High performance achieved via core engineering and side-chain engineering in organic solar cells based on the penta-fused-ring acceptor. Issue 19 (5th May 2022)
- Record Type:
- Journal Article
- Title:
- High performance achieved via core engineering and side-chain engineering in organic solar cells based on the penta-fused-ring acceptor. Issue 19 (5th May 2022)
- Main Title:
- High performance achieved via core engineering and side-chain engineering in organic solar cells based on the penta-fused-ring acceptor
- Authors:
- Li, Fengting
Chen, Yongjie
Fan, Xin-Heng
Gao, Cai-Yan
Zhu, Xiaozhang
Yang, Lian-Ming - Abstract:
- Abstract : Compared with the thiophene-based acceptor, the pyrrole-based acceptor exhibits a strong red-shift and the related device efficiency is significantly improved. Abstract : Recently, low-band gap non-fullerene acceptors (NFAs) have achieved rapid development and proven to be an effective means to improve the performance of organic photovoltaics (OPVs) because of their adjustable energy levels and strong near-infrared (NIR) absorption. In order to enhance light capture in the NIR region, strong electron donating and electron withdrawing units were introduced to enhance intramolecular charge transfer (ICT). However, the commonly used end-group engineering often fails to achieve a simultaneous enhancement of short-circuit current ( J sc ) and open-circuit voltage ( V oc ). In contrast, the strategy of core engineering can enhance both J sc and V oc . Moreover, among five-membered aromatic heterocycles, pyrrole has the highest electron density, and thus multi-pyrrole could be a strong electron donating unit. Therefore, we designed and synthesized a novel pyrrole-based NFA (DPBT-2Cl) for comparison with a thiophene-based NFA (TPBT-2Cl). Red shifts of 55 nm (in solution) and 75 nm (in film) of the absorption peaks were achieved through core engineering by substituting pyrrole for thiophene. The morphology of the active layer also plays a crucial role in the performance. By modifying the N atom of pyrrole with alkyl chain as the side-chain engineering, the phase separationAbstract : Compared with the thiophene-based acceptor, the pyrrole-based acceptor exhibits a strong red-shift and the related device efficiency is significantly improved. Abstract : Recently, low-band gap non-fullerene acceptors (NFAs) have achieved rapid development and proven to be an effective means to improve the performance of organic photovoltaics (OPVs) because of their adjustable energy levels and strong near-infrared (NIR) absorption. In order to enhance light capture in the NIR region, strong electron donating and electron withdrawing units were introduced to enhance intramolecular charge transfer (ICT). However, the commonly used end-group engineering often fails to achieve a simultaneous enhancement of short-circuit current ( J sc ) and open-circuit voltage ( V oc ). In contrast, the strategy of core engineering can enhance both J sc and V oc . Moreover, among five-membered aromatic heterocycles, pyrrole has the highest electron density, and thus multi-pyrrole could be a strong electron donating unit. Therefore, we designed and synthesized a novel pyrrole-based NFA (DPBT-2Cl) for comparison with a thiophene-based NFA (TPBT-2Cl). Red shifts of 55 nm (in solution) and 75 nm (in film) of the absorption peaks were achieved through core engineering by substituting pyrrole for thiophene. The morphology of the active layer also plays a crucial role in the performance. By modifying the N atom of pyrrole with alkyl chain as the side-chain engineering, the phase separation of PM6/DPBT-2Cl in the active layer is more ideal than that of PM6/TPBT-2Cl. The best power conversion efficiency (PCE) increases from 1.0% for TPBT-2Cl to 11.5% for DPBT-2Cl, which is one of the high performances we know of for reported OSCs based on the penta-fused-ring (PFR), with J sc increasing from 3.56 mA cm −2 to 23.1 mA cm −2 and V oc from 0.74 V to 0.78 V. We demonstrate that core engineering by replacing thiophene with pyrrole enables low-band gap NFAs and side chain engineering enables a more ideal phase separation in the active layer, which is an excellent strategy to realize a simultaneous enhancement in both V oc and J sc and maximize the performance of OPVs. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 10:Issue 19(2022)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 10:Issue 19(2022)
- Issue Display:
- Volume 10, Issue 19 (2022)
- Year:
- 2022
- Volume:
- 10
- Issue:
- 19
- Issue Sort Value:
- 2022-0010-0019-0000
- Page Start:
- 7724
- Page End:
- 7730
- Publication Date:
- 2022-05-05
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2tc00725h ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21540.xml