Gauge-invariant perturbation theory is an extension of ordinary perturbation theory which describes strictly gauge-invariant states in theories with a Brout-Englert-Higgs effect. Such gaugeinvariant states are composite operators which have necessarily only global quantum numbers. As a consequence, flavor is exchanged for custodial quantum numbers in the standard model, recreating the fermion spectrum in the process. Here, we study the implications of such a description, possibly also for the generation structure of the standard model.In particular, this implies that scattering processes are essentially bound-state-bound-state interactions, and require a suitable description. We analyze the implications for the pair-production process e + e − →f f at a linear collider to leading order. We show how ordinary perturbation theory is recovered as the leading contribution. Using a PDF-type language, we also assess the impact of sub-leading contributions. To lowest order we find that the result is mainly influenced by how large the contribution of the Higgs at large x is. This gives an interesting, possibly experimentally testable, scenario for the formal field theory underlying the electroweak sector of the standard model.
Whether intentional or unintentional, thin dielectric interlayers can be found in technologies ranging from catalysis to organic electronics. While originally considered as passive decoupling layers, recently it has been shown that they can actively promote charge transfer from the underlying metal to adsorbates. This charging can have profound effects on the surface chemistry of atoms, atomic clusters, and molecules, their magnetic moments, and charge injection at the contacts of organic devices. Yet, controlled studies required to understand the charge transfer process in depth are still lacking. Here, a comprehensive analysis of the phenomenon of charge transfer using the atomically controlled system of pentacene on ultrathin MgO(100) films on Ag(100) is presented. It is shown that the charge transfer process is governed by the charged and uncharged molecular species with distinct energy levels in the first monolayer. The experimental approach applied in this work allows to observe and control their ratio through direct tuning of either the work function or the thickness of the dielectric interlayer.
The determination of reaction pathways and the identification of reaction intermediates are key issues in chemistry. Surface reactions are particularly challenging, since many methods of analytical chemistry are inapplicable at surfaces. Recently, atomic force microscopy has been employed to identify surface reaction intermediates. While providing an excellent insight into the molecular backbone structure, atomic force microscopy is less conclusive about the molecular periphery, where adsorbates tend to react with the substrate. Here we show that photoemission tomography is extremely sensitive to the character of the frontier orbitals. Specifically, hydrogen abstraction at the molecular periphery is easily detected, and the precise nature of the reaction intermediates can be determined. This is illustrated with the thermally induced reaction of dibromo-bianthracene to graphene which is shown to proceed via a fully hydrogenated bisanthene intermediate. We anticipate that photoemission tomography will become a powerful companion to other techniques in the study of surface reaction pathways.
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