journal article·2017-12

Novel dithienopyrrole-based molecular donor materials for organic solar cells

Zong-Bing Zhang, Jia-Wei Xu, Xin-Yu Zhang, Shi-Xin Sun, Rong Xing

Functional Materials Letters· Volume 10· Issue 06
Publisher page

Abstract

A new molecule with dithieno[3,2-b:2’,3’-d]pyrrole (DTP) as central moiety and two terminal diketopyrrolopyrrole (DPP) units named DPP-DTPC8 has been designed and synthesized. The push–pull molecule exhibits excellent thermal stability, strong absorption in visible region, and matched energy levels. Devices fabricated from DTPC8:PC[Formula: see text]BM blend films exhibit the maximum power conversion efficiency of 2.75%, with Voc of 0.63 V, Jsc of 9.94 mA[Formula: see text] cm[Formula: see text], and FF of 43.8%. The active layers undergo thermal annealing or solvent vapor annealing treatments, exhibiting inconspicuous influence on the aggregation of the molecule. This study demonstrates that the new molecule DPP-DTPC8 tailored with DTP and DPP units could affect the thermal stability, absorption, energy levels and morphology that manage the photovoltaic performances.
Source: crossref · 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

College of Chemical and Environmental Engineering, Yancheng Teachers University, Yancheng 224002, P. R. China

College of Chemistry and Chemical Engineering, Nanjing Tech University, Nanjing 210009, P. R. China

Funding

Qing-Lan Project of Jiangsu Provinc

References (25)

Show source-provided references
1. 10.1002/adma.20130599910.1002/adma.201305999 ↗
2. 10.1142/S179360471540013510.1142/S1793604715400135 ↗
3. 10.1038/nphoton.2014.26910.1038/nphoton.2014.269 ↗
4. 10.1002/adma.20160051210.1002/adma.201600512 ↗
5. 10.1002/adma.20140207210.1002/adma.201402072 ↗
6. 10.1038/ncomms241110.1038/ncomms2411 ↗
7. 10.1002/adma.20160277610.1002/adma.201602776 ↗
8. 10.1038/nchem.142210.1038/nchem.1422 ↗
9. 10.1039/C4CS00250D10.1039/C4CS00250D ↗
10. 10.1002/adfm.20150502010.1002/adfm.201505020 ↗
11. 10.1007/s10853-016-0070-x10.1007/s10853-016-0070-x ↗
12. 10.1021/ol500809e10.1021/ol500809e ↗
13. 10.1021/acsami.6b1457210.1021/acsami.6b14572 ↗
14. 10.1021/jacs.5b0374010.1021/jacs.5b03740 ↗
15. 10.1016/j.matlet.2016.04.00910.1016/j.matlet.2016.04.009 ↗
16. 10.1002/aenm.20130018110.1002/aenm.201300181 ↗
17. 10.1021/am500622310.1021/am5006223 ↗
18. 10.1002/adma.20160001310.1002/adma.201600013 ↗
19. 10.1002/adma.20150564510.1002/adma.201505645 ↗
20. 10.1021/cm901487f10.1021/cm901487f ↗
21. 10.1021/cm501814710.1021/cm5018147 ↗
22. 10.1021/ja310483w10.1021/ja310483w ↗
23. 10.1021/acsami.5b0348810.1021/acsami.5b03488 ↗
24. 10.1142/S179360471750049710.1142/S1793604717500497 ↗
25. 10.1002/aenm.20140053810.1002/aenm.201400538 ↗