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Two Compatible Polymer Donors Enabling Ternary Organic Solar Cells with a Small Nonradiative Energy Loss and Broad Composition Tolerance
Southern Univ Sci & Technol SUSTech, Peoples R China.
Linköping University, Department of Physics, Chemistry and Biology, Biomolecular and Organic Electronics. Linköping University, Faculty of Science & Engineering.
Southern Univ Sci & Technol SUSTech, Peoples R China.
Southern Univ Sci & Technol SUSTech, Peoples R China; Korea Univ, South Korea.
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2020 (English)In: Solar RRL, E-ISSN 2367-198X, Vol. 4, no 11, article id 2000396Article in journal (Refereed) Published
Abstract [en]

High-performance nonfullerene ternary organic solar cells (OSCs) with two polymer donors are less frequently reported because of the limited numbers of efficient polymer donors with good compatibility. Herein, a wide-bandgap polymer P1 with a deep-lying highest occupied molecular orbital (HOMO) level is incorporated as the third component into the benchmark PM6:Y6 binary system to fabricate ternary OSCs. The introduction of P1 not only leads to extended absorption coverage and forms a cascade-like energy level alignment but also shows excellent compatibility with PM6, resulting in a favorable morphology in the ternary blend. More importantly, P1 possesses a deeper HOMO level (-5.6 eV) than most well-known donor polymers, which enables resulting ternary OSCs with an improved open-circuit voltage. As a result, the optimized ternary OSCs with 40 wt% P1 in donors achieve a power conversion efficiency (PCE) of 16.2% with a small nonradiative recombination loss of 0.23 eV, which is among the highest values of ternary OSCs based on two polymer donors. In addition, the ternary OSCs show a broad composition tolerance with a high PCE of over 14% throughout the whole blend ratios. These results provide an effective approach to fabricate efficient ternary OSCs by synergizing two wide-bandgap polymer donors.

Place, publisher, year, edition, pages
Wiley-VCH Verlagsgesellschaft, 2020. Vol. 4, no 11, article id 2000396
Keywords [en]
compatibility; composition tolerance; energy loss; ternary organic solar cells; wide-bandgap polymer donors
National Category
Polymer Chemistry
Identifiers
URN: urn:nbn:se:liu:diva-170560DOI: 10.1002/solr.202000396ISI: 000571638800001Scopus ID: 2-s2.0-85091150596OAI: oai:DiVA.org:liu-170560DiVA, id: diva2:1476941
Note

Funding Agencies|National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21801124]; Shenzhen Science and Technology Innovation Commission [JCYJ20170817105905899, JCYJ20180504165709042]; National Research Foundation of KoreaNational Research Foundation of Korea [NRF-2016M1A2A2940911, 2019R1A6A1A11044070]; Center for Computational Science and Engineering of SUSTech

Available from: 2020-10-16 Created: 2020-10-16 Last updated: 2022-11-18Bibliographically approved
In thesis
1. The Influence of Energy Levels on Voltage Losses and Charge Generation in Organic Solar Cells
Open this publication in new window or tab >>The Influence of Energy Levels on Voltage Losses and Charge Generation in Organic Solar Cells
2022 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Organic solar cells (OSCs) are a next-generation photovoltaic technology that convert solar energy to electrical energy. They have attracted great attention due to their advantages of low cost, ease of synthesis, light weight, mechanical flexibility, and roll-to-roll processability. In the past decades, owing to the development of the materials, device optimization and the understanding of the working mechanism, the power conversion efficiency (PCE) has been boosted to ~19%. However, the efficiency of the OSCs is still not comparable to the conventional inorganic solar cells and emerging perovskite solar cells due to the large open-circuit voltage loss (Vloss). In addition, it is also important to obtain efficient charge generation while reducing the Vloss. Thus, understanding the loss mechanisms in the OSCs is significant for achieving further improvement.

In this thesis, a novel small-molecule donor named ZR1 was used to fabricate all-small-molecule OSCs (SM-OSCs), which shows efficient charge separation and transport with the optimized hierarchical morphologies, obtaining a breakthrough efficiency of 13.34% with a low Vloss (0.54 eV) in SM-OSCs. In this system, the energy offsets between the donor and acceptor (ΔHOMO or ΔLUMO) play an important role in the open-circuit voltage (VOC) of the OSCs. According to the optoelectronic reciprocity introduced in this thesis, the sub-gap absorption and emission by charge transfer (CT) states lead to large radiative and non-radiative recombination losses. The results show that the decreased HOMO offsets between donor and acceptor can effectively reduce both radiative and non-radiative recombination losses from the CT states, resulting in a suppressed Vloss.

In addition to the SM-OSCs, we also study the Vloss and charge generation in the all-polymer OSCs (all- PSCs). A series of polymer acceptors were designed and applied in all-PSCs. In this work, all devices with negligible LUMO offsets show high VOCs of 1.02-1.15 V and good short-circuit currents (JSCs) of 8.87-15.16 mA cm−2 as well as small Vlosss. This study reveals that the small Vloss and the effective charge generation can also be realized simultaneously in all-PSCs with small energy offsets.

Next, we found that introducing a third component can also reduce Vloss. In this work, we start with the fundamental photophysical processes which determine the VOCs of the devices and provide a universal approach framework well explaining the VOC of ternary OSCs (TOSCs) in different situations. By combining experimental investigations with theoretical simulations, we highlight the significant influence of the thermal population arising from the guest component-related CT states and local excited (LE)states on the non-radiative recombination losses in TOSCs. Firmly based on our new understanding, we provide design rules for enhancing the VOC in TOSCs: 1) high emission yield for the guest binary system; close charge-transfer energies between two binary systems; 2) high miscibility of the guest component with the low-optical-gap component in the host binary blends.

In the all-PSCs work we did before, we find the small Vloss and the effective charge generation can be achieved simultaneously with small energy offsets, which can be also observed in other non-fullerene based OSCs. It was found that some of non-fullerene acceptors based OSCs can realize an efficient charge generation and a suppressed charge recombination process with small energy offsets (< 0.3 eV) between the donor and the acceptor, leading to a low Vloss, a high JSC, and a high fill factor (FF) simultaneously. Here, we investigate a series of OSCs blends with different HOMO offsets between donor and in a large range of ~ 0 to 0.50 eV. Along with decreasing HOMO offsets, the blends show reduced Vlosss. For the JSC and the FF, we observe a maximum value at an optimal energetic offset around 0.2-0.3 eV and the optimal energetic offset appears at different values for different non-fullerene acceptors. Through the analysis of the ultrafast transient absorption, we find inefficient charge generation when the HOMO offset is close to zero, which attributed to the back transfer of a hole from the donor to the acceptor. The affected charge generation at the small HOMO offsets is probably the main reason for the deceased JSC and FF. This study demonstrates the existence of optimal energy offsets for achieving high-performance OSCs.

Place, publisher, year, edition, pages
Linköping: Linköping University Electronic Press, 2022. p. 64
Series
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 2261
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:liu:diva-190046 (URN)10.3384/9789179294984 (DOI)978-91-7929-497-7 (ISBN)978-91-7929-498-4 (ISBN)
Public defence
2022-12-13, Planck, Fysikhuset, Campus Valla, Linköping, 10:15 (English)
Opponent
Supervisors
Note

2022-11-18 The thesis was first published online. Incorrect series number was printed in the thesis. The series no should be 2261, which is corrected in the online version. The PDF ISBN was also added to the online version.

Available from: 2022-11-18 Created: 2022-11-18 Last updated: 2022-11-21Bibliographically approved

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