Issue 10, 2016

Investigation of thermochromic photoluminescent, dielectric and crystal structural properties for an inorganic–organic hybrid solid of [1-hexyl-3-methylimidazolium][PbBr3]

Abstract

The thermochromic photoluminescence, dielectric and impedance spectra, as well as temperature dependent crystal structures were investigated for the hybrid solid of [1-hexyl-3-methylimidazolium][PbBr3] (1). The hybrid crystal, belonging to a monoclinic system with the space group P21/c, is composed of one-dimensional [PbBr3] chains where the neighboring PbBr6 coordination octahedra are connected via face-sharing mode; the organic cations are incorporated in the space of the inorganic chains. The dynamic motion of the cations strongly influences the dielectric and emission features of 1. The platform-type dielectric anomaly, accompanied by a thermal event, occurs at an onset temperature of around 250 K, which is related to the alkyl chain swing motion. The dielectric relaxation appears at temperatures above 240 K and results from the alkyl chain swing motion and imidazole ring libration motion. Another fascinating feature of 1 is its dual emissions, arising from the π ← π* transition within the imidazole ring and the exciton luminescence of the [PbBr3] semiconducting chain. The two emission bands have different sensitivities to temperature, leading to 1 showing photoluminescent thermochromism, which may have a potential application in thermosensitive devices.

Graphical abstract: Investigation of thermochromic photoluminescent, dielectric and crystal structural properties for an inorganic–organic hybrid solid of [1-hexyl-3-methylimidazolium][PbBr3]

Supplementary files

Article information

Article type
Paper
Submitted
12 May 2016
Accepted
22 Aug 2016
First published
22 Aug 2016

New J. Chem., 2016,40, 8664-8672

Investigation of thermochromic photoluminescent, dielectric and crystal structural properties for an inorganic–organic hybrid solid of [1-hexyl-3-methylimidazolium][PbBr3]

K. Wan, Y. Tong, . Li-Li, Y. Zou, H. Duan, J. Liu and X. Ren, New J. Chem., 2016, 40, 8664 DOI: 10.1039/C6NJ01508E

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