スルホベタインが蛋白質のダイナミクスに及ぼす効果の解析

学位記番号:工博乙12

Micro/Nano Liquid Crystal Layer–Based Tunable Optical Fiber Interferometers

Miniaturization and integration are the main trends in modern photonic technology. In this chapter, two kinds of micro-/nano liquid crystal (LC) layer–based tunable optical fiber interferometers are proposed. One fiber interferometer is the optical fiber gratings (LPGs), and the other one is the locally bent microfiber taper (LBMT). The working principles of the devices are theoretically analyzed. The preparation process and the functional properties of the devices are experimentally investigated as well

Criterions, Prediction and Prevention of Loess Liquefaction

Although loess liquefaction is not very common during earthquakes in Northwest of China, it is disastrous if it happens. Both study and valid evidence from Haiyuan 8.5 Earthquake in 1920 and Tajikistan 5.9 Earthquake in 1989 have proved that loess liquefaction could be very disastrous under certain conditions. In this paper, the criterions of loess liquefaction are discussed to show that unlike typical liquefaction of sand, loess which falls into the category of both silt clay and clayey silt has unique characteristics during liquefaction test. To predict liquefaction of loess, a simple method based on laboratory test and field evidences using GIS is proposed. The prediction results and corresponding measure have been adopted in Seismic Design Code for Buildings in Lanzhou Urban Area. Finally, recent approach of treatment of loess with chemicals methods is developed, which may have some application implication as an simple and feasible treatment method against liquefaction of loess

Dynamic deformability of individual PbSe nanocrystals during superlattice phase transitions

The behavior of individual nanocrystals during superlattice phase transitions can profoundly affect the structural perfection and electronic properties of the resulting superlattices. However, details of nanocrystal morphological changes during superlattice phase transitions are largely unknown due to the lack of direct observation. Here, we report the dynamic deformability of PbSe semiconductor nanocrystals during superlattice phase transitions that are driven by ligand displacement. Real-time high-resolution imaging with liquid-phase transmission electron microscopy reveals that following ligand removal, the individual PbSe nanocrystals experience drastic directional shape deformation when the spacing between nanocrystals reaches 2 to 4 nm. The deformation can be completely recovered when two nanocrystals move apart or it can be retained when they attach. The large deformation, which is responsible for the structural defects in the epitaxially fused nanocrystal superlattice, may arise from internanocrystal dipole-dipole interactions

Strong structural and electronic coupling in metavalent PbS moire superlattices

Moire superlattices are twisted bilayer materials, in which the tunable interlayer quantum confinement offers access to new physics and novel device functionalities. Previously, moire superlattices were built exclusively using materials with weak van der Waals interactions and synthesizing moire superlattices with strong interlayer chemical bonding was considered to be impractical. Here using lead sulfide (PbS) as an example, we report a strategy for synthesizing of moire superlattices coupled by strong chemical bonding. We use water-soluble ligands as a removable template to obtain free-standing ultra-thin PbS nanosheets and assemble them into direct-contact bilayers with various twist angles. Atomic-resolution imaging shows the moire periodic structural reconstruction at superlattice interface, due to the strong metavalent coupling. Electron energy loss spectroscopy and theoretical calculations collectively reveal the twist angle26 dependent electronic structure, especially the emergent separation of flat bands at small twist angles. The localized states of flat bands are similar to well-arranged quantum dots, promising an application in devices. This study opens a new door to the exploration of deep energy modulations within moire superlattices alternative to van der Waals twistronics

In Situ TEM Study of the Degradation of PbSe Nanocrystals in Air

PbSe nanocrystals have attracted widespread attention due to a variety of potential applications. However, the practical utility of these nanocrystals has been hindered by their poor air stability, which induces undesired changes in the optical and electronic properties. An understanding of the degradation of PbSe nanocrystals when they are exposed to air is critical for improving the stability and enhancing their applications. Here, we use in situ transmission electron microscopy (TEM) with an environmental cell connected to air to study PbSe nanocrystal degradation triggered by air exposure. We have also conducted a series of complementary studies, including in situ environmental TEM study of PbSe nanocrystals exposed to pure oxygen and PbSe nanocrystals in H2O using a liquid cell, and ex situ experiments, such as O2 plasma treatment and thermal heating of PbSe nanocrystals under different air exposure. Our in situ observations reveal that when PbSe nanocrystals are exposed to air (or oxygen) under electron beam irradiation, they experience a series of changes, including shape evolution of individual nanocrystals with the cuboid intermediates, coalescence between nanocrystals, and formation of PbSe thin films through drastic solid-state fusion. Further studies show that the PbSe thin films transform into an amorphous Pb rich phase or eventually pure Pb, which suggest that Se reacts with oxygen and can be evaporated under electron beam illumination. These various in situ and ex situ experimental results indicate that PbSe nanocrystal degradation in air is initiated by the dissociation and removal of ligands from the PbSe nanocrystal surface

Revealing of the Activation Pathway and Cathode Electrolyte Interphase Evolution of Li-Rich 0.5Li2MnO3·0.5LiNi0.3Co0.3Mn0.4O2 Cathode by in Situ Electrochemical Quartz Crystal Microbalance.

The first-cycle behavior of layered Li-rich oxides, including Li2MnO3 activation and cathode electrolyte interphase (CEI) formation, significantly influences their electrochemical performance. However, the Li2MnO3 activation pathway and the CEI formation process are still controversial. Here, the first-cycle properties of xLi2MnO3·(1- x) LiNi0.3Co0.3Mn0.4O2 ( x = 0, 0.5, 1) cathode materials were studied with an in situ electrochemical quartz crystal microbalance (EQCM). The results demonstrate that a synergistic effect between the layered Li2MnO3 and LiNi0.3Co0.3Mn0.4O2 structures can significantly affect the activation pathway of Li1.2Ni0.12Co0.12Mn0.56O2, leading to an extra-high capacity. It is demonstrated that Li2MnO3 activation in Li-rich materials is dominated by electrochemical decomposition (oxygen redox), which is different from the activation process of pure Li2MnO3 governed by chemical decomposition (Li2O evolution). CEI evolution is closely related to Li+ extraction/insertion. The valence state variation of the metal ions (Ni, Co, Mn) in Li-rich materials can promote CEI formation. This study is of significance for understanding and designing Li-rich cathode-based batteries

Carbon nanocages with nanographene shell for high-rate lithium ion batteries

Carbon nanocages with a nanographene shell have been prepared by catalytic decomposition of p-xylene on a MgO supported Co and Mo catalyst in supercritical CO2 at a pressure of 10.34 MPa and temperatures ranging from 650 to 750 °C. The electrochemical performance of these carbon nanocages as anodes for lithium ion batteries has been evaluated by galvanostatic cycling. The carbon nanocages prepared at a temperature of 750 °C exhibited relatively high reversible capacities, superior rate performance and excellent cycling life. The advanced performance of the carbon nanocages prepared at 750 °C is ascribed to their unique structural features: (1) nanographene shells and the good inter-cage contact ensuring fast electron transportation, (2) a porous network formed by fine pores in the carbon shell and the void space among the cages facilitating the penetration of the electrolyte and ions within the electrode, (3) thin carbon shells shortening the diffusion distance of Li ions, and (4) the high specific surface area providing a large number of active sites for charge-transfer reactions. These carbon nanocages are promising candidates for application in lithium ion batteries