The recent developments in material sciences and rational structural designs have advanced the field of compliant and deformable electronics systems. However, many of these systems are limited in either overall stretchability or areal coverage of functional components. Here, we design a construct inspired by Kirigami for highly deformable micro-supercapacitor patches with high areal coverages of electrode and electrolyte materials. These patches can be fabricated in simple and efficient steps by laser-assisted graphitic conversion and cutting. Because the Kirigami cuts significantly increase structural compliance, segments in the patches can buckle, rotate, bend and twist to accommodate large overall deformations with only a small strain (<3%) in active electrode areas. Electrochemical testing results have proved that electrical and electrochemical performances are preserved under large deformation, with less than 2% change in capacitance when the patch is elongated to 382.5% of its initial length. The high design flexibility can enable various types of electrical connections among an array of supercapacitors residing in one patch, by using different Kirigami designs.

Almost ten years ago, energetic neutral hydrogen atoms were detected after a strong-field double ionization of H2. This process, called 'frustrated tunneling ionization', occurs when an ionized electron is recaptured after being driven back to its parent ion by the electric field of a femtosecond laser. In the present study we demonstrate that a related process naturally occurs in clusters without the need of an external field: we observe a charge hopping that occurs during a Coulomb explosion of a small helium cluster, which leads to an energetic neutral helium atom. This claim is supported by theoretical evidence. As an analog to 'frustrated tunneling ionization', we term this process 'frustrated Coulomb explosion'.

Energy distribution of high-power, short-pulse laser produced fast electrons was experimentally and numerically studied using high-energy bremsstrahlung x-rays. The hard x-ray photons and escaping electrons from various metal foils, irradiated by the 50 TW Leopard laser at Nevada Terawatt Facility, were recorded with a differential filter stack spectrometer that is sensitive to photons produced by mainly 0.5–2 MeV electrons and an electron spectrometer measuring >2 MeV electrons. The experimental bremsstrahlung and the slope of the measured escaped electrons were compared with an analytic calculation using an input electron spectrum estimated with the ponderomotive scaling. The result shows that the electron spectrum entering a Cu foil could be continuous single slope with the slope temperature of ∼1.5 MeV in the detector range. The experiment and analytic calculation were then compared with a 2D particle-in-cell code, PICLS, including a newly developed radiation transport module. The simulation shows that a two-temperature electron distribution is generated at the laser interaction region, but only the hot component of the fast electrons flow into the target during the interaction because the low energy electron component is trapped by self-generated magnetic field in the preformed plasma. A significant amount of the photons less than 100 keV observed in the experiment could be attributed to the low energy electrons entering the foil a few picoseconds later after the gating field disappears.

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The double photoionization of a molecule by one photon ejects two electrons and typically creates an unstable dication. Observing the subsequent fragmentation products in coincidence can reveal a surprisingly detailed picture of the dynamics. Determining the time evolution and quantum mechanical states involved leads to deeper understanding of molecular dynamics. Here in a combined experimental and theoretical study, we unambiguously separate the sequential breakup via D+ + OD+ intermediates, from other processes leading to the same D+ + D+ + O final products of double ionization of water by a single photon. Moreover, we experimentally identify, separate, and follow step by step, two pathways involving the b 1Σ+ and a 1Δ electronic states of the intermediate OD+ ion. Our classical trajectory calculations on the relevant potential energy surfaces reproduce well the measured data and, combined with the experiment, enable the determination of the internal energy and angular momentum distribution of the OD+ intermediate.