Perovskite chalcogenides are gaining substantial interest as an emerging class of semiconductors for optoelectronic applications. High-quality samples are of vital importance to examine their inherent physical properties. We report the successful crystal growth of the model system, BaZrS 3 and its Ruddlesden–Popper phase Ba 3 Zr 2 S 7 by a flux method. X-ray diffraction analyses showed the space group of Pnma with lattice constants of a = 7.056(3) Å, b = 9.962(4) Å, and c = 6.996(3) Å for BaZrS 3 and P 4 2 / mnm with a = 7.071(2) Å, b = 7.071(2) Å, and c = 25.418(5) Å for Ba 3 Zr 2 S 7 . Rocking curves with full width at half maximum of 0.011° for BaZrS 3 and 0.027° for Ba 3 Zr 2 S 7 were observed. Pole figure analysis, scanning transmission electron microscopy images, and electron diffraction patterns also establish the high quality of the grown crystals. The octahedral tilting in the corner-sharing octahedral network is analyzed by extracting the torsion angles.
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Time-resolved photoluminescence studies of perovskite chalcogenides
Chalcogenides in the perovskite and related crystal structures (“chalcogenide perovskites” for brevity) may be useful for future optoelectronic and energy-conversion technologies inasmuch as they have good excited-state, ambipolar transport properties. In recent years, several studies have suggested that semiconductors in the Ba–Zr–S system have slow non-radiative recombination rates. Here, we present a time-resolved photoluminescence (TRPL) study of excited-state carrier mobility and recombination rates in the perovskite-structured material BaZrS 3 , and the related Ruddlesden–Popper phase Ba 3 Zr 2 S 7 . We measure state-of-the-art single crystal samples, to identify properties free from the influence of secondary phases and random grain boundaries. We model and fit the data using a semiconductor physics simulation, to enable more direct determination of key material parameters than is possible with empirical data modeling. We find that both materials have Shockley–Read–Hall recombination lifetimes on the order of 50 ns and excited-state diffusion lengths on the order of 5 μm at room temperature, which bodes well for ambipolar device performance in optoelectronic technologies including thin-film solar cells.
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- Award ID(s):
- 1751736
- PAR ID:
- 10433100
- Date Published:
- Journal Name:
- Faraday Discussions
- Volume:
- 239
- ISSN:
- 1359-6640
- Page Range / eLocation ID:
- 146 to 159
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Chalcogenide perovskites have attracted increasing research attention in recent years due to their promise of unique optoelectronic properties combined with stability. However, the synthesis and processing of these materials has been constrained by the need for high temperatures and/or long reaction times. In this work, we address the open question of a low-temperature growth mechanism for BaZrS3. Ultimately, a liquid-assisted growth mechanism for BaZrS3 using molten BaS3 as a flux is demonstrated at temperatures ≥540 °C in as little as 5 min. The role of Zr-precursor reactivity and S(g.) on the growth mechanism and the formation of Ba3Zr2S7 is discussed, in addition to the purification of resulting products using a straightforward H2O wash. The extension of this growth mechanism to other Ba-based chalcogenides is shown, including BaHfS3, BaNbS3, and BaTiS3. In addition, an alternative vapor-transport growth mechanism is presented using S2Cl2 for the growth of BaZrS3 at temperatures as low as 500 °C in at least 3 h. These results demonstrate the feasibility of scalable processing for the formation of chalcogenide perovskite thin-films. (DOI: 10.1021/acs.chemmater.3c00494)more » « less
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