journal article·2018-07-25Open access

Triptycene as a Supramolecular Additive in PTB7:PCBM Blends and Its Influence on Photovoltaic Properties

Lethy Krishnan Jagadamma, Liam J. McCarron, Alan A. Wiles, Victoria Savikhin, Muhammad T. Sajjad, Mahdieh Yazdani, Vincent M. Rotello, Michael F. Toney, Graeme Cooke, Ifor D. W. Samuel

ACS Applied Materials & Interfaces· Volume 10· Issue 29

Abstract

Additives play an important role in modifying the morphology and phase separation of donor and acceptor molecules in bulk heterojunction (BHJ) solar cells. Here, we report triptycene (TPC) as a small-molecule additive for supramolecular control of phase separation and concomitant improvement of the power conversion efficiency (PCE) of PTB7 donor and fullerene acceptor-based BHJ polymer solar cells. An overall 60% improvement in PCE is observed for both PTB7:PC61BM and PTB7:PC71BM blends. The improved photovoltaic (PV) performance can be attributed to three factors: (a) TPC-induced supramolecular interactions with donor:acceptor components in the blends to realize a nanoscale phase-separated morphology; (b) an increase in the charge transfer state energy that lowers the driving force for electron transfer from donor to acceptor molecules; and (c) an increase in the charge carrier mobility. An improvement in efficiency using TPC as a supramolecular additive has also been demonstrated for other BHJ blends such as PBDB-T:PC71BM and P3HT:PCBM, implying the wide applicability of this new additive molecule. A comparison of the photostability of TPC as an additive for PTB7:PCBM solar cells to that of the widely used 1,8-diiodooctane additive shows ∼30% higher retention of PV performance for the TPC-added solar cells after 34 h of AM 1.5G illumination. The results obtained suggest that the approach of using additives that can promote supramolecular interactions to modify the length scale of phase separation between donor and acceptor is very promising and can lead to the development of highly efficient and stable organic photovoltaics.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · solar cell performance optimization

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

Affiliations

Organic Semiconductor Centre, SUPA, School of Physics and Astronomy, University of St. Andrews, St. Andrews, Fife KY16 9SS, U.K.

Glasgow Centre for Physical Organic Chemistry (GCPOC), WestCHEM, School of Chemistry, University of Glasgow, Glasgow G12 8QQ, U.K..

Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park, California 94025, United States

Electrical Engineering Department, Stanford University, 350 Serra Mall, Stanford, California 94305, United States

Department of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, Massachusetts 01003, United States

Funding

Royal Society · Engineering and Physical Sciences Research Council · FP7 Ideas: European Research Council · Wolfson Foundation

References (62)

Show source-provided references
1. 10.1002/adma.20160405910.1002/adma.201604059 ↗
2. 10.1002/adma.20160028110.1002/adma.201600281 ↗
3. 10.1016/j.progpolymsci.2013.08.00810.1016/j.progpolymsci.2013.08.008 ↗
4. 10.1021/acsami.6b1648710.1021/acsami.6b16487 ↗
5. 10.1002/adfm.20130213410.1002/adfm.201302134 ↗
6. 10.1021/jp512721e10.1021/jp512721e ↗
7. 10.1002/adfm.20100097510.1002/adfm.201000975 ↗
8. 10.1039/c4tc00994k10.1039/c4tc00994k ↗
9. 10.1002/aenm.20150257910.1002/aenm.201502579 ↗
10. 10.1038/srep2006210.1038/srep20062 ↗
11. 10.1016/j.mattod.2013.08.01310.1016/j.mattod.2013.08.013 ↗
12. 10.1039/c6ta07105h10.1039/c6ta07105h ↗
13. http://www.molbase.com/en/properties_24772-63-2-moldata-48193.html (accessed Feb 19, 2018).
14. 10.1021/acs.chemmater.5b0434610.1021/acs.chemmater.5b04346 ↗
15. 10.1039/c5ta04129e10.1039/c5ta04129e ↗
16. 10.1002/aenm.20160097010.1002/aenm.201600970 ↗
17. 10.1039/c7tc04358a10.1039/c7tc04358a ↗
18. 10.1002/adma.20160206710.1002/adma.201602067 ↗
19. 10.1039/c6tc05066b10.1039/c6tc05066b ↗
20. 10.7567/apex.8.02430110.7567/apex.8.024301 ↗
21. 10.1039/c5ee02871j10.1039/c5ee02871j ↗
22. 10.1039/c0cc04852f10.1039/c0cc04852f ↗
23. 10.1002/ejoc.20110068410.1002/ejoc.201100684 ↗
24. 10.1246/cl.2010.65810.1246/cl.2010.658 ↗
25. 10.1021/ar800107v10.1021/ar800107v ↗
26. 10.1080/10610278.2012.69160710.1080/10610278.2012.691607 ↗
27. 10.1016/s0022-2860(00)00406-310.1016/s0022-2860(00)00406-3 ↗
28. 10.1039/a904457d10.1039/a904457d ↗
29. 10.1039/c4ta02276a10.1039/c4ta02276a ↗
30. 10.1107/s002188981200403710.1107/s0021889812004037 ↗
31. 10.1021/acs.chemmater.7b0006710.1021/acs.chemmater.7b00067 ↗
32. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Petersson, G. A.; Nakatsuji, H.; Li, X.; Caricato, M.; Marenich, A. V.; Bloino, J.; Janesko, B. G.; Gomperts, R.; Mennucci, B.; Hratchian, H. P.; Ortiz, J. V.; Izmaylov, A. F.; Sonnenberg, J. L.; Williams; Ding, F.; Lipparini, F.; Egidi, F.; Goings, J.; Peng, B.; Petrone, A.; Henderson, T.; Ranasinghe, D.; Zakrzewski, V. G.; Gao, J.; Rega, N.; Zheng, G.; Liang, W.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Throssell, K.; Montgomery, J. A., Jr.; Peralta, J. E.; Ogliaro, F.; Bearpark, M. J.; Heyd, J. J.; Brothers, E. N.; Kudin, K. N.; Staroverov, V. N.; Keith, T. A.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A. P.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Millam, J. M.; Klene, M.; Adamo, C.; Cammi, R.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Farkas, O.; Foresman, J. B.; Fox, D. J. Gaussian 16, Wallingford, CT, 2016.
33. 10.1002/aenm.20140031110.1002/aenm.201400311 ↗
34. 10.1038/ncomms386710.1038/ncomms3867 ↗
35. 10.1021/acs.jpcc.6b0154810.1021/acs.jpcc.6b01548 ↗
36. 10.1039/c6ta07705f10.1039/c6ta07705f ↗
37. 10.1021/nn204589u10.1021/nn204589u ↗
38. 10.1016/j.orgel.2016.04.01410.1016/j.orgel.2016.04.014 ↗
39. 10.1039/c4cp05826g10.1039/c4cp05826g ↗
40. 10.1021/jz501559q10.1021/jz501559q ↗
41. 10.1088/0953-8984/20/18/18400110.1088/0953-8984/20/18/184001 ↗
42. 10.1039/b200178k10.1039/b200178k ↗
43. 10.1039/b900754g10.1039/b900754g ↗
44. 10.1021/ma401421k10.1021/ma401421k ↗
45. 10.1021/cr300005u10.1021/cr300005u ↗
46. 10.1021/am402744k10.1021/am402744k ↗
47. 10.1146/annurev-physchem-040215-11214410.1146/annurev-physchem-040215-112144 ↗
48. 10.1002/adfm.20080005610.1002/adfm.200800056 ↗
49. 10.1002/aenm.20170281610.1002/aenm.201702816 ↗
50. 10.1021/ar300132r10.1021/ar300132r ↗
51. 10.1021/ja961211010.1021/ja9612110 ↗
52. 10.1002/chem.20100051710.1002/chem.201000517 ↗
53. 10.1021/acs.jpcc.6b0075310.1021/acs.jpcc.6b00753 ↗
54. 10.1021/ma201158d10.1021/ma201158d ↗
55. 10.1021/acsomega.7b0046810.1021/acsomega.7b00468 ↗
56. 10.1002/aenm.20150233810.1002/aenm.201502338 ↗
57. 10.1039/c7ta03144k10.1039/c7ta03144k ↗
58. 10.1002/adfm.20130261210.1002/adfm.201302612 ↗
59. 10.1021/acs.chemmater.5b0234110.1021/acs.chemmater.5b02341 ↗
60. 10.1016/j.solmat.2016.12.02110.1016/j.solmat.2016.12.021 ↗
61. 10.1021/acsami.7b0129610.1021/acsami.7b01296 ↗
62. 10.1002/aenm.20160071210.1002/aenm.201600712 ↗