In order to investigate the thermal and chemical (in)stabilities of MAPbI3 incorporated with graphene and silver nanowire (AgNW) electrodes, we employed the terahertz (THz) time-domain spectroscopy, which has a unique ability to deliver the information of electrical properties and the intermolecular bonding and crystalline nature of materials. In in situ THz spectroscopy of MAPbI3, we observed a slight blue-shift in frequency of the 2 THz phonon mode as temperatures increase across the tetragonal-cubic structural phase transition. For MAPbI3 with the graphene top electrode, no noticeable frequency shift is observed until the temperature reaches the maximum operating temperature of solar cells (85 °C). Phonon frequency shift is sensitive to the strain-induced tilt of PbI6 octahedra and our results indicate that graphene forms a stable interface with MAPbI3 and is also effective in suppression of the undesirable phase transition. Meanwhile, for MAPbI3 coupled with the AgNW bottom electrode, the THz conductivity was found to be as low as that of the MAPbI3 single layer, attributed to the chemical reaction between Ag atoms and iodide ions. The THz conductivity is greatly increased when an ultrathin Al2O3 interlayer is introduced to cover the AgNW network via the atomic layer deposition (ALD) method. ALD of Al2O3 on the AgNW surfaces at low temperature guarantees a conformal coating, which strongly affects the ohmic contacts between the NWs. Our results demonstrate the advantage of THz spectroscopy for the comprehensive analysis of thermal and chemical stabilities of perovskites associated with the electrode materials.Flexible sensing materials have attracted tremendous attention in recent years because of their potential applications in the fields of health monitoring, artificial intelligence, and so on. However, the preparation of rate sensing materials with self-healing performance is always a huge challenge. Herein, we first report the design and synthesis of a highly stretchable, recyclable, self-healing polysiloxane elastomer with rate sensing capability. The elastomer is composed of a dynamic dual network with boron/oxygen dative bonds and hydrogen bonds, which overcomes the structural instability of conventional solid-liquid materials. It exhibits certain adhesion, satisfactory mechanical robustness, and superior elongation at break (up to 1171%). After heating treatment at 80 °C for 2-4 h, the mechanical properties of damaged materials can be almost completely restored. Because of the “solid-liquid” property of the elastomer, it has irreplaceable functions which can sense different rates by resistance change after blending with multiwalled carbon nanotubes, principally in the range of 10 mm/min-150 mm/min. Especially, this rate sensing elastomer can be personalized by 3D printing at room temperature. This rate sensing strategy coupled with the introduction of dynamic dual-network structure is expected to help design advanced wearable devices for human rhythmic movement.Basic carboxypeptidases (basic CPs) cleave the C-terminal basic amino acid of peptides, and their activity is upregulated in some types of cancers. Therefore, detecting the activity of basic CPs in living cells would be important not only for studying the physiological functions of these enzymes but also for visualization of cancerous tissues. Here, we report two fluorescein diacetate (FDA)-based activatable fluorescence probes, named 5ArgAF-FDA and 5LysAF-FDA, in which the substrate amino acid arginine or lysine is conjugated to the benzene moiety via an azoformyl linker. In live-cell fluorescence imaging of CPM, one of the seven basic CPs, 5ArgAF-FDA showed a larger intracellular fluorescence increase than did 5LysAF-FDA within a few minutes. This increase was inhibited by coincubation with 2-mercaptomethyl-3-guanidinoethylthiopropanoic acid (MGTA), an inhibitor of basic CPs. When 5ArgAF-FDA was applied to a coculture of two breast cancer cell lines with different CPM activities, the fluorescence increase in individual cells was correlated with the expression level of CPM, suggesting that 5ArgAF-FDA has the ability to distinguish cell lines having different levels of CPM activity, owing to its high intracellular retention. We believe these probes will be useful for imaging cancers with upregulated basic CP activity.A broad array of imaging and diagnostic technologies employs fluorophore-labeled antibodies for biomarker visualization, an experimental technique known as immunofluorescence. Significant performance advantages, such as higher signal-to-noise ratio, are gained if the appended fluorophore emits near-infrared (NIR) light with a wavelength >700 nm. However, the currently available NIR fluorophore antibody conjugates are known to exhibit significant limitations, including low chemical stability and photostability, weakened target specificity, and low fluorescence brightness. These fluorophore limitations are resolved by employing a NIR heptamethine cyanine dye named s775z whose chemical structure is very stable, charge-balanced, and sterically shielded. Using indirect immunofluorescence for imaging and visualization, a secondary IgG antibody labeled with s775z outperformed IgG analogues labeled with the commercially available NIR fluorophores, IRDye 800CW and DyLight800. Comparison experiments include three common techniques immunocytochemistry, immunohistochemistry, and western blotting. Specifically, the secondary IgG labeled with s775z was 3-8 times brighter, 3-6 times more photostable, and still retained excellent target specificity when the degree of antibody labeling was high. The results demonstrate that antibodies labeled with s775z can emit total photon counts that are 1-2 orders of magnitude higher than those currently possible, and thus enable unsurpassed performance for NIR fluorescence imaging and diagnostics. They are especially well suited for analytical applications that require sensitive NIR fluorescence detection or use modern photon-intense methods that require high photostability.Promoting the generation of intermediate active species (superoxide radical (•O2-)) is an important and challenging task for water purification by photoelectrocatalytic (PEC) oxidation. learn more Herein, we have constructed hierarchical cationic sulfur-doped Co3O4 architectures with controllable morphology and highly exposed reactive facets by introducing l-cysteine as a capping reagent and sulfur resource via a one-step hydrothermal reaction. The as-obtained cationic sulfur (1.8 mmol l-cysteine) source doped Co3O4 (SC-1.8) architectures with highly exposed (112) facets exhibited superior PEC activities and long-term stability (∼25,000 s) in 1.0 mol·L-1 sulfuric acid for an accelerated reactive brilliant blue KN-R degradation test. Our experimental and theoretical results confirmed that the superior PEC performance of the SC-1.8 architectures could be ascribed the following factors (1) the highly exposed reactive (112) facets of SC-1.8 promoted carrier transport and diffusion during the PEC process and facilitated separating the electron/hole pairs and producing the predominant active species (•O2-) compared with currently used other electrodes.