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溶液介导的SnSe向SbSe薄膜的转变

Solution-Mediated Inversion of SnSe to SbSe Thin-Films.

作者信息

Polivtseva Svetlana, Kois Julia, Kruzhilina Tatiana, Kaupmees Reelika, Klopov Mihhail, Molaiyan Palanivel, van Gog Heleen, van Huis Marijn A, Volobujeva Olga

机构信息

Department of Materials and Environmental Technology, School of Engineering, TalTech, Ehitajate tee 5, 19086 Tallinn, Estonia.

Auramet Solutions OÜ, Kalliomäentie 1B, 02920 Espoo, Finland.

出版信息

Nanomaterials (Basel). 2022 Aug 23;12(17):2898. doi: 10.3390/nano12172898.

Abstract

New facile and controllable approaches to fabricating metal chalcogenide thin films with adjustable properties can significantly expand the scope of these materials in numerous optoelectronic and photovoltaic devices. Most traditional and especially wet-chemical synthetic pathways suffer from a sluggish ability to regulate the composition and have difficulty achieving the high-quality structural properties of the sought-after metal chalcogenides, especially at large 2D length scales. In this effort, and for the first time, we illustrated the fast and complete inversion of continuous SnSe thin-films to SbSe using a scalable top-down ion-exchange approach. Processing in dense solution systems yielded the formation of SbSe films with favorable structural characteristics, while oxide phases, which are typically present in most SbSe films regardless of the synthetic protocols used, were eliminated. Density functional theory (DFT) calculations performed on intermediate phases show strong relaxations of the atomic lattice due to the presence of substitutional and vacancy defects, which likely enhances the mobility of cationic species during cation exchange. Our concept can be applied to customize the properties of other metal chalcogenides or manufacture layered structures.

摘要

制备具有可调性质的金属硫族化物薄膜的新型简便且可控的方法,能够显著拓展这些材料在众多光电器件和光伏器件中的应用范围。大多数传统方法,尤其是湿化学合成途径,在调节成分方面能力不足,并且难以实现所需金属硫族化物的高质量结构性能,特别是在大二维长度尺度上。在这项工作中,我们首次展示了使用可扩展的自上而下离子交换方法将连续的SnSe薄膜快速且完全转化为SbSe。在致密溶液体系中进行处理,得到了具有良好结构特征的SbSe薄膜,同时消除了大多数SbSe薄膜中通常存在的氧化物相,无论使用何种合成方案。对中间相进行的密度泛函理论(DFT)计算表明,由于存在替代和空位缺陷,原子晶格发生了强烈弛豫,这可能增强了阳离子交换过程中阳离子物种的迁移率。我们的概念可用于定制其他金属硫族化物的性质或制造层状结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/308d/9458253/11f181ea958e/nanomaterials-12-02898-g001.jpg

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