Photoelectron spectroscopy study of Pb/Ag(1 1 1) in the submonolayer range

The vacuum deposition of Pb onto Ag(1 1 1) gives rise to two different surface structures depending on coverage and deposition temperature. At room temperature (RT), low energy electron diffraction (LEED) reveals a sharp reconstruction completed at 1/3 Pb monolayer (ML). Beyond, a close-packed Pb(1 1 1) incommensurate overlayer develops. At low temperature (LT, ∼100 K) the incommensurate structure is directly observed whatever the coverage, corresponding to the growth of close-packed two-dimensional Pb(1 1 1) islands. Synchrotron radiation Pb 5d core-level spectra clearly demonstrate that in each surface structure all Pb atoms have essentially a unique, but different, environment. This reflects the surface alloy formation between the two immiscible metals in the reconstruction and a clear signature of the de-alloying process at RT beyond 1/3 ML coverage.     

InAs单层和亚单层结构中的自旋动力学研究

利用偏振时间分辨光谱和时间分辨Kerr旋转谱，研究了GaAs中的InAs单层和亚单层的电子自旋动力学.实验发现，在非共振激发条件下，厚度为1/3单层的InAs亚单层中电子自旋弛豫寿命长达3.4ns，而1个单层厚的InAs层的电子自旋寿命只有0.48ns；而在共振激发条件下，亚单层结构中的电子自旋寿命大大减少，只有70ps，单层InAs中电子自旋寿命没有显著变化.分析表明，低温下InAs单层和亚单层结构中，Bir-Aronov-Pikus(BAP)自旋弛豫机理占主导地位.通过改变材料结构特性和激发条件来改变电子空穴的空间相关性，从而达到控制自旋弛豫的目的. 关键词： InAs亚单层 自旋弛豫 BAP机理     

Photoelectron spectroscopy of azulenes

The photoelectron spectra of azulene and ten of its derivatives (halo-, methyl-, phenyl-, acetyl- and benzoylazulenes) are presented and assigned. Assignments based on a composite-molecule view are validated by computations (CNDO/S). Conjugative interactions in the phenylazulenes lead to an inversion of the usual order of the two phenyl group e_1g component orbitals. Many of the azulenes have very low ionization energies, and it is suggested that they constitute a class of excellent π-electron donor molecules.     

Photoelectron spectroscopy of phosphites and phosphates

The ultraviolet photoelectron spectra (UPS) of trimethyl and triethyl phosphite, trimethyl and triethyl phosphate and four substituted phosphates are presented. Assignments are based on analogies to the UPS of phosphorus trichloride and phosphoryl trichloride and are substantiated by CNDO/2 computations. The mechanism of PO (axial) bond formation is discussed.     

A study of nitric oxide adsorbed on nickel oxide,cobalt oxide,and graphite by X-ray photoelectron spectroscopy

The nitrogen 1s binding energy of nitric oxide adsorbed on nickel oxide, cobalt oxide and graphite was measured at several temperatures by X-ray photoelectron spectroscopy. For the oxides, a temperature dependent range of binding energies was observed, but for graphite the nitrogen 1s binding energy was independent of temperature. The values obtained suggest that significant back donation of electrons occurs from the oxides to the adsorbed nitric oxides, but no back donation occurs from graphite to adsorbed nitric oxide. However, adsorption did not cause changes in the binding energy of substrate core electrons. It is believed that unless the mean free path of electrons is short, the total photoelectron signal will not reveal changes in binding energy of electrons from substrate atoms at the surface.     

Synthesis of zinc oxide nanostructures catalytically active in the optical range without irradiation

A technique for synthesizing catalytically active zinc oxide-based nanostructures is described. The synthesis product represents a blue-gray powder. When it is introduced into a water solution of methyl orange the latter bleaches out both under daylight and in the dark. The activity of the material is measured by the Kubelka-Munk formula in the wavelength range 0.3–1.8 μm. As follows from X-ray phase analysis data, the synthesized material is a composite consisting of hexagonal structures with the parameters ZnO [a: 3.2491, c: 5.2046] and Zn [a: 2.6639, c: 4.9397]. A mechanism underlying the formation of a ZnO-Zn nanocomposite is suggested.     

Complex impedance spectroscopy of Mn-doped zinc oxide nanorod films

The frequency-dependent properties of Mn-doped (3-5 at.%) aligned zinc oxide (Mn-ZnO) nanorods, synthesized by hybrid wet chemical route onto glass substrates, were investigated by bias-dependent impedance spectroscopy. No peak of Mn cluster/secondary phases was detected in the X-ray diffraction traces of the samples. XPS studies show the presence of oxygen vacancies in Mn-ZnO nanorods and Mn in Mn²⁺ and Mn⁴⁺ charge states. Although X-ray diffraction/X-ray photoelectron spectroscopy does not give any indication of the presence of metal clusters in the samples, bias-dependent impedance spectroscopy demonstrates significant sensitivity to the formation of Mn clusters in Mn-ZnO nanorods.     

Photoelectron spectroscopy of 9,10-dihaloanthracenes

The photoelectron spectra of anthracene and its 9,10-dichloro- and dibromo-derivatives have been obtained. Analysis of the spectra is based mainly on the shifts in the anthracene molecular orbital ionization energies observed upon substitution. These shifts are interpreted on the basis of a perturbation model comprising short-range and long-range inductive terms and a mesomeric term. The electronic perturbation caused by the halogen atom is observed to depend largely on the unperturbed energy of the halogen np electrons and the charge distribution in the anthracene molecular orbitals. It has been possible to separate out Coulombic interactions and mesomeric interactions which depend on the energy gap between hydrocarbon and substituent orbitals. Although the observations are not conclusive, owing to the fact that only two orbitals have measurable mesomeric shifts, results indicate that α_Cl′, the Coulombic perturbation parameter, may well be negative, in contrast to previous work.     

Evidence from photoelectron spectroscopy for dissociative adsorption of oxygen on nickel oxide

XPS and UPS spectra from oxygen adsorption at high temperature on polycrystalline nickel oxide surfaces pre-heated at 700°C and 1450°C are presented. Adsorption results in complete loss of surface charge on both surfaces. There is an increase in intensity of the 0(1s) 529.7 eV peak, attributed to O^2? ions, and the $\text{Ni}\text{(2p}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{)}$ spectra show a shift of intensity to the 854.6 eV peak due to Ni²⁺ ions. The results are compared with previous data from kinetic, conductivity and electrochemical measurements. Agreement with a model of O^2? and nickel vacancy production is demonstrated. UPS spectra indicate considerable reorganisation of electronic charge in the surface of the 1450°C pre-heated oxide, after oxygen adsorption, giving an almost stoichiometric surface similar to that of a cleaved single crystal.     

Effect of doping with nickel ions on the structural state of a zinc oxide crystal

The fine structure of a hexagonal zinc oxide crystal doped with nickel ions of the composition Zn_{1 − x} Ni _x O has been studied using neutron diffraction and magnetic measurements. It is established that even at very low doping levels (x = 0.0004), the crystal undergoes local distortions in basal planes of the initial hexagonal lattice. The local distortions are assumed to be sources of the formation of ferromagnetism in compounds of this class.     

Incorporation of nano zinc oxide for improvement of electroless nickel plating

The advantages of electroless nickel plating (EN) include excellent corrosion resistance, wear resistance, solderability, low porosity and uniform thickness even on complex parts and ability to plate on nonconductors. In the present study nano ZnO particles were synthesized by using an electrochemical technique and incorporated the particles into Ni-P plates. An alkaline bath was selected and used for nano zinc oxide incorporation. The electrochemical and metallurgical properties of the Ni-nano ZnO-P plates were evaluated and compared with that of the un-reinforced Ni-P plates. The incorporation of the nano ZnO particles resulted in improvement of metallurgical and corrosion resistance characteristics of the plates.     

Photovoltaic cells based on nickel phthalocyanine and zinc oxide formed by atomic layer deposition

The introduction of an ultrathin zinc oxide (ZnO) layer formed by the atomic layer deposition (ALD) technique was found to improve the operation parameters of nickel phthalocyanine (NiPc) based photovoltaic cells with a transparent bottom electrode, indium tin oxide (ITO). This improvement is attributed to several reasons, such as I) increase of photovoltaic yield in ITO/p-NiPc/n-ZnO/Al cells incorporating a hybrid heterojunction as compared to single-layer ITO/NiPc/Al cells, II) enhancement of the overall spectral response in the double-layer cells and III) extension of long-term operational stability.     

Photoelectron spectroscopy of some biological molecules

The ultraviolet photoelectron spectra (UPS) of the following biologically-active compounds are reported and/or assigned: 2,4-dinitrophenol, nicotinic acid, nicotinamide, barbituric acid, xanthine, hypoxanthine, uric acid, uracil, thymine, cytosine, adenine, guanine, β-carotene, menadione, purine and pyrimidine. The importance of UPS data is exemplified in two ways: First, by investigating the validity of the Pullman k-index approach ¹⁴ to ionization energies; and, second, by generating an experimental scale of electron-donating ability.     

Photoelectron spectroscopy of doped helium nanodroplets

The photoionization dynamics of aniline doped helium droplets has been investigated by photoelectron spectroscopy. The photoelectron spectra resemble closely that of gas phase aniline, except for a droplet-size-dependent shift. This shift is caused by lowering of the ionization threshold upon solvation and can be readily estimated. The individual peaks in the photoelectron spectrum are broadened towards lower kinetic energy which is attributed to the relaxation of the photoelectrons as they pass through the helium droplet.     

Empirical formula for work function changes during deposition in the submonolayer range

It has been shown that Δφ−θ curves observed for several systems can be described within a wide range of temperatures and coverages with a simple formula. The formula enables the attainment of the minimum which frequently appears in the experimental curve.     

Analysis of protective oxide films on copper—nickel alloys by photoelectron spectroscopy

Photoelectron spectroscopy was used to determine the elemental composition of thin films formed on 70:30 cupronickel exposed to sodium chloride solutions at different impressed electrochemical potentials. At anodic potentials below the passivation potential, ?0.350 V versus SCE under the experimental conditions, either no film or a film containing copper and nickel in the same ratio as the alloy existed on the alloy. At the passivation potential the spectrum of the passive film indicated primarily nickel oxide and was very similar to the spectrum obtained from a pure nickel specimen passivated in the same environment.     

Impedance spectroscopy study of zinc oxide incorporated iron borate glass-ceramic

Here, the effects of zinc oxide (ZnO) on impedance and dielectric properties of the ZnO incorporated iron borate (Fe₃BO₆) glass-ceramics were studied using impedance spectroscopy in a wide range of frequency (1 Hz – 1 MHz) and temperature (25 °C–250 °C). With ZnO addition, the ε′ and tanδ values were reduced significantly, the strength of the relaxation process also decreased, along with a decrease in conductivity. Activation energies associated with modulus and conductivity plots suggest that similar type of charge carriers was responsible for the relaxation and conduction processes. The analysis of both complex impedance and conductivity show the negative temperature coefficient of resistance (NTCR) behavior of the samples. The thermistor constant B-values of 5ZnO and 10ZnO were found to be 7223 and 7088 respectively. The study of the NTCR properties suggests a potential candidate for thermistor applications.     

Electronic response in mesoscopically disordered zinc oxide probed by terahertz spectroscopy

Terahertz spectroscopy is applied for characterizing the high frequency transport of electrons in polycrystalline ZnO films deposited by spray pyrolysis. Electromodulation of the charge carrier density provides the frequency dependent conductivity of the electron gas. Amplitude and phase of the high frequency response are well reproduced by the Drude–Smith model.     

Surface state spectroscopy on zinc oxide crystals by means of modulated photoconductivity measurements

The spectral distribution of photoconductivity for photon energies between 0.2 and 2.5 eV was measured on ZnO crystals at low temperatures in ultrahigh vacuum (UHV). The prism surfaces (∥c axis) were cleaned by heating whereas the polar surfaces (⊥c axis) were prepared by cleavage in UHV. The spectra obtained on the three types of ZnO surfaces are different. Exposure to oxygen and to atomic hydrogen influences the absolute amount of photoconductivity. Therefore, an excitation from surface states is concluded and transition energies are derived.