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Facile combustion synthesis, structural, morphological, optical and antibacterial studies of Bi1-xAlxFeO3 (0.0 = x = 0.15) nanoparticles

机译:Bi1-XalxFeO3(0.0 <0.0 <= 0.015)纳米颗粒的嵌合燃烧合成,结构,形态学,光学和抗菌和抗菌研究

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摘要

In this study, undoped and Al-doped BiFeO3 (Bi1-xAlxFeO3 : x = 0.0, 0.05, 0.1 and 0.15) nanoparticles were successfully prepared by solution combustion method using urea as the fuel. The obtained product was sintered at 550 degrees C for 2 h to obtain pure phase. The as-prepared samples were characterized by powder XRD, FT-IR, FE-SEM, EDX, TEM, UV-Vis absorption and PL spectroscopic analysis. Powder XRD study revealed that the synthesized nano-powders exhibit rhombohedral structure. The average crystallite size of the samples decreased from 56.25 to 48.55 nm with "x". Surface morphology of the samples were analyzed by FE-SEM and TEM micrograph technique and the grain distribution was not quite homogeneous and observed agglomeration, which is mainly due to the magnetic interaction among the particles. EDX analysis showed that the presence of Bi, Fe, O and Al peaks only without any form of impurity peak in all products. PL spectroscopy showed a high intense peak at 464 nm, which was attributed to blue emission. Antibacterial activity of Bi1-xAlxFeO3 nanoparticles was found to be enhanced with increase in Al doping concentration as it caused a reduction in the grain size of the samples.
机译:在该研究中,通过使用尿素作为燃料,通过溶液燃烧方法成功地制备了未掺杂的和抗铝异种3(Bi1-XalxFeO 3:X = 0.05,0.1和0.15)。将所得产物在550℃下烧结2小时以获得纯相。通过粉末XRD,FT-IR,Fe-SEM,EDX,TEM,UV-Vis吸收和PL光谱分析表征了如制备的样品。粉末XRD研究表明,合成的纳米粉末表现出菱形结构。样品的平均微晶尺寸从56.25降至48.55nm,“x”减少。通过Fe-SEM和TEM显微照片技术分析样品的表面形态,并且晶粒分布不是非常均匀的并且观察到的聚集,这主要是由于颗粒之间的磁相互作用。 EDX分析表明,只有在所有产品中没有任何形式的杂质峰值,Bi,Fe,O和Al峰的存在。 PL光谱显示在464nm处显示出高强度峰,归因于蓝色排放。发现BI1-XALXFEO3纳米颗粒的抗菌活性随着Al掺杂浓度的增加而增强,因为它导致样品的晶粒尺寸的降低。

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