The emerging field of free-electron quantum optics enables electron-photon entanglement and holds the potential for generating nontrivial photon states for quantum information processing. Although recent experimental studies have entered the quantum regime, rapid theoretical developments predict that qualitatively unique phenomena only emerge beyond a certain interaction strength. It is thus pertinent to identify the maximal electron-photon interaction strength and the materials, geometries, and particle energies that enable one to approach it. We derive an upper limit to the quantum vacuum interaction strength between free electrons and single-mode photons, which illuminates the conditions for the strongest interaction. Crucially, we obtain an explicit energy selection recipe for electrons and photons to achieve maximal interaction at arbitrary separations and identify two optimal regimes favoring either fast or slow electrons over those with intermediate velocities. We validate the limit by analytical and numerical calculations on canonical geometries and provide near-optimal designs indicating the feasibility of strong quantum interactions. Our findings offer fundamental intuition for maximizing the quantum interaction between free electrons and photons and provide practical design rules for future experiments on electron-photon and electron-mediated photon-photon entanglement. They should also enable the evaluation of key metrics for applications such as the maximum power of free-electron radiation sources and the maximum acceleration gradient of dielectric laser accelerators.
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http://dx.doi.org/10.1103/PhysRevLett.134.043803 | DOI Listing |
Small
March 2025
Multidisciplinary Platform of Advanced Engineering, Department of Chemical Engineering, School of Engineering, Monash University Malaysia, Jalan Lagoon Selatan, Bandar Sunway, Selangor, 47500, Malaysia.
The design of highly efficient photocatalysts to photoreduce nitrogen (N) to ammonia (NH) under mild conditions is extremely challenging. In this work, various molar ratio of molybdenum (Mo) is incorporated into BiOCl via a hydrothermal process. The resulting Mo-doped BiOCl exhibits remarkable solar-driven activity for N photo fixation without any scavengers or sacrificial agents.
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March 2025
University of Leuven, KU Leuven), LOMAC Celestijnenlaan 200F, B-3001, Leuven, Belgium.
Photosynthesis in plants has inspired photochemical reactions in organic chemistry. Synthetic organic chemists always seek cost-effective, operationally simple, averting the use of toxic and difficult-to-remove metallic catalysts, atom economical, and high product purity in organic reactions. In the last few decades, the use of light as a catalyst in organic reactions has increased exponentially as literature has exploded with examples, particularly by using toxic and expensive metal complexes, photosensitizers like organic dyes, hypervalent iodine, or by using inorganic semiconductors.
View Article and Find Full Text PDFSmall
March 2025
The Centre of Nanoscale Science and Technology and Key Laboratory of Functional Polymer Materials, State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China.
Photocatalytic hydrogen production through water splitting represents a promising strategy to store solar energy as chemical energy. Current photocatalysts primarily focus on traditional semiconductor materials, such as metal oxides, sulfides, nitrides, g-CN, etc. However, these materials often suffer from large bandgap and fast charge recombination, which limit sunlight utilization and result in unsatisfactory photon conversion efficiency.
View Article and Find Full Text PDFNanomaterials (Basel)
March 2025
Department of Biotechnology and Bioinformatics, Yogi Vemana University, Kadapa 516005, India.
The use of metal nanoparticles is gaining popularity owing to their low cost and high efficacy. We focused on green synthesis of silver nanoparticles (AgNPs) using (Tc) leaf extracts. The structural characteristics of Tc nanoparticles (TcAgNPs) were determined using several advanced techniques.
View Article and Find Full Text PDFAdv Mater
March 2025
Beijing Advanced Innovation Center for Materials Genome Engineering, Department of Applied Physics, University of Science and Technology Beijing, Beijing, 100083, China.
Pb-free dielectric energy storage capacitors are core components in advanced pulse-power electronic systems and devices. However, the relatively low energy density (W) for the industrial pillar BaTiO (BT)-based capacitors remains a significant obstacle for their cutting-edge applications, due to their low intrinsic polarization and breakdown strength (E). Herein, through chemical composition and local structure design, a giant W of 15.
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