14%-efficiency fullerene-free ternary solar cell enabled by designing a short side-chain substituted small-molecule acceptor. (October 2019)
- Record Type:
- Journal Article
- Title:
- 14%-efficiency fullerene-free ternary solar cell enabled by designing a short side-chain substituted small-molecule acceptor. (October 2019)
- Main Title:
- 14%-efficiency fullerene-free ternary solar cell enabled by designing a short side-chain substituted small-molecule acceptor
- Authors:
- Chang, Yuan
Zhang, Xin
Tang, Yabing
Gupta, Monika
Su, Dan
Liang, Jiaen
Yan, Dong
Li, Kun
Guo, Xuefeng
Ma, Wei
Yan, He
Zhan, Chuanlang - Abstract:
- Abstract: A new fused-ring electron acceptor (FREA) IEICF-DMOT was designed and synthesized with 3, 4-dimethoxylthiophene (DMOT) as the π−bridges to link the IDT core and the end IC-2F units. Compared to IEICO-4F which uses 3-(2-ethylhexyloxyl)thiophene as the bridge, IEICF-DMOT with two much shorter side chains (methoxyl) on the π−bridge exhibits a higher level of the lowest unoccupied molecular orbital (LUMO) (−3.85 vs. −3.93 eV), broadening absorption band, larger absorptivity, and a larger bandgap (1.38 vs. 1.27 eV), but reduced crystallinity in both the in-plane (100) and out-of-plane (010) directions, which makes a 0.13 V-larger open-circuit voltage ( V oc ) with a 10%-higher external quantum efficiency (EQE) and 9%-higher fill factor (FF), and thereby, a power conversion efficiency (PCE) of 13% in comparison with the IEICO-4F 10% efficiency. Adding the crystalline and narrower bandgap IEICO-4F as the near infrared absorber, the PBDB-T:IEICF-DMOT:IEICO-4F (1:1:0.1) ternary blend shows increased crystallinity for both donor and acceptor phases with increased hole and electron mobilities, achieving increased short-circuit current-density ( J sc ) and FF, and therefore, a promising PCE of 14%. These results indicate that DMOT with short side-chains on the thiophene-3, 4-positions is a promise bridge unit to design nonfullerene small-molecule acceptors with tunable energy levels, optical bandgap, and crystallinity to simultaneously increase V oc, EQE, and FF, andAbstract: A new fused-ring electron acceptor (FREA) IEICF-DMOT was designed and synthesized with 3, 4-dimethoxylthiophene (DMOT) as the π−bridges to link the IDT core and the end IC-2F units. Compared to IEICO-4F which uses 3-(2-ethylhexyloxyl)thiophene as the bridge, IEICF-DMOT with two much shorter side chains (methoxyl) on the π−bridge exhibits a higher level of the lowest unoccupied molecular orbital (LUMO) (−3.85 vs. −3.93 eV), broadening absorption band, larger absorptivity, and a larger bandgap (1.38 vs. 1.27 eV), but reduced crystallinity in both the in-plane (100) and out-of-plane (010) directions, which makes a 0.13 V-larger open-circuit voltage ( V oc ) with a 10%-higher external quantum efficiency (EQE) and 9%-higher fill factor (FF), and thereby, a power conversion efficiency (PCE) of 13% in comparison with the IEICO-4F 10% efficiency. Adding the crystalline and narrower bandgap IEICO-4F as the near infrared absorber, the PBDB-T:IEICF-DMOT:IEICO-4F (1:1:0.1) ternary blend shows increased crystallinity for both donor and acceptor phases with increased hole and electron mobilities, achieving increased short-circuit current-density ( J sc ) and FF, and therefore, a promising PCE of 14%. These results indicate that DMOT with short side-chains on the thiophene-3, 4-positions is a promise bridge unit to design nonfullerene small-molecule acceptors with tunable energy levels, optical bandgap, and crystallinity to simultaneously increase V oc, EQE, and FF, and ultimately, efficiency. Graphical abstract: Image 1 Highlights: 3, 4-dimethoxylthiophene (DMOT), a new π-bridge for designing nonfullerene acceptor with improved absorption property. A new fused-ring electron acceptor, IEICF-DMOT reported. The use of DMOT enables LUMO level upshifted and absorption broadened, helpful for obtaining increased V oc and J sc . The use of short methoxyl side chains on the π−thiophene enables to reduce the crystallinity. 13% and 14% efficiencies fullerene-free binary and ternary solar cells obtained. … (more)
- Is Part Of:
- Nano energy. Volume 64(2019)
- Journal:
- Nano energy
- Issue:
- Volume 64(2019)
- Issue Display:
- Volume 64, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 64
- Issue:
- 2019
- Issue Sort Value:
- 2019-0064-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-10
- Subjects:
- Small-molecule acceptor -- Ternary solar cell -- Fullerene-free -- Nonfullerene -- Organic photovoltaic
Nanoscience -- Periodicals
Nanotechnology -- Periodicals
Nanostructured materials -- Periodicals
Power resources -- Technological innovations -- Periodicals
Nanoscience
Nanostructured materials
Nanotechnology
Power resources -- Technological innovations
Periodicals
621.042 - Journal URLs:
- http://www.sciencedirect.com/science/journal/22112855 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.nanoen.2019.103934 ↗
- Languages:
- English
- ISSNs:
- 2211-2855
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11646.xml