亚乙基亚胺
超顺磁性
纳米颗粒
透射电子显微镜
化学
化学工程
水溶液
材料科学
纳米技术
有机化学
聚合物
磁化
工程类
物理
量子力学
磁场
复合材料
作者
Francis Y. Acquaye,Rabin Mahat,Shane C. Street
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-09-30
卷期号:37 (40): 11750-11758
被引量:2
标识
DOI:10.1021/acs.langmuir.1c01662
摘要
Using poly(ethyleneimine) (PEI) polymer substrates, spherical FePt nanoparticles (NPs) with diameter <10 nm have been synthesized by photoreduction and chemical reduction in aqueous media at room temperature. In the photoreduction approach, PEvI acts as both the template into which the metal ions are coordinated and as a reductant when irradiated by ultraviolet light. In the chemical reduction method, PEI acts as only a template, with NaBH4 as the reductant. The as-prepared NPs were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), and vibrating sample magnetometry (VSM). Starting from the same precursor state and relative concentrations, the as-prepared NPs from both methods are spherical, crystalline solid solutions with a chemically disordered face-centered cubic (fcc) structure. The as-prepared NPs from both methods are superparamagnetic with some contribution from a ferromagnetic phase. The photoreduced NPs have broad size distribution of (5 ± 1.0 nm), an expanded lattice (3.913 Å), and relatively lower magnetic moment (0.02 emu/g) compared to the narrower size distribution (4 ± 0.7 nm), shortened lattice (3.890 Å), and a dominant moment (15 emu/g) of the chemically reduced NPs. The difference in the rate of particle formation apparently leads to a low efficiency of FePt NP formation via photoreduction compared to chemical reduction.
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