Palade Petru, Comanescu Cezar, Kuncser Andrei, Berger Daniela, Matei Cristian, Iacob Nicusor, Kuncser Victor
National Institute of Materials Physics, Atomistilor 405A, 077125 Magurele, Romania.
Polytechnic University of Bucharest, Faculty of Applied Chemistry and Materials Science 1-7 Polizu St, Bucharest 011061, Romania.
Nanomaterials (Basel). 2020 Mar 6;10(3):476. doi: 10.3390/nano10030476.
A facile and cheap surfactant-assisted hydrothermal method was used to prepare mesoporous cobalt ferrite nanosystems with BET surface area up to 151 m/g. These mesostructures with high BET surface areas and pore sizes are made from assemblies of nanoparticles (NPs) with average sizes between 7.8 and 9.6 nm depending on the initial pH conditions. The pH proved to be the key factor for controlling not only NP size, but also the phase purity and the porosity properties of the mesostructures. At pH values lower than 7, a parasite hematite phase begins to form. The sample obtained at pH = 7.3 has magnetization at saturation M = 38 emu/g at 300 K (54.3 emu/g at 10 K) and BET surface area S = 151 m/g, whereas the one obtained at pH = 8.3 has M = 68 emu/g at 300 K (83.6 emu/g at 10 K) and S = 101 m/g. The magnetic coercive field values at 10 K are high at up to 12,780 Oe, with a maximum coercive field reached for the sample obtained at pH = 8.3. Decreased magnetic performances are obtained at pH values higher than 9. The iron occupancies of the tetrahedral and octahedral sites belonging to the cobalt ferrite spinel structure were extracted through decomposition of the Mössbauer patterns in spectral components. The magnetic anisotropy constants of the investigated NPs were estimated from the temperature dependence of the hyperfine magnetic field. Taking into consideration the high values of BET surface area and the magnetic anisotropy constants as well as the significant magnetizations for saturation at ambient temperature, and the fact that all parameters can be adjusted through the initial pH conditions, these materials are very promising as recyclable anti-polluting agents, magnetically separable catalysts, and targeted drug delivery vehicles.
采用一种简便且廉价的表面活性剂辅助水热法制备了比表面积高达151 m²/g的介孔钴铁氧体纳米体系。这些具有高比表面积和孔径的介观结构由平均尺寸在7.8至9.6 nm之间的纳米颗粒(NP)组装而成,具体尺寸取决于初始pH条件。事实证明,pH不仅是控制NP尺寸的关键因素,也是控制介观结构的相纯度和孔隙率特性的关键因素。在pH值低于7时,会开始形成寄生赤铁矿相。在pH = 7.3时获得的样品在300 K下的饱和磁化强度M = 38 emu/g(在10 K下为54.3 emu/g),比表面积S = 151 m²/g,而在pH = 8.3时获得的样品在300 K下的M = 68 emu/g(在10 K下为83.6 emu/g),S = 101 m²/g。在10 K时的磁矫顽场值高达12,780 Oe,其中在pH = 8.3时获得的样品达到最大矫顽场。在pH值高于9时,磁性能会下降。通过将穆斯堡尔谱分解为光谱成分,提取了属于钴铁氧体尖晶石结构的四面体和八面体位点的铁占有率。根据超精细磁场的温度依赖性估算了所研究NP的磁各向异性常数。考虑到比表面积、磁各向异性常数的高值以及室温下显著的饱和磁化强度,并且所有参数都可以通过初始pH条件进行调节,这些材料作为可回收的抗污染剂、磁分离催化剂和靶向药物递送载体非常有前景。