One-step inkjet printing of tungsten oxide-poly(3,4-ethylenedioxythiophene):polystyrene sulphonate hybrid film and its applications in electrochromic devices
Hybrid film comprised tungsten oxide and poly (3,4-ethylenedioxythiophene):polystyrene sulphonate (WO3–PEDOT:PSS) was developed by applying one-step inkjet printing from an office inkjet printer. The WO3 nanoparticles were synthesized from commercial crystalline WO3 powder through a wet ball-milling...
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Published in | Thin solid films Vol. 603; pp. 276 - 282 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
31.03.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Hybrid film comprised tungsten oxide and poly (3,4-ethylenedioxythiophene):polystyrene sulphonate (WO3–PEDOT:PSS) was developed by applying one-step inkjet printing from an office inkjet printer. The WO3 nanoparticles were synthesized from commercial crystalline WO3 powder through a wet ball-milling process, which is a simple, environmentally friendly, and cost-effective method of using water as a green solvent and low-energy milling. The WO3–PEDOT:PSS inkjet ink was prepared by dispersing the as-milled WO3 and PEDOT:PSS in n-propanol and deionized water. The inkjet-printed WO3–PEDOT:PSS thin films show marked improvements of cathodic electrochromism over WO3 films: the transmittance change of 20% at 550nm (visible region) and 35% at 900nm (infrared region) along with the response time of 5.67/0.30s in their colored/bleached state, and the electrochromic coloration efficiency of 27.86cm2/C at 550nm and 69.64cm2/C at 900nm.
•WO3 nanoparticles were synthesized by milling commercial crystalline WO3.•Wet ball-milling was carried out by using water as a green solvent and low energy.•WO3–PEDOT:PSS hybrid ink was simply prepared by adding n-propanol and DI water.•WO3–PEDOT:PSS hybrid films were inkjet-printed via an office inkjet printer.•WO3–PEDOT:PSS films show better electrochromic performances than WO3 films. |
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ISSN: | 0040-6090 1879-2731 |
DOI: | 10.1016/j.tsf.2016.02.031 |