Khammang Alex, Wright Joshua T, Meulenberg Robert W
Department of Physics and Astronomy and Frontier Institute for Research in Sensor Technologies, University of Maine, Orono, ME, 04469, USA.
Department of Physics, Illinois Institute of Technology, Chicago, IL, USA.
Nat Commun. 2021 Jan 19;12(1):438. doi: 10.1038/s41467-020-20712-0.
In terms of producing new advances in sustainable nanomaterials, cation exchange (CE) of post-processed colloidal nanocrystals (NCs) has opened new avenues towards producing non-toxic energy materials via simple chemical techniques. The main processes governing CE can be explained by considering hard/soft acid/base theory, but the detailed mechanism of CE, however, has been debated and has been attributed to both diffusion and vacancy processes. In this work, we have performed in situ x-ray absorption spectroscopy to further understand the mechanism of the CE of copper in solution phase CdSe NCs. The x-ray data indicates clear isosbestic points, suggestive of cooperative behavior as previously observed via optical spectroscopy. Examination of the extended x-ray absorption fine structure data points to the observation of interstitial impurities during the initial stages of CE, suggesting the diffusion process is the fundamental mechanism of CE in this system.
在可持续纳米材料取得新进展方面,后处理胶体纳米晶体(NCs)的阳离子交换(CE)通过简单的化学技术为生产无毒能源材料开辟了新途径。支配阳离子交换的主要过程可以通过硬/软酸碱理论来解释,然而,阳离子交换的详细机制一直存在争议,并且被认为与扩散过程和空位过程有关。在这项工作中,我们进行了原位X射线吸收光谱分析,以进一步了解溶液相CdSe纳米晶体中铜的阳离子交换机制。X射线数据显示出明显的等吸收点,这表明存在协同行为,正如之前通过光谱学观察到的那样。对扩展X射线吸收精细结构数据的研究表明,在阳离子交换的初始阶段观察到了间隙杂质,这表明扩散过程是该体系中阳离子交换的基本机制。