Investigating the chemical and physical aspects: optical and electrical properties of TiO2, TiO2: Fe, and Fe/TiO2 (111) through DFT analysis

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23640%2F24%3A43974567" target="_blank" >RIV/49777513:23640/24:43974567 - isvavai.cz</a>

Výsledek na webu

<a href="https://doi.org/10.1007/s11696-023-03078-7" target="_blank" >https://doi.org/10.1007/s11696-023-03078-7</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/s11696-023-03078-7" target="_blank" >10.1007/s11696-023-03078-7</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Investigating the chemical and physical aspects: optical and electrical properties of TiO2, TiO2: Fe, and Fe/TiO2 (111) through DFT analysis

Popis výsledku v původním jazyce

The development of a thin film titanium dioxide (TiO2) depends on an understanding of complex electronic structure and charge transport properties. The utilization of simulation studies will help us understand the complicated system at the atomic level. Here, utilizing Hubbard&apos;s modified first-principles density functional theory (DFT + U), a theoretically created thin film TiO2 (111) interface model is provided. Generalized gradient approximation with Perdew-Burke-Ernzerhof assistance (GGA + PBE) was used to model structural properties, while Hubbard&apos;s modified (GGA + U) exchange correlation functional was used to simulate optoelectronic properties. The addition, i.e., doping and adsorption, of Fe to the TiO2 rutile (111) surface transfers its bandgap energy from 2.95 eV to a metallic nature, thereby enhancing its responsiveness to visible light by lowering the energy required for electron transitions. The enhanced visible light absorption and efficient charge separation worked together to significantly improve the hybrid photo catalyst&apos;s photocatalytic performance. The research utilized the DFT method along with the (GGA + U) technique to evaluate both the band structure and density of states (DOS). The analysis of the electronic structure shows that the band gap for the pristine but for the doped and adsorbed systems the nature of the materials changes to metallic. The DOS calculations indicate hybridization between O-orbitals and Fe-orbitals in the vicinity of the conduction band minimum for both channels due to the doped system, and for the maximum in the case of the adsorbed system, the impurity introduces an energy level that lowers the band gap. The research carried out computations to determine the band structure and density of states for (TiO2) doped with Fe and Fe-adsorbed. The results demonstrate that the doped and adsorption is considered to be a more advantageous approach than the pristine because of the maximum absorption in visible region. When the Fe atoms are adsorbed on TiO2 (111), there is a maximum increase in the adsorption energy. The study examines the photo activity mechanism by investigating the impact of Fe on the semiconductor&apos;s absorption edge. This type of semiconductor, with Fe adsorbed on TiO2 (111), has potential applications in the fields of photovoltaic, photocells, and electronics.

Název v anglickém jazyce

Investigating the chemical and physical aspects: optical and electrical properties of TiO2, TiO2: Fe, and Fe/TiO2 (111) through DFT analysis

Popis výsledku anglicky

The development of a thin film titanium dioxide (TiO2) depends on an understanding of complex electronic structure and charge transport properties. The utilization of simulation studies will help us understand the complicated system at the atomic level. Here, utilizing Hubbard&apos;s modified first-principles density functional theory (DFT + U), a theoretically created thin film TiO2 (111) interface model is provided. Generalized gradient approximation with Perdew-Burke-Ernzerhof assistance (GGA + PBE) was used to model structural properties, while Hubbard&apos;s modified (GGA + U) exchange correlation functional was used to simulate optoelectronic properties. The addition, i.e., doping and adsorption, of Fe to the TiO2 rutile (111) surface transfers its bandgap energy from 2.95 eV to a metallic nature, thereby enhancing its responsiveness to visible light by lowering the energy required for electron transitions. The enhanced visible light absorption and efficient charge separation worked together to significantly improve the hybrid photo catalyst&apos;s photocatalytic performance. The research utilized the DFT method along with the (GGA + U) technique to evaluate both the band structure and density of states (DOS). The analysis of the electronic structure shows that the band gap for the pristine but for the doped and adsorbed systems the nature of the materials changes to metallic. The DOS calculations indicate hybridization between O-orbitals and Fe-orbitals in the vicinity of the conduction band minimum for both channels due to the doped system, and for the maximum in the case of the adsorbed system, the impurity introduces an energy level that lowers the band gap. The research carried out computations to determine the band structure and density of states for (TiO2) doped with Fe and Fe-adsorbed. The results demonstrate that the doped and adsorption is considered to be a more advantageous approach than the pristine because of the maximum absorption in visible region. When the Fe atoms are adsorbed on TiO2 (111), there is a maximum increase in the adsorption energy. The study examines the photo activity mechanism by investigating the impact of Fe on the semiconductor&apos;s absorption edge. This type of semiconductor, with Fe adsorbed on TiO2 (111), has potential applications in the fields of photovoltaic, photocells, and electronics.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2024

Kód důvěrnosti údajů

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

Název periodika

Chemical Papers

ISSN

0366-6352

e-ISSN

2585-7290

Svazek periodika

78

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

CH - Švýcarská konfederace

Počet stran výsledku

13

Strana od-do

283-294

Kód UT WoS článku

001075352700001

EID výsledku v databázi Scopus

2-s2.0-85172987784