光致发光
共沉淀
材料科学
煅烧
纳米技术
核化学
分析化学(期刊)
化学
无机化学
有机化学
光电子学
催化作用
作者
S. Deepthi,Y.S. Vidya,H.C. Manjunatha,K.N. Sridhar,S. Manjunatha,R. Munirathnam,T. Ganesh
标识
DOI:10.1016/j.inoche.2023.111101
摘要
The water soluble Fe2O3 and Fe3O4 nanoparticles (NPs) were synthesized by coprecipitation method followed by calcination. The Bragg reflections confirm the formation of hexagonal α-Fe2O3 and cubic inverse spinel structure Fe3O4 NPs. The surface morphology consists of irregular shaped agglomerated NPs. The direct energy band gap estimated from Wood and Tauc's plot was found to be 1.75 and 1.81 eV for α-Fe2O3 and Fe3O4 NPs respectively. The photoluminescence spectra and CIE clearly show the blue emission from both samples whereas high intensity is observed for Fe3O4 NPs. The cytotoxic properties of Fe2O3 and Fe3O4 NPs were studied and analyzed against MDA-MB-231 breast cancer cell line and compared with standard drug Cisplatin. Compared to Fe2O3,Fe3O4 NPs shows good cytotoxic property more than Cisplatin. Thus, the present synthesized water soluble Fe2O3 and Fe3O4 NPs might be a good candidate as a nanophosphor in display technology and a anticancer drug carrier.
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