Beckhoff Burkhard
Physikalisch-Technische Bundesanstalt, Abbestraße 2-12, 10587 Berlin, Germany.
Nanomaterials (Basel). 2022 Jun 30;12(13):2255. doi: 10.3390/nano12132255.
Traceable characterization methods allow for the accurate correlation of the functionality or toxicity of nanomaterials with their underlaying chemical, structural or physical material properties. These correlations are required for the directed development of nanomaterials to reach target functionalities such as conversion efficiencies or selective sensitivities. The reliable characterization of nanomaterials requires techniques that often need to be adapted to the nano-scaled dimensions of the samples with respect to both the spatial dimensions of the probe and the instrumental or experimental discrimination capability. The traceability of analytical methods revealing information on chemical material properties relies on reference materials or qualified calibration samples, the spatial elemental distributions of which must be very similar to the nanomaterial of interest. At the nanoscale, however, only few well-known reference materials exist. An alternate route to establish the required traceability lays in the physical calibration of the analytical instrument's response behavior and efficiency in conjunction with a good knowledge of the various interaction probabilities. For the elemental analysis, speciation, and coordination of nanomaterials, such a physical traceability can be achieved with X-ray spectrometry. This requires the radiometric calibration of energy- and wavelength-dispersive X-ray spectrometers, as well as the reliable determination of atomic X-ray fundamental parameters using such instrumentation. In different operational configurations, the information depths, discrimination capability, and sensitivity of X-ray spectrometry can be considerably modified while preserving its traceability, allowing for the characterization of surface contamination as well as interfacial thin layer and nanoparticle chemical compositions. Furthermore, time-resolved and hybrid approaches provide access to analytical information under operando conditions or reveal dimensional information, such as elemental or species depth profiles of nanomaterials. The aim of this review is to demonstrate the absolute quantification capabilities of SI-traceable X-ray spectrometry based upon calibrated instrumentation and knowledge about X-ray interaction probabilities.
可溯源的表征方法能够准确地将纳米材料的功能或毒性与其潜在的化学、结构或物理材料特性关联起来。为了有针对性地开发纳米材料以实现诸如转换效率或选择性灵敏度等目标功能,需要建立这些关联。可靠地表征纳米材料需要一些技术,这些技术通常需要在探针的空间尺寸以及仪器或实验分辨能力方面适应样品的纳米尺度。揭示化学材料特性信息的分析方法的可溯源性依赖于参考材料或经过鉴定的校准样品,其空间元素分布必须与所关注的纳米材料非常相似。然而,在纳米尺度上,已知的参考材料很少。建立所需可溯源性的另一条途径在于结合对各种相互作用概率的充分了解,对分析仪器的响应行为和效率进行物理校准。对于纳米材料的元素分析、形态分析和配位分析,可以通过X射线光谱法实现这种物理可溯源性。这需要对能量色散和波长色散X射线光谱仪进行辐射校准,以及使用此类仪器可靠地确定原子X射线基本参数。在不同的操作配置中,X射线光谱法的信息深度、分辨能力和灵敏度可以在保持其可溯源性的同时进行显著调整,从而能够表征表面污染物以及界面薄层和纳米颗粒的化学成分。此外,时间分辨和混合方法能够在操作条件下获取分析信息或揭示尺寸信息,例如纳米材料的元素或物种深度分布。本综述的目的是基于经过校准的仪器和关于X射线相互作用概率的知识,展示国际单位制可溯源X射线光谱法的绝对定量能力。