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新型微波辅助合成法制备的高效催化活性BiFeO₃纳米颗粒

Efficient Catalytic Activity BiFeO3 Nanoparticles Prepared by Novel Microwave-Assisted Synthesis.

作者信息

Zou Jing, Gong Wanyun, Ma Jinai, Li Lu, Jiang Jizhou

出版信息

J Nanosci Nanotechnol. 2015 Feb;15(2):1304-11. doi: 10.1166/jnn.2015.9074.

Abstract

A novel microwave-assisted sol-gel method was applied to the synthesis of the single-phase perovskite bismuth ferrite nanoparticles (BFO NPs) with the mean diameter ca. 73.7 nm. The morphology was characterized by scanning electron microscope (SEM). The X-ray diffraction (XRD) revealed the rhombohedral phase with R3c space group. The weak ferromagnetic behavior at room temperature was affirmed by the vibrating sample magnetometer (VSM). According to the UV-vis diffuse reflectance spectrum (UV-DSR), the band gap energy of BFO NPs was determined to be 2.18 eV. The electrochemical activity was evaluated by BFO NPs-chitosan-glassy carbon electrode (BFO-CS-GCE) sensor for detection of p-nitrophenol contaminants. The material showed an efficient oxidation catalytic activity by degrading methylene blue (MB). It was found that the degradation efficiency of 10 mg L-1 MB at pH 6.0 was above 90.9% after ultrasound- and microwave-combined-assisted (US-MW) irradiation for 15 min with BFO NPs as catalyst and H202 as oxidant. A possible reaction mechanism of degradation of MB was also proposed.

摘要

一种新型微波辅助溶胶-凝胶法被应用于合成平均直径约为73.7 nm的单相钙钛矿型铋铁氧体纳米颗粒(BFO NPs)。通过扫描电子显微镜(SEM)对其形貌进行了表征。X射线衍射(XRD)表明其为具有R3c空间群的菱方相。振动样品磁强计(VSM)证实了其在室温下的弱铁磁行为。根据紫外-可见漫反射光谱(UV-DSR),确定BFO NPs的带隙能量为2.18 eV。通过BFO NPs-壳聚糖-玻碳电极(BFO-CS-GCE)传感器评估了其电化学活性,用于检测对硝基苯酚污染物。该材料通过降解亚甲基蓝(MB)表现出高效的氧化催化活性。结果发现,以BFO NPs为催化剂、H2O2为氧化剂,在超声和微波联合辅助(US-MW)照射15 min后,pH 6.0时10 mg L-1 MB的降解效率高于90.9%。还提出了MB降解的可能反应机理。

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