BiFe0.5Cr0.5O3纳米催化剂用于可持续太阳能光驱动制药废水净化

IF 4.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2025-05-15 DOI:10.1039/D5RA01638J
Titas Vincent Rozario, Mohasin Tarek and M. A. Basith
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引用次数: 0

摘要

制药废水污染,特别是来自抗生素的污染,由于抗生素耐药细菌和常规治疗无效,造成严重的环境和健康风险。本研究采用溶胶-凝胶法制备了BiFe0.5Cr0.5O3 (BFCO)纳米颗粒,并研究了其作为可见光驱动光催化剂在太阳照射下降解环丙沙星(CIP)和左氧氟沙星(LFX)。结构分析证实了Cr3+掺入的单相钙钛矿结构,增强了电荷分离和可见光吸收。通过XPS和拉曼光谱发现,氧空位的存在对电荷转移和活性氧(ROS)的产生起着至关重要的作用。综合电化学和光电化学分析,包括CV、LSV和EIS,证实了光照下电荷输运增强和界面电阻降低。带隙为1.87 eV的BFCO具有较高的太阳能利用效率,在240分钟内达到70.35%的CIP和94%的LFX降解,符合准一级动力学。活化能从33.61±5.88降低到19.69±3.94 kJ mol−1 K−1,证实了催化效率的提高。LFX的表观量子收益率(AQY)为34.9%,进一步突显了其优越的活性。清除剂研究发现,电子(e−)和超氧化物(O2−)自由基是驱动抗生素降解的关键活性氧,而氧空位促进了电荷分离和活性氧的形成。可重用性测试证实了BFCO在多个循环中的稳定性,保持了其结构、形态和光学完整性。降解机制包括太阳诱导的电子-空穴对生成,电荷转移到氧空位,以及随后的氧化还原反应,将抗生素分解成无毒副产物。Cr取代、氧空位和混合价态的协同作用显著提高了BFCO的光催化效率,表明BFCO具有大规模环境修复的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

BiFe0.5Cr0.5O3 nanocatalysts for sustainable solar-light-driven purification of pharmaceutical wastewater†

BiFe0.5Cr0.5O3 nanocatalysts for sustainable solar-light-driven purification of pharmaceutical wastewater†

Pharmaceutical wastewater contamination, particularly from antibiotics, poses severe environmental and health risks due to antibiotic-resistant bacteria and the inefficacy of conventional treatments. In this study, BiFe0.5Cr0.5O3 (BFCO) nanoparticles were synthesized via the sol–gel method and investigated as a visible-light-driven photocatalyst for ciprofloxacin (CIP) and levofloxacin (LFX) degradation under solar irradiation. The structural analysis confirmed a single-phase perovskite structure with Cr3+ incorporation, enhancing charge separation and visible-light absorption. The presence of oxygen vacancies, identified through XPS and Raman spectroscopy, played a crucial role in charge transfer and reactive oxygen species (ROS) generation. Comprehensive electrochemical and photoelectrochemical analyses, including CV, LSV, and EIS, confirmed enhanced charge transport and reduced interfacial resistance under illumination. BFCO, with a bandgap of 1.87 eV, exhibited efficient solar energy utilization, achieving 70.35% CIP and 94% LFX degradation within 240 minutes, following pseudo-first-order kinetics. The activation energy decreased from 33.61 ± 5.88 to 19.69 ± 3.94 kJ mol−1 K−1, confirming enhanced catalytic efficiency. An apparent quantum yield (AQY) of 34.9% for LFX further underscored its superior activity. Scavenger studies identified electron (e) and superoxide (˙O2) radicals as key ROS driving antibiotic degradation, while oxygen vacancies improved charge separation and ROS formation. Reusability tests confirmed BFCO's stability across multiple cycles, maintaining its structural, morphological, and optical integrity. The degradation mechanism involves solar-induced electron–hole pair generation, charge transfer to oxygen vacancies, and subsequent redox reactions that break down antibiotics into non-toxic byproducts. The synergistic effects of Cr substitution, oxygen vacancies, and mixed-valence states significantly enhanced photocatalytic efficiency, demonstrating BFCO's potential for large-scale environmental remediation.

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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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