In recent years, the fundamental researches on nanocrystals have been received increasing attentions for the novel applications, especially the nonvolatile memory technology. Adoption of nanocrystals technology could solve the serious limitation suffered by the conventional nonvolatile memory, flash, while scaling down. Once the thin tunneling oxide of flash device has been created a leaky path, all the stored charge in the floating gate will be lost after numerous counts of data reading and writing. Hence, the thinning of tunneling oxide will become one of important keys to the scaling limitation. Furthermore, if the tunneling oxide can not be thinned any more, both the operation voltage and speed of memory can not be improved. These drawbacks will restrict the development of nonvolatile memory. Replacement of floating gate structure with nanocrystals could effectively avoid the data losing due to the leaky path in the thin tunneling oxide. All stored charges can¡¦t be lost through the few leaky paths since the charges are stored in distributed nanocrystals. The charges stored nearby the leaky path will be lost, but others are still kept in the distributed and independent nanocrystals. The advantages of metal nanocrystals has have higher density of states around Fermi level, stronger coupling with conduction channel, wide range of available work functions and smaller energy perturbation due to carrier confinement. So metal nanocrystals can reduce operate voltage, and increase write/erase speed and endurance. In this thesis, we will study of cobalt and cobalt-silicide as the memory storage element. The nanocrystals were formed by high temperature oxidation or metal rapid thermal annealing with all kinds of conditions. And we analyze the effect of electron storage at metal nanocrystals by means of material and electrical analysis.

Yes / Understanding the effect of physical parameters (e.g., temperature) on crystallisation dynamics is of paramount importance for the synthesis of nanocrystals of well‐defined sizes and geometries. However, imaging nucleation and growth is an experimental challenge owing to the resolution required and the kinetics involved. Here, by using an aberration‐corrected transmission electron microscope, we report the fabrication of precious metal nanocrystals from nuclei and the identification of the dynamics of their nucleation at three different temperatures (20, 50, and 100 °C). A fast, and apparently linear, acceleration of the growth rate is observed against increasing temperature (78.8, 117.7, and 176.5 pm min−1, respectively). This work appears to be the first direct observation of the effect of temperature on the nucleation and growth of metal nanocrystals. / The Royal Society. Grant Number: UF150295 Leverhulme Trust. Grant Number: ECF-2013-414 The Academy of Medical Sciences. Grant Number: SBF003\1170

Thesis advisor: Chia-Kuang F. Tsung / Thesis advisor: Dunwei Wang / In order to understand the lattice strain effect and its relationship to size, shape, composition, and catalytic performance, novel well-defined nanocrystal archetypes were designed and synthesized by taking advantage of wet chemical, seed-mediated (mild) reduction routes developed by our lab. First, the current synthesis challenges are addressed in creating smaller monometallic shape-controlled metal nanocrystals, and novel cuboctopods via a hybrid nanoparticle stabilizer. A look at the relationship between lattice strain and morphology is then shown in a single-component system, where still new features have been observed for the first time by the traditional technique of powder x-ray diffraction. Synthesis methods for differently strained Pd surfaces are described and catalysis by these surfaces is discussed. Finally, studies of the synthesis, characterization, electrocatalytic activity, and restructuring of novel and more sophisticated strained architectures are presented: core-island-shell nanocrystals, phase-segregated nanoboxes, island nanoframeworks, and core-sandwich-shell nanoparticles. Lattice strain and composition effects were studied in carbon monoxide, small alcohol, and formic acid electrocatalytic oxidations as well as in oxygen reduction, the latter of which, governs the commercial viability of automotive fuel cells, a sustainable energy and zero-emission technology. Here it is demonstrated how a tunable thickness of Ni sandwich layers can be used to improve catalytic performance by increasing lattice strain on the Pt surface. The sandwich archetype offers a new platform for the investigation of lattice strain and could be a promising, industrially relevant, catalyst design concept, to help address the need for a more sustainable energy future. The results help paint a new picture of catalysis by metal nanocrystals; one which brings lattice strain to the forefront of the discussion, as an important parameter for further study and for use in developing higher-performing catalysts. / Thesis (PhD) — Boston College, 2015. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

In recently years, nonvolatile memory with nanocrystals cell have widely applied to overcome the issue of operation and reliability for conventional floating gate memory. The excellent electrical characteristics of memory device need good endurance, long retention time and small operation voltage. Among numerous memory devices with nanocrystals, the memory device with metal nanocrystals was widely researched. It will be new candidate for flash memory. The advantages of metal nanocrystals has have higher density of states around Fermi level, stronger coupling with conduction channel, wide range of available work functions and smaller energy perturbation due to carrier confinement. So metal nanocrystals can reduce operate voltage, and increase write/erase speed and endurance. Most important of all, we can control the sizes of nanocrystals dot and manufacture at low temperature¡CThis advantage can apply to thin film transistor liquid crystal display; it fabricates driving IC and logical IC on panel for diverseness and adds memory beside switch TFT as image storage to reduce power consumption for portability. In this thesis, we will discuss metal nanocrystals as memory storage medium. And we can use high temperature oxidation, low temperature annealing with oxygen to form nanocrystals. Besides we analyze the effect of electron storage at metal nanocrystals by means of material and electrical analysis.

Yes / The fabrication of precious metal (ruthenium, osmium, gold, and iridium) nanocrystals from single atoms has been studied in real-time. The dynamics of the first stage of the metal nanocrystallisation on a doped (B,S)-graphitic surface are identified, captured, and reported. / We thank the Leverhulme Trust (Early Career Fellowship No. ECF-2013-414 to NPEB), the ERC (Grant No. 247450 to PJS), EPSRC (EP/F034210/1 to PJS).

Yes / Metal nanocrystals offer new concepts for the design of nanodevices with a range of potential applications. Currently the formation of metal nanocrystals cannot be controlled at the level of individual atoms. Here we describe a new general method for the fabrication of multi-heteroatom-doped graphitic matrices decorated with very small, ångström-sized, three-dimensional (3D)-metal crystals of defined size. We irradiate boron-rich precious-metal-encapsulated self-spreading polymer micelles with electrons and produce, in real time, a doped graphitic support on which individual osmium atoms hop and migrate to form 3D-nanocrystals, as small as 15 Å in diameter, within 1 h. Crystal growth can be observed, quantified and controlled in real time. We also synthesize the first examples of mixed ruthenium–osmium 3D-nanocrystals. This technology not only allows the production of ångström-sized homo- and hetero-crystals, but also provides new experimental insight into the dynamics of nanocrystals and pathways for their assembly from single atoms. / We thank the Leverhulme Trust (Early Career Fellowship No. ECF-2013-414 to NPEB), the University of Warwick (Grant No. RDF 2013-14 to NPEB), the Swiss National Science Foundation (Grant No. PA00P2_145308 to NPEB and PBNEP2_142949 to APB), the ERC (Grant No. 247450 to PJS), EPSRC (EP/G004897/1 to RKOR, and EP/F034210/1 to PJS) and Science City (AWM/ERDF) for support. We thank the Wellcome Trust (Grant No. 055663/Z/98/Z) for funding the Electron Microscopy Facility, School of Life Sciences, University of Warwick. We also thank COST Action CM1105 for stimulating discussions, Thomas Wilks for supplying the micelle image for Figure 1, and the Australian Synchrotron and the University of Monash for allocation of time on the SAXS/ WAXS beamline and funding. The 2000FX Gatan Orius digital TEM camera used in this research was funded by Science City: Creating and Characterizing Next Generation Advanced Materials, with support from Advantage West Midlands and part funded by the European Regional Development Fund.

Nanotechnology builds devices from the bottom up with atomic accuracy. Among the basic nano-components to fabricate such devices, semiconductor nanoparticle quantum dots (QDs), metal nanocrystals, proteins, and nucleic acids have attracted most interests due to their potential in optical, biomedical, and electronic areas. The major objective of this research was to prepare nano-components in order to fabricate functional nano-scale devices. This research consisted of three projects. In the first two projects, we incorporated two desirable characteristics of QDs, which are their abilities to serve as donors in fluorescence energy transfer (FRET) and surface energy transfer (SET) as well as to do multiplexing, to engineer QD-based nanoconjugates for optical and biomedical applications. Immobilizing luminescent semiconductor CdSe/ZnS QDs to a solid platform for QD-based biosensors offers advantages over traditional solution-based assays. In the first project, we designed highly sensitive CdSe/ZnS QD SET-based probes using gold nanoparticles (AuNPs) as FRET acceptors on polystyrene (PS) microsphere surfaces. The emission of PS-QD was significantly quenched and restored when the AuNPs were attached to and then removed from the surface. The probes were sensitive enough to analyze signals from a single bead and for use in optical applications. The new PS-QD-AuNP SET platform opens possibilities to carry out both SET and FRET assays in microparticle-based platforms and in microarrays. In the second project, we applied the QD-encoded microspheres in FRET-based analysis for bio-applications. QDs and Alexa Fluor 660 (A660) fluorophores are used as donors and acceptors respectively via a hairpin single stranded DNA. FRET between QD and A660 on the surface of polystyrene microspheres resulted in quenching of QD luminescence and increased A660 emission. QD emission on polystyrene x microspheres was restored when the targeted complementary DNA hybridized the hairpin strand and displaced A660 away from QDs. The third project involved fabrication of different nanoconjugates via self-assembly of template-based metal nanowires and metal nanoparticles using oligonucleotides as linkers. These nanoconjugates can serve as building blocks in nano-electronic circuits. The template method restricted the oligonucleotides attachment to the tip of the nanowires. Nanowires tagged with hybridizable DNA could connect to complementary DNA-modified metal crystals in a position-specific manner.