Large Crystal Size Research Articles

Removal of artificial anionic dye by electrocoagulation and electro-oxidation combined system using aluminum and nano (Cu-Mn-Ni) composite electrodes

The combined system of electrocoagulation (EC) and electro-oxidation (EO) is one of the most promising methods in dye removal. In this work, a solution of 200 mg/l of Congo red was used to examine the removal of anionic dye using an EC-EO system with three stainless steel electrodes as the auxiliary electrodes and an aluminum electrode as anode for the EC process, Cu-Mn-Ni Nanocomposite as anode for the EO process. This composite oxide was simultaneously synthesized by anodic and cathodic deposition of Cu (NO3)2, MnCl2, and Ni (NO3)2 salts with 0.075 M as concentrations of each salt with a fixed molar ratio (1:1:1) at a constant current density of 25 mA/cm2. The characteristics structure and surface morphology of the deposited nano oxides onto the graphite substrates were determined by (XRD), (FE-SEM), (AFM), and (EDX). The results shown that nano Cu-Mn-Ni oxides were successfully deposited onto the anode and cathode. The crystal size and root mean square for the cathode were 30.79 nm and 79.36 nm, respectively, while for the anode, they were 24.19 nm and 41.88 nm, respectively. Furthermore, the combined system was examined for C.D, NaCl concentration, and time. In the EC-EO combined system, the cathode and anode were efficient when used as anodes for the EO process, besides aluminum. The cathode was more effective in the removal process than the anode due to its larger crystal size and the rough, granular shape of its surface. When current density (C.D) increased from 3 to 6 mA/cm², the removal efficiency shifted from 95% to 98%. However, excellent removal of 98% and 96.5% was attained with 1.665 and 2.0859 kWh/kg of dye as energy consumption in the presence and absence of NaCl salt, respectively by applying 6 mA/cm2 within 20 min of electrolysis.

Comparison of ZnO Nanoparticles Prepared by Spray Pyrolysis and Consecutive Method for UV-Driven Photocatalytic Degradation of Methylene Blue

ZnO is a semiconductor material that is widely used for many applications in industries such as solar cells, dye-sensitized solar cells, food packaging, photocatalytic, anti-microbial, light-emitting diode devices, and gas sensors. In this study, ZnO nanoparticles (NPs) have been successfully synthesized using two methods, namely spray pyrolysis and a consecutive method. The consecutive method is a combination of sol-gel and spray drying methods. The objective of this study is to investigate the photocatalytic performance of ZnO fabricated using those methods. Both methods used the same precursor, zinc acetate dehydrate as a source of zinc, but with different solvents and additives. Based on the X-ray diffraction pattern, the ZnO NPs synthesized using spray pyrolysis and a consecutive method exhibited similar polycrystalline hexagonal wurtzite structures. The large crystal sizes of ZnO NPs were obtained using a consecutive method, sol-gel followed by spray drying, in comparison with those from the ZnO spray pyrolysis. In contrast, the particle size of ZnO prepared by the consecutive method was in a smaller range. The SEM analysis implied that the ZnO structures had surface defects. In the UV-driven photocatalytic degradation of methylene blue, ZnO produced by the consecutive method exhibited slightly higher degradation performance than ZnO spray pyrolysis. This performance was attributed to the larger crystal size of ZnO NPs, which provided a longer carrier movement at semiconductor surfaces and reduced electron-hole recombination. Additionally, ZnO NPs produced using the consecutive method underwent agglomeration that leads to a smaller contact surface with methylene blue, obstructing the degradation process.

Composition Determination of Heterometallic Trinuclear Clusters via Anomalous X-ray and Neutron Diffraction.

Anomalous X-ray diffraction (AXD) and neutron diffraction can be used to crystallographically distinguish between metals of similar electron density. Despite the use of AXD for structural characterization in mixed metal clusters, there are no benchmark studies evaluating the accuracy of AXD toward assessing elemental occupancy in molecules with comparisons with what is determined via neutron diffraction. We collected resonant diffraction data on several homo and heterometallic clusters and refined their anomalous scattering components to determine metal site occupancies. Theoretical resonant scattering terms for Fe0, Co0, and Zn0 were compared against experimental values, revealing theoretical values are ill-suited to serve as references for occupancy determination. The cluster featuring distinct cation and anion metal compositions [CoCp2*][(tbsL)Fe3(μ3-NAr)] was used to assess the accuracy of different f' references for occupancy determination (f'theoretical ± 15-17%; f'experimental ± 10%). This methodology was applied toward calculating the occupancy of three different clusters: (tbsL)Fe2Zn(py) (6), (tbsL)Fe2Zn(μ3-NAr)(py) (7), and [CoCp*2][(tbsL)Fe2Zn(μ3-NAr)] (8). The first two clusters maintain 100% Fe/Zn site isolation, whereas 8 showed metal mixing within the sites. The large crystal size of 8 enabled collection of neutron diffraction data which was compared against the results found with AXD. The ability of AXD to replicate the metal occupancies as determined by neutron diffraction supports the AXD occupancy methodology developed herein. Furthermore, the advantages innate to AXD (e.g., smaller crystal sizes, shorter collection times, and greater availability of synchrotron resources) versus neutron diffraction further support the need for its development as a standard technique.

Study on the mechanism of crystal-induced plasticity enhancement in Ni-Zr crystal/amorphous composites by molecular dynamics simulation

The industrial applications of metallic glass (MGs) are limited by poor plasticity, which crystal/amorphous composites (CACs) can effectively address. This study simulates the compression of Ni-Zr MGs with embedded fcc crystal phases by molecular dynamics to elucidate the mechanism of crystal-induced plasticity enhancement. The plasticity of CACs improves with larger crystal sizes. Atoms at the crystal-amorphous interfaces (CAIs) are classified as CAIfcc and CAIMGs for fcc and MGs, respectively. The transformation of CAIfcc to CAIMGs at the CAIs is crucial for plastic flow during compression. The connection between CAIfcc and CAIMGs clusters is less stable than that of fcc, making it more prone to damage and leading to multiple shear bands (SBs). These SBs offer additional pathways for plastic flow, reducing stress concentration and enhancing material plasticity. This research provides an atomic-level understanding of crystal-induced plasticity in CACs, offering valuable insights for designing high-performance CACs.

Establishment of Multi-Physics coupling model and analysis on thermal stress and crack risk in directional growth of TiAl alloys under electromagnetic confinement

The electromagnetic confinement directional solidification (EMCDS) technique is an optimal method for preparing large-size and non-contamination directional TiAl alloy crystals. Despite its advantages, the high temperature gradient inherent to this process induces thermal stress within the ingot, which increases the risk of cracking. To address this challenge, an innovative Integrated Multi-Physics Coupling Model was established to map and study the thermal stress field during EMCDS in this study. It synchronized the computation of the electromagnetic field, temperature field, solute field, flow field, and stress field during the crystal growth of TiAl alloy, and its high accuracy was proved by the micro-indentation experiment. Our analysis reveals that transverse temperature differences are crucial in inducing thermal stresses, and identifies that hot cracks and cold cracks are prone to occur respectively at the area of radial 23R along the sample (X = 23R) and on the sample surface, which aligns with experimental observations impressively. This model can more accurately and efficiently optimize the process parameters of the EMCDS process to avoid cracks and promote its industrial application.

Surface treatment processed electron transport layers for efficient Sb2S3 solar cells

Solution-processed Sb2S3 thin films and solar cell devices have recently gained popularity due to their easy procedure and outstanding final device performance. Nevertheless, although the substrate has a significant influence on thefollowing functional films, the effect of the substrate in the Sb-based solar cells appears to have not been adequately examined. In this study, we performed an interesting thioacetamide (TA)-assisted surface treatment strategy on the electron transport layer (ETL) to achieve high-quality development of Sb2S3 thin films and based solar devices. The surface treatment of ETLs resulted in a uniform surface, Zn(OH)2 impurity reduction, and excellent wettability. The above enhanced the growth of Sb2S3 thin films with features like extremely large crystal sizes (∼8 um), more homogeneous and dense film morphology, preferred crystal orientation, reduced oxygen content, and fewer defects, which benefits carrier transport. Finally, a device structure constructed of FTO/TiO2/Zn(O,S)/Sb2S3/Spiro/Au was created, resulting in an almost 30 % increase in efficiency, from 4.05 % to 5.21 %. The proposed approach not only gives new insights into generating higher-quality Sb2S3 thin films and devices, but it also presents new concepts and methods for future high-quality sulfide thin film preparation.

Optimizing crucible geometry to improve the quality of AlN crystals by the physical vapor transport method

In the conventional crucible structure for AlN crystal growth by physical vapor transport, owing to the long molecular transport path of Al vapor and the disruption of the gas flow by the presence of a deflector, the Al vapor easily forms polycrystals in the growth domain. The result is increased internal stress in the crystals and increased difficulty in growing large-sized crystals. On this basis, with the help of finite element simulations, a novel crucible structure is designed. This crucible not only optimizes the gas transport but also increases the radial gradient of the AlN crystal surface, making the enhanced growth rate in the central region more obvious. The thermal stresses between the deflector and the crystal are also reduced. High-quality AlN crystals with an FWHM of 79 arcsec were successfully grown with this structure, verifying the accuracy of finite element simulation of the growth of AlN crystals. Our work has important guiding significance for the growth of high-quality AlN crystals.

Phyto-mediated synthesis of ZnO nanoparticles and their sunlight-driven photocatalytic degradation of cationic and anionic dyes

Abstract In this study, zinc oxide-based nanocatalysts were biosynthesized using Ocimum basilicum (OB) and Olea africana (OA) leaf aqueous extracts, termed OB-ZnO and OA-ZnO, as a simple, affordable, and environmentally friendly approach. Their characteristics and efficacy in photodegrading cationic dyes (crystal violet and methylene blue) and anionic dyes (methyl orange and naphthol blue black) were investigated. The catalyst’s properties were analyzed using various techniques, including Fourier transform infrared, X-ray diffraction, photoluminescence, thermogravimetric analysis, UV-Vis, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and Brunauer–Emmett–Teller. Analysis revealed pure products having a hexagonal wurtzite structure, crystallite sizes of 15.04 and 21.46 nm, surface areas of 23.65 and 7.97 m2/g, particle sizes of 35 and 170 nm with spherical (uniform) and oval-like (non-uniform) shapes, and optical bandgaps of 3.15 and 3.05 eV, respectively. Photocatalytic applications under sunlight indicated excellent activity of both catalysts against targeted cationic and anionic dyes. Most notably, even though OA-ZnO has a lower surface area than OB-ZnO, it demonstrated greater efficiency. The variation in effectiveness is explained by the lower bandgap value of OA-ZnO and its ability to reduce electron–hole recombination due to its larger crystal size, which accelerates the degradation process. Additionally, both catalysts exhibited high stability after being used four times.

Impact of repeated heat-pressing on the microstructure and flexural strength of lithium disilicate glass-ceramics

BackgroundThe leftover material from the heat-pressing of IPS e.max Press ceramic is often discarded, despite some laboratories exploring its potential for reuse. However, there is a lack of data on the performance of IPS e.max Press ceramic when combined with the button portions. This study investigated the impact of repeated heat-pressing on the crystal structure and flexural strength of lithium disilicate glass-ceramic (LDGC).MethodsSpecimens (N = 30, n = 10 per group) were categorized based on the number of heat-pressing cycles: G0 (control group, no heat-pressing), G1 (one cycle of heat-pressing), and G2 (two cycles of heat-pressing). The crystal structure of LDGC bars was characterized using X-ray diffraction (XRD). Flexural strength was tested, and microstructures were analyzed via scanning electron microscopy (SEM) and the ImageJ processing program. Data were analyzed using one-way analysis of variance (ANOVA), and multiple pairwise comparisons of means were performed with Tukey’s post-hoc test.ResultsG2 exhibited significantly lower flexural strength and crystallinity, as well as larger crystal size, compared to G1 and G0 (p < 0.05). Flexural strength values decreased significantly with an increased number of heat-pressing cycles.ConclusionsThe mechanical properties of LDGC significantly degraded after repeated heat pressing. Therefore, it is not clinically advisable to repeatedly press the lithium disilicate ingot together with the leftover material.

Synthesis of submillimeter-size two-dimensional metal iodides single crystal via undercooling control strategy

Two-dimensional (2D) metal iodides have attracted significant attention in recent years due to their superior optoelectronic properties. However, the current synthesis methods for 2D metal iodides are either time-consuming or not able to synthesize large size crystal. Here we develop an undercooling control strategy based on hot plate assisted vertical vapor deposition for the synthesis of submillimeter-size 2D bismuth iodide (BiI3) single crystal. The whole synthesis process is efficient and only takes one minute in atmosphere. The problem of high nucleation density can be addressed by undercooling control, avoiding the collide of crystals before they grow into large size. This general approach is versatility and can be expanding to synthesize other 2D metal iodides. In addition, nonlinear optical property investigation of BiI3 crystal reveals a thickness-dependent and power-dependent second harmonic response. Our strategy presents a new solution for facile preparation of large-size 2D metal iodides, facilitating their fundamental physics studies and next-generation optoelectronics development.

Crystal Structure, Microstructure, and Dielectric and Electrical Properties of Ceramic Material Prepared Using Volcanic Ash

In the present work, the electrical and dielectric properties of ceramic samples prepared from volcanic ash were investigated. For this purpose, ceramic samples were prepared using milled volcanic ash with a binder material at a sintering temperature of 950 °C for 2 h. The chemical content of the milled volcanic ash was investigated using XRF. Differential thermal analysis and thermogravimetry were performed to determine the firing conditions. The crystalline phases and microstructures of the ceramic samples were investigated using XRD and SEM, respectively. Finally, the electrical and dielectric properties of the obtained samples were evaluated at a frequency ranging from 1 × 102 to 4 × 106 Hz and temperatures ranging from room temperature to 800 °C. The XRD results revealed that the ceramic samples contained three main phases: albite, hematite, and augite. Moreover, the microstructures of the samples exhibited a large crystal size with a dense surface. The conductivities and dielectric constants of the samples remained stable up to 500 °C. The real and imaginary parts of the dielectric constant decreased with an increase in frequency and increased with an increase in temperature. The results indicated that ceramics based on volcanic ash are promising for use in technological applications such as high-voltage power insulators.

Investigation into “hair” inclusions in large-sized KDP crystals grown by traditional method

Potassium dihydrogen phosphate (KDP) crystals are widely used in high-energy laser facilities for harmonic generation. An important defect observed in KDP crystals, known as "hair" inclusions in large-size crystals grown by traditional methods, was investigated using ultra-microscopy. Most of the "hair" inclusions within the crystals have a straight chain structure, while only a few displays a curved formation. The "hair" inclusions consist of multiple liquid inclusions and exhibit a chain-like structure with quasi-periodic features. The size of these liquid inclusions varies, ranging from 17.54 to 56.90 μm, and show a chain density between 0.90 mm−1 and 20.77 mm−1. The angles of the "hair" inclusion orientations about the c-axis range from 30° to 79°, corresponding to the dislocations in KDP crystals. Furthermore, the study examined the impact of "hair" inclusions on the transmittance of the crystals. This investigation aims to enhance the understanding of “hair” inclusions in traditionally grown KDP crystals and attempts to clarify the factors leading to the formation of these inclusions. It also offers a theoretical and experimental basis for reducing these inclusions in KDP crystals.

Development of large-volume 130TeO2 bolometers for the CROSS 2β decay search experiment

We report on the development of thermal detectors based on large-size tellurium dioxide crystals (45 × 45 × 45 mm), containing tellurium enriched in 130Te to about 91%, for the CROSS double-beta decay experiment. A powder used for the crystals growth was additionally purified by the directional solidification method, resulting in the reduction of the concentration of impurities by a factor 10, to a few ppm of the total concentration of residual elements (the main impurity is Fe). The purest part of the ingot (the first ∼ 200 mm, about 80% of the total length of the cylindrical part of the ingot) was determined by scanning segregation profiles of impurities and used for the 130TeO2 powder production with no evidence of re-contamination. The crystal growth was verified with precursors produced from a powder with natural Te isotopic composition, and two small-size (20 × 20 × 10 mm) samples were tested at a sea-level laboratory showing high bolometric and spectrometric performance together with acceptable 210Po content (below 10 mBq/kg). This growth method was then applied for the production of six large cubic 130TeO2 crystals and 4 of them were taken randomly to be characterized at the Canfranc underground laboratory, in the CROSS-dedicated low-background cryogenic facility. Two 130TeO2 samples were coated with a thin, 𝒪(100 nm), metal film in form of Al layer (on 4 sides) or AlPd grid (on a single side) to investigate the possibility to tag surface events by pulse-shape discrimination. Similarly to the small natural precursors, large-volume 130TeO2 bolometers show high performance and even better internal purity (210Po activity ∼ 1 mBq/kg, while activities of 228Th and 226Ra are below 0.01 mBq/kg), satisfying requirements for the CROSS and, potentially, next-generation experiments.

Tailoring structural and optical properties of Ti1-xMxO2 (M = Fe, Co, Ni, Cu, and Zn) nanoparticles for enhanced antimicrobial activity: a sol-gel synthesis study

Titanium dioxide (TiO2) nanoparticles possess intriguing properties and have been extensively utilized in medical applications due to their exceptional antimicrobial characteristics. The antimicrobial efficacy can be heightened by altering the structural morphology, size, and optical properties through the introduction of transition metal ions (M: Fe, Co, Ni, Cu, and Zn) with a concentration of x = 0.02 into TiO2, thereby producing Ti1 -xMxO2 powder via the sol-gel method at a sintering temperature ranging from 500 °C to 600 °C. The morphological characteristics of Ti1 - xMxO2 were analyzed using FT-IR, UV-DRS, XRD, TGA, BET, and SEM-EDAX techniques. Substituting M-doped TiO2 at a sintering temperature of 500 °C results in all doping ions yielding the Ti1 -xMxO2 anatase phase. Conversely, at 600 °C, the doping ions M: Cu, Co, Zn exhibit a tendency to substitute the TiO2 structure, destabilizing the anatase phase and leading to the formation of an anatase-rutile dual phase with larger crystal size. At elevated temperatures, ions with larger radii than Ti (0.61), namely Cu (0.73), Co (0.75), and Zn (0.74), tend to be substituted, thereby altering the structure of TiO2. The antimicrobial efficacy, evaluated based on the inhibition zone, demonstrates that Ti1 -xMxO2 effectively inhibits the cellular activity of Salmonella typhimurium (Gram -) and Staphylococcus aureus (Gram +) bacteria compared to TiO2.

In situ synthesis of nanosized ZSM-12 zeolite isomorphously substituted by gallium for the n-hexadecane hydroisomerization

The ZSM-12 zeolite has attracted attention as the promising acid component of bifunctional catalysts for the n -alkane hydroisomerization because of its large size of micropore openings (0.57 nm × 0.61 nm) with 12-membered-ring and one-dimensional channels. However, the larger crystal size and stronger Brønsted acid strength of microsized ZSM-12 zeolite will lead to cracking of iso -olefin intermediates and decrease the iso -alkane yield. In this study, ZSM-12 zeolite samples partially and completely isomorphously substituted with gallium ([Ga,Al]Z12 and GaZ12) were in situ synthesized. The characteristic results indicate that isomorphous substitution by Ga can effectively reduce the crystal size to increase the mesoporosity and weaken the Brønsted acidity of the [Ga,Al]Z12 and GaZ12 samples. In addition, bifunctional catalysts with more appropriate metal-acid proximity for n -hexadecane hydroisomerization were prepared by mixing the 0.6Pd/A sample with 0.6 wt.% Pd loaded on γ-Al2O3 and the ZSM-12, [Ga,Al]Z12 and GaZ12 samples, respectively. The 0.3Pd/A-[Ga,Al]Z12 and 0.3Pd/A-GaZ12 catalysts both promote the maximum iso -hexadecane yield and distribution of multi-branched iso -hexadecane products due to their enhanced mesoporosity, reduced Brønsted acid strength, increased CPd/CH+ ratios and improved metal-acid balance. Especially for the 0.3Pd/A-GaZ12 catalyst, when the n -hexadecane conversion is 93.5%, the maximum iso -hexadecane yield reaches 80.6%, and the proportion of multi-branched iso -hexadecane products is 64.6%, which are both the highest among all investigated catalysts. Accordingly, Ga isomorphous substitution is an effective strategy to develop the efficient bifunctional catalysts for hydroisomerization.

Electrospun poly(lactic acid) membranes with defined pore size to enhance cell infiltration

Electrospun membranes are compact structures with small pore sizes that hinder cell infiltration, resulting in membranes with cells attached only to the external surface rather than throughout the entire volume. Thus, there is a need to increase the pore size of electrospun membranes maintaining their structural similarity to the extracellular matrix. In this work, we used glucose crystals embedded in polyethylene oxide (PEO) fibers to create large pores in poly(lactic acid) (PLA) electrospun membranes to allow for cellular infiltration. The PEO fibers containing glucose crystals of different sizes (>50, 50–100 and 100–150 μm) and in varying concentrations (10, 15 and 20 %) were co-electrospun with PLA fibers and subsequently leached out using distilled water. PLA fibrous membranes without glucose crystals were also produced as controls. The membranes were examined for their morphology, mechanical properties, and potential to support the proliferation of fibroblasts. In addition, the immune response to the membranes was evaluated using monocyte-derived macrophages. The glucose crystals were uniformly distributed in the PLA membranes and their removal created open pores without collapsing the structure. Although a reduced Young's modulus was observed for membranes produced using higher glucose crystal concentrations and larger crystal sizes, the structural integrity remained intact, and the values are still suitable for tissue engineering. In vitro results showed that the scaffolds supported the adhesion and proliferation of fibroblasts and the pores created in the PLAmembranes were large enough for fibroblasts infiltration and colonization of the entire scaffold without inducing an inflammatory response.

Active methane release from the early Cambrian seafloor? Clues from Ba isotopes

The Cambrian Explosion coincided with a global greenhouse climate, but the mechanism behind this warming event remains unclear, impeding our understanding of their essential link. To address this, an integrated study of δ138Ba, δ34S, Scanning Electron Microscopy, and Energy Dispersive Spectroscopy was carried out on the lower Cambrian shales from a range of water depths in the Nanhua Basin of South China. These shales are characterized by variably elevated Ba concentrations (>10,000 ppm), primarily hosted by barite and Ba-feldspar, with the latter found only in a deep-water setting. The Ba-isotopic compositions of the study shales (δ138Ba, −0.15‰ to +0.60‰), along with the large size and euhedral shape of barite crystals and associated soft-sediment deformation, indicate that barite and Ba-feldspar were formed in porewaters close to the sulfate-methane-transition zone during early diagenesis under sulfate-rich and sulfate-poor conditions, respectively. We propose that low sulfate in the early Cambrian ocean, coupled with the high organic matter content of the sediment, may have resulted in large methane emissions from the sediment to the atmosphere, generating an early Cambrian greenhouse climate at the time of the Cambrian Explosion.

Carbon/copper oxide electrode materials with high atomic utilization constructed by in-situ induced growth strategy of nano metal-organic frameworks

Carbon/metal composites derived from metal-organic frameworks (MOFs) have attracted widespread attention due to their excellent electronic conductivity, adjustable porosity, and outstanding stability. However, traditional synthesis methods are limited by the dense stereo geometry and large crystal grain size of MOFs, resulting in many metals active sites are buried in the carbon matrix. While the common strategy involves incorporating additional dispersed media into material, this leads to a decrease in practical metal content. In this study, nanosized copper-metal-organic frameworks (Cu-MOFs) are in-situ grown on surface of carbon spheres by pre-anchoring copper ions, and the hybrid composite of porous carbon/copper oxide with high copper atom utilization rate is prepared through activation and pyrolysis methods. This strategy effectively addresses the issue of insufficient exposure of metal sites, and the obtained composite material exhibits high effective copper atom utilization rate, large specific surface area (2052.3 m2·g−1), diverse pore structure, outstanding specific capacity (1076.5F·g−1 at 0.5 A·g−1), and excellent cycle stability. Furthermore, this highly atom-economical universal method has positive significance in application fields of catalysis, energy storage, and adsorption.

Preparation of Highly Efficient and Stable All-Inorganic CsPbBr3 Perovskite Solar Cells Using Pre-Crystallization Multi-Step Spin-Coating Method

All-inorganic CsPbBr3 perovskite solar cells have garnered extensive attention in the photovoltaic domain due to their remarkable environmental stability. Nevertheless, CsPbBr3 prepared using the conventional sequential deposition method suffers from issues such as inferior crystallinity, low phase purity, and poor film morphology. Herein, we propose a pre-crystallization methodology by introducing a minute quantity of CsBr into the PbBr2 precursor solution to generate a small amount of CsPb2Br5 crystals within the PbBr2 film, leading to a porous PbBr2 film with enhanced crystallinity. Under the influence of more pores and CsPb2Br5 crystals as nucleation sites for inducing growth, a CsPbBr3 film with a larger crystal size, lower grain boundary density, stronger crystallinity, and higher phase purity is formed. Compared with untreated devices, photovoltaic devices prepared using the pre-crystallization method achieved a champion photovoltaic conversion efficiency (PCE) of 8.62%. Furthermore, pre-crystallized devices demonstrate higher stability than untreated ones and can still retain 94% of the original PCE after being exposed to air for 1000 h without encapsulating.

Nickel phosphorous trisulfide: A ternary 2D material with an ultra-low coefficient of friction

Ultra-low friction is crucial for the anti-friction, anti-wear, and long-life operation of nanodevices. However, very few two-dimensional materials can achieve ultra-low friction, and they have some limitations in their applications. Therefore, exploring novel materials with ultra-low friction properties is greatly significant. The emergence of ternary two-dimensional materials has opened new opportunities for nanoscale ultra-low friction. This study introduced nickel phosphorous trisulfide (NiPS3, referred to as NPS), a novel two-dimensional ternary material capable of achieving ultralow friction in a vacuum, into the large nanotribology family. Large-size and high-quality NPS crystals with up to 14 mm × 6 mm × 0.3 mm dimensions were grown using the chemical vapor transport method. The NPS nanosheets were obtained using mechanical exfoliation. The dependence of the NPS nanotribology on layer, velocity, and angle was systematically investigated using lateral force microscopy. Interestingly, the coefficient of friction (COF) of NPS with multilayers was decreased to about 0.0045 under 0.005 Pa vacuum condition (with load up to 767.8 nN), achieving the ultra-low friction state. The analysis of the frictional dissipation energy and adhesive forces showed that NPS with multilayers had minimum frictional dissipation energy and adhesive forces since the interlayer interactions were weak and the meniscus force was excluded under vacuum conditions. This study on the nanoscale friction of a ternary two-dimensional material lays a foundation for exploring the nanoscale friction and friction origin of other two-dimensional materials in the future.