Kim Eun-Kyung, Park Dasom, Shrestha Nabeen K, Chang Jinho, Yi Cheol-Woo, Han Sung-Hwan
Institute of Materials Design, Department of Chemistry, Hanyang University, Seongdong-gu, 133791 Seoul, Republic of Korea.
Department of Chemistry, Sungshin W. University, 55 Dobong-ro, 76ga-gil, Gangbuk-gu, Seoul 142-732, Republic of Korea.
Dalton Trans. 2016 Nov 1;45(43):17312-17318. doi: 10.1039/c6dt03038f.
The present work demonstrates a highly controllable, facile and environmentally friendly aqueous solution based synthetic method for oxide contamination-free AgTe thin films on desired substrates at room temperature using ion exchange induced chemical transformation of Ag/AgO thin films. The films before and after chemical transformation reaction are characterized using an energy dispersive X-ray analyzer, field emission scanning electron microscopy, X-ray photoelectron spectroscopy, thin film X-ray diffraction technique, high resolution transmission electron microscopy, and the selected area electron diffraction analysis technique. The as-deposited AgTe films show a highly crystalline nature even without thermal treatment. Furthermore, the electrochemistry for lithiation/delithiation of the AgTe film is studied for exploring its feasibility in the application as an anode material in a Li-ion battery. The experimentally estimated capacity of the AgTe electrode for Li storage is found to be about two and half fold larger than the theoretical capacity of the AgTe material. This implies that the binder-free AgTe film prepared by the current method could find a potential application in the Li-ion or other similar charge storing devices.
本工作展示了一种高度可控、简便且环境友好的基于水溶液的合成方法,该方法可在室温下,通过银/氧化银薄膜的离子交换诱导化学转化,在所需衬底上制备无氧化物污染的碲化银薄膜。利用能量色散X射线分析仪、场发射扫描电子显微镜、X射线光电子能谱、薄膜X射线衍射技术、高分辨率透射电子显微镜以及选区电子衍射分析技术,对化学转化反应前后的薄膜进行了表征。所沉积的碲化银薄膜即使未经热处理也呈现出高度结晶的性质。此外,研究了碲化银薄膜锂化/脱锂的电化学过程,以探索其作为锂离子电池负极材料应用的可行性。实验估计碲化银电极的锂存储容量比碲化银材料的理论容量大约大两倍半。这意味着通过当前方法制备的无粘结剂碲化银薄膜在锂离子或其他类似的电荷存储装置中可能具有潜在应用。