Low energy electron irradiation induced deep level defects in 6H-SiC: the implication for the microstructure of the deep levels E1/E2

N-type 6H-SiC samples irradiated with electrons having energies of E(e)=0.2, 0.3, 0.5, and 1.7 were studied by deep level transient technique. No deep level was detected at below 0.2 MeV irradiation energy while for E(e)>/=0.3 MeV, deep levels ED1, E(1)/E(2), and E(i) appeared. By considering the minimum energy required to displace the C atom or the Si atom in the SiC lattice, it is concluded that generation of the deep levels E(1)/E(2), as well as ED1 and E(i), involves the displacement of the C atom in the SiC lattice.     

Enhanced self-diffusion on Cu(111) by trace amounts of s: chemical-reaction-limited kinetics

We find that less than 0.01 monolayer of S can enhance surface self-diffusion on Cu(111) by several orders of magnitude. The measured dependence of two-dimensional island decay rates on S coverage (theta(S)) is consistent with the proposal that Cu3S3 clusters are responsible for the enhancement. Unexpectedly, the decay and ripening are diffusion limited with very low and very high theta(S) but not for intermediate theta(S). To explain this result we propose that surface mass transport in the intermediate region is limited by the rate of reaction to form Cu3S3 clusters on the terraces.     

Facile fabrication and characterization of hierarchically porous calcium carbonate microspheres

Higher-order porous calcite microspheres exhibiting high specific surface areas, unusual morphologies and textures were fabricated by a simple precipitation reaction of CaCO3 in the presence of PSMA as a crystal modifier.     

Absolute potassium cation affinities (PCAs) in the gas phase

The potassium cation affinities (PCAs) of 136 ligands (20 classes) in the gas phase were established by hybrid density functional theory calculations (B3-LYP with the 6-311+G(3df,2p) basis set). For these 136 ligands, 70 experimental values are available for comparison. Except for five specific PCA values-those of phenylalanine, cytosine, guanine, adenine (kinetic-method measurement), and Me(2)SO (by high-pressure mass spectrometric equilibrium measurement)-our theoretical estimates and the experimental affinities are in excellent agreement (mean absolute deviation (MAD) of 4.5 kJ mol(-1)). Comparisons with previously reported theoretical PCAs are also made. The effect of substituents on the modes of binding and the PCAs of unsubstituted parent ligands are discussed. Linear relations between Li+/Na+ and K+ affinities suggest that for the wide range of ligands studied here, the nature of binding between the cations and a given ligand is similar, and this allows the estimation of PCAs from known Li+ and/or Na+ affinities. Furthermore, empirical equations relating the PCAs of ligands with their dipole moments, polarizabilities (or molecular weights), and the number of binding sites were established. Such equations offer a simple method for estimating the PCAs of ligands not included in the present study.     

Lu8Te and Lu7Te. Novel substitutional derivatives of lutetium metal

Monocrystals of Lu8Te are synthesized by disproportionation of Lu7Te at 1000-1200 degrees C or by direct reaction of Lu plus Lu2Te3 at 1000 degrees C for 2 weeks. Lu7Te is produced by arc-melting of a suitable Lu-Lu2Te3 mixture, with good crystals being formed by subsequent annealing at 1300 degrees C. The structures of Lu8Te (P2m, Z = 1) and Lu7Te (Cmcm, Z = 4) exhibit simple AB... packing of distorted, not close-packed, layers along one short axis (, , respectively). Puckered Lu, Te layers are stacked normal to (010) or (001) in six- or eight-layer repeat sequences, with Te substituting for every third or every other Lu in every third or fourth layer, respectively. Strong Lu-Te bonding is indicated. Both Te substitutions decrease the volume per atom from that in hcp. Lu and also decrease the coordination number of all atoms from 12 to 9-11.     

A Novel Gelatin–Carbon Nanotubes Hybrid Hydrogel

This letter focuses on the first result of the preparation and the swelling behavior of a novel hybrid gelatin hydrogel with carbon nanotubes. A novel hybrid gelatin hydrogel with carbon nanotubes was synthesized by a physical mixing method. The structure of the novel hydrogel obtained was characterized by SEM. Besides, the swelling behavior of the synthesized hydrogel was measured at two different temperatures. The results indicate that carbon nanotubes added could maintain the stability of the hybrid hydrogel without cross‐linking at 37 °C. This suggests that the hybrid gelatin hydrogel with carbon nanotubes could be used in biomedical field. Besides, its application in protein separation is discussed.

SEM image of the gelatin‐MWNTs hybrid gel at 10 000 × magnification.