Surface and Aqueous Geochemistry Group, Department of Geological & Environmental Sciences, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):2787-92. doi: 10.1073/pnas.0910170107. Epub 2010 Feb 1.
The natural nanomineral ferrihydrite is an important component of many environmental and soil systems and has been implicated as the inorganic core of ferritin in biological systems. Knowledge of its basic structure, composition, and extent of structural disorder is essential for understanding its reactivity, stability, and magnetic behavior, as well as changes in these properties during aging. Here we investigate compositional, structural, and magnetic changes that occur upon aging of "2-line" ferrihydrite in the presence of adsorbed citrate at elevated temperature. Whereas aging under these conditions ultimately results in the formation of hematite, analysis of the atomic pair distribution function and complementary physicochemical and magnetic data indicate formation of an intermediate ferrihydrite phase of larger particle size with few defects, more structural relaxation and electron spin ordering, and pronounced ferrimagnetism relative to its disordered ferrihydrite precursor. Our results represent an important conceptual advance in understanding the nature of structural disorder in ferrihydrite and its relation to the magnetic structure and also serve to validate a controversial, recently proposed structural model for this phase. In addition, the pathway we identify for forming ferrimagnetic ferrihydrite potentially explains the magnetic enhancement that typically precedes formation of hematite in aerobic soil and weathering environments. Such magnetic enhancement has been attributed to the formation of poorly understood, nano-sized ferrimagnets from a ferrihydrite precursor. Whereas elevated temperatures drive the transformation on timescales feasible for laboratory studies, our results also suggest that ferrimagnetic ferrihydrite could form naturally at ambient temperature given sufficient time.
天然纳米矿物水铁矿是许多环境和土壤系统的重要组成部分,并且被认为是生物系统中铁蛋白的无机核心。了解其基本结构、组成和结构无序程度对于理解其反应性、稳定性和磁行为以及这些性质在老化过程中的变化至关重要。在这里,我们研究了在高温下吸附柠檬酸存在下“2 线”水铁矿老化时发生的组成、结构和磁性变化。虽然在这些条件下老化最终会导致赤铁矿的形成,但原子对分布函数的分析以及补充的物理化学和磁性数据表明,形成了具有较大粒径、缺陷较少、结构弛豫和电子自旋有序性更强、反铁磁性更强的中间水铁矿相,与无序水铁矿前体相比。我们的结果代表了在理解水铁矿结构无序的性质及其与磁结构的关系方面的重要概念进展,也验证了最近提出的该相有争议的结构模型。此外,我们确定的形成亚铁磁性水铁矿的途径可能解释了在好氧土壤和风化环境中赤铁矿形成之前通常会出现的磁性增强现象。这种磁性增强归因于从水铁矿前体形成了难以理解的纳米级亚铁磁体。虽然高温会在实验室研究可行的时间尺度上驱动转化,但我们的结果还表明,在足够的时间内,亚铁磁性水铁矿也可能在环境温度下自然形成。