Abstract
Ionically bonded organic metal halide hybrids have emerged as versatile multicomponent material systems exhibiting unique and useful properties. The unlimited combinations of organic cations and metal halides lead to the tremendous structural diversity of this class of materials, which could unlock many undiscovered properties of both organic cations and metal halides. Here we report the synthesis and characterization of a series benzoquinolinium (BZQ) metal halides with a general formula (BZQ)Pb2X5 (X = Cl, Br), in which metal halides form a unique two-dimensional (2D) structure. These BZQ metal halides are found to exhibit enhanced photoluminescence and stability as compared to the pristine BZQ halides, due to the scaffolding effects of 2D metal halides. Optical characterizations and theoretical calculations reveal that BZQ+ cations are responsible for the emissions in these hybrid materials. Changing the halide from Cl to Br introduces heavy atom effects, resulting in yellow room temperature phosphorescence (RTP) from BZQ+ cations.
Original language | English |
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Pages (from-to) | 8229-8236 |
Number of pages | 8 |
Journal | Journal of Physical Chemistry Letters |
Volume | 12 |
Issue number | 34 |
DOIs | |
State | Published - Sep 2 2021 |
Externally published | Yes |
Funding
This work was supported by the Air Force Office of Scientific Research under Contract No. FA9550-18-1-0231 and the Florida State University Office of Research. This work made use of the Rigaku Synergy-S single-crystal X-ray diffractometer acquired through the NSF MRI program (Award CHE-1828362) and the Edinburgh Instruments LP980-KS transient absorption system acquired through the NSF MRI program (Grant No. CHE-1531629). A portion of the work was conducted in the FSU Department of Chemistry & Biochemistry’s MAC (FSU075000MAC) and X-ray (FSU075000XRAY) Laboratories. The theoretical calculations are based upon work supported by the Department of Energy Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division (M.-H.D.), and National Nuclear Security Administration through the Nuclear Science and Security Consortium under Award Number DE-NA0003180 (C.J.D. and J.P.H.). This work was supported by the Air Force Office of Scientific Research under Contract No. FA9550-18-1-0231 and the Florida State University Office of Research. This work made use of the Rigaku Synergy-S single-crystal X-ray diffractometer acquired through the NSF MRI program (Award CHE-1828362) and the Edinburgh Instruments LP980-KS transient absorption system acquired through the NSF MRI program (Grant No. CHE-1531629). A portion of the work was conducted in the FSU Department of Chemistry & Biochemistry's MAC (FSU075000MAC) and X-ray (FSU075000XRAY) Laboratories. The theoretical calculations are based upon work supported by the Department of Energy Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division (M.-H.D.), and National Nuclear Security Administration through the Nuclear Science and Security Consortium under Award Number DE-NA0003180 (C.J.D. and J.P.H.).
Funders | Funder number |
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Florida State University Office of Research | |
National Science Foundation | CHE-1828362, FSU075000XRAY, FSU075000MAC, CHE-1531629 |
U.S. Department of Energy | |
Air Force Office of Scientific Research | FA9550-18-1-0231 |
Basic Energy Sciences | |
National Nuclear Security Administration | DE-NA0003180 |
Division of Materials Sciences and Engineering |