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Using the improved quantitative rescattering (QRS) model, we simulate the correlated two-electron momentum distributions (CMD) for nonsequential double ionization (NSDI) of Ar by near-single-cycle laser pulses with a wavelength of 750 nm at an intensity of 2.8 × 10¹⁴W/cm². With the accurate cross sections obtained from fully quantum mechanical calculations for both electron impact excitation and electron impact ionization of Ar⁺, we unambiguously identify the contributions from recollision direct ionization (RDI) and recollision excitation with subsequent ionization (RESI). Our analysis reveals that RESI constitutes the main contribution to NSDI of Ar under the conditions considered here. The simulated results are directly compared with experimental measurements [Bergueset al.,Nat. Commun.3,813(2012)10.1038/ncomms1807] in which each NSDI event is tagged with the carrier-envelope phase (CEP). It is found that the overall pattern of both the CEP-resolved and the CEP-averaged CMDs measured in experiment are well reproduced by the QRS model, and the cross-shaped structure in the CEP-averaged CMD is attributed to the strong forward scattering of the recolliding electron as well as the depletion effect in tunneling ionization of the electron from an excited state of the parent ion.

Using the quantitative rescattering model, we simulate the correlated two-electron momentum distributions for nonsequential double ionization of helium by 800 nm laser pulses at intensities in the range of (2 − 15) × 10¹⁴W/cm². The experimentally observed V-shaped structure at high intensities [Phys. Rev. Lett.99,263003(2007)10.1103/PhysRevLett.99.263003] is attributed to the strong forward scattering in laser-induced recollision excitation and the asymmetric momentum distribution of electrons that are tunneling-ionized from the excited states. The final-state electron repulsion also plays an important role in forming the V-shaped structure.

We consider and analyze a single‐server multiqueue polling model with inner arrivals. Customers arriving at the queue before polling instant could receive service in the current polling round; furthermore, each one could be retried (turns into an inner arrival) a given number of times with a specified probability. Such polling model can be used to study the performance of certain scheduling data transmission in the Internet of Things (IoT) and the relationship between data retransmission and delay. We obtain the closed‐form expression for the generating function of the amount of customers, which are presented at polling instants. Then, it is used to derive the precise closed‐form formula of mean queue length and mean waiting time in symmetric system.

In recent years, hybrid perovskite solar cells (HPSCs) have received considerable research attention due to their impressive photovoltaic performance and low‐temperature solution processing capability. However, there remain challenges related to defect passivation and enhancing the charge carrier dynamics of the perovskites, to further increase the power conversion efficiency of HPSCs. In this work, the use of a novel material, phenylhydrazinium iodide (PHAI), as an additive in MAPbI₃perovskite for defect minimization and enhancement of the charge carrier dynamics of inverted HPSCs is reported. Incorporation of the PHAI in perovskite precursor solution facilitates controlled crystallization, higher carrier lifetime, as well as less recombination. In addition, PHAI additive treated HPSCs exhibit lower density of filled trap states (10¹⁰cm⁻²) in perovskite grain boundaries, higher charge carrier mobility (≈11 × 10⁻⁴cm²V⁻¹s), and enhanced power conversion efficiency (≈18%) that corresponds to a ≈20% improvement in comparison to the pristine devices.

Photovoltaic power‐conversion systems can harvest energy from sunlight almost perpetually whenever sunrays are accessible. Meanwhile, as indispensable energy storage units used in advanced technologies such as portable electronics, electric vehicles, and renewable/smart grids, batteries are energy‐limited closed systems and require constant recharging. Fusing these two essential technologies into a single device would create a sustainable power source. Here, it is demonstrated that such an integrated device can be realized by fusing a rear‐illuminated single‐junction perovskite solar cell with Li₄Ti₅O₁₂‐LiCoO₂Li‐ion batteries, whose photocharging is enabled by an electronic converter via voltage matching. This design facilitates a straightforward monolithic stacking of the battery on the solar cell using a common metal substrate, which provides a robust mechanical isolation between the two systems while simultaneously providing an efficient electrical interconnection. This system delivers a high overall photoelectric conversion‐storage efficiency of 7.3%, outperforming previous efforts on stackable integrated architectures with organic–inorganic photovoltaics. Furthermore, converter electronics facilitates system control with battery management and maximum power point tracking, which are inevitable for efficient, safe, and reliable operation of practical loads. This work presents a significant advancement toward integrated photorechargeable energy storage systems as next‐generation power sources.