Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81877
Title: One-pot sequential electrochemical deposition of multilayer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic acid)/tungsten trioxide hybrid films and their enhanced electrochromic properties
Authors: Ling, Han
Lu, Jinlin
Phua, Silei
Liu, Hai
Liu, Liang
Huang, Yizhong
Mandler, Daniel
Lee, Pooi See
Lu, Xuehong
Keywords: Electrochemical deposition
Multilayers
Issue Date: 2014
Source: Ling, H., Lu, J., Phua, S., Liu, H., Liu, L., Huang, Y., et al. (2014). One-pot sequential electrochemical deposition of multilayer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic acid)/tungsten trioxide hybrid films and their enhanced electrochromic properties. Journal of Materials Chemistry A, 2(8), 2708-2717.
Series/Report no.: Journal of Materials Chemistry A
Abstract: Hybrid thin films composed of multilayer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic acid) (PEDOT:PSS) and tungsten trioxide (WO3) were electrochemically deposited on indium tin oxide (ITO) from a one-pot solution using a square-wave galvanostatic method. The morphology of the hybrid thin films could be easily manipulated to optimize their electrochromic properties by adjusting deposition conditions. In the hybrids, both components can be simultaneously switched to coloured or bleached states. The hybrid film obtained with very short deposition times of PEDOT:PSS and WO3 in each cycle exhibits significantly enhanced electrochromic properties. The optical contrast of the hybrid film is higher than that of PEDOT:PSS or WO3 films of the same thickness. Moreover, the stability of the hybrid film is also drastically enhanced. The enhancement may be attributed to the favourable interactions between the two components, i.e., PEDOT:PSS may enter the defect sites in electrodeposited WO3, preventing surface-defect-induced anodic dissolution during cycling, while the surface functional groups of WO3 may act as dopants to inhibit over-oxidation of PEDOT, as well as the large interfacial area created using this unique one-pot multilayer deposition method.
URI: https://hdl.handle.net/10356/81877
http://hdl.handle.net/10220/39701
ISSN: 2050-7488
DOI: 10.1039/c3ta14781a
Rights: © 2014 The Royal Society of Chemistry. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of Materials Chemistry A, The Royal Society of Chemistry. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1039/c3ta14781a].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles
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