Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 120, Issue 20, Pages 11170-11179Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b00142
Keywords
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Funding
- German Science Foundation (DFG) through the cluster of excellence Nanosystems Initiative Munich (NIM)
- Center for Nanoscience (CeNS)
- Elite Network of Bavaria
- Austrian Science Funds (FWF) [SFB-F41]
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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)](+)[Ca2Nb3O10](-) nanosheets obtained through intercalation exfoliation of the layered bulk phase KCa2Nb3O10 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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