scholarly journals Rate-Limiting Steps of Dye Degradation over Titania-Silica Core-Shell Photocatalysts

Catalysts ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 583 ◽  
Author(s):  
Ariane Giesriegl ◽  
Jakob Blaschke ◽  
Shaghayegh Naghdi ◽  
Dominik Eder

In this work, we employed a step-by-step sol-gel process to controllably deposit ultra-thin layers of SiO2 on anatase nanoparticles in the range between 0 and 1 nm. The deposition was confirmed by TEM, EDX, and ATR-FTIR (e.g., Ti-O-Si band at 960 cm-1). Zeta potential measurements unravelled a continuous change in surface charge density with increasing silica shell thickness. The photocatalysts were evaluated towards adsorption and degradation of positively-charged and negatively-charged dyes (methylene blue, methyl orange) under UV illumination. The growth mechanism follows the Stranski–Krastanov model with three thickness regimes: (a) Flat islands (first step), (b) mono/bilayers (second/third step), and (c) regular thick films (fourth/fifth step). The results suggest different rate limiting processes for these regimes: (a) For the thinnest scenario, acidic triple-phase boundaries (TPBs) increase the activity for both dyes with their accessibility being the rate limiting step; (b) for continuous mono/bilayers, dye adsorption on the negatively-charged SiO2 shells becomes the rate liming step, which leads to a stark increase in activity for the positively-charged MB and a decrease for MO; (c) for thicker shells, the activity decreases for both dyes and is limited by the charge transport through the isolating shells.

1986 ◽  
Vol 73 ◽  
Author(s):  
Bruce D. Kay ◽  
Roger A. Assink

ABSTRACTHigh resolution 1H NMR spectroscopy at high magnetic fields is employed to study the reaction kinetics of the Si(OCH3)4:CH3OH:H2O sol-gel system. Both the overall extent of reaction as a function of time and the equilibrium distribution of species are measured. In acid catalyzed solution, condensation is the rate limiting step while in base catalyzed solution, hydrolysis becomes rate limiting. A kinetic model in which the rate of hydrolysis is assumed to be independent of the adjacent functional groups is presented. This model correctly predicts the distribution of product species during the initial stages of the sol-gel reaction.


1994 ◽  
Vol 77 (4) ◽  
pp. 891-896 ◽  
Author(s):  
Seung-Young Bae ◽  
Masaru Miyayama ◽  
Hiroaki Yanagida

1995 ◽  
Vol 10 (10) ◽  
pp. 2626-2630 ◽  
Author(s):  
Brian G. Dixon ◽  
Myles A. Walsh ◽  
Peter G. Phillips ◽  
R. Scott Morris

Thin amorphous films of ceramic capacitor materials were successfully deposited using sol-gel chemistry onto titanium wire using a continuous, computer-controlled process. By repeatedly depositing and calcining very thin layers of material, smooth and even coats can be produced. Surface analyses revealed the layered nature of these thin coats, as well as the amorphous nature of the ceramic. The electrical properties of the better coatings, all composed of niobrium, bismuth, and zinc oxides, were then evaluated.


1984 ◽  
Vol 32 ◽  
Author(s):  
J. Livage

ABSTRACTTransition metal oxide gels can be obtained, through a polycondensation process, by acidification of aqueous solutions. Thin layers can be easily deposited onto a substrate. Their electronic and ionic properties could lead to new developments of the sol-gel process. The semiconducting properties of V2O gels can be used for antistatic coatings or electrical switching devices. These gels exhibit a lamellar structure and can be described as particle hydrates. They are fast proton conductors and could behave as a host lattice for intercalation.


Author(s):  
H. Piombini ◽  
F. Compoint ◽  
C. Ambard ◽  
K. Vallé ◽  
Ph. Belleville ◽  
...  

2018 ◽  
Vol 18 (3) ◽  
pp. 2235-2240 ◽  
Author(s):  
Bing-Shun Huang ◽  
En-Chin Su ◽  
Yun-Ya Huang ◽  
Hui-Hsin Tseng

ChemInform ◽  
2010 ◽  
Vol 25 (35) ◽  
pp. no-no
Author(s):  
S.-Y. BAE ◽  
M. MIYAYAMA ◽  
H. YANAGIDA

2018 ◽  
Author(s):  
Hardeli ◽  
Harry Sanjaya ◽  
Rahadian Zainul

In this research we has investigated synthesis and electrical properties of ITO (Indium Tin Oxide) thin layers doping Aluminum (Al) and ZnO with spin-coating technique through sol-gel process and calcined at ±550 ºC for 1 hour. Effect of Al and ZnO doping on the conductivity of ITO with 0%, 1%, 3% and 5% w/v dopant concentration and the number of coating (4 and 5 layers) has reported. ITO-Al has 2 phases, these are rhombohedral and cubic, the crystal size is 67.31 nm. Meanwhile, ITO-ZnO are rhombohedral, cubic (bixbyite) and hexagonal (wurtzite), with crystallite size value was 67.4 nm. The surface morphology data indicated film thickness was 3.4 µm (ITO-Al) and 0.974 nm (ITO-ZnO). The electrical properties shows that the optimum film in 4 layers coating with the addition of 5% doping value was 17 kΩ/cm2 (ITO-Al) and 5-layered by addition of 5% of doping ZnO (80.800 kΩ/cm2). Meanwhile, ITO-Al thin film with 4 layers coating without doping was 9.331 kΩ / cm2, and for ITO-ZnO (5 layers) coating without doping was 11.796 kΩ/cm2. Al and ZnO doping decrease the electrical conductivity of ITO.


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