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用于光催化降解氧氟沙星的钆和锆共掺杂铋铁氧体磁性纳米颗粒

Gd and Zr Co-Doped BiFeO Magnetic Nanoparticles for Piezo-Photocatalytic Degradation of Ofloxacin.

作者信息

Liu Xuan, Chao Jie, Guo Feifei, Chang Liangliang, Zhang Xinyang, Long Wei, Xi Zengzhe

机构信息

Shaanxi Key Laboratory of Photoelectric Functional Materials and Devices, School of Materials and Chemical Engineering, Xi'an Technological University, Xi'an 710021, China.

Shaanxi Engineering Research Center for Mineral Resources Clean & Efficient Conversion and New Materials, Research Centre of Grapheme Technology and Application, Shangluo University, Shangluo 726000, China.

出版信息

Nanomaterials (Basel). 2025 May 24;15(11):792. doi: 10.3390/nano15110792.

Abstract

Addressing the limitations of poor piezoelectric photocatalytic activity and insufficient magnetic recovery in pure BiFeO nanoparticles, Gd and Zr co-doped BiFeO nanoparticles were synthesized via the sol-gel method. The structural characterization revealed a rhombohedral-to-orthorhombic phase transition with reduced grain size (~35 nm) and lattice distortion due to dopant incorporation. An XPS analysis confirmed Fe dominance and oxygen vacancy enrichment, while optimized BGFZ9 exhibited enhanced remanent magnetization (0.1753 emu/g, 14.14 increase) compared to undoped BFO. The synergistic piezo-photocatalytic system achieved 81.08% Ofloxacin degradation within 120 min (rate constant: 0.0136 min, 1.26 higher than BFO) through stress-induced piezoelectric fields that promoted electron transfer for ·O/·OH radical generation via O reduction. The Ofloxacin degradation efficiency decreased to 24.36% after four cycles, with structural integrity confirmed by XRD phase stability. This work demonstrates a triple-optimization mechanism (crystal phase engineering, defect modulation, and magnetic enhancement) for designing magnetically recoverable multiferroic catalysts in pharmaceutical wastewater treatment.

摘要

针对纯BiFeO纳米颗粒中压电光催化活性差和磁回收不足的局限性,通过溶胶 - 凝胶法合成了Gd和Zr共掺杂的BiFeO纳米颗粒。结构表征显示,由于掺杂剂的掺入,发生了从菱面体到正交晶相的转变,晶粒尺寸减小(约35 nm)且晶格畸变。XPS分析证实了Fe的优势和氧空位的富集,而优化后的BGFZ9与未掺杂的BFO相比,剩磁增强(0.1753 emu/g,增加了14.14)。协同压电光催化系统通过应力诱导的压电场在120分钟内实现了81.08%的氧氟沙星降解(速率常数:0.0136 min,比BFO高1.26倍),该压电场通过O还原促进电子转移以产生·O/·OH自由基。四个循环后,氧氟沙星降解效率降至24.36%,XRD相稳定性证实了结构完整性。这项工作展示了一种用于设计用于制药废水处理的磁可回收多铁性催化剂的三重优化机制(晶相工程、缺陷调制和磁增强)。

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