Extensive studies are conducted on perovskite solar cells (PSCs) with significant performance advances (mainly spin coating techniques), which have encouraged recent efforts on scalable coating techniques for the manufacture of PSCs. However, devices fabricated by blade coating techniques are inferior to state-of-the-art spin-coated devices because the power conversion efficiency (PCE) is highly dependent on the morphology and crystallization kinetics in the controlled environment and the delicate solvent system engineering. In this study, based on the widely studied perovskite solution system dimethylformamide-dimethyl sulfoxide, air-knife-assisted ambient fabrication of PSCs at a high relative humidity of 55 ± 5% is reported. In-depth time-resolved UV-vis spectrometry is carried out to investigate the impact of solvent removal and crystallization rate, which are critical factors influencing the crystallization kinetics and morphology because of adventitious moisture. UV-vis spectrometry enables accurate determination of the thickness of the wet precursor film. Anti-solvent-free, high-humidity ambient coatings of hysteresis-free PSCs with PCEs of 21.1% and 18.0% are demonstrated for 0.06 and 1 cm2 devices, respectively. These PSCs exhibit comparable stability to those fabricated in a glovebox, thus demonstrating their high potential.At the organic-inorganic interface of nanocrystals, electron-phonon coupling plays an important but intricate role in determining the diverse properties of nanomaterials. Here, it is reported that highly doping of Yb3+ ions within the nanocrystal host can form an energy-migration network. https://www.selleckchem.com/products/10074-g5.html The networking state Yb3+ shows both distinct Stark splitting peak ratios and lifetime dynamics, which allows quantitative investigations of quenching and thermal activation of luminescence, as the high-dimensional spectroscopy signatures can be correlated to the attaching and de-attaching status of surface molecules. By in-situ surface characterizations, it is proved that the Yb-O coordination associated with coordinated water molecules has significantly contributed to this reversible effect. Moreover, using this approach, the prime quencher -OH can be switched to -CH in the wet-chemistry annealing process, resulting in the electron-phonon coupling probability change. This study provides the molecular level insights and dynamics of the surface dark layer of luminescent nanocrystals.Selective separation of organic species, particularly that of intermediate-size ones from their analogs, remains challenging because of their similar structures and properties. Here, a novel strategy is presented, cooperatively (thermodynamically and kinetically) controlled crystallization for the highly selective separation of intermediate-size anionic pollutants from their analogs in water through one-pot construction of cationic metal-organic frameworks (CMOFs) with higher stabilities and faster crystallization, which are based on the target anions as charge-balancing anions. 4,4'-azo-triazole and Cu2+ are chosen as suitable ligand and metal ion for CMOF construction because they can form stronger intermolecular interaction with p-toluenesulfonate anion (Ts-) compared to its analogs. For this combination, a condition is established, under which the crystallization rate of a Ts--based CMOF is remarkably high while those of analog-based CMOFs are almost zero. As a result, the faster crystallization and higher stability cooperatively endow the cationic framework with a close-to-100% selectivity for Ts- over its analogs in two-component mixtures, and this preference is retained in a practical mixture containing more than seven competing (analogs and inorganic) anions. The nature of the free Ts- anion in the cationic framework also allows the resultant CMOF to be recyclable via anion exchange.The industrial application of lithium metal anode requires less side reaction between active lithium and electrolyte, which demands the sustainability of the electrolyte-induced solid-electrolyte interface. Here, through a new diluted lithium difluoro(oxalato)borate-based (LiDFOB) high concentration electrolyte system, it is found that the oxidation behavior of aggregated LiDFOB salt has a great impact on solid-electrolyte interphase (SEI) formation and Li reversibility. Under the operation window of Cu/LiNi0.8Co0.1Mn0.1O2 full cells (rather than Li/Cu configuration), a polyether/coordinated borate containing solid-electrolyte interphase with inner Li2O crystalline can be observed with the increasing concentration of salt, which can be ascribed to the reaction between aggregated electron-deficient borate species and electron-rich alkoxide SEI components. The high Li reversibility (99.34%) and near-theoretical lithium deposition enable the stable cycling of LiNi0.8Co0.1Mn0.1O2/Li cells (N/P less then 2, 350 Wh kg-1) under high cutoff voltage condition of 4.6 V and lean electrolyte condition (E/C ≈ 3.2 g Ah-1).Cells are able to perceive complex mechanical cues from their microenvironment, which in turn influences their development. Although the understanding of these intricate mechanotransductive signals is evolving, the precise roles of substrate microtopography in directing cell fate is still poorly understood. Here, UV nanoimprint lithography is used to generate micropillar arrays ranging from 1 to 10 µm in height, width, and spacing to investigate the impact of microtopography on mechanotransduction. Using mesenchymal stem cells (MSCs) as a model, stark pattern-specific changes in nuclear architecture, lamin A/C accumulation, chromatin positioning, and DNA methyltransferase expression, are demonstrated. MSC osteogenesis is also enhanced specifically on micropillars with 5 µm width/spacing and 5 µm height. Intriguingly, the highest degree of osteogenesis correlates with patterns that stimulated maximal nuclear deformation which is shown to be dependent on myosin-II-generated tension. The outcomes determine new insights into nuclear mechanotransduction by demonstrating that force transmission across the nuclear envelope can be modulated by substrate topography, and that this can alter chromatin organisation and impact upon cell fate. These findings have potential to inform the development of microstructured cell culture substrates that can direct cell mechanotransduction and fate for therapeutic applications in both research and clinical sectors.