K. P. Mohanchandra

Giant electric-field-induced reversible and permanent magnetization reorientation on magnetoelectric Ni/(011) [Pb(Mg1/3Nb2/3)O3](1−x)–[PbTiO3]x heterostructure

We report here an atomic resolution study of the structure and composition of the grain boundaries in polycrystalline Sr0.6K0.4Fe2As2 superconductor. A large fraction of grain boundaries contain amorphous layers larger than the coherence length, while some others contain nanometer-scale particles sandwiched in between amorphous layers. We also find that there is significant oxygen enrichment at the grain boundaries. Such results explain the relatively low transport critical current density (Jc) of polycrystalline samples with respect to that of bicrystal films.We report giant reversible and permanent magnetic anisotropy reorientation in a magnetoelectric polycrystalline Ni thin film and (011)-oriented [Pb(Mg1/3Nb2/3)O3](1−x)–[PbTiO3]x heterostructure. The electric-field-induced magnetic anisotropy exhibits a 300 Oe anisotropy field and a 50% change in magnetic remanence. The important feature is that these changes in magnetization states are stable without the application of an electric field and can be reversibly switched by an electric field near a critical value (±Ecr). This giant reversible and permanent magnetization change is due to remanent strain originating from a non-180° ferroelectric polarization reorientation when operating the ferroelectric substrate in a specific non-linear regime below the electric coercive field.

Domain engineered switchable strain states in ferroelectric (011) [Pb(Mg1/3Nb2/3)O3](1−x)-[PbTiO3]x (PMN-PT, x≈0.32) single crystals

The ferroelectric properties of (011) [Pb(Mg1/3Nb2/3)O3](1−x)-[PbTiO3]x (PMN-PT, x≈0.32) single crystals with focus on piezoelectric strain response were reported. Two giant reversible and stable remanent strain states and tunable remanent strain properties are achieved by properly reversing the electric field from the depolarized direction. The unique piezoelectric strain response, especially along the [100] direction, mainly stems from the non-180° ferroelectric polarization reorientation in the rhombohedral phase crystal structure. Such giant strain hysteresis with tunable remanent strain properties may be useful for magnetoelectric based memory devices as well as a potential candidate for other applications.

Reversible magnetic domain-wall motion under an electric field in a magnetoelectric thin film

We report direct microscopic measurements that confirm the magnetic stripe-domain patterns can be reversibly changed under an electric field due to the converse magnetoelectric effect in a bilayer thin film ferromagnetic-Ni/ferroelectric-lead zirconate titanate (100nm∕1.28μm) heterostructure. Electric field-induced curving, bending, branching, and elongation of magnetic stripe-domain patterns in the Ni layer are observed with the use of magnetic force microscopy. Upon removal of the electric field, the magnetic stripe-domain patterns return to their original configuration, i.e., reversible.

Examination of the sputtering profile of NiTi under target heating conditions

In this paper we have examined compositional shifts in NiTi film sputter-deposited from a heated and a cooled target. Substrates were radially placed at 18° intervals to capture the semicircular sputtering profile. The composition of the film was measured using Rutherford backscattering spectroscopy (RBS). Film thickness values were measured and the atomic flux captured was calculated. Results indicate that the target temperature significantly influences the composition of the sputtered film. It was found that, for cold targets, Ni and Ti sputter at different angles, producing a compositional shift in the film when compared with the target. For hot targets the sputtering angle is influenced to a lesser degree, such that the compositional shift is negligible. Therefore, target temperature appears to represent an approach to alter the stoichiometry of films deposited.

Thin-film nitinol (NiTi): A feasibility study for a novel aortic stent graft material

OBJECTIVE Although technological improvements continue to advance the designs of aortic stent grafts, miniaturization of the required delivery systems would allow their application to be available to a wider range of patients and potentially decrease the access difficulties that are encountered. We performed this feasibility study to determine if thin-film NiTi (Nitinol) could be used as a covering for stent grafts ranging from 16 mm to 40 mm in diameter. Specifically, we wished to determine the profile reduction attainable and improve the flexibility of our design. METHODS Using a novel hot-sputter deposition technique, we created sheets of thin-film NiTi (TFN) with a tensile strength of >500 Megapascal (MPa) and thickness of 5-10 microns. TFN was used to cover stents, which were then deployed in vitro. Patterned thin film was fabricated via a lift-off technique; grafts were constructed with stents ranging from 16-40 mm and deployed in a pulsatile flow system from the smallest diameter polymer tubing into which the stent and TFN would fit. The bending/stiffness ratio vs similar sized expanded polytetrafluoroethylene (ePTFE)-covered stents was also determined. RESULTS TFN was created in both non-patterned and patterned forms, with a tensile strength of >100 MPa for the latter. We created devices that were successfully deployed via delivery systems half the size of fabric-covered stent grafts (ie, the 16 mm stent graft that originally was delivered via a 16French (F) system was reduced to 8F, and the 40 mm stent graft delivered via a 24F system was reduced to 12F). No migration of the devices was observed with deployment in both straight and curved tubing, which was sized so that the stent grafts were oversized by 20%. Both forms of the thin-film were noted to be more flexible than the same sized ePTFE stent graft, and the patterned graft had an additional 15-30% flexibility vs the non-patterned film. CONCLUSION These in vitro results demonstrate the feasibility of TFN for covering stent grafts designed for placement in the aorta. The delivery profile can be significantly reduced across a wide range of sizes, while the material remained more flexible than ePTFE.

Super Hydrophilic Thin Film Nitinol Demonstrates Reduced Platelet Adhesion Compared with Commercially Available Endograft Materials

BACKGROUND Thin film nitinol (TFN) is a novel material with which to cover stents for the treatment of a wide range of vascular disease processes. This study aimed to show that TFN, if treated to produce a super hydrophilic surface, significantly reduces platelet adhesion, potentially rendering covered stents more resistant to thrombosis compared to commercially available materials. MATERIALS AND METHODS TFN was fabricated using a sputter deposition process to produce a 5-μ thin film of uniform thickness. TFN then underwent a surface treatment process to create a super hydrophilic layer. Platelet adhesion studies compared surface treated TFN (S-TFN) to untreated TFN, polytetrafluoroethylene, Dacron, and bulk nitinol. In vivo swine studies examined the placement of an S-TFN covered stent in a 3.5 mm diameter external iliac artery. Angiography confirmed placement, and repeat angiography was performed at 2 wk followed by post mortem histopathology. RESULTS S-TFN significantly reduced platelet adhesion without any evidence of aggregation compared with all materials studied (P < 0.05). Furthermore, in vivo swine studies demonstrated complete patency of the S-TFN covered stent at 2 wk. Post mortem histopathology showed rapid endothelialization of the S-TFN without excessive neointimal hyperplasia. CONCLUSIONS These results demonstrate that S-TFN significantly reduces platelet adhesion and aggregation compared with commercially available endograft materials. Furthermore, the hydrophilic surface may confer thromboresistance in vivo, suggesting that S-TFN is a possible superior material for covering stents.

In vitro hemocompatibility of thin film nitinol in stenotic flow conditions.

Because of its low profile and biologically inert behavior, thin film nitinol (TFN) is ideally suited for use in construction of endovascular devices. We have developed a surface treatment for TFN designed to minimize platelet adhesion by creating a superhydrophilic surface. The hemocompatibility of expanded polytetrafluorethylene (ePTFE), untreated thin film nitinol (UTFN), and a surface treated superhydrophilic thin film nitinol (STFN) was compared using an in vitro circulation model with whole blood under flow conditions simulating a moderate arterial stenosis. Scanning electron microscopy analysis showed increased thrombus on ePTFE as compared to UTFN or STFN. Total blood product deposition was 6.3 ± 0.8 mg/cm(2) for ePTFE, 4.5 ± 2.3 mg/cm(2) for UTFN, and 2.9 ± 0.4 mg/cm(2) for STFN (n = 12, p < 0.01). ELISA assay for fibrin showed 326 ± 42 μg/cm(2) for ePTFE, 45.6 ± 7.4 μg/cm(2) for UTFN, and 194 ± 25 μg/cm(2) for STFN (n = 12, p < 0.01). Platelet deposition measured by fluorescent intensity was 79,000 20,000 AU/mm(2) for ePTFE, 810 ± 190 AU/mm(2) for UTFN, and 1600 ± 25 AU/mm(2) for STFN (n = 10, p < 0.01). Mass spectrometry demonstrated a larger number of proteins on ePTFE as compared to either thin film. UTFN and STFN appear to attract significantly less thrombus than ePTFE. Given TFNs low profile and our previously demonstrated ability to place TFN covered stents in vivo, it is an excellent candidate for use in next-generation endovascular stents grafts.

Thermoelectric power of CdS and CdSe films deposited on vibrating substrates

Abstract The effect of substrate vibration at ultrasonic frequencies on thermoelectric properties (TEP) during the evaporation of CdS and CdSe films has been studied in detail. The temperature variation of the TEP has been explained. The carrier concentration n c and Fermi energy E F of the films deposited on vibrating and nonvibrating substrates are compared. It is found that the effect of in situ substrate vibration during deposition is to decrease the extrinsic behaviour of the films by improving the stoichiometry.

Deposition and characterization of Ti–Ni–Pd and Ti–Ni–Pt shape memory alloy thin films

Thin films of Ti–Ni–Pd and Ti–Ni–Pt shape memory alloys were produced by a DC magnetron sputtering process. Targets with the following compositions were studied: Ti54Ni16Pd30, Ti54Ni6Pd40, Ti54Ni3Pd43 and Ti54Ni26Pt20. The films were deposited on SiO2/Si substrates at ambient temperature and were crystallized in situ at 550 °C for 1 h. X-ray diffraction data show that the crystal structure of the martensitic phase is orthorhombic (B19) for all films and texturing is present in the Ti–Ni–Pt films. TEM micrographs show that both Ti–Ni–Pd and Ti–Ni–Pt films have a well defined twin structure at ambient temperature. Transformation temperatures were determined by both DSC and wafer curvature methods. The results indicate that as the Pd content increases to 43 at.% the transformation temperature Af, austenite finish temperature, increases up to 516 °C. For the Ti–Ni–Pt film, at 20 at.% Pt, the austenite finish temperature is 422 °C compared to 273 °C for Ti–Ni–Pd at 30 at.% Pd. Experimental data also demonstrate that all the films fabricated exhibit the classic shape memory effect.

In vitro and in vivo testing of a novel, hyperelastic thin film nitinol flow diversion stent.

A flexible, low profile, flow diversion stent could replace endovascular coiling for the treatment of intracranial aneurysms. Micropatterned-thin film nitinol (TFN) is a novel biomaterial with high potential for use in next-generation endovascular devices. Recent advancements in micropatterning have allowed for fabrication of a hyperelastic thin film nitinol (HE-TFN). In this study, the authors describe in vitro and in vivo testing of novel HE-TFN based flow diverting stents. Two types of HE-TFN with expanded pores having long axes of 300 and 500 μm were used to fabricate devices. In vitro examination of the early thrombotic response in whole blood showed a possible mechanism for the devices function, whereby HE-TFN serves as a scaffold for blood product deposition. In vivo testing in swine demonstrated rapid occlusion of model wide-neck aneurysms. Average time to occlusion for the 300-μm device was 10.4 ± 5.5 min. (N = 5) and 68 ± 30 min for the 500-μm device (N = 5). All aneurysms treated with bare metal control stents remained patent after 240 min (N = 3). SEM of acutely harvested devices supported in vitro results, demonstrating that HE-TFN serves as a scaffold for blood product deposition, potentially enhancing its flow-diverting effect. Histopathology of devices after 42 days in vivo demonstrated a healthy neointima and endothelialization of the aneurysm neck region. HE-TFN flow-diverting stents warrant further investigation as a novel treatment for intracranial aneurysms.