The relation between the energy-dependent particle and wave descriptions of electron–matter interactions on the nanoscale was analyzed by measuring the delocalization of an evanescent field from energy-filtered amplitude images of sample/vacuum interfaces with a special aberration-corrected electron microscope. The spatial field extension coincided with the energy-dependent self-coherence length of propagating wave packets that obeyed the time-dependent Schrödinger equation, and underwent a Goos–Hänchen shift. The findings support the view that wave packets are created by self-interferences during coherent–inelastic Coulomb interactions with a decoherence phase close to Δφ = 0.5 rad. Due to a strictly reciprocal dependence on energy, the wave packets shrink below atomic dimensions for electron energy losses beyond 1000 eV, and thus appear particle-like. Consequently, our observations inevitably include pulse-like wave propagations that stimulate structural dynamics in nanomaterials at any electron energy loss, which can be exploited to unravel time-dependent structure–function relationships on the nanoscale.
The relation between the energy-dependent particle and wave descriptions of electron–matter interactions on the nanoscale was analyzed by measuring the delocalization of an evanescent field from energy-filtered amplitude images of sample/vacuum interfaces with a special aberration-corrected electron microscope. The spatial field extension coincided with the energy-dependent self-coherence length of propagating wave packets that obeyed the time-dependent Schrödinger equation, and underwent a Goos–Hänchen shift. The findings support the view that wave packets are created by self-interferences during coherent–inelastic Coulomb interactions with a decoherence phase close to Δφ = 0.5 rad. Due to a strictly reciprocal dependence on energy, the wave packets shrink below atomic dimensions for electron energy losses beyond 1000 eV, and thus appear particle-like. Consequently, our observations inevitably include pulse-like wave propagations that stimulate structural dynamics in nanomaterials at any electron energy loss, which can be exploited to unravel time-dependent structure–function relationships on the nanoscale.
The correlation between particle and wave descriptions of electron-matter interactions is analyzed by measuring the delocalization of an evanescent field using electron microscopy. Its spatial extension coincides with the energy-dependent, self-coherence length of propagating wave packets that obey the time-dependent Schrödinger equation and undergo a Goos-Hänchen shift. In the Heisenberg limit they are created by self-interferences during coherent-inelastic Coulomb interactions with a decoherence phase Δϕ = 0.5 rad and shrink to particle-like dimensions for energy losses of more than 1000 eV.
Intensities in high-resolution phase-contrast images from electron microscopes build up discretely in time by detecting single electrons. A wave description of pulse-like coherent-inelastic interaction of an electron with matter implies a time-dependent coexistence of coherent partial waves. Their superposition forms a wave package by phase decoherence of 0.5 - 1 radian with Heisenbergs energy uncertainty ΔEH = ħ/2 Δt-1 matching the energy loss ΔE of a coherent-inelastic interaction and sets the interaction time Δt. In these circumstances, the product of Planck's constant and the speed of light hc is given by the product of the expression for temporal coherence λ2/Δλ and the energy loss ΔE. Experimentally, the self-coherence length was measured by detecting the energy-dependent localization of scattered, plane matter waves in surface proximity exploiting the Goos-Hänchen shift. Chromatic-aberration Cc-corrected electron microscopy on boron nitride (BN) proves that the coherent crystal illumination and phase contrast are lost if the self-coherence length shrinks below the size of the crystal unit cell at ΔE > 200 eV. In perspective, the interaction time of any matter wave compares with the lifetime of a virtual particle of any elemental interaction, suggesting the present concept of coherent-inelastic interactions of matter waves might be generalizable.
Atomic resolution transmission electron microscopy (TEM) is an indispensable tool for interdisciplinary investigations of radiation soft or hard materials that evolves rapidly because emerging technologies enable remarkable new experiments [1, 2]. Nowadays, many of them embrace the time domain [2-4]. Beyond materials research, electron microscopy is uniquely suited to study fundamental quantum-mechanical aspects. In fact, it remains concerning that aspects addressing the wave-particle duality, time-dependent measurements, or the entanglement of wave functions and their collapse at a detector still require detailed investigations to guide progress. Certainly, this is no academic matter because such aspects become the bottleneck for the deployment of microscopes that enable studying dynamic processes at high spatiotemporal resolution. It is established practice to describe the scattering of electron ensembles by either a particle picture (Figure 1a) or a wave picture (Figure 1b). Sometimes both pictures are mixed. In spite of calls for solving Schrödinger’s time dependent equation [5], the static Schrödinger equation of wave functions is almost exclusively used to reliably simulate the image formation process using multislice calculations for coherent-elastically scattered electron ensembles [6, 7]. Moreover, the Copenhagen convention of quantum mechanics [8] is adopted, which emphasizes the importance of an observation for the collapse of wave functions (Figure 1b). In order to foster further insight into fundamental quantum-mechanical aspects we pursue a series of experiments with low electron dose rates that guarantee the presence of single electrons in the microscope column at any given time [9]. Consequently, we address the scattering of single electrons (Figure 1c) and build up intensities from electron ensembles over time. In such conditions energy filtered TEM recently revealed the presence of image intensity at sample/vacuum interfaces that cannot be simulated using the established (static) calculation tools even if frozen phonon excitations are considered [10]. In contrast, these intensities can be explained by the time-dependent Schrödinger equation assuming that an energy exchange ΔE occurs during any interaction of the electron with the sample in the Heisenberg limit ΔE = ℏ/2 Δt−1 (coherent-inelastic scattering). In this process a wave package is formed by the superposition of partial waves and a decoherence phase of 0.5-1 radian [10]. The time-dependent Schrödinger equation yields two parameters that characterize the static and the dynamic behavior of any wave function ψ(r, t) = ψ(r) ϕ(t), namely xstatic = ℏ/(2mΔE)1/2 and xdynamic = ℏc/ΔE [11]. The former is the de Broglie wavelength if ΔE is a kinetic energy and the latter becomes an expression for self-coherence if the scattering process is coherent-inelastic in the Heisenberg limit. In these circumstances, the product of Planck’s constant and the speed of light hc is given by the product of the expression for temporal coherence λ2/Δλ and the energy loss ΔE (hc = (λ2/Δλ) ΔE). The validity of the relation is shown in Figure 2 [11]. Thus, the temporal part of Schrödinger’s equation adds contributions of a finite self-coherence length (or time if the electron velocity is considered) to any scattering process, which is neglected if only the static expression is exploited. Further, the formation of wave packages rationalizes the wave-particle duality. The width of wave packages is described by a self-coherence length ls that can vary by over 40 orders of magnitude depending on the strength of interactions [11]. For Coulomb interactions, ls explains the vanishing phase contrast from EF-HRTEM images when the energy loss exceeds values of ΔE > 200 eV [11]. A procedure to experimentally determine the self-coherence length was established earlier by measuring the energy dependent localization of scattered matter waves in surface proximity [10]. Therefore, electron microscopy can be used as a general tool to measure the self-coherence length in real space images on a scale of nanometers and relate this these values to a self-coherence time that reaches attoseconds [12]. Particle and wave descriptions of electron scattering. a) Scattering of electron ensembles in a particle picture. The process is often described by Feynman diagrams, which involves the emission of a virtual photon of lifetime given by Heisenbergs Uncertainty Principle. b) Scattering of electron ensembles in a wave picture that underlies the multi-slice calculations. Infinite wave functions entangle source, sample and detector. The Copenhagen convention requires a wave function collapse upon observation. c) Proposed scattering process of a single electron wave function. The energy exchange occurs in the Heisenberg limit ΔEloss = E2-E1= ℏ/2 (t2-t1)−1= ℏ/2 Δt−1 when a wave package is formed during Δt because of existing energy (wavelength) differences ΔEloss of partial waves [11]. Measurements of self-coherence length and the related self-coherence time at the calculated Heisenberg limit. The colored background marks the quantum realm. The solid lines represent the Heisenberg limit in space and time, which includes the constant ℏc [11].
Electron beams are a formidable tool for probing nanophotonic systems [1]. Combining electron microscopy with external optical excitation in ultrafast transmission electron microscopes has enabled the mapping of optical near-fields [2] and the bunching of electrons in attosecond pulses [3, 4]. These developments are based on the stimulated inelastic scattering between electrons and light [5, 6], in which the electrons gain energy from or lose energy to the optical field. Recently, the underlying interaction strength of this process has been increased significantly by harnessing resonant enhancement of the optical field and velocity phase matching [7]. Such an increased interaction strength also benefits the spontaneous scattering of electrons with light, thus promising applications like generating complex quantum states of light [8]. In this presentation, we discuss a set of experiments on free electron quantum optics that investigate single-electron-single-photon interactions and probe the resulting entanglement. Specifically, we consider scenarios in which optical waveguide structures are placed inside a transmission electron microscope (TEM) facilitating the interaction. Electrons passing by, for example, an integrated photonic structure (cf. Fig. 1a) can inelastically scatter with the optical mode, leading to the emergence of electron-photon pair states [9]. The resulting correlation between energy-loss electrons and photons, illustrated in Fig. 1b, can be probed employing time- and energy-resolved detection of both particles, revealing a pronounced coincidence peak between their arrival times, schematically shown in Fig. 1c. Extending the photon detection setup by a second detector to allow for Hanbury Brown and Twiss (HBT) measurements, the photon statistics heralded by such energy-loss electrons can be studied [10]. The observed anti-bunching behavior indicates a nonclassical optical state with single-photon properties. The inelastic electron-light scattering underlying the electron-photon pair generation is further expected to induce entanglement in the particle energies [11], however, direct observation of quantum entanglement would be exceedingly difficult given the large number of independent quantum states available in these degrees of freedom. Therefore, we propose experiments based on the quantum eraser scheme to demonstrate this free-electron-photon entanglement in different degrees of freedom [12,13]. Specifically, we consider a double-slit geometry coherently illuminated by an electron beam such that an interference pattern can be observed on a distant screen (cf. Fig. 2a). If electrons passing through the left or right (denoted |Land |R, respectively) slit generate distinct marker photons with vertical (|V)or horizontal (|H) polarization, this interference pattern would disappear due to the entanglement of electron path and photon polarisation (cf. Fig. 2b). However, if this which-path information carried by the marker photon is erased, e.g. by mixing the polarisation states, the interference pattern can be recovered when detecting electrons and photons in coincidence. We describe an extension of this idea to an entanglement test, before discussing possible realistic implementations and presenting preliminary results on several experimental key aspects. In summary, we discuss the inelastic electron-light scattering at integrated photonic structures with applications ranging from coherent electron beam modulation using continuous-wave optical fields to the electron-driven generation of quantum optical states of light. Delving deeper into single electron-single photon interactions, we outline feasible experiments to generate and verify electron-photon entanglement with a potential extension to electron pairs based on entanglement swapping. All this adds to the toolbox of free electron quantum optics, potentially enabling novel sources of quantum light as well as quantum-enhanced sensing in electron microscopy. Generation of correlated electron-photon pairs. (a) Electrons pass over a photonic integrated circuit placed in the sample plane of a TEM, generating photons in the optical waveguides via inelastic scattering. Energy-loss electrons are detected and time-tagged behind an imaging spectrometer in coincidence with photons exiting the waveguide. (b) Inelastic scattering links the electron energy loss (green, right ladder) to the generation of photons (red, left ladder), creating correlations in energy and time. (c) A strong temporal correlation between the loss electrons and detected photons, indicated by the red dot, is observed relative to the uncorrelated zero-loss background electrons (blue line). Free-electron-photon quantum eraser. (a) Coherent electron illumination of a double-slit structure results in interference between the two pathways |Land |R.(b) If the electrons generate distinguishable marker photons, e.g. of orthogonal polarizations |Vand |H, no interference pattern can be observed due to the electron-photon entanglement. (c) Collecting these marker photons and erasing the which-path information, e.g. using a half-wave plate (λ/2), the electron interference can be recovered using electron-photon coincidence detection with single-photon detectors (SPDs) placed behind a polarizing beam splitter (PBS).
Abstract In Copenhagen’s interpretation, a self-interference mechanism is assumed for a wave function to split and to pass through the slits simultaneously, then recombine and collapse to generate a dot signal on a detector. Its use of a single wave function to describe a whole ensemble without accounting for a particle’s individuality is incomplete. To better understand the single-electron double-slit interference, we use a wave-packet trajectory approach to track each electron’s dynamics and calculate the time-dependent interference intensity. We analyze the self-interference and cross-interference mechanisms to illustrate how an electron’s coherence length affects the self-interference and how it dictates the wave packet overlaps between adjacent electrons for the cross-interference mechanism to be effective. To circumvent a conflicting dilemma between the electron’s indivisibility and its wave-packet split while passing through the slits, we consider an alternate mechanism involving slit-induced quantized momentum. This mechanism preserves the electron’s indivisibility and avoids the illusive split, recombination and mysterious collapse of a single particle’s wave function.
Wave-particle duality is widely regarded as one of the conceptual pillars of modern quantum theory, providing the framework through which the behavior of microscopic matter can be consistently interpreted. According to this principle, microscopic entities such as electrons, photons, atoms and even complex molecules exhibit both wave-like and particle-like properties depending on the experimental configuration used to observe them. This duality is quantitatively formalized through the De Broglie relation, which associates a wavelength with any particle possessing momentum. The present work provides a comprehensive theoretical analysis of the physical and mathematical foundations of wave-particle duality, focusing particularly on the De Broglie wavelength and the kinetic energy of the electron in both non-relativistic and relativistic regimes. The connection between the De Broglie hypothesis and Schrödinger’s equation is discussed in detail, highlighting the role of the kinetic energy operator and the interpretation of matter waves in terms of quantum wave packets. Experimental evidence supporting the wave nature of matter, including electron diffraction experiments and interferometry techniques, is also reviewed. Beyond their conceptual importance, these principles underpin several modern technologies, including electron microscopy, nanoscale semiconductor devices and quantum metrology. The analysis demonstrates that the De Broglie relation provides a unifying framework connecting momentum, wavelength and kinetic energy, thereby forming a fundamental bridge between classical mechanics, quantum theory and modern technological applications.