Regulating the crystal phase and morphology of XMoO4 through adjusting the ratio of iron and cobalt for significantly boosted photocatalytic degradation of methylene blue and tetracycline

IF 2.8 4区 工程技术 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC Journal of Materials Science: Materials in Electronics Pub Date : 2024-11-30 DOI:10.1007/s10854-024-13977-4
Baoxuan Hou, Chen Chen, Ting Cheng, Fei Wu, Youzhi Dai, Xiao Zhang, Yuan Tian, Jiarui Zhu, Liangliang Wu
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Abstract

Regulating the mineral phase and morphology, as one kind of new strategy for the enhancement of photocatalytic properties, displayed notable advantages in promoting the charge transfer efficiency and achieving low recombination probability of photo-generated electron and hole. Herein, novel composite photocatalysts of XMoO4 (X = Fe and Co) were systematically regulated and synthesized successfully via adjusting the proportion of iron and cobalt. The photocatalytic degradation of methylene blue (MB) and tetracycline (TE) was conducted under visible light. It was proved that the composite photocatalyst (C7F3), with the optimal cobalt/iron ratio 7:3, displayed nanosheet morphology and notable visible light absorption, and the band gap was 1.60 eV. Besides, compared to other materials, C7F3 demonstrated the most robust photodegradation ability to remove MB and TE, which was attributed to the excellent photoelectric efficiency of C7F3. Also, the composite exhibited favorable photocatalytic stability. Furthermore, photoelectric testing and density functional theory (DFT) calculations illustrated that C7F3 photocatalyst exhibited the strongest photocurrent response, the lowest charge transfer resistance and probability of photo-generated electron–hole recombination, and the most suitable bandgap width and band position (− 0.1902 to 1.4098 V). Additionally, the superoxide radicals, photo-generated electrons and holes synergistically contributed to pollutants degradation in photocatalytic system.

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通过调节铁钴比调节XMoO4的晶相和形貌,显著提高了光催化降解亚甲基蓝和四环素的效果
调节矿物相和形态作为一种增强光催化性能的新策略,在提高电荷转移效率和光生电子和空穴的低复合概率方面具有显著的优势。本文通过调节铁和钴的比例,对XMoO4 (X = Fe和Co)复合光催化剂进行了系统调控并成功合成。在可见光下进行了亚甲基蓝(MB)和四环素(TE)的光催化降解。结果表明,复合光催化剂(C7F3)在最佳钴铁比为7:3时,具有纳米片状形貌和显著的可见光吸收,带隙为1.60 eV。此外,与其他材料相比,C7F3对MB和TE的光降解能力最强,这归功于C7F3优异的光电效率。该复合材料具有良好的光催化稳定性。光电测试和密度泛函理论(DFT)计算表明,C7F3光催化剂具有最强的光电流响应、最低的电荷转移电阻和光生电子-空穴复合概率,以及最合适的带隙宽度和带隙位置(- 0.1902 ~ 1.4098 V)。在光催化系统中,光生电子和空穴协同作用促进了污染物的降解。
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来源期刊
Journal of Materials Science: Materials in Electronics
Journal of Materials Science: Materials in Electronics 工程技术-材料科学:综合
CiteScore
5.00
自引率
7.10%
发文量
1931
审稿时长
2 months
期刊介绍: The Journal of Materials Science: Materials in Electronics is an established refereed companion to the Journal of Materials Science. It publishes papers on materials and their applications in modern electronics, covering the ground between fundamental science, such as semiconductor physics, and work concerned specifically with applications. It explores the growth and preparation of new materials, as well as their processing, fabrication, bonding and encapsulation, together with the reliability, failure analysis, quality assurance and characterization related to the whole range of applications in electronics. The Journal presents papers in newly developing fields such as low dimensional structures and devices, optoelectronics including III-V compounds, glasses and linear/non-linear crystal materials and lasers, high Tc superconductors, conducting polymers, thick film materials and new contact technologies, as well as the established electronics device and circuit materials.
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