Low‐dimensional (low‐D) organic metal halide hybrids (OMHHs) have emerged as fascinating candidates for optoelectronics due to their integrated properties from both organic and inorganic components. However, for most of low‐D OMHHs, especially the zero‐D (0D) compounds, the inferior electronic coupling between organic ligands and inorganic metal halides prevents efficient charge transfer at the hybrid interfaces and thus limits their further tunability of optical and electronic properties. Here, using pressure to regulate the interfacial interactions, efficient charge transfer from organic ligands to metal halides is achieved, which leads to a near‐unity photoluminescence quantum yield (PLQY) at around 6.0 GPa in a 0D OMHH, [(C6H5)4P]2SbCl5.
Organic metal halide hybrids (OMHHs) have attracted great research attention owing to their exceptional structure and property tunability. Using appropriate organic and inorganic metal halide components, OMHHs with controlled dimensionalities at the molecular level, from 3D to 2D, 1D, and 0D structures, can be obtained. In 0D OMHHs, anionic metal halide polyhedrons are surrounded and completely isolated by organic cations to form single crystalline “host–guest” structures. These ionically bonded organic–inorganic hybrid systems often exhibit the intrinsic properties of individual metal halide species, for instance, highly efficient Stokes‐shifted broadband emissions. In this progress report, the recent advances in the development and study of luminescent 0D OMHHs are discussed: from synthetic structural control to fundamental understanding of the structure–property relationship and device integration.
more » « less- Award ID(s):
- 1709116
- NSF-PAR ID:
- 10446380
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Optical Materials
- Volume:
- 9
- Issue:
- 18
- ISSN:
- 2195-1071
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Low‐dimensional (low‐D) organic metal halide hybrids (OMHHs) have emerged as fascinating candidates for optoelectronics due to their integrated properties from both organic and inorganic components. However, for most of low‐D OMHHs, especially the zero‐D (0D) compounds, the inferior electronic coupling between organic ligands and inorganic metal halides prevents efficient charge transfer at the hybrid interfaces and thus limits their further tunability of optical and electronic properties. Here, using pressure to regulate the interfacial interactions, efficient charge transfer from organic ligands to metal halides is achieved, which leads to a near‐unity photoluminescence quantum yield (PLQY) at around 6.0 GPa in a 0D OMHH, [(C6H5)4P]2SbCl5.
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