Davisson-Germer taken to the limit

If you can diffract electrons off a crystal, you can put them through a two-slit analogue and look at the interference fringes. Jönsson did exactly this in 1961, building a nano-fabricated double slit for electrons. Later experiments used pairs of thin-wire biprisms (Möllenstedt biprisms) to split and recombine electron waves, producing interference fringes visible on a screen — the literal equivalent of Young's double slit with matter instead of light. The current frontier is atom interferometers, in which beams of cold atoms are split, steered, and recombined using lasers, and the interference is sensitive enough to measure gravitational acceleration to parts in 10^{11} or to probe space-time curvature. All of this is the direct legacy of the accidental 1927 experiment in Bell Labs.

Where this leads next