Crystal Orientation Research Articles

Effects of cold plastic deformation on microstructure and magnetic susceptibility of Au-Pt alloys

Formation of the alloys of paramagnetic gold (Au) and diamagnetic platinum (Pt) holds promise for developing materials with ultra-low magnetic susceptibility. This study investigates the effects of cold plastic deformation on the mechanical properties and magnetic susceptibility of Au-29Pt alloys by microstructure characterization. After cold rolling, the Vickers hardness of the Au-Pt alloy increases from 138.35 HV to 218.28 HV at 80 % deformation. Meanwhile, the volume magnetic susceptibility exhibits a change from −19.10 ppm to −28.60 ppm with minor difference between the results measured from different orientations. The crystal orientation of the Au-29Pt alloys changes but no new phases or no textures are formed. With the increase of the deformation level from 0 % to 60 %, EBSD measurements demonstrates a ∼40-fold increment in average geometric dislocation density. The results indicate the formation of new defects, which are identified as edge dislocations and stacking faults via HRTEM. Consequently, the larger diamagnetic susceptibility at a higher deformation level is mainly correlated with the formation of defects. The results of this study could provide useful guidelines for the design of ultra-low magnetic susceptibility alloys.

Tin-Lead Perovskite Solar Cells with Preferred Crystal Orientation by Buried Interface Approach.

Mixed tin-lead perovskite solar cells (PSCs) have garnered much attention for their ideal bandgap and high environmental research value. However, poly (3,4-ethylenedioxythiophene): poly (styrene sulfonate) (PEDOT: PSS), widely used as a hole transport layer (HTL) for Sn-Pb PSCs, results in unsatisfactory power conversion efficiency (PCE) and long-term stability of PSCs due to its acidity and moisture absorption. A synergistic strategy by incorporating histidine (HIS) into the PEDOT: PSS HTL is applied to simultaneously regulate the nucleation and crystallization of perovskite (PVK). HIS neutralizes the acidity of PEDOT: PSS and enhances conductivity. Especially, the coordination of the C═N and -COO- functional groups in the HIS molecule with Sn2+ and Pb2+ induces vertical growth of PVK film, resulting in the release of residual surface stress. Additionally, this strategy also optimizes the energy level alignment between the perovskite layer and the HTL, which improves charge extraction and transport. With these cooperative effects, the PCE of Sn-Pb PSCs reaches 21.46% (1 sun, AM1.5), maintaining excellent stability under a nitrogen atmosphere. Hence, the buried interface approach exhibits the potential for achieving high-performance and stable Sn-Pb PSCs.

A polycrystal plasticity-cellular automaton integrated modeling method for continuous dynamic recrystallization and its application to AA2196 alloy

Continuous dynamic recrystallization usually dominates the microstructural evolution in hot working of aluminum alloys, in which the high-angle grain boundaries of new grains mainly originate from the gradual increase in subgrain misorientation angles. In this work, an integrated computational method is proposed to simulate continuous dynamic recrystallization process of aluminum alloys by coupling three-dimensional cellular automaton and visco-plastic self-consistent models. The stress response, dislocation accumulation and recovery, and evolution of crystal orientations are computed in the context of polycrystal plasticity; the formation and rotation of subgrains, followed by stored energy and curvature-driven boundary migration, are captured and visualized by cellular automaton. The non-octahedral slip mode {110}<110> is additionally introduced to capture the 〈001〉 texture during hot compression. A universal cell topology deformation method is adopted to achieve an effective track of grain morphology evolution during plastic deformation. The proposed simulation framework is validated through simulating the isothermal uniaxial compression process of AA2196 alloy under different temperatures and strain rates. The orientation dependence of CDRX during compression is numerically reproduced by correlating the subgrain formation and rotation process with the activation state of slip systems. The simulated macroscopic flow stress, 3D microstructure and inherent microstructural characteristics such as subgrain size, subgrain boundaries and textures are in good agreement with the experimental results. The proposed method provides an effective and efficient tool for multi-scale simulation of hot forming process of aluminum alloys.

One-step in situ doping of Sb achieves enhanced performance of [001]-oriented nano-LiFe0.6Mn0.4PO4/C cathode high-rate materials

The LiFe0.6Mn0.4PO4/C composite has become a cost-effective and reliable material for lithium battery storage in commercial applications, due to its significant safety benefits. However, its industrial application is limited by its suboptimal high-rate capacity and unsatisfactory cycling performance. To address this issue, Li(Fe0.6Mn0.4)1-xSbxPO4 (x = 0, 0.01, 0.03, 0.04, 0.05) materials were synthesized using a one-step solvothermal method in this study, aiming to modulate the microstructure and achieve Sb doping, thereby enhancing the electrochemical performance. The electrochemical test results indicate that LFMP/C doped with Sb (designated as LFMP/C-Sb0.04) displays exceptional electrochemical performance, with remarkable capacities of 166.6 mAh·g−1 and 146.8 mAh·g−1 at 0.2C and 1C, respectively. Notably, it achieves a capacity of 126.1 mAh·g−1 at a high rate (5C) and maintains an impressive capacity retention rate of 93.6 % after 300 cycles, outperforming the original LMFP/C (109.5 mAh·g−1), which retains only 61.5 % of its initial capacity. Further characterization of the samples reveals that in situ Sb doping promotes the growth of the [001] crystal orientation, enhancing the lithium-ion diffusion rate and effectively reducing electrode polarization and charge transfer resistance, thereby contributing to its exceptional rate performance. Moreover, Sb doping increases the M − O binding energy, strengthens the metal-oxygen framework, mitigates the Jahn-Teller effect caused by Mn3+ dissolution, and enhances its cycling stability.

Comparison on Hysteresis Loops and Dislocation Configurations in Fatigued Face-Centered Cubic Single Crystals

The aggregation and evolution of dislocations form different configurations, which are the preferred locations for fatigue crack initiation. To analyze the spatial distribution of the same dislocation configuration and the resulting configuration morphologies on different observation planes, several typical hysteresis loops and dislocation configurations in fatigued face-centered cubic single crystals with various orientations were compared. The crystal orientations of these specimens were determined by the electron back-scattering diffraction technique in a Cambridge S360 Scanning Electron Microscope. It is well known that dislocation ladder and wall structures, as well as patch and vein structures, are distributed on their respective observation planes, (12¯1) and (111). These correspond to the point defect direction and line defect direction of dislocations, respectively. Therefore, the wall structures on the (12¯1) and (111) planes consist of point defects and line defects, which can be defined as point walls and line walls, respectively. Furthermore, the walls on the (12¯1) plane consist of Persistent Slip Band ladders connected with each other, corresponding to the formation of deformation bands. The evolution of dislocation patterns follows a process from patch to ladder and from vein to wall. The formation of labyrinths and dislocation cells originates from the activation of different secondary slip systems. In one word, it can help us better understand the physical nature of metal fatigue and failure by studying the distribution and evolution of different configurations.

Crystallization-Based Modification of Ammonium Perchlorate Heat Release.

Composite propellants use the decomposition of crystalline oxidizers, such as ammonium perchlorate (AP), to produce oxidizing species that can combust with fuels. Controlled crystal microstructure must be leveraged to tailor reactivity to minimize the use of exotic energetic materials. This work uses meniscus-guided coating (MGC) to fabricate films of AP with a high degree of control over the AP crystal microstructure. Exploring a wide range of crystallization parameters resulted in film thickness ranging from 200 nm to 14 μm, particle size ranging from 18 to 110 μm, variable preferential orientation with respect to the substrate, and relative defect density ranging from 2.74 × 105 to 6.78 × 105 μm-3. Increasing coating blade speed and substrate temperature within the MGC process shifts the preferential orientation of the AP crystals from predominantly exhibiting (002) and (210) crystal planes parallel to the substrate to (200)/(011) crystal planes parallel to the substrate. This shift in orientation is accompanied by an increase in defect density, which is shown to increase the heat release from the low-temperature decomposition regime and decrease the heat release from the high temperature regime. These results demonstrate the ability to use recrystallization, defect density control, and orientation control to tune the heat release profiles of energetic materials to augment propellant performance.

On the Sources of Discrepancies Between Grain Size Measurements

Accurate quantification of grain size in polycrystals is extraordinarily important for quality assurance and the development of structure-property relationships, as grain size affects nearly all engineering properties of structural alloys, from strength and fatigue life to corrosion resistance and thermal conductivity. Despite nearly a century of the existence of standards for measuring grain size, issues persist in obtaining consistent grain size measurements across several techniques. Of particular interest is comparing optical microscopy or scanning electron microscopy on an etched surface with mapping of crystal orientations using electron backscatter diffraction (EBSD). In this work, discrepancies between methods in the ASTM E 112 and ASTM E 2627 standards are explored through simulated measurements on synthetic microstructures. It is concluded that a small but systematic discrepancy exists between planimetric and lineal intercept-based approaches, and a new empirical relationship between the ASTM grain size number G and lineal intercepts is proposed.

Interaction of defects, martensitic transformation and slip in metastable body centred cubic crystals of Ti-10V-2Fe-3Al: A study via crystal plasticity finite element methods (CPFEM)

Metastable β titanium alloys are widely applied in many industries. These alloys can have plastic deformation via dislocation slip, twinning, stress-induced martensite (SIM), or a combination of these. These alloys fail in a ductile manner via a process of void nucleation, growth, and coalescence. Inherent defects, such as voids, are commonly attributed to poor mechanical properties. In this study, aspects of plastic anisotropy in damage accumulation are investigated for metastable crystals that deform by combined slip and SIM. The focus of this study is to understand the evolution of damage due to inherent voids in metastable Ti-10V-2Fe-3Al single crystals. This investigation is conducted using crystal plasticity-based 3D finite element (FE) calculations. A unit-cell FE model involving a spherical void is deformed under constant stress triaxiality and lode parameter. We investigated four triaxiality values at differing lode parameters in three crystal orientations. The void growth was found to be heavily dependent on crystal orientation at low triaxialities. At higher triaxialities, SIM is found to inhibit the void growth via accommodation of the required deformation in the surrounding material. Orientations aligned favourable with SIM undergo significantly less void growth. The accommodation of deformation in the surrounding matrix was found to help preserve the integrity of the void, preventing the localisation of deformation around the void. At lower lode parameter and at higher stress triaxiality this impedes the exponential growth of the void. While, at higher lode parameter with low triaxiality SIM was found to delay the collapse of the void into a crack like morphology. This study not only deepens our understanding of the mechanical behaviour of metastable β titanium alloys, but also unveils the complex interplay between inherent defects, stress-induced martensite, and slip-based plasticity within their crystalline structure, offering fresh perspectives on enhancing material performance.

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.

Growth orientation control in rapid solid-state crystal growth of (K,Na)NbO3 single crystals using plate-like NaNbO3 single crystal particles

The rolling-extended orientation technique and plate-like NaNbO3 (NN) single crystal particles prepared by a single-step molten salt synthesis, both of which have been developed to fabricate (K, Na)NbO3 (KNN) textured ceramics, were utilized to control the growth orientation of KNN single crystals synthesized by a rapid solid-stated crystal growth (RSSCG) method. As the seed crystals, two kinds of NN single crystal particles were synthesized using pure NaCl and KCl-NaCl mixed molten salts. Plate-like KNN single crystals of about 1 cm squares with the upper and lower faces almost parallel to the (100) (001) planes were obtained with a probability exceeding 50% when NN single crystal particles were synthesized from mixed salts and were subsequently thermal-treated again in Na2CO3-NaCl mixed molten salts under appropriate conditions to remove the Bi element, which is known as the suppression factor of the crystal growth. The average crystal growth rate was 0.6–1.2 mm h−1. Controlling the growth orientation of KNN single crystals produced by the SSCG method using seed crystals other than KTaO3 single crystals was successfully accomplished for the first time.

Frictional properties and environmental adaptability of Ti-MoS2/WC multilayer films

Magnetron-sputtered molybdenum disulfide films are extensively utilized as solid lubricating coatings in space applications as a result of their low friction coefficient and minimal contamination. However, MoS2-based films are sensitive to hygrothermal and oxidation environment, and are easily oxidized to form MoO3, which results in high friction and wear of the films, significantly reducing their operational lifespan. Especially when the spacecraft adopts the launching mode of coastal launch or ocean platform, the performance deterioration caused by oxidation of MoS2 films during transportation, storage and launch is more serious. Therefore, to enhance the frictional performance and oxidation resistance of the films in humid and salt spray environments, the Ti-MoS2/WC multilayer films with preferred (002) crystal plane orientation were prepared, achieving a friction coefficient of 0.009 in a vacuum environment and a wear rate of 1.1×10-7 mm3/N∗m. In particular, the film can maintain this extremely low coefficient of friction even after exposure to moisture or salt spray. These findings demonstrate that the dual doping of Ti and WC and the design of multilayer structures enable MoS2 films to achieve outstanding frictional performance and oxidation resistance. This is crucial for designing MoS2 films with excellent environmental adaptability.

Relative molecular orientation can impact the onset of plasticity in molecular crystals

Abstract Creating or moving dislocations is the first step to dissipating mechanical energy via plastic deformation under contact loading. In molecular crystals there is both a lattice that defines crystal orientation and a relative orientation of the basis of the molecules. We define a normalization parameter which relates strain at yield, the hardness of the bulk crystal, and a distance parameter analogous to a Burgers vector that nominally predicts the relative ease of initiating plasticity in this broad class of materials. Analyzing the yield behavior of 10 different molecular crystals of varying space groups shows the inter-molecular orientation predicts the experimentally observed applied stress needed to nucleate dislocations. When molecules are oriented ‘parallel’ relative to one another the normalized maximum shear stress at the onset of plasticity is on the order of 3–5 times lower than when molecules within the crystal are ‘anti-parallel’, and molecules with a more equiaxed shape fall in between these bounds. This provides an initial indication of a structural feature which predicts the relative ease of initiating plasticity during contact loading in molecular crystals.

Substrate orientation influence on nanotwinning in magnetron sputtered CoCrFeMnNi and Ni coatings

This study reveals the influence of crystal orientation on formation of growth twins in magnetron-sputtered coatings. A comparison between materials with low and high stacking fault energy (SFE) was made: CoCrFeMnNi (25 mJ/m2) and Ni (125 mJ/m2). The coatings were grown on a polycrystalline 316L stainless-steel substrate with near-random crystal texture, providing a comprehensive selection of samples on a single substrate. Electron backscatter diffraction was used to identify the film orientation, followed by transmission electron microscopy of selected regions.The presence and density of twins depended on both the material and the growth orientation. For Ni, nanotwins were observed on < 5 % of the substrate grains, on growth directions closest to 〈111〉 . All other film orientations grew epitaxially with a cube-on-cube relationship. For CoCrFeMnNi, nanotwinning was observed on 50 % of the substrate grains, deviating < 35° from 〈111〉 . In the nanotwinned regions, the twin spacing was 10–100 nm for Ni and 2–20 nm for CoCrFeMnNi. The presence of nanotwins increased hardness in both materials. The mechanism behind these differences is discussed, together with other parameters for controlling twin density. Our results show that control of the growth process can be used for nanotwin-engineering in magnetron-sputtered materials with low SFE.

Defect-Free Nanowelding of Bilayer SnSe Nanoplates.

Nanowelding is a bottom-up technique to create custom-designed nanostructures and devices beyond the precision of lithographic methods. Here, a new technique is reported based on anisotropic lubricity at the van der Waals interface between monolayer and bilayer SnSe nanoplates and a graphene substrate to achieve precise control of the crystal orientation and the interface during the welding process. As-grown SnSe monolayer and bilayer nanoplates are commensurate with graphene's armchair direction but lack commensuration along graphene's zigzag direction, resulting in a reduced friction along that direction and a rail-like, 1D movement that permits joining nanoplates with high precision. This way, molecular beam epitaxially grown SnSe nanoplates of lateral sizes 30-100nm are manipulated by the tip of a scanning tunneling microscope at room temperature. In situ annealing is applied afterward to weld contacting nanoplates without atomic defects at the interface. This technique can be generalized to any van der Waals interfaces with anisotropic lubricity and is highly promising for the construction of complex quantum devices, such as field effect transistors, quantum interference devices, lateral tunneling junctions, and solid-state qubits.

Low-Frequency Vibrational Spectra of 4-Fluorophenol Studied by THz Spectroscopy and Solid-State Density Functional Theory.

Hydrogen bonds serve as important intermolecular interactions organizing the spatial arrangement of molecular crystals. Determining the hydrogen-bond orientations remains a challenging task. In the previous XRD study, the authors assumed a single crystal structure of 4-fluorophenol in which molecules form hexamer-ring clusters via anticlockwise hydrogen bonding. However, the existence of the other structure, which adopts clockwise hydrogen bonding, remains uncertain and warrants further exploration. We unveil distinctive fingerprint information associated with both structures by using high-resolution terahertz spectroscopy. The distinct structures result in different intramolecular geometries of 4-fluorophenol regarding the O-H bond configurations, which are manifested by a noticeable peak splitting in the 20-200 cm-1 frequency range. This result illustrates the sensitivity of THz spectroscopy to hydrogen-bond conformational polymorphism. Our findings represent a significant advancement in utilizing high-resolution THz spectroscopy to resolve hydrogen-bond orientations in molecular crystals with possible broad applicability across diverse hydrogen-bonded organic and inorganic framework materials.

Fabrication of TiN metal hard masks via very-high-frequency-direct-current superimposed sputtering

In high-end logic devices, TiN films have attracted increasing attention as metal hard masks (MHMs) for scaling trenches and vias of Cu back-end of line. In this study, we investigated the application of very-high-frequency-direct-current (VHF)-DC superimposed magnetron sputtering for fabricating TiN MHM films and compared these films with TiN MHM films deposited via DC magnetron sputtering. The X-ray diffraction (XRD) pattern of deposited TiN MHs showed crystalline orientations corresponding to the (111), (200), and (220) orientations of NaCl TiN. The films deposited using DC magnetron sputtering exhibited high density (<5.2 g/cm³) and significant compressive stress (1.477 GPa) when the TiN film thickness ranged from 29 to 30 nm. The films deposited via VHF-DC superimposed sputtering exhibited a higher density (5.25 g/cm³) and tensile stress (0.928 GPa). As revealed by XRD, the films deposited via DC sputtering exhibited the (111) crystal orientation, whereas those deposited via VHF-DC superimposed sputtering exhibited the (200) crystal orientation. The film deposited by VHF-DC superimposed sputtering at a frequency of 60 MHz and a substrate temperature of 350 °C exhibited good resistivity (93.0–143.3 μΩ cm). Furthermore, the TiN films exhibited exceptional smoothness with a surface roughness of less than 0.5 nm. These results show that VHF-DC superimposed sputtering is a promising technique for fabricating TiN-based MHMs.

Microwaves induced epitaxial growth of urchin like MIL-53(Al) crystals on ceramic supports

Shaping Metal–Organic Frameworks (MOFs) poses a significant challenge for their widespread application on a large scale. In particular, a precise control over crystal orientation and arrangement on substrates are expected to provide exiting opportunities for novel materials with customized characteristics and enhanced performance in catalysis, gas storage, sensing, optics and electronics. Here we demonstrated for the first time that microwave irradiation can induce well controlled epitaxial growth of urchin-like MIL-53(Al) crystals via the hydrothermal conversion of Atomic Layer Deposition alumina layers on SiC foams. The resulting large, ordered crystals feature specific size, homogeneity, dispersion, and quantity that strongly correlate with the nature of the ceramic support and its ability to absorb microwaves. Furthermore, the supported MIL-53(Al) urchins were considered as templates for generating nanostructured alumina fibers on SiC foams, providing attractive catalyst carriers with high specific surface areas.

Correlation between grain orientation and corrosion performance of different tantalum crystal facets in 3.5 wt% NaCl aqueous solution

To investigate the influence of different crystal orientations of tantalum on corrosion performance, this study explored the diverse corrosion behaviors exhibited by the (110), (200), and (211) crystal planes of monocrystalline tantalum in a 3.5 wt% NaCl aqueous solution. The electrochemical behavior of the three crystal planes was characterized using open circuit potential, potentiodynamic polarization, and electrochemical impedance spectroscopy tests. The results revealed that the corrosion potential of the (110) crystal plane was slightly higher than that of the other two crystal planes, suggesting that this can be attributed to the influence of surface energy. The corrosion current density and corrosion rate of the (110) crystal plane were measured to be 0.269 μA cm−2 and 1.911 × 10−3 mm/y, respectively, significantly exceeding those of the other two crystal planes. Additionally, the electrochemical impedance spectroscopy results indicated that the modulus impedance and polarization resistance of the (110) crystal plane were much lower compared to the other two crystal planes, suggesting inferior corrosion resistance. A comprehensive analysis indicates that the (110) crystal plane exhibits poorer corrosion resistance compared to the (200) and (211) planes, with the interplanar spacing identified as the primary factor influencing its corrosion resistance.

Synthesis of Multifunctional Organic Molecules via Michael Addition Reaction to Manage Perovskite Crystallization and Defect.

Additive engineering plays a pivotal role in achieving high-quality light-absorbing layers for high-performance and stable perovskite solar cells (PSCs). Various functional groups within the additives exert distinct regulatory effects on the perovskite layer. However, few additive molecules can synergistically fulfill the dual functions of regulating crystallization and passivating defects. Here, we custom-synthesized 2-ureido-4-pyrimidone (UPy) organic small molecules with diverse functional groups as additives to modulate crystallization and defects in perovskite films via the Michael addition reaction. Theoretical and experimental investigations demonstrate that the -OH groups in UPy exhibit significant effects in fixing uncoordinated Pb2+ ions, passivation of lead-iodide antisite defects, alleviating hysteresis, and reducing non-radiative recombination. Furthermore, the enhanced C=O and -NH2 motifs interact with the A-site cation via hydrogen bonding, which relieves residual strain and adjusts crystal orientation. This strategy effectively controls perovskite crystallization and passivates defects, ultimately enhancing the quality of perovskite films. Consequently, the open-circuit voltage of the UPy-based p-i-n PSCs reaches 1.20 V, and the fill factor surpasses 84%. The champion device delivers a power conversion efficiency of 25.75%. Remarkably, the unencapsulated device maintained 96.9% and 94.5% of its initial efficiency following 3,360 hours of dark storage and 1,866 hours of 1-sun illumination, respectively.

Strain localisation and grain boundary-mediated deformation in pure titanium at low and high temperatures: In-situ optical microscopy and digital image correlation

Heterogeneous deformation occurs between grains in polycrystalline α-titanium. Understanding the role of temperature in local deformation is essential for its applications in extreme environments such as cryo- or high-temperature, but the underlying mechanism still remains elusive. Here we report a study of grain-scale deformation behaviour in CP-Ti plate at the temperature range from −60 °C to 280 °C. The full-field strain measurements were conducted on the tensile samples loaded parallel (RD) and transverse (TD) to the rolling direction, using in-situ optical microscopy and digital image correlation (OM-DIC). The DIC local strain maps were coupled with scanning electron microscopy and electron backscatter diffraction analysis. The grain boundary sliding and slip transfer occurred depending on the geometric relationship (i.e., deformation compatibility) between adjacent grains at 20 °C, and a micro-crack was observed at the {101‾1} twist boundary. The strain was recovered in the grains in the RD sample favourable for slip, whilst more accumulated in the grains in TD sample unfavourable for slip at 280 °C. The plasticity of grains differs with decreasing temperature to −40 °C, resulting in the presence of soft/hard grain pairs. The strong strain localisation between the soft and hard grains led to the cracking along the GBs (RD) and cross the grains (TD). Interestingly, the cracking was significantly reduced with decreasing temperature to −60 °C due probably to the temperature dependence of the plasticity of grains. The strain-hardening behaviour of α-Ti polycrystals was significantly affected by the temperature and crystal orientation dependence of grain-scale deformation mechanism.