Radiation chemistry of water and aqueous solutions has always been an interesting scientific issue owing to involving electronic excitations, ionization of solvated species, and formation of radiolytic species and many elementary reactions, but the underlying mechanisms are still poorly understood. Here, we for the first time molecular dynamics characterize the hydration dynamics of two correlated electrons and their triggered unique phenomena in liquid water associated with radiolysis of water using the combined hybrid functional and nonlocal dispersion functional. Hydration of two electrons may experience two distinctly different mechanisms, one forming a spin-paired closed-shell unicaged dielectron hydrate (e22-aq) and the other forming a spin-paired metastable open-shell bicaged hydrated electron pair (e-aq···e-aq) which exhibits intriguing antiferromagnetic spin coupling dynamics (in a range of -40 cm-1 to -500 cm-1). e-aq···e-aq can recombine to e22-aq through a unique solvent fluctuation-controlled gradual-flowing mechanism, and enlarging fluctuation can promote the conversion. Interestingly, we directly observe that e22-aq as the precursor can trigger hydrogen evolution via unique continuous spontaneous double proton transfer to the dielectron with a short-lived H-aq intermediate, but e-aq···e-aq does not directly. This is the first direct observation for the connection between e22-aq and spontaneous hydrogen evolution including participation of H-aq in aqueous solution, bridging relevant experimental phenomena. This work also evidences an unnoticed process, the double proton transfer mediated charge separation, and presents the first detailed analysis regarding the evolution dynamics of e22-aq for the understanding of the radiolysis reactions in aqueous solutions.Droplet evaporation on surfaces is ubiquitous and affects areas as diverse as climate, microbiology, the chemical industry, and materials science. While solute concentration is the universally taken-for-granted behavior in drop evaporation, the present work shows that saline droplets evaporating on nanoporous thin-film surfaces can get diluted rather than concentrated. The driving mechanism of this phenomenon is attributed to the flow drawn from the drop through the nanopores by an annular peripheral evaporation. This fluid transport can continuously collect the salt solution from a concentrated region of the droplet, which is induced by radial microflows during drop evaporation. The coupling of these processes leads to the overall drop dilution effect. The influence of substrate temperature and drop volume was also investigated. This study opens up new perspectives on many natural phenomena and offers alternatives for physicochemical applications in small dimensions as well as for water desalination technologies.All-inorganic lead halide perovskites, for example, CsPbI3, are becoming more attractive for applications as light absorbers in perovskite solar cells because of higher thermal and photochemical stability as compared to their hybrid analogues. However, a specific drawback of the CsPbI3 absorber consists of the rapid phase transition from black to yellow nonphotoactive phase at low temperatures (e.g., 30) of metal cations in a wide range of concentration has allowed us to establish a set of Pb2+ substitutes, facilitating the crystallization of the photoactive black CsPbI3 phase at low temperatures. Importantly, the appropriate Pb2+ substitution with Ca2+, Sr2+, Ce3+, Nd3+, Gd3+, Tb3+, Dy2+, Er3+, Yb2+, Lu3+, and Pt2+ cations has led to a spectacular enhancement of the film stability under realistic solar cell operation conditions (∼1 sun equivalent light exposure, 50 °C). Optoelectronic, structural, and morphological effects of partial Pb2+ substitution were investigated, providing a deeper insight into the processes underlying the stabilization of the CsPbI3 films. Several CsPb1-xM x I∼3 systems were evaluated as absorber materials in perovskite solar cells, demonstrating encouraging light power conversion efficiency of 11.4% in preliminary experiments. The obtained results feature the potential of designing efficient and stable all-inorganic perovskite solar cells using novel absorber materials rationally designed via compositional engineering.SARS-CoV-2, the virus responsible for the current COVID-19 pandemic, displays a corona-shaped layer of spikes which play a fundamental role in the infection process. Recent structural data suggest that the spikes possess orientational freedom and the ribonucleoproteins segregate into basketlike structures. How these structural features regulate the dynamic and mechanical behavior of the native virion are yet unknown. By imaging and mechanically manipulating individual, native SARS-CoV-2 virions with atomic force microscopy, here, we show that their surface displays a dynamic brush owing to the flexibility and rapid motion of the spikes. The virions are highly compliant and able to recover from drastic mechanical perturbations. Their global structure is remarkably temperature resistant, but the virion surface becomes progressively denuded of spikes upon thermal exposure. The dynamics and the mechanics of SARS-CoV-2 are likely to affect its stability and interactions.Krypton (Kr) and xenon (Xe) are nowadays widely applied in technical and industrial fields. Separating and collecting highly pure Xe from nuclear facilities are necessary and urgent. However, the technology is limited due to the inert nature of Xe and other interferential factors. In this work, a calcium-based metal-organic framework, Ca-SINAP-1, which comprises a three-dimensional microporous framework with a suitable pore width, was researched for xenon and krypton separation through both experimental and theoretical methods. Ca-SINAP-1, synthesized in solvothermal and gamma ray conditions, features accessible open-metal sites, exhibits a high Xe/Kr selectivity of 10.32, and owns a Xe adsorption capacity of 2.87 mmol/g at room temperature (1.0 bar). AZD9291 Particularly, its excellent chemical stability (from pH 2 to 13) and thermal stability (up to 550 °C), as well as radiation-resistance (up to 400 kGy β irradiations), render this material a promising candidate for radioactive inert gases treatment.