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Clinton Davisson and Lester Germer measured strong angular structure in electron scattering from a nickel crystal. Its dependence on incident electron energy agreed with a wavelength set by the electron momentum through the de Broglie wavelength. The crystal therefore supplied a periodic structure against which electron wave behavior could be tested. The Davisson–Germer experiment linked a tunable electron source and angularly resolved detector with the theoretical idea of matter waves.^[ref]

A physicist whose route into research included a telephone-company job when he could not afford to continue at Chicago. He later worked at Bell Telephone Laboratories, retiring in 1946 after 29 years, and taught physics at Virginia in 1947–1949.^[ref] The Davisson–Germer experiment connects that industrial-laboratory work to electron diffraction and matter waves.

The Davisson–Germer experiment turned elastic scattering from nickel into evidence for a matter wave. The search became a deliberate wave test in 1926, with diffraction beams found early in 1927. The earlier crystal investigation had begun in 1925; the de Broglie wavelength proposal was already present in the 1924 thesis.^[ref]

A heated tungsten ribbon supplied electrons; gun apertures selected a narrow beam. Two $1\mathrm{mm}$ apertures were $8\mathrm{mm}$ apart; the gun ended $7\mathrm{mm}$ from a nickel crystal cut parallel to its $\{111\}$ planes. An adjustable electric potential difference set the speed. The beam struck normally inside an evacuated, field-free enclosure with target and outer electrodes at one potential. A double-box collector, $11\mathrm{mm}$ from the target with a $1\mathrm{mm}$ entrance, selected directions. A retarding electric potential difference rejected slower electrons; the inner collector fed a sensitive galvanometer. Moving the collector scanned colatitude; rotating the crystal scanned azimuth.^[ref]

The readout was collected electric current, not a photograph of electron paths. Voltage scans held the gun-plate current constant because incident-beam current could not be held constant; the overall current trend therefore needed caution. A strong feature developed at $54\mathrm{V}$ near $50^{\circ }$ colatitude. Surface heating distinguished crystal beams from adsorbed-gas beams; finite apertures and background shifted or broadened apparent peaks.^[ref]

At the bright beam's colatitude, an azimuth scan revealed three companion directions, matching crystal symmetry. The test compared wavelengths inferred from diffraction angles and known crystal spacings with wavelengths inferred from accelerating voltage and momentum; the 1937 lecture displayed this comparison against $U^{-1/2}$. Agreement across beam directions supplied more evidence than one angular peak.^[ref]

The inference is about coherent quantum phases in scattering probabilities. It does not establish a wavy particle trajectory, and a collector-current experiment does not resolve individual detection events. Predicting the full intensity additionally requires the material's scattering amplitude, its surface condition, and instrumental angular acceptance; the de Broglie wavelength alone predicts none of those strengths. The following finite-row electron diffraction model isolates phase addition without attempting to reproduce the nickel measurements.

In the 1923 note Waves and Quanta, Louis de Broglie proposed a periodic process associated with rest energy, remaining in phase with a wave along the moving particle's path. He distinguished the internal frequency slowed by time dilation from the wave frequency based on total energy.^[ref] The proposal developed into his 1924 thesis.^[ref] In the 1929 lecture The wave nature of the electron, he reconstructed the argument using a Lorentz transformation.^[ref]

Here is that quantum phase argument in modern notation. Set ${\omega }_0=m{c}^2/\hslash$ in the rest frame. A Lorentz transformation to a frame where the particle has velocity $v$ givesAlong $x=vt$, proper time is $\tau =t/\gamma$, soThis is the harmony: evaluating the spatial wave at the moving particle gives the slower clock phase. At fixed $x$, its angular frequency is instead $E/\hslash =\gamma {\omega }_0$. Since $k=p/\hslash$, the de Broglie wavelength follows as $\lambda =2\pi /k=h/p$. The proposed clock was a theoretical construction, not an observed mechanical vibration.

The de Broglie wavelength is the distance over which a matter wave accumulates one full spatial quantum phase cycle in its propagation direction:Here $h$ is the Planck constant, $\mathbf{p}$ is the momentum, and $\mathbf{k}$ is the angular wavevector. The scalar $p$ in $\lambda =h/p$ means the positive momentum magnitude, not a signed component. Reversing a momentum reverses the wavevector without making the wavelength negative. At zero momentum there is no finite spatial phase period: the limiting wavelength diverges.

This relation makes microscopic diffraction accessible with particles: increasing the momentum shortens the wavelength until it is comparable with the spacings in a crystal scattering problem. The electron accelerating-voltage wavelength gives a practical way to tune this scale, while the Davisson–Germer experiment tests it by comparing electron diffraction directions with independently known crystal geometry. The same relation applies to neutral particles in a neutron interferometer; electric charge is not a requirement for a matter wave.

The wavelength belongs to the wavefunction, not to a sinusoidal path of a particle. A free-particle momentum convention makes the distinction especially clear: a plane wave has a rotating complex quantum phase but a constant probability density. A localized wave packet contains a range of momenta and therefore generally has a range of wavelengths, rather than one exact spatial period.

Let an electron start with negligible kinetic energy and move through an increase $U>0$ in electric potential. Its electric charge is $q=-e$, where $e>0$ is the elementary charge, so the decrease in potential energy is $eU$. In a field-free region after acceleration,This is an electron formula, not a universal conversion from voltage to wavelength. It assumes negligible initial kinetic energy, negligible losses, and $eU\ll m_e{c}^2$, where $c$ is the speed of light. It describes the de Broglie wavelength outside the crystal; the potential energy inside a material can change the local kinetic momentum.

For $U=54\mathrm{V}$, take $h=6.62607015\times 10^{-34}\mathrm{J}\mathrm{s}$, $e=1.602176634\times 10^{-19}\mathrm{C}$, and $m_e\simeq 9.1093837\times 10^{-31}\mathrm{kg}$. The rounded electron mass is consistent with the 2022 recommended constants.^[ref]The electronvolt is an energy unit: $54\mathrm{eV}$ must be converted to joules before combining it with $m_e$ in SI units. Dimensional analysis checks both steps:The resulting velocity is about $4.3584\times 10^6\mathrm{m}{\mathrm{s}}^{-1}$, or $0.01454c$, so the nonrelativistic assumption is consistent. For a larger accelerating voltage, the relativistic energy-momentum relation gives $pc=\sqrt{K(K+2m_e{c}^2)}$, with $K=eU$, while $\lambda =h/p$ still holds. At $54\mathrm{V}$ the relativistic wavelength is shorter by about $0.00264\%$.

Explicitly, the exact special relativity formula and its nonrelativistic quantum mechanics limit areHere $K=eU$ is the gained kinetic energy; the total energy is $E=m_e{c}^2+K$. At $80\mathrm{kV}$, the nonrelativistic quantum mechanics expression gives $4.336\mathrm{pm}$, about $3.84\%$ larger than the exact $4.176\mathrm{pm}$. This difference matters when using electron diffraction ring positions to infer lattice plane spacings.

Electron diffraction is interference between scattered electron probability amplitudes. It connects the de Broglie wavelength of the incident beam to the arrangement of the scattering material. In elastic scattering from a fixed crystal, $|{\mathbf{k}}_{\mathrm{out}}|=|{\mathbf{k}}_{\mathrm{in}}|=2\pi /\lambda$, and constructive crystal scattering selects wavevector transfers $\mathbf{Q}={\mathbf{k}}_{\mathrm{out}}-{\mathbf{k}}_{\mathrm{in}}$ in the reciprocal lattice. The physical momentum transfer to the electron is $\hslash \mathbf{Q}$ in this convention.

Bragg's law expresses the same condition as $2d\sin {\theta }_B=n\lambda$, where $d$ is the spacing of the chosen lattice planes, $n$ the diffraction order, and ${\theta }_B$ the angle to those planes. The angle between incoming and outgoing propagation directions is $\chi =2{\theta }_B$ for that reflection geometry. In normal-incidence backscattering, a detector's angle $\varphi$ from the outward surface normal instead gives $\chi =\pi -\varphi$; neither detector colatitude nor angle to the surface normal should silently replace ${\theta }_B$. A finite-row electron diffraction model uses a different spacing, the spacing between sites along a surface row, and makes that distinction explicit.

An electron microscope forms a spatially enlarged representation of a specimen using electrons, electron lenses, and a detector. Its appeal is access to structure too fine for an ordinary optical microscope, but a short de Broglie wavelength alone does not guarantee fine electron microscope resolution. Increasing magnification can enlarge an existing blur without revealing any additional structure.

In transmission electron microscopy, an electron gun illuminates a thin specimen; magnetic electron lenses form and enlarge its transmitted image on a fluorescent screen or detector. A vacuum reduces collisions with gas. Lens electric currents control focusing and magnification.^[ref]

Electron microscope resolution concerns distinguishable specimen detail under a specified contrast criterion. It depends on diffraction, lens defects, electron energy spread, specimen motion and detection. A smaller de Broglie wavelength permits finer detail in principle, but neither wavelength nor magnification is the instrument's measured resolution.

For an electron accelerated from negligible initial kinetic energy through a positive electric potential difference $U$, combine $K=eU$, the relativistic energy-momentum relation and the de Broglie wavelength:Here $h$ is the Planck constant, $m_e$ the electron mass, $e$ the elementary charge, and $c$ the speed of light. This includes the relativistic correction omitted by the low-voltage electron accelerating-voltage wavelength approximation. With $m_e\simeq 9.1093837\times 10^{-31}\mathrm{kg}$ and SI defining values of $h,e,c$, calculated wavelengths are approximately $6.979$, $3.701$ and $1.969\mathrm{pm}$ at $30$, $100$ and $300\mathrm{kV}$ respectively. The rounded mass agrees with the recommended value.^[ref]

For a circular aperture admitting a small semi-angle $\alpha$, the Rayleigh criterion suggests a diffraction-limited resolution scale $d_D=0.61\lambda /\alpha$. At $100\mathrm{kV}$ and $\alpha =10\mathrm{mrad}$, this gives $0.226\mathrm{nm}$, already much larger than the $0.00370\mathrm{nm}$ wavelength. This is an ideal aperture estimate. Transmission electron microscopy with coherent illumination and a particular specimen requires its own image-contrast analysis; this scale alone is not a universal two-feature resolution test.

An original illustrative blur model adds competing effects:Define $C_s{\alpha }^3$ as a characteristic transverse blur from the electron-lens analogue of spherical aberration, and $C_c\alpha \Delta K/K$ as one from energy-dependent focusing, the analogue of chromatic aberration. The coefficients $C_s,C_c$ have units of length, $\Delta K$ is a chosen characteristic kinetic energy spread, and $b_0$ is a fixed residual blur. Adding their squares is a declared heuristic, not a measured point spread function or a rigorous resolution theorem. The model omits contrast transfer, specimen scattering and signal statistics, so its minimum is only an estimate within its assumptions.

Choose $C_s=C_c=1\mathrm{mm}$, $\Delta K=0.7\mathrm{eV}$ and $b_0=0.10\mathrm{nm}$ at $K=100\mathrm{keV}$. At $5\mathrm{mrad}$, the four contributions are about $0.452$, $0.125$, $0.035$ and $0.100\mathrm{nm}$, giving $b\simeq 0.480\mathrm{nm}$. At $10\mathrm{mrad}$, the diffraction contribution falls to $0.226\mathrm{nm}$ but the assumed spherical aberration contribution grows to $1.00\mathrm{nm}$. Thus opening the aperture indefinitely worsens this model's image. All these values are calculations with chosen parameters, not observations of any microscope.

Electron optics studies how electric fields and magnetic fields guide electrons and form images. The Lorentz force supplies a trajectory description, while the de Broglie wavelength supplies the wave scale needed for diffraction. Both descriptions matter: steering a narrow beam and resolving two nearby specimen features are different achievements.

For a magnetic electron lens,Here $e>0$ is the elementary charge, $\mathbf{v}$ the electron velocity, and $\mathbf{B}$ the magnetic field. The second equality follows because a cross product is perpendicular to each factor: a static magnetic field bends the trajectory without increasing the kinetic energy. Acceleration instead requires work by an electric field. This distinction lets an electron microscope adjust imaging with magnetic fields while an accelerating voltage sets the electron momentum.

For a free particle of mass $m>0$ in nonrelativistic quantum mechanics, choose the potential energy zero and writeApplying the momentum operator $-i\hslash \nabla$ returns $\mathbf{p}\psi$; this fixes the sign convention. The angular frequency is measured relative to this chosen energy zero. Adding a constant energy changes only a time-dependent global phase, leaving the spatial de Broglie wavelength unchanged. No rest-energy term is included in this nonrelativistic quantum mechanics convention.

The plane wave has $|\psi {|}^2=|A{|}^2$ and probability current $\mathbf{j}=(\mathbf{p}/m)|A{|}^2$. Its real part can be drawn as a sine or cosine, but that graph is a component of a probability amplitude, not a transverse displacement. On infinite space this is a generalized momentum eigenstate, not a state satisfying wavefunction normalization. A narrow wave packet instead moves with group velocity ${\nabla }_{\mathbf{k}}\omega =\mathbf{p}/m$; the phase velocity $\omega /|\mathbf{k}|=|\mathbf{p}|/(2m)$ is not its transport speed.

The equality of canonical momentum and kinetic momentum here assumes a field-free region with the magnetic vector potential chosen zero. For a charged particle in a magnetic field, the kinetic momentum is $\mathbf{\Pi }=\mathbf{p}-q\mathbf{A}$. An arbitrary canonical phase gradient must not then be substituted into $m\mathbf{v}$; the free particle formula needs its stated assumptions.

George Paget Thomson demonstrated wave behavior of electrons by passing an electron beam through thin material and recording diffraction patterns. Many crystal orientations in a thin polycrystalline film produce rings, whose geometry can be compared with the wavelength associated with the electron momentum. The experiment connects a photographic pattern with the de Broglie wavelength, making electron interference observable at energies and in a geometry different from a reflected crystal beam.^[ref]

Physics.^[ref]

Lester Germer and Clinton Davisson observed electron diffraction from a nickel crystal. The intensity of scattered electrons varied strongly with direction and incident electron energy, as expected when a crystal's periodic structure acts on a wave. Agreement between the inferred wavelength and the de Broglie wavelength connected a particle's momentum with observable interference. The experiment made electron wave behavior a measured property of a material-scattering apparatus.^[ref]

The momentum operator generates spatial translations. In a one-dimensional position representation in quantum mechanics, it acts asApplying it to a plane wave $e^{ikx}$ gives momentum eigenvalue $\hslash k$, connecting momentum with the de Broglie wavelength. A localized wave packet generally contains several such momenta.

A differential expression alone does not define a self-adjoint operator: its domain and boundary conditions matter. On a periodic interval, the allowed momentum eigenvalues are discrete; on the whole real line they form a continuous spectrum. In a magnetic field, this operator is the canonical momentum. The mechanical momentum entering the kinetic energy is instead $P-qA$ in SI units, where $A$ is the vector potential.

Treat the incident and outgoing neutrons as free nonrelativistic particles outside the specimen. Their wave vectors, de Broglie wavelengths, momenta and kinetic energies obeyHere $k_i=|{\mathbf{k}}_i|$, $k_f=|{\mathbf{k}}_f|$, $m_n$ is the neutron mass, and $\hslash =h/(2\pi )$ uses the Planck constant. Subtracting the outgoing projectile quantities from the incoming ones gives the momentum transfer and energy delivered to the specimen:Thus $\mathbf{Q}$ has units of inverse length, rather than momentum. A positive $\omega$ means the specimen gains energy; negative $\omega$ means it supplies energy to the neutron. If the angle between incident and outgoing propagation directions is $2\theta$, the law of cosines givesKnowing the detector angle alone therefore leaves $Q$ undetermined unless the outgoing energy is known or an elastic scattering assumption is justified.

For a reproducible unit conversion choose $m_n=1.67492750056\times 10^{-27}\mathrm{kg}$, $h=6.62607015\times 10^{-34}\mathrm{J}\mathrm{s}$ and $1\mathrm{eV}=1.602176634\times 10^{-19}\mathrm{J}$. The first is a recommended central value; the latter two conversions are exact.^[ref] With $1$ ångström equal to $10^{-10}\mathrm{m}$ and $1\mathrm{meV}=10^{-3}$ electronvolts, substitution into $E=h^2/(2m_n{\lambda }^2)$ givesSquare brackets here mean the numerical value in the indicated unit. For an original chosen example, ${\lambda }_i=2$ ångströms and ${\lambda }_f=2.5$ ångströms give $E_i\simeq 20.451\mathrm{meV}$, $E_f\simeq 13.089\mathrm{meV}$ and $\hslash \omega \simeq 7.362\mathrm{meV}$. At $2\theta =60^{\circ }$, $Q\simeq 2.879{\mathring{\mathrm{A}}}^{-1}$. These values stipulate an allowed projectile geometry; they do not assert that any particular specimen has an excitation there.

Awarded to Louis de Broglie for the wave nature of electrons. The de Broglie wavelength connects momentum to observable diffraction.^[ref]

A free particle whose kinetic energy equals the ground-state total energy $\hslash \omega /2$ has momentum $\hslash /a$ and de Broglie wavelength $\lambda =2\pi a$, where $a=\sqrt{\hslash /(m\omega )}$. Substitution into the normalized bound-state Gaussian yields the title density. The comparison wavelength is a useful length scale; it is not a claim that the bound state has a single free momentum or spatially uniform probability density.

At incident wave number $k$, low kinetic energy means $ka\ll 1$: the de Broglie wavelength is much larger than the scattering region. A generic finite-range scatterer can then be described to leading order without resolving its angular structure. In partial-wave scattering, this is leading S-wave scattering. The $\ell =0$ spherical harmonic is constant, whereas the centrifugal term ${\hslash }^2\ell (\ell +1)/(2m{r}^2)$ impedes penetration to the potential for $\ell >0$.

For a central potential with regular threshold behaviour, the finite-range partial-wave threshold law gives ${\delta }_{\ell }=O(k^{2\ell +1})$. Thuswhich is independent of scattering angle. For finite nonzero scattering length $a_s$, $f\to -a_s$ and $d\sigma /d\Omega \to a_s^2$ is isotropic. The potential range $a$ and scattering length $a_s$ are different quantities. The claim describes the generic leading S-wave scattering limit; tuned vanishing S-wave scattering amplitude or exceptional threshold resonances require separate analysis rather than a universal angular conclusion.

Atomic-resolution cryo-electron microscopy became possible by retaining high-frequency structural information through the whole experiment: specimen preparation, electron optics, detection and computation. The decisive advances improved the information obtained per damaging electron and made it possible to align and average many weak images without averaging away structural differences. A short de Broglie wavelength had always been available; the practical limit was preserving and extracting the information carried by those electrons.

First, vitrification preserves hydrated biological material in a thin noncrystalline layer of water. Rapid freezing avoids the strong periodic scattering and disruption associated with ordinary ice crystals, while cryogenic imaging slows some damage processes. The specimen still suffers radiation damage, and a thicker layer adds background and multiple scattering. Reproducible thin ice, clean grids, stable supports and reduced mechanical drift are therefore prerequisites. The specimen must remain structurally intact and occupy enough orientations for a three-dimensional reconstruction. Adsorption at the air–water interface, preferred orientation and variable thickness can defeat an otherwise excellent microscope. Sample optimization should include independent checks of assembly integrity and activity where feasible.

Second, direct electron detection greatly improved the useful signal relative to earlier indirect cameras. In a counting detector, individual electron events can be localized and recorded without treating the deposited signal merely as a continuous intensity. detective quantum efficiency measures how efficiently the detector preserves the input signal-to-noise ratio as a function of spatial frequency. High efficiency matters particularly because the permissible exposure is limited. At excessive event rates, overlapping events cause coincidence losses, so faster readout permits useful counting at practical collection rates. A nominally smaller camera pixel alone cannot replace a detector that preserves high-frequency information.

Fast detectors also turn an exposure into a sequence of movie frames. Aligning those frames corrects specimen drift and beam-induced movement; local correction handles different movements across the imaged area. Uncorrected movement preferentially smears fine features. dose weighting then combines early and later frames according to the information they retain: later exposure can help low-frequency alignment even after fine structural details have been damaged. ^[ref] exemplifies this computational use of detector movies. Frame alignment cannot restore chemistry already destroyed by radiation damage, and extremely noisy individual frames require constrained motion estimates.

Third, stable and coherent electron optics increase contrast transfer at the finest spacings. A narrow source energy spread reduces chromatic aberration, because electrons with different energies otherwise focus differently. A cold field emission gun provides one route; a monochromator provides another. An energy filter removes many inelastically scattered electrons that otherwise contribute background. This does not remove all damage or every unwanted scattering event. Improved mechanical and electrical stability, reproducible lens settings, accurate coma-free alignment and calibrated magnification make the information more consistent across images.

The 2020 apoferritin reconstructions illustrate the final hardware step. One study combined a cold source, improved energy filtering and a fast direct camera with advanced correction to obtain a map at about $1.22\text{A˚}$. Another used an instrument with monochromation and aberration correction to reach about $1.25\text{A˚}$.^[ref][ref] The two instruments demonstrate complementary ways of preserving coherent high-frequency information. These unusually rigid, symmetric particles are favorable test specimens; their resolutions do not imply that a flexible cellular assembly will reach the same limit.

Fourth, modern reconstruction treats the noisy images statistically. single-particle analysis estimates how many randomly oriented projections correspond to a common three-dimensional structure. Bayesian inference and maximum likelihood estimation permit uncertainty in image orientations and class membership to be handled rather than committing every weak image to a single exact alignment from the beginning. ^[ref] provides a concrete implementation. Two-dimensional classes reject many damaged or overlapping particles; three-dimensional classification can separate different compositions or conformations. Appropriate symmetry increases the effective information, but an incorrect symmetry assumption can erase a real asymmetric feature.

Refinement increasingly corrects individual particle movements and optical imperfections. Per-particle defocus estimates accommodate height differences in ice. Beam tilt, higher-order aberrations and anisotropic magnification need correction when their accumulated phase errors become important. The contrast transfer function changes the magnitude and sign of Fourier components; combining images recorded with different defocus values recovers information suppressed at particular transfer-function zeros. Near atomic spacings, accounting for Ewald sphere curvature can further improve reconstruction. Such corrections require adequate signal and calibration; simply adding more adjustable parameters to weak data risks fitting noise.

Automation and fast computation make these methods practical. Stable automated acquisition and beam-image-shift strategies collect large image sets; parallel computation permits repeated alignment, classification and refinement. More particles improve the average only if they carry consistent signal. Under an ideal independent-noise model, the amplitude signal-to-noise ratio improves in proportion to $\sqrt{N}$; a systematic alignment error or persistent structural heterogeneity will not disappear by this scaling. For a target spacing $d$ and real-space pixel size $a$, Nyquist–Shannon sampling theorem requires $a\le d/2$. For $d=1.2\text{A˚}$ this gives $a\le 0.6\text{A˚}$ per pixel, a necessary sampling condition rather than a guarantee of such resolution.

Validation is part of the technological achievement. Split particles into independent halves and refine them independently; calculate their Fourier shell correlation, commonly reporting the spacing at the $0.143$ criterion for independently refined half-maps. Shared high-resolution references, poorly handled masks or correlated data can inflate agreement, so independence and mask correction matter. Inspect directional coverage and local resolution, compare models against held-out map information, and check stereochemistry. The global resolution is a summary: flexible loops, bound lipids and minor components may be much worse than the ordered core.

Finally, distinguish an atomistic model from atomically resolved data. At ordinary near-atomic resolution, side chains and backbone features can support building an atomic model while individual neighboring chemical atoms are not all separated. At true atomic resolution, many individual atomic peaks become distinguishable and some hydrogen contributions may be detectable under favorable conditions. cryo-electron microscopy reconstructs scattering electrostatic potential, so interpretation of very fine features is not identical to interpreting X-ray crystallography electron-density maps. The breakthrough was the combined improvement of specimen quality, counting movies, optical coherence and statistical reconstruction, with independent validation showing that the fine detail was supported by the data.

The neutron is nonrelativistic at this kinetic energy. Its de Broglie wavelength isIn elastic scattering, Bragg's law gives $2d\sin \theta =\lambda$. The measured total deflection is $2\theta$, so it must be halved before taking the sine. The reflection order is absorbed into the Miller indices of the diffracting lattice planes. In the order of the four measured rings, the interplanar spacings areThe last digits give the numerical calculation, rather than accuracy beyond the supplied angular precision.

For a neutron in the Earth's Newtonian gravitational potential ${\Phi }_E$, the Schrödinger equation isNear the surface, ${\Phi }_E(z)=gz$ up to an additive constant.

The Colella–Overhauser–Werner experiment uses crystal slabs as coherent beam splitters and mirrors in a neutron interferometer. The two paths contain horizontal segments of length $s$ separated vertically by $r$, then recombine. The gravitational potential energy difference is $m_{n}gr$. A neutron of speed $v$ spends time $s/v$ on a horizontal segment, so the gravitationally induced relative quantum phase isUsing the de Broglie wavelength $\lambda =h/(m_{n}v)$ and $\hslash =h/(2\pi )$ givesRotating the apparatus changes the vertical projection of its enclosed area from zero to $rs$. The number of full interference oscillations is thereforeHere $rs=(\sqrt{10}\mathrm{cm}{)}^2=10^{-3}{\mathrm{m}}^2$, soThe expected change is therefore $\boxed{9}$ oscillations to the nearest integer.