Copper and Platinum Doped Titania for Photocatalytic Reduction of Carbon Dioxide
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27710%2F18%3A10240188" target="_blank" >RIV/61989100:27710/18:10240188 - isvavai.cz</a>
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0169433217319621" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0169433217319621</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.apsusc.2017.06.307" target="_blank" >10.1016/j.apsusc.2017.06.307</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Copper and Platinum Doped Titania for Photocatalytic Reduction of Carbon Dioxide
Popis výsledku v původním jazyce
The parent TiO2, platinum and copper doped TiO2 photocatalysts with 0.5-2 wt. % of Pt, 0.5-2 wt. %Cu and 1 wt. % Pt combined with 1 wt. % Cu were prepared by the sol-gel method. All the prepared photocatalysts were tested for the CO2 photocatalytic reduction in a stirred batch reactor. The main reaction product was methane, however, hydrogen and carbon monoxide were also detected. The textural, (micro)structural, optical and electronic properties of photocatalysts were characterized in detailby low-temperature nitrogen physisorption, X-ray powder diffraction, EDX, HRTEM, X-ray fluorescence,X-ray photon spectroscopy, scanning electron microscope, transmission electron microscope and diffuse reflectance UV-vis spectroscopy. The photoelectrochemical characteristics of the photocatalysts were determined using photoelectric spectrometry. The highest yields of CH4, H2 and CO were achieved in the presence of 2 wt. % Cu/TiO2, 0.5 wt. % Cu/TiO2 and pure, amorphous TiO2. Based on the conducted experiments it was suggested that both the amount of chemisorbed oxygen or/and hydroxyl species onthe TiO2 surface and specific surface area of photocatalyst highly influence its photocatalytic activity.
Název v anglickém jazyce
Copper and Platinum Doped Titania for Photocatalytic Reduction of Carbon Dioxide
Popis výsledku anglicky
The parent TiO2, platinum and copper doped TiO2 photocatalysts with 0.5-2 wt. % of Pt, 0.5-2 wt. %Cu and 1 wt. % Pt combined with 1 wt. % Cu were prepared by the sol-gel method. All the prepared photocatalysts were tested for the CO2 photocatalytic reduction in a stirred batch reactor. The main reaction product was methane, however, hydrogen and carbon monoxide were also detected. The textural, (micro)structural, optical and electronic properties of photocatalysts were characterized in detailby low-temperature nitrogen physisorption, X-ray powder diffraction, EDX, HRTEM, X-ray fluorescence,X-ray photon spectroscopy, scanning electron microscope, transmission electron microscope and diffuse reflectance UV-vis spectroscopy. The photoelectrochemical characteristics of the photocatalysts were determined using photoelectric spectrometry. The highest yields of CH4, H2 and CO were achieved in the presence of 2 wt. % Cu/TiO2, 0.5 wt. % Cu/TiO2 and pure, amorphous TiO2. Based on the conducted experiments it was suggested that both the amount of chemisorbed oxygen or/and hydroxyl species onthe TiO2 surface and specific surface area of photocatalyst highly influence its photocatalytic activity.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10403 - Physical chemistry
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Applied Surface Science
ISSN
0169-4332
e-ISSN
—
Svazek periodika
430
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
13
Strana od-do
475-487
Kód UT WoS článku
000416961500044
EID výsledku v databázi Scopus
2-s2.0-85023600854