煅烧温度对溶胶-凝胶法制备纳米钴铁氧体结构、形貌、磁性、电学和光学性能的影响

IF 4.7 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Md. Farid Ahmed, Afia Yasmin, Bristy Biswas, Md. Lutfor Rahman, Juliya Khanam, Rabeya Jahan Rakhi, Mahmuda Hakim, Md. Sahadat Hossain, Firoz Ahmed, Israt Jahan Lithi and Nahid Sharmin
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引用次数: 0

摘要

溶胶-凝胶法制备铁酸钴纳米颗粒(CoFe2O4)是一种高效、经济的制备方法。在不同的煅烧温度(500℃、600℃、700℃、800℃、900℃和1000℃)下,用硝酸钴[Co(NO3)2·6H2O]、硝酸铁[Fe(NO3)3·9H2O]、柠檬酸(C6H8O7·H2O)、甘油(C3H8O3)和氢氧化铵(NH4OH)进行煅烧。结果表明,不同的煅烧温度会影响结晶的大小,即温度越高,晶体的大小越大。为了研究溶胶-凝胶法制备的钴铁氧体纳米颗粒的结构、光学、磁性和介电性能,采用x射线衍射(XRD)、同步热分析(STA)、振动样品磁强计(VSM)、扫描电镜(SEM)和傅里叶变换红外(FTIR)光谱等表征技术进行表征。XRD证实了NPs的面心立方结构。在1000℃时,样品T6表现出较高的zeta电位,证明了溶液的稳定性。采用Debye-Scherrer (D-S)法、Williamson-Hall (W-H)法、Halder-Wagner (H-W)法和尺寸-应变图(SSP)技术测量晶体尺寸和晶格应变。XRD数据证实所有样品均存在钴铁素体NPs的单尖晶石相。T1样品的晶粒尺寸最小,T6样品的晶粒尺寸在33 ~ 169 nm之间。在402 ~ 403 cm−1和576 ~ 580 cm−1处观察到的两个FTIR吸收带分别是由于尖晶石钴铁素体中八面体的M-O键和四面体部位的M-O键。SEM显微图显示,制备的NPs呈球形,分布均匀。经800℃退火后,样品的平均粒径为46.72 nm。最大饱和磁化强度约为85 ~ 62 emu g−1。利用Kubelka-Munk方法计算了带隙能,发现随着退火温度的升高,晶体尺寸增大,带隙能在3.00 ~ 3.52 eV之间变化。因此,溶胶-凝胶法可以在不同的煅烧温度下改变晶体的大小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of calcination temperature on nano-cobalt ferrite synthesized by a sol–gel method for modification of its structural, morphological, magnetic, electrical and optical properties

Effect of calcination temperature on nano-cobalt ferrite synthesized by a sol–gel method for modification of its structural, morphological, magnetic, electrical and optical properties

Synthesis of cobalt ferrite (CoFe2O4) nanoparticles (NPs) through a sol–gel process is an efficient and cost-effective approach. This process is carried out at different calcination temperatures (500 °C, 600 °C, 700 °C, 800 °C, 900 °C and 1000 °C) using cobalt nitrate [Co(NO3)2·6H2O], ferric nitrate [Fe(NO3)3·9H2O], citric acid (C6H8O7·H2O), glycerol (C3H8O3), and ammonium hydroxide (NH4OH). It is found that different calcination temperatures affect the size of the crystallite produced, i.e., at higher temperature the size of the crystals increases. To study the structural, optical, magnetic and dielectric properties of the cobalt ferrite nanoparticles synthesized by a sol–gel method, characterization techniques such as X-ray diffraction (XRD), simultaneous thermal analysis (STA), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy were carried out. XRD proved the face centered cubic structure of the NPs. At 1000 °C the sample T6 exhibited a higher zeta potential proving the stability of the solution. The crystallite size and lattice strain were measured by the Debye–Scherrer (D–S) method, Williamson–Hall (W–H) process, Halder–Wagner (H–W) method and size–strain plot (SSP) technique. XRD data confirm the presence of the single spinel phase of cobalt ferrite NPs for all the samples. The sample T1 showed the lowest crystallite size, and the crystallite size ranged from 33 nm to 169 nm for the T6 sample. Two FTIR absorption bands observed at about 402–403 cm−1 and 576–580 cm−1 are due to the octahedral M–O bond and the M–O bond at the tetrahedral site in the spinel cobalt ferrite, respectively. The SEM micrographs showed that the produced NPs are spherical in shape and homogenously distributed. The average particle size is found to be 46.72 nm for the sample annealed at 800 °C. The maximum saturation magnetization was found to be around 85–62 emu g−1. The band gap energy was found using the Kubelka–Munk method, and it was found that as the annealing temperature increases the size of crystals increases and band gap energy ranges from 3.00 to 3.52 eV, respectively. Thus the sol–gel method can be used to modify the crystallite size at different calcination temperatures.

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Materials Advances
Materials Advances MATERIALS SCIENCE, MULTIDISCIPLINARY-
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