原位小角x射线散射监测金属氢氧化物薄膜电化学生长过程中的纳米结构动力学

IF 3.6 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jonas Schwan, Dr. Sabine Rosenfeldt, Prof. Anna S. Schenk
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引用次数: 0

摘要

了解纳米尺度上的结构动力学对于催化、储能和纳米技术等当前研究领域的进展至关重要。在这项研究中,我们介绍了一个内部电化学流动电池,用于实时小角度x射线散射(SAXS)实验,以监测可控条件下氢氧化钴(Co(OH)2)的电结晶。以Co(NO3)2溶液为原料,采用阴极电化学沉积法制备了Co(OH)2薄膜。SAXS数据,结合电子显微镜和光谱学,揭示了纳米级Co(OH)2血小板的形成,平均厚度为~13 nm,横向尺寸为~600 nm。时间分辨原位SAXS跟踪这些血小板的稳定生长,在120分钟内从7.8 nm到15.7 nm的厚度。此外,SAXS测量表明柠檬酸盐配体的影响,其最初抑制血小板形成并稳定球形纳米结构。随着电解质中柠檬酸盐的消耗,血小板开始形成,表明结晶机制发生了动态变化。通过采用原位SAXS,我们成功地监测了纳米级结构的时间演变,为在电化学控制条件下控制结晶的机制提供了见解。这些发现强调了内部SAXS装置在实时分析材料形成和生长过程中的多功能性,这意味着可以针对各种技术应用定制具有专用纳米结构的材料的合成参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Monitoring Nanostructural Dynamics During the Electrochemical Growth of Metal Hydroxide Thin Films by in-situ Small-Angle X-Ray Scattering

Monitoring Nanostructural Dynamics During the Electrochemical Growth of Metal Hydroxide Thin Films by in-situ Small-Angle X-Ray Scattering

Monitoring Nanostructural Dynamics During the Electrochemical Growth of Metal Hydroxide Thin Films by in-situ Small-Angle X-Ray Scattering

Monitoring Nanostructural Dynamics During the Electrochemical Growth of Metal Hydroxide Thin Films by in-situ Small-Angle X-Ray Scattering

Understanding structural dynamics on the nanoscale is essential for progress in current research areas such as catalysis, energy storage, and nanotechnology. In this study, we introduce an in-house electrochemical flow cell for real-time small-angle X-ray scattering (SAXS) experiments to monitor cobalt hydroxide (Co(OH)2) electrocrystallization under controlled conditions. Co(OH)2 films were produced via cathodic electrochemical deposition (CED) from a Co(NO3)2 solution. SAXS data, complemented by electron microscopy and spectroscopy, reveal the formation of nanoscale Co(OH)2 platelets with an average thickness of ~13 nm and a lateral size of ~600 nm. Time-resolved in-situ SAXS tracks the steady growth of these platelets, from 7.8 nm to 15.7 nm thickness over 120 min. In addition, SAXS measurements demonstrate the influence of citrate ligands, which initially suppress platelet formation and stabilize spherical nanostructures. As citrate depletes in the electrolyte, platelets begin to form, indicating a dynamic shift in crystallization mechanism. By employing in-situ SAXS, we successfully monitor the temporal evolution of nanoscale structures, offering insights into the mechanisms governing crystallization under electrochemically controlled conditions. These findings underscore the versatility of in-house SAXS setups for real-time analysis of material formation and growth processes, with implications for tailoring the synthetic parameters towards materials with dedicated nanostructures for various technological applications.

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CiteScore
7.30
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