Professor Ming-Chang
Lin,
Fellow of Academia Sinica,
Taiwan (R.W. Woodruff Professor Emeritus of Emory
University, USA)
Title
of Plenary Speech
Quantum Chemical
Simulations of Processes Occurring in
ComplexChemical Systems from Combustion
to Water Splitting
Abstract of Plenary Speech
Selected examples on
the merit of quantum chemical
simulations for elucidation of complex
mechanisms involved in combustion,
propulsion and solar water splitting
systems will be presented. Specifically,
the kinetics and mechanisms for nitrogen
oxide formation in hydrocarbon
combustion, the combustion initiation
reactions in N2O4-hydrazines
and ammonium perchlorate propulsion
systems, and the synergistic effects of
metal doping in TiO2
nanoparticles with hydrogenation for
water splitting will be discussed, based
on the results from state-of-the-art
quantum chemical calculations for
comparison with available experimental
data.
Professor Kahar
Bin Osman,
Chair of School of Biomedical Engineering &
Health Sciences,
Universiti Teknologi Malaysia, Malaysia
Title
of Plenary Speech
Customised Stent Design
Abstract of Plenary Speech
In some cases, especially in neonates,
ductus arteriosus needs to remain patent
for multiple medical purposes. In order
to achieve this, current practice
involves inserting stent in the ductus
arteriosus. This condition is called
patent ductus arteriosus (PDA). For this
process, stents such as coronary stent
are commonly used due to unavailability
of customized stent for PDA in neonates.
The usage of coronary stent however,
opens the possibility of acute stent
thrombosis and other complications.
Therefore, there is a high need of
special and customized stents to be used
for PDA in neonates. This customized
stent has to be able to sustain the
hemodynamic effects of the flow inside
the PDA. The stent has to be able to
support the ductus wall compression and
contraction due to arterial compliance.
What is more important is that the stent
must properly fit into various
morphologies of the ductus. In addition,
the stent has to be tested for
biocompatibility and practicality.
Therefore, the customized design of the
PDA stents can be derived from the
concept of coronary stents and in
compliance with all the mentioned
characteristics. However, further
analysis has to be completed ensure
proper compatibility with neonates. In
conclusion, the biggest challenge is to
customize a stent that fits all the PDA
morphologies.
Dong-Sing Wuu*
Fellows of SPIE, OSA, IOP
Lifetime Distinguished Professor
Department of Materials
Science and Engineering,
National Chung Hsing
University, Taichung 40227, Taiwan
*E-mail address: dsw@nchu.edu.tw
Title of
Keynote Speech
Passive-Matrix Micro-LED
Displays with Advanced Process Integration
Abstract of
Keynote Speech
The light-emitting diode
(LED) is a self-emissive device with high
response time, brightness, and color saturation
properties. It possesses the high thermal and
humid stability, which is suitable as a next
generation displays. However, for achieving the
high resolution, the pixel size should be
downsized into a few micron scale. In this
study, the pixel size of micro-LED was
investigated from 100×100
μm2 to a 10×10
μm2, where a laser direct writing
technique was employed. The direct writing
technique does not need the photomask and can
improve the exposure accuracy with minimized
image distortion. However, for the smaller pixel
sizes, the plasma damage from the dry-etched
sidewall of pixel became more evident and would
degrade the light extraction efficiency.
Therefore, the surface passivation processes
e.g. spin coating, PECVD, ALD have plays an
important role in determining the leakage
current levels. As a result, the external
quantum efficiency of 10×10
μm2 pixel size can achieve 18.81%
under a current density of 136.8 A/cm2.
The brightness of blue micro-LED display with a
pixel size of 20 x 20 μm2 was 516 cd/m2 at 3 V under the full lighting
state. Using the advanced process integration,
the performance of the blue, green and red
passive-matrix micro-LED displays with 150-250
pixel-per-inch resolution will be described.
Future applications of these small-size
micro-LED displays will also be discussed.
Dr. Srinath Rajagopal,
Senior Research Scientist of National Physical
Laboratory,
United Kingdom
Title of
Keynote Speech
Metrology in Medical Ultrasound
Abstract of
Keynote Speech
The earliest application of ultrasound in
medicine dates back to 1940s when its
therapeutic effects were demonstrated by
successfully destroying brain tissue in animals.
It was nearly after a decade later the first
diagnostic capability of ultrasound in the
detection of breast carcinoma was reported. The
ultrasound-induced damage to tissue in therapy
did not go unnoticed as the diagnostic use of
ultrasound continued to rise in the 1950s and
1960s especially in monitoring of foetal
development. In 1980s US Food and Drug
Administration initiated the regulation of
diagnostic ultrasound equipment. The regulation
placed restriction on the ultrasound exposure
level, which has been adopted by the
manufacturers globally.
The ultrasound exposure levels are quantified by
the measurement of the two key quantities,
pressure and power. These two quantities
represent potential mechanical and thermal
damage to tissue under certain excitation
conditions. Manufacturers are required to
perform measurements under a number of different
operational conditions to demonstrate equipment
safety. The devices used to make measurements of
pressure and power must be traceable to
International System of Units (SI) via their
calibration at a National Measurement Institute
(NMI) for example, National Physical Laboratory,
U.K or National Measurement Laboratory, Taiwan.
Hydrophones are used to make the measurement of
the dynamic pressure of ultrasound and whereas
Radiation Force Balance (RFB) is to measure the
ultrasound power. The highest measurement
standards applied in the determination of a
physical quantity is known as a primary
standard. The primary standards for ultrasound
pressure and power along with systematic
effects, which affect the measurement quality,
traceability and dissemination will be
described. The emerging technologies in medical
ultrasound poses new challenges to measurement
and recent efforts to address these challenges
will also be covered.