Physics of Discrete Impurities under the Frameworkof Device Simulations for Nanostructure Devices.

Localized impurities doped in the semiconductor substrate of nanostructure devices play anessential role in understanding and resolving transport and variability issues in device characteristics.Modeling discrete impurities under the framework of device simulations is, therefore, an urgent needfor reliable prediction of device performance via device simulations. In the present paper, we discussthe details of the physics associated with localized impurities in nanostructure devices, which areinherent, yet nontrivial, to any device simulation schemes: The physical interpretation and the roleof electrostatic Coulomb potential in device simulations are clarified. We then show that a naiveintroduction of localized impurities into the Poisson equation leads to a logical inconsistency withinthe framework of the drift-diffusion simulations. We describe a systematic methodology for how totreat the Coulomb potential consistently with both the Poisson and current-continuity (transport)equations. The methodology is extended to the case of nanostructure devices so that the effects of theinterface between different materials are taken into account.

Material challenges for solar cells in the twenty-first century: directions in emerging technologies.

Photovoltaic generation has stepped up within the last decade from outsider status to one of the important contributors of the ongoing energy transition, with about 1.7% of world electricity provided by solar cells. Progress in materials and production processes has played an important part in this development. Yet, there are many challenges before photovoltaics could provide clean, abundant, and cheap energy. Here, we review this research direction, with a focus on the results obtained within a Japan-French cooperation program, NextPV, working on promising solar cell technologies. The cooperation was focused on efficient photovoltaic devices, such as multijunction, ultrathin, intermediate band, and hot-carrier solar cells, and on printable solar cell materials such as colloidal quantum dots.

Analyzing the Vacuolar Membrane (Tonoplast) Proteome.

A large number of proteins in the vacuolar membrane (VM; tonoplast), including transporters and receptors, support the various functions of the vacuole. Molecular analysis of membrane proteins is an essential step in understanding how the vacuole operates but so far only a small number of tonoplast proteins have been identified at the molecular level. Accordingly, mutant lines with altered level of tonoplast proteins for characterizing their physiological roles have been developed sparsely. Also, detecting activities of tonoplast proteins remains difficult as it requires a certain degree of enrichment of this organelle fraction. In order to extend our understanding of the vacuole, several groups have turned to proteomic analysis of tonoplast membrane proteins. A primary requirement of any organelle analysis by proteomics is that the purity of the isolated organelle needs to be high so that its composition can be accurately analyzed with mass spectrometry. In this chapter, we describe a simple method for the isolation of intact vacuoles and subsequent proteome analysis of the VM fraction of cells from Arabidopsis suspension cultures.

Intermediate-band dynamics of quantum dots solar cell in concentrator photovoltaic modules.

We report for the first time a successful fabrication and operation of an InAs/GaAs quantum dot based intermediate band solar cell concentrator photovoltaic (QD-IBSC-CPV) module to the IEC62108 standard with recorded power conversion efficiency of 15.3%. Combining the measured experimental results at Underwriters Laboratory (UL®) licensed testing laboratory with theoretical simulations, we confirmed that the operational characteristics of the QD-IBSC-CPV module are a consequence of the carrier dynamics via the intermediate-band at room temperature.

Studies on vacuolar membrane microdomains isolated from Arabidopsis suspension-cultured cells: local distribution of vacuolar membrane proteins.

The local distribution of both the vacuolar-type proton ATPase (V-ATPase) and the vacuolar-type proton pyrophosphatase (V-PPase), the main vacuolar proton pumps, was investigated in intact vacuoles isolated from Arabidopsis suspension-cultured cells. Fluorescent immunostaining showed that V-PPase was distributed evenly on the vacuolar membrane (VM), but V-ATPase localized to specific regions of the VM. We hypothesize that there may be membrane microdomains on the VM. To confirm this hypothesis, we prepared detergent-resistant membranes (DRMs) from the VM in accordance with well established conventional methods. Analyses of fatty acid composition suggested that DRMs had more saturated fatty acids compared with the whole VM in phosphatidylcholine and phosphatidylethanolamine. In the proteomic analyses of both DRMs and detergent-soluble mebranes (DSMs), we confirmed the different local distributions of V-ATPase and V-PPase. The observations of DRMs with an electron microscope supported the existence of different areas on the VM. Moreover, it was observed using total internal reflection fluorescent microscopy (TIRFM) that proton pumps were frequently immobilized at specific sites on the VM. In the proteomic analyses, we also found that many other vacuolar membrane proteins are distributed differently in DRMs and DSMs. Based on the results of this study, we discuss the possibility that VM microdomains might contribute to vacuolar dynamics.

Dynamic aspects of ion accumulation by vesicle traffic under salt stress in Arabidopsis.

The intracellular membrane dynamics of Arabidopsis cells under high salt treatment were investigated. When Arabidopsis was treated with high levels of NaCl in hydroponic culture, root tip cells showed rapid changes in the vacuolar volume, a decrease in the number of small acid compartments, active movement of vesicles and accumulation of Na(+) both in the central vacuole and in the vesicles around the main vacuole observed with the Na(+)-dependent fluorescence of Sodium Green. Detailed observation of Arabidopsis suspension-cultured cells under high salt treatment showed a similar pattern of response to that observed in root tip cells. Immunostaining of suspension-cultured cells with antibodies against AtNHX1 clearly showed the occurrence of dotted fluorescence in the cytoplasm only under salt treatment. We also confirmed the existence of AtNHX1 in the vacuolar membrane isolated from suspension-cultured cells with immunofluorescence. Knockout of the vacuolar Q(a)-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) protein VAM3/SYP22 caused an increase in salt tolerance. In mutant plants, the distribution of Na(+) between roots and shoots differed from that of wild-type plants, with Na(+) accumulating more in roots and less in the shoots of the mutant plants. The role of vesicle traffic under salt stress is discussed.

Involvement of actin filaments in rhizoid morphogenesis of Spirogyra.

The role of actin filaments in rhizoid morphogenesis was studied in Spirogyra. When the algal filaments were severed, new terminal cells started tip growth and finally formed rhizoids. Actin inhibitors, latrunculin B and cytochalasin D, reversibly inhibited the process. A mesh-like structure of actin filaments (AFs) was formed at the tip region. Gd(3+) inhibited tip growth and decreased AFs in the tip region. Either a decrease in turgor pressure or lowering of the external Ca(2+) concentration also induced similar results. It was suggested that the mesh-like AF structure is indispensable for the elongation of rhizoids. A possible organization mechanism of the mesh-like AF structure was discussed.

Adjustment of osmotic pressure coupled with change of growth mode in Spirogyra.

Spirogyra living in running water forms a rhizoid which anchors it to the substratum. Rhizoid differentiation can be induced in the laboratory by severing algal filaments. The terminal cell changes the growth mode from diffuse growth to tip growth, and finally differentiates to be a rhizoid. We found that the intracellular osmolarity of the rhizoid was significantly lower than that of other interjacent cells which did not form rhizoids. The decrease in the intracellular osmolarity began before the start of tip growth. TEA, a K+ channel blocker, inhibited the decrease in the intracellular osmolarity of the terminal cells; increase in the external K+ also inhibited this. It was suggested that K+ efflux through K+ channel is involved in the adjustment of osmotic pressure. When the adjustment of osmotic pressure was inhibited, tip growth did not start, inevitably, no rhizoid was formed. In Spirogyra sp. which was unable to form rhizoids, the terminal cell did not show the adjustment of osmotic pressure. Thus, this adjustment seems to be intimately coupled with the rhizoid differentiation. Possible roles of the adjustment of osmotic pressure in rhizoid differentiation are discussed.