The growth mechanism of PtS2 single crystal.

PtS2, a member of the group 10 transition metal dichalcogenides (TMDs), has received extensive attention because of its excellent electrical properties and air stability. However, there are few reports on the preparation of single-crystal PtS2 in the literature, and the growth mechanism of single crystal PtS2 is not well elucidated. In this work, we proposed a method of preparation that combines magnetron sputtering and chemical vapor transport to obtain monocrystalline PtS2 on a SiO2/Si substrate. By controlling the growth temperature and time, we have synthesized a single crystalline PtS2 of hexagonal shape and size of 1-2 µm on a silicon substrate. Combining the molecular dynamics simulation, the growth mechanism of single crystal PtS2 was investigated both experimentally and theoretically. The synthesis method has a short production cycle and low cost, which opens the door for the fabrication of other TMDs single crystals.

Bird's Nest-Shaped Sb2 WO6 /D-Fru Composite for Multi-Stage Evaporator and Tandem Solar Light-Heat-Electricity Generators.

Herein, an integrated solar-thermal-power protocol is presented at a micro-nanoscopic level to maximize the energy utilization efficiency involving utilization period and utilization patterns, and the nexus of freshwater production and nanogeneration is realized. This sophisticated vaporization device is constructed with the merits of thermally confined evaporation space in favor of recycling latent heat of condensation and optimizing light absorption based on the local sunlight angle of incidence. Inspired by a bird's nest, Sb2 WO6 /D-Fructose composites are prepared as photothermal absorbers to achieve a superior water evaporation rate of 2.78 kg m-2  h-1 in the Multi-stage evaporator. In addition, a synergistic tandem photo thermal-electric device with a combination of solar-driven water evaporation and further waterflow-driven hydrovoltaic generation, which can output a stable voltage of up to 360.8 mV with effective utilization of steam energy and a limited water source, is exploited. Such integrated configurations pave a pathway for clean water production and renewable power generation simultaneously toward energy issues.

Spatial Patterned Interfacial Solar Evaporators toward Recovering Heat Loss.

The novel freshwater production technology, such as interface solar-steam conversion (ISSC) technology, has advanced so rapidly recently, where its energy capture and conversion process was localized at the air-water interface so as to achieve high efficiency of energy utilization and transformation. However, when enlarging the evaporation surface and application scale, the inevitably increased heat loss and reduced conversion efficiency put it in a dilemma: should we exploit innovative steamer constructs for practical applications. In order to effectively mitigate heat loss from the evaporator to the surrounding environment, a series of spatial pattern evaporators (SPEs) are specifically designed in this article. By recovering the energy of radiation and convection heat loss, SPEs achieved low heat loss in an open evaporator through unequal height auxiliary heat exchange platforms. In an open environment, it achieves a maximum evaporation rate of 1.68 kg m-2 h-1, with approximately 52.41% of the heat loss being reabsorbed. This sophisticated pattern design provides a promising guideline for optimizing thermal management strategies and promoting practically scalable applications.

Centimeter-Scale Few-Layer PdS2: Fabrication and Physical Properties.

To develop next-generation electronic devices, novel semiconductive materials are urgently required. The transition metal dichalcogenides (TMDs) hold the promise of next generation of semiconductor materials for emerging electronic applications. As a member of the group-10 TMDs, PdS2 has a notable layer-number-dependent band structure and tremendously high carrier mobility at room temperature. Here, we demonstrate the experimental realization of centimeter-scale synthesis of the few-layer PdS2 by the combination of physical vapor deposition (PVD) and chemical vapor deposition (CVD) methods. For the first time, the optical anisotropic properties of the few-layer PdS2 were investigated through angle-resolved polarized Raman spectroscopy. Also, the evolution of Raman spectra was studied depending on the temperature in the range of 12-300 K. To further understand the electronic properties of the few-layer PdS2, the field-effect transistor (FET) devices were fabricated and investigated. The electronic measurements of such FET devices reveal that the PdS2 materials exhibit a tunable ambipolar transport mechanism with field-effect mobility of up to ∼388 cm2 V-1 s-1 and the on/off ratio of ∼800, which were not reported before in the literature. To well understand the experimental results, the electronic structure of PdS2 was determined using density functional theory (DFT) calculations. These excellent physical properties are very helpful in developing high-performance opto-electronic applications.

Hierarchy in Au nanocrystal ordering in supracrystals: III. Competition between van der Waals and dynamic processes.

Au nanocrystals coated with thiol derivatives of varying chain sizes ranging from C12 to C16 were produced; two different size nanocrystals have been synthesized (5 and 7 nm in diameter) for each coating agent. All of those specimens are characterized by a low size distribution (below 7%). Those Au nanocrystals were used as building blocks to grow larger self-assembled crystalline structures or supracrystals. These crystalline growths were carried out by slow and controlled solvent evaporation at different temperatures and under non-null partial solvent vapor pressure (Pt). We show that the order within the supracrystals is temperature-dependent when they are made of hexadecanethiol-coated gold nanocrystals, regardless of the size of the nanocrystals. The interparticle distances within the various supracrystals that were produced were determined by small-angle X-ray diffraction (SAXRD). We demonstrate that the interparticle distance is controlled not only by the presence of physisorbed thiol residues, as previously reported, but also, at higher temperatures, by the dynamics of the organic chains and the van der Waals forces involved between the metallic cores of the nanocrystals forming the structure.

Hierarchy in Au nanocrystal ordering in a supracrystal: II. Control of interparticle distances.

Au nanocrystals coated with thiol derivatives differing by the length of their alkyl chains are used to build 3D superlattices called supracrystals. In this study, we used two sets of Au nanocrystals differing by their sizes and size distributions. The average sizes are 5 nm (Au5) and 7 nm (Au7). From one experiment to the other, the size distribution slightly changes. For Au5 nanocrystals, it evolves from 6 to 8%, and for Au7 nanocrystals, it varies from 5 to 6%. The Au nanocrystals (Au5 and Au7) are first dispersed in toluene and produce fcc supracrystals by solvent evaporation. Here, by small-angle grazing X-ray diffraction, we observe a control in the average interparticle distance within the supracrystals. When the supracrystals are grown at zero toluene vapor pressure, the interparticle distances increase linearly with the alkyl chain length of the nanocrystals' coating agent regardless of their diameters. Furthermore, the dry supracrystals can swell and the interparticle distance within the superstructure be increased by subjecting the material to toluene vapor pressure after initial growth. This swelling process is reversible, and retraction occurs when the toluene vapor pressure drops. This indicates a strong ability of the dried supracrystals to trap toluene molecules. On increasing the toluene vapor pressure during the solvent evaporation process, the slope of the linear dependency of the interparticle distances to the alkyl chain length is markedly decreased and the interparticle distance reaches a quasi-plateau. This is explained by the influence of depletion forces created by the presence of thiol-containing molecules physisorbed on the coating molecules on the internal structure of these supracrystals. Recently, we demonstrated that, by using the same nanocrystals (Au5 and Au7), a hierarchy in the supracrystal growth process takes place from heterogeneous nucleation with the formation of a layer-by-layer film to homogeneous nucleation in solution with the formation of shaped supracrystals. Here it is shown that the interparticle distance is independent of the supracrystal growth mechanisms.