Strain-induced Changes Research Articles

Reshaping precipitate structure and morphology in an Al-Zn-Mg-Cu alloy through dislocation-precipitate interactions

Mechanical properties of age-hardenable alloys are significantly influenced by the intricate interplay between precipitates and mobile dislocations. This study examined how dislocations interact with nanosized precipitates at the atomic scale in an under-aged Al-Zn-Mg-Cu alloy. Results revealed that precipitates hinder dislocation movement but are also sheared by them during deformation. Furthermore, the sheared precipitates experienced structural collapse and deviated from their usual evolutionary path, forming ordered but non-periodic topologically close-packed structures and altered morphologies. The discoveries provide insights into dislocation-precipitate interactions and strain-induced structural changes, which could inspire strategies to modulate precipitates with tailored microstructures and thereby improved alloy properties.

Effective control of magnetism and transport properties of monolayer WV2N4 with two magnetic atomic layers and its van der Waals heterostructure

The large magneto-resistance (MR) effect produced by electric control of the magnetic state for van der Waals (vdW) heterostructures composed of vdW intrinsic magnets holds great significance for low-dissipation spintronic devices. Our first-principles calculations reveal that the proposed monolayer WV2N4 is a ferromagnetic (FM) metal with two magnetic V atomic layers, and the interlayer magnetic coupling between two V atomic layers can be switched from FM to antiferromagnetic coupling by applying a small compressive strain. Interestingly, a large MR ratio of 253% is achieved in the proposed graphite/monolayer WV2N4/graphite vdW heterostructure using a −1.5% compressive strain. Combining the strain-induced change in magnetism of monolayer WV2N4 and the graphite/monolayer WV2N4/graphite vdW heterostructure with the inverse piezoelectricity of piezoelectric materials, a feasible strategy is proposed to achieve electric control of the interlayer magnetic coupling of monolayer WV2N4 in the graphite/monolayer WV2N4/graphite vdW heterostructure clamped by piezoelectric materials by utilizing the inverse piezoelectricity, thereby generating a large MR ratio in the graphite/monolayer WV2N4/graphite vdW heterostructure clamped by the piezoelectric material. Our work presents a promising avenue for developing energy-efficient spintronic devices.

Exploration of near room temperature magnetoelectric coupling in BaFe10Sc[formula omitted]O19:KNbO[formula omitted] composite

The consequential experimental endeavour has been undertaken to investigate and control the strain-mediated coupling of the magnetic and electric properties of the composite systems composed of Sc-doped BaFe12O19 and KNbO3. A distinct non-disperse ferroelectric-like anomaly is observed Tkink∼ 265 K, which concomitantly coincides with the magnetic Tcone transition. The observation of external magnetic field dependence dielectric response shows a noticeable decrease in permittivity values, indicating a negative magnetodielectric response. The maximum intrinsic magnetodielectric response is seen in the vicinity of room temperature with the magnetodielectric ratio of 5.4% @ 1 kHz. The linearity of −Δɛ′(H)% vs. M2 plot is phenomenologically described with the Ginzburg–Landau theory with the magnetoelectric coupling term γP2M2. The magnetoelectric coupling relies on strain to induce crystal deformations (flexomagnetoelectric response) on either the ferroelectric phase through magnetostriction or in the magnetic phase through the converse piezoelectric effect. Strain-induced changes in the magnetic as well as dielectric properties of the composites lead to strong magnetoelectric coupling to throw more light exploring a potential candidate for room-temperature multiferroic materials.

Strain-dependent dynamic re-alignment of collagen fibers in skeletal muscle extracellular matrix

Collagen fiber architecture within the skeletal muscle extracellular matrix (ECM) is significant to passive muscle mechanics. While it is thought that collagen fibers re-orient themselves in response to changes in muscle length, this has not been dynamically visualized and quantified within a muscle. The goal of this study was to measure changes in collagen alignment across a range of muscle lengths and compare the corresponding alignment to muscle mechanics. We hypothesized that collagen fibers dynamically increase alignment in response to muscle stretching, and this change in alignment is related to passive muscle stiffness. Further, we hypothesized that digesting collagen fibers with collagenase would reduce the re-alignment response to muscle stretching. Using DBA/2J and D2.mdx mice, we isolated extensor digitorum longus (EDL), soleus, and diaphragm muscles for collagenase or sham treatment and decellularization to isolate intact or collagenase-digested decellularized muscles (DCMs). These DCMs were mechanically tested and imaged using second harmonic generation microscopy to measure collagen alignment across a range of strains. We found that collagen alignment increased in a strain-dependent fashion, but collagenase did not significantly affect the strain-dependent change in alignment. We also saw that the collagen fibers in the diaphragm epimysium (surface ECM) and perimysium (deep ECM) started at different angles, but still re-oriented in the same direction in response to stretching. These robust changes in collagen alignment were weakly related to passive DCM stiffness. Overall, we demonstrated that the architecture of muscle ECM is dynamic in response to strain and is related to passive muscle mechanics. Statement of significanceOur study presents a unique visualization and quantification of strain-induced changes in muscle collagen fiber alignment as they relate to passive mechanics. Using dynamic imaging of collagen in skeletal muscle we demonstrate that as skeletal muscle is stretched, collagen fibers re-orient themselves along the axis of stretch and increase their alignment. The degree of alignment and the increase in alignment are each weakly related to passive muscle stiffness. Collagenase treatments further demonstrate that the basis for muscle Extracellular matrix stiffness is dependent on factors beyond collagen crosslinking and alignment. Together the study contributes to the knowledge of the structure-function relationships of muscle extracellular matrix to tissue stiffness relevant to conditions of fibrosis and aberrant stiffness.

Substrate Charge Transfer Induced Ferromagnetism in MnSe/SrTiO3 Ultrathin Films.

The observation of superconductivity in MnSe at 12 GPa motivated us to investigate whether superconductivity could be induced in MnSe at ambient conditions. A strain-induced structural change in the ultrathin film could be one route to the emergence of superconductivity. In this report, we present the physical property of MnSe ultrathin films, which become tetragonal (stretched ab-plane and shortened c-axis) on a (001) SrTiO3 (STO) substrate, prepared by the pulsed laser deposition (PLD) method. The physical properties of the tetragonal MnSe ultrathin films exhibit very different characteristics from those of the thick films and polycrystalline samples. The tetragonal MnSe films show substantial conductivity enhancement, which could be associated with the presence of superparamagnetism. The optical absorption data indicate that the electron transition through the indirect bandgap to the conduction band is significantly enhanced in tetragonal MnSe. Furthermore, the X-ray Mn L-edge absorption results also reveal an increase in unoccupied state valance bands. This theoretical study suggests that charge transfer from the substrate plays an important role in conductivity enhancement and the emergence of a ferromagnetic order that leads to superparamagnetism.

Detection of indentation damage in carbon fiber/epoxy composites via EIT during the application of bending loads

Electrical impedance tomography (EIT) is a method of spatially mapping the conductivity distribution of a domain and has been studied as a potential embedded sensing or nondestructive evaluation (NDE) tool. An often touted advantage of EIT is that it can be used in-situ; that is, because the method only requires the application of unobtrusive electrodes, it can conceivably be used while the component or structure is in operation. This material-as-the-sensor philosophy strongly aligns with key components of the NDE 4.0 vision such as the realization of intelligent cyber–physical systems (CPS) and digital twins. To date, however, the claim of in-situ sensing via EIT has not been significantly substantiated. This is problematic because operational loads induce strains that often change the conductivity of the material. Establishing that EIT can detect damage-induced conductivity changes through the presence of unrelated strain-induced conductivity changes is therefore important. To that end, we herein study the application of EIT for detecting indentation damage in a carbon fiber/epoxy composite as the composite is loaded in a four-point bend. It was found that the bending load changes the contact impedance of the electrodes, which resulted in poor EIT images when solving the EIT inverse problem with the ℓ2-norm on the error term. Using the ℓ1-norm on the error term, solved via the primal–dual interior point method (PDIPM), significantly improved image quality. Image quality was even further improved through the use of a mixed prior for regularization, and EIT images were compared to thermography with good agreement. These results show that EIT can indeed detect damage through the presence of an applied load, but care must be taken to account for factors such as outlier data arising from electrode degradation and changing contact impedance. Use of the ℓ1-norm on the error term is therefore highly recommended for in-situ imaging via EIT.

Mechanism of strain-induced magnetic signal change in ferromagnetic materials under weak magnetic environment

Weak magnetic detection based on force-magnetic coupling effect is widely used in nondestructive testing of ferromagnetic materials, but the weak magnetic signals caused by the deformation of ferromagnetic materials under the action of external load show nonlinear changes, and the existing theories can not make a unified conclusion on the mechanism of nonlinear changes of magnetic signals, which limits the further application of weak magnetic detection. In this paper, a microscopic model of ferromagnetic material is established with the strain of the material as the independent variable. Firstly, the reasonableness of the established model is verified by the stress–strain relationship, and the stress concentration phenomenon generated by the change of the microscopic structure of the model is studied in depth by using the XRD diffraction method, so as to put forward the idea of characterizing the macroscopic stress with microscopic dislocations; secondly, the mechanism of the change of the magnetic signals of the ferromagnetic material caused by strain is analyzed by using the atomic magnetic moments and the density of states. The model explains the mechanism of strain-induced magnetic signal change in ferromagnetic materials, and has a guiding role in the further application and promotion of the weak magnetic method.

Strain-induced changes of electronic and optical properties of Zr-based MXenes

Zr-based MXenes recently attracted attention because of its experimental preparation showing temperature stability, mechanical strength, and promising energy, sensoric, and electrochemistry applications. However, necessary theoretical predictions at a precise/predictive level are complicated due to essential excitonic features and strong electron correlation (i.e., a necessity to go beyond standard density functional theory, DFT). Contrary to the prevailing focus on oxygen-terminated MXenes and standard predictions of other Zr-based MXenes as conductors, based on the hybrid DFT and GW many-body perturbational theory, we were able to find seven different semiconductors (five of them for their equilibrium geometry and two others under slight tensile biaxial strain) in the case of two- and three-layered Zr2CT2 and Zr3C2T2 configurations with various terminations (T = O, F, S, Cl). We observed semiconductor-to-conductor transition induced by strain in the majority of such Zr-based MXenes at an experimentally achievable strain range. Furthermore, using the Bethe–Salpeter equation (BSE), we demonstrated that selected semiconducting Zr-based MXenes possess high optical absorption efficiency (20%–30%) in the visible light range, underscoring their potential in photonic applications. The high sensitivity of Zr-based MXenes to external conditions and functionalization combined with the thermal stability makes the materials promising for applications at operational temperatures in electronic and optical technologies.

A novel investigation into strain-induced changes in the physical properties and solar cell performances of lead-free Ca3NCl3 perovskite

The first-principle calculations were employed to analyze the structural, thermodynamic, electronic, optical, and mechanical properties of calcium-based halide perovskites, Ca3NCl3, under pressure variations from +6 % to −6%. The Ca3NCl3 materials are thermodynamically and dynamically stable, as indicated by the negative final enthalpy values obtained under pressures ranging from −6% to +6 %. The charge density maps confirm the existence of both ionic and covalent bonding features. The unstressed Ca3NCl3 has a direct bandgap of 1.66 eV with PBE functions, 2.32 eV with HSE functions and 1.48 eV with spin-orbit coupling (SOC) at the Γ point. When subjected to compressive strain, the bandgap reduces to 1.37 eV(PBE), 1.93 eV(HSE) and 1.08 eV(SOC) at −6% strain, causing a redshift in absorption coefficient peaks. Conversely, under tensile strain, the bandgap slightly rises to 1.92 eV(PBE), 2.60 eV(HSE) and 1.73 eV(SOC) at +6 % strain, resulting in a blueshift in absorption coefficient peaks. The Ca3NCl3 materials show enhanced optical absorption, loss function, conductivity, dielectric function, refractive index and reflectivity under applied pressure, making them more appropriate for use in solar absorbers, surgical tools, and optoelectronic devices. The investigation of the mechanical properties reveals that the Ca3NCl3 perovskite is mechanically stable. Moreover, with rising pressure (tensile to compressive), elastic constants, elastic moduli, ductility, machinability index, bulk modulus, shear modulus, pugh's ratio, young modulus and anisotropy all rise. The photovoltaic (PV) performance of novel cell configurations, featuring Ca3NCl3 as an absorber and CdS as an Electron Transport Layer (ETL), was systematically studied using the SCAPS-1D simulator. This structure achieved a maximum power conversion efficiency (PCE) of 20.88 %, with a current density (JSC) of 19.184 mAcm−2, a voltage (VOC) of 1.22 V, and a fill factor (FF) of 89.06. The valuable findings from our simulations will aid in the experimental design of an efficient Ca3NCl3-based new inorganic perovskite solar cell in the near future.

Influence of chemical strains on the electrocaloric response, polarization morphology, tetragonality, and negative-capacitance effect of ferroelectric core-shell nanorods and nanowires

Using Landau-Ginzburg-Devonshire (LGD) approach, we proposed the analytical description of the influence of chemical strains on spontaneous polarization and the electrocaloric response in ferroelectric core-shell nanorods. We postulate that the nanorod core presents a defect-free single-crystalline ferroelectric material, and elastic defects are accumulated in the ultrathin shell, where they can induce tensile or compressive chemical strains. Finite-element modeling (FEM) based on the LGD approach reveals transitions of domain-structure morphology induced by chemical strains in the BaTiO3 nanorods. Namely, tensile chemical strains induce and support the single-domain state in the central part of the nanorod, while the curled domain structures appear near the unscreened or partially screened ends of the rod. The vortexlike domains propagate toward the central part of the rod and fill it entirely, when the rod is covered by a shell with compressive chemical strains above some critical value. The critical value depends on the nanorod sizes, aspect ratio, and screening conditions at its ends. Both analytical theory and FEM predict that the tensile chemical strains in the shell increase the nanorod polarization, lattice tetragonality, and electrocaloric response well above the values corresponding to the bulk material. The physical reason for the increase is strong electrostriction coupling between the mismatch-type elastic strains induced in the core by chemical strains in the shell. Comparison with earlier XRD data confirmed an increase of the tetragonality ratio in tensile BaTiO3 nanorods compared to the bulk material. Obtained analytical expressions, which are suitable for the description of strain-induced changes in a wide range of multiaxial ferroelectric core-shell nanorods and nanowires, can be useful for strain engineering of advanced ferroelectric nanomaterials for energy storage, harvesting, electrocaloric applications, and negative capacitance elements. Published by the American Physical Society 2024

Strain-modulated electronics enabled by surface piezoelectricity

The strain-induced polarization in a piezoelectric semiconductor is an effective strategy to modulate its current transport. However, the piezoelectricity is degraded by the free charges, and the inevitable compromise of piezoelectricity and semiconductivity severely limits the material choice and device performance. We tackle this dilemma by investigating the polarization caused by broken translational symmetry of a material surface. The ubiquitous surface piezoelectricity of solid materials enables the strain-induced polarization change to control the electrical transport effectively in crystals without bulk piezoelectricity. The Schottky barrier is shown to prohibit the bulk charges from screening the surface polarization. The strain engineering of the barrier height leads to an exponential modulation of the current, and an unprecedented gauge factor of 3.10×108 and an on/off ratio of 2.53×105 are demonstrated. The outstanding tunability of current with the synergistic effect of the surface piezoelectricity and metal-semiconductor contact unlocks the device development from various materials.

Density functional theory study on the formation mechanism and electrical properties of two-dimensional electron gas in biaxial-strained LaGaO3/BaSnO3 heterostructure

The two-dimensional electron gas (2DEG) in BaSnO3-based heterostructure (HS) has received tremendous attention in the electronic applications because of its excellent electron migration characteristic. We modeled the n-type (LaO)+/(SnO2)0 interface by depositing LaGaO3 film on the BaSnO3 substrate and explored strain effects on the critical thickness for forming 2DEG and electrical properties of LaGaO3/BaSnO3 HS system using first-principles electronic structure calculations. The results indicate that to form 2DEG in the unstrained LaGaO3/BaSnO3 HS system, a minimum thickness of approximately 4 unit cells of LaGaO3 film is necessary. An increased film thickness of LaGaO3 is required to form the 2DEG for -3%-biaxially-strained HS system and the critical thickness is 3 unit cells for 3%-baxially-strained HS system, which is caused by the strain-induced change of the electrostatic potential in LaGaO3 film. In addition, the biaxial strain plays an important role in tailoring the electrical properties of 2DEG in LaGaO3/BaSnO3 HS syestem. The interfacial charge carrier density, electron mobility and electrical conductivity can be optimized when a moderate tensile strain is applied on the BaSnO3 substrate in the ab-plane.

Stress-induced phase stability and optoelectronic property changes in cesium lead halide perovskites

Over the past decade, the certified power conversion efficiency of perovskite solar cells (PSCs) has increased to 26.1%. However, phase instability originating from lattice strains, has limited their commercialization. Strains will inevitably be generated during the PSC fabrication and service process due to the “soft lattice” nature of halide perovskites. In particular, flexible PSCs are subjected to not only mechanical tensile and compressive loads, but also suffer from thermal stresses. In this study, strain-induced changes in the phase stability and the corresponding optoelectronic properties of CsPbI3−xBrx (CsPbI3, CsPbBr3, and CsPbI2Br) systems under tensile and compressive stresses were investigated using first-principles calculations. The results showed that compressive stresses reduce the bandgap value and increase the light absorption coefficient; thus, the optoelectronic performance is improved, whereas the light absorption coefficient decreases regardless of how the bandgap changes under tensile stresses. Moreover, under the same stress, the tensile strain value was twice that of the compressive strain, and the critical value of the transition from the cubic to tetragonal phase was lower, indicating that phase stability was worse under tensile stresses. Therefore, during the fabrication of PSCs, the tensile stress state should be adjusted to the compressive stress state, which is favorable for enhancing PSCs photovoltaic performance and phase stability. The results not only provide direct evidence of tensile and compressive strains influencing the phase stability and optoelectronic property changes in halide perovskites, but also highlight lattice-strain tailoring for the composition design, process optimization, and interface engineering of efficient and stable PSCs.

Phase-separated porous nanocomposite with ultralow percolation threshold for wireless bioelectronics.

Realizing the full potential of stretchable bioelectronics in wearables, biomedical implants and soft robotics necessitates conductive elastic composites that are intrinsically soft, highly conductive and strain resilient. However, existing composites usually compromise electrical durability and performance due to disrupted conductive paths under strain and rely heavily on a high content of conductive filler. Here we present an in situ phase-separation method that facilitates microscale silver nanowire assembly and creates self-organized percolation networks on pore surfaces. The resultant nanocomposites are highly conductive, strain insensitive and fatigue tolerant, while minimizing filler usage. Their resilience is rooted in multiscale porous polymer matrices that dissipate stress and rigid conductive fillers adapting to strain-induced geometry changes. Notably, the presence of porous microstructures reduces the percolation threshold (Vc = 0.00062) by 48-fold and suppresses electrical degradation even under strains exceeding 600%. Theoretical calculations yield results that are quantitatively consistent with experimental findings. By pairing these nanocomposites with near-field communication technologies, we have demonstrated stretchable wireless power and data transmission solutions that are ideal for both skin-interfaced and implanted bioelectronics. The systems enable battery-free wireless powering and sensing of a range of sweat biomarkers-with less than 10% performance variation even at 50% strain. Ultimately, our strategy offers expansive material options for diverse applications.

Evaluating the effect of unidirectional loading on the piezoresistive characteristics of carbon nanoparticles

The piezoresistive effect of materials can be adopted for a plethora of sensing applications, including force sensors, structural health monitoring, motion detection in fabrics and wearable, etc. Although metals are the most widely adopted material for sensors due to their reliability and affordability, they are significantly affected by temperature. This work examines the piezoresistive performance of carbon nanoparticle (CNP) bulk powders and discusses their potential applications based on strain-induced changes in their resistance and displacement. The experimental results are correlated with the characteristics of the nanoparticles, namely, dimensionality and structure. This report comprehensively characterizes the piezoresistive behavior of carbon black (CB), onion-like carbon (OLC), carbon nanohorns (CNH), carbon nanotubes (CNT), dispersed carbon nanotubes (CNT-D), graphite flakes (GF), and graphene nanoplatelets (GNP). The characterization includes assessment of the ohmic range, load-dependent electrical resistance and displacement tracking, a modified gauge factor for bulk powders, and morphological evaluation of the CNP. Two-dimensional nanostructures exhibit promising results for low loads due to their constant compression-to-displacement relationship. Additionally, GF could also be used for high load applications. OLC’s compression-to-displacement relationship fluctuates, however, for high load it tends to stabilize. CNH could be applicable for both low and high loading conditions since its compression-to-displacement relationship fluctuates in the mid-load range. CB and CNT show the most promising results, as demonstrated by their linear load-resistance curves (logarithmic scale) and constant compression-to-displacement relationship. The dispersion process for CNT is unnecessary, as smaller agglomerates cause fluctuations in their compression-to-displacement relationship with negligible influence on its electrical performance.

Strain-induced changes in the electronic, optical and mechanical properties of the inorganic cubic halide perovskite Sr3PBr3 with FP-DFT

In recent years, inorganic perovskite materials have garnered significant attention in solar technology due to their outstanding structural, optical, mechanical, and electronic properties. A comprehensive investigation, employing first-principles density-functional theory, was conducted to assess the impact of compressive and tensile strain on the optical and electrical properties of cubic perovskite Sr3PBr3. The unstrained Sr3PBr3 exhibits a direct bandgap of 1.528 eV/2.32 eV with PBE/HSE functions at the Γ point. Under compressive strain, the bandgap decreases (1.23 eV at −4% strain), leading to a redshift in the absorption coefficient spikes, while tensile strain results in a slight bandgap increase (1.723 eV at +4 % strain) and a blueshift in absorption coefficient spikes. Total density of states was computed as 18.75 and 1.60 electrons/eV at VB and CB without strain. The value of static dielectric constant was measured as 5.24. The initial critical point of dielectric constant, large absorption peak, and maximum loss function were calculated at 1.47, 7.28, and 9.15 eV without strain. The material demonstrates excellent light absorption in the range of visible light, aligning with its electronic properties. The Sr3PBr3 perovskite is therefore thought to be perfect for usage in solar cells for the generation of power and light control.

Mechanical Stretch α-Cyclodextrin Pseudopolyrotaxane Elastomer with Reversible Phosphorescence Behavior.

Polyethylene glycol chains in two terminals of the naphthalene functional group are threaded into α-cyclodextrin cavities to form the pseudopolyrotaxane (NPR), which not only effectively induces the phosphorescence of the naphthalene functional group by the cyclodextrin macrocycle confinement, but also provides interfacial hydrogen bonding assembly function between polyhydroxy groups of cyclodextrin and waterborne polyurethane (WPU) chains to construct elastomers. The introduction of NPR endows the elastomer with enhanced mechanical properties and excellent room temperature phosphorescent(RTP) emission (phosphorescence remains in water, acid, alkali, and organic solvents, even at 160 °C high temperatures). Especially, the reversible mechanically responsive room temperature phosphorescence behavior (phosphorescence intensity increased three times under 200% strain) can be observed in the mechanical stretch and recover process, owing to strain-induced microstructural changes further inhibiting the non-radiative transition and the vibration of NPR. Therefore, changing the phosphorescence behavior of supramolecular elastomers through mechanical stretching provides a new approach for supramolecular luminescent materials.

Strain-Modulated and Nanorod-Waveguided Fluorescence in Single Zinc Oxide Nanorod-Based Immunodetection.

Mechanical strain has been shown to be a versatile and tunable means to control various properties of nanomaterials. In this work, we investigate how strain applied to individual ZnO nanorods (NRs) can affect the fluorescence signals originated from external sources of bioanalytes, which are subsequently coupled and guided onto the NRs. Specifically, we determine how factors such as the NR length and protein concentration can influence the strain-induced changes in the waveguided fluorescence intensity along the NRs. We employ a protein of tumor necrosis factor-α (TNF-α) and a fluorophore-labeled antibody in a model immunoassay reaction, after which Alexa488-TNF-α immunocomplex is formed on ZnO NRs. We elucidate the relationships between the types as well as amounts of strain on the NRs and the fluorescence intensity originated from the Alexa488-TNF-α immunocomplexes. We show that tensile (compressive) strain applied to the NR leads to an increase (decrease) in the waveguided fluorescence signals. By assessing important optical phenomena such as fluorescence intensification on nanorod ends (FINE) and degree of FINE (DoF), we confirm their linear dependence with both the types and amounts of strain. Furthermore, the strain-induced changes in both FINE and DoF are found to be independent of protein concentration. We determine that NR length plays a critical role in obtaining high strain-dependence of the measured fluorescence signals. Particularly, we ascertain that longer NRs yield larger changes in both FINE and DoF in response to the applied strain, relative to shorter ones. In addition, longer NRs permit higher linear correlation between the protein concentration and the waveguided fluorescence intensity. These outcomes provide valuable insight into exploiting strain to enhance the detection of optical signals from bioanalytes, thus enabling their quantifications even at ultra-trace levels. Coupled with the use of individual ZnO NRs demonstrated in our measurements, this work may contribute to the development of a miniaturized, highly sensitive biosensor whose signal transduction is best optimized by the application of strain.

Uniaxial Strain-Induced Stacking Order Change in Trilayer Graphene.

The layer stacking order in two-dimensional heterostructures, like graphene, affects their physical properties and potential applications. Trilayer graphene, specifically ABC-trilayer graphene, has captured significant interest due to its potential for correlated electronic states. However, achieving a stable ABC arrangement is challenging due to its lower thermodynamic stability compared to the more stable ABA stacking. Despite recent advancements in obtaining ABC graphene through external perturbations, such as strain, the stacking transition mechanism remains insufficiently explored. In this study, we unveil a universal mechanism to achieve ABC stacking, applicable for understanding ABA to ABC stacking changes induced by any mechanical perturbations. Our approach is based on a novel strain engineering technique that induces interlayer slippage and results in the formation of stable ABC domains. We investigate the underlying interfacial mechanisms of this stacking change through computational simulations and experiments. Our findings demonstrate a highly anisotropic and significant transformation of ABA stacking to large and stable ABC domains facilitated by interlayer slippage. Through atomistic simulations and local energy analysis, we systematically demonstrate the mechanism for this stacking transition, that is dependent on specific loading orientation. Understanding such a mechanism allows this material system to be engineered by design compatible with industrial techniques on a device-by-device level. We conduct Raman studies to validate and characterize the formed ABC stacking, highlighting its distinct features compared to the ABA region. Our results contribute to a clearer understanding of the stacking change mechanism and provide a robust and controllable method for achieving stable ABC domains, facilitating their use in developing advanced optoelectronic devices.

Stretchable hierarchical metal wire networks for neuromorphic emulation of nociception and anti-nociception.

Among biomimetic technologies, the incorporation of sensory hardware holds exceptional utility in human-machine interfacing. In this context, devices receptive to nociception and emulating antinociception gain significance as part of pain management. Here we report, a stretchable two-terminal resistive neuromorphic device consisting of a hierarchical Ag microwire network formed using a crack templating protocol. The device demonstrates sensitivity to strain, where the application of strain induces the formation of gaps across active elements, rendering the device electrically open. Following activation by voltage pulses, the device exhibits potentiated states with finite retentions arising from filamentary growth across these gaps due to field migration. Remarkably, the strain-induced functioning alongside controllable gaps enables achieving user-controlled neuromorphic properties, desired for self-adaptive intelligent systems. Interestingly, in the neuromorphic potentiated state, the response to strain is enhanced by ∼106 due to higher sensitivities associated with nanofilaments. The device emulates basic neuromorphic functionalities such as threshold switching, and short-term (STP) and long-term potentiations (LTP). Furthermore, the sensitivity has been exploited in mimicking nociception through strain-induced changes in the potentiated state. Interestingly, repetition of the strain stimulus leads to endurance making the device restore its conductance, thereby emulating adaptation and habituation representing the antinociceptive behavior.