scholarly journals Formation of stable Si–O–C submonolayers on hydrogen-terminated silicon(111) under low-temperature conditions

2015 ◽  
Vol 6 ◽  
pp. 19-26 ◽  
Author(s):  
Yit Lung Khung ◽  
Siti Hawa Ngalim ◽  
Andrea Scaccabarozzi ◽  
Dario Narducci

In this letter, we report results of a hydrosilylation carried out on bifunctional molecules by using two different approaches, namely through thermal treatment and photochemical treatment through UV irradiation. Previously, our group also demonstrated that in a mixed alkyne/alcohol solution, surface coupling is biased towards the formation of Si–O–C linkages instead of Si–C linkages, thus indirectly supporting the kinetic model of hydrogen abstraction from the Si–H surface (Khung, Y. L. et al. Chem. – Eur. J. 2014, 20, 15151–15158). To further examine the probability of this kinetic model we compare the results from reactions with bifunctional alkynes carried out under thermal treatment (<130 °C) and under UV irradiation, respectively. X-ray photoelectron spectroscopy and contact angle measurements showed that under thermal conditions, the Si–H surface predominately reacts to form Si–O–C bonds from ethynylbenzyl alcohol solution while the UV photochemical route ensures that the alcohol-based alkyne may also form Si–C bonds, thus producing a monolayer of mixed linkages. The results suggested the importance of surface radicals as well as the type of terminal group as being essential towards directing the nature of surface linkage.

Author(s):  
Irwing M. Ramírez-Sánchez ◽  
Erick R. Bandala

Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (&bull;OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide&reg; TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.


Molecules ◽  
2021 ◽  
Vol 26 (20) ◽  
pp. 6166
Author(s):  
Serge Ismael Zida ◽  
Yue-Der Lin ◽  
Yit Lung Khung

While the sonochemical grafting of molecules on silicon hydride surface to form stable Si–C bond via hydrosilylation has been previously described, the susceptibility towards nucleophilic functional groups during the sonochemical reaction process remains unclear. In this work, a competitive study between a well-established thermal reaction and sonochemical reaction of nucleophilic molecules (cyclopropylamine and 3-Butyn-1-ol) was performed on p-type silicon hydride (111) surfaces. The nature of surface grafting from these reactions was examined through contact angle measurements, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Cyclopropylamine, being a sensitive radical clock, did not experience any ring-opening events. This suggested that either the Si–H may not have undergone homolysis as reported previously under sonochemical reaction or that the interaction to the surface hydride via a lone-pair electron coordination bond was reversible during the process. On the other hand, silicon back-bond breakage and subsequent surface roughening were observed for 3-Butyn-1-ol at high-temperature grafting (≈150 °C). Interestingly, the sonochemical reaction did not produce appreciable topographical changes to surfaces at the nano scale and the further XPS analysis may suggest Si–C formation. This indicated that while a sonochemical reaction may be indifferent towards nucleophilic groups, the surface was more reactive towards unsaturated carbons. To the best of the author’s knowledge, this is the first attempt at elucidating the underlying reactivity mechanisms of nucleophilic groups and unsaturated carbon bonds during sonochemical reaction of silicon hydride surfaces.


2008 ◽  
Vol 55 ◽  
pp. 56-61
Author(s):  
L. Minati ◽  
Giorgio Speranza ◽  
Yoann Jestin ◽  
Cristina Armellini ◽  
Andrea Chiappini ◽  
...  

Two series of xHfO2 - (100-x) SiO2 (x=10, 20, 30 mol%) glass-ceramics planar waveguides doped with 0.3 mol% Er3+ ions were prepared by the sol-gel route. A thermal treatment at 1000°C was applied to the second series of samples to nucleate HfO2 crystals. The waveguides were analyzed by X-ray photoelectron spectroscopy to study the effect of the Hf concentration and of the annealing on the material structure. XPS shows that in the first series of samples a Hf concentration threshold exists. Above this threshold the material undergoes a spinodal decomposition with formation of HfO2 rich domains. In the second series of samples the presence of thermal treatment lowers the concentration threshold so that the phase separation occurs also at a Hf concentration of 10%mol. In the waveguides where spinodal decomposition in present, the emission spectra from the Er3+ ions reveal a sensible narrowing of the 4I13/2 → 4I15/2 line. This demonstrates the presence of a crystalline environment for the Er3+ ions since the inhomogeneous broadening due to the disordered glassy network is suppressed. These results may have important implications for the fabrication of photonic devices with increased efficiency.


Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2139 ◽  
Author(s):  
Chukwuka Bethel Anucha ◽  
Ilknur Altin ◽  
Zekeriya Biyiklioglu ◽  
Emin Bacaksiz ◽  
Ismail Polat ◽  
...  

ZnWO4MnPc was synthesized via a hydrothermal autoclave method with 1 wt.% manganese (iii) phthalocyanine content. The material was characterized for its structural and morphological features via X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission emission microscopy (TEM), scanning electron microscopy-Energy dispersive X-ray spectroscopy (SEM-EDX), N2 adsorption–desorption at 77K, X-ray photoelectron spectroscopy (XPS), and UV-visible/diffuse reflectance spectroscopy(UV-vis/DRS). ZnWO4MnPc photocatalytic performance was tested on the degradation of bisphenol A (BPA). The ZnWO4MnPc material removed 60% of BPA after 4 h of 365 nm UV irradiation. Degradation process improved significantly to about 80% removal in the presence of added 5 mM H2O2 after 4 h irradiation. Almost 100% removal was achieved after 30 min under 450 nm visible light irradiation in the presence of same concentration of H2O2. The effect of ions and humic acid (HA) towards BPA removal was also investigated.


2000 ◽  
Vol 612 ◽  
Author(s):  
G.P. Beyer ◽  
M. Baklanov ◽  
T. Conard ◽  
K. Maex

AbstractIt was found that copper surfaces, which had been exposed to a clean room atmosphere, were covered by a layer, whose chemical composition can be described by Cu(OH)2·CuCO3. This layer can effectively be removed by either a short thermal treatment in vacuum at 350°C, a hydrogen plasma treatment, or a combination of both. Ex-situ photoelectron spectroscopy measurements show little difference of the chemical composition of the surface after the respective treatments. The thermal treatment, however, gives rise to re-crystallisation of the copper film due to the difference in temperature of deposition and the anneal. Ex-situ ellipsometry measurements indicate that the hydrogen plasma not only removes Cu(OH)2·CuCO3 but also passivates the copper surface.


2020 ◽  
Vol 842 ◽  
pp. 214-222
Author(s):  
Chu Wen Rao ◽  
Wei Zhang ◽  
Zheng Fa Hu ◽  
Zu Yong Feng ◽  
Ying Jun Chen ◽  
...  

In this paper, ZnWO4: La3+, Y3+ photocatalysts were synthesized by a high-temperature solid state reaction method. The effects of La3+ and Y3+ doping contents on the phase, morphologies and optical properties of the samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Diffuse reflectance spectra (DRS), photoluminescence spectra (PL), Raman and UV-visible spectroscopy, respectively. The as-prepared ZnWO4:La3+, Y3+ photocatalysts showed photoluminescence with a broad band emission, and high photocatalytic activity in degradation of rhodamine B (RhB) under simulated UV irradiation. The results showed that co-doping in ZnWO4 can enhance light harvesting capability to generate more electron-hole pairs, and acted as a trap center by decreasing the recombination of photogenerated electrons and holes. All the results obtained by the work suggest that ZnWO4: La3+, Y3+ photocatalysts are promising materials for the photocatalytic decomposition of pollutants.


2020 ◽  
Vol 32 (7) ◽  
pp. 761-774
Author(s):  
Lopamudra Das ◽  
John C Poutsma ◽  
Michael J Kelley

Polyimides (PIs) have a wide range of industrial and scientific applications due to their excellent thermal and mechanical stability and chemical resistance. Their response to ultraviolet (UV) irradiation is of further interest in high-value applications such as spacecraft technology and electronics packaging. In this work, we investigated the effect of 172-nm UV xenon excimer lamp irradiation on samples of pyromellitimido-oxydianiline (PMDA-ODA) commercial films in the absence of oxygen. The average irradiance received at the sample position was 90 mW/cm2, and the total radiation dosage varied from 0 to 64 J/cm2. X-Ray photoelectron spectroscopy, time-of-flight-secondary ion mass spectrometry, atomic force microscopy, and contact angle measurements were used to characterize the effect. Calculated UV-visible spectroscopy absorption spectra were obtained using the ZINDO//B3LYP/3-21G method to give an indication of which orbitals are involved in the transitions near 172 nm. The reactivity of the different UV-treated PI samples toward nitrogen-borne heptafluorodecene vapor was then investigated using the above techniques. Grafting reactions occurred on the surface of the photochemically activated polymer. This study explored the potential for modification of PI surfaces using UV-light-assisted grafting to impart valuable functionalities.


Nanomaterials ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 163 ◽  
Author(s):  
Reza Katal ◽  
Saeideh Kholghi Eshkalak ◽  
Saeid Masudy-panah ◽  
Mohammadreza Kosari ◽  
Mohsen Saeedikhani ◽  
...  

In this report, the photocatalytic activity of P25 has been explored and the influence of thermal treatment under various atmospheres (air, vacuum and hydrogen) were discussed. The samples’ characteristics were disclosed by means of various instruments including X-ray diffraction (XRD), Electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS) and UV–vis. This study also accentuates various states of the oxygen vacancy density formed inside the samples as well as the colour turning observed in treated P25 under various atmospheres. Produced coloured TiO2 samples were then exploited for their photocatalytic capability concerning photodegradation of methylene blue (MB) using air mass (AM) 1.5 G solar light irradiation. Our findings revealed that exceptional photocatalytic activity of P25 is related to the thermal treatment. Neither oxygen vacancy formation nor photocatalytic activity enhancement was observed in the air-treated sample. H2-treated samples have shown better photoactivity which even could be further improved by optimizing treatment conditions to achieve the advantages of the positive role of oxygen vacancy (O-vacancy at higher concentration than optimum acts as electron trapping sites). The chemical structure and stability of the samples were also studied. There was no sign of deteriorating of O2-vacancies inside the samples after 6 months. High stability of thermal treated samples in terms of both long and short-term time intervals is another significant feature of the produced photocatalyst.


2014 ◽  
Vol 92 (7/8) ◽  
pp. 832-837
Author(s):  
J. Molina ◽  
C. Zúñiga ◽  
M. Moreno ◽  
W. Calleja ◽  
P. Rosales ◽  
...  

In this work, rutile-phase TiO2 particles (r-TiO2, about 360 nm in size) are embedded within a silicon oxide matrix using different concentration ratios of r-TiO2 with respect to SiO2:H2O, so that suspensions of mixed TiO2:SiO2 oxides were obtained and analyzed. These TiO2:SiO2 suspensions were deposited on previously-cleaned crystalline silicon and quartz substrates so that thin films of TiO2:SiO2 were obtained. All films were then exposed to relatively high-temperature thermal treatments in nitrogen and different characterization techniques were used to determine their physical and electrical properties before and after ultraviolet (UV) irradiation. Before high thermal treatment, X-ray diffraction patterns show that the main diffraction peaks for the obtained TiO2:SiO2 films correspond to the crystalline phase of rutile-TiO2. Infrared analyses before and after thermal treatment show significant changes in the chemical bonding of the final films relative to the temperatures used during annealing. Also, UV–visible spectra provide a constant optical band gap for the films, independent of different TiO2 concentrations as expected. On the other hand, atomic-force microscopy measurements before and after UV irradiation show an appreciable difference in the grain size and surface morphology of the resulting TiO2:SiO2 oxides annealed at 1000 °C. Finally, photoelectrical I–V properties were obtained for all TiO2:SiO2 films by depositing ultrathin titanium stripes on top of the photoactive material and then, measuring the total current flowing through the metal electrode before and after UV irradiation. From these last measurements, a detectable increase in the I–V slope (lower resistance of the titanium stripe) is found for all samples during UV exposure, thus making this device to act as a simple photoresistor based on r-TiO2 particles.


1988 ◽  
Vol 129 ◽  
Author(s):  
C.J. Kiely ◽  
C. Jones ◽  
V. Tavitian ◽  
J.G. Eden

ABSTRACTThe viability of ammonia as a sensitiser for the epitaxial growth of Ge on GaAs by laser photochemical vapour deposition (LPVD) has been investigated. Specifically NH3/GeH4/He (0.8/5/95 sccm, 5.5 Torr total pressure) mixtures have been irradiated by a 193nm ArF excimer laser in parallel geometry for substrate temperatures, Ts<400°C. As evidenced by a dramatic acceleration in Ge film growth rate, the NH3 efficiently couples the laser radiation to the GeH4 precursor molecule. The microstructures of LPVD Ge films grown with and without NH3 have been examined by TEM, and the epitaxial nature of both types of films has been verified, although some subtle differences are noted. Chemical analysis of the deposited films has been carried out using Auger spectroscopy, X-ray photoelectron spectroscopy and secondary ion mass spectroscopy. Our results show that there is little or no nitrogen incorporation into the Ge films grown in the presence of NH3, and that hydrogen contamination in our films is minimal. The beneficial effect of NH3 on the growth rate of LPVD Ge films is attributed to the photolytic production of hydrogen atoms which efficiently decompose GeH4 by hydrogen abstraction collisions.


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