In this chapter, we will restrict our attention to the ferrites and a few other closely related materials. The great interest in ferrites stems from their unique combination of a spontaneous magnetization and a high electrical resistivity. The observed magnetization results from the difference in the magnetizations of two non-equivalent sub-lattices of the magnetic ions in the crystal structure. Materials of this type should strictly be designated as “ferrimagnetic” and in some respects are more closely related to anti-ferromagnetic substances than they are to ferromagnetics in which the magnetization results from the parallel alignment of all the magnetic moments present. We shall not adhere to this special nomenclature except to emphasize effects, which are due to the existence of the sub-lattices.

Ferromagnetic materials

Two-photon excitation provides a means of activating chemical or physical processes with high spatial resolution in three dimensions and has made possible the development of three-dimensional fluorescence imaging, optical data storage, and lithographic microfabrication. These applications take advantage of the fact that the two-photon absorption probability depends quadratically on intensity, so under tight-focusing conditions, the absorption is confined at the focus to a volume of order λ3 (where λ is the laser wavelength). Any subsequent process, such as fluorescence or a photoinduced chemical reaction, is also localized in this small volume. Although three-dimensional data storage and microfabrication have been illustrated using two-photon-initiated polymerization of resins incorporating conventional ultraviolet-absorbing initiators, such photopolymer systems exhibit low photosensitivity as the initiators have small two-photon absorption cross-sections (δ). Consequently, this approach requires high laser power, and its widespread use remains impractical. Here we report on a class of π;-conjugated compounds that exhibit large δ (as high as 1, 250 × 10−50 cm4 s per photon) and enhanced two-photon sensitivity relative to ultraviolet initiators. Two-photon excitable resins based on these new initiators have been developed and used to demonstrate a scheme for three-dimensional data storage which permits fluorescent and refractive read-out, and the fabrication of three-dimensional micro-optical and micromechanical structures, including photonic-bandgap-type structures.

Two-photon polymerization initiators for three-dimensional optical data storage and microfabrication

http://www.cdi-electrosorption.org/wp-content/uploads/2014/06/Porada-et-al.-2013-Review-on-the-Science-and-Technology-of-Water-Desalination-by-Capacitive-Deionization.pdf

Review on the science and technology of water desalination by capacitive deionization

Capacitive deionization (CDI) is an emerging technology for the facile removal of charged ionic species from aqueous solutions, and is currently being widely explored for water desalination applications. The technology is based on ion electrosorption at the surface of a pair of electrically charged electrodes, commonly composed of highly porous carbon materials. The CDI community has grown exponentially over the past decade, driving tremendous advances via new cell architectures and system designs, the implementation of ion exchange membranes, and alternative concepts such as flowable carbon electrodes and hybrid systems employing a Faradaic (battery) electrode. Also, vast improvements have been made towards unraveling the complex processes inherent to interfacial electrochemistry, including the modelling of kinetic and equilibrium aspects of the desalination process. In our perspective, we critically review and evaluate the current state-of-the-art of CDI technology and provide definitions and performance metric nomenclature in an effort to unify the fast-growing CDI community. We also provide an outlook on the emerging trends in CDI and propose future research and development directions.

/pdf/water-desalination-via-capacitive-deionization-what-is-it-p45le9ivut.pdf

Water desalination via capacitive deionization : What is it and what can we expect from it?

We show that the Raman scattering technique can give complete structural information for one-dimensional systems, such as carbon nanotubes. Resonant confocal micro-Raman spectroscopy of an (n,m) individual single-wall nanotube makes it possible to assign its chirality uniquely by measuring one radial breathing mode frequency omega(RBM) and using the theory of resonant transitions. A unique chirality assignment can be made for both metallic and semiconducting nanotubes of diameter d(t), using the parameters gamma(0) = 2.9 eV and omega(RBM) = 248/d(t). For example, the strong RBM intensity observed at 156 cm(-1) for 785 nm laser excitation is assigned to the (13,10) metallic chiral nanotube on a Si/SiO2 surface.

Structural (n,m) determination of isolated single wall carbon nanotubes by resonant Raman scattering

Electrosorptive desalination by carbon nanotubes and nanofibres electrodes and ion-exchange membranes.

The electron field emission performance of screen-printed graphene cathode was studied. High-yield graphene was prepared by a modified Hummers method and hydrazine hydrate reduction process, and screen printing technology was used to prepare the graphene field emission cathode. This cathode structure satisfies the requirements of both good electrical conductivity and a high surface field enhancement factor, leading to excellent and stable field emission properties with a low threshold field (~1.5 V µm−1). Our work introduced a simple and convenient method suitable for large scale on different substrates, paving the way for more applications of graphene films.

Electron field emission from screen-printed graphene films.

Electrosorption behavior of cations with carbon nanotubes and carbon nanofibres composite film electrodes

Electrosorption of anions with carbon nanotube and nanofibre composite film electrodes

The combinations of hollow MoS2 micro@nano-spheres were successfully fabricated through a one-step hydrothermal method. A possible growth mechanism was presented in detail based on time-dependent experimental facts. Besides, the photocatalytic activities of the samples were evaluated by monitoring the photodegradation of methylene blue (MB). The adsorption value of 150 mg g−1 shows a strong adsorption capability in the dark. After irradiation for only 30 min, the remaining MB in solution is about 9.7%. Moreover, the humidity sensing properties of the samples were measured for the first time. The results revealed high sensitivity at high RH, small humidity hysteresis, fast response and recovery times, and good stability. The greatest sensitivity is 32.19 nF/% RH and the maximum hysteresis is ∼6.3% RH. For humidity cycling of 17.2–89.5–17.2% RH, the response and recovery times are ∼140 s and ∼80 s, respectively. Capacitance fluctuations for one month are less than ±7% at various relative humidities (RHs).

Yiwei Chen

Papers

Electrosorptive desalination by carbon nanotubes and nanofibres electrodes and ion-exchange membranes.

Electron field emission from screen-printed graphene films.

Electrosorption behavior of cations with carbon nanotubes and carbon nanofibres composite film electrodes

Electrosorption of anions with carbon nanotube and nanofibre composite film electrodes

The combinations of hollow MoS2 micro@nano-spheres: one-step synthesis, excellent photocatalytic and humidity sensing properties