摘要
The “self-trap state” in low demensional halide perovskites usually induces highly efficient below-gap broadband luminescence, which makes them promising fluorescence emitting materials. However, the luminescence mechanism based on the “self-trap state” is not well understood as yet. In this work, solution-grown quasi-one-dimensional RbPbI3crystals reveal a large Stokes shift of ∼0.57 eV, wide and strong luminescence, and a linear power-dependent luminescence, whose luminescence mechanism was attributed to the formation of a “self-trap state” in RbPbI3. Furthermore, Cs substitutional counterpart (RbxCs1−x)PbI3crystals were found to adjust the distortions of the PbI6octahedron and the self-trap-state-induced luminescence properties. Our work provides a new strategy to control the “self-trap-state”-induced luminescence in low demensional halide perovskite materials.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 12108-12112 |
| 页数 | 5 |
| 期刊 | Journal of Materials Chemistry C |
| 卷 | 8 |
| 期 | 35 |
| DOI | |
| 出版状态 | 已出版 - 21 9月 2020 |
指纹
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