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1.
Nanotechnology ; 28(48): 485601, 2017 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-29105645

RESUMO

GaN microrods are used as a basis for subsequent InGaN quantum well (QW) and quantum dot deposition by metal-organic vapor phase epitaxy. The coverage of the shell along the sidewall of rods is dependent on the rod growth time and a complete coverage is obtained for shorter rod growth times. Transmission electron microscopy measurements are performed to reveal the structural properties of the InGaN layer on the sidewall facet and on the top facet. The presence of layers in the microrod and on the microrod surface will be discussed with respect to GaN and InGaN growth. A detailed model will be presented explaining the formation of multiple SiN layers and the partial and full coverage of the shell around the core. Cathodoluminescence measurements are performed to analyze the InGaN emission properties along the microrod and to study the microresonator properties of such hexagonal core-shell structures. High quality factor whispering gallery modes with [Formula: see text] are reported for the first time in a GaN microrod/InGaN non-polar QW core-shell geometry. The GaN/InGaN core-shell microrods are expected to be promising building blocks for low-threshold laser diodes and ultra-sensitive optical sensors.

2.
Nano Lett ; 16(6): 3415-25, 2016 06 08.
Artigo em Inglês | MEDLINE | ID: mdl-27187840

RESUMO

Vertically aligned hexagonal InN nanorods were grown mask-free by conventional metal-organic vapor phase epitaxy without any foreign catalyst. The In droplets on top of the nanorods indicate a self-catalytic vapor-liquid-solid growth mode. A systematic study on important growth parameters has been carried out for the optimization of nanorod morphology. The nanorod N-polarity, induced by high temperature nitridation of the sapphire substrate, is necessary to achieve vertical growth. Hydrogen, usually inapplicable during InN growth due to formation of metallic indium, and silane are needed to enhance the aspect ratio and to reduce parasitic deposition beside the nanorods on the sapphire surface. The results reveal many similarities between InN and GaN nanorod growth showing that the process despite the large difference in growth temperature is similar. Transmission electron microscopy, spatially resolved energy-dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Raman spectroscopy have been performed to analyze the structural properties. Spatially resolved cathodoluminescence investigations are carried out to verify the optical activity of the InN nanorods. The InN nanorods are expected to be the material of choice for high-efficiency hot carrier solar cells.

3.
Nanoscale ; 8(8): 4529-36, 2016 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-26661036

RESUMO

High-quality fabrication of plasmonic devices often relies on wet-chemically grown ultraflat, presumably single-crystalline gold flakes due to their superior materials properties. However, important details about their intrinsic structure and their optical properties are not well understood yet. In this study, we present a synthesis routine for large flakes with diameters of up to 70 µm and an in-depth investigation of their structural and optical properties. The flakes are precisely analyzed by transmission electron microscopy, electron backscatter diffraction and micro-ellipsometry. We found new evidence for the existence of twins extending parallel to the Au flake {111} surfaces which have been found to not interfere with the presented nanopatterning. Micro-Ellipsometry was carried out to determine the complex dielectric function and to compare it to previous measurements of bulk single crystalline gold. Finally, we used focused ion beam milling to prepare smooth crystalline layers and high-quality nanostructures with desired thickness down to 10 nm to demonstrate the outstanding properties of the flakes. Our findings support the plasmonics and nano optics community with a better understanding of this material which is ideally suited for superior plasmonic nanostructures.

4.
Gene Ther ; 14(3): 191-202, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16957769

RESUMO

We examined the efficacy and host response to the adenovirus (Ad)-mediated delivery of human apolipoprotein A-I (APOA1) gene to the liver of APOA1(-/-) mice. Administration of a first-generation vector (FGAd-AI) resulted in a transient appearance of APOA1 in plasma and induced an anti-APOA1 antibody titer, whereas treatment with a helper-dependent vector (HDAd-AI) resulted in sustained APOA1 expression without inducing an antibody titer. With these results, we studied the effects of FGAd vectors on APOAI expression by HDAd-AI vector. Co-treatment with an FGAd vector inhibited HDAd-AI- mediated APOA1 expression independent of transgene cassettes, but only FGAd-AI induced a humoral response. Furthermore, APOA1 mRNA levels in mice co-treated with FGAd vectors were much lower than those expected from the vector copy number, suggesting that DNA of FGAd vectors interferes with the HDAd-AI vector's APOA1 promoter. A single treatment with an HDAd-AI vector produced a supraphysiological plasma APOA1 level that gradually declined to about half the normal human level over the course of 2 years, associated with a plasma cholesterol level that is persistently higher than that in controls. This investigation provides the proof of principle that liver-directed HDAd gene delivery is effective for the long-term phenotypic correction of monogenic hypoalphalipoproteinemia.


Assuntos
Adenoviridae/genética , Apolipoproteína A-I/genética , Terapia Genética/métodos , Vetores Genéticos/administração & dosagem , Vírus Auxiliares/genética , Hipoalfalipoproteinemias/terapia , Adenoviridae/imunologia , Animais , Apolipoproteína A-I/análise , Apolipoproteína A-I/imunologia , Autoanticorpos/sangue , Colesterol/sangue , Feminino , Expressão Gênica , Vetores Genéticos/genética , Vetores Genéticos/imunologia , Humanos , Hipoalfalipoproteinemias/imunologia , Hipoalfalipoproteinemias/metabolismo , Injeções , Fígado/metabolismo , Fígado/patologia , Fígado/virologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Modelos Animais , Fenótipo , Transdução Genética/métodos , Transgenes , Carga Viral
5.
J Phys Chem B ; 110(1): 58-61, 2006 Jan 12.
Artigo em Inglês | MEDLINE | ID: mdl-16471499

RESUMO

This communication reports on the growth of highly uniform KNbO3 nanowires exhibiting a narrow diameter distribution around 60 nm and a length-to-width ratio up to 100. The nanowires were prepared by a hydrothermal route, which enables simple, gram-scale production. A systematic study of the synthesized nanowires in terms of the morphological and chemical characteristics was carried out by varying the temperature-pressure conditions and the composition of the starting mixture. The results indicate that highly uniform single-crystalline nanowires form within a narrow window of the ternary phase diagram of KOH-Nb2O5-H2O.


Assuntos
Nanoestruturas/química , Nióbio/química , Óxidos/química , Potássio/química , Cristalização , Tamanho da Partícula , Difração de Pó , Pressão , Temperatura
6.
Gene Ther ; 11(20): 1540-8, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15269711

RESUMO

We tested the efficacy of low-density lipoprotein receptor (LDLR) therapy using helper-dependent adenovirus (HD-Ad), comparing it with that of very low-density lipoprotein receptor (VLDLR), an LDLR homolog. We treated high cholesterol diet fed LDLR-/- mice with a single intravenous injection of HD-Ad expressing monkey LDLR (1.5 x 10(13) or 5 x 10(12) VP/kg) or VLDLR. Throughout the 24-week experiment, plasma cholesterol of LDLR-treated mice was lower than that of VLDLR-treated mice, which was in turn lower than that of PBS-treated mice. Anti-LDLR antibodies developed in 2/10 mice treated with high-dose HD-Ad-LDLR but in none (0/14) of the other treatment groups. HD-Ad-treated mice displayed significant retardation of atherosclerotic lesion progression. We next tested the long-term efficacy of low-dose HD-Ad-LDLR injected into 12-week-old LDLR-/- mice. After 60 weeks, atherosclerosis lesions covered approximately 50% of the surface of aortas of control mice, whereas aortas of treated mice were essentially lesion-free. The lipid lowering effect of HD-Ad-LDLR lasted at least 108 weeks (>2 years) when all control mice had died. In addition to retarding lesion progression, treatment caused lesion remodeling from a vulnerable-looking to a more stable-appearing phenotype. In conclusion, HD-Ad-mediated LDLR gene therapy is effective in conferring long-term protection against atherosclerosis in a mouse model of familial hypercholesterolemia.


Assuntos
Arteriosclerose/prevenção & controle , Terapia Genética/métodos , Hiperlipoproteinemia Tipo II/terapia , Receptores de LDL/genética , Transdução Genética/métodos , Adenoviridae/genética , Adenoviridae/imunologia , Animais , Sequência de Bases , Progressão da Doença , Vetores Genéticos/administração & dosagem , Vetores Genéticos/genética , Hiperlipoproteinemia Tipo II/imunologia , Hiperlipoproteinemia Tipo II/metabolismo , Camundongos , Camundongos Knockout , Modelos Animais , Dados de Sequência Molecular , Receptores de LDL/metabolismo , Linfócitos T Auxiliares-Indutores/imunologia , Fatores de Tempo
7.
Opt Lett ; 26(11): 792-4, 2001 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-18040452

RESUMO

La/B(4)C multilayers have been fabricated by magnetron sputtering for use as x-ray mirrors at energies below 190 eV, particularly for detection of boron K and alpha x rays at 183 eV, their performance has been compared with that of Mo/B(4)C multilayers, which are currently the best-performing multilayers for this energy range. Transmission electron microscopy and synchrotron soft-x-ray reflectometry were used to study the structural quality of the multilayers and their performance as x-ray mirrors. The results show a significant improvement of the peak reflectivity and the spectral purity, indicating that La/B(4)C has a high potential to replace Mo/B(4)C in many x-ray optical applications below 190 eV.

8.
Phys Rev B Condens Matter ; 51(24): 17780-17794, 1995 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-9978811
11.
Phys Rev B Condens Matter ; 40(2): 1277-1281, 1989 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-9991954
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