Aminosilane as a Molecular Linker between the Electron-Transport Layer and Active Layer for Efficient Inverted Polymer Solar Cells
Source abstract
Abstract
Interfacial modification is crucial for improving the photovoltaic performance. In this work, we present an aminosilane as a molecular linker between the ZnO electron-transport layer and fullerene derivative phenyl-C 71 -butyric acid methyl ester (PC 71 BM)-based active layer for efficient inverted polymer solar cells. An enhancement in the power-conversion efficiency (PCE), from 8.47 to 9.46%, was achieved on using PTB7-Th as donors. The aminosilane molecular linker provides dual functionalities for enhanced PCE, including (1) passivating the ZnO surface and decreasing the surface work function of ZnO for energy-level alignment and (2) bonding onto the fullerene derivative PC 71 BM-based active layer to reduce the interface contact resistance.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China
Graduate University of Chinese Academy of Sciences, Beijing 100049, China
Funding
Chinese Academy of Sciences · Central Committee of the Communist Party of China · Collaborative Innovation Center of Chemistry for Energy Materials
References (29)
Show source-provided references
1. 10.1126/science.121882910.1126/science.1218829 ↗
2. 10.1002/adma.20120059410.1002/adma.201200594 ↗
3. 10.1002/adma.20110026610.1002/adma.201100266 ↗
4. 10.1039/c2ee22296e10.1039/c2ee22296e ↗
5. 10.1039/c3ta10537g10.1039/c3ta10537g ↗
6. 10.1002/adfm.20130416310.1002/adfm.201304163 ↗
7. 10.1039/C4EE03802A10.1039/C4EE03802A ↗
8. 10.1002/adma.20130299110.1002/adma.201302991 ↗
9. 10.1002/adma.20160116110.1002/adma.201601161 ↗
10. 10.1021/acsami.5b0775910.1021/acsami.5b07759 ↗
11. 10.1002/aenm.20130169210.1002/aenm.201301692 ↗
12. 10.1039/C6TA07105H10.1039/C6TA07105H ↗
13. 10.1016/j.nanoen.2015.02.03210.1016/j.nanoen.2015.02.032 ↗
14. 10.1016/j.apsusc.2014.11.16110.1016/j.apsusc.2014.11.161 ↗
15. 10.1021/la802621n10.1021/la802621n ↗
16. 10.1016/j.electacta.2009.03.00610.1016/j.electacta.2009.03.006 ↗
17. 10.1021/am800081k10.1021/am800081k ↗
18. 10.1021/am500666e10.1021/am500666e ↗
19. 10.1021/ja512559410.1021/ja5125594 ↗
20. 10.1007/s00289-011-0685-710.1007/s00289-011-0685-7 ↗
21. 10.1038/ncomms1280610.1038/ncomms12806 ↗
22. 10.1002/1099-0690(200202)2002:4<640::AID-EJOC640>3.0.CO;2-U10.1002/1099-0690(200202)2002:4<640::AID-EJOC640>3.0.CO;2-U ↗
23. 10.1021/ja027200q10.1021/ja027200q ↗
24. 10.1016/j.apsusc.2007.06.06110.1016/j.apsusc.2007.06.061 ↗
25. 10.1016/0021-9797(80)90209-X10.1016/0021-9797(80)90209-X ↗
26. 10.1021/j150568a00410.1021/j150568a004 ↗
27. 10.1039/c3ee42440e10.1039/c3ee42440e ↗
28. 10.1002/adfm.20080128610.1002/adfm.200801286 ↗
29. 10.1021/am501920z10.1021/am501920z ↗