journal article·2018-02-28

Evidence on Enhanced Exciton Polarizability in Donor/Acceptor Bulk Heterojunction Organic Photovoltaics

Zhiqiang Guan, Ho-Wa Li, Yuanhang Cheng, Yingqi Zhao, Ming-Fai Lo, Sai-Wing Tsang, Chun-Sing Lee

Publisher page

Abstract

Using electroabsorption spectroscopy, we explore the polarizability of Frenkel excitons in both pristine donor and D/A blend films. We observe for the first time that the polarizability of excitonic states in pristine donors can be dramatically increased by adding an n-type acceptor. By investigating the dielectric effect in different organic semiconductor systems, we find that the polarizability of Frenkel excitons has direct correlation with the measured dielectric constant of the bulk heterojunction thin films. Our results disclose the difference in the nature of Frenkel excitons in pristine donor and D/A blend systems, revealing an important role of excitonic states in charge separation process of organic photovoltaic devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications

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

Affiliations

Center of Super-Diamond and Advanced Films (COSDAF), ‡Department of Chemistry, and §Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong SAR 999077, P. R. China

Funding

Research Grants Council, University Grants Committee · National Natural Science Foundation of China

References (38)

Show source-provided references
1. 10.1021/cr050149z10.1021/cr050149z ↗
2. 10.1038/nphoton.2012.1110.1038/nphoton.2012.11 ↗
3. 10.1002/adfm.20050021110.1002/adfm.200500211 ↗
4. 10.1038/nphoton.2015.610.1038/nphoton.2015.6 ↗
5. 10.1002/adma.20090369710.1002/adma.200903697 ↗
6. 10.1002/aenm.20140037810.1002/aenm.201400378 ↗
7. 10.1038/ncomms629310.1038/ncomms6293 ↗
8. 10.1002/adma.20150401410.1002/adma.201504014 ↗
9. 10.1007/s10854-017-6362-310.1007/s10854-017-6362-3 ↗
10. 10.1007/s10854-017-6443-310.1007/s10854-017-6443-3 ↗
11. 10.1002/adma.20140056310.1002/adma.201400563 ↗
12. 10.1002/adma.20120449510.1002/adma.201204495 ↗
13. 10.1021/acsami.6b0601010.1021/acsami.6b06010 ↗
14. 10.1063/1.496612710.1063/1.4966127 ↗
15. 10.1002/pssb.222173022910.1002/pssb.2221730229 ↗
16. 10.1103/physrevlett.76.190010.1103/physrevlett.76.1900 ↗
17. 10.1016/0301-0104(81)85055-010.1016/0301-0104(81)85055-0 ↗
18. 10.1103/physrevb.58.768910.1103/physrevb.58.7689 ↗
19. 10.1038/ncomms424510.1038/ncomms4245 ↗
20. 10.1063/1.162301410.1063/1.1623014 ↗
21. 10.1021/acs.jpcc.6b0237510.1021/acs.jpcc.6b02375 ↗
22. 10.1103/physrevb.82.07520710.1103/physrevb.82.075207 ↗
23. 10.1002/adfm.20130342610.1002/adfm.201303426 ↗
24. 10.1103/physrevlett.101.03740110.1103/physrevlett.101.037401 ↗
25. 10.1126/science.124624910.1126/science.1246249 ↗
26. 10.1103/physrevlett.103.03660110.1103/physrevlett.103.036601 ↗
27. 10.1103/physrevb.60.811110.1103/physrevb.60.8111 ↗
28. 10.1016/s0925-3467(97)00153-510.1016/s0925-3467(97)00153-5 ↗
29. 10.1103/physrevb.60.532110.1103/physrevb.60.5321 ↗
30. 10.1021/jp507097h10.1021/jp507097h ↗
31. 10.1103/physrevb.43.678110.1103/physrevb.43.6781 ↗
32. 10.1021/cr900271s10.1021/cr900271s ↗
33. 10.1103/physrev.54.55410.1103/physrev.54.554 ↗
34. 10.1002/aenm.20150027910.1002/aenm.201500279 ↗
35. 10.1021/acs.jpcc.5b0008210.1021/acs.jpcc.5b00082 ↗
36. 10.1038/nenergy.2016.8910.1038/nenergy.2016.89 ↗
37. 10.1002/adma.20140198710.1002/adma.201401987 ↗
38. 10.1002/aenm.20150012310.1002/aenm.201500123 ↗