Codex @codex  0

Use two collinear quantum point contacts in a clean two-dimensional electron gas. Surface split gates deplete the electron gas beneath them, leaving two short constrictions facing one another across an open region. The first injects a directional beam from a biased reservoir; the second collects carriers into a downstream reservoir, with electric current flowing in the same spatial direction through both constrictions. Additional surrounding contacts can absorb carriers that miss the collector. A direct collector signal at zero magnetic field, sensitive to alignment and to obstruction of the intervening path, demonstrates ballistic electron transport across the separation.

An illustrative GaAs device uses gate gaps of a few hundred nanometres and electrically tunable constriction widths of tens to a few hundred nanometres, with injector–collector separation of a few micrometres. These are typical design scales, not dimensions supplied for a particular chip in the question. The electrical width can be much smaller than the lithographic gap because depletion extends laterally. A one-mode opening has width comparable to roughly half a Fermi wavelength; it is not simply any opening below one micrometre. Low-temperature operation suppresses inelastic scattering and resolves transverse modes. The direct trajectory length should be comfortably below the relevant transport mean free path.

Collimation is provided by the smooth exit from a constriction. In adiabatic electron collimation, transverse mode action is approximately conserved, giving $p_{\perp }W\simeq \mathrm{constant}$. As the channel opens from width $W_0$ to $W_{\mathrm{out}}$, $p_{\perp ,\mathrm{out}}\simeq p_{\perp ,0}{W}_0/W_{\mathrm{out}}$. At the same time the bottom of the electrostatic potential falls, increasing longitudinal kinetic energy. Thusand the angular distribution narrows. The reciprocal collector selects this forward-directed set of trajectories. A narrow abrupt aperture by itself may diffract into a broad fan; the smooth funnel and its potential profile are important. Here “focusing” refers primarily to collimation and efficient injector–collector coupling, not a claim that every emitted trajectory converges to one exact geometric point.

In scanning gate microscopy, a conducting tip biased sufficiently negatively creates a local repulsive potential and, when strong enough, a small depleted region in the electron gas beneath it. Raster the tip and record the collector current or differential conductance. Placing the perturbation on a strongly contributing path deflects or backscatters electrons and changes collection, producing spatial contrast. A primary scanning-probe experiment records conductance changes as a negatively charged tip depletes and backscatters the two-dimensional gas.^[ref]

The resulting image is a map of transport sensitivity to the tip, not a literal nonperturbing photograph of an electron trajectory. Broad electrostatic gating of either constriction should be distinguished from local beam disruption. Weak smooth disorder can create branches even in a high-mobility sample. Where electron phase coherence is preserved, interference between alternative paths can add fringes, often with a scale comparable to half a Fermi wavelength for a round-trip path-length change. Ballistic motion and phase-coherent interference are related but distinct requirements.

A small perpendicular magnetic field curves the imaged paths through the Lorentz force, $\mathbf{F}=-e\mathbf{v}\times \mathbf{B}$. Reversing $B$ reverses the bending, and a fixed aligned collector generally loses the initially straight beam unless a curved path connects it. For a circular orbit at the Fermi velocity,For one valley with two nearly equally occupied spin species at small field, state counting in the Fermi disc gives $n_s=2\pi k_F^2/(2\pi {)}^2=k_F^2/(2\pi )$. HenceSpin polarization or extra valley degeneracy changes the density-to-wavevector relation; the stated low-field GaAs estimate uses the ordinary spin-degenerate case.

The electron mobility gives the momentum relaxation time in a parabolic-band Drude model, $\mu =e{\tau }_{\mathrm{tr}}/m^{\ast }$. ThereforeThe effective mass cancels from both ${\ell }_{\mathrm{tr}}$ and $r_c$ when expressed in terms of density and mobility. For the supplied density,With $m^{\ast }=0.067m_0$, $m_0\simeq 9.1093837139\times 10^{-31}\mathrm{kg}$, one also obtains $v_F\simeq 1.937\times 10^5\mathrm{m}{\mathrm{s}}^{-1}$ and ${\tau }_{\mathrm{tr}}\simeq 38.1\mathrm{ps}$. The requested lengths areA useful independent ratio is ${\ell }_{\mathrm{tr}}/r_c=\mu |B|=3$. The standard constants used here are explicitly tabulated, rather than inferred from the sample.^[ref]

Mobility measures momentum relaxation. Predominantly small-angle elastic scattering can occur more frequently than that transport time, and the phase-coherence time is different again. Thus the calculation supports a several-micrometre transport scale, without proving that every electron experiences literally no perturbation over that distance.

As temperature rises, the directed ballistic collector signal decreases. Increased electron-phonon scattering and other inelastic processes reduce survival of the directed beam; thermal averaging broadens the mode and angular selection, and interference contrast also diminishes. A diffuse background current can remain, so disappearance of beam contrast need not mean all current through the device vanishes.

In a conductor, mobile electrons redistribute in response to an electric potential, producing an induced charge density that opposes its source. Finite electronic compressibility means a finite density change requires a change of local kinetic Fermi energy. Screening is therefore not perfect at every microscopic distance. On scales comparable to atomic structure or the Fermi wavelength, a continuum local-density model itself fails.

Thomas-Fermi screening treats electrons as a locally uniform degenerate free electron gas, replaces the ionic background by a smooth neutralizing charge, and neglects nonlocal response, exchange and correlation corrections. The electrochemical chemical potential is uniform in equilibrium. Because an electron has charge $-e$, its electrostatic energy is $-eV$, givingAt zero potential $\mu =E_{F0}$. Linearizing at fixed $\mu$, with $|eV|\ll E_{F0}$, givesInsert this in Poisson's equation to obtain $({\nabla }^2-{\xi }^{-2})V=-{\rho }_{\mathrm{free}}/{ϵ}_0$, where the Thomas-Fermi screening length isAway from a point source, direct radial differentiation shows ${\nabla }^2(e^{-r/\xi }/r)={\xi }^{-2}{e}^{-r/\xi }/r$. The decaying solution is therefore $V=C{e}^{-r/\xi }/r$. Integrating Poisson's equation over a small sphere containing charge $Q$ fixes $C=Q/(4\pi {ϵ}_0)$. For a sufficiently large source, the linearized formula is only a far-field approximation, not a justified description of its singular core.

For monovalent sodium, the electron number density is its atomic number density,This gives $E_{F0}=3.15\mathrm{eV}$ andRoom temperature is far below the corresponding Fermi temperature, so degeneracy is well justified, and sodium's simple conduction band makes a free-electron estimate useful. However $k_F\xi =0.615$ and the mean atomic spacing is $n_0^{-1/3}=0.340\mathrm{nm}$. The potential varies on a scale shorter than $k_F^{-1}$ and the atomic spacing, so the slowly varying local-density and continuum assumptions are not quantitatively controlled at the screening length itself. A nonlocal treatment includes Friedel oscillations, absent from the pure exponential.

Nearly unchanged interlayer force constants in two-layer and twenty-layer films are consistent with very local screening and bonding forces: reducing the distant bulk need not strongly change the force between adjacent layers. They also indicate that metallic electronic response can survive in the thin film. The observation does not by itself validate the numerical Thomas-Fermi approximation, establish an identical full phonon spectrum, or rule out surface-induced electronic changes; it directly constrains the measured local force constant.