Please use this identifier to cite or link to this item:
For citation please use:
Main Title: Unfolding the role of B site-selective doping of aliovalent cations on enhancing sacrificial visible light-induced photocatalytic H2 and O2 evolution over BaTaO2N
Author(s): Hojamberdiev, Mirabbos
Vargas, Ronald
Kadirova, Zukhra C.
Kato, Kosaku
Sena, Hadi
Krasnov, Aleksei G.
Yamakata, Akira
Teshima, Katsuya
Lerch, Martin
Type: Article
Abstract: The doping of foreign cations and anions is one of the effective strategies for engineering defects and modulating the optical, electronic, and surface properties that directly govern the photocatalytic O2 and H2 evolution reactions. BaTaO2N (BTON) is a promising 600 nm-class photocatalyst because of its absorption of visible light up to 660 nm, small band gap (Eg = 1.9 eV), appropriate valence band-edge position for oxygen evolution, good stability under light irradiation in concentrated alkaline solutions, and nontoxicity. Although the photocatalytic and photoelectrochemical water-splitting efficiencies of BaTaO2N have been progressively improved, it is still far from the requirements set for practical applications. Here, we employ a 5% B site-selective doping of aliovalent metal cations (Al3+, Ga3+, Mg2+, Sc3+, and Zr4+) to enhance sacrificial visible light-induced photocatalytic H2 and O2 evolution over BaTaO2N. The results of physicochemical characterizations reveal that no significant change in crystal structure, crystal morphology, and optical absorption edge is observed upon cation doping. Therefore, the difference observed in O2 and H2 evolution during the photocatalytic reactions over pristine and doped BaTaO2N photocatalysts is explained by examining optical, electronic, and surface properties. Also, molecular dynamics (MD) is used to gain insights into the respective effect of cation doping on adsorption energy of water molecules and formed intermediates (H* for H2 evolution and HO*, O*, and HOO* for O2 evolution) on the BaTaO2N surfaces terminated with TaO6, TaN6, and TaO4N2 octahedra. Finally, the experimental reaction rates for H2 and O2 evolution are correlated well using a linear energy–performance relationship, elucidating the doping and surface-termination trends observed in the BaTaO2N photocatalysts.
Subject(s): adsorption
Issue Date: 10-Jan-2022
Date Available: 5-May-2022
Language Code: en
DDC Class: 540 Chemie und zugeordnete Wissenschaften
Sponsor/Funder: EC/H2020/793882/EU/Carbon-Oxynitride Coupled Artificial Photosynthesis System For Solar Water Splitting Beyond 600 nm/H2O-SPLIT
Journal Title: ACS Catalysis
Publisher: American Chemical Society
Volume: 12
Issue: 2
Publisher DOI: 10.1021/acscatal.1c04547
Page Start: 1403
Page End: 1414
EISSN: 2155-5435
TU Affiliation(s): Fak. 2 Mathematik und Naturwissenschaften » Inst. Chemie » FG Anorganische Chemie - Festkörper- und Materialchemie
Appears in Collections:Technische Universität Berlin » Publications

Files in This Item:
Hojamberdiev_etal_Unfolding_2022.pdf   Until 2023-01-11

Format: Adobe PDF | Size: 1.79 MB
Download   Request a copy

Item Export Bar

Items in DepositOnce are protected by copyright, with all rights reserved, unless otherwise indicated.