Nanoparticles and Nanotechnology Research
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Nanoparticles, Nanocrystals, and Quantum Dots What They Are, Why They’Re Interesting, and What We Can Do with Them J
Nanoparticles, nanocrystals, and quantum dots What they are, why they’re interesting, and what we can do with them J. Nadeau, Department of Biomedical Engineering [email protected] Colloidal nanocrystals of different materials… …And different geometries From: Science. 2005 January 28; 307(5709): 538544. Medieval Nanotechnology! The colors in some stained- glass windows from medieval cathedrals are probably due to nanocrystals of compouds of Zn, Cd, S, and Se. History of nanoparticles 1980 Ekimov observed quantum confinement on a sample of glass containing PbS. 1982 Brus L.’s group conducted CdS colloid preparation and investigation of band-edge luminescence properties. 1993 Murray C., Norris D., Bawendi M., Synthesis and Characterization of Nearly Monodisperse CdE (E=S, Se, Te) Semiconductor Nano- crystallites. 1995 Hines M., Guyot-Sionnest P., reported synthesis and Characterization of Strongly Luminescent ZnS-Capped CdSe Nanocrystals 1998 Alivisatos and Nie independently reported Bio-application for core shell dots. 2001 Nie’s group described Quantum dot-tagged microbeads for multiplexed optical coding of biomolecules. 2003 T. Sargent at UOT observed electroluminescence spanning 1000 – 1600 nm originating from PbS nanocrystals embedded in a polymer matrix. What is a quantum dot? • Synthesis • Quantum mechanics • Optical properties WhatWhat isis itit goodgood for?for? ••InterestingInteresting physicsphysics ••ApplicationsApplications inin optoelectronicsoptoelectronics ••ApplicationsApplications inin biologybiology Synthesis Quick -
Charge Transport in Semiconductors Assembled from Nanocrystal Quantum Dots
ARTICLE https://doi.org/10.1038/s41467-020-16560-7 OPEN Charge transport in semiconductors assembled from nanocrystal quantum dots Nuri Yazdani1, Samuel Andermatt2, Maksym Yarema 1, Vasco Farto1, Mohammad Hossein Bani-Hashemian 2, Sebastian Volk1, Weyde M. M. Lin 1, Olesya Yarema 1, ✉ Mathieu Luisier 2 & Vanessa Wood 1 The potential of semiconductors assembled from nanocrystals has been demonstrated for a 1234567890():,; broad array of electronic and optoelectronic devices, including transistors, light emitting diodes, solar cells, photodetectors, thermoelectrics, and phase change memory cells. Despite the commercial success of nanocrystal quantum dots as optical absorbers and emitters, applications involving charge transport through nanocrystal semiconductors have eluded exploitation due to the inability to predictively control their electronic properties. Here, we perform large-scale, ab initio simulations to understand carrier transport, generation, and trapping in strongly confined nanocrystal quantum dot-based semiconductors from first principles. We use these findings to build a predictive model for charge transport in these materials, which we validate experimentally. Our insights provide a path for systematic engineering of these semiconductors, which in fact offer previously unexplored opportunities for tunability not achievable in other semiconductor systems. 1 Materials and Device Engineering Group, Department of Information Technology and Electrical Engineering, ETH Zurich, 8092 Zurich, Switzerland. 2 Nano ✉ TCAD Group, Department -
RSC NC-2Edn Contents 23..36
Contents List of Acronyms xxxvii Teaching (Nano) Materials xli Learning (Nano) Materials xliii Guessing (Nano) Materials xliv About the Authors xlv Acknowledgements l Nanofood for Thought–Thinking about Nanochemistry, Nanoscience, Nanotechnology and Nanosafety lii Chapter 1 Nanochemistry Basics 3 1.1 The Roots of Nanochemistry in Materials Chemistry 3 1.2 Synthesis of Materials and Nanomaterials 5 1.3 Materials Self-Assembly 9 1.4 Big Bang to the Universe 10 1.5 Why Nano? 10 1.6 What Do we Mean by Large and Small Nanomaterials? 11 1.7 Do it Yourself Quantum Mechanics 12 1.8 What is Nanochemistry? 13 1.9 Molecular vs. Materials Self-Assembly 13 1.10 What is Hierarchical Assembly? 14 Nanochemistry: A Chemical Approach to Nanomaterials By Geoffrey A. Ozin, Andre´C. Arsenault and Ludovico Cademartiri r Geoffrey A. Ozin, Andre´C. Arsenault and Ludovico Cademartiri 2009 Published by the Royal Society of Chemistry, www.rsc.org xxiii xxiv Contents 1.11 Directing Self-Assembly 15 1.12 Supramolecular Vision 15 1.13 Genealogy of Self-Assembling Materials 16 1.14 Unlocking the Key to Porous Solids 19 1.15 Learning from Biominerals – Form is Function 22 1.16 Can You Curve a Crystal? 24 1.17 Patterns, Patterns Everywhere 25 1.18 Synthetic Creations with Natural Form 26 1.19 Two-Dimensional Assemblies 28 1.20 SAMs and Soft Lithography 31 1.21 Clever Clusters 32 1.22 Extending the Prospects of Nanowires 34 1.23 Coercing Colloids 35 1.24 Mesoscale Self-Assembly 38 1.25 Materials Self-Assembly of Integrated Systems 40 References 41 Nanofood for Thought – -
1. INTRODUCTION Geometric Structure
1. INTRODUCTION Clusters, in general, are aggregates of atoms that are too large compared to atoms and molecules and too small compared to small pieces of crystals (bulk materials). Generally, clusters does not have the same structure or atomic arrangements as a bulk solid and can change its structure with the addition of just one or few atoms. As the number of atoms in the cluster increase, the bulk structure is established and the addition of atoms has no more effect on the structure. Of course there will be some rearrangement of the atoms on the surface of this bulk structure, but since the surface to volume ratio is very low in bulk material it can be neglected with a good approximation. However, in case of clusters, most of the atoms lie on the surface (extremely high surface to volume ratio) and such rearrangement produce a drastic effect. Owning to their high surface to volume ratio, the surface science from both chemical and physical point of view has become crucial in order to collect data and information about such systems. The ways to study such small cluster is nearly the same as the way they have been fabricated. With Bottom-up approach (chemical point of view) these clusters are formed from atoms and/or molecules by assembling it together to form the cluster, and there were many calculation based on this view point. Also these clusters can be fabricated, starting from the bulk material by reducing its dimension somehow, which is the Top-down approach. Geometric structure Usually the crystal structure of a large nanocluster is the same as the bulk structure of the material, with somewhat different lattice parameters (in general clusters are slightly contracted as compared to bulk). -
Gelation of Plasmonic Metal Oxide Nanocrystals by Polymer-Induced Depletion Attractions
Gelation of plasmonic metal oxide nanocrystals by polymer-induced depletion attractions Camila A. Saez Cabezasa, Gary K. Onga,b, Ryan B. Jadricha, Beth A. Lindquista, Ankit Agrawala, Thomas M. Trusketta,c,1, and Delia J. Millirona,1 aMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712; bDepartment of Materials Science and Engineering, University of California, Berkeley, CA 94720; and cDepartment of Physics, The University of Texas at Austin, Austin, TX 78712 Edited by Catherine J. Murphy, University of Illinois at Urbana–Champaign, Urbana, IL, and approved July 26, 2018 (received for review April 22, 2018) Gelation of colloidal nanocrystals emerged as a strategy to preserve silver fuse into wire-like networks when assembled into self-supported inherent nanoscale properties in multiscale architectures. However, nanoparticle gels, obliterating the LSPR optical response char- available gelation methods to directly form self-supported nano- acteristic of the isolated nanoparticles (22, 23). We sought a new crystal networks struggle to reliably control nanoscale optical strategy for gelation using physical bonding interactions, which phenomena such as photoluminescence and localized surface plas- we hypothesized could maintain the discrete morphology of LSPR- mon resonance (LSPR) across nanocrystal systems due to processing active metal oxides intact, to target LSPR-active nanocrystal gels. variabilities. Here, we report on an alternative gelation method based Our approach is not specific to the chemistry of the nanocrystals on physical internanocrystal interactions: short-range depletion at- employed and could potentially enable a broad class of gels as- tractions balanced by long-range electrostatic repulsions. The latter sembled from diverse nanoscale components capable of reflect- are established by removing the native organic ligands that passivate ing their individual properties. -
Quantitative Theories of Nanocrystal Growth Processes
QUANTITATIVE THEORIES OF NANOCRYSTAL GROWTH PROCESSES Michael D. Clark Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Columbia University Graduate School of Arts and Sciences COLUMBIA UNIVERSITY 2013 © 2012 Michael D. Clark All Rights Reserved ABSTRACT Quantitative Theories of Nanocrystal Growth Processes Michael D. Clark Nanocrystals are an important field of study in the 21 st century. Crystallites that are nanometers in size have very different properties from their bulk analogs because quantum mechanical effects become dominant at such small length scales. When a crystallite becomes small enough, the quantum confinement of electrons in the material manifests as a size-dependence of the nanocrystal's properties. Electrical and optical properties such as absorbance, surface plasmon resonance, and photoluminescence are sensitive to the size of the nanocrystal and proffer an array of technological applications for nanocrystals in such fields as biological imaging, laser technology, solar power enhancement, LED modification, chemical sensors, and quantum computation. The synthesis of size-controlled nanocrystals is critical to using nanocrystal in applications for their size-dependent properties. The development of nanocrystal synthesis techniques has been its own entire field of study for two decades or more, and several successes have established novel, utilitarian protocols for the mass-production of nanocrystals with controlled size and very low polydispersity. However, the experimental successes are generally poorly understood and no theoretical framework exists to explain the dynamics of these processes and how to better control or optimize them. It is the goal of this thesis to develop novel theories of nanocrystal synthesis processes to describe these phenomena in theoretical detail and extract meaningful correlations and driving forces that provide the necessary insight to improve the technology and enhance our understanding of nanocrystal growth. -
How to Dope a Semiconductor Nanocrystal? Uri Banin Institute Of
Abstract #2152, 224th ECS Meeting, © 2013 The Electrochemical Society How to dope a semiconductor nanocrystal? Uri Banin Institute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel Doping of bulk semiconductors, the process of intentional introduction of impurity atoms into a crystal discovered back in the 1940s, is a key enabling route for tuning their properties. Its introduction allowed the wide-spread application of semiconductors in electronic and electro- optic components. Controlling the size and dimensionality of semiconductor structures is an additional powerful way to tune their properties via quantum confinement effects. In this respect, colloidal semiconductor nanocrystals have emerged as a family of materials with size dependent optical and electronic properties that have attracted significant attention due to their unique attributes and potential applications. Impurity doping in such colloidal nanocrystals still remains an open challenge. From the Figure 1: Effects of doping in semiconductor synthesis side, the introduction of a few impurity atoms nanocrystals. Shown is a sketch for n-doped into a nanocrystal which contains only a few hundred nanocrystal quantum dot with confined energy atoms may lead to their expulsion to the surface or levels, red and green lines correspond to the compromise the crystal structure. From a physical QD and impurity levels, respectively. Left: viewpoint, impurities inherently create a heavily doped The level diagram for a single impurity nanocrystal under strong quantum confinement, and the effective mass model, Right: Impurity levels electronic and optical properties in such circumstances are develop into impurity bands as the number of still unresolved. -
Transformation of Doped Graphite Into Cluster- Encapsulated Fullerene Cages
ARTICLE DOI: 10.1038/s41467-017-01295-9 OPEN Transformation of doped graphite into cluster- encapsulated fullerene cages Marc Mulet-Gas1, Laura Abella2, Maira R. Cerón 3, Edison Castro 3, Alan G. Marshall1,4, Antonio Rodríguez-Fortea 2, Luis Echegoyen3, Josep M. Poblet 2 & Paul W. Dunk 1 An ultimate goal in carbon nanoscience is to decipher formation mechanisms of highly ordered systems. Here, we disclose chemical processes that result in formation of high- 1234567890 symmetry clusterfullerenes, which attract interest for use in applications that span biome- dicine to molecular electronics. The conversion of doped graphite into a C80 cage is shown to occur through bottom-up self-assembly reactions. Unlike conventional forms of fullerene, the iconic Buckminsterfullerene cage, Ih-C60, is entirely avoided in the bottom-up formation mechanism to afford synthesis of group 3-based metallic nitride clusterfullerenes. The effects of structural motifs and cluster–cage interactions on formation of compounds in the solvent- extractable C70–C100 region are determined by in situ studies of defined clusterfullerenes under typical synthetic conditions. This work establishes the molecular origin and mechanism that underlie formation of unique carbon cage materials, which may be used as a benchmark to guide future nanocarbon explorations. 1 National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310, USA. 2 Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, Tarragona 43007, Spain. 3 Department of Chemistry, University of Texas at El Paso, El Paso, TX 79968, USA. 4 Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306, USA. Marc Mulet-Gas and Laura Abella contributed equally to this work. -
DOD Report to Congree
Defense Nanotechnology Research and Development Program December 2009 Department of Defense Director, Defense Research & Engineering Table of Contents Executive Summary .................................................................................... ES-1 I. Introduction ....................................................................................................... 1 II. Goals and Challenges ........................................................................................ 2 III. Plans .................................................................................................................. 4 IV. Progress ............................................................................................................. 6 A. The United States Air Force ........................................................................ 6 1. Air Force Devices and Systems ............................................................. 6 Photon-Plasmon-Electron Conversion Enables a New Class of Imaging Cameras ................................................................................ 6 2. Air Force Nanomaterials ........................................................................ 6 Processing of Explosive Formulations With Nano-Aluminum Powder ................................................................................................ 6 3. Air Force Manufacturing ....................................................................... 7 Uncooled IR Detector Made Possible With Controlled Carbon Nanotube Array .................................................................... -
Clusters: Structure, Energetics, and Dynamics of Intermediate States of Matter A
Subscriber access provided by Johns Hopkins Libraries Article Clusters: Structure, Energetics, and Dynamics of Intermediate States of Matter A. W. Castleman, and K. H. Bowen J. Phys. Chem., 1996, 100 (31), 12911-12944• DOI: 10.1021/jp961030k • Publication Date (Web): 01 August 1996 Downloaded from http://pubs.acs.org on May 8, 2009 More About This Article Additional resources and features associated with this article are available within the HTML version: • Supporting Information • Links to the 42 articles that cite this article, as of the time of this article download • Access to high resolution figures • Links to articles and content related to this article • Copyright permission to reproduce figures and/or text from this article The Journal of Physical Chemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 J. Phys. Chem. 1996, 100, 12911-12944 12911 Clusters: Structure, Energetics, and Dynamics of Intermediate States of Matter A. W. Castleman, Jr.* Department of Chemistry, PennsylVania State UniVersity, 152 DaVey Laboratory, UniVersity Park, PennsylVania 16802 K. H. Bowen, Jr. Department of Chemistry, The Johns Hopkins UniVersity, 3400 N. Charles Street, Baltimore, Maryland 21218 ReceiVed: April 4, 1996; In Final Form: June 20, 1996X The field of cluster research can trace its origins back to the mid-nineteenth century when early studies of colloids, aerosols, and nucleation phenomena were reported. The field underwent a resurgence of interest several decades ago when well-defined clusters were observed in supersonic expansions that could be investigated using mass spectrometers. The advent of the laser provided a new dimension, enabling detailed spectroscopic observations through the probing of systems of varying size and degree of solvation. -
Transformation of Doped Graphite Into Cluster- Encapsulated Fullerene Cages
ARTICLE DOI: 10.1038/s41467-017-01295-9 OPEN Transformation of doped graphite into cluster- encapsulated fullerene cages Marc Mulet-Gas1, Laura Abella2, Maira R. Cerón 3, Edison Castro 3, Alan G. Marshall1,4, Antonio Rodríguez-Fortea 2, Luis Echegoyen3, Josep M. Poblet 2 & Paul W. Dunk 1 An ultimate goal in carbon nanoscience is to decipher formation mechanisms of highly ordered systems. Here, we disclose chemical processes that result in formation of high- 1234567890 symmetry clusterfullerenes, which attract interest for use in applications that span biome- dicine to molecular electronics. The conversion of doped graphite into a C80 cage is shown to occur through bottom-up self-assembly reactions. Unlike conventional forms of fullerene, the iconic Buckminsterfullerene cage, Ih-C60, is entirely avoided in the bottom-up formation mechanism to afford synthesis of group 3-based metallic nitride clusterfullerenes. The effects of structural motifs and cluster–cage interactions on formation of compounds in the solvent- extractable C70–C100 region are determined by in situ studies of defined clusterfullerenes under typical synthetic conditions. This work establishes the molecular origin and mechanism that underlie formation of unique carbon cage materials, which may be used as a benchmark to guide future nanocarbon explorations. 1 National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310, USA. 2 Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, Tarragona 43007, Spain. 3 Department of Chemistry, University of Texas at El Paso, El Paso, TX 79968, USA. 4 Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306, USA. Marc Mulet-Gas and Laura Abella contributed equally to this work. -
A Unified View of Ligand-Protected Gold Clusters As Superatom Complexes
A unified view of ligand-protected gold clusters as superatom complexes Michael Walter†, Jaakko Akola†‡, Olga Lopez-Acevedo†, Pablo D. Jadzinsky§¶, Guillermo Calero§, Christopher J. Ackerson§ʈ, Robert L. Whetten††, Henrik Gro¨ nbeck‡‡, and Hannu Ha¨ kkinen†§§¶¶ Departments of †Physics and §§Chemistry, Nanoscience Center, University of Jyva¨skyla¨, FI-40014 Jyva¨skyla¨, Finland; ‡Institut fu¨r Festko¨rperforschung, Forschungszentrum Ju¨lich, D-52425 Ju¨lich, Germany; §Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305; ¶Department of Applied Physics, Stanford University, Stanford, CA 94305; ††School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332; and ‡‡Competence Centre for Catalysis and Department of Applied Physics, Chalmers University of Technology, SE-41296, Go¨teborg, Sweden Edited by Royce W. Murray, University of North Carolina, Chapel Hill, NC, and approved April 10, 2008 (received for review January 31, 2008) Synthesis, characterization, and functionalization of self-assembled, 6s orbitals (10, 11), representing a finite-system analogy to the ligand-stabilized gold nanoparticles are long-standing issues in the bulk conduction electron states, which have 6s-character close to chemistry of nanomaterials. Factors driving the thermodynamic the Fermi surface. Exceptional stability is associated with a total stability of well documented discrete sizes are largely unknown. count of Herein, we provide a unified view of principles that underlie the stability of