scholarly journals Comparison of Photoelectrochemical Current in Amorphous and Crystalline Anodized TiO2 Nanotube Electrodes

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Candy C. Mercado ◽  
Michael Eric L. Lubrin ◽  
Hazel Anne J. Hernandez ◽  
Reynaldo A. Carubio

The interest in TiO2 nanotubes has resulted in a lot of studies including the effects of various parameters on the properties and performance for different applications. This study investigated the effect of anodization at a low temperature on the properties and photoelectrochemical performance. The effects of varied anodization settings on morphology, crystallinity, and PEC response were studied. Low-temperature anodization resulted in smaller pore diameter and shorter tube length. Annealing temperature affected the presence of varied phases of TiO2 such as the prominence of anatase and amounts of rutile and amorphous TiO2 at 125°C. To observe photoelectrochemical response, annealing at 450°C is necessary. However, a cathodic response was observed for TiO2 nanotubes synthesized with low voltage at low temperature. Hence, amorphous titania nanotubes annealed at 125°C with thickness achieved in the anodization can be a potential material used for photocatalytic applications due to its determined cathodic photoelectrochemical response.

Author(s):  
Huang Min ◽  
P.S. Flora ◽  
C.J. Harland ◽  
J.A. Venables

A cylindrical mirror analyser (CMA) has been built with a parallel recording detection system. It is being used for angular resolved electron spectroscopy (ARES) within a SEM. The CMA has been optimised for imaging applications; the inner cylinder contains a magnetically focused and scanned, 30kV, SEM electron-optical column. The CMA has a large inner radius (50.8mm) and a large collection solid angle (Ω > 1sterad). An energy resolution (ΔE/E) of 1-2% has been achieved. The design and performance of the combination SEM/CMA instrument has been described previously and the CMA and detector system has been used for low voltage electron spectroscopy. Here we discuss the use of the CMA for ARES and present some preliminary results.The CMA has been designed for an axis-to-ring focus and uses an annular type detector. This detector consists of a channel-plate/YAG/mirror assembly which is optically coupled to either a photomultiplier for spectroscopy or a TV camera for parallel detection.


Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3515
Author(s):  
Weikang Wang ◽  
Xuanchun Wei ◽  
Xinhua Cai ◽  
Hongyang Deng ◽  
Bokang Li

: The early-age carbonation curing technique is an effective way to improve the performance of cement-based materials and reduce their carbon footprint. This work investigates the early mechanical properties and microstructure of calcium sulfoaluminate (CSA) cement specimens under early-age carbonation curing, considering five factors: briquetting pressure, water–binder (w/b) ratio, starting point of carbonation curing, carbonation curing time, and carbonation curing pressure. The carbonization process and performance enhancement mechanism of CSA cement are analyzed by mercury intrusion porosimetry (MIP), thermogravimetry and derivative thermogravimetry (TG-DTG) analysis, X-ray diffraction (XRD), and scanning electron microscope (SEM). The results show that early-age carbonation curing can accelerate the hardening speed of CSA cement paste, reduce the cumulative porosity of the cement paste, refine the pore diameter distribution, and make the pore diameter distribution more uniform, thus greatly improving the early compressive strength of the paste. The most favorable w/b ratio for the carbonization reaction of CSA cement paste is between 0.15 and 0.2; the most suitable carbonation curing starting time point is 4 h after initial hydration; the carbonation curing pressure should be between 3 and 4 bar; and the most appropriate time for carbonation curing is between 6 and 12 h.


Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 850 ◽  
Author(s):  
Ladislav Svoboda ◽  
Nadia Licciardello ◽  
Richard Dvorský ◽  
Jiří Bednář ◽  
Jiří Henych ◽  
...  

In the majority of photocatalytic applications, the photocatalyst is dispersed as a suspension of nanoparticles. The suspension provides a higher surface for the photocatalytic reaction in respect to immobilized photocatalysts. However, this implies that recovery of the particles by filtration or centrifugation is needed to collect and regenerate the photocatalyst. This complicates the regeneration process and, at the same time, leads to material loss and potential toxicity. In this work, a new nanofibrous membrane, g-C3N4/PMMA/PUR, was prepared by the fixation of exfoliated g-C3N4 to polyurethane nanofibers using thin layers of poly(methyl methacrylate) (PMMA). The optimal amount of PMMA was determined by measuring the adsorption and photocatalytic properties of g-C3N4/PMMA/PUR membranes (with a different PMMA content) in an aqueous solution of methylene blue. It was found that the prepared membranes were able to effectively adsorb and decompose methylene blue. On top of that, the membranes evinced a self-cleaning behavior, showing no coloration on their surfaces after contact with methylene blue, unlike in the case of unmodified fabric. After further treatment with H2O2, no decrease in photocatalytic activity was observed, indicating that the prepared membrane can also be easily regenerated. This study promises possibilities for the production of photocatalytic membranes and fabrics for both chemical and biological contaminant control.


2012 ◽  
Vol 535-537 ◽  
pp. 894-898 ◽  
Author(s):  
Chien Chon Chen ◽  
Po Chun Chen ◽  
Jun Zou ◽  
Sheng Jen Hsieh

In this paper, we used a simple process of anodization fabrication TiO2, TiO2, TiO2-MoO3, and TiO2-Ta2O5 nanotubes. Those high dielectric constant and large surface area of NT materials are suitable used for the ultracapacitors. Based on the nanotube structural characteristics such as pore diameter, porosity, and tube length, we also investigated and calculated the NT specific capacitance.


2001 ◽  
Vol 7 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Patrick Echlin

Abstract A brief description is given of the events surrounding the development of biological X-ray microanalysis during the last 30 years, with particular emphasis on the contribution made by research workers in Cambridge, UK. There then follows a broad review of some applications of biological X-ray microanalysis. A more detailed consideration is given to the main thrust of current procedures and applications that are, for convenience, considered as four different kinds of samples. Thin frozen dried sections which are analyzed at ambient temperatures in a transmission electron microscope (TEM); semithin frozen dried sections which are analyzed at low temperature in a scanning transmission electron microscope (STEM); thick frozen hydrated sections which are analyzed at low temperature in a scanning electron microscope (SEM), and bulk samples which are analyzed at low temperature in the same type of instrument. A brief outline is given of the advantages and disadvantages of performing low-voltage, low-temperature X-ray microanalysis on frozen hydrated bulk biological material. The article concludes with a consideration of alternative approaches to in situ analysis using either high-energy beams or visible and near-visible photons.


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