Phénomènes de pulvérisation et de distribution en profondeur. Partie IV. Pulvérisation cathodique des oxydes Nb2O5, Ta2O5 et WO3

1970 ◽  
Vol 48 (2) ◽  
pp. 137-145 ◽  
Author(s):  
L. Q. Nghi ◽  
Roger Kelly

Three different methods have been used to determine the sputtering yield (S) for 2–30 keV Kr ions on the amorphous anodic oxides Nb2O5, Ta2O5, and WO3. The methods were based on (a) the change of interference colors due to ion bombardment, (b) the perforation of a film of free oxide by an intense ion beam, and (c) the loss of weight of the target. Although S for Kr–WO3 was larger than expected, S for Kr–Nb2O5 and Kr–Ta2O5 was similar to what has been found for other oxides. For example, at 4 keV, S lies between 1.1 and 2.4 atoms/ion for Ar or Kr bombardment of Al2O3, Nb2O5, SiO2, Ta2O5, TiO2, and UO2, whereas it is 6.2 atoms/ion for WO3. The results were interpreted first with a modified form of the theory of Rol et al., in which S is equated to K′E/Rm, where K′ is a constant in Å/keV and Rm is the experimental median range. A good fit between experiment and theory was obtained for K′ equal to 25 for Nb2O5, 13 for Ta2O5, and 51 for WO3. The recently formulated theory of Sigmund, which is in principle completely analytical, was also considered. The observed values of S could be made compatible with the predictions of the theory by taking the following values for Eb, the surface binding energy (units of kcal/gram atom): 100–150 for Nb2O5, 200–250 for Ta2O5, and 45–60 for WO3, We would point out that these latter values are similar to the heats of atomization.

2021 ◽  
Author(s):  
Yunchang Liang ◽  
Karla Banjac ◽  
Kévin Martin ◽  
Nicolas Zigon ◽  
Seunghwa Lee ◽  
...  

A sustainable future requires highly efficient energy conversion and storage processes, where electrocatalysis plays a crucial role. The activity of an electrocatalyst is governed by the binding energy towards the reaction intermediates, while the scaling relationships prevent the improvement of a catalytic system over its volcano-plot limits. To overcome these limitations, unconventional methods that are not fully determined by the surface binding energy can be helpful. Here, we use organic chiral molecules, i.e., hetero-helicenes, to boost the oxygen evolution reaction (OER) by ca. 131.5 % (at the potential of 1.65 V vs. RHE) at state-of-the-art 2D catalysts via a spin-polarization mechanism. Our results show that chiral molecule-functionalization is able to increase the OER activity of catalysts beyond the volcano limits. A guideline for optimizing the catalytic activity via chiral molecular functionalization of hybrid 2D electrodes is given.


2020 ◽  
Vol 8 (11) ◽  
pp. 5671-5678 ◽  
Author(s):  
Xinxin Zhao ◽  
Fengjiao Chen ◽  
Junqing Liu ◽  
Mingren Cheng ◽  
Hai Su ◽  
...  

A SnO2-coated carbon fiber mat is fabricated and used to guide uniform K nucleation/deposition for dendrite free K metal anodes.


2021 ◽  
Author(s):  
Yunchang Liang ◽  
Karla Banjac ◽  
Kévin Martin ◽  
Nicolas Zigon ◽  
Seunghwa Lee ◽  
...  

Abstract A sustainable future requires highly efficient energy conversion and storage processes, where electrocatalysis plays a crucial role. The activity of an electrocatalyst is governed by the binding energy towards the reaction intermediates, while the scaling relationships prevent the improvement of a catalytic system over its volcano-plot limits. To overcome these limitations, unconventional methods that are not fully determined by the surface binding energy can be helpful. Here, we use organic chiral molecules, i.e., hetero-helicenes, to boost the oxygen evolution reaction (OER) by ca. 131.5% (at the potential of 1.65 V vs. RHE) at state-of-the-art 2D catalysts via a spin-polarization mechanism. Our results show that chiral molecule-functionalization is able to increase the OER activity of catalysts beyond the volcano limits. A guideline for optimizing the catalytic activity via chiral molecular functionalization of hybrid 2D electrodes is given.


2019 ◽  
Vol 1299 ◽  
pp. 012022 ◽  
Author(s):  
Akinwumi Akinpelu ◽  
Oluwole E. Oyewande ◽  
Adaeze ◽  
Arijaje T. Emuobor ◽  
C Olawole ◽  
...  

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