Non-Classical Crystallization of Thin Films and Nanostructures in CVD and PVD Processes

Non-Classical Crystallization of Thin Films and Nanostructures in CVD and PVD Processes

Author: Nong Moon Hwang

Publisher: Springer

Published: 2016-06-14

Total Pages: 338

ISBN-13: 9401776164

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This book provides a comprehensive introduction to a recently-developed approach to the growth mechanism of thin films and nanostructures via chemical vapour deposition (CVD). Starting from the underlying principles of the low pressure synthesis of diamond films, it is shown that diamond growth occurs not by individual atoms but by charged nanoparticles. This newly-discovered growth mechanism turns out to be general to many CVD and some physical vapor deposition (PVD) processes. This non-classical crystallization is a new paradigm of crystal growth, with active research taking place on growth in solution, especially in biomineralization processes. Established understanding of the growth of thin films and nanostructures is based around processes involving individual atoms or molecules. According to the author’s research over the last two decades, however, the generation of charged gas phase nuclei is shown to be the rule rather than the exception in the CVD process, and charged gas phase nuclei are actively involved in the growth of films or nanostructures. This new understanding is called the theory of charged nanoparticles (TCN). This book describes how the non-classical crystallization mechanism can be applied to the growth of thin films and nanostructures in gas phase synthesis. Based on the author’s graduate lecture course, the book is aimed at senior undergraduate and graduate students and researchers in the field of thin film and nanostructure growth or crystal growth. It is hoped that a new understanding of the growth processes of thin films and nanostructures will reduce trial-and-error in research and in industrial fabrication processes.


Phase Transitions, Transfer and Nanoscale Growth of Epitaxial Bi and Bi1̳-̳x̳Sbx̳ Thin Films

Phase Transitions, Transfer and Nanoscale Growth of Epitaxial Bi and Bi1̳-̳x̳Sbx̳ Thin Films

Author: Emily Susan Walker

Publisher:

Published: 2018

Total Pages: 270

ISBN-13:

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Bismuth (Bi) and Bismuth-Antimony (Bi [subscript 1-x] Sb [subscript x]) alloys are considered very promising for emerging spintronic devices due to their large spin-orbit coupling, high mobility, and conductive, spin-split surface states, which are topologically non-trivial in Bi [subscript 1-x] Sb [subscript x]. Due to the long mean free path in Bi, quantum confinement effects become significant in relatively thick (~100 nm) films, resulting in the opening of a small, indirect band gap and enabling tuning of the electronic properties through the film thickness. Quantum confinement effects are expected to occur in Bi [subscript 1-x] Sb [subscript x] films at a similar length scale, which may enlarge the bulk band gap and extend the topologically insulating composition regime. When the film thickness of epitaxial Bi on Si(111) is reduced below a few nanometers, a puckered-layer allotropic structure similar to black phosphorus is stable. This puckered-layer structure is expected to exhibit unique properties, including a larger band gap and increased spin splitting, which may be useful for 2-D spintronics; however, the tendency of this structure to grow in small islands inhibits characterization. This dissertation explores the growth of both bulk-like and puckered-layer Bi and Bi [subscript 1-x] Sb [subscript x] on Si(111), and discusses how the unique properties of this system may be controlled through the growth parameters, film thickness, and composition. We find that while alloying bulk-like Bi with Sb in the quantum confinement thickness regime may increase the band gap, the crystalline orientation changes with increasing concentrations of Sb. This effect has not been observed in epitaxial Bi [subscript 1-x] Sb [subscript x] on other substrates, and significantly impacts the electronic properties of the films. In contrast, alloying Sb with nanoscale puckered-layer Bi improves the crystallinity and continuity, suggesting a promising route towards tuning the band structure of puckered-layer Bi and producing large-area films for electrical measurements. Finally, we demonstrate that epitaxial Bi and Bi [subscript 1-x] Sb [subscript x] films exhibit surprisingly weak adhesion to the Si(111) growth substrate, which may originate from the early allotropic transition. This weak adhesion enables the straightforward transfer of these films, opening a route toward the integration of epitaxial-quality Bi and Bi [subscript 1-x] Sb [subscript x] films with arbitrary substrates for novel heterostructures.


Temperature Impact on Thermal Evolution of Advanced PVD Ceramic and Metallic Glass Thin Films

Temperature Impact on Thermal Evolution of Advanced PVD Ceramic and Metallic Glass Thin Films

Author: Mihai Apreutesei

Publisher:

Published: 2015

Total Pages: 0

ISBN-13:

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In the recent years the industrial requirements to develop new functional materials able to overcome the severe conditions during machining operation are continuously increasing. Researchers then must find novel solutions to respond to their severe industrial requirements. To coat the tool surface with advanced coatings is the most efficient solution. New nanostructured materials may nowadays exhibit unique mechanical, physical and chemical properties ensuring notable degradation resistance where the surface protection of materials against corrosion, wear, friction or oxidation is a key issue, particularly when operating in hostile environments. Within the scope of this Ph.D. thesis the influence of the temperature on the structural stability of two different PVD ceramic and metallic glass thin films is proposed. The main goal consists in the development of two distinct classes of thin films, with a wide range of properties. In order to prepare these films, the project will be focused on the study on the influence of PVD deposition conditions in the particular film's growth characteristics: chemical composition, structure, morphology and the subsequent changes in the main properties of the thin films, namely oxidation and crystallization resistance, especially. For that purpose we adopted the multiscale approach. The first part is related to the ceramic CrN-based coatings to give new functionalities and improve the tools' surface with the primary aim to increase their lifetime. Secondly, new protective materials able to better protect the exposed surfaces against high temperature oxidation have been proposed, namely CrAlN and CrAlYN coatings as will be evidenced in this manuscript. The second part of the manuscript is dedicated to the innovative Zr-Cu thin films metallic glasses prepared by a PVD magnetron co-sputtering method with the objective to investigate the amorphization ability and their structural properties. Their excellent properties at room temperature have recently attracted attention as a new class of materials with great potential for engineering applications due to unique mechanical and physico-chemical characteristics (high elastic strain limit, corrosion resistance...). Finally, an important approach during the course of this thesis was the real time observation of the structure and surface modifications during heating by means of in situ methods. The thin films proposed during the course of the work could be straightforward used as surface engineering solutions to protect and extend the lifetime of the materials and components.


Chemical Physics of Thin Film Deposition Processes for Micro- and Nano-Technologies

Chemical Physics of Thin Film Deposition Processes for Micro- and Nano-Technologies

Author: Y. Pauleau

Publisher: Springer Science & Business Media

Published: 2012-12-06

Total Pages: 372

ISBN-13: 940100353X

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An up-to-date collection of tutorial papers on the latest advances in the deposition and growth of thin films for micro and nano technologies. The emphasis is on fundamental aspects, principles and applications of deposition techniques used for the fabrication of micro and nano devices. The deposition of thin films is described, emphasising the gas phase and surface chemistry and its effects on the growth rates and properties of films. Gas-phase phenomena, surface chemistry, growth mechanisms and the modelling of deposition processes are thoroughly described and discussed to provide a clear understanding of the growth of thin films and microstructures via thermally activated, laser induced, photon assisted, ion beam assisted, and plasma enhanced vapour deposition processes. A handbook for engineers and scientists and an introduction for students of microelectronics.


Deposition and Characterisation of Bismuth Layer-structured Ferroelectric Films

Deposition and Characterisation of Bismuth Layer-structured Ferroelectric Films

Author: Xiaobing Hu

Publisher:

Published: 2006

Total Pages:

ISBN-13:

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Bismuth layer-structured ferroelectrics have been recognised as promising film materials for ferroelectric random access memory application due to their excellent fatigue resistance and other electrical properties. This work deals with the deposition and characterisation of epitaxial and polycrystalline W-doped SrBi2Ta2O9 (SBT) and lanthanide-doped bismuth titanate (BiT) films. SBT and W-doped SBT films were fabricated by pulsed laser deposition (PLD) on platinised silicon substrates. The effects of fabrication temperature and W-doping level on film properties were studied. The crystallinity of SBTW films improved with increasing fabrication temperatures, resulting in enhanced ferroelectric properties and dielectric properties above the fabrication temperature of 750 °C. Dense ceramic samples of Nd- and Sm-doped BiT (BNdT and BSmT) were successfully fabricated for PLD targets by solid state processing. Highly epitaxially (001)-, (118)-, and(104)-oriented Nd-doped bismuth titanate (BNdT) films were grown by PLD on (001)-, (011)-, and (111)-oriented SrTiO3 (STO) single crystal substrates, respectively. A three-dimensional orientation relationship between films and substrates was derived as: BNdT(001)//STO(001), BNdT[110]//STO[100]. Films showed strong dependence of structural and ferroelectric properties on the crystal orientation. PLD-grown BSmT films on platinised silicon substrates were studied as a function of fabrication temperature, effects of Pt bottom layer orientation, Sm doping level, and LaNiO3 buffer layer. An alkoxide-salt chemical solution deposition (CSD) method was adopted to prepare the precursors for BSmT (BNdT) film fabrication. Precursors of Bi-Sm(Nd)-Ti which were stable for at least eight months in air ambient were successfully developed. In-situ FT-IR studies suggest that acetic acid serves as chelating agent to improve the homogeneity of the precursor solution by generating a dense and homogeneous Ti-O-Ti polymeric network. The electrical properties of the films fabricated in this study (dielectric and ferroelectric properties, leakage current characteristics and electrical fatigue properties), are comparable or superior to these previously reported for similar films developed by other techniques or with other doping elements. Low temperature electrical properties of BSmT films suggest that the films are very promising for extremely low temperature nonvolatile memory applications. The results of BNdT films annealed at different oxygen partial pressure (O2, air, N2) showed that oxygen ambience affected structural properties of the films by enhancing the growth of perovskite phase (phase formation), increasing grain size (grain growth), and assisting the growth of (117)-oriented grains (crystallographic orientations). Piezoresponse force microscopy (PFM) was adopted to characterise BSmT films. Domain structures were clearly observed in a PLD-grown BSmT film, which were closely related to the grain structures. Domain manipulation was carried out in a CSD-derived BSmT film, showing that the film can be nearly uniformly polarised, which can be used in nanoscale device fabrication. Clear hysteresis loops were measured by PFM, which was an important proof of ferroelectricity. Large spatial variations of piezoelectric hysteresis loops of a CSD-derived BSmT film were observed across the film surface. Effective electrostriction coefficient (Qeff) of a PLD-grown BSmT film was measured, showing that BSmT films had better piezoelectric properties (higher Qeff, higher dzz) than SBT films, un-doped BiT ceramics and films. It suggests that BSmT films are promising piezoelectric materials for MEMS use.


Bismuth Magnesium Titante - Lead Titanate Thin FIlms for High Temperature Ferroelectric Memory

Bismuth Magnesium Titante - Lead Titanate Thin FIlms for High Temperature Ferroelectric Memory

Author: Carl Sebastian Morandi

Publisher:

Published: 2018

Total Pages:

ISBN-13:

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This work provides a comprehensive study on the development of 35Bi(Mg1/2Ti1/2)O3-65PbTiO3 thin films deposited by pulsed laser deposition, detailing the effects of processing variables on the film composition and resulting electrical properties. The primary application focus is on a potential high temperature ferroelectric layer for ferroelectric random access memory (FeRAM) devices. To assess whether 35BiMT-65PT thin films are of interest for this application, the films were assessed by determining the switchable polarization, the dielectric properties and their thickness dependence, the high temperature polarization and dielectric properties, and the retention characteristics.For pulsed-laser deposited 35BiMT-65PT films on 36 nm thick PbTiO3 or 16 nm thick 5 mol% La-doped PbTiO3 seed layers, the processing window for developing a perovskite structure was found to be wide. Within the detection limits of x-ray diffraction, scanning electron microscopy and transmission electron microscopy, the films were found to be phase pure perovskite for growth temperatures from 600 C to 700 C at O2(90%)/O3(10%) background pressures of 100-300 mTorr. Target compositions from 10 mol% to 85 mol% excess Pb produced phase pure perovskite films when depositing at 700 C and a 10 Hz laser repetition rate. The film composition was found to vary as a function of processing parameters. As the chamber pressure during deposition decreased, the film Mg and Pb concentration decreased, while the concentration of Bi increases. For films on 36 nm PbTiO3 seed layers, the remanent polarization, Pr, increased 64% to 21 C/cm2 and the polarization electric field loops rotated counterclockwise as the deposition pressure increased from 60 mTorr to 340 mTorr. Decreasing the seed layer thickness from 36 to 16 nm led to a decrease in Pr to 14 C/cm2. Adjusting the target composition allowed the deposition of films which had near-stoichiometric Bi and Mg concentrations, but in all cases, the grown films were lead deficient. These films had remanent polarizations of 18 to 20 C/cm2. If the lead content of the target was increased too far, the remanent polarization decreased, possibly due to the need to evolve more PbO from defective growth layers. Finally, the deposition rate showed no substantial effect on the film composition, but did have a significant impact on the ferroelectric properties. As the deposition rate decreased, the Pr increased to 22 C/cm2 presumably due to enhanced crystalline quality and time for atomic rearrangement. At laser frequencies of 5 Hz, a Mg-rich pyrochlore phase begins to form and films showed a maximum Pr 22 C/cm2. The optimal processing window for the maximum in ferroelectric properties shifts to higher PbO excess contents in the target as the deposition rate decreased. A film deposited at 5 Hz with a 65 mol% Pb, 20 mol% Bi, and 10 mol% Mg excess target had the maximum Pr 25 C/cm2. The processing-composition behavior is explained via preferential adsorption of Bi on the A-site, which results in lead vacancies.The dielectric, polarization and leakage properties of 35BiMT-65PT thin films with varying levels of A-site deficiency were investigated as a function of thickness and/or temperature. PbTiO3 seed layers utilized to nucleate the perovskite phase in A-site deficient films induced a thickness dependence to the ferroelectric hysteresis and dielectric permittivity. Adjusting for this, the dielectric response of the 35BiMT-65PT films is 960. The dielectric permittivity maximum was 430 C at 1 MHz for A-site deficient films. The transition temperature is independent of film thickness to 85 nm. Tan() remains less than 15% at 1 MHz, regardless of film thickness and temperature up to 585 C. High temperature polarization-electric field hysteresis measurements show charge injection with is exacerbated on increasing temperature, while PUND measurements show little temperature dependence of Pr up to temperatures of 200 C. Poole-Frenkel emission dominated the high field leakage behavior. The refractive index measured by ellipsometry is 2.58 at 633 nm. All samples show significant retention loss. As the stoichiometry improves, retention improves such that >40% of the initial P is retained over 280 min. at room temperature. To remove the influence of the PbTiO3 seed layers on the apparent thickness dependence of 35BiMT-65PT, films without a PbTiO3 seed layer were deposited. Similar to their seed layer counterparts, seedless films show phase purity within the same target composition range investigated for films on seed layers. Phase pure films show somewhat reduced thickness dependent dielectric properties with respect to seeded films. Pr measured at 10 kHz for seedless films was 22-25 C/cm2 until thicknesses of 200 nm and decreased to 15.5 C/cm2 for films that were 100 nm thick. I-V measurements of seedless films deposited under nominally the same conditions as seeded films resulted in higher leakage compared to seeded films. Deposition under an Ar/O2 atmosphere decreased the leakage behavior by up to five times. Films grown under the optimum 50%O2/50%Ar atmosphere demonstrate little temperature dependence in Pr up to 200 C. As temperature increases, the DC dielectric breakdown of strength of seedless films decreases faster compared to seeded films. Retention analysis shows similar behavior to that of seeded films.


Bismuth Oxide Thin Films for Optoelectronic and Humidity Sensing Applications

Bismuth Oxide Thin Films for Optoelectronic and Humidity Sensing Applications

Author: Simona Condurache-Bota

Publisher:

Published: 2018

Total Pages:

ISBN-13:

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Bismuth oxide thin films still prove attractive to both scientists and engineers due to their semiconducting behavior, large energy bandgap and high refractive index, despite their often complex structure, both polymorphic and polycrystalline. We present here a summary and a comparison of the morpho-structural and optical properties of such films prepared through three physical vapor deposition (PVD) techniques on several types of substrates kept at different temperatures. Thermal vapor deposition, thermal oxidation in air and pulsed laser deposition are discussed as largely used PVD methods. It is proved that the physical properties of the bismuth oxide thin films can be tailored by changing the substrate nature and its temperature during the deposition process in a way even more relevant than even the chosen deposition method. Thus, bismuth oxide thin films with energy bandgaps ranging from the infrared up to near-ultraviolet can be obtained, depending on their structure and morphology. High refractive index of the films can be also attained for specific spectral ranges. When deposited on certain conductive substrates, the films have much lower electrical resistance and even became sensitive to water vapor. Therefore, humidity sensing and optoelectronic applications of the analyzed bismuth oxide thin films can be easily found and used in both science and technology.