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We present experimental results showing a laser-accelerated proton beam maximum energy cutoff of 67.5 MeV, with more than 5 × 106 protons per MeV at that energy, using flat-top hollow microcone targets. This result was obtained with a modest laser energy of ∼80 J, on the high-contrast Trident laser at Los Alamos National Laboratory. From 2D particle-in-cell simulations, we attribute the source of these enhanced proton energies to direct laser-light-pressure acceleration of electrons along the inner cone wall surface, where the laser light wave accelerates electrons just outside the surface critical density, in a potential well created by a shift of the electrostatic field maximum with respect to that of the magnetic field maximum. Simulations show that for an increasing acceleration length, the continuous loading of electrons into the accelerating phase of the laser field yields an increase in high-energy electrons.

Laser-plasma wakefield accelerators have seen tremendous progress, now capable of producing quasi-monoenergetic electron beams in the GeV energy range with few-femtoseconds bunch duration. Scaling these accelerators to the nanocoulomb range would yield hundreds of kiloamperes peak current and stimulate the next generation of radiation sources covering high-field THz, high-brightness X-ray and γ-ray sources, compact free-electron lasers and laboratory-size beam-driven plasma accelerators. However, accelerators generating such currents operate in the beam loading regime where the accelerating field is strongly modified by the self-fields of the injected bunch, potentially deteriorating key beam parameters. Here we demonstrate that, if appropriately controlled, the beam loading effect can be employed to improve the accelerator’s performance. Self-truncated ionization injection enables loading of unprecedented charges of ∼0.5 nC within a mono-energetic peak. As the energy balance is reached, we show that the accelerator operates at the theoretically predicted optimal loading condition and the final energy spread is minimized.

Summary Efg1 is a central transcriptional regulator of morphogenesis and metabolism in

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