Details
| Original language | English |
|---|---|
| Pages (from-to) | 375-384 |
| Number of pages | 10 |
| Journal | Applied Catalysis B: Environmental |
| Volume | 241 |
| Early online date | 21 Sept 2018 |
| Publication status | Published - Feb 2019 |
Abstract
Different studies to unravel the nature of the activity of TiO 2 photocatalysts modified with rGO were carried out. The band edge potentials and the band gap energy of the nanocomposites were determined by performing electrochemical impedance and UV–vis diffuse reflectance measurements, respectively. However, no changes were observed when TiO 2 is modified with rGO. Nevertheless, the presence of rGO in the hybrid composite led to a low charge transfer resistance across the electrode-electrolyte interface, observing even a tenfold increase in the photocurrent values in methanol photo-oxidation for P25-rGO 1%. Moreover, a higher oxygen reduction current was found when increasing the rGO concentration that could lead to a higher ROS formation. In order to analyze the beneficial properties of the hybrid materials, the influence of rGO doping ratio on oxalic acid photocatalytic degradation and on oxalic acid adsorption onto the nanocomposites surface was studied, both of them under UV-A light irradiation. In addition, the photoactivity of the conduction band electrons and the valence band holes was investigated by performing EPR and transient absorption spectroscopy measurements under UV-A illumination in O 2 or N 2 atmospheres. It was demonstrated that rGO behaved as an electron acceptor. Finally, TAS results under O 2 and N 2 atmospheres proved that the role played by rGO was not as crucial in excess of dissolved O 2 as in N 2 atmosphere. These findings agree with the observed photocatalytic activity and EPR measurements. Nevertheless, generation of HO [rad] in N 2 saturated suspensions was highly increased with the addition of rGO.
Keywords
- ATR-FTIR, Mechanism, Oxalic acid, Reduced graphene oxide, TiO -rGO
ASJC Scopus subject areas
- Chemical Engineering(all)
- Catalysis
- Environmental Science(all)
- Chemical Engineering(all)
- Process Chemistry and Technology
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In: Applied Catalysis B: Environmental, Vol. 241, 02.2019, p. 375-384.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Nature and photoreactivity of TiO2-rGO nanocomposites in aqueous suspensions under UV-A irradiation
AU - Tolosana-Moranchel, A.
AU - Casas, J.A.
AU - Bahamonde, A.
AU - Pascual, L.
AU - Granone, L.I.
AU - Schneider, J.
AU - Dillert, R.
AU - Bahnemann, D.W.
N1 - Funding Information: This work has been supported by the Spanish Plan Nacional de I+D+i through the project CTM2015-64895-R and CTM2016-76454-R. Alvaro Tolosana-Moranchel thanks to Ministerio de Educación, Cultura y Deporte for his FPU grant ( FPU14/01605 ).
PY - 2019/2
Y1 - 2019/2
N2 - Different studies to unravel the nature of the activity of TiO 2 photocatalysts modified with rGO were carried out. The band edge potentials and the band gap energy of the nanocomposites were determined by performing electrochemical impedance and UV–vis diffuse reflectance measurements, respectively. However, no changes were observed when TiO 2 is modified with rGO. Nevertheless, the presence of rGO in the hybrid composite led to a low charge transfer resistance across the electrode-electrolyte interface, observing even a tenfold increase in the photocurrent values in methanol photo-oxidation for P25-rGO 1%. Moreover, a higher oxygen reduction current was found when increasing the rGO concentration that could lead to a higher ROS formation. In order to analyze the beneficial properties of the hybrid materials, the influence of rGO doping ratio on oxalic acid photocatalytic degradation and on oxalic acid adsorption onto the nanocomposites surface was studied, both of them under UV-A light irradiation. In addition, the photoactivity of the conduction band electrons and the valence band holes was investigated by performing EPR and transient absorption spectroscopy measurements under UV-A illumination in O 2 or N 2 atmospheres. It was demonstrated that rGO behaved as an electron acceptor. Finally, TAS results under O 2 and N 2 atmospheres proved that the role played by rGO was not as crucial in excess of dissolved O 2 as in N 2 atmosphere. These findings agree with the observed photocatalytic activity and EPR measurements. Nevertheless, generation of HO [rad] in N 2 saturated suspensions was highly increased with the addition of rGO.
AB - Different studies to unravel the nature of the activity of TiO 2 photocatalysts modified with rGO were carried out. The band edge potentials and the band gap energy of the nanocomposites were determined by performing electrochemical impedance and UV–vis diffuse reflectance measurements, respectively. However, no changes were observed when TiO 2 is modified with rGO. Nevertheless, the presence of rGO in the hybrid composite led to a low charge transfer resistance across the electrode-electrolyte interface, observing even a tenfold increase in the photocurrent values in methanol photo-oxidation for P25-rGO 1%. Moreover, a higher oxygen reduction current was found when increasing the rGO concentration that could lead to a higher ROS formation. In order to analyze the beneficial properties of the hybrid materials, the influence of rGO doping ratio on oxalic acid photocatalytic degradation and on oxalic acid adsorption onto the nanocomposites surface was studied, both of them under UV-A light irradiation. In addition, the photoactivity of the conduction band electrons and the valence band holes was investigated by performing EPR and transient absorption spectroscopy measurements under UV-A illumination in O 2 or N 2 atmospheres. It was demonstrated that rGO behaved as an electron acceptor. Finally, TAS results under O 2 and N 2 atmospheres proved that the role played by rGO was not as crucial in excess of dissolved O 2 as in N 2 atmosphere. These findings agree with the observed photocatalytic activity and EPR measurements. Nevertheless, generation of HO [rad] in N 2 saturated suspensions was highly increased with the addition of rGO.
KW - ATR-FTIR
KW - Mechanism
KW - Oxalic acid
KW - Reduced graphene oxide
KW - TiO -rGO
UR - http://www.scopus.com/inward/record.url?scp=85053780164&partnerID=8YFLogxK
U2 - 10.1016/j.apcatb.2018.09.070
DO - 10.1016/j.apcatb.2018.09.070
M3 - Article
VL - 241
SP - 375
EP - 384
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
SN - 0926-3373
ER -