Synergetic Surface Sensitivity of Photoelectrochemical Water Oxidation on TiO2 (Anatase) Electrodes

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F18%3A00493586" target="_blank" >RIV/61388955:_____/18:00493586 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/49777513:23640/17:43931748

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>

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 splitting—oxygen evolution—dominates 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 splitting—oxygen evolution—dominates 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.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Projekt

<a href="/cs/project/GA13-07724S" target="_blank" >GA13-07724S: Materiálové inženýrství pro inovativní Graetzelovy solární články</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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

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