Relevant bibliographies by topics / Structure of nanoscale materials

Contents

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

Academic literature on the topic 'Structure of nanoscale materials'

Author: Grafiati
Published: 17 September 2021
Last updated: 18 February 2022

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Journal articles on the topic "Structure of nanoscale materials"

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Bentley, Cameron L., Minkyung Kang, and Patrick R. Unwin. "Nanoscale Structure Dynamics within Electrocatalytic Materials." Journal of the American Chemical Society 139, no. 46 (October 23, 2017): 16813–21. http://dx.doi.org/10.1021/jacs.7b09355.

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Lookman, Turab, and Peter Littlewood. "Nanoscale Heterogeneity in Functional Materials." MRS Bulletin 34, no. 11 (November 2009): 822–31. http://dx.doi.org/10.1557/mrs2009.232.

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AbstractThe physical properties that make “functional” materials worthy of their moniker frequently arise because of a phase transition that establishes a new kind of order as the material is cooled from a parent state. Such ordered states include ferroelectrics, ferromagnets, and structurally ordered martensites; because these states all break an orientational symmetry, and it is rare that one can produce the conditions for single domain crystallinity, the observed configuration is generally heterogeneous. However, the conditions under which domain structures form are highly constrained, especially by elastic interactions within a solid; consequently, the observed structures are far from fully random, even if disorder is present. Often the structure of the heterogeneity is important to the function, as in shape-memory alloys. Increasingly, we are surprised to discover new phases inside solids that are themselves a heterogeneous modulation of their parents.
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Stan, Gheorghe, Richard S. Gates, Qichi Hu, Kevin Kjoller, Craig Prater, Kanwal Jit Singh, Ebony Mays, and Sean W. King. "Relationships between chemical structure, mechanical properties and materials processing in nanopatterned organosilicate fins." Beilstein Journal of Nanotechnology 8 (April 13, 2017): 863–71. http://dx.doi.org/10.3762/bjnano.8.88.

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The exploitation of nanoscale size effects to create new nanostructured materials necessitates the development of an understanding of relationships between molecular structure, physical properties and material processing at the nanoscale. Numerous metrologies capable of thermal, mechanical, and electrical characterization at the nanoscale have been demonstrated over the past two decades. However, the ability to perform nanoscale molecular/chemical structure characterization has only been recently demonstrated with the advent of atomic-force-microscopy-based infrared spectroscopy (AFM-IR) and related techniques. Therefore, we have combined measurements of chemical structures with AFM-IR and of mechanical properties with contact resonance AFM (CR-AFM) to investigate the fabrication of 20–500 nm wide fin structures in a nanoporous organosilicate material. We show that by combining these two techniques, one can clearly observe variations of chemical structure and mechanical properties that correlate with the fabrication process and the feature size of the organosilicate fins. Specifically, we have observed an inverse correlation between the concentration of terminal organic groups and the stiffness of nanopatterned organosilicate fins. The selective removal of the organic component during etching results in a stiffness increase and reinsertion via chemical silylation results in a stiffness decrease. Examination of this effect as a function of fin width indicates that the loss of terminal organic groups and stiffness increase occur primarily at the exposed surfaces of the fins over a length scale of 10–20 nm. While the observed structure–property relationships are specific to organosilicates, we believe the combined demonstration of AFM-IR with CR-AFM should pave the way for a similar nanoscale characterization of other materials where the understanding of such relationships is essential.
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Ariga, Katsuhiko. "Progress in Molecular Nanoarchitectonics and Materials Nanoarchitectonics." Molecules 26, no. 6 (March 15, 2021): 1621. http://dx.doi.org/10.3390/molecules26061621.

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Although various synthetic methodologies including organic synthesis, polymer chemistry, and materials science are the main contributors to the production of functional materials, the importance of regulation of nanoscale structures for better performance has become clear with recent science and technology developments. Therefore, a new research paradigm to produce functional material systems from nanoscale units has to be created as an advancement of nanoscale science. This task is assigned to an emerging concept, nanoarchitectonics, which aims to produce functional materials and functional structures from nanoscale unit components. This can be done through combining nanotechnology with the other research fields such as organic chemistry, supramolecular chemistry, materials science, and bio-related science. In this review article, the basic-level of nanoarchitectonics is first presented with atom/molecular-level structure formations and conversions from molecular units to functional materials. Then, two typical application-oriented nanoarchitectonics efforts in energy-oriented applications and bio-related applications are discussed. Finally, future directions of the molecular and materials nanoarchitectonics concepts for advancement of functional nanomaterials are briefly discussed.
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Conradson, Steven, Francisco Espinosa-Faller, and Phillip Villella. "Local structure probes of nanoscale heterogeneity in crystalline materials." Journal of Synchrotron Radiation 8, no. 2 (March 1, 2001): 273–75. http://dx.doi.org/10.1107/s0909049500018999.

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Yu, Edward T., and Stephen J. Pennycook. "Nanoscale Characterization of Materials." MRS Bulletin 22, no. 8 (August 1997): 17–21. http://dx.doi.org/10.1557/s0883769400033753.

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One of the dominant trends in current research in materials science and related fields is the fabrication, characterization, and application of materials and device structures whose characteristic feature sizes are at or near the nanometer scale. Achieving an understanding of—and ultimately control over—the properties and behavior of a wide range of materials at the nanometer scale has therefore become a major theme in materials research. As our ability to synthesize materials and fabricate structures in this size regime improves, effective characterization of materials at the nanometer scale will continue to increase in importance.Central to this activity are the development and application of effective experimental techniques for performing characterization of structural, electronic, magnetic, optical, and other properties of materials with nanometer-scale spatial resolution. Two classes of experimental methods have proven to be particularly effective: scanning-probe techniques and electron microscopy. In this issue of MRS Bulletin, we have included eight articles that illustrate the elucidation of various aspects of nanometer-scale material properties using advanced scanningprobe or electron-microscopy techniques. Because the range of both experimental techniques and applications is extremely broad—and rapidly increasing—our intent is to provide several examples rather than a comprehensive treatment of this extremely active and rapidly growing field of research.
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Azat, Seitkhan, Valodia V. Pavlenko, Almagul R. Kerimkulova, and Zulkhair A. Mansurov. "Synthesis and Structure Determination of Carbonized Nano Mesoporous Materials Based on Vegetable Raw Materials." Advanced Materials Research 535-537 (June 2012): 1041–45. http://dx.doi.org/10.4028/www.scientific.net/amr.535-537.1041.

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This article presents the results of the synthesis of carbon nanomaterials: Nanoscale materials obtained by carbonization of waste agricultural products (apricot kernel, walnut, rice husk). The results of physico-chemical characteristics of the obtained nanomaterials.
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Cui, Tianyu, Qingsuo Liu, Xin Zhang, Dawei Zhang, and Jinman Li. "Characterization of a Nanocrystalline Structure Formed by Crystal Lattice Transformation in a Bulk Steel Material." Metals 9, no. 1 (December 20, 2018): 3. http://dx.doi.org/10.3390/met9010003.

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The formation of nanocrystalline structures in bulk metal materials is of great significance for both investigating the structural features of nanocrystalline materials and enhancing the value of bulk metal materials in engineering applications. Herein, we report a nanocrystalline structure formed by lattice transformation in a three-dimensional bulk metal material. We characterized its phase composition, three-dimensional features, and boundary structure. This nanocrystalline structure had microscale length and height and nanoscale width, which gave it a “nanoplate” structure in three-dimensional space. We observed edge dislocations in the interior of the nanocrystalline structure. A unique transitional boundary that contributed to maintaining its nanoscale size was found at the border between the parent phase and the nanocrystalline structure.
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Chen, Si-Ming, Huai-Ling Gao, Yin-Bo Zhu, Hong-Bin Yao, Li-Bo Mao, Qi-Yun Song, Jun Xia, et al. "Biomimetic twisted plywood structural materials." National Science Review 5, no. 5 (July 30, 2018): 703–14. http://dx.doi.org/10.1093/nsr/nwy080.

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Abstract Biomimetic designs based on micro/nanoscale manipulation and scalable fabrication are expected to develop new-style strong, tough structural materials. Although the mimicking of nacre-like ‘brick-and-mortar’ structure is well studied, many highly ordered natural architectures comprising 1D micro/nanoscale building blocks still elude imitation owing to the scarcity of efficient manipulation techniques for micro/nanostructural control in practical bulk counterparts. Herein, inspired by natural twisted plywood structures with fascinating damage tolerance, biomimetic bulk materials that closely resemble natural hierarchical structures and toughening mechanisms are successfully fabricated through a programmed and scalable bottom-up assembly strategy. By accurately engineering the arrangement of 1D mineral micro/nanofibers in biopolymer matrix on the multiscale, the resultant composites display optimal mechanical performance, superior to many natural, biomimetic and engineering materials. The design strategy allows for precise micro/nanostructural control at the macroscopic 3D level and can be easily extended to other materials systems, opening up an avenue for many more micro/nanofiber-based biomimetic designs.
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Schubert, Ulrich, Guido Kickelbick, and Nicola Hüsing. "Nanoscale Structures of Sol-Gel Materials." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 354, no. 1 (December 2000): 107–22. http://dx.doi.org/10.1080/10587250008023607.

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Dissertations / Theses on the topic "Structure of nanoscale materials"

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Kuna, Jeffrey James. "The effect of nanoscale structure on interfacial energy." Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/62744.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2011.
Vita. Cataloged from PDF version of thesis.
Includes bibliographical references.
Interfaces are ubiquitous in nature. From solidification fronts to the surfaces of biological cells, interfacial properties determine the interactions between a solid and a liquid. Interfaces, specifically liquid-solid interfaces, play important roles in many fields of science. In the field of biology, interfaces are fundamental in determining cell-cell interactions, protein folding behavior and assembly, and ligand binding. In chemistry, heterogeneous catalysts greatly increase reaction rates of reactions occurring at the interface. In materials science, crystallization and the resulting crystal habit are determined by interfacial properties, and interfaces affect diffusion through polycrystalline materials. In nanotechnology, much work on self-assembly, molecular recognition, catalysis, electrochemistry and numerous other applications depends on the properties of interfaces. The structure and properties of interfaces have been studied experimentally using a variety of techniques including various forms of microscopy, wetting measurements, and scattering techniques. Conventionally, the typical interface considered was highly homogeneous and exhibited a uniform composition and roughness. In contrast, many of the interfaces encountered in biological or nanotechnological systems have surfaces with a greater degree of complexity. While the surface may be compositionally homogeneous over a large area, these surfaces are structured and have a complex surface topology. On a mixed interface, several different chemical groups may be present on the surface, and the chemical composition can vary on a sub-nanometer length scale. Structured systems are inherently difficult to experimentally measure. Most techniques available to characterize interfaces average properties over the entire surface and are not sensitive to nanoscale variations. Furthermore, many of these techniques are incapable of distinguishing global, surface-dependent properties from artifactual influences. Many surface characterization techniques require a large, flat, smooth surface. Preparation of mixed interfaces is an experimental challenge as well as many mixed interfaces with nanoscale structure are present on objects that are themselves nanoscale, such as proteins. Several technological hurdles exist that limit the ability to produce nanoscale mixed interfaces large enough for conventional measurements. In this thesis, the effect of surface structure on wetting behavior was investigated. Interfaces can be characterized by the energy required to form them, a quantity called interfacial energy. Models have been developed to describe the interfacial energy of mixed interfaces for a wide range of surfaces. These models only account for the composition of the surface. The wetting behavior of mixed surfaces has also been related to artifact-dependent wetting effects (namely the effect of a boundary or asperity). No attempt has been made to incorporate surface structure into a global expression of interfacial energy. This thesis will study how the structure of an interface determines the resulting interfacial energy. Surfaces prepared with chemical domains of different length scales demonstrate and interfacial energy trend with significant deviation from the current best model. Specifically, the observed trend is non-linear, unlike the conventional model, and furthermore in some cases, is non-monotonic. These deviations are shown to stem from the surfaces' intrinsic structure and are not an artifact of the measurement process or surface defects. The deviations from the predicted trend are explained by the molecular scale structure of the solvent. The two proposed mechanisms, cavitation and confinement, arise when surface features are smaller than a solvent-dependent length. With cavitation, nonwetting surface features below a size threshold are more wetting than would be expected. With confinement, wetting patches become less wetting as their dimensions are decreased. Molecular dynamics simulations support the proposed mechanisms. Additional experimental results provide further experimental evidence of the proposed molecular-scale wetting phenomena.
by Jeffrey James Kuna.
Ph.D.
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Janko, Marek. "Structure and stability of biological materials – characterisation at the nanoscale." Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-143453.

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Tuchband, Michael R. "Revealing the Nanoscale Structure and Behavior of the Twist-Bend Nematic Liquid Crystal Phase." Thesis, University of Colorado at Boulder, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10752109.

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The nematic phases of liquid crystals have been the most thoroughly investigated since the founding of the liquid crystal field in the early 1900’s. The resulting technologies, most notably the liquid crystal display, have changed our world and spawned an entire industry. Consequently, the recent identification of a new type of nematic – the twist-bend nematic – was met with as much surprise as excitement, as it melds the fluid properties and environmental responsiveness of conventional nematics with the intrinsic polarization and complex ordering of bent-core liquid crystals. I summarize the history of the twist-bend nematic phase, charting the development of our understanding from its first identification to the present day. Furthermore, I enumerate and highlight my own efforts in the field to characterize the behavior and nanoscale organization of the twist-bend phase.

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Ehrlich, Deborah J. C. "Synthetic strategies for control of structure from individual macromolecules to nanoscale materials to networks." Thesis, Massachusetts Institute of Technology, 2019. https://hdl.handle.net/1721.1/122451.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2019
Cataloged from PDF version of thesis.
Includes bibliographical references.
Chapter 1. Aqueous self-assembly of prodrug macromonomers. A series of highly tunable micelles for drug delivery were made from norbornene based poly(ethylene glycol) macromonomers with covalently linked drugs. A total of five macromonomers were made using three different drugs (telmisartan, paclitaxel, and SN-38) and three different drug loadings. Combinations of these macromonomers were then allowed to self assemble into micellar aggregates. The size, stability, and shape of these micellar aggregates were controlled with the highly versatile structure. Chapter 2. Post micellization modification of norbornene-containing prodrug macromonomers. Highly tunable micelles for drug delivery were functionalized after their selfassembly. Post-micellization inverse electron demand Diels-Alder reactions of norbornenes and tetrazines were used to signal changes in micelle size and stability through the addition of either hydrophilic or hydrophobic tetrazines.
Thiol-ene additions reactions were used to increase micelle size and form chemically crosslinked nanoparticles. These modifications of norbornene-containing prodrug macromonomer assemblies illustrate their versatility. Chapter 3. Synthesis of polymers by iterative exponential growth. A scalable synthetic route that enables absolute control over polymer sequence and structure has remained a key challenge in polymer chemistry. Here, we report an iterative exponential growth plus side-chain functionalization (IEG+) strategy for the production of macromolecules with defined sequence, length, and stereoconfiguration. Each IEG+ cycle begins with the azide opening of an enantiopure epoxide, followed by side chain functionalization, alkyne deprotection, and copper-catalyzed azide-alkyne cycloaddition (CuAAC). These cycles have been conducted to form unimolecular macromolecules with molar masses of over 6,000 g/mol.
Subsequent modifications to IEG+ allow for the functionalization of monomers prior to the IEG+ cycle, expanding the library of compatible side chain chemistries. Chapter 4. Introduction to elastomer toughening strategies. Silicone elastomers are ubiquitous. Here, silicone elastomers are discussed in terms of network structure, the impact of network structure upon physical properties, and modifications of network structure in order to achieve desired physical properties. Fillers, the standard toughening strategy, are discussed in conjunction with entanglement density. Focus is placed on the impact of entanglement density on material properties. Topological networks are discussed and noted for their stress dissipative properties. Chapter 5. Topology modification of polydimethylsiloxane elastomers through loop formation. Topological networks are well known for their stress dissipation through the pulley effect leading to soft, extensible materials.
Combining these properties with a traditionally crosslinked network to produce a hybrid material allows for enhanced extensibility without a loss in modulus. Here, such hybrid networks were made with poly(dimethyl siloxane) polymers of a range of molecular weights. Side-loop polymer brushes were synthesized and then crosslinked to create hybrid networks with the statistical formation of topological bonds. These materials were characterized through tensile testing. Elastomers formed with the same molecular weight polymer in both side-loops and network formation did not show mechanical properties that depended upon the fraction of networks used for brush formation. Elastomers made with long polymers in brush formation and shorter polymers for network formation resulted in highly extensible systems without significant loss in modulus.
by Deborah J.C. Ehrlich.
Ph. D.
Ph.D. Massachusetts Institute of Technology, Department of Chemistry
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Salahshoor, Pirsoltan Hossein. "Nanoscale structure and mechanical properties of a Soft Material." Digital WPI, 2013. https://digitalcommons.wpi.edu/etd-theses/924.

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"Recently, hydrogel have found to be promising biomaterials since their porous structure and hydrophilicity enables them to absorb a large amount of water. In this study the role of water on the mechanical properties of hydrogel are studied using ab-initio molecular dynamics (MD) and coarse-grained simulations. Condensed-Phased Optimized Molecular Potential (COMPASS) and MARTINI force fields are used in the all-atom atomistic models and coarse-grained simulations, respectively. The crosslinking process is modeled using a novel approach by cyclic NPT and NVT simulations starting from a high temperature, cooling down to a lower temperature to model the curing process. Radial distribution functions for different water contents (20%, 40%, 60% and 80%) have shown the crosslinks atoms are more hydrophilic than the other atoms. Diffusion coefficients are quantified in different water contents and the effect of crosslinking density on the water diffusion is studied. Elasticity parameters are computed by constant strain energy minimization in mechanical deformation simulations. It is shown that an increase in the water content results in a decrease in the elastic. Finally, continuum hyper elastic model of contact lens is studied for three different loading scenarios using Finite Element Model. "
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Janko, Marek [Verfasser], and Robert [Akademischer Betreuer] Stark. "Structure and stability of biological materials – characterisation at the nanoscale / Marek Janko. Betreuer: Robert Stark." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2012. http://d-nb.info/1022791176/34.

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Hatton, Hilary J. "Magnetic and structural studies of nanoscale multilayer and granular alloy systems of Ag and FeCo." Thesis, University of Sheffield, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286916.

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Schiffrin, Agustin. "Self-assembly of amino acids on noble metal surfaces : morphological, chemical and electronic control of matter at the nanoscale." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/798.

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Designing novel nanostructures which exploit the self-assembly capabilities of biomolecules yields a promising approach to control matter at the nanoscale. Here, the homochiral molecular self-assemblies of the methionine and tyrosine amino acids on the monocrystalline Ag(111) and Cu(111) surfaces are characterized by means of scanning tunneling microscopy (STM) and spectroscopy (STS), helium atom scattering (HAS), x-ray photoelectron spectroscopy (XPS) and near-edge x-ray absorption fine structure (NEXAFS) in ultrahigh vacuum (UHV). On Ag(111), methionine self-assembles into supramolecular chains following the <110> substrate axis, forming regular nanogratings with tunable periodicity. Within the nanowires, a zwitterionic dimerization scheme is revealed. STS shows that the biomolecular nanostructures act as tunable one-dimensional quantum resonators for the surface state electrons. Zero-dimensional electronic confinement is achieved by positioning single iron atoms in the molecular trenches. This shows a novel approach to control the dimensionality of surface state electrons. The nanogratings were exploited to steer the spontaneous one-dimensional ordering of cobalt and iron atoms. For T > 15 K, the metal species self-align into homogeneously distributed chains in between the biomolecular trenches with ~25 Å interatomic distace. For Co, the dynamics of the self-alignment was monitored, revealing a reduced mobility in comparison with isolated Co atoms on bare Ag(111). On Cu(111), the self-assembly of methionine is influenced by the substrate reactivity and its temperature during molecular deposition. For T < 273 K, the biomolecules assemble in anisotropic extended clusters oriented with a -10° rotation off the <110> substrate orientations, whereas above 283 K a regularly ordered 1D phase arises with a +10° rotation off these high-symmetry axis. XPS reveals a structural transformation triggered by a thermally activated deprotonation of the zwitterionic ammonium group. On Ag(111), tyrosine self-assembles above a critical temperature into linear structures primarily following the substrate crystalline symmetry. A zwitterionic non-covalent molecular dimerization is demonstrated, NEXAFS data providing evidence of a non-flat adsorption of the phenyl ring. This recalls the geometrical pattern of methionine on Ag(111) and supports a universal self-assembling scheme for amino acids on close-packed noble metal surfaces, the different mesoscopic ordering being determined by the side chain reactivity.
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Ohmura, Jacqueline (Jacqueline Frances). "Utilizing viruses to probe the material process - structure - property relationship : controlling catalytic properties via protein engineering and nanoscale synthesis." Thesis, Massachusetts Institute of Technology, 2018. http://hdl.handle.net/1721.1/115761.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biological Engineering, 2018.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 136-146).
From the fabrication of fine chemicals, to the increasing attainability of a non-petrochemical based energy infrastructure, catalysts play an important role in meeting the increasing energy and consumable demands of today without compromising the global health of tomorrow. Development of these catalysts relies on the fundamental understanding of the effects individual catalyst properties have on catalytic function. Unfortunately, control, and therefore deconvolution of individual parameter effects, can be quite challenging. Due to the nanoscale formfactor and wide range of available surface chemistries, biological catalyst fabrication affords one solution to this challenge. To this end, this work details the processing of M13 bacteriophage as a synthetic toolbox to modulate key catalyst parameters to elucidate the relationship between catalyst structure and performance. With respect to electrocatalysis, a biotemplating method for the development of tunable 3D nanofoams is detailed. Viral templates were rationally assembled into a variety of genetically programmable architectures and subsequently templated into a variety of material compositions. Subsequently, this synthetic method was employed to examine the effects of nanostructure on electro-catalytic activity. Next, nanoparticle driven heterogeneous catalysis was targeted. Nanoparticle-protein binding affinities were leveraged to explore the relationship between nanoparticles and their supports to identify a selective, base free alcohol oxidation catalyst. Finally, the surface proteins of the M13 virus were modified to mirror homogeneous copper-ligand chemistries. These viruses displayed binding pocket free copper complexation and catalytic efficacy in addition to recyclability and solvent robustness. Subsequently, the multiple functional handles of the viron were utilized to create catalytic ensembles of varying ratios. Single and dendrimeric TEMPO (4-Carboxy-2,2,6,6-tetramethylpiperidine 1-oxyl) were chemically conjugated to the surface of several catalytically active phage clones further tailoring catalytic function. Taken together, these studies provide strong evidence of the utility of biologically fabricated materials for catalytic design.
by Jacqueline Ohmura.
Ph. D.
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Leininger, Wyatt Christopher. "Design and Control of a Micro/Nano Load Stage for In-Situ AFM Observation and Nanoscale Structural and Mechanical Characterization of MWCNT-Epoxy Composites." Thesis, North Dakota State University, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10680380.

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Nanomaterial composites hold improvement potential for many materials. Improvements arise through known material behaviors and unique nanoscale effects to improve performance in areas including elastic modulus and damping as well as various processes, and products. Review of research spurred development of a load-stage. The load stage could be used independently, or in conjunction with an AFM to investigate bulk and nanoscale material mechanics.

The effect of MWCNT content on structural damping, elastic modulus, toughness, loss modulus, and glass transition temperature was investigated using the load stage, AMF, and DMA. Initial investigation showed elastic modulus increased 23% with 1wt.% MWCNT versus pure epoxy and in-situ imaging observed micro/nanoscale deformation.

Dynamic capabilities of the load stage were investigated as a method to achieve higher stress than available through DMA. The system showed energy dissipation across all reinforce levels, with ~480% peak for the 1wt.% MWCNT material vs. the neat epoxy at 1Hz.

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Books on the topic "Structure of nanoscale materials"

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Fan, Chunhai. DNA Nanotechnology: From Structure to Function. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013.

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Bellucci, Stefano. Physical Properties of Ceramic and Carbon Nanoscale Structures: The INFN Lectures, Vol. II. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

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Scherer, Maik Rudolf Johann. Double-Gyroid-Structured Functional Materials: Synthesis and Applications. Heidelberg: Springer International Publishing, 2013.

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name, No. Nanoscale materials. Boston, MA: Kluwer Academic Publishers, 2003.

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Liz-Marzán, Luis M., and Prashant V. Kamat, eds. Nanoscale Materials. Boston: Kluwer Academic Publishers, 2004. http://dx.doi.org/10.1007/b101855.

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Mukhopadhyay, Sharmila M., ed. Nanoscale Multifunctional Materials. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118114063.

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Symposium, A. on Microstructuring and Microsystems (1995 Strasbourg France). Small scale structures: Proceedings of Symposium A on Microstructuring and Microsystems, Symposium B on Materials for Sensors: Functional Nanoscaled Structures, and Symposium E on Structure and Properties of Metallic Thin Films and Multilayers of the 1995 E-MRS Spring Conference, Strasbourg, France, May 22-26, 1995. Amsterdam: Elsevier, 1996.

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Nanoscale materials in chemistry. New York: Wiley-Interscience, 2001.

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Klabunde, Kenneth J. Nanoscale Materials in Chemistry. New York: John Wiley & Sons, Ltd., 2004.

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Tu, King-Ning, and Andriy M. Gusak. Kinetics in Nanoscale Materials. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118743140.

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Book chapters on the topic "Structure of nanoscale materials"

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Trellakis, Alex, and Peter Vogl. "Electronic Structure and Transport for Nanoscale Device Simulation." In Materials for Tomorrow, 123–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-47971-0_5.

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Resasco, Daniel E. "Carbon Nanotubes and Related Structures." In Nanoscale Materials in Chemistry, 441–91. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470523674.ch13.

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Tiedke, S., and T. Schmitz. "Electrical Characterization of Nanoscale Ferroelectric Structures." In Nanoscale Characterisation of Ferroelectric Materials, 87–114. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08901-9_3.

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Yarin, Alexander L., Min Wook Lee, Seongpil An, and Sam S. Yoon. "Characterization of Self-Healing Phenomena on Micro- and Nanoscale Level." In Advanced Structured Materials, 121–34. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-05267-6_5.

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Webb, J., T. G. St. Pierre, and D. J. Macey. "New Materials and Nanoscale Structures derived from Biominerals." In Main Group Elements and their Compounds, 18–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-52478-3_3.

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Pierre, T. G. St, P. Sipos, P. Chan, W. Chua-Anusorn, K. R. Bauchspiess, and J. Webb. "Synthesis of Nanoscale Iron Oxide Structures Using Protein Cages and Polysaccharide Networks." In Nanophase Materials, 49–56. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1076-1_6.

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Campi, Gaetano. "Structural Fluctuations at Nanoscale in Complex Functional Materials." In Synchrotron Radiation Science and Applications, 181–89. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-72005-6_14.

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Moon, S. M., and Nam Hee Cho. "Synthesis and Structural Characterization of Nanoscale BaTiO3 Powders." In Materials Science Forum, 1323–27. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-443-x.1323.

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Yanagisawa, Susumu, and Ikutaro Hamada. "Nanoscale First-Principles Electronic Structure Simulations of Materials Relevant to Organic Electronics." In Theoretical Chemistry for Advanced Nanomaterials, 89–131. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-0006-0_4.

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Schneider, Wolf-Dieter. "Fabrication and Characterization of Ordered Atomic-scale Structures – A Step towards Future Nanoscale Technology." In Engineering Materials, 3–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-12070-1_1.

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Conference papers on the topic "Structure of nanoscale materials"

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Liu, Yong, Ruiqing Chu, Zhijun Xu, Qian Chen, and Guorong Li. "Structure and electrical properties of (La,Ta)-doped (K0.5Na0.5)0.94Li0.06Nb0.95Ta0.05O3 ceramic." In Nanoscale Phenomena in Polar Materials. IEEE, 2011. http://dx.doi.org/10.1109/isaf.2011.6014003.

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Chen, Qian, Zhijun Xu, Ruiqing Chu, Yong Liu, Mingli Chen, Lin Shao, and Guorong Li. "Structure and electrical properties of Ho-modified Sr2Bi4Ti5O18 Lead-free piezoelectric ceramics." In Nanoscale Phenomena in Polar Materials. IEEE, 2011. http://dx.doi.org/10.1109/isaf.2011.6014004.

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Xing, Zhijiu, Li Li, Yuling Su, Dongmei Deng, Zhenjie Feng, Shixun Cao, and Jincang Zhang. "Effect of divalent Ca ions substitution on structure and properties in multiferroic YbCrO3 chromites." In Nanoscale Phenomena in Polar Materials. IEEE, 2011. http://dx.doi.org/10.1109/isaf.2011.6013987.

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Do, D., J. W. Kim, G. H. Kim, Y. R. Bae, E. S. Kim, S. S. Kim, M. H. Lee, et al. "EuMnO3 effects on structure and electrical properties of chemical solution deposited BiFeO3 thin films." In Nanoscale Phenomena in Polar Materials. IEEE, 2011. http://dx.doi.org/10.1109/isaf.2011.6014145.

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Yamazoe, Seiji, Akihiro Kohori, Hiroyuki Sakurai, Takahiro Wada, Yuuki Kitanaka, Yuji Noguchi, and Masaru Miyayama. "Study on domain structure of NaNbO3 films by laser beam scanning microscope and piezoresponse force microscope." In Nanoscale Phenomena in Polar Materials. IEEE, 2011. http://dx.doi.org/10.1109/isaf.2011.6014111.

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Ho, Dean, Ben Chu, Hyeseung Lee, and Carlo D. Montemagno. "Nanoscale hybrid protein/polymer functionalized materials." In Smart Structures and Materials, edited by Vijay K. Varadan. SPIE, 2004. http://dx.doi.org/10.1117/12.539315.

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Tang, Xiaoduan, Shen Xu, and Xinwei Wang. "Far-field nanoscale thermal and structure imaging." In ICALEO® 2012: 31st International Congress on Laser Materials Processing, Laser Microprocessing and Nanomanufacturing. Laser Institute of America, 2012. http://dx.doi.org/10.2351/1.5062395.

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Gromov, Victor, Yurii Ivanov, Elena Nikitina, Krestina Aksenova, and Olga Semina. "Nanoscale level of the deformation band formation in bainite steel." In ADVANCED MATERIALS WITH HIERARCHICAL STRUCTURE FOR NEW TECHNOLOGIES AND RELIABLE STRUCTURES 2016: Proceedings of the International Conference on Advanced Materials with Hierarchical Structure for New Technologies and Reliable Structures 2016. Author(s), 2016. http://dx.doi.org/10.1063/1.4966361.

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Maheshwari, Gunjan, Nilanjan Mallik, Jandro Abot, Albert Song, Emily Head, Mitul Dadhania, Vesselin Shanov, et al. "Nanoscale materials for engineering and medicine." In The 15th International Symposium on: Smart Structures and Materials & Nondestructive Evaluation and Health Monitoring, edited by Vijay K. Varadan. SPIE, 2008. http://dx.doi.org/10.1117/12.782591.

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Asmatulu, Ramazan, William B. Spillman, Jr., and Richard O. Claus. "Dielectric constant measurements of nanoscale thickness polymeric films." In Smart Structures and Materials, edited by William D. Armstrong. SPIE, 2005. http://dx.doi.org/10.1117/12.592928.

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Reports on the topic "Structure of nanoscale materials"

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Wirth, Brian. Modeling investigation of the stability and irradiation-induced evolution of nanoscale precipitates in advanced structural materials. Office of Scientific and Technical Information (OSTI), April 2015. http://dx.doi.org/10.2172/1178434.

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Pearton, S. J., P. H. Holloway, R. K. Singh, A. F. Hebard, and S. Hershfield. Nanoscale Devices and Novel Engineered Materials. Fort Belvoir, VA: Defense Technical Information Center, June 2001. http://dx.doi.org/10.21236/ada388032.

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Son, Steven F., Richard A. Yetter, and Alexander S. Mukasyan. Silicon-Based Nanoscale Composite Energetic Materials. Fort Belvoir, VA: Defense Technical Information Center, February 2013. http://dx.doi.org/10.21236/ada573851.

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Cooper, Stephen Lance. Quantum Materials at the Nanoscale - Final Report. Office of Scientific and Technical Information (OSTI), January 2016. http://dx.doi.org/10.2172/1234220.

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Grulke, Eric A., and Mahendra K. Sunkara. Nanoscale Materials and Architectures for Energy Conversion. Office of Scientific and Technical Information (OSTI), May 2011. http://dx.doi.org/10.2172/1171604.

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Vasudevan, Vijay K., and Jainagesh A. Sekhar. Lightweight, High-Strength, Age-Hardenable Nanoscale Materials. Fort Belvoir, VA: Defense Technical Information Center, March 2004. http://dx.doi.org/10.21236/ada422041.

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Castleman Jr, A. W. Cluster Dynamics: Foundations for Developing Nanoscale Materials. Fort Belvoir, VA: Defense Technical Information Center, December 2003. http://dx.doi.org/10.21236/ada423029.

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Kuljanishvili, Irma, and Venkat Chandrasekhar. Novel Nanoscale Materials for Energy Conversion Applications. Fort Belvoir, VA: Defense Technical Information Center, March 2011. http://dx.doi.org/10.21236/ada544921.

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Kostecki, Robert, Xiang Yun Song, Kim Kinoshita, and Frank McLarnon. Nanoscale fabrication and modification of selected battery materials. Office of Scientific and Technical Information (OSTI), June 2001. http://dx.doi.org/10.2172/834264.

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Blair, Steve. Engineered Photonic Materials for Nanoscale Optical Logic Devices. Fort Belvoir, VA: Defense Technical Information Center, February 2004. http://dx.doi.org/10.21236/ada422569.

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