An electronic system distorted externally by a photon or a charged particle impact can integrally respond by the simultaneous emission of two electrons into the vacuum. The vacuum states of these two correlated electrons can be then determined using an angular and energy-resolved coincidence technique. The spectra of low-energy electron pairs, the subject of this study, carry the signature of their mutual correlations and their coupling to other degrees of freedom of the environment while in the high energy regime information on the initial-momentum components of the pair can be extracted from the recorded spectra [1‐ 4]. These observations have been made in diverse areas of physics, such as plasma, atomic, molecular, and condensed matter physics [3,5,6]. For pair emission from localized electronic states, such as atomic and molecular orbitals, it turns out that the spectra are dominated by the interelectronic interaction of the pair, in particular at lower energies (with respect to the initial orbital energies) [6]. Thus, an adequate theoretical description of these phenomena must go beyond an independent particle description. For delocalized electronic states, as present in metallic crystals and surfaces, it is established that delocalization does not preclude correlations. E.g., in transition metals the d electrons are delocalized, yet correlation between them is far from weak. In this work it is shown theoretically and experimentally that an electron pair can be regarded as a “two-electron quasiparticle.” The scattering of this quasi-single-particle from a crystal potential results in characteristic diffraction pattern that is, for the first time, experimentally observed. The positions of the diffraction peaks are governed by a von Laue‐ like diffraction condition for the center-ofmass wave vector of the electron pair. The relative intensities of the diffraction maxima are largely determined by the internal degree of freedom of the pair, i.e., by interelectronic correlations. The experimental setup used for the angular and energy-resolved detection of the pairs, i.e., for the projection of the two-electron initial state onto the two-electron vacuum state, is schematically depicted in Fig. 1. A more detailed description can be found in Refs. [7 ‐ 9]. The sample surface defines the x-y plane, while the z axis coincides with the surface normal. In the z-x plane two position sensitive microchannel plate electron detectors are located at a distance of 160 mm to the sample surface, such that the relative angle between the detector axes and the surface normal is given by 6a . The angular acceptance of each electron detector within the scattering plane is 613.2 ‐ . A parallel electron beam of about 1 mm diameter impinges onto the sample surface including the angle g with the surface normal. For investigating the Cu(001) sample, the angles a and g are chosen to be 40 ‐ and 0 ‐ , respectively, while in the case of Fe(110) (BCC), a was set to be 50 ‐ and g › 5 ‐ . Correlated electron pairs emitted from the sample upon excitation by a primary electron are detected in coincidence. Their energies have been measured using a time-of-flight technique. In the range of electron energies detected here, we achieve an energy resolution of DE › 0.4 0.8 eV. Standard cleaning procedure of the surface is applied before each measurement under a base pressure in the range of 10 211 mbar. The probability for the two electrons to be detected with asymptotic momenta k1 and k2 is derived from an