Photocatalytic Optimization of ATiO3 Codoped with Se/Zr: A DFT Study for Hydrogen Production.

IF 3.2 3区 材料科学 Q3 CHEMISTRY, PHYSICAL
Materials Pub Date : 2025-09-19 DOI:10.3390/ma18184389
Abdellah Bouzaid, Younes Ziat, Hamza Belkhanchi
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引用次数: 0

Abstract

Recent advances in energy conversion technologies, especially solar-driven photocatalytic water splitting, are vital for satisfying the increasing global need for sustainable and clean energy. Perovskite oxides have attracted considerable attention among photocatalytic materials due to their tunable electronic structures, exceptional stability, and promise for effective hydrogen generation and environmental remediation. In this study, the optoelectronic and photocatalytic (PC) characteristics of ATiO3 (A = Ca, Mg) perovskites, undoped and codoped with Se and Zr, have been analyzed using ab initio simulations based on the density functional theory (DFT). The calculated formation energies for codoped systems range from -1.01 to -3.32 Ry/atom, confirming their thermodynamic stability. Furthermore, band structure calculations indicate that the undoped compounds CaTiO3 and MgTiO3 possess indirect band gaps of 2.766 eV and 2.926 eV, respectively. In contrast, codoping alters the electronic properties by changing the band gap from indirect to direct and reducing its energy, resulting in the direct band gap values 2.153 eV, 1.374 eV, 2.159 eV, and 1.726 eV for the compounds Ca8Ti7Zr1O23Se1, Ca8Ti6Zr2O22Se2, Mg8Ti7Zr1O23Se1, and Mg8Ti6Zr2O22Se2, respectively. Additionally, this codoping improves light absorption and optical conductivity in the visible and ultraviolet ranges. These enhancements become increasingly evident with elevated dopant concentrations, leading to intensified light-matter interactions. Analysis of the band edge potentials reveals that the Se-/Zr-codoped CaTiO3 compounds satisfy the necessary criteria for the photodissociation of water, conferring on them an ability to generate H2 and O2 under light irradiation. However, under different pH conditions, Se-/Zr-codoped MgTiO3 is expected to perform better at higher pH levels, while Se-/Zr-codoped CaTiO3 is more effective at lower pH levels. These findings highlight the promise of codoped materials for renewable energy applications, such as solar-driven hydrogen production and optoelectronic devices, with pH being a critical factor in enhancing their photocatalytic performance.

Se/Zr共掺杂ATiO3光催化制氢的DFT研究。
能源转换技术的最新进展,特别是太阳能驱动的光催化水分解,对于满足全球对可持续和清洁能源日益增长的需求至关重要。钙钛矿氧化物由于其可调谐的电子结构、优异的稳定性以及在有效制氢和环境修复方面的前景,在光催化材料中引起了相当大的关注。本研究基于密度泛函理论(DFT),利用从头算模拟分析了未掺杂和共掺杂Se和Zr的ATiO3 (A = Ca, Mg)钙钛矿的光电和光催化(PC)特性。共掺杂体系的形成能在-1.01 ~ -3.32 Ry/原子之间,证实了其热力学稳定性。此外,带结构计算表明,未掺杂的化合物CaTiO3和MgTiO3的间接带隙分别为2.766 eV和2.926 eV。相比之下,共掺杂通过将带隙从间接改变为直接改变并降低其能量来改变电子性质,使得ca8ti7zr1023se1、Ca8Ti6Zr2O22Se2、mg8ti7zr1023se1和Mg8Ti6Zr2O22Se2的直接带隙分别为2.153 eV、1.374 eV、2.159 eV和1.726 eV。此外,这种共掺杂改善了可见光和紫外线范围内的光吸收和光电导率。随着掺杂剂浓度的升高,这些增强变得越来越明显,导致光-物质相互作用加剧。带边电位分析表明,Se-/ zr -共掺杂CaTiO3化合物满足水光解的必要条件,使其具有在光照射下生成H2和O2的能力。然而,在不同的pH条件下,Se-/ zr共掺杂的MgTiO3在较高的pH值下表现更好,而Se-/ zr共掺杂的CaTiO3在较低的pH值下表现更好。这些发现突出了共掺杂材料在可再生能源应用中的前景,例如太阳能驱动制氢和光电子器件,pH值是提高其光催化性能的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Materials
Materials MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
5.80
自引率
14.70%
发文量
7753
审稿时长
1.2 months
期刊介绍: Materials (ISSN 1996-1944) is an open access journal of related scientific research and technology development. It publishes reviews, regular research papers (articles) and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Materials provides a forum for publishing papers which advance the in-depth understanding of the relationship between the structure, the properties or the functions of all kinds of materials. Chemical syntheses, chemical structures and mechanical, chemical, electronic, magnetic and optical properties and various applications will be considered.
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