journal article·2019-10-30

Oligomer Electrolytes for Light-Emitting Electrochemical Cells: Influence of the End Groups on Ion Coordination, Ion Binding, and Turn-on Kinetics

Isabelle Gerz, E. Mattias Lindh, Pall Thordarson, Ludvig Edman, Jolla Kullgren, Jonas Mindemark

ACS Applied Materials & Interfaces· Volume 11· Issue 43
Publisher page

Abstract

The electrolyte is an essential constituent of the light-emitting electrochemical cell (LEC), since its operating mechanism is dependent on the redistribution of mobile ions in the active layer. Recent developments of new ion transporters have yielded high-performance devices, but knowledge about the interactions between the ionic species and the ion transporters and the influence of these interactions on the LEC performance is lacking. We therefore present a combined computational and experimental effort that demonstrates that the selection of the end group in a star-branched oligomeric ion transporter based on trimethylolpropane ethoxylate has a paramount influence on the ionic interactions in the electrolyte and thereby also on the performance of the corresponding LECs. With hydroxyl end groups, the cation from the salt is strongly coordinated to the ion transporter, which leads to suppression of ion pairing, but the penalty is a hindered ion release and a slow turn-on for the LEC devices. With methoxy end groups, an intermediate coordination strength is seen together with the formation of contact ion pairs, but the LEC performance is very good with fast turn-on. Using a series of ion transporters with alkyl carbonate end groups, the ion transporter:cation coordination strength is lowered further, but the turn-on kinetics are slower than what is seen for devices comprising the methoxy end-capped ion transporter.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Conducting polymers and applications · Organic Electronics and Photovoltaics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry—Ångström Laboratory, Uppsala University, Box 538, SE-751 21 Uppsala, Sweden

The Organic Photonics and Electronics Group, Department of Physics, Umeå University, SE-901 87 Umeå, Sweden

School of Chemistry, the Australian Centre for Nanomedicine and the ARC Centre of Excellence in Convergent Bio-Nano Science & Technology, University of New South Wales, Sydney, NSW 2052, Australia

Funding

Vetenskapsr?det · Stiftelsen Lars Hiertas Minne · Energimyndigheten · Stiftelsen L?ngmanska Kulturfonden · Australian Research Council · Stiftelsen f?r?Strategisk Forskning · Stiftelsen Olle Engkvist Byggm?stare · StandUP for ENERGY · eSSENCE · Bertil & Britt Svenssons stiftelse f?r belysningsteknik

References (59)

Show source-provided references
1. 10.1126/science.269.5227.108610.1126/science.269.5227.1086 ↗
2. 10.1039/c3cc40942b10.1039/c3cc40942b ↗
3. 10.1002/anie.20120147110.1002/anie.201201471 ↗
4. 10.1002/adma.20140128610.1002/adma.201401286 ↗
5. 10.1002/adfm.20150052810.1002/adfm.201500528 ↗
6. 10.1038/nphoton.2015.3710.1038/nphoton.2015.37 ↗
7. 10.1063/1.218740810.1063/1.2187408 ↗
8. 10.1103/PhysRevB.78.24520210.1103/PhysRevB.78.245202 ↗
9. 10.1021/ja104555510.1021/ja1045555 ↗
10. 10.1016/j.orgel.2011.07.00510.1016/j.orgel.2011.07.005 ↗
11. 10.1039/C5TC03429A10.1039/C5TC03429A ↗
12. 10.1016/S0379-6779(02)00470-810.1016/S0379-6779(02)00470-8 ↗
13. 10.1021/jz200071b10.1021/jz200071b ↗
14. 10.1016/j.orgel.2012.11.02910.1016/j.orgel.2012.11.029 ↗
15. 10.1002/admt.20180022910.1002/admt.201800229 ↗
16. 10.1063/1.221912210.1063/1.2219122 ↗
17. 10.1063/1.36431310.1063/1.364313 ↗
18. 10.1016/S0379-6779(00)00964-410.1016/S0379-6779(00)00964-4 ↗
19. 10.1002/adfm.20030543110.1002/adfm.200305431 ↗
20. 10.1016/j.tsf.2007.04.03310.1016/j.tsf.2007.04.033 ↗
21. 10.1021/acssuschemeng.6b0195310.1021/acssuschemeng.6b01953 ↗
22. 10.1038/srep3664310.1038/srep36643 ↗
23. 10.1002/adfm.20170579510.1002/adfm.201705795 ↗
24. 10.1021/jz101079710.1021/jz1010797 ↗
25. 10.1021/cm502290510.1021/cm5022905 ↗
26. 10.1002/adfm.20180129510.1002/adfm.201801295 ↗
27. 10.1016/j.ssi.2012.09.02010.1016/j.ssi.2012.09.020 ↗
28. 10.1039/C6CP00757K10.1039/C6CP00757K ↗
29. 10.1021/acs.macromol.6b0085110.1021/acs.macromol.6b00851 ↗
30. 10.1021/acs.chemmater.5b0484710.1021/acs.chemmater.5b04847 ↗
31. Supramolecular.org - Binding Constant Calculators. http://supramolecular.org/.
32. 10.1039/C0CS00062K10.1039/C0CS00062K ↗
33. Case, D. A.; Berryman, J. T.; Betz, R. M.; Cerutti, D. S.; Cheatham, T. E., III; Darden, T. A.; Duke, R. E.; Giese, T. J.; Gohlke, H.; Goetz, A. W.; Homeyer, N.; Izadi, S.; Janowski, P.; Kaus, J.; Kovalenko, A.; Lee, T. S.; LeGrand, S.; Li, P.; Luchko, T.; Luo, R.; Madej, B.; Merz, K. M.; Monard, G.; Needham, P.; Nguyen, H.; Nguyen, H. T.; Omelyan, I.; Onufriev, A.; York, D. M.; Kollman, P. A. AMBER 2015. University of California, San Francisco; 2015.
34. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G. A.; Nakatsuji, H.; Caricato, M.; Li, X.; Hratchian, H. P.; Izmaylov, A. F.; Bloino, J.; Zheng, G.; Sonnenberg, J. L.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Montgomery, J. A. J.; Peralta, J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Rega, N.; Millam, J. M.; Klene, M.; Knox, J. E.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Zakrzewski, V. G.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Dapprich, S.; Daniels, A. D.; Farkas, Ö.; Foresman, J. B.; Ortiz, J. V.; Cioslowski, J.; Fox, D. J. Gaussian09, revision B.01; Gaussian, Inc.: Wallingford, CT, 2009.
35. 10.1063/1.46491310.1063/1.464913 ↗
36. 10.1103/PhysRevB.37.78510.1103/PhysRevB.37.785 ↗
37. 10.1139/p80-15910.1139/p80-159 ↗
38. 10.1021/j100096a00110.1021/j100096a001 ↗
39. 10.1139/v68-56910.1139/v68-569 ↗
40. 10.1021/acs.jpcc.6b0327710.1021/acs.jpcc.6b03277 ↗
41. 10.1002/aenm.20180070310.1002/aenm.201800703 ↗
42. 10.1021/ed060p93310.1021/ed060p933 ↗
43. 10.1146/annurev.pc.40.100189.00050510.1146/annurev.pc.40.100189.000505 ↗
44. 10.1016/0013-4686(92)87120-O10.1016/0013-4686(92)87120-O ↗
45. 10.1007/s10953-007-9146-110.1007/s10953-007-9146-1 ↗
46. 10.1021/jp501319e10.1021/jp501319e ↗
47. 10.1016/0032-3861(92)91108-E10.1016/0032-3861(92)91108-E ↗
48. 10.1002/polb.2422710.1002/polb.24227 ↗
49. 10.1021/jp902276b10.1021/jp902276b ↗
50. 10.1039/C6CP08852J10.1039/C6CP08852J ↗
51. 10.1038/s41598-018-25287-x10.1038/s41598-018-25287-x ↗
52. 10.1021/ja711329410.1021/ja7113294 ↗
53. 10.1002/adfm.20090047910.1002/adfm.200900479 ↗
54. 10.1021/ja953695q10.1021/ja953695q ↗
55. 10.1063/1.166760110.1063/1.1667601 ↗
56. 10.1021/acsami.6b1416210.1021/acsami.6b14162 ↗
57. 10.1021/acsami.8b1419810.1021/acsami.8b14198 ↗
58. 10.1063/1.242287710.1063/1.2422877 ↗
59. 10.1002/adfm.20060098410.1002/adfm.200600984 ↗