High-definition and robust visualization of latent fingerprints utilizing ultrabright aggregation-induced emission of iridium developer.

Creation of AIEgens with high brightness is compactly related to acquiring optimum AIE capabilities and still faces challenges. This study proposes an ingenious structurally regulative approach for preparing ultrabright AIEgens, taking iridium complexes as the model. The incremental rotational activity of substituents obtained by fine adjustment of the stereoscopic configuration efficaciously activates the AIE of iridium complexes and synchronously imparts high-brightness luminescence. Subsequently, benefitting from the ultrabright AIE, high-resolution visualization of latent fingerprints (LFPs) is achieved on diverse substrates by transient immersion in a solution of the AIE-active iridium complex (Ir3) for 60 s. The LFPs stained by Ir3 are integral and distinct enough to possess level 1-3 detail features, which allow precisely realizing personal identification. The LFP photograph emerges inconspicuous attenuation of contrast when aged under ambient light for 10 days and then being continuously irradiated with high-power ultraviolet light for 1 h, reflecting extraordinary aging resistance. Notably, the ultrabright AIE of Ir3 with room-temperature phosphorescence feature successfully achieves enhanced visualization of local fingerprint details with ultrahigh contrast. This LFP visualization protocol based on the ultrabright AIEgens is practical and provides a reliable solution for forensic investigations in actual scenarios.

Discovering the direct evidence of photocatalytic sterilization mechanism on bimetallic sulfides heterostructures.

Despite the development of sterilization, the study of reactive oxygen species (ROS) based disinfection mechanism is still under restrictions due to the lack of direct evidence. In this work, DiI is used to explore the sterilization mechanism in-depth. The mechanism is directly proven to be that the generated ROS would seriously damage the lipid of the cell membrane. It provides direct evidence for the destruction of cell membrane for the first time. These ROS can cause the death of more than 99% of both Gram-negative and Gram-positive bacteria within 120 min under visible light. What's more, MoS2/MSy (MSy = MnS, CuS, and CeS2) are successfully synthesized by employing Mo/M-MOF (M = Mn, Cu, and Ce) as precursors. Since bigger Fermi lever difference and smaller work function bring better photocatalytic activity, MoS2/MnS composites display superb photocatalytic activity than others. Therefore, the as-prepared materials can be widely used in environmental protection, biotechnology, and clinical therapy.

Tannic acid-polypyrrole multifunctional coating layer enhancing the interface effect and efficient Li-ion transport of a phosphorus anode.

Phosphorus has been considered a promising anode material for lithium-ion batteries because of its high specific capacity of 2596 mA h g-1 and safe lithiation voltage of 0.7 V. However, the practical application of the phosphorus anode is challenged by its poor cyclability associated with the dissolution of phosphorus intermediates, the enormous volume expansion and the sluggish lithiation reaction kinetics during the cycling process. Herein, a multifunctional coating layer is designed and fabricated on the surface of a phosphorus-carbon nanotube (P-CNT) electrode via the facile in situ polymerization of plant-derived tannic acid (TA) and pyrrole (Py). This coating layer shows strong adsorption of phosphorus and its derivatives, buffers the volumetric expansion of phosphorus and facilitates efficient Li-ion transport, thus enhancing phosphorus utilization during the cycling process. As a result, the P-CNT@TA-PPy hybrid exhibits a stable coulombic efficiency of 99.0% at 520 mA g-1 after 100 cycles and a reduced volumetric expansion of 50% at 260 mA g-1, superior to P-CNT with its unstable coulombic efficiency and large electrode expansion of 329%. This study sheds light on the rational design of advanced phosphorus-based anodes for alkali metal-ion batteries.

Facile Separator Modification Strategy for Trapping Soluble Polyphosphides and Enhancing the Electrochemical Performance of Phosphorus Anode.

Phosphorus anode is one of the most promising candidates for high-energy-density lithium-ion batteries. Recent studies found the lithiation process of phosphorus is accompanied by the soluble intermediates of lithium polyphosphides. The trans-separator diffusion of polyphosphides is responsible for the capacity decay. Herein, a facile separator modification strategy is proposed for improving the performance of phosphorus anode. The lightweight CNT-modified layer that has a continuous conductive skeleton, a dense structure, and a strong interaction with the soluble lithium polyphosphides can trap, stabilize, and reactivate the active material. Without sophisticated electrode structure design, the cyclability and high-rate performance of the phosphorus anode has been significantly improved, leading to a higher specific capacity of 1505 mAh/g at 250 mA/g (200th cycle) and 1312 mAh/g at 2 A/g. With the advantages of simplicity and low cost, the separator modification strategy provides a new feasible way for further improvement of the phosphorus-based anode.

Manipulating the Zinc Deposition Behavior in Hexagonal Patterns at the Preferential Zn (100) Crystal Plane to Construct Surficial Dendrite-Free Zinc Metal Anode.

Zinc metal has a severe dendrite issue caused by the uneven Zn plating/stripping during continual cycles, which hinders the practical application of ZIBs. The surficial atomic structure of zinc anode plays a decisive role in solving dendrites and improving the electrochemical performance. According to the density functional theory results, Zn (100) plane possesses a much stronger adsorption energy of zinc atom compared with the (002), thus zinc atom preferentially nucleates on the (100) surface. It subsequently continues to grow vertically on (100). Herein, the zinc anode is designed with hexagonal-hole patterns (h-Zn) through a phosphoric acid etching reaction. An abundance of Zn (100) crystal planes are exposed perpendicularly to the anode surface, while the (002) surfaces are at the bottom of these hexagonal holes. Zinc prefers to deposit in hexagonal holes at the (100) surfaces, favoring the restraining of the surficial dendrite growth and accelerating the Zn deposition kinetics. Thus, the symmetric cell using h-Zn exhibits a long cycling lifespan for over 1200 h and extremely low polarization voltage of ≈80 mV at 5 mA cm-2 and 1 mAh cm-2 . This work provides an insight into the surficial structure design and crystal plane regulation to fabricate brilliant zinc metal anodes.

Cationic intermediates assisted self-assembly two-dimensional Ti3C2Tx/rGO hybrid nanoflakes for advanced lithium-ion capacitors.

Two-dimensional (2D) material MXenes have been intensively concerned in energy-storage field due to these unique properties of metallic-like conductivity, good hydrophilicity and high volumetric capacity. However, the self-restocking of ultra-thin 2D materials seriously hinders these performances, which significantly inhibits the full exploitation of MXenes in the field of energy storage. To solve this issue, a strategy to prepare delaminated Ti3C2Tx (MXene) nanoflakes/reduced graphene oxide (rGO) composites is proposed using the electrostatic self-assembly between positively charged Ti3C2Tx with tetrabutylammonium ion (TBA+) modification and negatively charged graphene. The nanoflakes of Ti3C2Tx/rGO are well dispersed and arranged in a face-to-face structure to effectively alleviate the self-restacking and provide more electroactive sites for accessible of electrolyte ions. The prepared delaminated Ti3C2Tx/rGO anode shows a high reversible capacity up to 1394 mAh g-1 at a current density of 50 mA g-1. Moreover, a lithium-ion capacitor (LIC) was assembled with delaminated Ti3C2Tx/rGO anode and activated carbon (AC) cathode which can exhibit a specific capacity of 70.7 F g-1 at a current density of 0.1 A g-1 and deliver an ultrahigh energy density of 114 Wh kg-1 at a relatively high power density of 3125 W kg-1. These good electrochemical performances demonstrate the potential of delaminated Ti3C2Tx/rGO as an anode material for lithium-ion capacitors.

K2Ti6O13/carbon core-shell nanorods as a superior anode material for high-rate potassium-ion batteries.

Bunches of oriented K2Ti6O13 nanorods coated by a thin carbon layer (4-7 nm) were prepared by combining hydrothermal and heat treatment in sequence. The K2Ti6O13 nanorods possess long- and short-axis crystal orientations of <010> and <001>, respectively, contributing to fast K+ diffusion, and the carbon-coating layer improves the electron conductivity. In addition, the obtained K2Ti6O13/carbon has a high compaction density, which is beneficial for realizing high volumetric specific capacity. When evaluated as a potassium-ion battery anode, the nanorods demonstrated a superior rate capability (122.5, 104.3, 92.3, 78.6 and 65.1 mA h g-1 at current densities of 20, 50, 100, 200 and 500 mA g-1, respectively), a favourable cycle life (118.5 mA h g-1 at 25 mA g-1 for 200 cycles) and high capacity retention.

Preparation of multi-functional magnetic-plasmonic nanocomposite for adsorption and detection of thiram using SERS.

Magnetic materials have been widely used for constructing substrate in surface enhanced Raman scattering (SERS) sensing due to the magnetic responsibility. Here, we reported a facile and effective approach to construct multi-functional SERS substrate based on assembling Ag nanoparticles (NPs) on porous Fe microspheres. The porous Fe microspheres were prepared through hydrogen reduction of Fe2O3 NPs with porous structure, in which the size and morphology of Fe could be well controlled. The surface of Fe was grafted with amino group, and then decorated with Ag NPs. The surface area and pore size of Fe microsphere were characterized by nitrogen adsorption and desorption. The Fe@Ag nanocomposite illustrated a good SERS activity. Furthermore, this substrate could be used for pesticide monitoring by portable Raman spectrometer. Especially, the porous Fe microsphere could adsorb analyte from target sample and the Fe@Ag could be concentrated by magnetic force to amplify the SERS signal for thiram detection.

The improvement of photocatalysis O2 production over BiVO4 with amorphous FeOOH shell modification.

A novel amorphous FeOOH modified BiVO4 photocatalyst (A-FeOOH/BiVO4) was successfully produced and characterized by various techniques. The results showed that amorphous FeOOH with about 2 nm thickness evenly covered on BiVO4 surface, which caused resultant A-FeOOH/BiVO4 exhibiting higher visible light photocatalytic performance for producing O2 from water than BiVO4. When the covered amount of amorphous FeOOH was 8%, the resultant photocatalyst possessed the best photocatalytic performance. To find the reasons for the improvement of photocatalytic property, electrochemical experiments, DRS, PL and BET, were also measured, the experimental results indicated that interface effect between amorphous FeOOH and BiVO4 could conduce to migration of photogenerated charge, and exhibit stronger light responded capacity. These positive factors promoted A-FeOOH/BiVO4 presenting improved the photocatalytic performance. In a word, the combination of amorphous FeOOH with BiVO4 is an effective strategy to conquer important challenges in photocatalysis field.

The dependence of oxygen sensitivity on the molecular structures of Ir(iii) complexes and their application for photostable and reversible luminescent oxygen sensing.

Three Ir(iii) complexes IrC1, IrC2, and IrC3 substituted with 4-(diphenylamino)phenyl (TPA), 4-(9H-carbazol-9-yl)phenyl (Cz1), and 9-phenyl-9H-carbazol-3-yl (Cz2) moieties were prepared and fully characterized as phosphorescent emitters. In comparison with Ir(ppy)3, introduction of TPA, Cz1, and Cz2 moieties strongly improved the oxygen sensitivities of IrC1-IrC3. Short-decayed IrC1 with I 0/I 100 of 168.6 and K app SV of 202.2 bar-1 in THF exhibited the highest sensitivity for oxygen. TPA and Cz moieties caused remarkable collision radius variations of the Ir(iii) complexes with 2.13 ± 0.08 for σ IrC1/σ Ir(ppy)3 , 1.24 ± 0.06 for σ IrC2/σ Ir(ppy)3 , and 1.54 ± 0.08 for σ IrC3/σ Ir(ppy)3 . For demonstrating the dependence of oxygen sensitivity on the molecular structure of the oxygen-sensitive probes (OSPs), the delocalization of spin populations (DSPs) has been applied for the first time to confirm the collision radius variations of Ir(iii) complexes. Remarkable DSPs were found on the TPA, Cz1, and Cz2 moieties with the spin population (percentage of the spin population) of 0.23210 (11.61%), 0.08862 (4.43%), and 0.13201 (6.60%), respectively. And strong linear correlations (R 2 = 0.997) between the collision radius variations and spin population on TPA and Cz moieties were apparent. The DSPs could be used to describe the dependence of oxygen sensitivity on the molecular structure of the OSPs. For achieving real-time oxygen sensing, the photostability, oxygen sensing performance, and operational stability of IrC1-IrC3 and Ir(ppy)3 immobilized in ethyl cellulose (EC) were investigated. The IrC1-EC film demonstrated outstanding photostability after 60 min of irradiation and excellent operational stability for continuous oxygen monitoring with no attenuation of the original emission intensity in 4000 s. This study quantified and analyzed the dependence of oxygen sensitivity on the molecular structure of Ir(iii) complexes for the first time and illustrated a feasible approach to achieve high-efficiency sensors for real-time monitoring of oxygen.

Selective sensing and visualization of pesticides by ABW-type metal-organic framework based luminescent sensors.

A new ABW-type luminescent metal-organic framework (MOF) namely (H3O)[Zn2L(H2O)]·3NMP·6H2O (1), constructed with eco-friendly Zn2+ and the multicarboxylate intraligand (LH5) was designed, synthesized and fully characterized by X-ray single-crystal diffraction, steady-state absorption and emission spectroscopy, and SEM observations. The MOF-based suspension sensor 1 (NMP) demonstrated high sensitivity to low-concentration pesticides of chlorothalonil (CTL), nitrofen (NF), trifluralin (TFL), and 2,6-dichloro-4-nitroaniline (DCN), which was assigned to the synergistic effect of the photoinduced electron transfer and the fluorescence resonance energy transfer. With the highest luminescent detection efficiency (K SV up to 11.194 µmol-1 and LOD down to 2.93 ppm) to DCN, 1 (NMP) was successfully applied for the selective sensing of DCN. The MOF-based film sensor 1 (film) illustrated the selective visualization sensing of trace amounts of DCN. In addition, based on the high saturated vapor pressure of TFL and the unique bathochromic shift effect to the emission maxima of 1, the MOF-based luminescent vapor sensing device 1 (LED) successfully exhibited operability for sensing of TFL vapor. The results illustrated a feasible approach to construct new MOF-based luminescent sensors for selective sensing and visualization of pesticides.