纳米片
带隙
材料科学
钙钛矿(结构)
光谱学
剥脱关节
电子能量损失谱
分析化学(期刊)
光电子学
纳米技术
透射电子显微镜
化学
结晶学
石墨烯
物理
有机化学
量子力学
作者
Kulpreet Singh Virdi,Yaron Kauffmann,Christian Ziegler,Pirmin Ganter,Peter Blaha,Bettina V. Lotsch,Wayne D. Kaplan,Christina Scheu
标识
DOI:10.1021/acs.jpcc.6b00142
摘要
Rapid progress in the synthesis of nanostructures with tailor-made morphologies necessitates adequate analytical tools to unravel their physical properties. In our study, we investigate, on the nanometer scale, the band gap of individual [TBA x H 1– x ] + [Ca 2 Nb 3 O 10 ] − nanosheets obtained through intercalation–exfoliation of the layered bulk phase KCa 2 Nb 3 O 10 with tetra- n -butylammonium hydroxide (TBAOH) using valence electron energy loss spectroscopy (VEELS) in the scanning transmission electron microscope (STEM). The nanosheets consist of an anionically charged perovskite layer with cationic organic ligands surrounding it. Because of the hybrid nature, a careful acquisition and analysis protocol is required since the nanosheets disintegrate easily under electron beam irradiation. The VEELS data reveal a fundamental band gap of an individual freely suspended perovskite nanosheet to be 2.9 ± 0.2 eV and optically allowed transitions above 3.8 ± 0.2 eV (optical band gap). The spatial resolution of the measurements is about 9 nm, taking into account 50% of the excitations when illuminating with an incident electron beam of 1 nm diameter. Our investigations reveal that the band gap of an individual nanosheet is not changed significantly compared to the bulk phase, which is confirmed by UV–vis data. This is rationalized by the quasi-2D electronic structure of the bulk material being preserved upon delamination.
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