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2D nanostructure

We also include in this class of quasi-2D nanostructured materials Titania deposited inside ordered mesoporous silica (because an inner coating of mesoporous silica may be realized), or nano-dot type Titania particles well dispersed in the ordered porous matrix. We do not consider here solids which contain linear or zig-zag type TiOTiO-nanowires in a microcrystalline porous framework, such as ETS-4 and ETS-10, notwithstanding the interest of these materials also as photocatalysts,146-151 because these nanowires are located inside the host matrix, and not fully accessible from the gas reactants (the reactivity is essentially at pore mouth). [Pg.369]

In conclusion, GaS and GaSe nanowalls have been obtained by thermal treatment of bulk powders, thereby demonstrating how these materials are quite similar to graphite in that they form 0D, ID and 2D nanostructures. It is noteworthy that we have obtained Ga203 and GaN nanowalls from GaS and GaSe nanowalls without the loss of dimensional integrity. [Pg.583]

Hossain MK, Shibamoto K, Ishioka K, Kitajima M, Mitani T, Nakashima S (2007) 2D nanostructure of gold nanoparticles an approach to SERS-active substrate. J Lumin 122-123 792-795... [Pg.133]

Fig.29 A STM image (27.1 nmx27.1 nm) of a monolayer of TTA-DIA after 30 minutes of UV light irradiation. A pulse (height - 3.2 V, width 500 ns) was applied at the position indicated with a white arrow. B STM image (27.1 nmx27.1 nm) of the monolayer of TTA-DIA at the same area after application of a single pulse. The white arrow in the image indicates the polydiacetylene backbone created by pulsing. C Molecular model of a 2D nanostructure formed by the covalent connection of adjacent parallel polydiacetylene chains. (Reproduced with permission from [89])... Fig.29 A STM image (27.1 nmx27.1 nm) of a monolayer of TTA-DIA after 30 minutes of UV light irradiation. A pulse (height - 3.2 V, width 500 ns) was applied at the position indicated with a white arrow. B STM image (27.1 nmx27.1 nm) of the monolayer of TTA-DIA at the same area after application of a single pulse. The white arrow in the image indicates the polydiacetylene backbone created by pulsing. C Molecular model of a 2D nanostructure formed by the covalent connection of adjacent parallel polydiacetylene chains. (Reproduced with permission from [89])...
EFFECTS OF SPATIAL REPRODUCTION AND MULTIPLICATION AT THE INTERFERENCE OF THE ELECTRON WAVES IN SEMICONDUCTOR 2D NANOSTRUCTURES WITH RECTANGULAR QUANTUM WELLS... [Pg.109]

Effects of spatial nonhomogeneity for the probability current density (or a quantum-mechanical current density) in the semiconductor 2D nanostructures in the form of joints in the direction of propagation of the electron wave of narrow and wide rectangular quantum wells have been theoretically studied. [Pg.109]

At present, advances in nanotechnology allow to create semiconductor nanostructures in which linear dimensions of the conductive channel in the direction of propagation of the electron wave are smaller than the mean free path of the electron. In such a channel particles move in a ballistic regime that allows to study experimentally the effects of ballistic transport in such structures, in particular, various electron interference effects [1]. A large number of theoretical works were devoted to the investigation of electron quantum ballistic transport in ID and 2D nanostructures whose common feature is the presence in quantum channels of regions of a sharp (nonadiabatic) variation either of the channel s geometry or a potential relief in it [2-4]. [Pg.109]

In Fig. 1 the results of a numerical calculation of the effects of spatial inhomogeneity for jx (x, z) in 2D nanostructures are presented. We have considered a problem of the scattering of a simple harmonic electron wave spreading in the lower subband from narrow rectangular QW (a = 42 A) on the... [Pg.111]

The simple hydrothermal method can be used to control the ID and 2D nanostructures of the oxides. The reaction was a conversion of nitrates mixture into carbonate hydrate phase, with the presence of ammonium hydrogen carbonate solution, at a reaction temperature of200 °C for 3 h. Morphological architectures of the rare earth oxides obtained were controlled by the thermal treatment at... [Pg.141]

It is first important to classify the different types of nanostructures and their relevant characteristics and morphological features at the nanoscale, according to their dimensionality, as illustrated in Fig. 4.1. One can clearly distinguish OD nanostructures with nanoparticles, clusters and mesoporous systems as MOFs (Metal Oxide Frameworks), ID nanostmctures with nanotubes and nanowires, 2D nanostructures with multilayers and 3D nanostructures with nanostructured and nanocrystalline materials. In this context, nanocrystalline materials are defined as single- or multi-phase polycrystaUine solids with a grain size of a few nanometres... [Pg.188]

The 2D nanostructures, or surface slabs, are suitable for the simulation of the apolar ZnO surfaces and might constitute the basis for the investigation of adsorption of dye-sensitizers onto ZnO [203] which are of interest for dye-sensitized solar cells. Here we performed a systematic investigation of the electronic and optical properties... [Pg.173]

Fig. 15 Left. Optimized geometrical structure of the [(ZnO)3o(H20)3], [(Zn0)42(H20>4], and [(Zn0)54(H20)5] 2D nanostructures. Red=0, yellow=Zxi, whi/e=H atoms. Right Optimized geometrical structure of the [(Zn0)i28(H20)i2] and [(ZnO)222(H20),2] 3D nanostructures. The dashed arrow indicates the c axis along the [1210] directiom Adapted fixjm [200] by pmnission of the PCCP Owner Societies... Fig. 15 Left. Optimized geometrical structure of the [(ZnO)3o(H20)3], [(Zn0)42(H20>4], and [(Zn0)54(H20)5] 2D nanostructures. Red=0, yellow=Zxi, whi/e=H atoms. Right Optimized geometrical structure of the [(Zn0)i28(H20)i2] and [(ZnO)222(H20),2] 3D nanostructures. The dashed arrow indicates the c axis along the [1210] directiom Adapted fixjm [200] by pmnission of the PCCP Owner Societies...
For the considered 2D nanostructures, we find the lowest TDDFT excitation energy in solution to be almost independent of the surface extension, with calculated values of 3.93,3.97, and 3.96 eV for [(ZnO)3o(H20)3], [(Zn0)42(H20>4], and [(Zn0)54(H20>5], respectively, which are, as expected, higher than the lowest excitation energy for the reference (ZnO)ni cluster (3.59 eV). Altogether, these results suggest that the main directions responsible for quantum ccmfinement correspond to the [1010] and [0001] crystal axes. [Pg.174]

The unique solvent properties of hydrazine have further been used to produce a range of 2D nanostructures of first and second row transition metal chalcogenides by the solvothermal method. Hydrazine, being a small volatile molecule, capable of forming coordinate complexes or... [Pg.247]


See other pages where 2D nanostructure is mentioned: [Pg.316]    [Pg.369]    [Pg.85]    [Pg.581]    [Pg.583]    [Pg.309]    [Pg.340]    [Pg.104]    [Pg.581]    [Pg.583]    [Pg.70]    [Pg.80]    [Pg.127]    [Pg.81]    [Pg.109]    [Pg.112]    [Pg.226]    [Pg.2376]    [Pg.363]    [Pg.501]    [Pg.439]    [Pg.2759]    [Pg.3737]    [Pg.1428]    [Pg.174]    [Pg.937]    [Pg.369]    [Pg.299]    [Pg.265]    [Pg.246]   
See also in sourсe #XX -- [ Pg.439 ]




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