A Study of the Initial Adsorption Processes of Oxygen on the Ti(1010) Surface by TOF-Type Electron Stimulated Desorption

Author(s):  
K. Ueda ◽  
A. Takano
Holzforschung ◽  
2000 ◽  
Vol 54 (3) ◽  
pp. 321-326 ◽  
Author(s):  
Cao Jinzhen ◽  
Zhao Guangjie

Summary In order to make clear the molecular mechanism of the dielectric relaxation based on adsorbed water in wood cell wall during moisture changing process, the temperature and frequency spectrums of dielectric processes of Sikkim spruce (Picea spinulosa Griff.) were measured in three different adsorption processes. Three levels of relative humidity used were 40, 80 and 100 %, respectively, and the temperature was kept at 20°C. In oven-dry state, relaxation process I based on the reorientation of CH2OH groups in amorphous region of wood cell wall was observed. While in moist state, relaxation process II based on ionic conductivity and relaxation process III based on the additive reorientation of CH2OH groups and adsorbed water molecules occurred. Within higher humidity region, relaxation process IV concerned with adsorbed water in lignin was observed in the initial adsorption period, but it vanished with further adsorption.


2010 ◽  
Vol 17 (04) ◽  
pp. 397-403 ◽  
Author(s):  
HUI HE ◽  
YAN GUO ◽  
SHOUFU WANG ◽  
YAQING JIANG

The kinetics of formation of self-assembled monolayers on gold generated by the adsorption of 1-octanethiol and 1,8-octanedithiol were explored by electrochemistry measurement. The time dependence of capacitance and surface coverage supported that the adsorption of thiols typically processed with a two-step adsorption consisted of a fast initial adsorption and a slowly following reorganization. From the function of surface coverage versus time, one could get rate constants of adsorption of thiols, and the adsorption process was demonstrated to follow a diffusion-controlled Langmuir model. A comparison of the adsorption rates for different concentration between 1-octanethiol and 1,8-octanedithiol revealed that their adsorption processes were almost identical and independent on the concentration, inferring that only one sulfur atom contributed to the self-assembly of dithiol molecule.


Author(s):  
M. R. McCartney ◽  
J. K. Weiss ◽  
David J. Smith

It is well-known that electron-beam irradiation within the electron microscope can induce a variety of surface reactions. In the particular case of maximally-valent transition-metal oxides (TMO), which are susceptible to electron-stimulated desorption (ESD) of oxygen, it is apparent that the final reduced product depends, amongst other things, upon the ionicity of the original oxide, the energy and current density of the incident electrons, and the residual microscope vacuum. For example, when TMO are irradiated in a high-resolution electron microscope (HREM) at current densities of 5-50 A/cm2, epitaxial layers of the monoxide phase are found. In contrast, when these oxides are exposed to the extreme current density probe of an EM equipped with a field emission gun (FEG), the irradiated area has been reported to develop either holes or regions almost completely depleted of oxygen. ’ In this paper, we describe the responses of three TMO (WO3, V2O5 and TiO2) when irradiated by the focussed probe of a Philips 400ST FEG TEM, also equipped with a Gatan 666 Parallel Electron Energy Loss Spectrometer (P-EELS). The multi-channel analyzer of the spectrometer was modified to take advantage of the extremely rapid acquisition capabilities of the P-EELS to obtain time-resolved spectra of the oxides during the irradiation period. After irradiation, the specimens were immediately removed to a JEM-4000EX HREM for imaging of the damaged regions.


2013 ◽  
Vol 5 (3) ◽  
pp. 153-173 ◽  
Author(s):  
Georgina Laredo ◽  
Fernando Trejo-Zarraga ◽  
Federico Jimenez-Cruz ◽  
Jose Garcia-Gutierrez

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