Materials, Interfaces, and Electrochemical Phenomena
Fabrication of an anionic polythiophene/layered double hydroxide ultrathin film showing red luminescence and reversible pH photoresponse
Article first published online: 17 SEP 2010
DOI: 10.1002/aic.12400
Copyright © 2010 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Yan, D., Lu, J., Ma, J., Wei, M., Evans, D. G. and Duan, X. (2011), Fabrication of an anionic polythiophene/layered double hydroxide ultrathin film showing red luminescence and reversible pH photoresponse. AIChE J., 57: 1926–1935. doi: 10.1002/aic.12400
Publication History
- Issue published online: 9 JUN 2011
- Article first published online: 17 SEP 2010
- Accepted manuscript online: 17 AUG 2010 08:18AM EST
- Manuscript Revised: 5 AUG 2010
- Manuscript Received: 17 JAN 2010
Funded by
- The National Natural Science Foundation of China
- The 973 Program. Grant Number: 2009CB939802
- 111 Project. Grant Number: B07004
Keywords:
- polythiophene;
- layered double hydroxide;
- polarized red luminescence;
- pH sensor;
- periodic density functional theory
Abstract
Luminescent ordered ultrathin films (UTFs) based on a sulfonated polythiophene (SPT) and Mg–Al-layered double hydroxide (LDH) nanosheets have been fabricated by the layer-by-layer assembly method. UV-visible absorption and fluorescence spectroscopy showed that there was a stepwise and regular growth of the films with increasing number of deposition cycles. XRD, AFM, and SEM showed that the films had a periodic layered structure with a period of ca. 3.0 nm, and that the thickness can be finely controlled within the range ca. 26–100 nm. The SPT/LDH UTFs show well-defined polarized photoemission with an anisotropy of ca. 0.3, and they show a reversible luminescence response to changes in pH. Periodic density functional theoretical calculations gave a band energy of 1.85 eV for the SPT/LDH system and showed that the valence electrons of SPT can be confined in the energy wells formed by the LDH monolayers, which effectively inhibits both the nonradiative relaxation and the π–π stacking interaction of the polymer chromophores. © 2010 American Institute of Chemical Engineers AIChE J, 2011

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