Umeå universitets logga

umu.sePublikationer
Driftstörningar
Det förekommer återkommande driftstörningar på några av sök-portalerna på grund av hög belastning. Vi arbetar på att lösa problemet, ni kan tillfälligt mötas av ett felmeddelande.
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
The influence of electrodes on the performance of light-emitting electrochemical cells
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik.
Department of Science and Technology, Linköpings Universitet, SE-601 74 Norrköping, Sweden.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik.ORCID-id: 0000-0003-2495-7037
2007 (Engelska)Ingår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 52, nr 23, s. 6456–6462-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

We demonstrate that the electrochemical properties of the electrode material can have a dramatic impact on the performance of light-emitting electrochemical cells (LECs). Specifically, we report results from planar wide-gap LECs containing a blend of poly(2-methoxy,5-(2’-ethylhexyloxy)-p-phenylene vinylene) (MEH-PPV), poly(ethylene oxide) and LiCF3SO3 as the active material. We find that Au electrodes are preferable over Al electrodes, since Au-electrode devices exhibit fast turn-on (i.e., p-n junction formation time) and clearly visible light emission during operation at 5 V and 360 K, while Al-electrode devices exhibit slow turn-on (due to a delayed onset of p-doping progression) and no visible light emission. These results are rationalized with a cyclic voltammetry study, which demonstrates that Al is oxidized at a lower potential than the p-doping (oxidation) potential of MEH-PPV, while Au is electrochemically inert over the entire voltage range spanned by the p- and n-doping potentials of MEH-PPV. Consequently, the oxidation charge injected into Al-electrode devices results in a combination of p-doping of MEH-PPV and formation of Al ions. The latter process is undesired since it results in a slow turn-on time and quenched light emission. Finally, we find that planar LECs in a bottom-electrode configuration exhibit a faster turn-on time than identical devices with the electrodes on top of the active material.

Ort, förlag, år, upplaga, sidor
Elsevier , 2007. Vol. 52, nr 23, s. 6456–6462-
Identifikatorer
URN: urn:nbn:se:umu:diva-6544DOI: 10.1016/j.electacta.2007.04.068Scopus ID: 2-s2.0-34249889089OAI: oai:DiVA.org:umu-6544DiVA, id: diva2:146213
Tillgänglig från: 2007-12-13 Skapad: 2007-12-13 Senast uppdaterad: 2024-07-02Bibliografiskt granskad
Ingår i avhandling
1. Polymer light-emitting electrochemical cells: Utilizing doping for generation of light
Öppna denna publikation i ny flik eller fönster >>Polymer light-emitting electrochemical cells: Utilizing doping for generation of light
2011 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

    The current implementation of conjugated polymers (“conducting plastics”) in a wide range of devices promises to bring the vision of a new generation of flexible, efficient and low-cost applications to reality. Plastic lightemitting devices in the form of polymer light-emitting diodes (PLEDs) are projected to be particularly close to the market in applications such as large area and conformable illumination panels and high-performance thin displays. However, two notable drawbacks of PLEDs are that they depend on vacuum deposition of a reactive metal for the negative electrode and that the active material must be extremely thin and uniform in thickness. As a consequence, PLEDs cannot be expected to allow for a low-cost continuous production using a roll-to-roll coating and/or printing process.

This thesis focuses on an alternative to the PLED: A light-emitting electrochemical cell (LEC). LECs comprise a mixture of a conjugated polymer and a solid-state electrolyte as the active material positioned between two electrodes. The existence of mobile ions in the active material allows for a number of interesting attributes, both from a fundamental science and an application perspective. Importantly, the ions and the related unique operation of LECs make these devices apt for the utilization of low-cost roll-to-roll fabrication of the entire device as the electrode materials can be air stable and solution-processible and the requirement on the thickness of the active material is much less stringent than in PLEDs.

   The herein presented “basic science” studies primarily focus on the operation of LECs. It is for instance firmly established that a light-emitting p-n junction can form in-situ in a LEC device during the application of a voltage. This dynamic p-n junction exhibits some similarities, but also distinct differences, in comparison to the static p-n junctions that are exploited in crystalline inorganic semiconductor devices. We have also systematically explored the role that the constituent materials (ions, conjugated polymer, ionic solvent, and electrode material) can have on the performance of LECs, and two of the more important findings are that the concentration of ions can influence the doping structure in a motivated fashion and that it is critically important to consider the electrochemical stability window of the constituent materials in order to attain stable device operation.

   With this knowledge at hand, we have executed a number of more “applied science” studies, where we have used the acquired information from the basic-science studies for the rational design of improved devices. We have demonstrated LEC devices with significantly improved device performance, as exemplified by an orange-red device that emitted significant light (> 100 cd/m2) for more than one month of uninterrupted operation, and a yellow-green device that emitted significant light for 25 days at a low voltage of 4 V and at relatively high efficiency (6 lm/W). Finally, we have conceptualized and realized a solely solution-processed and metal-free LEC comprising graphene as the negative electrode and the conducting polymer PEDOT-PSS as the positive electrode. This type of devices represents a paradigm shift in the field of solid-state lighting as they demonstrate that it is possible to fabricate an entire light-emitting device from solution-processible and “green” carbon-based materials in a process that is akin to printing.

Ort, förlag, år, upplaga, sidor
Umeå: Department of Physics, Umeå University, 2011. s. 67
Identifikatorer
urn:nbn:se:umu:diva-38953 (URN)978-91-7459-124-8 (ISBN)
Disputation
2011-02-04, Mit-huset, MA 121, Umeå universitet, Umeå, 09:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2011-01-13 Skapad: 2011-01-11 Senast uppdaterad: 2024-07-02Bibliografiskt granskad

Open Access i DiVA

Fulltext saknas i DiVA

Övriga länkar

Förlagets fulltextScopus

Person

Matyba, PiotrEdman, Ludvig

Sök vidare i DiVA

Av författaren/redaktören
Matyba, PiotrEdman, Ludvig
Av organisationen
Institutionen för fysik
I samma tidskrift
Electrochimica Acta

Sök vidare utanför DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetricpoäng

doi
urn-nbn
Totalt: 632 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf