Oriented attachment (OA) is a particle-based crystallization pathway in which nanocrystals self-assemble in solution and attach along certain crystallographic direction often forming highly organized three-dimensional crystal morphologies. The pathway offers the potential for a general synthetic approach of hierarchical nanomaterials, in which multiscale structural control is achieved by manipulating the interfacial nucleation and self-assembly of nanoscale building blocks. Here, the current status of the development of a predictive theoretical framework for modeling crystallization by OA is reviewed. A particular emphasis is made on recent developments in understanding the microscopic details of solvent-mediated forces that drive nanocrystal reorientation and alignment for face-selective attachment. Interactions arising from the correlated solvent dynamics at particle interfaces emerge as the main sources of long-range face-specific interparticle forces and short-range torque for fine particle alignment into lattice matching configuration. These findings shift the focus of the experimental and theoretical research of OA onto the detailed study of interfacial solvent structure and dynamics.

A facile one-pot and environmentally friendly method was developed to synthesize multi-branched flowerlike gold (Au) nanostructures by reducing chlorate gold (HAuCl4) with hydrogen peroxide (H2O2) in the presence of sodium citrate. The multibranched Au nanostructures were characterized by transmission electron microscopy and Ultraviolet-visible (UV-vis) absorption spectroscopy. The molar ratio of sodium citrate to HAuCl4 and the concentrations of the reacted reagents play important roles in the formation of multibranched Au nanostructures. The multibranched Au nanostructures with sharp tips exhibit excellent surface-enhanced Raman scattering (SERS) ability of 4-aminothiophenol (PATP). The experimental and simulated results both confirm that the photoinduced catalytic coupling reaction of PATP transformation to 4,4′-dimercaptoazobenzene occurs on the surface of multibranched Au nanostructures at a high power during the SERS measurement. It is believed that these multibranched Au nanostructures may find potential applications in SERS, biosensors, and the photoinduced surface catalytic application fields.

Conventional methods for determination of trace drug residues are either time consuming or labor intensive or require large specialized instruments, which hamper their practical applications in field analysis. Here, we present a rapid and quantitative surface-enhanced Raman scattering (SERS) detection method coupled with a portable Raman spectrometer for determination of trace drug residues on fish surface. Graphene oxide (GO) decorated popcorn-like Ag nanoparticles (NPs) on Cu plate (GO/AgNPs/Cu) were fabricated by a facile approach and directly employed as a robust SERS detection substrate. For practical SERS detections, trace-level residues of crystal violet (10−8 M, 4.1 ng/g) and malachite green (10−8 M, 3.6 ng/g) could be readily detected by simply swabbing the contaminated fish scale surface with the SERS substrate. Importantly, SERS detection was quantitatively realized in the broad linear concentrations. Compared with lab-based Raman spectrometer with large footprints, our method has potential applications in practical rapid, accurate, and on-site SERS determination.

The hierarchical Au-loaded SnO2 nanoflowers were synthesized using a new developed self-reductive hydrothermal method, of which the gas-sensing properties were enhanced significantly. The SnO2 hierarchical nanoflowers were composed of well-defined nanosheets with a specific surface area of around 84 m2/g. Gas sensors made of pure and Au-doped SnO2 were fabricated, and their gas-sensing properties were characterized. The 1.0 at.% Au-loaded SnO2 sensor prepared by the new developed self-reductive method showed much more excellent selectivity toward ethanol at 200 °C than the one prepared with the conventional hydrothermal method. Its response to ethanol was around 3 times higher than that of the pure SnO2 sensor. A very wide detection range of 1–500 ppm for ethanol, good repeatability, and long-term stability were also approved.

Regular WO3 nanocubes have been prepared on a large scale through a convenient hydrothermal route at the temperature of 200 °C. The products were characterized by powder X-ray diffraction (XRD), field-emission scanning electron microscopy, UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. A crystal growth process for WO3 nanocubes was simply proposed based on the comparative experiments. The band gap energy (Eg) was determined to be 2.58 eV based on the UV-vis DRS analysis, and the PL spectrum exhibited a strong blue light emission band centered at 469 nm. The as-prepared WO3 nanocubes showed higher visible light photocatalytic performance for degrading rhodamine B compared with WO3·H2O and WO3·0.33H2O/WO3 which were obtained at 80 °C and 140 °C, respectively, suggesting potential application in the region of wastewater purification.

Three-dimensional graphene (3D-GN)/Cu/Fe3O4 composite support materials were synthesized by a modified chemical reduction method using graphene oxide precursor. A 3D-GN/Cu/Fe3O4 biosensor was prepared by coating the electrode with laccase. The electrochemical properties of the biosensor were investigated by cyclic voltammetry (CV) and differential pulse voltammetry using potassium ferricyanide, phosphate-buffered saline (PBS) solution, and bisphenol A (BPA) solution. The current response of 3D-GN/Cu/Fe3O4 biosensors presents a remarkable sensitivity based on CV. The linear range of BPA is 7.2–18 μM using differential pulse voltammetry in PBS solution (pH = 4.0). A linear fitting equation of the laccase biosensor was observed for the current response as a function of BPA concentration. The detection limit was decreased to 1.7 μM. The detection approach herein turns out to be highly sensitive, has a wide linear range, and exhibits excellent stability.

Nowadays, hierarchical materials have received tremendous interests because of their unique physical and chemical properties. In this article, a novel and facile particle aggregation method was used to fabricate vertically aligned diamondoid nanowires and hierarchical branched nanowire cluster array by using an electrophoresis template method. Triamantane, a three-cage diamondoid, was applied as raw material in current research. Diamondoids are nanometer-sized, hydrogen-terminated diamond-like, saturated hydrocarbons, which process great potential in nanotechnology due to biocompatibility and ultrahard nature. By electrophoresis template method, triamantane molecules dissolved in toluene were transferred into a porous alumina template by electric field and form the one-dimensional (1D) nanostructure with high aspect ratio. After that, a two-step thermal treatment was applied to the nanowires to achieve hierarchical branched nanowires. The surface morphologies of triamantane nanowire array with different treatments were characterized by scanning electron microscopy. This approach opens a new avenue for mass production of the vertically aligned diamondoid nanowires and hierarchical branched nanowire cluster arrays.

Ceramic–metal composites are an important group of materials that have gained interest recently because of their peculiar properties. There have been numerous studies on the reinforcement of alumina through the incorporation of various ductile metals in it. However, these studies have been limited to determining the effect of the addition of metals on the mechanical properties of ceramics, without determining the effect of these metal additions on other physical properties of the resulting composite. In this way, in agreement with the obtained results, we have that because of the conductive nature of metals, there is a considerable decrease in the electrical resistivity of alumina, mainly when copper is added to it. However, in terms of optical performance, alumina matrix composites showed significant changes in absorbance in the visible spectra. The addition of iron, titanium, and yttrium enhanced the absorbance of alumina, whereas manganese addition significantly decreased the optical absorption.

Hierarchically porous poly(L-lactic acid) (PLLA)/poly(ε-caprolactone) (PCL) monolithic composites were fabricated by nonsolvent-induced phase separation (NIPS) method without any template for the first time. A homogeneous hierarchical porous structure with relatively large specific surface area containing both mesopores and macropores was confirmed by pore size distribution plots and scanning electron microscopy images, respectively. Fourier transform infrared analysis (FTIR) revealed that PLLA and PCL were physically blended. Differential scanning calorimeter (DSC) analysis further showed that the two components were physically blended but had a slight thermal compatibility. Meanwhile, X-ray diffraction (XRD) tests indicated that the addition of PCL hindered the crystallization of PLLA. Herein, the formation of the mesopores and macropores during the phase separation process was explained from the microscopic point of view according to the results of XRD and DSC. The present monolithic composites with hierarchically porous structures had promising prospect for applications of tissue engineering.

In this work, a new phenylethylene derivative, named 2-((3,5-di(9H-carbazol-9-yl)phenyl)(p-tolyl)methylene)malononitrile (DCPTMM), is synthesized and characterized by 1H NMR, 13C NMR spectroscopies, mass spectrum, and X-ray crystallography. Its photophysical properties are systematically studied and the result illustrates that DCPTMM shows aggregation-induced emission (AIE). The X-ray single crystal diffraction shows that the individual structure of crystals is monoclinic system with space group symbol P21/c and presents a twisted propeller-type structure as well as the packing structure of crystals has multiple types of hydrogen bonds (C–H⋯π and C–H⋯N) formed between adjacent molecules, and there is no π–π interaction between the aromatic rings, which is the main reason for the formation of AIE. Nondoped OLED fabricated with DCPTMM as light emitting layer emits greenish yellow light with a maximum emission peak of 554 nm and has relatively good performance with a maximum current efficiency of 5.53 cd/A and a maximum brightness of 6936 cd/m2.

In this contribution, we devoted ourselves to fabricating aggregation-induced emission (AIE) activity copolymers via one-pot combination of RAFT polymerization and Biginelli reaction for the first time. When the feeding ratio of TPB was 33.5%, the molar fraction of TPB was, respectively, about 14.2 and 22.5% in PEG-PTE1 copolymers by two-step strategy and PEG-PTE2 copolymers by one-pot strategy with the similar structure. The Mn of PEG-PTE1 increased to 59,300 from 52,800 of PEG-AE presoma with narrow PDI, which was more than Mn of PEG-PTE2 with 52,300. As compared with PEG-PTE2, when the feeding ratio of TPB was 48.6%, the molar fraction of TPB increased to 32.6% in PEG-PTE3. In aqueous solution, the as-obtained PEG-PTE2 copolymers can self-assemble into fluorescent organic nanoparticles (FONs) with 100–180 nm spherical morphology, the maximal emission peak of which presented at 460 nm with the obvious AIE phenomenon. Moreover, due to the low toxicity and excellent cell dyeing behavior, the as-prepared PEG-PTE2 copolymers displayed great potential for biomedical applications.

Nano/mesoporous carbon was prepared from pine wood sawdust via the pretreatment of acid and hydrothermal process, followed by potassium hydroxide (KOH) activation. This study proposed the enhancement of activated carbon (AC) adsorption capacity by utilizing the vacant sites and phenomena of opposite charge attraction via multilayer adsorption of Cr(VI) ions and dyes with positive and negative charges. On the first layer, the maximum adsorption capacities for Cr(VI) ions, methylene blue (MB) molecules, and acid red 18 (AR18) molecules onto AC were found to be 7.91 mg/g, 476.19 mg/g, and 434.78 mg/g, respectively. For multiple adsorption, after Cr(VI) ions uptake saturation, the sequential adsorption of MB and AR18 on the second layer, the maximum adsorption capacity, reached 322.58 mg/g and 333.33 mg/g. After MB and AR18 uptake saturation, the maximum Cr(VI) adsorption capacity reached 2.92 mg/g and 4.39 mg/g.

Wire-shaped supercapacitors (WSSCs) hold great promise in portable and wearable electronics. Herein, a novel kind of high-performance coaxial WSSCs has been demonstrated and realized by scrolling porous carbon dodecahedrons/Al foil film electrode on vertical FeOOH nanosheets wrapping carbon fiber tows (FeOOH NSs/CFTs) yarn electrode. Remarkably, ionogel is utilized as solid-state electrolyte and exhibits a high thermal/electrochemical stability, which effectively ensures the great reliability and high operating voltage of coaxial WSSCs. Benefiting from the intriguing configuration, the coaxial WSSCs with superior flexibility act as efficient energy storage devices and exhibit low resistance, high volumetric energy density (3.2 mW h/cm3), and strong durability (82% after 10,000 cycles). Importantly, the coaxial WSSCs can be effectively recharged by harvesting sustainable wind source and repeatedly supply power to the lamp without a decline of electrochemical performance. Considering the facile fabrication technology with an outstanding performance, this work has paved the way for the integration of sustainable energy harvesting and wearable energy storage units.

Polypropylene plastic (PP) was chosen as additives for the preparation of activated carbon (AC), considering that PP promotes pore formation during the preparation of AC. When the addition ratio of PP was 20%, AC having a maximum specific surface area of 1916.1 m2/g was prepared. Fourier transform–infrared spectroscopy (FT-IR) analysis exhibited the types of functional groups on the surface of AC, such as–OH, C=O, C–C, and –CH. The SEM analysis revealed the formation of disordered pores over the AC. Furthermore, iodine value of the AC is 1460 mg/g. Additionally, adsorption test revealed the AC is suitable for adsorbing methylene blue (MB). The adsorption equilibrium data of MB onto AC were most suitable for Redlich–Peterson model. The maximum adsorption capacity of the single layer was 476.88 mg/g, indicating that AC has high adsorption capacity. The kinetic data fitted well with the pseudo-second-order model.

Biochar conversion from corn stover was evaluated under various process conditions, and the absorption capacity of biochar was investigated for the removal of oxytetracycline in wastewater. Biochar was prepared at lower carbonization temperatures (200–500 °C) and was used in three different concentrations of chemical oxygen wastewater. The results showed that the biochar prepared at the temperature range of 200–500 °C had a faster sorption rate and shorter sorption equilibrium time compared to biochar produced at higher temperatures. The longest time to reach sorption equilibrium was 9 h for biochar obtained at 200 °C. However, the biochar prepared at 500 °C required only 0.5 h to reach the sorption equilibrium. The corn stover-biochar had the highest sorption capacity of 246.3 mg/g for oxytetracycline at 30 °C. The adsorption kinetics was consistent with pseudo–second-order kinetics. This study provides a theoretical basis for the conversion of corn stover into biochar as efficient sorbents.