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产热钴取代磁铁矿纳米颗粒的合成、表面改性及磁性分析

Synthesis, Surface Modification and Magnetic Properties Analysis of Heat-Generating Cobalt-Substituted Magnetite Nanoparticles.

作者信息

Ognjanović Miloš, Bošković Marko, Kolev Hristo, Dojčinović Biljana, Vranješ-Đurić Sanja, Antić Bratislav

机构信息

VINČA Institute of Nuclear Sciences, National Institute of the Republic of Serbia, University of Belgrade, 11351 Belgrade, Serbia.

Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.

出版信息

Nanomaterials (Basel). 2024 Apr 30;14(9):782. doi: 10.3390/nano14090782.

Abstract

Here, we present the results of the synthesis, surface modification, and properties analysis of magnetite-based nanoparticles, specifically CoFeO (S1) and CoFeO (S2). These nanoparticles were synthesized using the co-precipitation method at 80 °C for 2 h. They exhibit a single-phase nature and crystallize in a spinel-type structure (space group 3¯). Transmission electron microscopy analysis reveals that the particles are quasi-spherical in shape and approximately 11 nm in size. An observed increase in saturation magnetization, coercivity, remanence, and blocking temperature in S2 compared to S1 can be attributed to an increase in magnetocrystalline anisotropy due to the incorporation of Co ions in the crystal lattice of the parent compound (FeO). The heating efficiency of the samples was determined by fitting the Box-Lucas equation to the acquired temperature curves. The calculated Specific Loss Power () values were 46 W/g and 23 W/g (under = 200 Oe and = 252 kHz) for S1 and S2, respectively. Additionally, sample S1 was coated with citric acid (CoFeO@CA) and poly(acrylic acid) (CoFeO@PAA) to obtain stable colloids for further tests for magnetic hyperthermia applications in cancer therapy. Fits of the Box-Lucas equation provided values of 21 W/g and 34 W/g for CA- and PAA-coated samples, respectively. On the other hand, X-ray photoelectron spectroscopy analysis points to the catalytically active centers Fe/Fe and Co/Co on the particle surface, suggesting possible applications of the samples as heterogeneous self-heating catalysts in advanced oxidation processes under an AC magnetic field.

摘要

在此,我们展示了基于磁铁矿的纳米颗粒,特别是CoFeO(S1)和CoFeO(S2)的合成、表面改性及性能分析结果。这些纳米颗粒采用共沉淀法在80°C下合成2小时。它们呈现单相性质,并结晶为尖晶石型结构(空间群3¯)。透射电子显微镜分析表明,颗粒形状为准球形,尺寸约为11nm。与S1相比,S2中观察到的饱和磁化强度、矫顽力、剩磁和阻塞温度的增加可归因于由于在母体化合物(FeO)晶格中掺入Co离子导致的磁晶各向异性增加。通过将Box-Lucas方程拟合到获取的温度曲线来确定样品的加热效率。对于S1和S2,计算得到的比损耗功率()值分别为46W/g和23W/g(在=200Oe和=252kHz下)。此外,样品S1用柠檬酸(CoFeO@CA)和聚丙烯酸(CoFeO@PAA)包覆,以获得稳定的胶体,用于癌症治疗中磁热疗应用的进一步测试。Box-Lucas方程的拟合分别给出了CA包覆样品和PAA包覆样品的值为21W/g和34W/g。另一方面,X射线光电子能谱分析表明颗粒表面存在催化活性中心Fe/Fe和Co/Co,这表明样品可能作为交流磁场下高级氧化过程中的非均相自热催化剂应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a49/11085861/2261843beff3/nanomaterials-14-00782-g001.jpg

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