Model-based deconvolution for particle analysis applied to a through-focus series of HAADF-STEM images.

This paper presents an approach for determining the sizes and three-dimensional (3D) positions of nanoparticles from a through-focus series of high-angle annular dark-field scanning transmission electron microscopy images. By assuming spherical particles with uniform density, the sizes and 3D positions can be derived via Wiener deconvolution using a series of kernels prepared by the convolution of the 3D point spread function of the electron beam and the 3D density distribution of spheres with different radii. This process is referred to as a model-based deconvolution. Four 3D datasets with a volume size of 148 × 148 × 560 nm3 were obtained from the four sets of 256 high-angle annular dark-field scanning transmission electron microscopy images of 256 × 256 pixels taken from the same field of view under the through-focus condition. The 3D positions and radii of 14 particles in each 3D dataset were derived using the model-based deconvolution for ∼8 min. The observation errors of the 3D position were estimated as σx ≅ σy ≅ 0.3 nm and σz < 1.6 nm.

Inelastic mean free path measurement by STEM-EELS technique using needle-shaped specimen.

Inelastic mean free path (IMFP) was determined by electron energy loss spectroscopy (EELS) to estimate the accurate thickness of TEM thin foil using needle-shaped specimen. From EELS measurements performed for 99.99% Al, Si wafer and 99.99% Fe, linear relationships were confirmed between the thickness of the TEM thin foil and the ratio of the total intensity of EELS spectrum to the total intensity of zero-loss spectrum for all samples. By weighted least-square fitting, the IMFP was estimated to be 143-150 nm for Al, 159-165 nm for Si with amorphous layer, and 92-94 nm for Fe with the collection semi-angle ß = 11.9 - 35.7 mrad, and accelerated voltage of 200 kV. Thus, the dependence of IMFP on ß is not dominant. The accuracy depends on the roundness of the cross-section of the needle-shaped specimen, and is observed to be low in terms of percentage in this work.

High-Pressure Synthesis and Crystal Structure of MoC-Type Tungsten Nitride by Nitridation with Ammonium Chloride.

A novel tungsten nitride, MoC-type WN, was synthesized at 6 GPa and 1200 °C via nitridation of tungsten by ammonium chloride as a nitrogen source. This compound is isostructural with γ'-MoC, which has a hexagonal structure with a space group of P63/mmc (No. 194). Micrometer-sized single crystals of MoC-type WN were grown in molten ammonium chloride flux. In addition, NaCl-type WN and WC-type WN were synthesized via nitridation by ammonium chloride at 6 GPa and 1000 °C. Ammonium chloride is appropriate as a nitrogen source for nitride synthesis under high pressure. The new WN phase crystallizes in the hexagonal structure with unit cell parameters of a = 2.89248(2) Å and c = 10.17069(7) Å. The chemical formula of MoC-type WN refined by the Rietveld analysis from powder X-ray diffraction data was WN0.60(1). The zero-pressure bulk modulus, K0, of MoC-type WN was determined to be 338(3) GPa, which can be expected to be a hard material.

Monolayer-to-bilayer transformation of silicenes and their structural analysis.

Silicene, a two-dimensional honeycomb network of silicon atoms like graphene, holds great potential as a key material in the next generation of electronics; however, its use in more demanding applications is prevented because of its instability under ambient conditions. Here we report three types of bilayer silicenes that form after treating calcium-intercalated monolayer silicene (CaSi2) with a BF4(-) -based ionic liquid. The bilayer silicenes that are obtained are sandwiched between planar crystals of CaF2 and/or CaSi2, with one of the bilayer silicenes being a new allotrope of silicon, containing four-, five- and six-membered sp(3) silicon rings. The number of unsaturated silicon bonds in the structure is reduced compared with monolayer silicene. Additionally, the bandgap opens to 1.08 eV and is indirect; this is in contrast to monolayer silicene which is a zero-gap semiconductor.

Organic dicarboxylate negative electrode materials with remarkably small strain for high-voltage bipolar batteries.

As advanced negative electrodes for powerful and useful high-voltage bipolar batteries, an intercalated metal-organic framework (iMOF), 2,6-naphthalene dicarboxylate dilithium, is described which has an organic-inorganic layered structure of π-stacked naphthalene and tetrahedral LiO4 units. The material shows a reversible two-electron-transfer Li intercalation at a flat potential of 0.8 V with a small polarization. Detailed crystal structure analysis during Li intercalation shows the layered framework to be maintained and its volume change is only 0.33%. The material possesses two-dimensional pathways for efficient electron and Li(+) transport formed by Li-doped naphthalene packing and tetrahedral LiO3C network. A cell with a high potential operating LiNi(0.5)Mn(1.5)O4 spinel positive and the proposed negative electrodes exhibited favorable cycle performance (96% capacity retention after 100 cycles), high specific energy (300 Wh kg(-1)), and high specific power (5 kW kg(-1)). An 8 V bipolar cell was also constructed by connecting only two cells in series.

Light-harvesting photocatalysis for water oxidation using mesoporous organosilica.

An organic-based photocatalysis system for water oxidation, with visible-light harvesting antennae, was constructed using periodic mesoporous organosilica (PMO). PMO containing acridone groups in the framework (Acd-PMO), a visible-light harvesting antenna, was supported with [Ru(II)(bpy)3(2+)] complex (bpy = 2,2'-bipyridyl) coupled with iridium oxide (IrO(x)) particles in the mesochannels as photosensitizer and catalyst, respectively. Acd-PMO absorbed visible light and funneled the light energy into the Ru complex in the mesochannels through excitation energy transfer. The excited state of Ru complex is oxidatively quenched by a sacrificial oxidant (Na2S2O8) to form Ru(3+) species. The Ru(3+) species extracts an electron from IrO(x) to oxidize water for oxygen production. The reaction quantum yield was 0.34 %, which was improved to 0.68 or 1.2 % by the modifications of PMO. A unique sequence of reactions mimicking natural photosystem II, 1) light-harvesting, 2) charge separation, and 3) oxygen generation, were realized for the first time by using the light-harvesting PMO.

Crystal-like periodic mesoporous organosilica bearing pyridine units within the framework.

Periodic mesoporous organosilica with densely packed pyridine units within the framework and crystal-like molecular-scale periodicity was synthesized. The framework pyridines were chemically active and fully accessible for protonation and Cu(2+) adsorption.

Visible-light-harvesting periodic mesoporous organosilica.

Highly ordered periodic mesoporous organosilica synthesized from a newly designed 9(10H)-acridone bridged organosilane precursor exhibited efficient light-harvesting antenna properties for visible light, at wavelengths up to 450 nm.

A periodic mesoporous organosilica-based donor-acceptor system for photocatalytic hydrogen evolution.

A new solid-sate donor-acceptor system based on periodic mesoporous organosilica (PMO) has been constructed. Viologen (Vio) was covalently attached to the framework of a biphenyl (Bp)-bridged PMO. The diffuse reflectance spectrum showed the formation of charge-transfer (CT) complexes of Bp in the framework with Vio in the mesochannels. The transient absorption spectra upon excitation of the CT complexes displayed two absorption bands due to radical cations of Bp and Vio species, which indicated electron transfer from Bp to Vio. The absorption bands slowly decayed with a half-decay period of approximately 10 mus but maintained the spectral shape, thereby suggesting persistent charge separation followed by recombination. To utilize the charge separation for photocatalysis, Vio-Bp-PMO was loaded with platinum and its photocatalytic performance was tested. The catalyst successfully evolved hydrogen with excitation of the CT complexes in the presence of a sacrificial agent. In contrast, reference catalysts without either Bp-PMO or Vio gave no or little hydrogen generation, respectively. In addition, a homogeneous solution system of Bp molecules, methylviologen, and colloidal platinum also evolved no hydrogen, possibly due to a weaker electron-donating feature of molecular Bp than that of densely packed Bp in Bp-PMO. These results indicated that densely packed Bp and Vio are essential for hydrogen evolution in this system and demonstrated the potential of PMO as the basis for donor-acceptor systems suitable for photocatalysis.

Reverse-selective microporous membrane for gas separation.

Reverse-selective membranes, through which bigger molecules selectively permeate, are attractive for developing chemical processes utilizing hydrogen because they can maintain the high partial pressure of hydrogen required for their further downstream utilization. Although several of these chemical processes are operated above 473 K, membranes with outstanding reverse-selective separation performance at these temperatures are still to be reported. Herein, we propose a new adsorption-based reverse-selective membrane that utilizes a Na cation occluded in a zeolitic framework. The membrane developed in this work, a compact Na(+)-exchanged ZSM-5 (NaZSM-5) type zeolite membrane, enables us to selectively permeate and separate bigger polar molecules, such as methanol and water, from a stream containing hydrogen, above 473 K. On the other hand, a Na(+)-free, H(+)-exchanged ZSM-5 (HZSM-5) type zeolite membrane did not show separation properties at these temperatures. The microporous zeolite membrane developed in this study can be applied to a variety of chemical reaction systems to minimize energy consumption.

Self-assembled double ladder structure formed inside carbon nanotubes by encapsulation of H8Si8O12.

Unique low-dimensional SiO(2)-based nanomaterials can be encapsulated and synthesized inside the nanometer-scale one-dimensional internal spaces of carbon nanotubes (CNTs). In this study, various single-walled CNTs (SWNTs) and double-walled CNTs (DWNTs) having different diameters are used as containers for cubic octameric H(8)Si(8)O(12) molecules. High-resolution transmission electron microscopy (HRTEM), Fourier transform infrared (FT-IR) spectroscopy, and Raman spectroscopy observations revealed that, depending on the diameter of the CNTs, two types of structures are formed inside the SWNTs and DWNTs: In the case of those CNTs having inner diameters ranging from 1.2 to 1.4 nm, a new ordered self-assembled structure composed of H(8)Si(4n)O(8n-4) molecules was formed through the transformation of H(8)Si(8)O(12); however, in the case of CNTs having inner diameters larger than 1.7 nm, a disordered structure was formed. This behavior may indicate that strong interactions occur between the CNTs and the encapsulated H(8)Si(4n)O(8n-4) molecules.

Design of molecularly ordered framework of mesoporous silica with squared one-dimensional channels.

Mesoporous silica with squared one-dimensional channels (KSW-2-type mesoporous silica), possessing a molecularly ordered framework arising from a starting layered polysilicate kanemite, was obtained through silylation of a surfactant (hexadecyltrimethylammonium, C16TMA)-containing mesostructured precursor with octoxytrichlorosilane (C8H17OSiCl3) and octylmethyldichlorosilane (C8H17(CH3)SiCl2). The presence of the molecular ordering in the silicate framework was confirmed by XRD and TEM. Octoxy groups grafted on KSW-2 can be eliminated by subsequent hydrolysis under very mild condition, and pure mesoporous silica was obtained with the retention of the kanemite-based framework. The framework is structurally stabilized by the attachment of additional SiO4 units to the framework, and the mesostructural ordering hardly changed under the presence of water vapor. A large number of silanol groups remained at the mesopore surfaces because C16TMA ions and octoxy groups can be removed without calcination. Octylmethylsilyl groups are regularly arranged at the mesopore surface due to the molecular ordering in the silicate framework. The molecularly ordered structural periodicity originating from kanemite is retained even after calcination at 550 degrees C, while that in the precursor without silylation disappeared. The synthetic strategy is quite useful for the design of the silicate framework of mesostructured and mesoporous materials with and without surface functional organic groups.

Insights into the crystal growth mechanisms of zeolites from combined experimental imaging and theoretical studies.

Detailed investigations into surface mediated crystal growth at zeolite external surfaces are presented. High resolution TEM is able to directly resolve surface and bulk crystallographic features and the unusual surface structural features are interpreted from simulation work. The growth of the double 4 ring is found to be a crucial and rate-determining step in the surface mediated, post-nucleation crystal growth mechanism of zeolite Beta C. Growth of 4 rings is found to be more favourable on fast growing rather than slow growing faces, explaining the relative growth rate of crystal faces in this materials. Similarly, the terminating structures of zeolite Y/Faujasite can be partly explained by considering the condensation of 6 ring and double 6 ring species at the crystal surface. Whilst 4-ring and double 4 rings are known solution species, 6 rings and double 6 rings are not, and hence it is speculated that post-nucleation crystal growth may involve competition between primary building unit and secondary building unit mediated crystal growth mechanisms.

Amino-functionalized SBA-15 type mesoporous silica having nanostructured hexagonal platelet morphology.

Amino-functionalized SBA-15 type mesoporous silicas having unique hexagonal platelet morphologies with short channels (100-300 nm) running parallel to the thickness of the nanostructured hexagonal platelet type morphologies have been directly synthesized by co-condensation of aminopropyltriethoxysilane (APTES) and sodium metasilicate as a silica source in the presence of Pluronic P123 triblock copolymer as a structure directing agent.

Complex zeolite structure solved by combining powder diffraction and electron microscopy.

Many industrially important materials, ranging from ceramics to catalysts to pharmaceuticals, are polycrystalline and cannot be grown as single crystals. This means that non-conventional methods of structure analysis must be applied to obtain the structural information that is fundamental to the understanding of the properties of these materials. Electron microscopy might appear to be a natural approach, but only relatively simple structures have been solved by this route. Powder diffraction is another obvious option, but the overlap of reflections with similar diffraction angles causes an ambiguity in the relative intensities of those reflections. Various ways of overcoming or circumventing this problem have been developed, and several of these involve incorporating chemical information into the structure determination process. For complex zeolite structures, the FOCUS algorithm has proved to be effective. Because it operates in both real and reciprocal space, phase information obtained from high-resolution transmission electron microscopy images can be incorporated directly into this algorithm in a simple way. Here we show that by doing so, the complexity limit can be extended much further. The power of this approach has been demonstrated with the solution of the structure of the zeolite TNU-9 (|H9.3|[Al9.3Si182.7O384]; ref. 10) with 24 topologically distinct (Si,Al) atoms and 52 such O atoms. For comparison, ITQ-22 (ref. 11), the most complex zeolite known to date, has 16 topologically distinct (Si,Ge) atoms.

An analytical approach to determine the pore shape and size of MCM-41 materials from X-ray diffraction data.

The pore shape and size of MCM-41 were studied analytically by comparing the observed powder X-ray diffraction intensities with that derived from the MCM-41 crystal structure models, with two different pore shapes, a hexagon and a circle. The powder diffraction patterns from the as-synthesized and the calcined MCM-41 were measured by a synchrotron radiation at SPring-8, Japan. The MCM-41 structure with circular and hexagonal pore shapes explains well for the as-synthesized and the calcined MCM-41 crystals, respectively. The pore size and boundary obtained by this approach agree with those obtained from an N2 gas adsorption measurement combined with the Fourier synthesized density map.

Formation of highly ordered mesoporous titania films consisting of crystalline nanopillars with inverse mesospace by structural transformation.

Highly ordered mesoporous titania films consisting of crystalline nanopillars with open-spaced, perpendicular, and continuous porosity have been prepared via structural transformation from a 3D hexagonal mesostructure during the thermal treatment. The mechanism of the structural transformation is explained by the crystallization of the titania framework and the large contraction of the initial 3D hexagonal mesostructured film upon calcination. This structural transformation provides a new approach to generate mesoporous thin-film materials with unique structures.

Self-assembly of designed oligomeric siloxanes with alkyl chains into silica-based hybrid mesostructures.

A novel self-assembly route to ordered silica-organic hybrids using well-defined siloxane oligomers with alkoxy functionality and covalently attached alkyl chains has been investigated. Various hybrid mesostructures were obtained by hydrolysis and polycondensation without the use of any structure-directing agents. The oligomers 1(Cn), having an alkylsilane core and three branched trimethoxysilyl groups, formed highly ordered lamellar phases when n = 14-18, while those with shorter alkyl chains formed cylindrical assemblies, slightly distorted two-dimensional (2D) hexagonal structures (n = 6-10), and a novel 2D monoclinic structure (n = 12). Furthermore, the mixtures of 1(Cn) with different chain lengths yielded well-ordered 2D hexagonal phases, possibly due to the better packing of the precursors. The hybrids consisting of cylindrical assemblies were converted to ordered porous silica with tunable pore sizes upon calcination to remove organic groups. The liquid-state 29Si NMR analysis of the hydrolysis and polycondensation processes of 1(Cn) revealed a unique intramolecular reaction yielding primarily the oligomer with a tetrasiloxane ring which is a new class of amphiphilic molecule having both self-assembling ability and high cross-linking ability. We also found that the mesostructure (lamellar or 2D hexagonal) was strictly controlled by varying the number of siloxane units per alkyl chain. These results provide a deeper understanding of the present self-assembly process that is strongly governed by the molecular packing of oligosiloxane precursors.