Crystalline Layer Research Articles

Layered hybrid superlattices as designable quantum solids.

Crystalline solids typically show robust long-range structural ordering, vital for their remarkable electronic properties and use in functional electronics, albeit with limited customization space. By contrast, synthetic molecular systems provide highly tunable structural topologies and versatile functionalities but are often too delicate for scalable electronic integration. Combining these two systems could harness the strengths of both, yet realizing this integration is challenging owing to distinct chemical bonding structures and processing conditions. Two-dimensional atomic crystals comprise crystalline atomic layers separated by non-bonding van der Waals gaps, allowing diverse atomic or molecular intercalants to be inserted without disrupting existing covalent bonds. This enables the creation of a diverse set of layered hybrid superlattices (LHSLs) composed of alternating crystalline atomic layers of variable electronic properties and self-assembled atomic or molecular interlayers featuring customizable chemical compositions and structural motifs. Here we outline strategies to prepare LHSLs and discuss emergent properties. With the versatile molecular design strategies and modular assembly processes, LHSLs offer vast flexibility for weaving distinct chemical constituents and quantum properties into monolithic artificial solids with a designable three-dimensional potential landscape. This opens unprecedented opportunities to tailor charge correlations, quantum properties and topological phases, thereby defining a rich material platform for advancing quantum information science.

Deformation Mechanism in Central China Revealed by Regional Earthquake Tomography

Abstract The central China region (CCN) has experienced significant deformation and complex structural arrangements. We conducted research on the deformation pattern of the CCN through the 3D velocity structure of the crust and uppermost mantle obtained via body-wave tomography. This velocity structure strongly correlates with the region’s topographic features. The relationship between velocity distributions and topography indicates that compression in the east–west direction, which can lead to crustal and mantle shortening, may play a crucial role in shaping topography. The various structures between the Qinling mountain range in the west and the Tongbai–Dabie mountain range in the east highlight distinct geological processes occurring along the Qinling–Dabie orogenic belt. In addition, we propose that reservoir water has infiltrated the crystalline basement rock layer up to 15–20 km beneath the Three Gorges Reservoir. Furthermore, the Three Gorges Dam serves as a solid foundation to prevent reservoir water from seeping downstream underground.

Self-activated epitaxial growth of ScN films from molecular nitrogen at low temperatures

Unlike naturally occurring oxide crystals such as ruby and gemstones, there are no naturally occurring nitride crystals because the triple bond of the nitrogen molecule is one of the strongest bonds in nature. Here, we report that when the transition metal scandium is subjected to molecular nitrogen, it self-catalyzes to break the nitrogen triple bond to form highly crystalline layers of ScN, a semiconductor. This reaction proceeds even at room temperature. Self-activated ScN films have a twin cubic crystal structure, atomic layering, and electronic and optical properties comparable to plasma-based methods. We extend our research to showcase Sc’s scavenging effect and demonstrate self-activated ScN growth under various growth conditions and on technologically significant substrates, such as 6H–SiC, AlN, and GaN. Ab initio calculations elucidate an energetically efficient pathway for the self-activated growth of crystalline ScN films from molecular N2. The findings open a new pathway to ultralow-energy synthesis of crystalline nitride semiconductor layers and beyond.

Toughening Immiscible Polymer Blends: The Role of Interface-Crystallization-Induced Compatibilization Explored Through Nanoscale Visualization.

This study explores the novel approach of interface-crystallization-induced compatibilization (ICIC) via stereocomplexation as a promising method to improve the interfacial strength in thermodynamically immiscible polymers. Herein, two distinct reactive interfacial compatibilizers, poly(styrene-co-glycidyl methacrylate)-graft-poly(l-lactic acid) (SAL) and poly(styrene-co-glycidyl methacrylate)-graft-poly(d-lactic acid) (SAD) are synthesized via reactive melt blending in an integrated grafting and blending process. This approach is demonstrated to enhance the interfacial strength of immiscible polyvinylidene fluoride/poly l-lactic acid (PVDF/PLLA) 50/50 blends via ICIC. IR nanoimaging indicates a cocontinuous morphology in the blends. The blend compatibilized with SAD exhibits a higher storage modulus, as unveiled by small amplitude oscillatory shear (SAOS) in the melt state at a temperature below the melting temperature of the stereocomplex (SC) crystals and by DMTA measurements in the solid state. This increase is attributed to the formation of a 200-300 nm thick rigid interfacial SC crystalline layer that is directly visible using AFM imaging and chemically characterized via IR nanospectroscopy. This ICIC also results in a significant toughening of the blend, with the elongation at break increasing more than 20-fold. Moreover, the fracture toughness factor obtained from single edge-notch bending (SENB) tests is doubled with ICIC as compared to the uncompatibilized blend, indicating the strong crack-resistance capability as a result of ICIC. This improvement is also evident in SEM images, where thinner and longer fibrillation is observed on the fractured surface in the presence of ICIC.

Effects of Surface Mesopores in the Newly Formed Crystalline Layer on Pore Structure Characterization of Water-Bearing Shale

Effects of Surface Mesopores in the Newly Formed Crystalline Layer on Pore Structure Characterization of Water-Bearing Shale

Nanoclay composites in electrochemical sensors

Nanoclays are layered structures in the nanoscale range with widespread application due to their unique properties such as swelling, cation exchange capacity, and ease of functionalisation using metals, metal oxides, and organic compounds such as carbon paste, polymers, and other biomolecules that form nanoclay composites. Nanoclay functionalisation with silver (Ag), zinc oxide (ZnO), and bimetallic silver–gold (Ag–Au) using hydrophilic and hydrophobic clays is here evaluated and discussed. The composites’ synthesis and morphological, crystallinity, and electroactive properties in comparison with pure nanoclay are also assessed. The layered structure and crystallinity of all these nanoclay composites were slightly changed. The clumped layered structures on the surface of the nanocomposites had dispersed white spots that indicated possible surface modification. The nano-films of the composites’ electroactivity were comparatively high, as seen from the increase in current in the cyclic voltammetry characterisation voltammograms and the differential pulse voltammograms of the pharmaceutical detection. Efavirenz, nevirapine, and zidovudine detection was improved by modification of the nanocomposite with human serum albumin (HSA), as shown by the higher current, thus indicating improved conductivity of the composites compared to the pure nanoclays. Applying HAS-modified nanocomposites in the analysis of efavirenz, nevirapine, and zidovudine on a glassy carbon electrode (GCE) showed good linearity and acceptable detection limits comparable to those of previous studies. Therefore, it has potential for application in pharmaceutical quality control and environmental monitoring.

In-vitro and thermal stability study of bioglass synthesized from biogenic sources

In this work, the bioactive glasses are derived from biowaste resources such as corn husk ash, sugarcane leaves ashes, and eggshell powder via the melt quench method. The raw materials were melted in a platinum rhodium crucible at 1550 °C, followed by rapid cooling to obtain a glassy phase. In order to assess the in-vitro bioactivity, glasses were soaked in simulated body fluid at 37 °C for different time durations, i.e., 7,14, 21, and 28 days. Biocompatibility of these glasses was also tested on MG-63 cell lines using a 3-(4,5-dimethylthiazol-2-yl) 2,5-diphenyl tetrazolium bromide (MTT) assay test. X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) were used to analyze the hydroxyapatite (HAp) layer formation and the thermal stability of soaked samples. SEM micrographs showed the cauliflower and flakes type morphology of hydroxyapatite (HAp) on the glass surfaces after 7 days of soaking in SBF. The EDS analysis also confirmed the formation of a hydroxyapatite layer with a Ca/P ratio that varies from 1.6 to 3.9. MTT assay revealed the biocompatibility for different dosages (1, 2, 5, and 10 mg/ml) of the as-prepared glasses with MG-63 cell lines. The heat treatment of soaked glasses converts the amorphous HAp layer into a crystalline HAp layer, followed by its conversion in stable diopside as main and Ca2.589Mg0.41(PO4)2 as minor phase. The tested glasses exhibited good bioactivity and biocompatibility particularly higher CaO content glass, suggesting for use in bone regeneration applications.

Hydrothermal carbonization of woody waste: Changes in the physicochemical properties and the structural evolution mechanisms of hydrochar during this process

The Chinese medicine residue (CMR) is composed of wet woody waste, including licorice and ephedra, so using hydrothermal carbonization (HTC) to recover renewable energy from the CMR is a suitable treatment method. An in-depth analysis of the physicochemical properties and structural evolution mechanism of hydrochars is helpful in fundamentally promoting the energy utilization of traditional Chinese medicine waste residue. Therefore, this study analyzed the physicochemical properties and morphological structure of hydrochar produced under varying HTC conditions using multiple testing methods. The evolution of the hydrochar's structural characteristics can be categorized into three stages: component decomposition, structural rearrangement, and carbonization. During the component decomposition and carbonization stages, numerous nanoscale micropores form within the hydrochar. These micropores' specific surface area and pore volume can reach up to 113.420 m2/g and 0.01913 cm3/g, respectively. The highest fractal dimension values for D1 and D2 are 2.6354 and 2.5565, while the maximum values for the microcrystalline stacking height (Lc) and the average number of crystalline layers (Nave) are 0.3354 and 1.9968, respectively. Consequently, the hydrochar produced during these stages exhibits a rougher pore surface and a more complex structure, making it more suitable for adsorbing heavy metals from soil and sequestering CO2. During the structural rearrangement stage, the hydrochar exhibits higher contents of fixed carbon (FC), MgO, P2O5, and a higher C/N atomic ratio, with maximum values of 38.51%, 0.99%, 1.12%, and 28.49, respectively. Thus, the hydrochar produced during this stage is more suitable for soil remediation and nutrient recovery.

Robust bilayer solid electrolyte interphase for Zn electrode with high utilization and efficiency

Construction of a solid electrolyte interphase (SEI) of zinc (Zn) electrode is an effective strategy to stabilize Zn electrode/electrolyte interface. However, single-layer SEIs of Zn electrodes undergo rupture and consequent failure during repeated Zn plating/stripping. Here, we propose the construction of a robust bilayer SEI that simultaneously achieves homogeneous Zn2+ transport and durable mechanical stability for high Zn utilization rate (ZUR) and Coulombic efficiency (CE) of Zn electrode by adding 1,3-Dimethyl-2-imidazolidinone as a representative electrolyte additive. This bilayer SEI on Zn surface consists of a crystalline ZnCO3-rich outer layer and an amorphous ZnS-rich inner layer. The ordered outer layer improves the mechanical stability during cycling, and the amorphous inner layer homogenizes Zn2+ transport for homogeneous, dense Zn deposition. As a result, the bilayer SEI enables reversible Zn plating/stripping for 4800 cycles with an average CE of 99.95% (± 0.06%). Meanwhile, Zn | |Zn symmetric cells show durable lifetime for over 550 h with a high ZUR of 98% under an areal capacity of 28.4 mAh cm−2. Furthermore, the Zn full cells based on the bilayer SEI functionalized Zn negative electrodes coupled with different positive electrodes all exhibit stable cycling performance under high ZUR.

Robust Imidazole-Linked Covalent Organic Framework Enabling Crystallization Regulation and Bulk Defect Passivation for Highly Efficient and Stable Perovskite Solar Cells.

The low crystallinity of the perovskite layers and many defects at grain boundaries within the bulk phase and at interfaces are considered huge barriers to the attainment of high performance and stability in perovskite solar cells (PSCs). Herein, a robust photoelectric imidazole-linked porphyrin-based covalent organic framework (PyPor-COF) is introduced to precisely control the perovskite crystallization process and effectively passivate defects at grain boundaries through a sequential deposition method. The 1D porous channels, abundant active sites, and high crystallization orientation of PyPor-COF offer advantages for regulating the crystallization of PbI2 and eliminating defects. Moreover, the intrinsic electronic characteristics of PyPor-COF endow a more closely matched energy level arrangement within the perovskite layer, which promotes charge transport and thereby suppresses the recombination of photogenerated carriers. The champion PSCs containing PyPor-COF achieved power conversion efficiencies of 24.10% (0.09 cm2) and 20.81% (1.0 cm2), respectively. The unpackaged optimized device is able to maintain its initial efficiency of 80.39% even after being exposed to air for 2000 h. The device also exhibits excellent heating stability and light stability. This work gives a new impetus to the development of highly efficient and stable PSCs via employing COFs.

Investigation on the machining mechanism of silicon modified by Au ion irradiation in elliptical vibration diamond cutting

Single-crystal silicon (Si) has important applications in semiconductor, infrared optics, and photovoltaic industries. However, Si is difficult to be machined precisely due to its hard and brittle characteristics. Ion irradiation is proposed as an advanced technology to reduce the hardness and brittleness for a covalent crystal, which is beneficial for the ductile machining process. In the present research, the simulation and experimental investigation of Si with Au ion irradiation were carried out firstly. As following, the grooving experiment is carried out by elliptical vibration cutting (EVC). the machining performance is compared with ordinary cutting (OC) and the material removal mechanism is elaborated. The critical depth of cut for brittle-to-ductile transition is nearly 7 times higher by EVC compared to OC. Initial verification of material modification was conducted by Raman spectra and cutting microgrooves. Finally, the ion irradiation damage mechanism and amorphous Si (a-Si)/crystalline Si (c-Si) machining deformation mechanism were analyzed in detail by transmission electron microscopy. The irradiated sample contains an amorphous layer of 1050 nm, a transition layer containing dislocations and nanocrystals, and a fully crystalline layer. During machining a-Si/c-Si interface, the machining defects in the amorphous layer will first absorb the energy and ensure that the crystalline layer does not produce subsurface damage. In summary, ion-irradiated Si can be achieved in the amorphous region at any depth position and the substrate ductile machining without subsurface damage generation by EVC.

Quantification of microstructural homogeneity in indium arsenide epilayers by X-ray diffraction

In this article a complete procedure to investigate thin semiconductor plates (epitaxial layers), including high-resolution X-ray diffraction measurements, mathematical modelling of both crystalline structure and crystalline microstructure and computations to approximate solving inverse problems, is proposed and described in detail. The method is successfully applied to estimate crystalline homogeneity of a square indium-arsenide plate epitaxially-grown on gallium-arsenide substrate. To this end, the specimen is tested in nine areas around points forming a square grid. It is demonstrated that whole specimen may be regarded as a single large crystalline grain consisting of crystallites separated by small-angle boundaries. The crystallites occur as rode-like cuboids elongated in the direction perpendicular to the plate surface, with different areas of the sample and with base sizes not much differing. The mean-absolute second-order strain is very small and almost constant in the whole sample. The first-order strain also appears and, effectively, the structure of the crystalline layer is tetragonal with unit-cell parameters being smaller parallelly and larger perpendicularly to the layer surface and varying slightly in the layer. The results are presented in tables and figures and commented.

CMAS resistance characteristics of Gd2(Hf0.7Ce0.3)2O7 thermal barrier material at 1300 °C and 1400 °C

The corrosion resistance to calcium‑magnesium‑aluminum-silicate (CMAS) is a key property affecting the long-term durability of thermal barrier coatings (TBCs). Meanwhile, rare-earth hafnates are considered promising TBC candidates due to their low thermal conductivity and suitable thermal expansion coefficients. Thus, this study explores the CMAS corrosion resistance of Gd2(Hf0.7Ce0.3)2O7 (GH7C3) ceramic material under different conditions and compares it with the binary system Gd2Hf2O7 (GH) ceramic material. The findings indicate that GH7C3 can react chemically with CMAS and rapidly form a dense apatite crystalline layer at the interface between GH7C3 ceramic and CMAS, providing excellent CMAS resistance. Furthermore, the composition of the remaining CMAS melt Furthermore, the composition of the remaining CMAS melt undergoes compositional changes upon interaction, ultimately forming spinel in Mg and Al-enriched regions. In the meantime, CeO2 can promote the rapid formation of apatite crystals, significantly enhancing the CMAS resistance of GH7C3 to CMAS at high temperatures compared to GH.

Friends not Foes: Exfoliation of Non-van der Waals Materials.

ConspectusTwo-dimensional materials have been a focus of study for decades, resulting in the development of a library of nanosheets made by a variety of methods. However, many of these atomically thin materials are exfoliated from van der Waals (vdW) compounds, which inherently have weaker bonding between layers in the bulk crystal. Even though there are diverse properties and structures within this class of compounds, it would behoove the community to look beyond these compounds toward the exfoliation of non-vdW compounds as well. A particular class of non-vdW compounds that may be amenable to exfoliation are the ionically bonded layered materials, which are structurally similar to vdW compounds but have alkali ions intercalated between the layers. Although initially they may have been more difficult to exfoliate due to a lack of methodology beyond mechanical exfoliation, many synthesis techniques have been developed that have been used successfully in exfoliating non-vdW materials. In fact, as we will show, in some cases it has even proven to be advantageous to start the exfoliation from a non-vdW compound.The method we will highlight here is chemical exfoliation, which has developed significantly and is better understood mechanistically compared to when it was first conceived. Encompassing many methods, such as acid/base reactions, solvent reactions, and oxidative extractions, chemical exfoliation can be tailored to the delamination of non-vdW materials, which opens up many more possibilities of compounds to study. In addition, beginning with intercalated analogues of vdW materials can even lead to more consistent and higher quality results, overcoming some challenges associated with chemical exfoliation in general. To exemplify this, we will discuss our group's work on the synthesis of a 1T'-WS2 monolayer ink. By starting with K0.5WS2, the exfoliated 1T'-WS2 nanosheets obtained were larger and more uniform in thickness than those from previous syntheses beginning with vdW materials. The crystallinity of the nanosheets was high enough that films made from this ink were superconducting. We will also show how soft chemical methods can be used to make new phases from existing compounds, such as HxCrS2 from NaCrS2. This material was found to have alternating amorphous and crystalline layers. Its biphasic structure improved the material's performance as a battery electrode, enabling reversible Cr redox and faster Na-ion diffusion. From these and other examples, we will see how chemical exfoliation of non-vdW materials compares to other methods, as well as how this technique can be further extended to known compounds that can be deintercalated electrochemically and to quasi-one-dimensional crystals.

Spin-coated BiFeO3 films on Si wafers: Low processing temperature but prominent piezoelectricity

The direct integration of crystalline oxide layers with industrial Si substrate, specifically compatible with CMOS technology, requires the development of relatively simple, low-temperature processing routes below 450 °C. Here, a novel nonstoichiometric approach is proposed to achieve fabrication of BiFeO3 films at 450 °C. Of particular importance is that, a saturation and remnant polarization of ∼80 μC/cm2 and ∼60 μC/cm2 and a strain as large as 1% are obtained. This strain stands as one of the most impressive values reported for thin films, comparable to the most superior strain obtained in ferroelectric films fabricated at temperatures exceeding 700 °C. The current work provides a new paradigm with significant simplicity and novel efficacy in reducing processing temperatures, as well offers a promising material for memory and piezo-driven actuating applications, especially meeting the increasing demand for precision position control systems at the nanometer scale.

A feasibility study of oil palm empty fruit bunch pulp as a substitution for radiata pine pulp for autoclave fibre cement composite production

The main objective of this study was to investigate the feasibility of using unbleached pulp from oil palm empty fruit bunches, produced via the Ethanolamine pulping process, to replace Radiata Pine pulp in autoclave fibre cement composite (AFCC) manufacturing. The Ethanolamine pulping process was chosen for its silica retention capability on empty fruit bunch surfaces. The research involves three key phases: an initial characterization of RPP and EFBP properties, including kappa numbers and pulp aspect ratios; subsequent AFCC production with varying RPP content levels (0%–13%) and different cement-to-silica (C/S) ratios (0.2–1.0); and the introduction of EFBP as a partial or complete substitute for RPP at a fixed C/S ratio. Results reveal RPP excels in fibre quality attributes like length, coarseness, fineness, width, and wet/dry zero span, while EFBP offers advantages in fibre count and macro fibrillation index. X-ray diffraction confirms silica presence on EFBP. The highest modulus of rupture (MOR), at 15.5 MPa, is achieved with 9% RPP and a C/S ratio of 1.0. Subsequent analysis, with 1% EFBP interval substitutions to total 13% pulp content, yields the highest MOR values under dry (16.7 MPa) and wet (9.9 MPa) conditions using recipes with 6% RPP and 3% EFBP. XRD confirms the presence of silica on EFBP, forming a crystalline flake layer post-autoclaving. Thus, EFBP proves suitable as a partial AFCC substitute.

Reactively Processed Poly(butylene adipate terephthalate) Composite–Based Multilayered Films with Improved Properties for Sustainable Packaging Applications: Structural Characterization and Biodegradation Mechanism

AbstractIn this study, it is attempted to enhance the properties and biodegradability of poly(butylene adipate terephthalate) (PBAT) using nanocomposite technology to meet the demand for sustainable packaging applications. Two nanoclays containing PBAT composites are reactively processed and integrated into the multilayered films. Reactive processing facilitates the dispersion and distribution of nanoclay particles in the PBAT matrix. The multilayered films comprising reactively processed PBAT composites exhibited a 24.5%–31.5% reduction in the oxygen transmission rate and improved dimensional stability and tensile properties. Moreover, the degradability of the multilayered film comprising reactively processed PBAT composites reached 82% in 180 days. In contrast, a neat PBAT film of similar thickness attained only 53% degradation in the same period. The biodegradation mechanism is proposed based on the topology of the disintegrated films studied using scanning electron microscopy, chemical bond vibrations determined by Fourier‐transform infrared spectroscopy, and structural evolution by small‐ and wide‐angle X‐ray scattering (SWAXS). The SWAXS analysis is used to understand the changes in the degree of crystallinity, long‐range periodic order, and crystalline and amorphous layer thickness of the multilayered films before and after degradation. Such multilayered films can find applications where packaging or biomedical devices cannot be recycled.

Control of the preferentially orientated growth of Sr2TiSi2O8 crystals in a SrO – TiO2 – SiO2 – Al2O3 – K2O parent glass

A polar glass-ceramic containing Sr-fresnoite Sr2TiSi2O8 (STS) as single crystalline phase was developed through the controlled crystallization of a parent glass composition containing SrO, TiO2, SiO2, K2O, and Al2O3. The objective of this work is to obtain a piezoelectric substrate exhibiting a well-defined orientation of the polar direction of the STS crystals over a depth suitable for the design of surface acoustic waves (SAW) devices. For that purpose, the crystallization mechanism of the parent glass was first studied by Differential Scanning Calorimetry (DSC). Based on this study, heat treatments were applied to transform the glass into glass-ceramics. Two aspects were investigated: i). The influence of the surface state of parent glass and of its environment on the nucleation of preferentially orientated STS crystals at the surface of the parent glass; ii). The growth of a preferentially orientated crystallized layer from the surface into the bulk. The microstructures of resulting glass ceramics were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM). We demonstrate that growth of the surface crystallized layer is governed by diffusion mechanisms through a transition glass composition separating the crystalized layer and the subjacent parent glass. The control of the growth rate of the crystalline layer plays the key role to keep a high and constant orientation of the (002) STS plans parallel to the surface of the substrate.

Exploring electron backscatter diffraction analysis as a tool for understanding stromatolite: Quantitative description of Cretaceous lacustrine stromatolite reveals formative processes and high‐resolution climatic cycles

AbstractLacustrine stromatolites serve as important archives for recording environmental changes, and the detailed examination of their microfabrics is essential for understanding their formative processes and the environmental changes embedded within them. This study explored the application of Electron Backscatter Diffraction combined with Energy‐Dispersive X‐ray Spectroscopy to investigate a well‐preserved middle Cretaceous lacustrine stromatolite from south‐eastern Korea, unveiling ultra‐high‐resolution sedimentary processes that are often challenging to observe using conventional methods. Two types of microsparitic layers and one type of crystalline layer are distinguished based on their texture, crystal morphology and elemental composition. Both microsparitic layers are micrometre‐thick and are characterized by poorly co‐oriented calcite grains, but differ in their composition. Type 1 is depleted in magnesium but enriched in detrital elements such as silicon and aluminium, likely originating from the trapping and binding of detrital sediments on microbial mats during rainy seasons. In contrast, type 2 is enriched in magnesium but devoid of detrital elements, interpreted to have formed by the precipitation of calcium carbonate during dry seasons. The crystalline layers comprise fan‐shaped calcite crystals (ca 500 μm in length) with radiating internal structures, with their c‐axes oriented perpendicular to the stromatolite layers. These structures resemble those observed in some modern freshwater stromatolites, which are interpreted as imprints of cyanobacterial fascicules. While the cyclic occurrence of types 1 and 2 microsparitic layers might imply annual seasonal cycles, the less frequent crystalline layers are interpreted as a result of environmental changes occurring every 27 to 30 years. This is the first study to apply Electron Backscatter Diffraction to stromatolites, showcasing its potential in unravelling both the formative and diagenetic processes of ancient stromatolites.

Thermochemical interaction of (Yb0.7Gd0.3)4Hf3O12 ceramic with CMAS melts

The molten calcium-magnesium alumino-silicate (CMAS) deposits degradation of thermal barrier coatings (TBCs) is increasingly severe in advanced turbine engines. In this study, the thermochemical interaction of a promising TBC candidate material, (Yb0.7Gd0.3)4Hf3O12, with CMAS melts at 1300 ℃ and 1500 ℃ was systematically investigated. The apatite and reprecipitated fluorite with high melting points were crystallized rapidly when the ceramic reacted with CMAS melts, resulting in the formation of a dense crystalline layer to suppress further infiltration of CMAS melts. Moreover, as the reaction proceeded, the formation of garnet and cuspidine occurred at 1300 ℃ and 1500 ℃, respectively. The CMAS resistance of (Yb0.7Gd0.3)4Hf3O12 was significantly higher compared to that of Yb4Hf3O12, which could be attributed to the greater volume fraction of apatite and reprecipitated fluorite in the reaction products. The (Yb0.7Gd0.3)4Hf3O12 exhibited high effectiveness in mitigating CMAS infiltration, making it a potential candidate material for thermal barrier coatings.