Layered Transition-Metal Ditellurides in Electrocatalytic Applications-Contrasting Properties
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F17%3A43913380" target="_blank" >RIV/60461373:22310/17:43913380 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61989592:15310/17:73584556
Výsledek na webu
<a href="http://pubs.acs.org/doi/abs/10.1021/acscatal.7b02080" target="_blank" >http://pubs.acs.org/doi/abs/10.1021/acscatal.7b02080</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acscatal.7b02080" target="_blank" >10.1021/acscatal.7b02080</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Layered Transition-Metal Ditellurides in Electrocatalytic Applications-Contrasting Properties
Popis výsledku v původním jazyce
The layered compounds and especially transition-metal dichalcogenides are at the forefront of current research on electrocatalytic materials. Despite the fact that electrocatalytical properties of molybdenum and tungsten disulfides are well-known, their tellurium analogues are significantly less explored. Here we show an effective method for MoTe2 and WTe2 chemical exfoliation based on alkali metal intercalation and subsequent reaction with water. The as-synthesized and exfoliated tellurides were characterized in detail and investigated for potential application in electrocatalysis. The inherent electrochemical activity related to both cation and anion was observed. This is dominantly related to the oxidation tendency of tellurium. The MoTe2 and WTe2 show significantly contrasting properties toward the hydrogen evolution reaction, where MoTe2 shows highly increased HER activity with little dependence on electrochemical treatment, whereas WTe2 shows slightly worse improvement and strong dependence on the electrochemical treatment. In particular, the exfoliated MoTe2 exhibits improved electrocatalytic activity for hydrogen evolution reaction and possesses a huge application potential.
Název v anglickém jazyce
Layered Transition-Metal Ditellurides in Electrocatalytic Applications-Contrasting Properties
Popis výsledku anglicky
The layered compounds and especially transition-metal dichalcogenides are at the forefront of current research on electrocatalytic materials. Despite the fact that electrocatalytical properties of molybdenum and tungsten disulfides are well-known, their tellurium analogues are significantly less explored. Here we show an effective method for MoTe2 and WTe2 chemical exfoliation based on alkali metal intercalation and subsequent reaction with water. The as-synthesized and exfoliated tellurides were characterized in detail and investigated for potential application in electrocatalysis. The inherent electrochemical activity related to both cation and anion was observed. This is dominantly related to the oxidation tendency of tellurium. The MoTe2 and WTe2 show significantly contrasting properties toward the hydrogen evolution reaction, where MoTe2 shows highly increased HER activity with little dependence on electrochemical treatment, whereas WTe2 shows slightly worse improvement and strong dependence on the electrochemical treatment. In particular, the exfoliated MoTe2 exhibits improved electrocatalytic activity for hydrogen evolution reaction and possesses a huge application potential.
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
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
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
ACS Catalysis
ISSN
2155-5435
e-ISSN
—
Svazek periodika
7
Číslo periodika v rámci svazku
9
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
11
Strana od-do
5706-5716
Kód UT WoS článku
000410005700017
EID výsledku v databázi Scopus
2-s2.0-85029055718