Studies on the hydrothermal synthesis of Cd(x)Zn(1-x)S compounds
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F18%3A10381902" target="_blank" >RIV/00216208:11310/18:10381902 - isvavai.cz</a>
Výsledek na webu
<a href="https://doi.org/10.2298/PAC1803287S" target="_blank" >https://doi.org/10.2298/PAC1803287S</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.2298/PAC1803287S" target="_blank" >10.2298/PAC1803287S</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Studies on the hydrothermal synthesis of Cd(x)Zn(1-x)S compounds
Popis výsledku v původním jazyce
In this study series of Cd(x)Zn(1-x)S solid solutions with different amounts of Cd and Zn were synthesized by the hydrothermal treatment of aqueous solutions containing CdCl2, Na2S . 9 H2O and ZnSO4 . 7 H2O. The aim was to examine the influence of Zn concentration and processing conditions (hydrothermal temperature and duration) on the structure of the obtained powders and their photocatalytic activity (in water splitting process). The obtained photocatalysts (with and without Pd co-catalyst) were analysed by X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), ultravioletvisible spectroscopy (UV-VIS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) method and gas chromatography (GC). The XRD results confirmed the crystallinity of the compounds and transition from hexagonal to cubic phase with increasing Zn content. Complete transformation from hexagonal to cubic phase did not take place, and both phases were present in almost all Samples. BET analysis showed the importance of the pore distribution and pore size, especially in the case of photocatalysts with different duration treatment. GC measurements of the photocatalysts without and with Pd co-catalyst confirmed the production of hydrogen for all tested compounds. The best photocatalytic performance was achieved by the sample Zn(50)230/72-Pd prepared at 230 degrees C, for 72 hours, with 50% Zn and in the presence of Pd co-catalyst. The synthesis implied no stabilizer neither organic compound.
Název v anglickém jazyce
Studies on the hydrothermal synthesis of Cd(x)Zn(1-x)S compounds
Popis výsledku anglicky
In this study series of Cd(x)Zn(1-x)S solid solutions with different amounts of Cd and Zn were synthesized by the hydrothermal treatment of aqueous solutions containing CdCl2, Na2S . 9 H2O and ZnSO4 . 7 H2O. The aim was to examine the influence of Zn concentration and processing conditions (hydrothermal temperature and duration) on the structure of the obtained powders and their photocatalytic activity (in water splitting process). The obtained photocatalysts (with and without Pd co-catalyst) were analysed by X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), ultravioletvisible spectroscopy (UV-VIS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) method and gas chromatography (GC). The XRD results confirmed the crystallinity of the compounds and transition from hexagonal to cubic phase with increasing Zn content. Complete transformation from hexagonal to cubic phase did not take place, and both phases were present in almost all Samples. BET analysis showed the importance of the pore distribution and pore size, especially in the case of photocatalysts with different duration treatment. GC measurements of the photocatalysts without and with Pd co-catalyst confirmed the production of hydrogen for all tested compounds. The best photocatalytic performance was achieved by the sample Zn(50)230/72-Pd prepared at 230 degrees C, for 72 hours, with 50% Zn and in the presence of Pd co-catalyst. The synthesis implied no stabilizer neither organic compound.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
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
Processing and Application of Ceramics
ISSN
1820-6131
e-ISSN
—
Svazek periodika
12
Číslo periodika v rámci svazku
3
Stát vydavatele periodika
CS - Srbsko a Černá Hora
Počet stran výsledku
8
Strana od-do
287-294
Kód UT WoS článku
000446121300011
EID výsledku v databázi Scopus
2-s2.0-85054540728