Rotation Curve of Galaxies by the Force Induced by Mass of Moving Particles

We suggest that there is a novel force which is generated by the mass of relatively moving particles. The new force which we named Mirinae Force is a counterpart of the magnetic force operating between electrically charged moving particles. Instead of using the conventional dark matter, we applied the mirinae force to a particular model system of the spiral galaxy in which most of the galaxy's mass is located within the central region where some portion of the inner mass is in revolving motion at a relativistic speed. The calculation yielded three important results that illustrate the existence of mirinae force and validate the proposed model: First, the mirinae force in this model explains why most of the matters in the galactic disk are in the circular motion which is similar to cycloid. Second, the mirinae force well explains not only the flat rotation curve but also the varied slope of the rotation curve observed in the spiral galaxies. Third, at the flat velocity of 220 Km/s, the inner mass of the Milky Way calculated by using the proposed model is 6.0\times10^11 M\odot, which is very close to 5.5\times10^11 M\odot (r <50 Kpc, including Leo I) estimated by using the latest kinematic information. This means that the mirinae force well takes the place of the dark matter of the Milky Way

Electrical Phase Transition of Poly(4,4&apos;-aminotriphenylene hexafluoroisopropy lidenediphthalimide) by Photogenerated Charged Carrier Injection

We show a set-up of poly(4,4&apos;-aminotriphenylene hexafluoroisopropylidenediphthalimide) (6F-TPA PI)/Al sample in which holes are injected by photoelectron emission process instead of direct charge carrier injection via metal electrode. In this process, an irreversible electrical phase transition of 6F-TPA PI is found in contrast to the Al/6F-TPA PI/Al structure, leading to a write-once-read-many behavior. The photoelectron spectroscopy results measured before and after the switching process revealed that the irreversible electrical phase transition of 6F-TPA PI is attributed to the chemical modification of the carbonyl group in phthalimide moiety. (C) 2012 American Institute of Physics. [doi:10.1063/1.3681776]X1122sciescopu

Thickness-insensitive properties of alpha-moo3 nanosheets by weak interlayer coupling

van der Waals (vdW) materials have shown unique electrical and optical properties depending on the thickness due to strong interlayer interaction and symmetry breaking at the monolayer level. In contrast, the study of electrical and tribological properties and their thickness-insensitivity of van der Waals oxides are lacking due to difficulties in the fabrication of high quality two-dimensional oxides and the investigation of nanoscale properties. Here we investigated various tribological and electrical properties, such as, friction, adhesion, work function, tunnel current, and dielectric constant, of the single-crystal alpha-MoO3 nanosheets epitaxially grown on graphite by using atomic force microscopy. The friction of atomically smooth MoO3 is rapidly saturated within a few layers. The thickness insensitivity of friction is due to very weak mechanical interlayer interaction. Similarly, work function (4.73 eV for 2 layers (hereafter denoted as L)) and dielectric constant (6 for 2L and 10.5-11 for &gt;3L) of MoO3 in MoO3 showed thickness insensitivity due to weak interlayer coupling. Tunnel current measurements by conductive atomic force microscopy showed that even 2L MoO3 of 1.4 nm is resistant to tunneling with a high dielectric strength of 14 MV/cm. The thickness-indifferent electrical properties of high dielectric constant and tunnel resistance by weak interlayer coupling and high crystallinity show a promise in the use of MoO3 nanosheets for nanodevice applications.OAIID:RECH_ACHV_DSTSH_NO:T201918311RECH_ACHV_FG:RR00200001ADJUST_YN:EMP_ID:A080876CITE_RATE:12.279FILENAME:acs.nanolett.9b03701.pdfDEPT_NM:재료공학부EMAIL:[email protected]_YN:YFILEURL:https://srnd.snu.ac.kr/eXrepEIR/fws/file/0d14e111-9761-492b-8321-20defa61a5a6/linkN

Influence of LaFeO3 Surface Termination on Water Reactivity.

The polarity of oxide surfaces can dramatically impact their surface reactivity, in particular, with polar molecules such as water. The surface species that result from this interaction change the oxide electronic structure and chemical reactivity in applications such as photoelectrochemistry but are challenging to probe experimentally. Here, we report a detailed study of the surface chemistry and electronic structure of the perovskite LaFeO3 in humid conditions using ambient-pressure X-ray photoelectron spectroscopy. Comparing the two possible terminations of the polar (001)-oriented surface, we find that the LaO-terminated surface is more reactive toward water, forming hydroxyl species and adsorbing molecular water at lower relative humidity than its FeO2-terminated counterpart. However, the FeO2-terminated surface forms more hydroxyl species during water adsorption at higher humidity, suggesting that adsorbate-adsorbate interactions may impact reactivity. Our results demonstrate how the termination of a complex oxide can dramatically impact its reactivity, providing insight that can aid in the design of catalyst materials

Digital Memory Characteristics of Aromatic Polyimides Based on Pyridine and Its Derivatives

Soluble aromatic polyimides and polyvinyls were prepared by incorporating pyridine moiety and its derivatives in the backbone and the side groups, respectively: 6F-Py-i polymers based on the polyimide backbone (6F-Py-1 to 6F-Py-7) and PVPy-i polymers based on the polyvinyl backbone (PVPy-1 to PVPy-4). All polymers were found to be amorphous. The 6F-Py-i polymers were thermally stable up to 511–545 °C; the PVPy-i polymers were stable up to 362–376 °C. Their glass transitions, thin film densities, molecular orbitals, and band gaps were determined. The electrical devices fabricated with the polymers in an electrode/polymer/electrode structure revealed p-type unipolar write-once-read-many times (namely, permanent) or dynamic random access memory or dielectric behavior, depending on the substituents of the pyridine unit and the film thicknesses. In particular, such digital memory characteristics were found to originate from the pyridine moieties possessing a high charge affinity in the polymers. However, the pyridine moieties were found to still need at least two or more aromatic substituents to get enough power to stabilize charges via utilizing the resonance effects provided by the substituents. Overall, this study demonstrated that the pyridine unit conjugated with two or more aromatic substituents is a very useful component to design and synthesize digital memory materials based on thermally stable polyimides and other high performance polymers. The 6F-Py-i polymers have potential for the low-cost mass production of high-performance programmable unipolar permanent memory devices with very low power consumption

High open-circuit voltage of graphene-based photovoltaic cells modulated by layer-by-layer transfer

Graphene has shown great application opportunities in future nanoelectronic devices because of its outstanding electronic properties. Moreover, its impressive optical properties have been attracting the interest of researchers, and, recently, the photovoltaic effects of a heterojunction structure embedded with few layer graphene (FLG) have been demonstrated. Here, we report the photovoltaic response of graphenesemiconductor junctions and the controlled open-circuit voltage (Voc) with varying numbers of graphene layers. After unavoidably adsorbed contaminants were removed from the FLGs by means of in situ annealing, prepared by layer-by-layer transfer of the chemically grown graphene layer, the work functions of FLGs showed a sequential increase as the graphene layers increase, despite random interlayer-stacking, resulting in the modulation of photovoltaic behaviors of FLGs/Si interfaces. The surface photovoltaic effects observed here show an electronic realignment in the depth direction in the FLG heterojunction systems, indicating future potential toward solar devices utilizing the excellent transparency and flexibility of FLG. Copyright (c) 2011 John Wiley & Sons, Ltd

Coating lithium titanate anodes with a mixed ionic-electronic conductor for high-rate lithium-ion batteries

Lithium titanate (Li4Ti5O12; LTO) is a promising anode material for fast (dis)charging Li-ion batteries (LIBs). However, its low Li diffusion coefficient and electronic conductivity limit its applications. Here, we uniformly coat the LTO surface with a 1.6 nm layer of partially lithiated titania (LixTiO2, x approximate to 0.5), which is found to be a mixed ionic-electronic conductor (MIEC), using a simple solid-state method. The MIEC layer simultaneously transfers electrons and Li-ions, facilitating efficient charge transfer to (de)lithiate LTO over the entire particle surface. MIEC-nanocoated LTO exhibits highly improved capacity retention and rate capability than pristine LTO; based on electrochemical simulations, MIEC nanocoating causes performance enhancement by maximum surface-area utilization for charge transfer. Furthermore, electrochemical impedance spectroscopy and density functional theory calculations confirm facile ionic transport and high electronic conductivity of LixTiO2 nano -layer. This general strategy of MIEC nanocoating can boost the electrochemical performances of various insu-lating electrodes, maximizing the materials utilization