Hydrogen Bond Induced Green Solvent Processed High Performance Ternary Organic Solar Cells with Good Tolerance on Film Thickness and Blend Ratios. (27th May 2019)
- Record Type:
- Journal Article
- Title:
- Hydrogen Bond Induced Green Solvent Processed High Performance Ternary Organic Solar Cells with Good Tolerance on Film Thickness and Blend Ratios. (27th May 2019)
- Main Title:
- Hydrogen Bond Induced Green Solvent Processed High Performance Ternary Organic Solar Cells with Good Tolerance on Film Thickness and Blend Ratios
- Authors:
- Du, Xiaoyang
Lu, Xi
Zhao, Juewen
Zhang, Yuqing
Li, Xinrui
Lin, Hui
Zheng, Caijun
Tao, Silu - Abstract:
- Abstract: For comprehensive development of organic solar cells (OSCs), some factors such as environmental stability, low cost, insensitive film thickness, component contents tolerance, and green preparation processes are equally crucial to achieve high power conversion efficiencies (PCEs). In this work, a small molecule 3‐(diethylamino)‐7‐imino‐7H‐benzo[4, 5]imidazo[1, 2‐a]chromeno[3, 2‐c]pyridine‐6‐carbonitrile (DIBC), which is commercially available at low cost, is utilized to realize high‐performance ternary OSCs. Demonstrated via Fourier transform infrared and 2D‐ 1 HNMR, DIBC can form hydrogen bond interactions with [6, 6]‐phenyl‐C71 ‐butyric acid methyl ester (PC71 BM) in solid films. Further electrostatic potential (ESP) calculations indicate that the hydrogen bond interaction enhances the ESP of PC71 BM and accelerates charge transport between donor and acceptor. As a result, poly(4, 8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1, 2‐b;4, 5‐b0]dithiophene‐2, 6‐diylalt‐(4‐(2‐ethylhexyl)‐3‐fluorothieno[3, 4‐b]thiophene‐)‐2‐carboxylate‐2‐6‐diyl (PTB7‐Th):DIBC:PC71 BM‐based ternary OSC achieves a maximum efficiency of 12.17%, which is the best result of green solvent processed fullerene OSCs at present. It is noteworthy that the ternary OSCs also show great tolerance to film thickness and blend ratios. These unique properties are attributed to the hydrogen‐bond‐linked DIBC and PC71 BM, which modulates molecule distribution and improves film morphology with anAbstract: For comprehensive development of organic solar cells (OSCs), some factors such as environmental stability, low cost, insensitive film thickness, component contents tolerance, and green preparation processes are equally crucial to achieve high power conversion efficiencies (PCEs). In this work, a small molecule 3‐(diethylamino)‐7‐imino‐7H‐benzo[4, 5]imidazo[1, 2‐a]chromeno[3, 2‐c]pyridine‐6‐carbonitrile (DIBC), which is commercially available at low cost, is utilized to realize high‐performance ternary OSCs. Demonstrated via Fourier transform infrared and 2D‐ 1 HNMR, DIBC can form hydrogen bond interactions with [6, 6]‐phenyl‐C71 ‐butyric acid methyl ester (PC71 BM) in solid films. Further electrostatic potential (ESP) calculations indicate that the hydrogen bond interaction enhances the ESP of PC71 BM and accelerates charge transport between donor and acceptor. As a result, poly(4, 8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1, 2‐b;4, 5‐b0]dithiophene‐2, 6‐diylalt‐(4‐(2‐ethylhexyl)‐3‐fluorothieno[3, 4‐b]thiophene‐)‐2‐carboxylate‐2‐6‐diyl (PTB7‐Th):DIBC:PC71 BM‐based ternary OSC achieves a maximum efficiency of 12.17%, which is the best result of green solvent processed fullerene OSCs at present. It is noteworthy that the ternary OSCs also show great tolerance to film thickness and blend ratios. These unique properties are attributed to the hydrogen‐bond‐linked DIBC and PC71 BM, which modulates molecule distribution and improves film morphology with an interpenetrating network structure. Furthermore, the DIBC containing device also exhibits good thermal and light radiation stability. These results illustrate that intermolecular hydrogen bond interaction has great potential for realizing high‐performance OSCs. Abstract : Intermolecular hydrogen bonding is a potential strategy for organic solar cells to realize low cost, high efficiency, good device and morphology stability, excellent composition, and film thickness tolerance. … (more)
- Is Part Of:
- Advanced functional materials. Volume 29:Number 30(2019)
- Journal:
- Advanced functional materials
- Issue:
- Volume 29:Number 30(2019)
- Issue Display:
- Volume 29, Issue 30 (2019)
- Year:
- 2019
- Volume:
- 29
- Issue:
- 30
- Issue Sort Value:
- 2019-0029-0030-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-05-27
- Subjects:
- electrostatic potential -- green solvents -- hydrogen bonds -- organic solar cells -- stability
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.201902078 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11244.xml