다중혈관 관상동맥 환자에서 y-문합을 이용하여 양쪽 내흉동맥만을 사용한 우회술의 조기 성적

The need to develop inexpensive renewable energy sources stimulates scientific research for efficient, low-cost photovoltaic devices.1 The organic, polymer-based photovoltaic elements have introduced at least the potential of obtaining cheap and easy methods to produce energy from light.2 The possibility of chemically manipulating the material properties of polymers (plastics) combined with a variety of easy and cheap processing techniques has made polymer-based materials present in almost every aspect of modern society.3 Organic semiconductors have several advantages: (a) lowcost synthesis, and (b) easy manufacture of thin film devices by vacuum evaporation/sublimation or solution cast or printing technologies. Furthermore, organic semiconductor thin films may show high absorption coefficients4 exceeding 105 cm-1, which makes them good chromophores for optoelectronic applications. The electronic band gap of organic semiconductors can be engineered by chemical synthesis for simple color changing of light emitting diodes (LEDs).5 Charge carrier mobilities as high as 10 cm2/V‚s6 made them competitive with amorphous silicon.7 This review is organized as follows. In the first part, we will give a general introduction to the materials, production techniques, working principles, critical parameters, and stability of the organic solar cells. In the second part, we will focus on conjugated polymer/fullerene bulk heterojunction solar cells, mainly on polyphenylenevinylene (PPV) derivatives/(1-(3-methoxycarbonyl) propyl-1-phenyl[6,6]C61) (PCBM) fullerene derivatives and poly(3-hexylthiophene) (P3HT)/PCBM systems. In the third part, we will discuss the alternative approaches such as polymer/polymer solar cells and organic/inorganic hybrid solar cells. In the fourth part, we will suggest possible routes for further improvements and finish with some conclusions. The different papers mentioned in the text have been chosen for didactical purposes and cannot reflect the chronology of the research field nor have a claim of completeness. The further interested reader is referred to the vast amount of quality papers published in this field during the past decade.

Conjugated polymer-based organic solar cells

Peptides or proteins convert under some conditions from their soluble forms into highly ordered fibrillar aggregates. Such transitions can give rise to pathological conditions ranging from neurodegenerative disorders to systemic amyloidoses. In this review, we identify the diseases known to be associated with formation of fibrillar aggregates and the specific peptides and proteins involved in each case. We describe, in addition, that living organisms can take advantage of the inherent ability of proteins to form such structures to generate novel and diverse biological functions. We review recent advances toward the elucidation of the structures of amyloid fibrils and the mechanisms of their formation at a molecular level. Finally, we discuss the relative importance of the common main-chain and side-chain interactions in determining the propensities of proteins to aggregate and describe some of the evidence that the oligomeric fibril precursors are the primary origins of pathological behavior.

/pdf/protein-misfolding-functional-amyloid-and-human-disease-2w386pwb7k.pdf

Protein Misfolding, Functional Amyloid, and Human Disease

Research in the use of organic polymers as the active semiconductors in light-emitting diodes has advanced rapidly, and prototype devices now meet realistic specifications for applications. These achievements have provided insight into many aspects of the background science, from design and synthesis of materials, through materials fabrication issues, to the semiconductor physics of these polymers.

Electroluminescence in conjugated polymers

We review the dynamical mean-field theory of strongly correlated electron systems which is based on a mapping of lattice models onto quantum impurity models subject to a self-consistency condition. This mapping is exact for models of correlated electrons in the limit of large lattice coordination (or infinite spatial dimensions). It extends the standard mean-field construction from classical statistical mechanics to quantum problems. We discuss the physical ideas underlying this theory and its mathematical derivation. Various analytic and numerical techniques that have been developed recently in order to analyze and solve the dynamical mean-field equations are reviewed and compared to each other. The method can be used for the determination of phase diagrams (by comparing the stability of various types of long-range order), and the calculation of thermodynamic properties, one-particle Green's functions, and response functions. We review in detail the recent progress in understanding the Hubbard model and the Mott metal-insulator transition within this approach, including some comparison to experiments on three-dimensional transition-metal oxides. We present an overview of the rapidly developing field of applications of this method to other systems. The present limitations of the approach, and possible extensions of the formalism are finally discussed. Computer programs for the numerical implementation of this method are also provided with this article.

Dynamical mean-field theory of strongly correlated fermion systems and the limit of infinite dimensions

Mechanism of thioflavin T binding to amyloid fibrils

Degradation-induced changes in the structural and optical properties of the polyfluorene-based blue emitting films and LEDs are examined using spectroscopic (FTIR, UV−vis, photo- and electroluminescence), analytical (FTIR and ESCA), and scanning probe microscopy techniques. The materials studied are oligomers (DP ∼ 10) of 9,9-di-n-hexylfluorene and its random copolymer with anthracene. In situ FTIR monitoring is used to characterize chemical changes in the active layer of operating LED devices. Two primary mechanisms of degradation are identified. In the first, photooxidation of the polymer matrix leads to the formation of an aromatic ketone, most likely fluorenone at the chain terminating monomer units, which quenches the fluorescence. The second process promotes aggregate formation, which then leads to loss of luminous intensity by exciton transfer and relaxation through excimers.

Electrical and Photoinduced Degradation of Polyfluorene Based Films and Light-Emitting Devices

We have studied polyaniline and polyethylenedioxythiophene transparent electrodes for use as hole-injecting anodes in polymer light emitting diodes. The anodes were doped with a variety of polymer and monomer-based acids and cast from either water or organic solvents to determine the effect of the dopant and solvent on the hole-injection properties. We find that the anodes with polymeric dopants have improved device quantum efficiency and brightness relative to those with small molecule dopants, independent of conductivity, solvent, or type of conducting polymer. For the most conducting polymer anodes [σ>2(Ωcm)−1], diodes could be made without an indium tin oxide underlayer. These diodes show substantially slower degradation.

/pdf/polymeric-anodes-for-improved-polymer-light-emitting-diode-1f6kjhs7rq.pdf

Polymeric anodes for improved polymer light-emitting diode performance

[19] Since the mixing ratio of the anions in the solution from which the crystals were grown was revealed to be almost identical to the stoichiometry determined by EPMA of the obtained crystal, the mixing ratio of the anions in the solution was adopted in the chemical formula of the crystal The results of EPMA of k-(BETS)2FexGa1‐xBr10Cl30 are: for x = 050, Fe/Ga/Br/Cl = 051:049:113:285 (050:050:100:300); for x = 040, Fe/Ga/Br/Cl = 040:060:096:287 (040:060:100:300); for x = 030, Fe/Ga/Br/Cl = 032:068:111:307 (030:070:100:300); for x = 020, Fe/Ga/Br/Cl = 024:076:111:316 (020:080:100:300); for x = 010, Fe/Ga/Br/Cl = 012:088:104:322 (010:090:100:300) [20] Recent susceptibility measurements revealed that the angle between the easy axis of the antiferromagnetic structure and the c axis is about 35 in k-(BETS)2FeCl4 (E Ojima, T Sasaki, private communication) While the easy axis of k-(BETS)2FeBr06Cl34 is approximately parallel to the b* axis

http://physics.ucsc.edu/~sacarter/arango2000.pdf

Efficient Titanium Oxide/Conjugated Polymer Photovoltaics for Solar Energy Conversion

We have studied the transport properties of electron- and hole-dominated MEH-PPV, poly(2-methoxy,5-(2′-ethyl-hexoxy)-p-phenylene vinylene), devices in the trap-free limit and have derived the temperature-dependent electron and hole mobilities (μ=μ0eγ√E) from the space-charge-limited behavior at high electric fields. Both the zero-field mobility μ0 and electric-field coefficient γ are temperature dependent with an activation energy of the hole and electron mobility of 0.38±0.02 and 0.34±0.02 eV, respectively. At 300 K, we find a zero-field mobility μ0 on the order of 1±0.5×10−7 cm2/V s and an electric-field coefficient γ of 4.8±0.3×10−4 (m/V)1/2 for holes. For electrons, we find a μ0 an order of magnitude below that for holes but a larger γ of 7.8±0.5×10−4 (m/V)1/2. Due to the stronger field dependence of the electron mobility, the electron and hole mobilities are comparable at working voltages in the trap-free limit, applicable to thin films of MEH-PPV.

Sue A. Carter

Papers

Mechanism of thioflavin T binding to amyloid fibrils

Electrical and Photoinduced Degradation of Polyfluorene Based Films and Light-Emitting Devices

Polymeric anodes for improved polymer light-emitting diode performance

Efficient Titanium Oxide/Conjugated Polymer Photovoltaics for Solar Energy Conversion

Temperature- and field-dependent electron and hole mobilities in polymer light-emitting diodes