相互作用的磁性纳米粒子群中的奈尔弛豫和布朗弛豫的非脱染行为

Materials Pub Date : 2024-08-09 DOI:10.3390/ma17163957
Cristian E. Botez, Jeffrey Knoop
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引用次数: 0

摘要

我们利用交流电感测量来研究不同浓度的 Fe3O4/Isopar M 纳米磁性流体中的超旋弛豫。在不同频率下收集的温度分辨数据(χ″ vs. T|f)揭示了载流体冰点(TF = 197 K)以下和冰点以上的磁事件:χ″在温度 Tp1 和 Tp2 分别约为 75 K 和 225 K 时显示峰值。在 TF 以下,内尔机制完全负责超旋弛豫(因为载流子流体是冻结的),我们发现弛豫时间 τN(Tp1)的温度依赖性可以用多尔曼-贝赛斯-菲奥拉尼(DBF)模型很好地描述:τNT=τrexpEB+EadkB T。然而,我们发现有证据表明,在高密度样品中观察到的 Tp2 峰对应的有效弛豫时间 τeff 并不遵循罗森斯韦格公式 1τeff=1τN+1τB 所描述的典型德拜行为。首先,τeff 在 225 K 时为 5 × 10-5 s,比通过上述 DBF 分析推断出的内尔对应值 τN~8 × 10-8 s 高出近三个数量级。因此,1τN≫1τeff 显然与罗森斯魏格公式不符。其次,观测到的有效弛豫时间 τeff(Tp2) 的温度依赖性可以用 τB-1T=Tγ0exp-E′kBT-T0′ 很好地描述,这个模型完全基于流体力学布朗弛豫,τB(T)=3ηTVHkBT,结合粘度温度变化的活化定律,ηT=η0expE′/kB(T-T0′。最佳拟合结果为 γ0=3ηVHkB = 1.6 × 10-5 s-K,E′/kB = 312 K,T0′ = 178 K。最后,在稀释程度较高的样品中,温度较高的 Tp2 峰消失了(δ ≤ 0.02)。这表明,稀释抑制了通过聚集形成较大的流体动力粒子,而聚集是在致密样品中观察到布朗弛豫的原因。我们的发现证实了之前蒙特卡洛计算的结果,这些发现非常重要,因为它们可能为合成生物医学应用的功能性磁性铁流体带来新的策略。
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Non-Debye Behavior of the Néel and Brown Relaxation in Interacting Magnetic Nanoparticle Ensembles
We used ac-susceptibility measurements to study the superspin relaxation in Fe3O4/Isopar M nanomagnetic fluids of different concentrations. Temperature-resolved data collected at different frequencies, χ″ vs. T|f, reveal magnetic events both below and above the freezing point of the carrier fluid (TF = 197 K): χ″ shows peaks at temperatures Tp1 and Tp2 around 75 K and 225 K, respectively. Below TF, the Néel mechanism is entirely responsible for the superspin relaxation (as the carrier fluid is frozen), and we found that the temperature dependence of the relaxation time, τN(Tp1), is well described by the Dorman–Bessais–Fiorani (DBF) model: τNT=τrexp⁡EB+EadkB T. Above TF, both the internal (Néel) and the Brownian superspin relaxation mechanisms are active. Yet, we found evidence that the effective relaxation times, τeff, corresponding to the Tp2 peaks observed in the denser samples do not follow the typical Debye behavior described by the Rosensweig formula 1τeff=1τN+1τB. First, τeff is 5 × 10−5 s at 225 K, almost three orders of magnitude more that its Néel counterpart, τN~8 × 10−8 s, estimated by extrapolating the above-mentioned DBF analysis. Thus, 1τN≫1τeff, which is clearly not consistent with the Rosensweig formula. Second, the observed temperature dependence of the effective relaxation time, τeff(Tp2), is excellently described by τB−1T=Tγ0exp⁡−E′kBT−T0′, a model solely based on the hydrodynamic Brown relaxation, τB(T)=3ηTVHkBT, combined with an activation law for the temperature variation of the viscosity, ηT=η0exp⁡E′/kB(T−T0′. The best fit yields γ0=3ηVHkB = 1.6 × 10−5 s·K, E′/kB = 312 K, and T0′ = 178 K. Finally, the higher temperature Tp2 peaks vanish in the more diluted samples (δ ≤ 0.02). This indicates that the formation of larger hydrodynamic particles via aggregation, which is responsible for the observed Brownian relaxation in dense samples, is inhibited by dilution. Our findings, corroborating previous results from Monte Carlo calculations, are important because they might lead to new strategies to synthesize functional magnetic ferrofluids for biomedical applications.
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