Raman Spectroscopy Measurements Research Articles

Investigation of overall water splitting process on the 1 T/2H-MxCS catalyst via in situ Raman and IR spectroscopy measurement

The decomposition and formation of water molecules determine the protonation and deprotonation processes at the catalyst surface. Detecting interfacial water is particularly challenging because it is located between two condensed phases. Herein, we combine electrochemical in situ Raman and infrared spectroscopy with computational techniques to study the interfacial water on snowflake-like 1 T/2H-xMoS2/Cu2S (1 T/2H-MxCS). The snowflake-like Cu2S prevents the aggregation of modified MoS2 nanoflowers. The 1 T/2H-M0.02CS electrocatalyst exhibits excellence electrochemical performance, with a low overpotential of 59 mV and Tafel slope of 56 mV dec−1. This outstanding property can be ascribed to the interface and the formation of 1 T-MoS2, which not only decreases the activation energy required for the reduction reaction but also provides additional active sites for the catalytic reaction. Density functional theory calculations (DFT), in-situ Raman, and FT-IR spectroscopy were used to further elucidate the mechanism of electrocatalytic performance. This strategy offers new insights into enhancing the electrocatalytic activity of transition metal sulfides and a deep understanding of the HER mechanism.

Intraoperative spectroscopic evaluation of sentinel lymph nodes in breast cancer surgery.

Sentinel lymph node (SLN) biopsy is a standard procedure for patients with breast cancer and normal axilla on imaging. Positive SLNs on histological examination can lead to a subsequent surgery for axillary lymph node clearance (ALNC). Here we report a non-destructive technique based on autofluorescence (AF) imaging and Raman spectroscopy for intra-operative assessment of SLNs excised in breast cancer surgery. A microscope integrating AF imaging and Raman spectroscopy modules was built to allow scanning of lymph node biopsy samples. During AF-Raman measurements, AF imaging determined optimal sampling locations for Raman spectroscopy measurements. After optimisation of the AF image analysis and training of classification models based on data from 85 samples, the AF-Raman technique was tested on an independent set of 81 lymph nodes comprising 58 fixed and 23 fresh specimens. The sensitivity and specificity of AF-Raman were calculated using post-operative histology as a standard of reference. The independent testset contained 66 negative lymph nodes and 15 positive lymph nodes according to the reference standard, collected from 78 patients. For this set of specimens, the area under the receiver operating characteristic (ROC) curve for the AF-Raman technique was 0.93 [0.83-0.98]. AF-Raman was then operated in a regime that maximised detection specificity, producing a 94% detection accuracy: 80% sensitivity and 97% specificity. The main confounders for SLN metastasis were areas rich in histiocytes clusters, for which only few Raman spectra had been included in the training dataset. This preliminary study indicates that with further development and extension of the training dataset by inclusion of additional Raman spectra of histiocytes clusters and capsule, the AF-Raman may become a promising technique for intra-operative assessment of SLNs. Intra-operative detection of positive biopsies could avoid second surgery for axillary clearance.

Promoting Electrochemical CO2 Reduction to Formate via Sulfur‐Assisted Electrolysis

AbstractElectrochemical CO2 reduction reaction (CO2RR) provides a renewable approach to transform CO2 to produce chemicals and fuels. Unfortunately, it faces the challenges of sluggish CO2 activation and slow water dissociation. This study reports the modification of Bi‐based electrocatalyst by S, which leads to a remarkable enhancement in activity and selectivity during electrochemical CO2 reduction to formate. Based on comprehensive in situ examinations and kinetic evaluations, it is observed that the presence of S species over Bi catalyst can significantly enhance its interaction with K+(H2O)n, facilitating fast dissociation of water molecules to generate protons. Further in situ attenuated total reflectance surface‐enhanced infrared absorption spectroscopy (ATR‐SEIRAS) and in situ Raman spectroscopy measurements reveal that S modification is able to decrease the oxidation state of Bi active site, which can effectively enhance CO2 activation and facilitate HCOO* intermediate formation while suppressing competing hydrogen evolution reaction. Consequently, the S‐modified Bi catalyst achieves impressive electrochemical CO2RR performance, reaching a formate Faradaic efficiency (FEformate) of 91.2% at a formate partial current density of ≈135 mA cm−2 and a potential of −0.8 V versus RHE in an alkaline electrolyte.

Iron-based graphene composite for oxygen reduction reaction in alkaline media: Electrocatalytic activity and lifetime evaluation

The development of electrocatalysts with high catalytic performance and low costs for oxygen reduction reaction (ORR) is still challenging. Herein, an overall solution for ORR in alkaline media, from the catalyst synthesis to catalyst regeneration and to the development of a rapid, reliable and easy approach for electrode surface evaluation, is presented. We focused on the development and characterization of an efficient material for ORR in alkaline media, α-Fe2O3 N-doped graphene (Fe-N-Gr). The associative pathway for the four electron transfer ORR mechanism is sustained by the Raman spectra recorded from the electrode surface. We highlighted the possibility of catalyst regeneration by a simple electrochemical method. After two regeneration rounds and 1500 cycles in O2-saturated 1 M NaOH, the catalyst still retains 40.8 % catalytic activity. Finally, as a part of the overall solution, we demonstrated that a methodology based on Raman spectroscopic measurements and machine learning algorithms can be applied for graphene-based catalysts lifetime investigation.

Copper tantalum nitride (CuTaN2) thin films prepared by reactive radio-frequency magnetron sputtering

RF reactive sputtering was used to deposit copper tantalum nitride (CuTaN2) films from a Cu/Ta target in an environment containing a mixture of argon and nitrogen at two different substrate temperatures: room temperature and 200 °C. The films were studied by SEM, EDS, XRD, Raman spectroscopy, spectrophotometry, and resistivity measurements. The deposition conditions significantly impacted the morphology of the films, which varied from smooth, void-free films at high nitrogen concentrations and at room temperature substrates to cauliflower-like grains with voids at low nitrogen contents and elevated substrate temperatures. Despite the target’s 1:1 Cu: Ta ratio, the stoichiometric analysis showed a lower Ta content in the deposited film. The films produced on silicon substrates were polycrystalline, whereas those deposited on glass substrates were amorphous. The band gap (0.9 eV to 1.55 eV) and film resistivity (20 kΩ-cm to 76 kΩ-cm) are strongly affected by the nitrogen fraction in the sputtering gas. Increasing the nitrogen percentage in semiconductor films results in smoother films with larger bandgaps (approximately 1.5 eV), higher resistivity, and compositions closest to those of stoichiometric CuTaN2.

Enhancing Carrier Mobility in Monolayer MoS2 Transistors with Process-Induced Strain.

Two-dimensional electronic materials are a promising candidate for beyond-silicon electronics due to their favorable size scaling of electronic performance. However, a major challenge is the heterogeneous integration of 2D materials with CMOS processes while maintaining their excellent properties. In particular, there is a knowledge gap in how thin film deposition and processes interact with 2D materials to alter their strain and doping, both of which have a drastic impact on device properties. In this study, we demonstrate how to utilize process-induced strain, a common technique extensively applied in the semiconductor industry, to enhance the carrier mobility in 2D material transistors. We systematically varied the tensile strain in monolayer MoS2 transistors by iteratively depositing thin layers of high-stress MgOx stressor. At each thickness, we combined Raman spectroscopy and transport measurements to unravel and correlate the changes in strain and doping within each transistor with their performance. The transistors displayed uniform strain distributions across their channels for tensile strains of up to 0.48 ± 0.05%, at 150 nm of stressor thickness. At higher thicknesses, mechanical instability occurred, leading to nonuniform strains. The transport characteristics systematically varied with strain, with enhancement in electron mobility at a rate of 130 ± 40% per % strain and enhancement of the channel saturation current density of 52 ± 20%. This work showcases how established CMOS technologies can be leveraged to tailor the transport in 2D transistors, accelerating the integration of 2D electronics into a future computing infrastructure.

Effect of Dual-Organic Cations on the Structure and Properties of 2D Hybrid Perovskites as Scintillators.

Two-dimensional (2D) hybrid organic-inorganic perovskite (HOIP) crystals show promise as scintillating materials for wide-energy radiation detection, outperforming their three-dimensional counterparts. In this study, we synthesized single crystals of (PEA2-xBZAx)PbBr4 (x ranging from 0.1 to 2), utilizing phenethylammonium (C6H5CH2CH2NH3+) and benzylammonium (C6H5CH2NH3+) cations. These materials exhibit favorable optical and scintillation properties, rendering them suitable for high light yield (LY) and fast-response scintillators. Our investigation, employing various techniques such as X-ray diffraction (XRD), photoluminescence (PL), time-resolved (TR) PL, Raman spectroscopy, radioluminescence (RL), thermoluminescence (TL), and scintillation measurements, unveiled lattice strain induced by dual-organic cations in powder X-ray diffraction. Density functional theory analysis demonstrated a maximal 0.13 eV increase in the band gap with the addition of BZA cation addition. Notably, the largest Stokes shift of 0.06 eV was observed in (BZA)2PbBr4. The dual-organic cation crystals displayed >80% fast component scintillation decay time, which is advantageous for the scintillating process. Furthermore, we observed a dual-organic cations-induced enhancement of electron-hole transfer efficiency by up to 60%, with a contribution of >70% to the fast component of scintillation decay. The crystal with the lowest BZA concentration, (PEA1.9BZA0.1)PbBr4, demonstrated the highest LYs of 14.9 ± 1.5 ph/keV at room temperature. Despite a 55-70% decrease in LY for BZA concentrations >5%, simultaneous reductions in scintillation decay time (12-32%) may work for time-of-flight positron emission tomography and photon-counting computed tomography. Our work underscores the crucial role of dual-organic cations in advancing our understanding of 2D-HOIP crystals for materials science and radiation detection applications.

Exploring the transformation: High-dosage gamma irradiation's role in tuning structural, optical, and electrical properties of cadmium-doped lead sulfide (PbS) nanoparticles

The effects of gamma irradiation on Cadmium-doped PbS (Cd-PbS) nanoparticles are thoroughly examined in this lattice study. The study sheds light on the changes in structural, morphological, and electrical properties brought about by Cd doping and gamma irradiation by employing a variety of methods such as X-ray diffraction, FESEM imaging, EDAX analysis, Raman spectroscopy, photoluminescence (PL) spectra, and Hall effect measurements. The Cd-doped PbS shows a fluctuating crystallite size as the average size first increases by ∼3 nm and then decreases by ∼3 nm with Cd concentration. This is due to the induced strain by the Cd dopant, which has a smaller ionic radius compared to Pb ions. With Cd substitution, the bandgap of PbS first decreases from 2.29 eV to 2.19 eV and then increases with mild fluctuations. Meanwhile, gamma irradiation causes these changes, decreasing the bandgap from 2.19 eV to 2.03 eV for lower Cd concentrations (x = 0.005) and increasing it to 2.41 eV for higher concentrations (x=0.01). The Hall data shows a wide range shift in electrical characteristics between the cadmium doped gamma-irradiated sample, and the pure sample, PS0. The electrical mobility increases from 6.05 V−1s−1 for PS0 to 4.95×102 V−1s−1 for GPS3 (higher cadmium concentration of x = 0.02), indicating a significant enhancement in which charge carriers can move through the material post-irradiation. Electrical resistivity shows a drastic increase from 4.42×101 Ωcm in PS0 to 9.41×102 Ωcm in GPS3, suggesting a marked increase in electrical conductivity post-irradiation. The findings demonstrate considerable changes in crystal characteristics, morphological transformations, increased crystallinity, and changed electrical properties, showing the promise of gamma-irradiated Cd-doped PbS in advanced optoelectronic device applications.

Study on heat-treated pyrolytic carbon deposited from methane on directly heated carbon fibres

The study investigated the morphology, microstructure, structure, texture, and mechanical properties of heat-treated at 1600 °C and 2000 °C pyrolytic carbon (PyC) deposited from methane using various methods such as scanning electron microscopy (SEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), Raman spectroscopy, and ultrasonic dynamic measurements of Young's modulus. The PyC was synthesised at 1100 °C using a chemical vapour deposition (CVD) method with direct electrical heating of the two types of carbon fibres (CFs). The results showed that the PyC had a low- and medium-texture (LT and MT PyC). Analysis of the graphitization trajectory allowed the determination of structural changes in the material as a function of temperature, including the growth of crystallites and an increase in the crystallinity proportion without the significant rearrangement within PyC. The crystallite size and the number of interstitial defects has increased with temperature that controlled mechanical properties. Therefore, based on the results obtained, the most suitable composites for further research in the context of electrodes for stimulation of nervous tissue were obtained at the temperature of their synthesis, i.e. at 1100 °C.

Rapid CO2 laser treatment of Pt–Fe MOF for efficient electrochemical hydrogen evolution reaction

The quest for efficient hydrogen production via electrochemical water splitting has led to extensive research on catalytic materials. This work focuses on enhancing the catalytic functionality of metal-organic frameworks (MOFs) by incorporating platinum (Pt) to improve the performance of the hydrogen evolution reaction (HER). Fe-based MOFs mixed with platinum precursors were altered through laser treatment, which caused considerable changes in their structure and catalytic activity in just 3 min. This was achieved without the need for vacuum or an inert atmosphere. Characterization techniques including X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and electrochemical measurements were used to characterize the synthesized materials. The laser-treated Pt–Fe MOF demonstrated outstanding HER performance with 3.5 wt% Pt content, outperforming commercial 20 wt% Pt/C catalysts, and exhibiting good stability even after prolonged cycling. These results highlight the potential of laser-treated MOFs for efficient and cost-effective electrochemical hydrogen generation.

Hydrothermal Destruction and Defluorination of Trifluoroacetic Acid (TFA).

Per- and polyfluoroalkyl substances (PFAS) have received increased attention due to their environmental prevalence and threat to public health. Trifluoroacetic acid (TFA) is an ultrashort-chain PFAS and the simplest perfluorocarboxylic acid (PFCA). While the US EPA does not currently regulate TFA, its chemical similarity to other PFCAs and its simple molecular structure make it a suitable model compound for studying the transformation of PFAS. We show that hydrothermal processing in compressed liquid water transforms TFA at relatively mild conditions (T = 150-250 °C, P < 30 MPa), initially yielding gaseous products, such as CHF3 and CO2, that naturally aspirate from the solution. Alkali amendment (e.g., NaOH) promotes the mineralization of CHF3, yielding dissolved fluoride, formate, and carbonate species as final products. Fluorine and carbon balances are closed using Raman spectroscopy and fluoride ion selective electrode measurements for experiments performed at alkaline conditions, where gas yields are negligible. Qualitative FTIR gas analysis allows for establishing the transformation pathways; however, the F-balance could not be quantitatively closed for experiments without NaOH amendment. The kinetics of TFA transformation under hydrothermal conditions are measured, showing little to no dependency on NaOH concentration, indicating that the thermal decarboxylation is a rate-limiting step. A proposed TFA transformation mechanism motivates additional work to generalize the hydrothermal reaction pathways to other PFCAs.

TiO2 multi-leg nanotubes for surface-enhanced Raman scattering

Abstract In the recent past, significant research efforts have been put forth to fabricate cost-effective substrates for surface-enhanced Raman scattering (SERS) applications. Here we propose semiconducting TiO2 multi-leg nanotubes and Au nanoparticle-coated TiO2 multi-leg nanotubes (TiO2 MLNTs and Au/TiO2 MLNTs) as SERS substrates. The unique multi-leg architecture of TiO2 nanotubes demonstrated enhanced light-harvesting properties facilitated by an induced photonic absorption edge. Remarkable high SERS sensitivity is observed towards the detection of Methylene blue (MB), up to nM concentration (E.F. ~104) using TiO2 MLNTs. The same is attributed to the resonantly matched photonic absorption edge of TiO2 MLNTs with the wavelength of incident laser probe light. On the other hand, the Au nanoparticle coating further leveraged the light absorption ability of TiO 2 MLNTs with the aid of localized surface plasmon resonance mode (LSPRs). As such, Au/TiO2 MLNTs showed excellent enhancement in SERS sensitivity (E.F. ~105, for nM of MB) facilitated by the synergy between the plasmonic modes of Au and the photonic absorption mode of TiO2 MLNTs. UV-Vis diffuse reflectance and Raman spectroscopy measurements are highlighted to elucidate the light absorption and SERS sensitivity of the TiO2 and Au/TiO2 MLNTs.

Silicon-tin thin-film anodes for low and high power-density lithium-ion batteries

Silicon (Si) is a promising replacement material for graphite, the commonly utilized anode material in lithium-ion batteries (LIBs). Si has a theoretical specific capacity up to 11 times higher than that of graphite. However, pure Si has two main issues: high electronic resistivity and significant volume change during charge/discharge cycling. To overcome these issues, Si was alloyed with high-conductivity materials. In this contribution, physical vapor deposition was utilized to produce binderless silicon-tin anodes for LIBs. Tin is a lithium-active alloying material that has high electrical conductivity and high specific capacity (i.e., up to three times that of graphite). Electronic resistivity, residual film stress, X-ray photoelectron spectroscopy, Raman spectroscopy, and cyclic voltammetry measurements were performed to thoroughly analyze the deposited Si-Sn films and help understand their charge/discharge cycling performance at low and high C-rates. At a low C-rate of 0.5 C, the alloyed films did not show any improvement compared to pure Si. However, the alloyed films showed better performance compared to pure Si when tested at a high C-rate of 10 C. Si-Sn films with (40 – 50 wt.% Sn) were able to retain a specific capacity of around 680 mAh g−1 after 1000 cycles.

Influence of multilayers Bernal and Rhombohedral graphene obtained by green chemistry on the acceleration in the germination process of tomato seeds

The environmental ramifications stemming from the application of graphene-based materials have sparked significant interest in recent years. This study delved into assessing the influence of multilayer graphene, specifically focusing on the Bernal (2H) and Rhombohedral (3R) phases, on the germination process of tomato (Solanum lycopersicum) seeds. Multilayers Bernal-Rhombohedral Graphene (MBRG) were synthesized employing green chemistry principles, utilizing the ultrasonication technique operating at 40 kHz within a deionized water solution. Systematic characterization of the phases was conducted via X-ray diffraction, Raman Spectroscopy, TEM, and conductivity measurements. Subsequent administration of MBRG at concentrations ranging from 10 to 500 mgL−1 on tomato seeds revealed an expedited germination process, achieving completion within 3 days. Noteworthy enhancements were observed, including a 12 % absolute increase in germination, a 3 % rise in relative root growth, and a 9 % elevation in the germination index compared to the control. Moreover, a discernible augmentation in root length was evident with escalating concentrations of MBRG, peaking at 50 mgL−1, albeit exhibiting a slight decrement at 500 mgL−1. Additionally, the antioxidant activities of root extracts were assessed across various MBRG concentrations, demonstrating no significant alterations. The outcomes posit that MBRG compositions, comprising 60.44 % (2H) and 39.55 % (3R) phases at specific concentrations, hold promise as a viable additive for expediting early seed germination, thereby presenting a potential sustainable solution in agricultural contexts.

Correlation of Structural Changes and Hydrogen Diffusion in Polycrystalline WO3 Thin Films by Combining In Situ Transmission Measurements and Raman Spectroscopy

AbstractDiffusion in polycrystalline tungsten trioxide (WO3) thin films is studied in a lateral geometry to better understand the impact of hydrogen‐induced structural phase transitions on the diffusion. WO3 thin films are coated with polymethylmethacrylate layer (PMMA). The latter is microstructured in such a way that a narrow stripe‐like gap occurs in the PMMA layer exposing the surface of the WO3 thin film. This stripe serves as the contact to the electrolyte in the intercalation experiment with hydrogen. After intercalation, the lateral diffusion of hydrogen inside WO3 below the PMMA layer can be observed, increasing the analyzable path and time scale by several orders of magnitude compared to the film thickness, thus, significantly improving spatial and temporal resolution of in situ transmission and Raman measurements. Spatially resolved transmission measurements in the wavelength range of 633±55 nm show that the diffusion process is dependent on hydrogen concentration and exhibits two regimes describable by different diffusion coefficients. Time‐resolved Raman spectroscopic measurements at different distances from the electrolyte contact area show that the switching between the two diffusion coefficients occurs at the phase transition from the orthorhombic to the tetragonal phase. The results are further supported by a simulation. The measurement approach is universally applicable for electrochromic films or multilayers.

Investigating the effects of Mn content on the morphology and dielectric properties of CdS nanoparticles

CdS nanoparticles doped with Mn were synthesized by chemical precipitation using varying concentrations of Mn at Cd1-xMnxS, where (x) = 0.00, 0.03, 0.05, and 0.07. The samples were examined using scanning electron microscopy (SEM), energy dispersive X-ray techniques (EDX), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, dielectric properties, and AC conductivity measurements. SEM micrograph shows that pure CdS nanomaterial has agglomerates primarily composed of nanoparticles, whereas the sample with a concentration of 0.03 contains smaller particles. In response to the phonon confinement effect, The Raman spectra of CdS nanoparticles exhibited peaks at 303 cm−1 and 603 cm−1. In contrast, the Raman spectra of Mn:CdS nanocomposites displayed a prominent fundamental mode at 301 cm−1 and a less pronounced overtone mode at 601 cm−1. The dielectric properties and the AC conductivity of CdS have been investigated over a wide frequency range of 0.1 Hz to 10 MHz and at a variety of temperatures ranging from 298 to 423K. The real and imaginary parts of the complex dielectric constant (εʹ, εʹʹ), the electric modulus, and AC conductivity of CdS were found to depend on Mn content at different temperatures.

Correlation of Visible Reflectance Spectrometry and Portable Raman Data for Red Pigment Identification

The accurate identification of pigments is of principal relevance in the field of cultural heritage conservation and restoration practices. In this preliminary study, a first attempt to set up a procedure for accurate red pigment identification, based on the assessment of the correlations existing between visible reflectance spectrometry (vis-RS) and Raman data, is presented. The proposed approach involved the realization of a library consisting of data acquired on a set of 35 pure red historical pigments supplied by ©Kremer Pigmente. In particular, vis-RS data, collected through a Konica Minolta CM-2600d spectrophotometer, were registered, together with the position of the Extrema Points (E.P.s) encompassing both the maximum and minimum points of the first derivative of the % spectral reflectance factor (SRF%) curves. Portable Raman spectroscopy measurements were collected by a B&amp;W Tek Inc. portable Raman spectrometer equipped with a 785 nm laser. For each tested pigment, the positions and relative intensities of the characteristic Raman peaks were considered. The library was then tested for the characterization of the red/reddish painted areas of the medieval wall painting located within The Norman Castle of Aci Castello (Catania, Italy), and was shown to be essential for the unambiguous identification of the pigment used. It is worth noting that this study represents the first novel attempt to establish a reliable and efficient methodology for pigment identification, offering promising prospects in reducing uncertainties and ambiguities arising from the application of a single stand-alone approach.

Gradient OH Desorption Facilitating Alkaline Hydrogen Evolution Over Ultrafine Quinary Nanoalloy

AbstractStrengthening OH adsorption on electrocatalyst is crucial to promote the rate‐determining water dissociation step of alkaline hydrogen evolution reaction (HER), whereas too‐intensified OH adsorption will poison the active sites instead. This dilemma remains one of the major challenges for improving the electrocatalysts’ alkaline HER activities. Herein, a surprising finding that the strongly adsorbed OH on an ultrafine quinary PtCoCuNiZn nanoalloy can be facilely desorbed via a unique gradient OH desorption pattern is reported, which tremendously boosts its alkaline HER activity. Theoretical simulations unravel that the ultrafine PtCoCuNiZn nanoalloy possesses versatile metal sites for adsorbing OH and the strongly adsorbed OH can be gradiently transferred to desorb from the ultrafine PtCoCuNiZn nanoalloy with moderate energy barriers for each transfer step that is the gradient OH desorption. In the meanwhile, the unique gradient OH desorption mode on the ultrafine PtCoCuNiZn nanoalloy is also experimentally evidenced by the in situ Raman spectroscopy and cyclic voltammetry measurements. This finding offers a fresh opportunity to expedite the alkaline HER without compromising the OH adsorption strength on electrocatalysts, which thus maximally promotes their water dissociation properties and unlocks the full potential of their alkaline HER activities.

Identification of compressive strain in thin ferroelectric Al1–x Sc x N films by Raman spectroscopy

Compressive strain in thin ferroelectric Al1–x Sc x N films with different Sc atom concentrations (x) on sapphire substrates was identified by Raman spectroscopy measurement. Both E2 H and A1(LO) spectra showed a blue shift while thinning the Al1–x Sc x N film thicknesses. The shift was enhanced with higher Sc atom concentration. A stress of the order of 200 MPa was applied from the substrate interface, resulting in a strain of the order of 10−4. The presence of the compressive strain at the bottom interface can be correlated to the increase in the coercive field for thinner Al1–x Sc x N films.

Epitaxial growth and characterization of (110)-oriented YBCO/PBCGO bilayer and YBCO/PBCGO/YBCO trilayer heterostructures

We have grown and characterized (110)-oriented YBa2Cu3O7−x (YBCO)/PrBa2(Cu0.8Ga0.2)3O7−x (PBCGO) bilayer and YBCO/PBCGO/YBCO trilayer heterostructures, which were deposited by pulsed laser deposition technique for the nanofabrication of (110)-oriented YBCO-based superconductor (S)/insulator (I)/superconductor (S) tunneling vertical geometry Josephson junction and other superconductor electronic devices. The structural properties of these heterostructures, investigated through various x-ray diffraction techniques (profile, x-ray reflectivity, pole figure, and reciprocal mapping), showed (110)-oriented epitaxial growth with a preferred c-axis-in-plane direction for all layers of the heterostructures. The atomic force microscopy measurement on the top surface of the heterostructures showed crack-free and pinhole-free, compact surface morphology with about a few nanometer root mean square roughness over the 5 × 5 μm2 region. The electrical resistivity measurements on the (110)-direction of the heterostructures showed superconducting critical temperature (Tc) values above 77 K and a very small proximity effect due to the interfacial contact of the superconducting YBCO layers with the PBCGO insulating layer. Raman spectroscopy measurements on the heterostructures showed the softening of the Ag-type Raman modes associated with the apical oxygen O(4) and O(2)-O(3)-in-phase vibrations compared to the stand-alone (110)-oriented PBCGO due to the residual stress and additional two Raman modes at ∼600 and ∼285 cm−1 frequencies due to the disorder at the Cu–O chain site of the PBCGO. The growth process and structural, electrical transport, and Raman spectroscopy characterization of (110)-oriented YBCO/PBCGO bilayer and YBCO/PBCGO/YBCO trilayer heterostructures are discussed in detail.