Synergetic Surface Sensitivity of Photoelectrochemical Water Oxidation on TiO2 (Anatase) Electrodes
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23640%2F17%3A43931748" target="_blank" >RIV/49777513:23640/17:43931748 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61388955:_____/18:00493586
Výsledek na webu
<a href="http://dx.doi.org/10.1021/acs.jpcc.6b09289" target="_blank" >http://dx.doi.org/10.1021/acs.jpcc.6b09289</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jpcc.6b09289" target="_blank" >10.1021/acs.jpcc.6b09289</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Synergetic Surface Sensitivity of Photoelectrochemical Water Oxidation on TiO2 (Anatase) Electrodes
Popis výsledku v původním jazyce
The paper compares photoelectrocatalytic activity and selectivity of nanocrystalline anatase dominated by {110}, {101}, and {001} faces in photo(electro)catalytic water splitting. Although the anodic half-reaction of water splittingoxygen evolutiondominates the overall photoelectrochemical behavior of the photoexcited anatase, simultaneous reduction under photoelectrochemical conditions is also observed on some anatase faces. The activity of individual facets in anodic half-reaction of water splitting (oxygen evolution) increases in the order {101} < {110} < {001}. The increasing oxidation activity tracks the tendency of the surface to generate the OH• radical producing intermediates (H2O2, ozone) on the trapped hole states. The activity in reduction processes increases in the reversed order. Particularly, the reduction activity of the {101} oriented anatase can be attributed to pronounced hydrogen evolution by a charge transfer of photogenerated electrons. The observed trends agree with DFT-based models which confirm the possibility of a rational design of the photocatalysts.
Název v anglickém jazyce
Synergetic Surface Sensitivity of Photoelectrochemical Water Oxidation on TiO2 (Anatase) Electrodes
Popis výsledku anglicky
The paper compares photoelectrocatalytic activity and selectivity of nanocrystalline anatase dominated by {110}, {101}, and {001} faces in photo(electro)catalytic water splitting. Although the anodic half-reaction of water splittingoxygen evolutiondominates the overall photoelectrochemical behavior of the photoexcited anatase, simultaneous reduction under photoelectrochemical conditions is also observed on some anatase faces. The activity of individual facets in anodic half-reaction of water splitting (oxygen evolution) increases in the order {101} < {110} < {001}. The increasing oxidation activity tracks the tendency of the surface to generate the OH• radical producing intermediates (H2O2, ozone) on the trapped hole states. The activity in reduction processes increases in the reversed order. Particularly, the reduction activity of the {101} oriented anatase can be attributed to pronounced hydrogen evolution by a charge transfer of photogenerated electrons. The observed trends agree with DFT-based models which confirm the possibility of a rational design of the photocatalysts.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10301 - Atomic, molecular and chemical physics (physics of atoms and molecules including collision, interaction with radiation, magnetic resonances, Mössbauer effect)
Návaznosti výsledku
Projekt
<a href="/cs/project/GA13-07724S" target="_blank" >GA13-07724S: Materiálové inženýrství pro inovativní Graetzelovy solární články</a><br>
Návaznosti
S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Physical Chemistry C
ISSN
1932-7447
e-ISSN
—
Svazek periodika
121
Číslo periodika v rámci svazku
11
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
9
Strana od-do
6024-6032
Kód UT WoS článku
000397546300020
EID výsledku v databázi Scopus
—