Evaluation of surface hydrogen desorption from Si–H terminated Si(100) surfaces by thermal desorption spectroscopy

1998 ◽  
Vol 135 (1-4) ◽  
pp. 254-258 ◽  
Author(s):  
F Hirose ◽  
H Sakamoto
Keyword(s):  
Thermal Desorption ◽  
Thermal Desorption Spectroscopy ◽  
Hydrogen Desorption ◽  
Surface Hydrogen

The Role of Cr in H Desorption Kinetics in Rapidly Solidified Al

2014 ◽  
Vol 783-786 ◽  
pp. 264-269 ◽  
Author(s):  
Iya I. Tashlykova-Bushkevich ◽  
Keitaro Horikawa ◽  
Goroh Itoh
Keyword(s):  
High Temperature ◽  
Thermal Desorption ◽  
High Purity ◽  
Thermal Desorption Spectroscopy ◽  
Secondary Phase ◽  
Hydrogen Desorption ◽  
Oxide Surface ◽  
Desorption Kinetics ◽  
Hydrogen Trapping ◽  
Rapidly Solidified

Hydrogen desorption kinetics for rapidly solidified high purity Al and Al-Cr alloy foils containing 1.0, 1.5 and 3.0 at % Cr were investigated by means of thermal desorption analysis (TDA) at a heating rate of 3.3°C/min. For the first time, it was found that oxide inclusions of Al2O3 are dominant high-temperature hydrogen traps compared with pores and secondary phase precipitates resulted in rapid solidification of Al and its alloys. The correspondent high-temperature evolution rate peak was identified to be positioned at 600°C for high purity Al and shifted to 630°C for Al-Cr alloys. Amount of hydrogen trapped by dislocations increases in the alloys depending on Cr content. Microstructural hydrogen trapping behaviour in low-and intermediate temperature regions observed here was in coincidence with previous data obtained for RS materials using thermal desorption spectroscopy (TDS). The present results on hydrogen thermal desorption evolution indicate that the effect of oxide surface layers becomes remarkable in TDA measurements and show advantages in combinations of both desorption analysis methods to investigate hydrogen desorption kinetics in materials.

scholarly journals Crystal structure change in multilayer GeH flakes by hydrogen desorption under ultrahigh vacuum environments

2021 ◽  
Author(s):  
Mai Itoh ◽  
Masaaki ARAIDAI ◽  
Akio OHTA ◽  
Osamu Nakatsuka ◽  
Masashi Kurosawa
Keyword(s):  
Crystal Structure ◽  
Mass Loss ◽  
Thermal Desorption ◽  
Ultrahigh Vacuum ◽  
Thermal Desorption Spectroscopy ◽  
Hydrogen Desorption ◽  
Structure Change ◽  
Spectroscopy Analysis ◽  
Free Standing ◽  
Short Time

Abstract To confirm the feasibility of the theoretically proposed method of forming free-standing germanene [Araidai et al., J. Appl. Phys. 128, 125301 (2020).], we have experimentally investigated hydrogen desorption properties from the hydrogen-terminated germanane (GeH) flakes. Thermal desorption spectroscopy analysis revealed that hydrogen desorption occurred during the heating under an ultrahigh vacuum environment, corresponding to mass loss of 1.0 wt%. Moreover, we have found that using an ultrahigh vacuum ambient and short-time annealing for hydrogen desorption is a key to sustain the crystal structures.

On the Methodology of Thermal Desorption Spectroscopy to Evaluate Hydrogen Embrittlement

2012 ◽  
Vol 706-709 ◽  
pp. 2354-2359 ◽  
Author(s):  
Diana Pérez Escobar ◽  
Kim Verbeken ◽  
Lode Duprez ◽  
Marc Verhaege
Keyword(s):  
Hydrogen Embrittlement ◽  
Thermal Desorption ◽  
Surface Preparation ◽  
Thermal Desorption Spectroscopy ◽  
Sample Surface ◽  
Hydrogen Desorption ◽  
Sample Geometry ◽  
Metal Interactions ◽  
Charging Time ◽  
The Impact

Thermal desorption spectroscopy (TDS) is a very important tool in hydrogen embrittlement (HE) related research and has been applied on many different materials over the last decades in order to improve knowledge on the HE phenomenon. TDS provides the opportunity to distinguish between different types of hydrogen traps based on the analysis of a spectrum with different peak temperatures each corresponding to hydrogen desorption from a specific trap. These peak temperatures, and consequently the different traps in a material, arise from the various microstructural characteristics of the material. However, TDS results are also influenced by many other parameters, such as the sample surface preparation, the electrolytes used for hydrogen charging, sample geometry, charging time, current density, charging temperature. Even though the use of thermal desorption to evaluate hydrogen-metal interactions has increased over the past years, a careful evaluation of the effect of these other parameters was not yet performed. In this work, the impact of some of the above mentioned parameters was studied. It was demonstrated that the sample geometry, the surface roughness, and the initial total pressure of the TDS chamber influenced significantly the obtained TDS spectrum.

Hydrogen Degradation Property of Electrochemically Charged Aluminum

2007 ◽  
Vol 1042 ◽  
Author(s):  
Hiroshi Suzuki ◽  
Daisuke Kobayashi ◽  
Kenichi Takai ◽  
Yukito Hagihara
Keyword(s):  
Aqueous Solution ◽  
Thermal Desorption ◽  
Hydrogen Molecule ◽  
Thermal Desorption Spectroscopy ◽  
Hydrogen Desorption ◽  
The Other ◽  
Hydrogen Degradation ◽  
Hydrogen Recombination ◽  
Free Hydrogen ◽  
Two Peaks

AbstractDegradation property of aluminum due to hydrogen is studied. Hydrogen is introduced by electrolysis charge in aqueous solution with addition of 0.1 mass % NH4SCN as a hydrogen recombination poison. The amount of hydrogen and its existing state in the material is analyzed by hydrogen desorption curves measured by the thermal desorption spectroscopy. The hydrogen desorption curves of charged aluminum showed two peaks, one at less than 100 °C and the other around 400 °C. The existing state of hydrogen relate to each peaks are identified as weakly trapped solute hydrogen to vacancy and free hydrogen molecule located in cavities that exists in the bulk of the material. Tensile properties are obtained to determine degradation property of the material due to hydrogen. The effect of hydrogen on degradation of charged aluminum is analyzed in terms of interaction between hydrogen and vacancy or dislocation. Solute hydrogen and cavities are found to affect ductility of aluminum, whereas hydrogen molecule in cavities has no effect.

Kinetics of subsurface hydrogen adsorbed on niobium: Thermal desorption studies

2002 ◽  
Vol 17 (10) ◽  
pp. 2698-2704 ◽  
Author(s):  
A. L. Cabrera ◽  
J. Espinosa-Gangas ◽  
Johan Jonsson-Akerman ◽  
Ivan K. Schuller
Keyword(s):  
Heat Treatment ◽  
Carbon Monoxide ◽  
Thermal Desorption ◽  
Hydrogen Adsorption ◽  
Thermal Desorption Spectroscopy ◽  
Hydrogen Desorption ◽  
X Ray Diffraction ◽  
Surface Sites ◽  
Adsorption Desorption ◽  
Kinetics Of

The adsorption/absorption of hydrogen and the adsorption of carbon monoxide by niobium foils, at room temperature, was studied using thermal desorption spectroscopy. Two hydrogen desorption peaks were observed with a maximum at 404 and 471 K. The first hydrogen desorption peak is regarded as hydrogen desorbing from surface sites while the second peak, which represents desorption from surface sites stronger bound to the surface, also has a component—due to its tailing to higher temperatures—of hydrogen diffusing from subsurface sites. Carbon monoxide adsorption was used to determine the number of surface sites, since it does not penetrate below the surface. Two carbon monoxide desorption peaks are observed in these experiments: at 425 and 608 K. The first peak is regarded as the adsorption of molecular carbon monoxide, and the second, as carbon monoxide dissociated on the niobium surface. The crystallographic orientation of the foils was determined by x-ray diffraction and showed a preferential (110) orientation of the untreated foil due to the effect of cold rolling. This preferential orientation decreased after hydrogen/heat treatment, appearing strong also in the (200) and (211) orientations. This change in texture of the foils is mainly due to the effect of heat treatment and not to hydrogen adsorption/desorption cycling. The kinetics of hydrogen and CO desorption is compared with that of Pd and Pd alloys.

The Kinetics of Hydrogen Desorption From Zirconium Hydride

2013 ◽  
Author(s):  
Mingwang Ma ◽  
Ruiyun Wan ◽  
Yuan Wang ◽  
Yanlin Cheng ◽  
Li Liang ◽  
...  
Keyword(s):  
Thermal Desorption ◽  
Thermal Desorption Spectroscopy ◽  
Hydrogen Desorption ◽  
Pressure Effects ◽  
Zirconium Hydride ◽  
Desorption Kinetics ◽  
Desorption Process ◽  
Exponential Factor ◽  
Predict Weight Loss ◽  
Kinetics Of

Thermal desorption spectroscopy (TDS) was used to study the thermal desorption kinetics of zirconium hydride films, which were deposited on molybdenum substrates and thermally charged with gas phase hydrogen. The observed desorption peaks were attributed to phase transforming steps. The activation energy and pre-exponential factor for desorption kinetics was estimated as 116 kJ/mol and 8762 s−1 according to Kissinger relation, respectively. A simulation of TDS spectra was made, which showed that the desorption process followed a first order kinetics. The kinetic parameters were then utilized to predict weight loss behavior at a temperature profile. Pressure effects that can potentially reduce the desorption rate were discussed.

scholarly journals Investigation of the Pressure Dependent Hydrogen Solubility in a Martensitic Stainless Steel Using a Thermal Agile Tubular Autoclave and Thermal Desorption Spectroscopy

Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 231
Author(s):  
Patrick Fayek ◽  
Sebastian Esser ◽  
Vanessa Quiroz ◽  
Chong Dae Kim
Keyword(s):  
Stainless Steel ◽  
Thermal Desorption ◽  
Hydrogen Diffusion ◽  
Martensitic Stainless Steel ◽  
Thermal Desorption Spectroscopy ◽  
Hydrogen Uptake ◽  
Hydrogen Solubility ◽  
Automotive Components ◽  
Set Up ◽  
Service Application

Hydrogen is nowadays in focus as an energy carrier that is locally emission free. Especially in combination with fuel-cells, hydrogen offers the possibility of a CO2 neutral mobility, provided that the hydrogen is produced with renewable energy. Structural parts of automotive components are often made of steel, but unfortunately they may show degradation of the mechanical properties when in contact with hydrogen. Under certain service conditions, hydrogen uptake into the applied material can occur. To ensure a safe operation of automotive components, it is therefore necessary to investigate the time, temperature and pressure dependent hydrogen uptake of certain steels, e.g., to deduct suitable testing concepts that also consider a long term service application. To investigate the material dependent hydrogen uptake, a tubular autoclave was set-up. The underlying paper describes the set-up of this autoclave that can be pressurised up to 20 MPa at room temperature and can be heated up to a temperature of 250 °C, due to an externally applied heating sleeve. The second focus of the paper is the investigation of the pressure dependent hydrogen solubility of the martensitic stainless steel 1.4418. The autoclave offers a very fast insertion and exertion of samples and therefore has significant advantages compared to commonly larger autoclaves. Results of hydrogen charging experiments are presented, that were conducted on the Nickel-martensitic stainless steel 1.4418. Cylindrical samples 3 mm in diameter and 10 mm in length were hydrogen charged within the autoclave and subsequently measured using thermal desorption spectroscopy (TDS). The results show how hydrogen sorption curves can be effectively collected to investigate its dependence on time, temperature and hydrogen pressure, thus enabling, e.g., the deduction of hydrogen diffusion coefficients and hydrogen pre-charging concepts for material testing.

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