Oxidation of metallic two-dimensional transition metal dichalcogenides: 1T-MoS(2)and 1T-TaS2

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F20%3A73603969" target="_blank" >RIV/61989592:15310/20:73603969 - isvavai.cz</a>

Výsledek na webu

<a href="https://iopscience.iop.org/article/10.1088/2053-1583/ab9dd4" target="_blank" >https://iopscience.iop.org/article/10.1088/2053-1583/ab9dd4</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1088/2053-1583/ab9dd4" target="_blank" >10.1088/2053-1583/ab9dd4</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Oxidation of metallic two-dimensional transition metal dichalcogenides: 1T-MoS(2)and 1T-TaS2

Popis výsledku v původním jazyce

Molybdenum disulphide (MoS2) and tantalum disulphide (TaS2) are well-known members of the transition metal dichalcogenide (TMD) family. They occur naturally in hexagonal (2H) forms but can also be synthesized in metallic trigonal (1T) phases that are active hydrogen evolution catalysts and exhibit interesting phenomena such as superconductivity and charge density waves. Sparse experimental evidence indicates that 2D crystals of metallic TMDs degrade rapidly in air via an unknown oxidation mechanism. Here we present a computational study on oxidation at the edges and surfaces of 1T-MoS(2)and 1T-TaS(2)monolayers based on density functional theory calculations. Our results suggest that both 1T-MoS(2)and 1T-TaS(2)are very susceptible to oxidation because there are negligible energetic barriers to the dissociation of oxygen molecules at edge sites. However, further oxidation requires the substitution of sulphur atoms by oxygen, the rate of which is limited in the case of 1T-TaS(2)because the detachment of SO(2)groups is disfavored by 1.2 eV. Conversely, oxygen molecules adsorbed on 1T-MoS(2)dissociate directly at molybdenum atoms at the edge, forming intermediate S-O-Mo structures that facilitate the subsequent formation and detachment of SO2. Oxidation is not harmful to the catalysis of the hydrogen evolution reaction on 1T-MoS(2)but is detrimental to that on 1T-TaS2, which explains some apparently inconsistent experimental results. These results provide new insights into the mechanism of ambient oxidative degradation of metallic TMDs and the effect of oxidation on their catalytic properties.

Název v anglickém jazyce

Oxidation of metallic two-dimensional transition metal dichalcogenides: 1T-MoS(2)and 1T-TaS2

Popis výsledku anglicky

Molybdenum disulphide (MoS2) and tantalum disulphide (TaS2) are well-known members of the transition metal dichalcogenide (TMD) family. They occur naturally in hexagonal (2H) forms but can also be synthesized in metallic trigonal (1T) phases that are active hydrogen evolution catalysts and exhibit interesting phenomena such as superconductivity and charge density waves. Sparse experimental evidence indicates that 2D crystals of metallic TMDs degrade rapidly in air via an unknown oxidation mechanism. Here we present a computational study on oxidation at the edges and surfaces of 1T-MoS(2)and 1T-TaS(2)monolayers based on density functional theory calculations. Our results suggest that both 1T-MoS(2)and 1T-TaS(2)are very susceptible to oxidation because there are negligible energetic barriers to the dissociation of oxygen molecules at edge sites. However, further oxidation requires the substitution of sulphur atoms by oxygen, the rate of which is limited in the case of 1T-TaS(2)because the detachment of SO(2)groups is disfavored by 1.2 eV. Conversely, oxygen molecules adsorbed on 1T-MoS(2)dissociate directly at molybdenum atoms at the edge, forming intermediate S-O-Mo structures that facilitate the subsequent formation and detachment of SO2. Oxidation is not harmful to the catalysis of the hydrogen evolution reaction on 1T-MoS(2)but is detrimental to that on 1T-TaS2, which explains some apparently inconsistent experimental results. These results provide new insights into the mechanism of ambient oxidative degradation of metallic TMDs and the effect of oxidation on their catalytic properties.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

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)<br>S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2020

Kód důvěrnosti údajů

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

Název periodika

2D Materials

ISSN

2053-1583

e-ISSN

—

Svazek periodika

7

Číslo periodika v rámci svazku

4

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

13

Strana od-do

"045005-1"-"045005-13"

Kód UT WoS článku

000553697300001

EID výsledku v databázi Scopus

2-s2.0-85088912563