Crack Resistance in Ceramics – From Thin Films to Bulk Materials

Author(s):  
Vladimir Vishnyakov ◽  
◽  
B.D. Beake ◽  
S.V. Chornobuk ◽  
O.Ju. Popov ◽  
...  
2000 ◽  
Vol 361-362 ◽  
pp. 130-134 ◽  
Author(s):  
M.E Beck ◽  
T Weiss ◽  
D Fischer ◽  
S Fiechter ◽  
A Jäger-Waldau ◽  
...  

2006 ◽  
Vol 05 (04n05) ◽  
pp. 627-631 ◽  
Author(s):  
M. J. SUN ◽  
G. P. ZHAO ◽  
J. LIANG ◽  
G. ZHOU ◽  
H. S. LIM ◽  
...  

A simplified micromagnetic model has been proposed to calculate the hysteresis loops of nanostructured permanent magnets for various configurations, including thin films, exchange-coupled double-layer systems and bulk materials. The reversal part of the hysteresis is based on the Stoner–Wohlfarth coherent rotational model and the coercivity mechanism is due mainly to the motion of the transition region (a domain wall like magnetic moment distribution in the grain boundary). The elements of nucleation and pinning models are also incorporated.


2005 ◽  
Vol 15 (2) ◽  
pp. 3585-3588 ◽  
Author(s):  
A. Verdyan ◽  
Y.M. Soifer ◽  
J. Azoulay ◽  
E. Rabkin ◽  
M. Kazakevich

Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1331 ◽  
Author(s):  
Franck Tessier

Nitrogen (and also oxygen) determination has become an important parameter to characterize (oxy)nitride materials for many properties and applications. Analyzing such anions with accuracy is still a challenge for some materials. However, to date, a large panel of methodologies is available to answer this issue with relevant results, even for thin films. Carrier gas hot extraction techniques and electron probe microanalysis with wavelength dispersive spectroscopy (EPMA-WDS) look attractive to analyze bulk materials and thin films, respectively. This paper gathers several techniques using chemical and physical routes to access such anionic contents. Limitations and problems are pointed out for both powders and films.


1991 ◽  
Vol 243 ◽  
Author(s):  
Jhing–Fang Chang ◽  
Chi Kong Kwok ◽  
Seshu B. Desu

AbstractBoth La and Nd–doped PZT, i.e., PLZT and PNZT, ferroelectric thin films were prepared by the metalorganic deposition (MOD) process. The precursor solutions used were derived from lead acetate, lanthanum acetylacetonate, neodymium acetate, zirconium n–propoxide, and titanium iso–propoxide. The dopant concentration of the films analyzed by electron microprobe indicated a one–to–one correspondence between film composition and the composition of the precursor from which the film was made. In this study, the effects of Nd and La dopants in PZT films on Curie temperature was determined by in–situ hot–stage TEM and compared with those of bulk materials. Lattice parameter and phase transformation were determined by both X–ray and electron diffraction. Our observations were: (1) Curie temperature decreases with increasing dopant concentration for both thin foils and bulk ceramics, (2) for a given dopant concentration, Curie temperature and crystal tetragonality of PNZT thin foils is lower than those of PLZT samples, (3) Curie temperature of thin foils was found to be less than those of the corresponding bulk materials, and (4) ferroelectric domains is easily observed in both PLZT and PNZT TEM specimens prepared by the spin–coating method.


2015 ◽  
Vol 2015 (DPC) ◽  
pp. 000827-000864
Author(s):  
Li-Anne Liew ◽  
David T. Read ◽  
Nicholas Barbosa

We describe bend testing on micro-scale specimens of 302 stainless steel, using a MEMS test instrument. Bend testing is a common way of measuring the flexural stiffness of structural materials across many size scales, from thin laminate sheets to large weldments. Whereas the stiffness of a material under tensile loading is given by the Young's Modulus, the flexural stiffness, or the stiffness in bending, is much lower. In the past two decades, conventional materials testing machines and the specimens themselves have undergone miniaturization for the purpose of evaluating the mechanical properties of miniaturized mechanical components such as sensors and biomedical implants, for which the smallest specimen dimension is typically around 1 mm [2]. Another driver for miniaturizing the testing apparatuses is to test materials with inherently small form factors such as wires and thin films [3]. Now the emerging 3D printing technology is creating another need for material property measurement at micrometer size scales, to accurately capture the property gradients resulting from the layered manufacturing. However, with ever increasing miniaturization comes increasing difficulty in specimen handling, gripping, and alignment. Concurrently, MEMS technology has been used over the past 2 decades to fabricate small actuators and sensors for mechanical testing of materials of thin films [4] or nanoscale materials such as nanowires. We seek to use the advantages of MEMS to study the mechanical properties of bulk materials rather than thin films, but at the micrometer scale. We believe this will result in greater accuracy and spatial resolution of property measurements of structural materials used in civil infrastructure, aerospace, transportation and energy industries, as well as characterizing manufacturing processes that lead to steep property gradients such as 3D printed components. Our approach is to use MEMS actuators as chip-scale re-useable test instruments into which small specimens sectioned from bulk materials can be inserted and tested [5], to reduce the cost and time to obtain large data sets and to allow the measurements to be done in-situ in harsh environments. We will describe the design of a micro-size 302 stainless steel specimen, and the use of a MEMS test instrument for performing the bend testing on the specimens. The specimen's gage section was 350 um long, 65 um wide and 25 um thick, and was made by lithographic etching of a foil. The MEMS test instrument was fabricated from silicon and glass wafers. The specimens were inserted into the MEMS test chip and the silicon actuator applied static bending loads to the specimen. Displacements were measured from optical microscope images, and the force was calculated from the applied voltage and the known (measured) stiffness of the silicon actuator. The applied force from the MEMS actuator was measured directly, without any specimen, using a custom table-top force probe and load cell apparatus, and was in agreement with the force calculated from the applied voltage. The flexural stiffness of the micro specimens were measured, using the MEMS test device, at 90 – 130 N/m. These values were validated by independently testing the specimens with the much larger table-top force probe. We thus show that our MEMS test chip can be used to perform bending tests on micro scale specimens of bulk materials, but with a 1000-fold reduction in size compared to table-top force-measuring apparatuses.


2002 ◽  
Vol 720 ◽  
Author(s):  
Daniel Potrepka ◽  
Steven Tidrow ◽  
Arthur Tauber ◽  
Kevin Kirchner ◽  
Bernard Rod ◽  
...  

AbstractThin films were prepared from bulk targets by pulsed-laser deposition techniques. The targets were composed of Ba0.6Sr0.4TiO3 with charge-compensated substitutions for Ti4+. Results of the dielectric characterization measurements will be discussed and compared to the results of similar measurements in bulk materials with the same composition.


2006 ◽  
Vol 950 ◽  
Author(s):  
Sabrina Jedlicka ◽  
Silas J. Leavesley ◽  
Kenneth M Little ◽  
J. Paul Robinson ◽  
David E. Nivens ◽  
...  

ABSTRACTFunctional relationships between the biomaterial interface and extracellular matrix (ECM) proteins are intimately involved in cellular adhesion and function. Structural changes of ECM proteins upon adsorption to a surface alter the protein's biological activity by varying the availability of molecular binding sites. Recent work using native and organically modified sol-gel silica as a neuronal biointerface revealed that changes in surface nanotopography of bulk versus thin film materials result in dramatic differences in fibronectin structure, cell survival, and neuronal differentiation. In order to further investigate interactions between chemical functionality and surface topography, we evaluated the global conformation of human fibronectin adsorbed to seven different organically modified silica gels and thin films. Chemical functional groups were introduced into the materials either by altering the starting precursor or by doping with poly-l-lysine or polyethylenimine. Surface topography measurements by atomic force microscopy show that films have surface features less than 25 nm while bulk materials of the same precursor chemistry have features ranging from 50 – 100 nm in size. Fluorescence resonance energy transfer spectroscopy (FRET) revealed a strong interaction between surface topography and chemical functionality. Fibronectin remain globular on all bulk materials regardless of chemical modification. The same changes in precursors or dopant chemistry, however, induced changes in the conformation of fibronectin on the thin films. The differentiation of PC12 cells on the surface indicated a strong impact of the surface features and suggest a possible optimal fibronectin folding state.


Sign in / Sign up

Export Citation Format

Share Document