Feld Artur, Weimer Agnes, Kornowski Andreas, Winckelmans Naomi, Merkl Jan-Philip, Kloust Hauke, Zierold Robert, Schmidtke Christian, Schotten Theo, Riedner Maria, Bals Sara, Weller Horst
Institute of Physical Chemistry , Hamburg University , Grindelallee 117 , D-20146 Hamburg , Germany.
The Hamburg Center for Ultrafast Imaging , Hamburg University , Luruper Chaussee 149 , D-22761 Hamburg , Germany.
ACS Nano. 2019 Jan 22;13(1):152-162. doi: 10.1021/acsnano.8b05032. Epub 2018 Dec 17.
Herein, we demonstrate that meticulous and in-depth analysis of the reaction mechanisms of nanoparticle formation is rewarded by full control of the size, shape, and crystal structure of superparamagnetic iron oxide nanocrystals during synthesis. Starting from two iron sources, iron(II) and iron(III) carbonate, a strict separation of oleate formation from the generation of reactive pyrolysis products and concomitant nucleation of iron oxide nanoparticles was achieved. This protocol enabled us to analyze each step of nanoparticle formation independently in depth. The progress of the entire reaction was monitored via matrix-assisted laser desorption ionization time-of-flight mass spectrometry and gas chromatography, thus providing insight into the formation of various iron oleate species prior to nucleation. Interestingly, due to the intrinsic strongly reductive pyrolysis conditions of the oleate intermediates and redox process in early stages of the synthesis, pristine iron oxide nuclei were composed exclusively from wüstite irrespective of the oxidation state of the iron source. Controlling the reaction conditions provided a very broad range of size- and shape-defined monodispersed iron oxide nanoparticles. Curiously, after nucleation, star-shaped nanocrystals were obtained that underwent metamorphism toward cubic-shaped particles. Electron energy loss spectroscopy tomography revealed ex post oxidation of the primary wustite nanocrystal, providing a full 3D image of Fe and Fe distribution within. Overall, we developed a highly flexible synthesis, yielding multi-gram amounts of well-defined iron oxide nanocrystals of different sizes and morphologies.
在此,我们证明,对纳米颗粒形成反应机制进行细致深入的分析,会在合成过程中对超顺磁性氧化铁纳米晶体的尺寸、形状和晶体结构实现完全控制时得到回报。从两种铁源,即碳酸亚铁(II)和碳酸铁(III)出发,实现了油酸酯形成与活性热解产物生成以及氧化铁纳米颗粒伴随成核的严格分离。该方案使我们能够深入独立地分析纳米颗粒形成的每一步。通过基质辅助激光解吸电离飞行时间质谱和气相色谱监测整个反应的进程,从而深入了解成核前各种油酸铁物种的形成。有趣的是,由于油酸酯中间体固有的强还原热解条件以及合成早期的氧化还原过程,无论铁源的氧化态如何,原始氧化铁核均仅由方铁矿组成。控制反应条件可提供非常广泛的尺寸和形状定义明确的单分散氧化铁纳米颗粒。奇怪的是,成核后获得了星形纳米晶体,其会向立方体形颗粒发生变质。电子能量损失谱断层扫描揭示了原生方铁矿纳米晶体的事后氧化,提供了其中铁和铁分布的完整三维图像。总体而言,我们开发了一种高度灵活的合成方法,可生产多克量的不同尺寸和形态的定义明确的氧化铁纳米晶体。