Self-assembled monolayers of benzylmercaptan and p-cyanobenzylmercaptan on Au(111) surfaces: structural and spectroscopic characterization

The formation of self-assembled monolayers of benzylmercaptan (BM) and p-cyanobenzylmercaptan (pCBM) on Au(111) surfaces is investigated by a combination of X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS), and scanning tunneling microscopy (STM). The NEXAFS results of pCBM are supported by ab initio calculations. It is found that BM as well as pCBM form well-ordered monolayers with the molecules oriented almost perpendicular to the surface. BM forms a ( radical 3 x radical 3)R30 degrees structure whereas pCBM forms a slightly different c(7 x 7) hexagonal structure. No phase separation is detected for the adsorption of a 1:1 mixture of the two molecules. The implications of the results for the covalent attachment of transition-metal complexes to thiol-functionalized surfaces are discussed.     

Use of Enzymatic Digestion and Chemical Methylation Followed by Matrix-assisted Laser Desorption/Ionisation (MALDI) Mass Spectrometry to Sequence a 60kDa Commercial Fraction of Cellulose Acetate

Cellulose acetate was characterized by using enzyme in both digestion and chemical derivation and acetolysis. The fragments were normalised and compared on an anhydroglucose scale, using mass spectrometry to identify the different sized fragments. It was determined that at least two sub-populations for cellulose acetate existed within the parent. The macroscopic effect of this variation in the degree of acetylation will be a modification of the structural properties of the polymer chains. It was found that through comparison with enzyme-based degradation, an estimation of the acetylation topography of the cellulose acetate fraction could be made. Enzyme degradation produced a number of oligosaccharides of more than 10 glucose units, presumably resistant to enzyme degradation because they contained acetate groups. Chemical hydrolysis gave a random ladder of short sequences of mainly 3–4 glucose units some of which had a high methyl ether content, that were analysed by mass and converted to an anhydroglucose mass scale. This approach could be used to demonstrate differences between large biopolymers of cellulose acetate that previously gave an overall average rather than a specific ladder average.     

Manganese-doped zinc sulfide binary nanostructures as binder-free electrode materials for supercapattery

Journal of Solid State Electrochemistry - Binary metal sulfide–based electrode materials with distinct nanoarchitecture, improved conductivities, and fascinating mechanical stabilities are...     

Nonlinear absorption properties correlated with the surface and structural changes of ultra short pulse laser irradiated CR-39

We have investigated femtosecond laser irradiation effects on the surface topography, structural changes and nonlinear absorption properties of CR-39. For this purpose, a CR-39 target was exposed in air to 25 fs, 800 nm Ti: sapphire laser radiation at fluences ranging from 0.25 J cm⁻² to 3.6 J cm⁻². The surface of irradiated CR-39 probed by an Atomic Force Microscope (AFM) exhibits the formation of several topographical structures, like bumps, explosions and nano cavities. Raman spectroscopy is performed to explore chemical and structural modification of the irradiated target. The spectroscopy reveals changes such as cross linking, bond breaking, formation of new bonds etc. in the fundamental structure of the polymer after irradiation. In order to establish a correlation between morphological and structural changes with the changes in the nonlinear absorption of the irradiated CR-39, a Z-scan technique was employed. A comparison of experimentally obtained data from Z-scan measurements with our calculations predicts the dominance of three-photon absorption in the case of pristine CR-39, whereas for irradiated targets concurrence of three- and two-photon absorption is probable. Nonlinear absorption increases with increasing laser fluences and is well correlated by surface and structural changes revealed by AFM and Raman spectroscopy.     

Crystal structures of bis(cyanido)bis(N,N′-diethylthiourea-κS) mercury(II) and bis(cyanido)bis(N,N′-dipropylthiourea-κS) mercury(II)

Two mercury(II) complexes containing cyanide and, N,N′-diethylthiourea (detu) and N,N′-dipropylthiourea (dprtu) ligands, [(detu)₂Hg(CN)₂] (1) and [(dprtu)₂Hg(CN)₂] (2), respectively, have been prepared and characterized by X-ray crystallography. In the both complexes Hg atom lies on a 2-fold rotation axis, and is coordinated to the sulfur atoms of two thiourea ligands and to two cyanide carbon atoms. Both have a distorted tetrahedral environment with bond angles about the Hg atoms in the range of 93.41(4)°–146.75(19)°. In the crystal structures symmetry related molecules are linked via N-H-N hydrogen bonds resulting in the formation of a two-dimensional network in 1, while in 2 a double stranded one-dimensional chain is formed.     

Necessary and sufficient conditions for oscillation of second‐order dynamic equations on time scales

In this paper, we establish necessary and sufficient conditions for oscillation of second‐order strongly superlinear and strongly sublinear dynamic equations. Our results unify and improve many known results in the literature.     

Instability criteria for impulsive hybrid state dependent delay integrodifferential systems

In this paper, we present the sufficient conditions ensuring the instability of the zero solution of an impulsive state dependent delay integrodifferential system for different conditions on the delay function. We assume the instability of the associated linear impulsive system and apply the idea of dichotomies together with Schauder–Tychonoff theorem to establish the sufficient conditions for the unstable solution of the problem.     

Identification of ultra-fast electronic and thermal processes during femtosecond laser ablation of Si

Ultra-fast electronic and thermal processes for the energy deposition mechanism during femtosecond laser ablation of Si have been identified by means of atomic force microscopy and Raman scattering techniques. For this purpose, Si targets were exposed with 800-nm, 25-fs Ti:sapphire laser pulses for different laser fluencies in air and under UHV (ultra high vacuum) conditions. Various nano- and microstructures on the surface of the irradiated samples are revealed by a detailed surface topography analysis. Ultra-fast electronic processes are dominant in the lower-fluence regime. Therefore, by starting from the ablation threshold three different fluence regimes have been chosen: a lower-fluence regime (0.06–0.5 J?cm^?2 single-shot irradiation under UHV condition and 0.25–2.5 J?cm^?2 single-shot irradiation in ambient condition), a moderate-fluence regime (0.25–1.5 J?cm^?2 multiple-shot irradiation), and a higher-fluence regime (2.5–3.5 J?cm^?2 multiple-shot irradiation). Around the ablation threshold fluence, most significant features identified at the Si surface are nanohillock-like structures. The appearance of these nanohillocks is regarded as typical features for fast electronic processes (correlated with existence of hot electrons) and is explained on the basis of Coulomb explosion. The growth of these typical features (nanohillocks) by femtosecond laser irradiation is an element of novelty. At moderate irradiation fluence, a ring-shaped ablation with larger bumps and periodic surface structures is observed and is considered as a footprint of ultra-fast melting. Further increase in the laser fluence, i.e. a higher-fluence regime, resulted in strong enhancement of the thermal process with the appearance of larger islands. The change in surface topography provides an innovative clue to differentiate between ultra-fast electronic processes, i.e. Coulomb explosion (sub-100 fs) at a lower-fluence regime and ultra-fast melting (hundreds of fs) at a moderate-fluence regime, and slow thermal processes (ps time scale) at a higher-fluence regime. These fast electronic and thermal processes are well correlated to structural and crystallographic alterations, inferred from Raman spectroscopy.