Ultra-stable single component organic solar cells under thermal and/or illumination pressure: the next superior organic photovoltaics?
Yakun He a b, Peter Bäuerle c, Weiwei Li d, Thomas Heumüller a e, Ning Li a e, Christoph Brabec a e
a Institute of Materials for Electronics and Energy Technology (i-MEET), Friedrich-Alexander-Universität Erlangen-Nürnberg, Martensstrasse 7, 91058 Erlangen, Germany
b Erlangen Graduate School in Advanced Optical Technologies (SAOT), Paul-Gordan-Straße 6, 91052 Erlangen, Germany
c Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, Ulm, Germany
d Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China
e Helmholtz-Institute Erlangen-Nürnberg (HI ERN), Immerwahrstraße 2, 91058 Erlangen, Germany
International Conference on Hybrid and Organic Photovoltaics
Proceedings of 13th Conference on Hybrid and Organic Photovoltaics (HOPV21)
Online, Spain, 2021 May 24th - 28th
Organizers: Marina Freitag, Feng Gao and Sam Stranks
Oral, Yakun He, presentation 007
Publication date: 11th May 2021

Stability issue is the core restriction for the application of organic solar cells (OSCs). However, state-of-the-art OSCs based on bulk-heterojunction concept suffer from stability problems caused by the severe morphological changes upon thermal or illumination stress [1]. Single-component concept, enabled by the covalently-bonded structure with donor and acceptor in one molecule, presents attractive advantages such as a simplification of device fabrication and a stabilization of microstructure [2]. Recently, with the rapid improvement of efficiency from 2-3% to 8.4% for single-component organic solar cells (SCOSCs), the reports on their stability however are scanty. In this work, we for the first time systematically investigated the stability under thermal and illumination stress of a series of SCOSCs based on polymeric (SCP3, PBDBPBI-Cl) and molecular (Dyad1, 2, 3, 4) materials. Under thermal pressure, double-cable polymer-based SCOSCs exhibited excellent thermal stability with no degradation at 90 oC for 3000 hours, partially attributed to the high temperatures (around 200 oC) for post-treating active layer during device fabrication. Such rather high annealing temperatures are plausible to create microstructure arrangements which are in thermodynamic equilibrium after cooling down. Furthermore, without precedent, we studied the thermal stability comparison among a series of SCOSCs based on D-A small molecules (Dyad1, 2 and 3) with the same donor and acceptor units but differently long alkyl space linkers. Since macroscopic diffusion of molecules is excluded in these dyads, the length of the spacer can only provide the necessary flexibility for sub-nm rearrangements caused by thermal stress. Interestingly, dyads showed a distinctly different behavior, Dyad1 with the shortest linker exhibiting the highest thermal stability, while Dyad3 with the longest linker showing the worst thermal stability [3]. This highlights the need for further in-depth studies on the dual importance of spacer length for performance and stability. Moreover, Dyad1-based SCOSCs exhibited extraordinary illumination stability, retaining 98% of the initial PCE under concentrated light equal to 7.5-suns for over 1000 hours, which could be among the highest illumination stability for solution-processed OSCs. Based on the outstanding stability, SCOSCs could be an ideal candidate to study the ultimate stability under extremely rugged accelerating conditions such as high temperature and concentrated light. Since the morphological evolution is excluded, SCOSCs could serve as a model system to selectively study interface degradation. In the near future, SCOSCs will see a prospective renaissance with 10% efficiency and 20 years lifetime for industrial applications.

Y.H. is grateful to the financial support from China Scholarship Council (CSC) and Erlangen Graduate School in Advanced Optical Technologies (SAOT). C.J.B. gratefully acknowledges funding by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under the project numbers 182849149 – SFB 953 and INST 90/917, INST 90/1093‐1, financial support through the “Aufbruch Bayern” initiative of the state of Bavaria (EnCN and SFF) and the Bavarian Initiative “Solar Technologies go Hybrid” (SolTech) and the grant “ELF‐PV Design and development of solution processed functional materials for the next generations of PV technologies” by the Bavarian State Government (No. 44‐6521a/20/4).

© FUNDACIO DE LA COMUNITAT VALENCIANA SCITO
We use our own and third party cookies for analysing and measuring usage of our website to improve our services. If you continue browsing, we consider accepting its use. You can check our Cookies Policy in which you will also find how to configure your web browser for the use of cookies. More info