Relevant bibliographies by topics / J-Aggregate

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'J-Aggregate'

Author: Grafiati
Published: 4 June 2021
Last updated: 29 May 2022

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Journal articles on the topic "J-Aggregate"

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MAITI, NAKUL C., SHYAMALAVA MAZUMDAR, and N. PERIASAMY. "J- and H-Aggregates of Porphyrins with Surfactants: Fluorescence, Stopped Flow and Electron Microscopy Studies." Journal of Porphyrins and Phthalocyanines 02, no. 05 (October 1998): 369–76. http://dx.doi.org/10.1002/(sici)1099-1409(199807/10)2:4/5<369::aid-jpp92>3.0.co;2-3.

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The interaction of cationic surfactants such as CTAB (cetyl trimethyl ammonium bromide) with tetrakis-(4-sulfonato phenyl) porphine ( H 4 TPPS 2−), a dianion, leads to the formation of two premicellar aggregates of porphyrin when [CTAB] is below CMC (critical micelle concentration) and a micellized monomer when [CTAB] is above CMC. The premicellar aggregates are labeled as J- and H-aggregates because of their characteristic spectroscopic properties. Simple inorganic cations such as K +, Ba 2+, Ca 2+ and Zr 4+ also induce the formation of the J-aggregate but not of the H-aggregate. The formation of the J-aggregate is preceded by kinetic intermediates, while no intermediate was observed prior to the formation of the H-aggregate. The rate of formation of the H-aggregate was faster than that of the J-aggregate. The fluorescence depolarization (anisotropy) properties of the monomer and the H- and J-aggregates were studied and compared. The size and structure of the J-aggregate were examined by transmission electron microscopy (TEM). The structure of the J-aggregate reveals a fiber-like (linear stacking) or domain-like (helical stacking) arrangement of the porphyrin molecules.
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Ma, Suqian, Yingjie Liu, Jibo Zhang, Bin Xu, and Wenjing Tian. "Polymorphism-Dependent Enhanced Emission in Molecular Aggregates: J-Aggregate versus X-Aggregate." Journal of Physical Chemistry Letters 11, no. 24 (December 7, 2020): 10504–10. http://dx.doi.org/10.1021/acs.jpclett.0c02917.

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Hu, Shu, Yang Liao, Yang Zhang, Xiaoliang Yan, Zhenlu Zhao, Weiqiang Chen, Xin Zhang, et al. "Effect of Thermal Annealing on Conformation of MEH-PPV Chains in Polymer Matrix: Coexistence of H- and J-Aggregates." Polymers 12, no. 8 (August 7, 2020): 1771. http://dx.doi.org/10.3390/polym12081771.

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In diluted solid solution using poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene) (MEH-PPV) and polymethyl methacrylate (PMMA) or polystyrene (PS), both aggregated and extended conformations could be formed according to the weight ratio. Aggregated conformation in as-cast MEH-PPV/PMMA film presented a J-aggregate-like photoluminescence (PL) emission. After annealing at 160 °C, its PL showed characteristics of both J- and H-aggregates at the same time; however, extended conformation showed an oligomer-like emission, which was not sensitive to either measurement temperature or annealing temperature. Thus, the conformation transition between aggregated and extended is unlikely to happen in MEH-PPV/PMMA blends during thermal annealing. On the contrary, in MEH-PPV/PS blends, extended conformation dominated in as-cast film with oligomer-like emissions; after annealing at 160 °C, both J- and H- aggregate-like PL emissions were observed, indicating the conformation transitioned from extended to aggregated. Therefore, our work may suggest a new method to manipulate photophysical properties of conjugated polymers by combining appropriate host matrix and thermal annealing processes.
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Belko, Nikita V., Michael P. Samtsov, and Anatoly P. Lugovski. "Controlling H*- and J-aggregation of an indotricarbocyanine dye in aqueous solutions of inorganic salts." Journal of the Belarusian State University. Physics, no. 2 (June 2, 2020): 19–27. http://dx.doi.org/10.33581/2520-2243-2020-2-19-27.

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Aggregation process of a symmetrical cationic indotricarbocyanine dye in aqueous medium was studied. It was shown that self-assembled H*-aggregates with an absorption peak at 514 nm as well as J-aggregates with an absorption peak at 777 nm can be obtained. Both of the aggregate types are non-fluorescent. High concentration of a desired aggregate type can be obtained and stabilized by changing ionic strength and pH of the solution. At ionic strength of 170 mmol/L and pH 7.4 J-aggregates are stable. Decreasing pH as well as ionic strength leads to demise of J-aggregates and concomitant formation of H*-aggregates. Increasing temperature leads to a faster H*-aggregate formation. The type of aggregates can be changed by heating and subsequent cooling of the solution. An organic compound forming both H*- and J-aggregates has never been observed before. The fact that the H*- and J-bands are narrow, the shift between them is significant, the J-band is located in the far-red spectral region, and the type of aggregates can be controlled makes these objects promising for future applications.
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Anantharaman, Surendra B., Daniel Messmer, Amin Sadeghpour, Stefan Salentinig, Frank Nüesch, and Jakob Heier. "Excitonic channels from bio-inspired templated supramolecular assembly of J-aggregate nanowires." Nanoscale 11, no. 14 (2019): 6929–38. http://dx.doi.org/10.1039/c8nr10357g.

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Kato, Noritaka, Keiji Yamamoto, and Yoshiaki Uesu. "Aqueous Dispersions of J-Aggregates and J-Aggregate-Doped Silica Bulk Gels." Japanese Journal of Applied Physics 46, no. 8A (August 6, 2007): 5318–20. http://dx.doi.org/10.1143/jjap.46.5318.

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Melnik, A. D., T. S. Zhebit, A. B. Krylov, S. G. Pukhovskaya, Yu B. Ivanova, and M. M. Kruk. "FORMATION OF J-AGGREGATES OF THE 21-THIA-5,10,15,20-TETRA-(4-SULFONATOPHENYL)-PORPHYRIN IN WATER SOLUTIONS." Journal of Applied Spectroscopy 89, no. 2 (March 18, 2022): 177–83. http://dx.doi.org/10.47612/0514-7506-2022-89-2-177-183.

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The formation of J-aggregates of 21-thia-5,10,15,20-tetra-(4-sulfonatophenyl)-porphyrin in acidified water solutions is herein revealed for the first time and their spectral-luminescent properties are measured. It is shown that the spectral-luminescent properties of J-aggregates are due to the excitonic interactions, and the number of coherent interacting monomeric porphyrin molecules in the aggregate is evaluated. It is found that J-aggregates of heteroporphyrin have fluorescence, and the fluorescence quantum yield Фfl is found to be as low as 1.8 . 10–4. The photolability of J-aggregates is found, namely, upon J-aggregate photoexcitation to the absorption band at 503 nm they collapse to the monomeric doubly protonated molecules. The process of photomonomerisation is reversible: upon keeping the solution in the dark, J-aggregates form again.
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Белько, Н. В., М. П. Самцов, and А. А. Луговский. "Спектральные свойства индотрикарбоцианинового красителя в процессе самоорганизации его H-=SUP=-*-=/SUP=-- и J-агрегатов." Журнал технической физики 128, no. 11 (2020): 1627. http://dx.doi.org/10.21883/os.2020.11.50165.84-20.

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Self-assembly of H*- and J-aggregates of an indotricarbocyanine dye in phosphate buffered saline was investigated. At pH value of 7.0 the dye studied was shown to form non-luminescent H*-aggregates with the absorption band peaked at 516 nm, its FWHM being 35 nm (1303 cm-1), whereas, J-aggregates are absent. At pH value of 7.4 the H*-aggregates are not formed, whereas, the J-aggregates are observed. The absorption band of the J-aggregates is peaked at 777 nm, its FWHM being 30 nm (497 cm-1). Photoluminescence quantum yield of the J-aggregates does not exceed 10-6. An increase in the solution temperature from 20 to 31oC results in a 25-fold decrease in the self-assembly time of the H*-aggregates. An increase in the solution temperature from 20 to 80oC is followed by a reversible decay of both the H*- and J-aggregates. The H*-aggregate (J-aggregate) absorption band is reduced two-fold at the solution temperature of 37oC (32oC). Thansitions of the dye aggregates to high-lying electronic excited states were evidenced in the steady-state absorption in the spectral range between 400 and 480 nm.
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Wojtyk, James, Andrew McKerrow, Peter Kazmaier, and Erwin Buncel. "Quantitative investigations of the aggregation behaviour of hydrophobic anilino squaraine dyes through UV/vis spectroscopy and dynamic light scattering." Canadian Journal of Chemistry 77, no. 5-6 (June 1, 1999): 903–12. http://dx.doi.org/10.1139/v99-073.

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In continuing studies of the aggregation behaviour of squaraine dyes in DMSO-water mixtures, we have examined a series of symmetrical anilino-based squaraines with increasing N-alkyl chain length (n-butyl, n-octyl, and n-dodecyl). The aggregation behaviour was assessed through UV/vis spectroscopic and Dynamic Light Scattering (DLS) studies with quantitative interpretation based on exciton theory. This class of N-alkyl squaraines forms two distinct solution aggregates, Type J and Type H, depending on the composition of the DMSO-water medium. DLS measurement of the aggregates in the Type J and Type H morphologies showed that (i) the particle diameter increased with increasing hydrophobicity; (ii) DMSO has a large effect on the aggregate size; (iii) Type J aggregates are of equal dimensions with Type H aggregates. Moreover, even though as the DMSO-water solvent composition is varied the UV/vis spectra of Type H and Type J aggregates remained unchanged, the number of molecules comprising each aggregate varies widely. It is proposed that the dynamic conversion (J →> H) results from intramolecular reorganization of individual molecules within the aggregate. Quantification of aggregation through DLS has further developed the "kinetic" versus "thermodynamic" control model of dye aggregation.Key words: squaraine, dynamic light scattering, DMSO-water mixtures, self-assembly, kinetic/thermodynamic control.
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Rhodes, Samuel, Wenlang Liang, Xiaochen Wang, Nitin Ramesh Reddy, and Jiyu Fang. "Transition from H-Aggregate Nanotubes to J-Aggregate Nanoribbons." Journal of Physical Chemistry C 124, no. 21 (May 1, 2020): 11722–29. http://dx.doi.org/10.1021/acs.jpcc.0c02908.

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Dissertations / Theses on the topic "J-Aggregate"

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Bradley, Michael Scott. "Engineering J-aggregate cavity exciton-polariton devices." Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/53196.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2009.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 143-159).
Research efforts in solution-based dye lasers and organic light-emitting devices (OLEDs) have led to advances in materials engineering and fabrication technology, propelling the field of organic solid-state photonics. Active areas of photonic research in organic systems include solid-state lasers (in both VCSEL and DFB form factor), low-threshold optical switches, and photodetectors. In all of these areas, thin films of "Jelley aggregates," or J aggregates, offer a promising materials platform thanks to their narrow linewidth and high oscillator strength at room temperature, properties resulting from delocalization of excitations across multiple strongly-coupled molecules. By placing these films in an optical microcavity, the aggregates exhibit additional strong-coupling to the cavity electric field, creating light-matter quasi-particles known as exciton-polaritons, even at room temperature. In this thesis, I discuss my research on the properties of J-aggregate thin films and on advancing the device and materials engineering of strongly-coupled devices based on J-aggregate thin films to the level of those in inorganic semiconductor systems. Exciton-polariton systems have been extensively studied at cryogenic temperatures in II-VI and III-V semiconductor quantum well systems in the past two decades as potential low-threshold VCSELs.
(cont.) J-aggregate-based exciton-polaritons systems, however, offer many device and engineering challenges, including: understanding the role of inhomogeneous vs. homogeneous broadening in the J-aggregate optical response, fabricating higher-quality microcavities with the ability to pump the polaritons at high intensities, and lateral patterning on the single-micron scale of organic microcavities. These topics are addressed and the outlook of organic exciton-polariton device research discussed.
by M. Scott Bradley.
Ph.D.
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Walker, Brian J. (Brian Jacob). "Nanocrystal/J-aggregate constructs : chemistry, energy transfer, and applications." Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/65479.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2011.
Vita. Cataloged from PDF version of thesis.
Includes bibliographical references (p. 119-128).
The interaction of light with matter is one of the most central subjects to modern chemistry. Two types of materials, semiconductor nanocrystals and J-aggregates of cyanine dyes, have been developed chiefly due to their potential for interacting with light in interesting and productive ways. At the same time, existing spectroscopy and microscopy tools enable the study of these photonic materials, their dynamics, and their interactions. Although semiconductor nanocrystals and J-aggregates have complementary physical properties, the coupling between them requires new methods to control the interface between the organic (J-aggregate) and inorganic (nanocrystal) material. This thesis is about the interfacial chemistry, photophysical characterization, and selected applications of J-aggregated cyanine dyes conjugated with semiconductor nanocrystals. Chapter 1 begins with a brief review of J-aggregates and semiconductor nanocrystals together with referrals to other scources and motivation for the present work. Because the electronic excited states of both J-aggregates and semiconductor nanocrystals are characterized by a bound electron-hole pair, they can be grouped under the class of excitonic materials, and the coupling of J-aggregates with excitonic inorganic materials is reviewed. To control J-aggregate/nanocrystal interactions, it is important to preserve the aggregate structure while achieving favorable energy transfer. This challenge is the subject of Chapters 2 and 3, in which new ligand chemistry was developed to achieve near-unity energy transfer efficiency from the J-aggregates to the nanocrystal quantum dots in solution (Ch. 2) and in a solid state thin film (Ch. 3). These hybrid J-aggregate/nanocrystal constructs result in emission enhancement through energy transfer across the organic/inorganic interface, with the strongly-coupled J-aggregates serving as optical antennae to the nanocrystals. In the process, it was discovered that the ligand directs formation of J-aggregates onto the nanocrystal surface. In Chapter 4, the template-directing ligand is used on semiconductor nanowires grown from solution to realize a new photodetector design. Here, the excitation energy transfers from J-aggregated dyes to the nanowires, enhancing the photocurrent of the device and creating an artificial solid-state photodetector whose self assembly and aggregated antenna molecules are analogous to a photosynthetic light harvesting complex. Additionally, the nanowire/J-aggregate self-assembly generalizes to J-aggregates of three different color dyes (red/green/blue), providing a wavelength selectivity absent in biological light harvesting. In Chapter 5, the kinetics of indium phosphide (InP) semiconductor nanocrystal synthesis is discussed. InP is benficial for nanocrystal applications in biology or display technologies, as it does not contain lead or cadmium. However, the molecular mechanism of InP nanocrystal synthesis had been essentially unexplored. By studying the reaction kinetics of InP synthesis, a mechanism is proposed for InP. As in the case of the chemistry described in Chapters 2-4, it is clear that non-covalent interactions are vital to achieving control during nanocrystal synthesis.
by Brian J. Walker.
Ph.D.
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Cao, Yumeng Melody. "Photostabilization of J-aggregate cyanine dyes for exciton-polariton based devices." Thesis, Massachusetts Institute of Technology, 2018. http://hdl.handle.net/1721.1/118061.

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Thesis: S.M., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2018.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 67-69).
Organic molecules are becoming a commonly used material in strongly coupled systems as they possess large exciton binding energies and huge oscillator strengths that have allowed for the creation of room temperature polariton condensates, superfluids, and other exotic phenomena. Using J-aggregates, the aggregated form of cyanine organic dyes, we have previously fabricated light-emitting devices that demonstrated the first ever electrically pumped polariton emission, as well as critically coupled resonators with record high effective absorption constants. Although there are many promising applications for organic exciton-polariton devices, state-of-the- art devices suffer from rapid photodegradation at higher photon densities, which presently limits their eventual implementation into a viable technology. To achieve stable devices, we need to isolate the causes of photodegradation. Specifically, we studied the photoluminescence stability of J-aggregate thin films under different atmospheric conditions. Our results indicated that J-aggregates maintain both better emission and stability in high humidity environments in comparison to oxygen-rich atmospheres. Furthermore, we show an order of magnitude improvement in the photostability via encapsulation of the film with a hygroscopic sugar encapsulant. These results are highly promising and suggest future pathways for the realization of functional and stable polariton-based devices which we will explore in this thesis.
by Yumeng Melody Cao.
S.M.
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Tischler, Jonathan Randall 1977. "Electrically pumped polariton emission in a J-aggregate organic light emitting device." Thesis, Massachusetts Institute of Technology, 2003. http://hdl.handle.net/1721.1/88358.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2003.
Includes bibliographical references (leaves 46-47).
by Jonathan Randall Tischler.
S.M.
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Fylymonova, I., Yu V. Malyukin, and A. V. Sorokin. "Migration of Frenkel Excitons in PIC J-aggregates." Thesis, Sumy State University, 2012. http://essuir.sumdu.edu.ua/handle/123456789/35095.

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Using luminescent exciton traps, an efficiency of the exciton migration in J-aggregates of pseudoisocyanine dye in solutions has been investigated. Applying a modified Stern-Volmer equation for an analysis of the J-aggregates luminescence quenching by the trap, the quenching of 50% of PIC J-aggregates luminescence at the ratio PIC/trap = 70:1 has been found. To increase the exciton migration efficiency, the Jaggregate structure was improved by the formation of a "J-aggregate-surfactant” complex. It results in 35% enhancement of the exciton migration efficiency in PIC J-aggregates. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35095
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Shirasaki, Yasuhiro. "Efficient Föster energy transfer : from phosphorescent organic molecules to J-aggregate thin film." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/46500.

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Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2008.
Includes bibliographical references (p. 53-54).
This thesis demonstrates the first ever use of Forster resonance energy transfer (FRET) to increase the quantum efficiency of a electrically pumped J-aggregate light emitting device (JLED). J-aggregate thin films are highly absorptive films that have potential applications in a new class of optoelectronic devices, known as polaritonic devices. These devices, which utilize strong coupling between light and matter, include room temperature low power optical switches and low threshold lasers. Recent work has shown that a J-aggregate strong-coupling device can be powered not just optically but also electrically. However, since J aggregates are engineered for their optical and not electrical properties, exciting them electrically is very inefficient. JLED efficiency can be improved by first exciting phosphors that readily form excitons and then employing FRET to excite the J aggregates. Attaining high efficiency can make electrical pumping a viable option to power polaritonic devices.
by Yasuhiro Shirasaki.
M.Eng.
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Steeg, Egon. "Investigations on growth and structure of silver and silver halide nanostructures formed on amphiphilic dye aggregates." Doctoral thesis, Humboldt-Universität zu Berlin, 2018. http://dx.doi.org/10.18452/19577.

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Diese Arbeit beschäftigt sich mit dem Wachstumsmechanismus von Silberjodid Nanodrähten. Das Wachstum wurde über einen Zeitraum von Minuten bis hin zu Tagen untersucht. Im frühen Stadium bilden sich Silbernanopartikel innerhalb der Farbstoffröhren, welche als Keime für das weitere Wachstum von isolierten Drahtstücken dienen. Der Durchmesser dieser Drähte wird durch den Innendurchmesser der Röhren definiert. Im letzten Stadium wachsen diese Drahtstücke zusammen bis sie das gesamte Aggregat füllen. Dieser Wachstumsprozess impliziert einen Transport von Silber Ionen durch die Wand der Röhre. Das Wachstum der Drähte setzt sich weiter fort nachdem das Template gleichmäßig mit Drähten gefüllt ist und zerstört die Röhren in der Folge. Die Kristallstruktur der Drähte wurde sowohl mit hochauflösender Elektronenmikroskopie als auch Elektronenbeugung untersucht. Das Silberjodid konnte aufgrund seiner charakteristischen Wurtzite Struktur in der beta-Phase identifiziert werden. Da der Lösung nur Silbernitrat beigesetzt wurde, konnte die Quelle der Jod-Ionen als Verunreinigung im Farbstoffpulver ausgemacht werden. Das fragmentierte Wachstum der Drähte von verschiedenen Startpunkten aus führt zu Kristallen mit einkristallinen Domänen von mehr als 100 nm Länge. Eine bevorzugte Orientierung der Kristallstruktur relativ zur Aggregatachse wurde gefunden und durch die Molekülstruktur der Aggregate erklärt. Basierend auf diesen Ergebnissen wurde ein Model zum Wachstum von Silberjodid Nanodrähten im Inneren eines röhrenförmigen Molekülaggregats entwickelt. Es wurde angenommen, dass das Wachstum an Silberkeimen beginnt, die durch Photooxidation der bereits vorhandenen Jod Ionen mit Silber Ionen während der Belichtung der Probe gebildet werden. Diese Silberkeime ermöglichen die Bildung von stabilen Silberjodid Kristalliten und das nachfolgende Wachstum zu Drähten. Die Ergebnisse zeigen einen möglichen Weg zur Synthese von Metall-Halogenid Strukturen innerhalb von Farbstoffröhren.
This thesis reports on the growth mechanism of silver iodide nanowires as revealed by conventional as well as cryogenic transmission electron microscopy. The growth, initiated by short illumination with UV light, has been observed over time scales ranging from minutes to days. In an early stage, within the tubular aggregates nanoparticles are formed which act as seeds for continuous growth of separate pieces of wires. The diameter of the wires is determined by the inner diameter of the tubes. In the final state, the pieces of wire totally fill the aggregate. The growth process indicates transport of at least silver ions through the tubular wall membrane. After homogeneously filling the template the wires grow onwards over the diameter of the nanotubes, destroying it in the process. The crystal structure of the wires was investigated by means of high resolution transmission electron microscopy and selected area electron diffraction. The silver iodide could be clearly identified in its beta-phase by its typical wurtzite structure. Since only silver nitrate was added to the solutions, the source of the iodide ions could be attributed to impurities within the dye powder itself. The fragmented growth of the wires from separate seeds leads to nanowires consisting of single crystalline domains exceeding 100 nm in length. A preferential orientation of the crystal lattice planes with respect to the aggregate axis was observed which is explained by the molecular structure of the aggregates. Based on these findings a model for the growth of silver iodide nanowires within the inner space of the tubular molecular aggregate is presented. The growth is assumed to start at silver seeds that are formed due to photo-oxidation of the already present iodide ions by the silver ions during the illumination of the sample. These silver seeds facilitate nucleation of silver iodide and subsequent growth into wires.
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Kaidel, Björn [Verfasser], and J. [Akademischer Betreuer] Müller-Quade. "Fault-Tolerance and Deaggregation Security of Aggregate Signatures / Björn Kaidel ; Betreuer: J. Müller-Quade." Karlsruhe : KIT-Bibliothek, 2020. http://d-nb.info/120500193X/34.

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Ovchinnikov, O. V., M. S. Smirnov, A. O. Dedikova, B. I. Shapiro, T. S. Shatskikh, and A. N. Latyshev. "Spectral Manifestation of Hybrid Association of Zn0.7Sd0.3S Colloidal Quantum Dots with J-Aggregates of Thiacarbocyanine Dye." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35329.

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Spectral properties of mixtures of Zn0.7Sd0.3S colloidal quantum dots with mean diameter value of 3.5 nm with the molecules of 3,3'-di(γ-sulfopropil)-9-ethyl-4,5,4',5'-dibenzo-thiacarbocyanine betaine pyridine salt (DEC), prepared in gelatin were investigated. The obtained data indicated that the formation of well-luminescent trans-J-aggregates and spectral tuning in the position of the absorption band of DEC and the luminescence band of quantum dots, providing requirements for resonant energy transfer in the hybrid associate are the determinant factors in the increase of the luminescent emission of DEC molecules, interacting with Zn0.7Cd0.3S colloidal quantum dots. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35329
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Schebsdat, Erik [Verfasser], and Daniel J. [Akademischer Betreuer] Strauss. "Neural Correlates of Binaural Interaction Using Aggregate-System Stimulation in Cochlear Implantees / Erik Schebsdat ; Betreuer: Daniel J. Strauss." Saarbrücken : Saarländische Universitäts- und Landesbibliothek, 2020. http://d-nb.info/1209947307/34.

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Books on the topic "J-Aggregate"

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Burnet, G. Experimental studies of the production of lightweight aggregate from fly ash/coal cleaning refuse mixtures / G. Burnet and A. J. Gokhale. S.l: s.n, 1987.

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Rotemberg, Julio. Money, output, and prices--evidence from a new monetary aggregate / by Julio J. Rotemberg, John C. Driscoll, and James M. Poterba. Cambridge, Mass: Sloan School of Management, Massachusetts Institute of Technology, 1991.

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Photographic Science: Advances in Nanoparticles, J-aggregates, Dye Sensitization, and Organic Devices. Oxford: Oxford University Press, 2011.

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Kobayashi, Takayoshi. J-Aggregates. World Scientific Publishing Co Pte Ltd, 2012.

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T, Kobayashi, ed. J-aggregates. Singapore: World Scientific, 1996.

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Kobayashi, T. J-Aggregates. WORLD SCIENTIFIC, 1996. http://dx.doi.org/10.1142/3168.

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Kobayashi, Takayoshi. J-Aggregates. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/8226.

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Aument, Lori Renée. Experimentation in concrete: John J. Earley at Meridian Hill Park, Washington, DC : history, technology, and characterization of exposed aggregate concrete. 1999.

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Book chapters on the topic "J-Aggregate"

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Konzett, Verena Maria. "Wettbewerbliche Banken fördern das Wachstum." In Die Wirtschaft im Wandel, 37–41. Wiesbaden: Springer Fachmedien Wiesbaden, 2021. http://dx.doi.org/10.1007/978-3-658-31735-5_6.

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ZusammenfassungWas nützen die besten Ideen, wenn Investitionen und neue Jobs mangels Zugang zu Bankkrediten nicht zustande kommen? Wachstum und Innovation brauchen einen leistungsfähigen Finanzsektor. Wettbewerb regt auch die Banken zu Höchstleistungen an. Indem sie mehr Informationen über ihre Kunden sammeln und ihre Prozesse bei der Auswahl und anschliessenden Überwachung optimieren, gelingt es ihnen besser, die besonders vielversprechenden Unternehmen zu identifizieren. Dadurch, dass die Banken die Kreditvergabe vor allem auf die innovativen und profitablen Unternehmen mit hohem Wachstumspotential lenken, fördern sie die Produktivitätssteigerungen und das Wachstum der Realwirtschaft.Bai, J., D. Carvalho, und G. M. Phillips (2018), The Impact of Bank Credit on Labor Reallocation and Aggregate Industry Productivity, Journal of Finance 63(6), 2787–2836.
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Losytskyy, Mykhaylo Yu, and Valeriy M. Yashchuk. "Fluorescent J-Aggregates and Their Biological Applications." In Advanced Fluorescence Reporters in Chemistry and Biology II, 135–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-04701-5_4.

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Gaizauskas, E., and K. H. Feller. "Annihilation Enhanced Four-Wave Mixing in J-Aggregates." In Ultrafast Processes in Spectroscopy, 467–69. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4615-5897-2_104.

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Feller, K. H., R. Gadonas, and V. Krasauskas. "Time-Resolved Absorption Spectroscopy of Polymethine J-Aggregates." In Springer Proceedings in Physics, 289–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75826-3_57.

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Tani, T. "Photophysics of Capped Nanocrystals and Molecular J-Aggregates." In Single Organic Nanoparticles, 185–202. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-55545-9_15.

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Bakalis, L. "Excitons in J-Aggregates: Beyond the Heitler-London Approximation." In Spectroscopy and Dynamics of Collective Excitations in Solids, 600. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5835-4_25.

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Kamalov, V. F., R. Inaba, I. A. Struganova, M. Tasumi, and K. Yoshihara. "Intermolecular Coherence and Vibrational Dephasing of BIC J-Aggregates." In Springer Proceedings in Physics, 39–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85060-8_9.

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Virgili, T., S. Ceccarelli, L. Lüer, G. Lanzani, G. Cerullo, and D. G. Lidzey. "Coherent phonons in cyanine dye monomers and J-aggregates." In Springer Series in Chemical Physics, 370–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-95946-5_120.

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Lidzey, D. G., D. D. C. Bradley, A. Armitage, T. Virgili, M. S. Skolnick, and S. Walker. "Strong Coupling in Organic Semiconductor Microcavities Based on J-Aggregates." In Multiphoton and Light Driven Multielectron Processes in Organics: New Phenomena, Materials and Applications, 357–70. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4056-0_26.

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Agranovich, V. M., and A. M. Kamchatnov. "Quantum Confinement and Superradiance of Self-Trapped Excitons from 1D J-Aggregates." In Multiphoton and Light Driven Multielectron Processes in Organics: New Phenomena, Materials and Applications, 109–22. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4056-0_9.

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Conference papers on the topic "J-Aggregate"

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Chovan, J., and I. E. Perakis. "Photoluminescence in J-aggregate microcavities." In 2006 Conference on Lasers and Electro-Optics and 2006 Quantum Electronics and Laser Science Conference. IEEE, 2006. http://dx.doi.org/10.1109/cleo.2006.4628967.

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Mal'tsev, Eugene I., Dmitry A. Lypenko, Boris I. Shapiro, Vladimir V. Bobonkin, Jeffrey Wright, and Anatoly V. Vannikov. "Electroluminescence in polymer/j-aggregate nanostructures." In Advanced Display Technologies:Basic Studies of Problems in Information Display (FLOWERS'2000), edited by Victor V. Belyaev and Igor N. Kompanets. SPIE, 2001. http://dx.doi.org/10.1117/12.431262.

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Mal'tsev, Eugene I., Dmitry A. Lypenko, Boris I. Shapiro, George H. W. Milburn, Jeffrey Wright, Andre Hendriksen, Vladimir I. Berendyaev, Boris V. Kotov, and Anatoly V. Vannikov. "J-aggregate electroluminescence in polymer matrices." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Zakya H. Kafafi. SPIE, 1999. http://dx.doi.org/10.1117/12.372716.

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Chovan, J., and I. E. Perakis. "Theory of photoluminiscence in J-aggregate microcavities." In 2007 European Conference on Lasers and Electro-Optics and the International Quantum Electronics Conference. IEEE, 2007. http://dx.doi.org/10.1109/cleoe-iqec.2007.4386841.

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Kobayashi, T., and K. Misawa. "Giant Static Dipole Moment In Pseudoisocyanine J-aggregate." In Technical Digest CLEO/Pacific Rim '97 Pacific Rim Conference on Lasers and Electro-Optics. IEEE, 1997. http://dx.doi.org/10.1109/cleopr.1997.610753.

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Michetti, Paolo, Giuseppe C. La Rocca, Marília Caldas, and Nelson Studart. "Excitation dynamics and photoluminescence of J-aggregate microcavities." In PHYSICS OF SEMICONDUCTORS: 29th International Conference on the Physics of Semiconductors. AIP, 2010. http://dx.doi.org/10.1063/1.3295452.

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Lienau, Christoph. "Ultrafast optical nonlinearities in hybrid metal-J-aggregate nanostructures." In Frontiers in Optics. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/fio.2009.fwp1.

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Vasa, P., R. Pomraenke, S. Schwieger, E. Runge, and C. Lienau. "Ultrafast optical nonlinearities in hybrid metal-J-aggregate nanostructures." In 11th European Quantum Electronics Conference (CLEO/EQEC). IEEE, 2009. http://dx.doi.org/10.1109/cleoe-eqec.2009.5194749.

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Vasa, Parinda, Robert Pomraenke, Stephan Schwieger, Erich Runge, and Chrsitoph Lienau. "Ultrafast Optical Nonlinearities in Hybrid Metal-J-Aggregate Nanostructures." In International Quantum Electronics Conference. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/iqec.2009.ituk3.

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Eizner, Elad, Ori Avayu, Ran Ditcovski, and Tal Ellenbogen. "Exciton-plasmon hybridization in J-aggregate-aluminum nanoantenna metasurfaces." In 2015 International Conference on Optical MEMS and Nanophotonics (OMN). IEEE, 2015. http://dx.doi.org/10.1109/omn.2015.7288878.

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