This dissertation is composed of seven chapters, detailing advances within the area of sulfur polymer chemistry and processing, and highlights the relevance of the work to the fields of polymer science, energy storage, and optics that are enabled through the development of novel high sulfur-content copolymers as discussed in the following chapters. The first chapter is a review summarizing both the historical forays into utilization of elemental sulfur in high sulfur-content materials and the current research on the incorporation of sulfur into novel copolymers and composites for high value added applications such as energy production/storage, polymeric optical components, and dynamic/self-healing materials. Although recent efforts by the materials and polymer chemistry communities have afforded innovative sulfur containing materials, many studies fail to take advantage of the low cost and incredible abundance of sulfur by incorporating only minimal quantities into the end products. A fundamental challenge in the preparation of sulfur-containing polymers is simultaneous incorporation of high sulfur-content through facile chemical methods, to truly use the element as a novel feedstock in copolymerizations. Contributing to the challenge are the intrinsic limitations of sulfur (i.e., low miscibility with organic solvents, high crystallinity, and poor processability). The emphasis in chapter 1 is the critical development of utilizing sulfur as both a reagent and solvent in a bulk reaction, termed inverse vulcanization. Through this methodology we can directly prepare materials which retain the advantageous properties of elemental sulfur (i.e., high electrochemical capacity, high refractive index, and liable bond character), obviate the processing challenges, and enable precise control over composition and properties in a facile manner. The second chapter focuses on advancement in colloid synthesis, specifically an example mediated by in-situ reduction of organometallic precursors (ClAu^IPPh₃) by elemental sulfur at high temperatures. In chapter 2, elemental sulfur is employed both as a reactant and novel solvent, generating composite composed of well-defined gold nanoparticles (Au NPs) fully dispersed in a sulfur matrix. While the synthesis of Au NPs in molten sulfur was a novel development the challenge of analyzing the particles directly within the sulfur composite matrix by microscopy techniques required improvement of the composites mechanical properties. To overcome this issue, a one-pot reaction in which the Au NPs were initially synthesized, was vulcanized through an ambient atmosphere-tolerant bulk copolymerization by the addition of a difunctional comonomer (divinylbenzene). The improved composite integrity enabled microtoming and transmission electron microscopy analysis of the particles within the crosslinked reaction matrix. Due to the facile capabilities of directly dissolving the comonomers within the molten sulfur the inverse vulcanization methodology provides a simple route to prepare stable, high sulfur-content copolymers in a single one-pot reaction. The third chapter expands upon the methodology for direct dissolution of difunctional comonomers into molten elemental sulfur to afford chemically stable copolymer. A major challenge associated with the high temperature (i.e., 185 °C) bulk copolymerization reactions between sulfur and vinyl comonomers (i.e., divinylbenzene, DVB) is the high volatility of the organic monomers at elevated temperatures (BP of DVB = 195 °C). To obviate this problem required a novel monomer with an increased boiling point for successful scaling of the inverse vulcanization methodology. The work presented in chapter 3 details the employment of 1,3-diisopropenylbenzene (DIB, BP = 231 °C) to enable larger scale bulk inverse vulcanization reactions, allowing facile control over thermomechanical properties by simple variation in copolymer composition (50–90-wt% S₈, 10–50-wt% DIB). Poly(Sulfur-random-1,3-diisopropenylbenzene) ((poly(S-r-DIB)) copolymers prepared via the inverse vulcanization methodology possess substantially improved processing capabilities compared with elemental sulfur. A facile demonstration of improved processability is the generation of free-standing micropatterned structures using a high sulfur content liquid pre-polymer resin that can be poured into a mold and cured into the desired final form. The highest weight percentage copolymer (i.e., 90-wt% S₈) was also demonstrated to improve cycle lifetimes and capacity retention (823 mAh•g⁻¹ at 100 cycles) of a Lithium-Sulfur (Li-S) cell when the copolymer was utilized as the active material instead of elemental sulfur. Chapter four focuses on the optimization of Li-S cell performance as a function of copolymer composition and provides a more thorough understanding of the means by which copolymer active material improves battery performance. A substantial challenge associated with Li-S cells is the fast capacity fade and short cycle lifetimes that result from loss of the active material (i.e., sulfur) during normal cycling processes. The field has generally addressed these issues by encapsulation of the sulfur in a protective shell (e.g., polymeric, carbonaceous, or metal oxide in nature) in an attempt to sequester the active material. However, encapsulation of sulfur is non-trivial and leads to low loadings of sulfur, resulting in a low energy density within the final cell. To address the challenges associated with maintaining high capacity and long cycle lifetimes while employing an active material which is low cost, generated in a facile manner, and has a high sulfur content required a novel approach. In the work presented in chapter 4 we prepared high sulfur content copolymers via the inverse vulcanization methodology, which meet all the requirements necessary of an active material, and investigated the performance of Li-S batteries as a function of the copolymer composition. A survey of several poly(S-r-DIB) copolymer compositions were prepared with DIB compositions ranging from 1-50-wt% DIB (i.e., 50-99 wt% sulfur) and screened to determine optimal compositions for optimal Li-S battery performance. From this analysis it was determined that copolymers with 10-wt% DIB (90-wt% S₈) were optimal for producing Li-S batteries with high capacity and long cycle lifetimes. 10-wt% DIB copolymers batteries ultimately achieved long cyclic lifetimes and maintained high capacity (>600 mAh/g at 500 cycles). Chapter five details the optimization of conditions necessary to generate large scale (>100 g) inversely vulcanized sulfur copolymers and their application towards Li-S batteries. As previously stated a significant challenge in the Li-S battery field is the production of a Li-S active material with improved performance that is low cost, synthesized in a facile manner, and possesses high sulfur content. To date poly(S-r-DIB) copolymers prepared via the inverse vulcanization methodology afford some of the longest cycle lifetimes and highest capacity retention for polymeric active materials. However, initial inverse vulcanization reactions investigated for preparing active materials were performed on 10 gram scales. The goal of the work presented in chapter 5 was to prepare materials on a scale applicable to fabrication of several prismatic Li-S cells, each of which requires several grams of active material. However, scaling up of the reaction to a kilogram and utilizing the traditional inverse vulcanization conditions (i.e., 185 °C) results in catastrophic degradation as a consequence of the Trommsdorf effect. To address this challenge required decreasing the radical concentration within the bulk copolymerization, which necessitated performing the kilogram scale inverse vulcanization reactions at lower temperatures (i.e., 130 °C) over a longer reaction period. Decreasing the temperature generates materials that are nearly identical in thermomechanical properties to smaller scale samples and the battery performance is likewise comparable (>600 mAh/g at 500 cycles). The key advantage of performing the inverse vulcanization reaction at lower temperatures is that additional monomers, with lower boiling points or degradation issues, can be utilized and the increased gelation time, enables facile incorporation of additives (e.g., carbon black or nanoparticles) into the reaction. Chapter six focuses on the development of poly(S-r-DIB) copolymers as novel mid-infrared (mid-IR) transmitting materials and the analysis of the optical properties as a function of copolymer composition. A challenge in the optical science community is the limited number of materials applicable to the development of innovative optical components capable of functioning in the mid and far-IR regions. Semi-conductor and chalcogenide glasses have been widely applied as device components in infrared optics due to their high refractive indices (n ~2.0–4.0) and high transparency in the infrared region (1–10 μm). However, such materials are also expensive, difficult to fabricate, and toxic in comparison to organic polymers. On the other hand organic polymers are easily processed, low cost, and generated from easily accessible raw materials. Unfortunately, polymeric materials generally have low refractive indices (n<1.65) and are prepared from monomers with functional groups that are highly absorbing at mid-IR and longer wavelengths. Chapter 6 details the realization through the inverse vulcanization methodology of the first example of a material that is high refractive index and low mid-IR absorption, but also low cost and easily processable. Critical to achieving a polymeric material which was appropriate for mid-IR applications was the high sulfur content and the absence of functional groups, both of which are afforded by the facile copolymerization process. By simply controlling copolymer composition the optical properties of the material were tailorable; allowing adjustment of the refractive index from ~1.75 (50-wt% DIB) to ~1.875 (20-wt% DIB). Finally, through facile techniques, high quality copolymers lenses were prepared and we demonstrated the high optical transparency over several regions of the optical spectrum, from the visible (400–700 nm) all the way to the mid-IR (3–5μm). Poly(S-r-DIB) copolymers demonstrated high transparency to mid-IR light, but still maintain the processing capabilities of an organic polymer, the first example of such a material to possess both qualities. Ultimately the inverse vulcanization methodology offers a novel route to low cost, high refractive index, IR transparent materials, opening up unique opportunities for polymeric optical components within the optical sciences field. The seventh chapter discusses utilization of the inverse vulcanization methodology as a means to prepare and control the dynamic behavior of sulfur copolymers for potential applications towards self-healing materials. The incorporation of dynamic covalent bonds into conventional polymer architectures, either directly within the backbone or as side-chain groups, offers the stability of covalent bonds but with the ability of stimuli-responsive behavior to afford a change in chemical makeup or morphology. Traditionally the installation of such functionality requires the use of disparate, orthogonally polymerizable functional groups (i.e., vinyl) and discrete design of the comonomers utilized to generate a responsive copolymer. Therefore, a challenge in developing novel dynamic copolymers is the ability to install stimuli-responsive functionality directly as a result of the copolymerization without the need for rigorous synthetic monomer design and complex copolymerization techniques. In chapter 7 we discuss the analysis of poly(S-r-DIB) copolymers with rheological techniques to assess the composition dependent dynamic behavior. Aided by the bulk nature of copolymerization, the feed ratio of S₈ and DIB directly dictates copolymer microstructure; thus the sulfur rank between the organic groups (i.e., DIB) was tailorable from a single sulfur (thioether) to multiple sulfurs (pentasulfide). Control over sulfur content and number of S–S enables control over the dynamic behavior, as monitored via in-situ rheological techniques. The highest sulfur-content copolymers (80-wt% S₈, 20-wt% DIB) showed the fastest response when under shear stress due to the large number of S–S bonds. On the other hand when no dynamic bonds were present in the copolymer (i.e.; 35-wt% S₈, 65-wt% DIB) there is no dynamic behavior and full recovery of the pristine mechanical properties was not observed. The facile synthesis and simple control over copolymer microstructure affords the inverse vulcanization methodology an advantage over other dynamic materials, and provides potential secondary qualities (i.e., high refractive index) built directly into the structure.

As the Ming dynasty (1368-1644) collapsed, two outstanding novels were authored, Supplement to the Journey to the West (Hsi-yu Pu) and Prayer Mat of Flesh (Jou P'u T'uan). Although modern critics have studied these two works, important aspects of each novel have been overlooked. Therefore, this study explores three elements of Jou P'u T'uan: the novel as a picaresque novel, the hero's character consistency, and the book's morality. Also examined are the Ch'an Buddhist aspects present in Hsi-yu Pu. Information on the authors, editions, and controversies of these novels has also been presented. An initial chapter is provided discussing the historical and intellectual background. Finally, a comparative study of the two authors and their works has been undertaken to further understanding of both novels. Thus, it is hoped that this work has made a valuable contribution to the study of these two novels.

Between 1950s and 1990s, Hong Kong had a frenzy for writing and re-writing materials from classical literature and myths. The myth of Madame White Snake is one of the most well known stories that survived a long period of time. The earliest known version of Madame White Snake was a supernatural story in 1550, which later became a prototype of numerous subsequent versions starting in 1624. This prototype was repeatedly re-written throughout history and was also made into different genres including plays, playlets, novels, films and television dramas. One of the latest versions was written by Li Pikwah, a popular novelist in Hong Kong, in 1993, titled, Green Snake. Green Snake is a parody of Madame White Snake written from the perspective of Little Green, the servant of Madame White and an auxiliary figure in the tradition. The novel is also an autobiography of Little Green, who satirically criticizes the story of Madame White Snake in retrospect. Little Green’s autobiography is a nostalgic reflection of the past as well as a critique of the structure of the story that has survived throughout history. These implications made in the story hint at the author’s personal yearning for traditional China as a Chinese resident in Hong Kong. Her nostalgia for traditional China is not idealistic but paradoxical, because her re-writing of the story was an avenue to understand and re-negotiate her identity. Li is also well-known for her other novels, which are parodies of classical literature, traditional myth and legend. Many of these works were also made into films in the 80’s and 90’s. These novels and films were part of a phenomenon in contemporary Hong Kong literary and popular culture that tried to grasp a cultural connection with traditional China in order to embrace the return to mainland China in 1997 after a hundred years of British colonial rule.

The improvement of volumetric energy density remains a key area of research to opti-mize Li-ion batteries for applications such as extending the range of electric vehicles. There is still improvement to be made in the energy density in the positive elec-trode materials. The current thesis deals with determining the phase diagrams of the Li-Mn-Ni-O and Li-Co-Mn-O systems in order to better understand the structures and the electrochemistry of these materials. The phase diagrams were made through careful analysis of hundreds of X-ray di raction patterns taken of milligram-scale combinatorial samples. A number of bulk samples were also investigated. The Li-Mn-Ni-O system is of particular interest as avoiding cobalt lowers the cost of the material. However, this system is very complex: there are two large solid-solution regions separated by three two-phase regions as well as two three-phase regions. Comparing quenched and slow cooled samples shows that the system trans-form dramatically when cooled at rates typically used to make commercial materials. The consequences of these results are that much of the system must be avoided in order to guarantee that the materials remain single phase during cooling. This work should therefore impact signi cantly researchers working on composite electrodes. Two new structures were found. The first was Li-Ni-Mn oxide rocksalt structures with vacancies and ordering of manganese which were previously mistakenly identi ed as LixNi2xO2. The other new structure was a layered oxide with metal site vacancies allowing manganese to order on two superlattices. The electrochemistry of both these materials is presented here. Finally, the region where layered-layered composites form during cooling has been determined. These materials were long looked for along the composition line from Li2MnO3 to LiNi0.5Mn0.5O2 and the most significant consequence of the actual locations of the end-members is that one of the structures contains a high concentration of nickel on the lithium layer. Layered-layered nano-composites formed in this system are therefore not ideal positive electrode materials and it will be demonstrated that single-phase layered materials lead to better electrochemistry.

This project is a translation of Liu Qingbang's novella 'Shénmù' from Chinese into English. It is also accompanied by an analysis of the text and Li Yang's movie 'Blind Shaft', which was based on the novella.

L'utilisation d'un électrolyte aqueux pour la technologie Li-ion devrait permettre des performances en termes de puissance et de coût tout en garantissant une sécurité de fonctionnement et un impact neutre vis-à-vis de l'environnement. Cette technologie utilise des composés d'insertion du lithium fonctionnant habituellement en milieu organique dont le choix doit être adapté à un électrolyte aqueux, présentant une fenêtre de stabilité électrochimique réduite. Le travail de thèse porte dans un premier temps sur la sélection des différents éléments constituant un accumulateur Li-ion aqueux: choix de l'électrolyte, des collecteurs de courant, des liants d'électrode et des matériaux d'électrode. Les performances électrochimiques en milieu aqueux de différents composés d'insertion du lithium ont été évaluées. Afin d'augmenter la fenêtre de stabilité électrochimique de l'électrolyte aqueux, la passivation des électrodes par réduction de sels de diazonium a été réalisée. L'influence de la nature des sels de diazonium et de l'épaisseur des films sur les performances électrochimiques des électrodes a été évaluée par diverses techniques, voltampérométrie et impédance électrochimique. Les résultats obtenus montrent l'impact positif des dépôts obtenus vis-à-vis de l'augmentation de la surtension de réduction de l'eau. Ces travaux ouvrent la voie à des perspectives prometteuses sur cette technologie Li-Ion aqueuse.

The Lithium-ion (Li-ion) battery is one of the major topics currently studied as a potential way to help in reducing greenhouse gas emissions. Major car manufacturers are interested in adapting the Li-ion battery in the power trains of Plug-in Hybrid Electric Vehicles (PHEV) to improve fuel efficiency. Materials currently used for Li-ion batteries are LiCoO2 (LCO) and graphite—the first materials successfully integrated by Sony into Li-ion batteries. However, due to the high cost and polluting effect of cobalt (Co), and the low volumetric capacity of graphite, new materials are being sought out. LiFePO4 (LFP) and SnO2 are both good alternatives for the cathode and anode materials in Li-ion batteries. But, to create high-performance batteries, nano-sized carbon-coated particles of LFP and SnO2 are required. The present work attempts to develop a new synthesis method for these materials: organic template-assisted synthesis for three-dimensionally ordered macroporous (3DOM) LFP and porous SnO2. With the newly developed synthesis, highly pure materials were successfully synthesized and tested in Li-ion batteries. The obtained capacity for LFP was 158m Ah/g, which is equivalent to 93% of the theoretical capacity. The obtained capacity for SnO2 was 700 mAh/g, which is equivalent to 90% of the theoretical capacity. Moreover, Hybrid Pulse Power Characterization (HPPC) was used to test LFP and LCO for comparison and feasibility in PHEVs. HPPC is generally used to test the feasibility and capacity fade for PHEVs. It simulates battery use in various driving conditions of PHEVs to study pulse energy consumption and regeneration. In this case, HPPC was conducted on a half-cell battery for the first time to study the phenomena on a single active material, LFP or LCO. Based on the HPPC results, LFP proved to be more practical for use in PHEVs.

No description available.

Rechargeable lithium sulfur (Li-S) batteries are potentially safe, environmentally friendly and economical alternative energy storage systems that can potentially be combined with renewable sources including wind solar and wave energy. Sulfur has a high theoretical specific capacity of ~1680 mAh/g, attainable through the reversible redox reaction denoted as S8+16Li ↔8Li¬2S, which yields an average cell voltage of ~2.2 V. However, two detrimental factors prevent the achievement of the full potential of the Li-S batteries. First, the poor electrical/ionic conductivity of elemental sulfur and Li2S severely hampers the utilization of active material. Second, dissolution of intermediate long-chain polysulfides (Li2Sn, 2<n<7) into the electrolyte and their shuttle between cathode and anode lead to fast capacity degradation and low Coulombic efficiency. As a result of this shuttle process, insoluble and insulating Li2S/Li2S2 precipitate on the surface of electrodes causing loss of active material and rendering the electrode surface electrochemically inactive. Extensive research efforts have been devoted to overcome the aforementioned problems, such as combination of sulfur with conductive polymers, and encapsulation or coating of elemental sulfur in different nanostructured carbonaceous materials. Noteworthy, sulfur-polyacrylonitrile (SPAN) composites, wherein sulfur is chemically bond to the polymer backbone and PAN acts as a conducting matrix, have shown some success in suppressing the shuttle effect. However, due to the limited electrical conductivity of polyacrylonitrile, the capacity retention and rate performance of the SPAN systems are still very modest, which shows only 67 % retention of the initial capacity after 50 cycles for the binary system. Recently, graphene has been intensively investigated for enhancing the rate and cycling performance of lithium sulfur batteries. Graphene, which has a two-dimensional, one-atom-thick nanosheet structure, offers extraordinary electronic, thermal and mechanical properties. Herein, a sulfur-polyacrylonitrile/reduced graphene oxide (SPAN/RGO) composite with unique electrochemical properties was prepared. PAN is deposited on the surface of RGO sheets followed by ball milling with sulfur and heat treatment. Infrared spectroscopy and microscopy studies indicate that the composite consists of RGO decorated with SPAN particles of 100 nm average size. The PAN/RGO composite shows good overall electrochemical performance when used in Li/S batteries. It exhibits ~85% retention of the initial reversible capacity of 1467 mAh/g over 100 cycles at a constant current rate of 0.1 C and retains 1100 mAh/g after 200 cycles. In addition, the composite displays excellent Coulombic efficiency and rate capability, delivering up to 828 mAh/g reversible capacity at 2 C. The improved performance stems from composition and structure of the composite, wherein RGO renders a robust electron transport framework and PAN acts as sulfur/polysulfide absorber.

Rechargeable lithium sulfur (Li-S) batteries are potentially safe, environmentally friendly and economical alternative energy storage systems that can potentially be combined with renewable sources including wind solar and wave energy. Sulfur has a high theoretical specific capacity of ~1680 mAh/g, attainable through the reversible redox reaction denoted as S8+16Li ↔8Li¬2S, which yields an average cell voltage of ~2.2 V. However, two detrimental factors prevent the achievement of the full potential of the Li-S batteries. First, the poor electrical/ionic conductivity of elemental sulfur and Li2S severely hampers the utilization of active material. Second, dissolution of intermediate long-chain polysulfides (Li2Sn, 2<n<7) into the electrolyte and their shuttle between cathode and anode lead to fast capacity degradation and low Coulombic efficiency. As a result of this shuttle process, insoluble and insulating Li2S/Li2S2 precipitate on the surface of electrodes causing loss of active material and rendering the electrode surface electrochemically inactive. Extensive research efforts have been devoted to overcome the aforementioned problems, such as combination of sulfur with conductive polymers, and encapsulation or coating of elemental sulfur in different nanostructured carbonaceous materials. Noteworthy, sulfur-polyacrylonitrile (SPAN) composites, wherein sulfur is chemically bond to the polymer backbone and PAN acts as a conducting matrix, have shown some success in suppressing the shuttle effect. However, due to the limited electrical conductivity of polyacrylonitrile, the capacity retention and rate performance of the SPAN systems are still very modest, which shows only 67 % retention of the initial capacity after 50 cycles for the binary system. Recently, graphene has been intensively investigated for enhancing the rate and cycling performance of lithium sulfur batteries. Graphene, which has a two-dimensional, one-atom-thick nanosheet structure, offers extraordinary electronic, thermal and mechanical properties. Herein, a sulfur-polyacrylonitrile/reduced graphene oxide (SPAN/RGO) composite with unique electrochemical properties was prepared. PAN is deposited on the surface of RGO sheets followed by ball milling with sulfur and heat treatment. Infrared spectroscopy and microscopy studies indicate that the composite consists of RGO decorated with SPAN particles of 100 nm average size. The PAN/RGO composite shows good overall electrochemical performance when used in Li/S batteries. It exhibits ~85% retention of the initial reversible capacity of 1467 mAh/g over 100 cycles at a constant current rate of 0.1 C and retains 1100 mAh/g after 200 cycles. In addition, the composite displays excellent Coulombic efficiency and rate capability, delivering up to 828 mAh/g reversible capacity at 2 C. The improved performance stems from composition and structure of the composite, wherein RGO renders a robust electron transport framework and PAN acts as sulfur/polysulfide absorber.