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 have attracted tremendous research interests owing to their outstanding optical and electronic properties suitable for various applications, including photovoltaics, light‐emitting diodes, and photodetectors. Recently, the multifunctionality of this class of materials has been further explored beyond their optical and electronic properties. Here, for the first time the microwave electromagnetic properties of a 1D organic metal halide hybrid, (C6H13N4)3Pb2Br7, a single crystalline bulk assembly of organic metal halide nanotubes, are reported. Good microwave absorption performance with a large reflection loss value of −18.5 dB and a threshold bandwidth of 1.0 GHz is discovered for this material, suggesting its potential as a new microwave absorber. This work reveals a new functionality of organic metal halide hybrids and provides a new material class for microwave absorption application studies.
more » « less- Award ID(s):
- 1709116
- NSF-PAR ID:
- 10454451
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials Interfaces
- Volume:
- 7
- Issue:
- 3
- ISSN:
- 2196-7350
- 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.
In situ experimental characterizations and theoretical simulations reveal that the pressure‐induced electronic coupling between the lone‐pair electrons of Sb3+and the π electrons of benzene ring (lp‐π interaction) serves as an unexpected “bridge” for the charge transfer. Our work opens a versatile strategy for the new materials design by manipulating the lp‐π interactions in organic–inorganic hybrid systems. -
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