Academic literature on the topic 'Nanopower'

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Journal articles on the topic "Nanopower"

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Feng, Jiandong, Michael Graf, Ke Liu, Dmitry Ovchinnikov, Dumitru Dumcenco, Mohammad Heiranian, Vishal Nandigana, Narayana R. Aluru, Andras Kis, and Aleksandra Radenovic. "Single-layer MoS2 nanopores as nanopower generators." Nature 536, no. 7615 (July 13, 2016): 197–200. http://dx.doi.org/10.1038/nature18593.

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Rodriguez-Villegas, Esther, Alexander J. Casson, and Phil Corbishley. "A Subhertz Nanopower Low-Pass Filter." IEEE Transactions on Circuits and Systems II: Express Briefs 58, no. 6 (June 2011): 351–55. http://dx.doi.org/10.1109/tcsii.2011.2158165.

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Cannillo, F., C. Toumazou, and T. S. Lande. "Nanopower Subthreshold MCML in Submicrometer CMOS Technology." IEEE Transactions on Circuits and Systems I: Regular Papers 56, no. 8 (August 2009): 1598–611. http://dx.doi.org/10.1109/tcsi.2008.2008275.

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Kulej, Tomasz, Fabian Khateb, and Montree Kumngern. "0.3-V Nanopower Biopotential Low-Pass Filter." IEEE Access 8 (2020): 119586–93. http://dx.doi.org/10.1109/access.2020.3005715.

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Marraccini, Francesco, Giuseppe De Vita, Stefano Di Pascoli, and Giuseppe Iannaccone. "Low-voltage nanopower clock generator for RFID applications." Microelectronics Journal 39, no. 12 (December 2008): 1736–39. http://dx.doi.org/10.1016/j.mejo.2008.05.008.

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Park, Chang-Bum, and Shin-Il Lim. "A Sub-1V Nanopower CMOS Only Bandgap Voltage Reference." Journal of IKEEE 20, no. 2 (June 30, 2016): 192–95. http://dx.doi.org/10.7471/ikeee.2016.20.2.192.

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Cucchi, F., S. Di Pascoli, and G. Iannaccone. "Design of a nanopower current reference with reduced process variability." Analog Integrated Circuits and Signal Processing 77, no. 1 (July 14, 2013): 45–53. http://dx.doi.org/10.1007/s10470-013-0105-z.

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Given, Robert Parker, Kyle S. Wenger, Virginia D. Wheeler, Brian C. Utter, and Giovanna Scarel. "Fabrication of nanopower generators using thin atomic layer deposited films." Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films 35, no. 1 (January 2017): 01B120. http://dx.doi.org/10.1116/1.4971403.

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Lin, Jing, and Xingyu Huang. "Application of clothing friction nanopower generators in human motion energy acquisition." Nanomaterials and Energy 9, no. 2 (December 1, 2020): 163–72. http://dx.doi.org/10.1680/jnaen.20.00031.

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Yan, W., W. Li, and R. Liu. "Nanopower CMOS sub-bandgap reference with 11 ppm/°C temperature coefficient." Electronics Letters 45, no. 12 (2009): 627. http://dx.doi.org/10.1049/el.2009.3705.

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Dissertations / Theses on the topic "Nanopower"

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Cabello-Aguilar, Simon. "Lecture de macromolécules par translocation au travers d'un nanopore unique." Thesis, Montpellier 2, 2014. http://www.theses.fr/2014MON20242.

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La translocation de macromolécules au travers d'un nanopore unique est utilisée dans un but de détection et d'identification. Au cours de ces travaux de thèse, un dispositif expérimental, permettant la mesure du courant ionique dans les nanopores de façon optimisée, a été mis en place. Nous avons développé des programmes qui permettent le filtrage du courant mesuré et l'analyse des signaux de translocation. Nous avons fabriqué des nanopores uniques de haut rapport d'aspect avec, un diamètre ajusté au nanomètre près, et à l'état de surface contrôlé, grâce à la combinaison de techniques d'attaque de trace et de dépôt de couches atomiques. A l'aide du dispositif expérimental fabriqué nous avons effectué des mesures de courant ionique dans les nanopores à différentes échelles (autour de 100 nm et en dessous de 10 nm), en utilisant des systèmes différents (solides et hybrides) en présence de macromolécules ou pas. L'interprétation et l'analyse des signaux de courant résultant nous ont permis de mettre en évidence l'importance (i) de l'état de surface du nanopore aussi bien pour le transport des ions au travers du pore que pour leur entrée (ii) et des interactions des ions organisés autour des molécules en translocation avec les ions organisés dans le pore particulièrement lorsque son diamètre est faible (< 10 nm). L'étude de la translocation des polynucléotides au travers d'un nanopore hybride nous a permis de montrer qu'une protéine complexe peut préserver ses propriétés biologiques dans un nanopore solide si son diamètre est proche du diamètre extérieur de la protéine et son état de surface est semblable au milieu dans lequel évolue la protéine
The translocation of macromolecules through a single nanopore is used for purposes of detection and identification. During this thesis, an experimental set-up for ionic current recording in nanopores has been created. We have developed programs that allow filtering of the measured current and signal analysis. We have made high aspect ratio single nanopores with a diameter adjusted at the nanometer scale, and a controlled surface state by using a combination of track-etching and atomic layer deposition techniques. Using the experimental device created we performed measurements of ionic current through the nanopores at different scales (around 100 nm and below 10 nm), using different systems (solid and hybrid) and in the presence of macromolecules or not. The interpretation and analysis of translocation signals allowed us to highlight the importance of (i) the surface state of the nanopore for both the transport of ions through the pore and their entry (ii) and the interactions of the ions organized around the translocating molecule with the ions organized in the nanopore (in particular when the pore diameter is below 10 nm). The study of the translocation of polynucleotides through a hybrid nanopore showed that a complex protein can preserve its biological properties in a solid nanopore if its diameter is close to the outer diameter of the protein and its surface state is similar to the biological environment of the protein
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Lepoitevin, Mathilde P. "Conception d'un nanopore unique pour mimer un canal biologique et pour la détection de bio-macromolécules." Thesis, Montpellier, 2016. http://www.theses.fr/2016MONTT226/document.

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Un nanopore artificiel est une ouverture de taille nanométrique faite dans un film mince synthétique (polymère ou inorganique). Un nanopore unique peut être considéré comme l’élément simple constitutif d’une membrane. Les récentes avancées dans ce domaine ont ouvert des opportunités pour développer des outils pour la détection de molécules cibles à faible concentration (fmol L-1), en temps réel. Les nanopores artificiels s’inspirent des canaux biologiques situés dans la membrane cellulaire. Ces derniers permettent le transport d’ions ou de molécules entre les milieux intra- et extra-cellulaires, grâce à leurs fortes sélectivités ou leurs propriétés d’ouverture/fermeture. Comparé à leurs homologues biologiques, les limitations des nanopores solides sont leurs manques de sélectivité et de réponse aux stimuli extérieurs. Toutefois, les nanopores solides ont l’avantage d’être beaucoup plus résistant, robuste et facile à manipuler que les pores biologiques. Ainsi la fonctionnalisation de leur surface, avec des systèmes plus ou moins complexes, permettrait d’améliorer à la fois leurs propriétés de transport sélectif, leurs capacités de détection de biomolécules ou encore d’étudier plus précisément les mécanismes fondamentaux du transport des macromolécules en milieu confiné.Dans cette thèse, nous avons conçu dans un premier temps des nanopores bi-fonctionnels, répondant au pH, et à l’attache d’un ligand. Pour fabriquer ces nanopores bi-fonctionnels, nous avons utilisé un système biotine-avidine fixé dans des nanopores polymères. Nous avons démontré qu’il est possible de moduler l’ouverture et la fermeture du nanopore avec le pH de façon réversible. De plus, il est possible de détecter des protéines biotinylées et des anticorps par l’analyse des rectifications de courant. Le principal défaut de cette stratégie est son irréversibilité. En utilisant une stratégie similaire combinée avec des polyélectrolytes, nous avons obtenu des fonctionnalisations réversibles. Ils permettent de moduler la sélectivité ionique du pore et les propriétés de conduction en fonction du pH et de ligand. Dans un second temps, nous nous sommes intéressés aux questions fondamentales de la translocation de polynucléotide, plus précisément de l’analyse de l’influence de l’état de surface du nanopore (hydrophobicité, charge), dans les conditions où la distance de Debye devient équivalente au diamètre du nanopore. Nous avons démontré que si le nanopore présente la même charge que la PolyAdénosine et la PolyCytosine, la vitesse de passage de la molécule augmente et la barrière globale d’énergie d’entrée du nanopore diminue par rapport au nanopore non-chargé hydrophobe. Ensuite, en modifiant la surface d’un nanopore en PET, nous avons montré qu’il est possible de détecter des brins simples et doubles d’ADN très courts (10 à 40 bases). Enfin, nous avons tenté une fonctionnalisation de nanopores pour éviter l’adsorption non spécifique des protéines afin d’étudier la translocation de longs fibrilles d’amyloïdes de lysozyme. Cet objectif n’a pas été complètement atteint compte tenu des résultats qui ne permettent pas d’affirmer quand au passage des molécules à travers le pore.Dans cette thèse nous nous sommes attachés à montrer l’intérêt et la nécessité de fonctionnaliser les pores, aussi bien pour obtenir des nanopores biomimétiques stimuli-répondants (pH et ligand) ou anti-bioadhérants que pour des études fondamentales de transport. Il est également facile de transposer cette technique à des membranes multipores. Il est donc possible de concevoir des membranes optimisées pour des applications de séparation ionique, de capture de molécules cibles ou plus généralement de filtration
Artificial nanopores are nanometer sized aperture made in synthetic thin films (polymer or inorganic). A single nanopore can be considered as a constitutive element from membranes. Recent advances in this field are bringing new tools for real time detection of target molecules at low concentration (fmol L-1). Biological channels inside the cell membrane are used as models to design solid-state nanopores. They allow ions or molecules transport through intra- and extra-cellular side, thanks to their high selectivity and their gating properties. Compared to their biological counterparts, limitations of the synthetic nanopores are their lack of selectivity and unresponsiveness towards external stimuli. However, the solid state presents several advantages compared to the biological ones, such as nanopores robustness, the control of the number of pores and a long lifetime (several days or weeks). Thus their surface functionalization would increase their selective transport properties, their abilities to detect biomolecules or to study more in details their fundamental mechanisms.In this thesis, we design first bi-functional nanopores, pH- and ligand-gated. To do it, we used biotin-avidin system grafted inside a polymeric nanopore. We demonstrated that it is possible to reversibly gate the nanopore with pH modulation. Moreover, we are able to detect protein labeled with biotin and antibodies by analyzing the current rectification. The major drawback comes from the irreversibility of its covalent bonds. By using a similar concept combined with polyelectrolytes, we obtain a reversible functionalization. Depending on the ligand, the ionic selectivity and the conduction properties can be modulated. Next, we focused on fundamental questions regarding polynucleotides translocation, and more precisely on the influence of the surface state of the nanopore (hydrophobicity, charge) when the Debye distance is similar to the pore diameter. We show that if the nanopore has the same charge as the polyAdenosine or polyCytosine, the translocation time decreases, and the energy barrier of entrance decreases compared to an uncharged hydrophobic nanopore. Then, by modifying the surface of the nanopore made in PET film, we are able to detect short single and double strand of DNA (10 to 40 bases). Finally, we tried to functionalize PET nanopores to avoid unspecific adsorption of proteins and to study the translocation of long fibrils of amyloids from lysozyme. This goal has not been entirely reach since we cannot claim that the fibrils translocate through the pore.In this thesis we show the interest and the need to functionalize the nanopores, to obtain biomimetic stimuli-responsive (pH and ligand), to avoid unspecific adsorption or to study transport properties with the nanopore. It is easy to upscale those techniques to multipores membranes. Thus it is possible to design membranes to enhance their ionic separation, target molecule detection or more generally filtration applications
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Vlassarev, Dimitar. "DNA Characterization with Solid-State Nanopores and Combined Carbon Nanotube across Solid-State Nanopore Sensors." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10310.

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A DNA molecule passing through a nanopore in a liner and sequential fashion allows for unprecedented interrogation of the polymer. Adding transverse electrodes that are comparable in size and sensitive to the DNA molecule, can further the attempts to rapidly sequence DNA. Carbon nanotubes are comparable in size and interact strongly with the DNA molecule. This makes them an excellent choice for integration with nanopores. Only the section of the carbon nanotube in immediate proximity to the nanopore should be sensitive to the DNA molecules. Atomic layer deposition of metal-oxides passivates the sections of the carbon nanotube that are not to interact with the DNA molecule. The coating also protects the thin film interconnects leading to the carbon nanotube. Hafnium oxide is superior to aluminum oxide in chemical resistance and electrical insulation but leads to a high failure rate of the carbon nanotube across nanopore devices. Aluminum oxide, combined with gold thin film interconnects to the carbon nanotube, produced the first functioning devices in electrolyte. These devices had concurrently functioning ionic (current across the nanopore) and transverse (current through the carbon nanotube) channels. No concurrent DNA translocation signal was recorded on the ionic and nanotube current traces. Analyzing the translocation events recorded on the ionic channel indicated that double-stranded DNA (dsDNA) passed through the carbon nanotube articulated nanopore an order of magnitude slower than it would have through a comparable unarticulated nanopore. The slower translocation observed is a necessary condition for sequencing. Investigating dsDNA translocation under various experimental conditions led to the discovery of a new interaction between the molecule and small nanopores. A dsDNA molecule is trapped when the electric field near the nanopore attracts and immobilizes a non-end segment of the molecule at the nanopore orifice without inducing folded translocation. In this work, the expression “trapped dsDNA” will exclusively refer to the immobilization of a dsDNA molecule at the orifice of the nanopore. The ionic current through the nanopore decreases when the dsDNA molecule is trapped by the nanopore. By contrast, a translocating dsDNA molecule under the same conditions causes an ionic current increase. Finite element modeling results predict this behavior for the conditions of the experiment.
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Manara, Richard. "Free energy calculations of DNA translocation through protein nanopores and nanopore design for DNA sequencing." Thesis, University of Southampton, 2015. https://eprints.soton.ac.uk/374791/.

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DNA sequencing has vastly opened up the world of molecular biology, leading to new areas of interest, especially in medical research. Unfortunately the methods of DNA sequencing have only ever seen gradual improvements, as Sanger sequencing is still very much the norm despite its high cost and slow speed. Nanopores present an exciting opportunity for DNA sequencing, however, despite the concept being presented in 1996 several problems have prevented the creation of a publicly available sequencing device. The two main focuses of research into nanopores so far have been improving the resolution between bases and the slowing down of DNA translocation through the pore so modern ammeters can read the sequence accurately. The simulation work presented in this thesis largely focuses on the energetics associated with DNA translocation. This is performed in several parts; an investigation into the probability of pore entry, study into the free energy of translocation for two proteins in addition to solvent contribution to this free energy, finally a theoretical project was undertaken to investigate bottom up nanopore design.
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Ahmadi, Amir. "Wafer-scale processing of arrays of nanopore devices." Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/47533.

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Nanopore-based single-molecule analysis of biomolecules such as DNA and proteins is a subject of strong scientific and technological interest. In recent years, solid state nanopores have been demonstrated to possess a number of advantages over biological (e.g., ion channel protein) pores due to the relative ease of tuning the pore dimensions, pore geometry, and surface chemistry. However, solid state fabrication methods have been limited in their scalability, automation, and reproducibility. In this work, a wafer-scale fabrication method is first demonstrated for reproducibly fabricating large arrays of solid-state nanopores. The method couples the high-resolution processes of electron beam lithography (EBL) and atomic layer deposition (ALD). Arrays of nanopores (825 per wafer) are successfully fabricated across a series of 4' wafers, with tunable pore sizes from 50 nm to sub-20 nm. The nanopores are fabricated in silicon nitride films with thicknesses varying from 10 nm to 50 nm. ALD of aluminum oxide is used to tune the nanopore size in the above range. By careful optimization of all the processing steps, a device survival rate of 96% is achieved on a wafer with 50 nm silicon nitride films on 60- 80 micron windows. Furthermore, a significant device survival rate of 88% was obtained for 20 nm silicon nitride films on order 100 micron windows. In order to develop a deeper understanding of nanopore fabrication-structure relationships, a modeling study was conducted to examine the physics of EBL, in particular: to investigate the effects of beam blur, dose, shot pattern, and secondary electrons on internal pore structure. Under the operating conditions used in pore production, the pores were expected to taper to a substantially smaller size than their apparent size in SEM. This finding was supported by preliminary conductance readings from nanopores.
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Edmonds, Christopher Michael. "Computational investigations of biopolymer translocation through nanopore devices." Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/50260.

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Nanopores (1 – 10 nm diameter) constructed in solid-state membranes, have shown promise as next-generation biopolymer analysis devices offering both high resolution and high throughput. One promising application of nanopores is in the analysis of nucleic acids, such as DNA. This involves translocation experiments in which DNA is placed in an ionic solution and is forced through a nanopore with the aid of an applied electric field. The modulation of ionic current through the pore during DNA translocation can then be correlated to various properties of the biopolymer such as the length. To optimally design and operate nanopore devices, it would be advantageous to develop an accurate computer simulation methodology to predict the physics of the translocation process. Hence, I have developed a physically accurate, computationally efficient simulation methodology to predict and analyze the physics of biopolymer translocation through solid-state (silicon nitride) nanopores. The overall theme of this thesis is to use this simulation methodology to thoroughly investigate important issues in the physics underlying translocation experiments and thereby determine the effects of key structural and operation parameters, such as nanopore dimensions, applied voltage, hydrodynamic interactions, solvent viscosity, and the polymer chain length. The results from these simulation studies can assist in not only proper nanopore design, but also help determine the proper experimental environments and parameters for nanopore operation.
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Tasserit, Christophe. "Transport d'ions et d'objets dans des nanopores." Phd thesis, Ecole Polytechnique X, 2011. http://pastel.archives-ouvertes.fr/pastel-00589602.

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Il existe différentes techniques de manipulation et de détection de molécules uniques. Parmi elles, la mesure du courant ionique traversant un pore nanométrique unique est la plus ancienne. Le travail effectué dans cette thèse utilise cette technique et s'articule autour de deux objectifs. Tout d'abord, l'utilisation d'un nanopore unique obtenu par attaque de trace permet d'imiter les expériences déjà faites dans la littérature avec d'autres types de pores. Certains phénomènes, tels que la rectification par exemple, ont pu être observés, mais d'autres comme la translocation n'ont pu l'être. Ensuite, une étude du bruit de conductance électrique démontre l'existence d'un phénomène qui n'avait jusqu'alors pas été soulevé dans la littérature. En effet, ce bruit ne peut pas être imputé aux fluctuations des caractéristiques de la géométrie du pore ou de sa paroi, mais plutôt à des effets coopératifs sur la mobilité des ions dans un milieu confiné.
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Fazi, Davide. "Progetto di un nodo sensore a nanocorrenti basato su microcontrollore." Bachelor's thesis, Alma Mater Studiorum - Università di Bologna, 2017. http://amslaurea.unibo.it/13141/.

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Le prestazioni e la densità di integrazione dei circuiti integrati hanno avuto una incredibile crescita negli ultimi decenni. Questo incredibile sviluppo ha portato ad una enorme crescita delle applicazioni dei circuiti elettronici, fino ad arrivare a pensare di poter rendere “smart” e connesso ad Internet ogni oggetto di uso comune, grazie alla cosiddetta “Internet of Things”. In questo panorama trovano dunque sempre maggior spazio i sensori, indispensabili al fine di monitorare i parametri d’interesse negli oggetti da controllare. Un altro aspetto molto importante è quello di ridurre il consumo dei dispositivi. Gli oggetti da connettere ad internet nella maggior parte dei casi saranno infatti da alimentare a batteria. Lo scopo di questo elaborato è quello di sviluppare un nodo sensore con annesso un datalogger mediante l’utilizzo di un microcontrollore. L’obiettivo principale è di ridurne il consumo al minimo, con correnti di standby dell’ordine delle decine di nA, così da poter alimentare tale circuito per un periodo di diversi anni con la batteria più piccola possibile. Il circuito sarà non solo progettato ma anche realizzato su PCB, al fine di poterne collaudare il funzionamento reale e di poterlo confrontare con quello previsto. Un dispositivo di questo tipo, oltre ad essere un utile caso di studio per mostrare i valori minimi di consumo verso i quali sia possibile spingersi, potrebbe trovare applicazione in situazioni in cui si renda necessario monitorare determinati parametri in condizioni tali da rendere difficoltosa la sostituzione della batteria e quindi anche il monitoraggio real-time che richiederebbe necessariamente un maggior consumo. Il progetto si compone di un microcontrollore che, oltre a gestire la lettura di un sensore, si occupa di implementare la funzione di datalogger. Un altro componente fondamentale è un timer, avente lo scopo di gestire il periodo di attività del µC.
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Kipnusu, Wycliffe Kiprop. "Effects of Nanoscale Confinement on the Structure and Dynamics of Glass-forming Systems." Doctoral thesis, Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-183530.

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Structure and dynamics of nanoconfined glass-forming oligomers and diblock coplymers (BPCs) are investigated by a combination of infrared transition moment orientational analysis (IR-TMOA), positron annihilation lifetime spectroscopy (PALS), grazing incidence small angle X-ray scattering (GISAXS), atomic force microscopy (AFM), scanning electron microscopy (SEM) and broadband dielectric spectroscopy (BDS). The oligomers probed are the van der Waals type, tris(2-ethyhexyl)phosphate (TEHP) and the self-associating molecules of 2-ethyl-1-hexanol (2E1H). Symmetric and asymmetric poly(styrene-b-1,4-isoprene) P(S-b-I) are studied for the case of BCPs. The samples are confined either in one-dimensional (1D) in form of thin films or in 2D (nanopores) geometrical constraints. The molecular order of TEHP in nanopores as studied by IR-TMOA shows that about 7% of the molecules are preferentially oriented perpendicular to the long axis of the pores due to their interaction with the pore walls. PALS results reveal that 2E1H confined in nanopores exhibit larger free volume with respect to the bulk. In thin films (1D), P(S-b-I) having volume fraction of isoprene blocks f(PI)= 0.55 exhibits randomly oriented lamellae and their thicknesses are directly proportional to the film thickness d(film). For f(PI) = 0.73, perpendicular cylinders with respect to the substrate are observed for d(film)>50 nm but they lie along the substrate plane when d(film) < 50 nm. In AAO pores (2D) with average pore diameter d(pore) of 150 nm, straight nanorods are formed which change to helical structures in 18 nm pores. Molecular dynamics of 2E1H and TEHP constrained in nanopores (2D), is influenced by the interplay between confinement and surface effects. Confinement effects show up as an increase in the structural relaxation rate with decreasing pore sizes at the vicinity of the glass transition temperature. This is attributed to the reduced packing density of the molecules in pores as quantified by PALS results for 2E1H. Whereas the orientation and morphologies of the domains in P(S-b-I) and the chain dynamics of isoprene chains are influenced by the finite--size and dimensionality of confinement, the segmental motion, related to the dynamic glass transition (DGT) of both styrene and isoprene blocks remains unaffected-in its relaxation time-within experimental accuracy. Effects of nanoscale confinement on the molecular dynamics therefore depend on a number of factors: the type of molecules (polymers, low molecular liquids), interfacial interactions and the dimensionality of the constraining geometries.
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Raghupathy, Bala Praveen Chakkravarthy. "Spray freeze-drying of zirconia nanopowder." Thesis, Loughborough University, 2007. https://dspace.lboro.ac.uk/2134/34738.

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Industrial exploitation of ceramic nanopowders is inhibited by their poor flowability and strong tendency to agglomerate. To achieve good flowability and die-filling characteristics, controlled agglomeration is required whilst the strength of the agglomerates is minimised so that they crush into primary particles when die pressed. Yttria stabilised zirconia nanopowders with a primary particle size of ~16 nm were obtained through different drying routes from an aqueous suspension and characterised in terms of flowability and agglomerate strength.
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Books on the topic "Nanopower"

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Iqbal, Samir M., and Rashid Bashir, eds. Nanopores. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0.

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Gromov, Alexander, and Ulrich Teipel, eds. Metal Nanopowders. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527680696.

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Fahie, Monifa A. V., ed. Nanopore Technology. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0806-7.

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Gracheva, Maria E., ed. Nanopore-Based Technology. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-773-6.

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Edel, Joshua, and Tim Albrecht, eds. Nanopores for Bioanalytical Applications. Cambridge: Royal Society of Chemistry, 2012. http://dx.doi.org/10.1039/9781849735278.

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Long, Yi-Tao, ed. Confining Electrochemistry to Nanopores. Cambridge: Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781788013260.

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Iqbal, Samir M. Nanopores: Sensing and Fundamental Biological Interactions. Boston, MA: Springer Science+Business Media, LLC, 2011.

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Sohn, Hong Yong. Chemical vapor synthesis of inorganic nanopowders. Hauppauge, N.Y: Nova Science Publishers, 2011.

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Nanopowders and nanocoatings: Production, properties and applications. New York: Nova Science Publishers, 2010.

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Cotler, V. F. Nanopowders and nanocoatings: Production, properties, and applications. Hauppauge, N.Y: Nova Science Publishers, 2009.

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Book chapters on the topic "Nanopower"

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Liu, Maoqiang, Kevin Pelzers, Rainier van Dommele, Arthur van Roermund, and Pieter Harpe. "Nanopower SAR ADCs with Reference Voltage Generation." In Low-Power Analog Techniques, Sensors for Mobile Devices, and Energy Efficient Amplifiers, 59–82. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-97870-3_4.

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Ivanov, Vadim. "Design of Powerful DCDC Converters with Nanopower Consumption." In Low-Power Analog Techniques, Sensors for Mobile Devices, and Energy Efficient Amplifiers, 31–57. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-97870-3_3.

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Romani, A., M. Dini, M. Filippi, M. Tartagni, and E. Sangiorgi. "Nanopower-Integrated Electronics for Energy Harvesting, Conversion, and Management." In Future Trends in Microelectronics, 275–89. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119069225.ch3-3.

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Wolf, D. E., L. Brendel, M. Fendrich, and R. Zinetullin. "Nanopowder Sintering." In Nanoparticles from the Gasphase, 161–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28546-2_7.

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Venkatesan, Bala Murali, and Rashid Bashir. "Solid-State Nanopore Sensors for Nucleic Acid Analysis." In Nanopores, 1–33. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0_1.

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Wanunu, Meni, Allison Squires, and Amit Meller. "Capture and Translocation of Nucleic Acids into Sub-5 nm Solid-State Nanopores." In Nanopores, 227–54. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0_10.

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Peng, Hongbo, Binquan Luan, and Gustavo Stolovitzky. "Nanopore-Based DNA Sequencing and DNA Motion Control." In Nanopores, 255–86. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0_11.

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Timp, Gregory, Utkur Mirsaidov, Winston Timp, Jiwook Shim, Deqiang Wang, Valentin Dimitrov, Jan Scrimgeour, et al. "Third Generation DNA Sequencing with a Nanopore." In Nanopores, 287–311. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0_12.

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Guan, Xiyun, Ranulu Samanthi S. de Zoysa, Dilani A. Jayawardhana, and Qitao Zhao. "Stochastic Detection of Terrorist Agents and Biomolecules in a Biological Channel." In Nanopores, 313–34. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0_13.

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Comer, Jeffrey, and Aleksei Aksimentiev. "Nanopore Force Spectroscopy: Insights from Molecular Dynamics Simulations." In Nanopores, 335–56. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8252-0_14.

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Conference papers on the topic "Nanopower"

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Koymen, Itir, and Emmanuel M. Drakakis. "CMOS-based nanopower memristor dynamics emulator." In 2014 14th International Workshop on Cellular Nanoscale Networks and their Applications (CNNA). IEEE, 2014. http://dx.doi.org/10.1109/cnna.2014.6888637.

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De Rose, Raffaele, Domenico Albano, Felice Crupi, and Marco Lanuzza. "Design of a sub-1-V nanopower CMOS current reference." In 2017 European Conference on Circuit Theory and Design (ECCTD). IEEE, 2017. http://dx.doi.org/10.1109/ecctd.2017.8093351.

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Pal, Pratosh Kumar, Avaneesh Kumar Dubey, Ankur Kumar, Vikrant Varshney, and Rajendra Kumar Nagaria. "A 0.55V, 28.6ppm/◦C Nanopower Subthreshold Voltage Reference with Body Biasing." In 2018 15th IEEE India Council International Conference (INDICON). IEEE, 2018. http://dx.doi.org/10.1109/indicon45594.2018.8987157.

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Vita, Giuseppe De, and Giuseppe Iannaccone. "A Sub-1 V, 10 ppm/°C, Nanopower Voltage Reference Generator." In ESSCIRC 2006. Proceedings of the 32nd European Solid-State Circuits Conference. IEEE, 2006. http://dx.doi.org/10.1109/esscir.2006.307592.

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Sawigun, Chutham, Michiel Grashuis, Ralf Peeters, and Wouter Serdijn. "Nanopower sampled data wavelet filter design using Switched Gain Cell technique." In 2009 IEEE International Symposium on Circuits and Systems - ISCAS 2009. IEEE, 2009. http://dx.doi.org/10.1109/iscas.2009.5117806.

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Pawarangkoon, Prajuab. "A Nanopower 4th-Order Chebyshev Lowpass Filter For ECG Detection System." In 2018 IEEE Asia Pacific Conference on Circuits and Systems (APCCAS). IEEE, 2018. http://dx.doi.org/10.1109/apccas.2018.8605626.

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Cordova, David, Arthur C. de Oliveira, Pedro Toledo, Hamilton Klimach, Sergio Bampi, and Eric Fabris. "A sub-1 V, nanopower, ZTC based zero-VT temperature-compensated current reference." In 2017 IEEE International Symposium on Circuits and Systems (ISCAS). IEEE, 2017. http://dx.doi.org/10.1109/iscas.2017.8050289.

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Yueming Sun, Jiana Lou, and Xiaobo Wu. "A nanopower single-trim voltage reference in a 0.13/im digital CMOS process." In 2010 IEEE Region 10 Conference (TENCON 2010). IEEE, 2010. http://dx.doi.org/10.1109/tencon.2010.5686401.

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Huang, Zhangcai, Qin Luo, and Yasuaki Inoue. "A CMOS Sub-l-V nanopower current and voltage reference with leakage compensation." In 2010 IEEE International Symposium on Circuits and Systems - ISCAS 2010. IEEE, 2010. http://dx.doi.org/10.1109/iscas.2010.5537636.

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Li, Jian, Jiancheng Li, and Li Yang. "A nanopower, high PSRR full CMOS voltage reference circuit consisting of subthreshold MOSFETs." In 2015 IEEE 11th International Conference on ASIC (ASICON ). IEEE, 2015. http://dx.doi.org/10.1109/asicon.2015.7517079.

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Reports on the topic "Nanopower"

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James V. Marzik. Plasma Synthesized Doped Boron Nanopowder for MgB2 Superconductors. Office of Scientific and Technical Information (OSTI), March 2012. http://dx.doi.org/10.2172/1036975.

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Aumann, C. E., G. L. Skofronick, and J. A. Martin. Oxidation behavior of aluminum nanopowders. Office of Scientific and Technical Information (OSTI), November 1994. http://dx.doi.org/10.2172/10194316.

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Leung, Kevin, Tina Maria Nenoff, Louise Jacqueline Criscenti, Z. Tang, and J. H. Dong. Capturing CO2 via reactions in nanopores. Office of Scientific and Technical Information (OSTI), October 2008. http://dx.doi.org/10.2172/1086827.

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Doyle, Barney Lee, David Martin Follstaedt, Paolo Rossi, and Adam K. Norman. Direct single ion machining of nanopores. Office of Scientific and Technical Information (OSTI), October 2004. http://dx.doi.org/10.2172/919651.

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Elabd, Yossef A., and Giuseppe R. Palmese. Selective and Responsive Nanopore-Filled Membranes. Fort Belvoir, VA: Defense Technical Information Center, March 2011. http://dx.doi.org/10.21236/ada545036.

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Golovchenko, Jene A., and Daniel Branton. Electrical Properties of Solid-State Nanopore Sensors. Fort Belvoir, VA: Defense Technical Information Center, September 2003. http://dx.doi.org/10.21236/ada417079.

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Patel, Kamlesh D. High-density nanopore array for selective biomolecule transport. Office of Scientific and Technical Information (OSTI), November 2011. http://dx.doi.org/10.2172/1035348.

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King, David M., Arrelaine Dameron, Paul Lichty, and James Trevey. Low-Cost Encapsulation of Silicon-Based Nanopowders Final Report. Office of Scientific and Technical Information (OSTI), March 2018. http://dx.doi.org/10.2172/1429761.

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Golovchenko, J. A., and D. Branton. Ion Beam Nanosculpting and Materials Science with Single Nanopores. Office of Scientific and Technical Information (OSTI), October 2009. http://dx.doi.org/10.2172/1040619.

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Ji, Qing, Y. Chen, Ximan Jiang, Lili Ji, and K. N. Leung. Formation of Nanopore-Arrays by Plasma-based Thin FilmDeposition. Office of Scientific and Technical Information (OSTI), March 2005. http://dx.doi.org/10.2172/932785.

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