1 / 17

Forming Conducting Polymers Utilising Room Temperature Ionic Liquids

Forming Conducting Polymers Utilising Room Temperature Ionic Liquids. PhD student: Lavinia Astratine Supervisors: Dr. Anthony Betts & Prof. John Cassidy (DIT) Prof. Edmond Magner (MSSI, Limerick). 1. Concept 2. Objectives 3. Lab Work 4.Other polymers: polythiophene

murray
Télécharger la présentation

Forming Conducting Polymers Utilising Room Temperature Ionic Liquids

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Forming Conducting Polymers Utilising Room Temperature Ionic Liquids PhD student: Lavinia Astratine Supervisors: Dr. Anthony Betts & Prof. John Cassidy (DIT) Prof. Edmond Magner (MSSI, Limerick)

  2. 1. Concept • 2. Objectives • 3. Lab Work • 4.Other polymers: polythiophene & Ionic Liquids • 5.Future work

  3. 1. Concept • The aim of this project is to use conducting polymers (CPs), in conjunction with Room Temperature Ionic Liquids (RTILs), to produce electrochromic films. • Such films, which change colour in response to electrical potential changes, could be used in electronic display devices and in light and energy-control applications (eg. smart windows which control light transmittance).

  4. 2. Objectives • Production of improved electrochromic devices, using a more environmentally-friendly “Green Chemistry” approach is a desirable goal. • Conducting polymers (CPs, such as polypyrrole, polythiophene, polyaniline and/or their derivatives) have been studied extensively. A promising CP for electrochromic applications is polypyrrole (PPy).

  5. Characteristics of polypyrrole: • Thin films of polypyrrole are yellow in the undoped insulating state and black in the doped conductive state • Electrochemical degradation has been reported in many studies • The electrode potential applied has been found to influence greatly the degradation process (electrode potential limit 0.6 V vs. Ag/AgCl) • Polypyrrole is a quite labile electrode material that undergoes a relatively fast electrochemical degradation, at least in aqueous solutions Electrochimica Acta 52 (2007) 4784–4791

  6. 3. Lab Work Method used: Cyclic Voltammetry • a) Form PPy films using organic solvents as Electrolyte Experimental set up Working Electrode (WE): Pt electrode (diameter 2mm) Counter Electrode (CE): Silver Wire Reference Electrode (RE): saturated Ag/AgCl Pyrrole used for synthesis of PPy films was purified by distillation and kept refrigerated in the dark. Monomer solution: 0.1 M Pyrrole and 0.1 M LiClO4 and H2O Electrolyte solution: 0.1 M LiClO4 and H2O

  7. Results and Discussion →Potential range: -1V to +0.8V →After 3 sweeps a yellow film was deposited on the electrode surface

  8. In order to change the polymer colour the electrode was placed in electrolyte solution • Potential range: -0.4V to +0.5V • CV in electrolyte for 10 cycles • The polymer changed colour to blue

  9. b)FormPPy on FTO glass (WE), [0.5cmx3cm] Monomer solution (deoxygenated for 10 minutes): 0.1 M Py, 0.1 M LiClO4, H2O Electrolyte solution: 0.1 M LiClO4, H2O Potential range: -0.9 V to 1.5 V Run for 6 sweeps → Results in a black oxidized film, which is unstable → Polypyrrole was overoxidized

  10. Observations: • PPy is oxidizing at ca. 0.6V. From 0.55V on, the current increases with each potential sweep. • No colour change of the polymer was observed on the FTO glass. • Probably 1 or 2 scans are enough in the region where the pyrrole starts to be oxidized (0.95 V). • The results are better with FTO glass when the monomer solution is degassed before starting polymer formation.

  11. 4.Other polymers: polythiophene Combines the flexibility, elasticity and malleability of plastics + electrical conductivity + also often exhibit colour (polychromism) as electrochromic materials Ionic Liquids ‘Green Solvents’ • Ionic liquids (ILs) are room temperature molten salts, composed mostly of organic ions that can undergo almost unlimited structural variations • ILs which function at room temperature, the most desirable operational temperature range, are termed “Room Temperature Ionic Liquids”, RTILs

  12. Examples include 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM PF6) and its borate counterpart (BMIM.BF4)

  13. Making polymers in ionic liquids 25cycles WE: Pt electrode CE: Pt coil Monomer Solution: RE: Pt wire Polymerization range: -1 V to +1 V Colours of the film: yellow→orange→red→Black 0.1 M Pyrrole & BMIM PF6

  14. WE: FTO glass (3cm x 0.5mm) Monomer Solution: CE: Pt coil RE: Pt wire Polymerization range: -1 V to +1 V Colours of the film: yellow→light Brown→Brown→Black 0.1 M Pyrrole & BMIM PF6 16 cycles

  15. 5. Future work • Combine conducting polymers (pyrrole, thiophene) with other RTILs such as [ChCl][EG], [BMIM][CF3SO3], [Py][CF3SO3] in order to get different colours during electropolymerization on optically transparent FTO and Au-sputtered glass substrates. • Conduct spectroelectrochemical studies of the polymer films, in order to detect colour changes in situ • Gain insight into the mechanisms of electrochromism • Construct simple Proof of Concept Device/Prototype illustrating potential of technology and transfer technology

  16. Papers • Electrochimica Acta 52 (2007) 4784–4791, A.Brazier et al. • Polymer Degradation and Stability 75 (2002) 255–258, R. Mazeikiene, A. Malinauskas • Synthetic Metals 157 (2007) 485-491, A. Alumaa et al. • Electrochimica Acta, Vol.42,No.2,pp. 203-210, 1997, Yongfang Li • Journal of Electroanalytical Chemistry 618 (2008) 87–93, by D. Asil et al. • Nature Materials, 8, (2009), 621-629, M. Armand, D.R. MacFarlane, H. Ohno and B. Scrosati • Polymer 45(2004) 1447-1453, J.M. Pringle et al.

  17. Aknowledgements - Dr. Anthony Betts & Prof. John Cassidy (DIT) - Prof. Edmond Magner (MSSI, Limerick) - Edmond Magner Research Group (MSSI,Limerick) Thank you for your attention!

More Related