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Kaihovirta, Nikolai
Publications (4 of 4) Show all publications
Mindemark, J., Tang, S., Wang, J., Kaihovirta, N., Brandell, D. & Edman, L. (2016). High-Performance Light-Emitting Electrochemical Cells by Electrolyte Design. Chemistry of Materials, 28(8), 2618-2623
Open this publication in new window or tab >>High-Performance Light-Emitting Electrochemical Cells by Electrolyte Design
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2016 (English)In: Chemistry of Materials, ISSN 0897-4756, E-ISSN 1520-5002, Vol. 28, no 8, p. 2618-2623Article in journal (Refereed) Published
Abstract [en]

Polymer light-emitting electrochemical cells (LECs) are inherently dependent on a suitable electrolyte for proper function. Here, we design and synthesize a series of alkyl carbonate-capped star-branched oligoether-based electrolytes with large electrochemical stability windows, facile ion release, and high compatibility with common light-emitting materials. LECs based on such designed electrolytes feature fast turn-on, a long operational lifetime of 1400 h at >100 cd m(-2) and a record-high power conversion efficiency of 18.1 lm W-1, when equipped with an external outcoupling film.

National Category
Polymer Chemistry
Identifiers
urn:nbn:se:umu:diva-121575 (URN)10.1021/acs.chemmater.5b04847 (DOI)000375244500018 ()
Available from: 2016-06-27 Created: 2016-06-03 Last updated: 2018-06-07Bibliographically approved
Kaihovirta, N., Longo, G., Gil-Escrig, L., Bolink, H. J. & Edman, L. (2015). Self-absorption in a light-emitting electrochemical cell based on an ionic transition metal complex. Applied Physics Letters, 106(10), Article ID 103502.
Open this publication in new window or tab >>Self-absorption in a light-emitting electrochemical cell based on an ionic transition metal complex
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2015 (English)In: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 106, no 10, article id 103502Article in journal (Refereed) Published
Abstract [en]

We report on the quantitative and qualitative effects of self-absorption in light-emitting electrochemical cells (LECs) based on ionic transition metal complexes (iTMCs), as measured in-situ during electric driving. A yellow-emitting iTMC-LEC comprising an active material thickness of 95 nm suffers a 4% loss of the emission intensity to self-absorption, whereas the same type of device but with a larger active-material thickness of 1 mu m will lose a significant 40% of the light intensity. We also find that the LEC-specific effect of doping-induced self-absorption can result in a drift of the emission spectrum with time for iTMC-LECs, but note that the overall magnitude of doping-induced self-absorption is much smaller than for conjugated-polymer LECs.

National Category
Physical Sciences
Identifiers
urn:nbn:se:umu:diva-102367 (URN)10.1063/1.4914307 (DOI)000351397600060 ()
Available from: 2015-05-28 Created: 2015-04-23 Last updated: 2018-06-07Bibliographically approved
Kaihovirta, N., Asadpoordarvish, A., Sandström, A. & Edman, L. (2014). Doping-Induced Self-Absorption in Light-Emitting Electrochemical Cells. ACS Photonics, 1(3), 182-189
Open this publication in new window or tab >>Doping-Induced Self-Absorption in Light-Emitting Electrochemical Cells
2014 (English)In: ACS Photonics, E-ISSN 2330-4022, Vol. 1, no 3, p. 182-189Article in journal (Refereed) Published
Abstract [en]

We report on the quantitative effects of doping-induced self-absorption in light-emitting electrochemical cells (LECs) as a function of active material (AM) thickness and doping concentration. For state-of-the-art polymer LECs with optimized doping concentration and comprising Super Yellow as the electroluminescent (EL) polymer and poly(ethylene oxide)-KCF3SO3 as the electrolyte, we find that the self-absorption loss at the EL peak wavelength is similar to 10% for a 100 nm thin AM and >70% for a 1 mu m thick AM. This implies that the utilization of micrometer-thick AMs fit for fault-tolerant large-scale fabrication can be concomitant with a notable penalty in device performance, and that spatial variations in AM thickness will be manifested in a corresponding spatial light-intensity variation. Moreover, we find that inclusion of a poly(ethylene oxide)-KCF3SO3 electrolyte can inhibit the out-coupling of light and suggest that the culprit is light scattering from dispersed crystalline-electrolyte domains. Finally, we demonstrate evidence for that the selected initial salt concentration in an LEC device dictates the maximum doping concentration that can be attained at steady-state operation.

Keywords
light-emitting device, organic electronics, electroluminescence, electrochemical doping, cyclic voltammetry, conjugated polymer
National Category
Physical Sciences
Identifiers
urn:nbn:se:umu:diva-90793 (URN)10.1021/ph400050t (DOI)000335802900006 ()
Available from: 2014-10-09 Created: 2014-07-01 Last updated: 2018-06-14Bibliographically approved
Kaihovirta, N., Larsen, C. & Edman, L. (2014). Improving the Performance of Light-Emitting Electrochemical Cells by Optical Design. ACS Applied Materials and Interfaces, 6(4), 2947-2954
Open this publication in new window or tab >>Improving the Performance of Light-Emitting Electrochemical Cells by Optical Design
2014 (English)In: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 6, no 4, p. 2947-2954Article in journal (Refereed) Published
Abstract [en]

The organic light-emitting electrochemical cell (LEG) has emerged as an enabling technology for a wide range of novel and low-cost emissive applications, but its efficiency is still relatively modest. The focus in the field has so far almost exclusively been directed toward limiting internal loss mechanisms, whereas external losses resulting from poor light-outcoupling have been overlooked. Here, we report a straightforward procedure for improving the efficiency and emission quality of LECs. We find that our high-performance glass-encapsulated LECs exhibit a near-ideal Lambertian emission profile but that total internal reflection at the glass/air interface and a concomitant edge emission and self-absorption represent a significant loss factor. We demonstrate a 60% improvement in the outcoupled luminance in the forward direction by laminating a light-outcoupling film, featuring a hexagonal array of hemispherical microlenses as the surface structure, onto the front side of the device and a large-area metallic reflector onto the back side. With this scalable approach, yellow-emitting LEC devices with a power conversion efficiency of more than 15 lm W-1 at a luminance of 100 cd m(-2) were realized. Importantly, we find that the same procedure also can mitigate problems with spatial variation in the light-emission intensity, which is a common and undesired feature of large-area LECs.

Keywords
light-emitting electrochemical cell, microlens array, light outcoupling, conjugated polymer, power conversion efficiency, Super Yellow
National Category
Atom and Molecular Physics and Optics
Identifiers
urn:nbn:se:umu:diva-88335 (URN)10.1021/am405530d (DOI)000332144600097 ()
Available from: 2014-06-11 Created: 2014-04-30 Last updated: 2018-06-07Bibliographically approved
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