Investigating and Correlating Photoelectrochemical, Photocatalytic, and Antimicrobial Properties of TiO2 Nanolayers

Author(s):  
Volker Seiß ◽  
Uta Helbig ◽  
Ralf Lösel ◽  
Maik Eichelbaum

Abstract Semiconducting transition metal oxides such as TiO2 are promising photo(electro)catalysts for solar water splitting and photoreduction of CO2. Titania admixtures are also used in paints and building materials or as coating on window glass and medical devices, giving the modified materials antimicrobial, self-or even air-cleaning properties. Although TiO2 is an effective catalyst for all these applications, it is mechanistically important to distinguish between photoelectrocatalytic, photocatalytic and antimicrobial processes. In the former, TiO2 is usually electrically contacted as photoanode, i.e. only the oxidation reaction takes place at the titania surface. In the two latter applications, TiO2 works as heterogeneous catalyst and has to catalyze a complete redox cycle. The underlying common and diverging rate-determining photochemical and photoelectrochemical mechanisms are still not well understood. Here, we thus present a systematic structural, photoelectrocatalytic, photocatalytic and antimicrobial study to directly compare and correlate these properties. We prepared TiO2 thin films on flourine-doped tin oxide (FTO) substrates by a sol-gel spin-coating technique. The materials were annealed at temperatures between 200 and 600°C and their morphologies were studied by GIXRD, FESEM and EDX. Photoelectrochemical properties were measured by linear sweep voltammetry, photoelectrochemical impedance spectroscopy, chopped light chronoamperometry, and intensity modulated photocurrent/ photovoltage spectroscopy. For comparison, photocatalytic rate constants were determined by methylene blue and Escherichea coli degradation and correlated with the deduced photoelectrocatalytic parameters.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Volker Seiß ◽  
Uta Helbig ◽  
Ralf Lösel ◽  
Maik Eichelbaum

AbstractSemiconducting transition metal oxides such as $$\hbox {TiO}_2$$ TiO 2 are promising photo(electro)catalysts for solar water splitting and photoreduction of $$\hbox {CO}_2$$ CO 2 as well as for antibacterial, self-, water and air-cleaning coatings and admixtures in paints, building materials, on window glass or medical devices. In photoelectrocatalytic applications $$\hbox {TiO}_2$$ TiO 2 is usually used as photoanode only catalyzing the oxidation reaction. In coatings and admixtures $$\hbox {TiO}_2$$ TiO 2 works as heterogeneous catalyst and has to catalyze a complete redox cycle. While photoelectrochemical charge transport parameters are usually quite well accessible by electrochemical measurements, the quantitative description of photocatalytic properties is more challenging. Here, we present a systematic structural, photoelectrocatalytic, photocatalytic and antimicrobial study to understand if and how photoelectrochemical parameters can be used to predict the photocatalytic activity of $$\hbox {TiO}_2$$ TiO 2 . For this purpose $$\hbox {TiO}_2$$ TiO 2 thin films on flourine-doped tin oxide substrates were prepared and annealed at temperatures between 200 and 600 $$^{\circ }\hbox {C}$$ ∘ C . The film morphologies and thicknesses were studied by GIXRD, FESEM, and EDX. Photoelectrochemical properties were measured by linear sweep voltammetry, photoelectrochemical impedance spectroscopy, chopped light chronoamperometry, and intensity modulated photocurrent/ photovoltage spectroscopy. For comparison, photocatalytic rate constants were determined by methylene blue degradation and Escherichea coli inactivation and correlated with the deduced photoelectrocatalytic parameters. We found that the respective photoactivities of amorphous and crystalline $$\hbox {TiO}_2$$ TiO 2 nanolayers can be best correlated, if the extracted photoelectrochemical parameters such as charge transfer and recombination rates, charge transfer efficiencies and resistances are measured close to the open circuit potential (OCP). Hence, the interfacial charge transport parameters at the OCP can be indeed used as descriptors for predicting and understanding the photocatalytic activity of $$\hbox {TiO}_2$$ TiO 2 coatings.


2019 ◽  
Vol 7 (1) ◽  
pp. 28
Author(s):  
KOMARAIAH DURGAM ◽  
RADHA EPPA ◽  
REDDY M. V. RAMANA ◽  
KUMAR J. SIVA ◽  
R. SAYANNA ◽  
...  

2011 ◽  
Vol 10 (2) ◽  
pp. 187-192 ◽  
Author(s):  
Ramona-Crina Suciu ◽  
Marcela Corina Rosu ◽  
Teofil Danut Silipas ◽  
Emil Indrea ◽  
Violeta Popescu ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1409
Author(s):  
Ofelia Durante ◽  
Cinzia Di Giorgio ◽  
Veronica Granata ◽  
Joshua Neilson ◽  
Rosalba Fittipaldi ◽  
...  

Among all transition metal oxides, titanium dioxide (TiO2) is one of the most intensively investigated materials due to its large range of applications, both in the amorphous and crystalline forms. We have produced amorphous TiO2 thin films by means of room temperature ion-plasma assisted e-beam deposition, and we have heat-treated the samples to study the onset of crystallization. Herein, we have detailed the earliest stage and the evolution of crystallization, as a function of both the annealing temperature, in the range 250–1000 °C, and the TiO2 thickness, varying between 5 and 200 nm. We have explored the structural and morphological properties of the as grown and heat-treated samples with Atomic Force Microscopy, Scanning Electron Microscopy, X-ray Diffractometry, and Raman spectroscopy. We have observed an increasing crystallization onset temperature as the film thickness is reduced, as well as remarkable differences in the crystallization evolution, depending on the film thickness. Moreover, we have shown a strong cross-talking among the complementary techniques used displaying that also surface imaging can provide distinctive information on material crystallization. Finally, we have also explored the phonon lifetime as a function of the TiO2 thickness and annealing temperature, both ultimately affecting the degree of crystallinity.


2017 ◽  
Author(s):  
Siti Noraini Abu Bakar ◽  
Huda Abdullah ◽  
Kamisah Mohamad Mahbor

2021 ◽  
Vol 7 (1) ◽  
pp. 14
Author(s):  
Dewi Suriyani Che Halin ◽  
Kamrosni Abdul Razak ◽  
Mohd Arif Anuar Mohd Salleh ◽  
Mohd Izrul Izwan Ramli ◽  
Mohd Mustafa Al Bakri Abdullah ◽  
...  

Ag/TiO2 thin films were prepared using the sol-gel spin coating method. The microstructural growth behaviors of the prepared Ag/TiO2 thin films were elucidated using real-time synchrotron radiation imaging, its structure was determined using grazing incidence X-ray diffraction (GIXRD), its morphology was imaged using the field emission scanning electron microscopy (FESEM), and its surface topography was examined using the atomic force microscope (AFM) in contact mode. The cubical shape was detected and identified as Ag, while the anatase, TiO2 thin film resembled a porous ring-like structure. It was found that each ring that coalesced and formed channels occurred at a low annealing temperature of 280 °C. The energy dispersive X-ray (EDX) result revealed a small amount of Ag presence in the Ag/TiO2 thin films. From the in-situ synchrotron radiation imaging, it was observed that as the annealing time increased, the growth of Ag/TiO2 also increased in terms of area and the number of junctions. The growth rate of Ag/TiO2 at 600 s was 47.26 µm2/s, and after 1200 s it decreased to 11.50 µm2/s and 11.55 µm2/s at 1800 s. Prolonged annealing will further decrease the growth rate to 5.94 µm2/s, 4.12 µm2/s and 4.86 µm2/s at 2400 s, 3000 s and 3600 s, respectively.


2012 ◽  
Vol 2 (1) ◽  
Author(s):  
Marek Nocuń ◽  
Sławomir Kwaśny

AbstractIn our investigation, V doped SiO2/TiO2 thin films were prepared on glass substrates by dip coating sol-gel technique. Chemical composition of the samples was studied by X-ray photoelectron spectroscopy (XPS). Transmittance of the samples was characterized using UV-VIS spectrophotometry. Subsequently band-gap energy (Eg) was estimated for these films. Powders obtained from sols were characterized by FTIR spectroscopy. It was found that vanadium decreases optical band gap of SSiO2/TiO2 films.


1999 ◽  
Author(s):  
Yongxiang Li ◽  
Muralihar K. Ghantasala ◽  
Kosmas Galatsis ◽  
Wojtek Wlodarski

Author(s):  
Kaykobad Md. Rezaul Karim ◽  
Huei Ruey Ong ◽  
Hamidah Abdullah ◽  
Abu Yousuf ◽  
Chin Kui Cheng ◽  
...  

In this work, p-type CuFe2O4 was synthesized by sol gel method. The prepared CuFe2O4 was used as photocathode catalyst for photoelectrochemical (PEC) CO2 reduction. The XRD, UV-Visible Spectroscopy (UV-Vis), and Mott-Schottky (MS) experiments were done to characterize the catalyst. Linear sweep voltammetry (LSV) was employed to evaluate the visible light (λ>400 nm) effect of this catalyst for CO2 reduction.  The band gap energy of the catalyst was calculated from the UV-Vis and was found 1.30 eV. Flat band potential of the prepared CuFe2O4 was also calculated and found 0.27 V versus Ag/AgCl. Under light irradiation in the CO2-saturated NaHCO3 solution, a remarkable current development associated with CO2 reduction was found during LSV for the prepared electrode from onset potential -0.89 V with a peak current emerged at -1.01 V (vs Ag/AgCl) representing the occurrence of CO2 reduction reaction. In addition, the mechanism of PEC was proposed for the photocathode where the necessity of a bias potential in the range of 0.27 to ~ -1.0 V vs Ag/AgCl was identified which could effectively inhibit the electron-hole (e-/h+) recombination process leading to an enhancement of CO2 reduction reactions. Copyright © 2018 BCREC Group. All rights reservedReceived: 4th July 2017; Revised: 5th November 2017; Accepted: 15th November 2017; Available online: 11st June 2018; Published regularly: 1st August 2018How to Cite: Karim, K.M.R., Ong, H.R., Abdullah, H., Yousuf, A., Cheng, C.K., Khan, M.K.R. (2018). Electrochemical Study of Copper Ferrite as a Catalyst for CO2 Photoelectrochemical Reduction. Bulletin of Chemical Reaction Engineering & Catalysis, 13 (2): 236-244 (doi:10.9767/bcrec.13.2.1317.236-244) 


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