Revealing the formation mechanism and band gap tuning of Sb2S3 nanoparticles

Sb2S3 is a promising nanomaterial for application in solar cells and in the fields of electronics and optoelectronics. Herein, Sb2S3 nanoparticles were prepared via the hot-injection approach. In contrast to earlier work, the reaction temperature was decreased to 150 °C so that the reaction was slowed down and could be stopped at defined reaction stages. Thereby, the formation mechanism of the nanomaterial and the associated kinetics could be revealed. Based on morphological and structural analyses, it is suggested that seed particles (type 0) formed immediately after injecting the antimony precursor into the sulfur precursor. These seeds fused to form amorphous nanoparticles (type I) that contained a lower percentage of sulfur than that corresponding to the expected stoichiometric ratio of Sb2S3. The reason for this possibly lies in the formation of an oxygen- or carbon-containing intermediate during the seeding process. Afterward, the type I nanoparticles aggregated into larger amorphous nanoparticles (type II) in a second hierarchical assembly process and formed superordinate structures (type III). This process was followed by the crystallization of these particles and a layer-like growth of the crystalline particles by an Ostwald ripening process at the expense of the amorphous particles. It was demonstrated that the kinetic control of the reaction allowed tuning of the optical band gap of the amorphous nanoparticles in the range of 2.2–2.0 eV. On the contrary, the optical band gap of the crystalline particles decreased to a value of 1.7 eV and remained constant when the reaction progressed. Based on the proposed formation mechanism, future syntheses for Sb2S3 particles can be developed, allowing tuning of the particle properties in a broad range. In this way, the selective use of this material in a wide range of applications will become possible.

Pressure-driven fusion of amorphous particles into integrated monoliths

Biological organisms can use amorphous precursors to produce inorganic skeletons with continuous structures through complete particle fusion. Synthesizing monoliths is much more difficult because sintering techniques can destroy continuity and limit mechanical strength. We manufactured inorganic monoliths of amorphous calcium carbonate by the fusion of particles while regulating structurally bound water and external pressure. Our monoliths are transparent, owing to their structural continuity, with a mechanical strength approaching that of single-crystal calcite. Dynamic water channels within the amorphous bulk are synergistically controlled by water content and applied pressure and promote mass transportation for particle fusion. Our strategy provides an alternative to traditional sintering methods that should be attractive for constructing monoliths of temperature-sensitive biominerals and biomaterials.

Revealing the formation mechanism and band gap tuning of Sb2S3 nanoparticles

Sb2S3 is a promising nanomaterial for application in solar cells and other fields of electronics and optoelectronics. Sb2S3 nanoparticles were prepared via the hot-injection approach. In contrast to earlier work, the reaction temperature was decreased to 150°C, so that the reaction was slowed down and could be stopped at defined reaction stages. Thereby, the formation mechanism of the nanomaterial and the associated kinetics could be revealed. Based on morphological and structural analysis, it is suggested that seed particles (type 0) form immediately after injecting the antimony precursor into the sulfur precursor. These seeds fuse to form amorphous nanoparticles (type I) that contain a lower percentage of sulfur than that corresponding to the expected stoichiometric ratio of Sb2S3. The reason for this possibly lies in the formation of an oxygen- or carbon-containing intermediate during the seeding process. Afterward, the type I nanoparticles aggregate into larger amorphous nanoparticles (type II) in a second hierarchical assembly process and form superordinated structures (type III). This process is followed by the crystallization of these particles and a layer-like growth of the crystalline particles by an Ostwald ripening process at the expense of the amorphous particles. It was demonstrated that the kinetic control of the reaction allows tuning of the optical bandgap of the amorphous nanoparticles in the range of 2.2 – 2.0 eV. On the contrary, the optical bandgap of the crystalline particles decreases to a value of 1.7 eV and remains constant when the reaction progresses. Based on the proposed formation mechanism, future syntheses for Sb2S3 particles can be developed, allowing tuning the particles' properties in a broad range. In this way, the selective use of this material in a wide range of applications will become possible.

Solubility of proteins

<p class="ADMETabstracttext">Solubility is a fundamental protein property that has important connotations for therapeutics and use in diagnosis. Solubility of many proteins is low and affect heterologous overexpression of proteins, formulation of products and their stability. Two processes are related to soluble and solid phase relations. Solubility refers to the process where proteins have correctly folded structure, whereas aggregation is related to the formation of fibrils, oligomers or amorphous particles. Both processes are related to some diseases. Amyloid fibril formation is one of the characteristic features in several neurodegenerative diseases, but it is related to many other diseases, including cancers. Severe complex V deficiency and cataract are examples of diseases due to reduced protein solubility. Methods and approaches are described for prediction of protein solubility and aggregation, as well as predictions of consequences of amino acid substitutions. Finally, protein engineering solutions are discussed. Protein solubility can be increased, although such alterations are relatively rare and can lead to trade-off with some other properties. The aggregation prediction methods mainly aim to detect aggregation-prone sequence patches and then making them more soluble. The solubility predictors utilize a wide spectrum of features.</p>

Possibility of Recycling SiOx Particles Collected at Silicon Ingot Production Process as an Anode Material for Lithium Ion Batteries

Recently, some studies have utilized silicon (Si) as an anode material of lithium ion battery by recycling Si from the slurry of wafer slicing dust. The filtration of Si particles condensed from Si vapors that were exhausted from the ingot growing furnace could propose another method of Si recycling. In this study, we investigated the possibility of using such collected silicon oxides (SiOx) particles as an anode material. After collecting SiOx particles, FE-SEM, TEM, EDS, XRD, XPS analysis, and charge/discharge test were carried out to investigate characteristics and usability of these particles. FE-SEM and FE-TEM images showed that these particles mainly consisted of spherical primary particles with a diameter of 10 nm or less. Agglomerates of these primary particles were larger than 300 nm in diameter. In TEM image and EDS analysis, crystalline particles were observed along with amorphous particles. As a result of XRD analysis, amorphous silica (SiO2) and crystalline Si were observed. Charge/discharge tests were carried out to determine the feasibility of using these particles as an anode material for lithium ion batteries. A cycle efficiency of 40.6% was obtained in the test in which the total number of charge/discharge cycle was 100 under the condition of C-rate 0.2 for the first three times and C-rate 1.0 for the remaining 97 times. Results showed that these collected particles could be used as an anode material for lithium ion batteries.

Reversed Crystal Growth

In the last decade, a reversed growth route has been found in many crystal growth processes. In these systems, a single crystal does not develop from a single nucleus. The precursor molecules/ions or nanocrystallites aggregate into some large amorphous or polycrystalline particles. Multiple-nucleation on the surface of the amorphous particles or surface re-crystallization of the polycrystalline particles then takes place, forming a single crystal shell with a regular morphology. Finally, the crystallization extends from the surface to the core to form single crystals. This non-classical crystal growth route often results in some special morphologies, such as core-shell structures, hollow single crystals, sandwich structures, etc. This article gives a brief review of the research into reversed crystal growth and demonstrates that investigation of detailed mechanisms of crystal growth enables us to better understand the formation of many novel morphologies of the crystals. Some unsolved problems are also discussed.