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17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO _x.

ABSTRACT: A charge transport layer based on transition metal-oxides prepared by an anhydrous sol-gel method normally requires high-temperature annealing to achieve the desired quality. Although annealing is not a difficult process in the laboratory, it is definitely not a simple process in mass production, such as roll-to-roll, because of the inevitable long cooling step that follows. Therefore, the development of an annealing-free solution-processable metal-oxide is essential for the large-scale commercialization. In this work, a room-temperature processable annealing-free "aqueous" MoO _x solution is developed and applied in non-fullerene PBDB-T-2F:Y6 solar cells. By adjusting the concentration of water in the sol-gel route, an annealing-free MoO _x with excellent electrical properties is successfully developed. The PBDB-T-2F:Y6 solar cell with the general MoO _x prepared by the anhydrous sol-gel method shows a low efficiency of 7.7% without annealing. If this anhydrous MoO _x is annealed at 200 °C, the efficiency is recovered to 17.1%, which is a normal value typically observed in conventional structure PBDB-T-2F:Y6 solar cells. However, without any annealing process, the solar cell with aqueous MoO _x exhibits comparable performance of 17.0%. In addition, the solar cell with annealing-free aqueous MoO _x exhibits better performance and stability without high-temperature annealing compared to the solar cells with PEDOT:PSS.

SUBMITTER: Tran HN

PROVIDER: S-EPMC7610336 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO <i><sub>x</sub></i>.

Tran Hong Nhan HN Park Sujung S Wibowo Febrian Tri Adhi FTA Krishna Narra Vamsi NV Kang Ju Hwan JH Seo Jung Hwa JH Nguyen-Phu Huy H Jang Sung-Yeon SY Cho Shinuk S

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20200921 21

A charge transport layer based on transition metal-oxides prepared by an anhydrous sol-gel method normally requires high-temperature annealing to achieve the desired quality. Although annealing is not a difficult process in the laboratory, it is definitely not a simple process in mass production, such as roll-to-roll, because of the inevitable long cooling step that follows. Therefore, the development of an annealing-free solution-processable metal-oxide is essential for the large-scale commerci ...[more]

PMID: 33173748

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Project description:The active layer in a solution processed organic photovoltaic device comprises a light absorbing electron donor semiconductor, typically a polymer, and an electron accepting fullerene acceptor. Although there has been huge effort targeted to optimize the absorbing, energetic, and transport properties of the donor material, fullerenes remain as the exclusive electron acceptor in all high performance devices. Very recently, some new non-fullerene acceptors have been demonstrated to outperform fullerenes in comparative devices. This Account describes this progress, discussing molecular design considerations and the structure-property relationships that are emerging. The motivation to replace fullerene acceptors stems from their synthetic inflexibility, leading to constraints in manipulating frontier energy levels, as well as poor absorption in the solar spectrum range, and an inherent tendency to undergo postfabrication crystallization, resulting in device instability. New acceptors have to address these limitations, providing tunable absorption with high extinction coefficients, thus contributing to device photocurrent. The ability to vary and optimize the lowest unoccupied molecular orbital (LUMO) energy level for a specific donor polymer is also an important requirement, ensuring minimal energy loss on electron transfer and as high an internal voltage as possible. Initially perylene diimide acceptors were evaluated as promising acceptor materials. These electron deficient aromatic molecules can exhibit good electron transport, facilitated by close packed herringbone crystal motifs, and their energy levels can be synthetically tuned. The principal drawback of this class of materials, their tendency to crystallize on too large a length scale for an optimal heterojunction nanostructure, has been shown to be overcome through introduction of conformation twisting through steric effects. This has been primarily achieved by coupling two units together, forming dimers with a large intramolecular twist, which suppresses both nucleation and crystal growth. The generic design concept of rotationally symmetrical aromatic small molecules with extended π orbital delocalization, including polyaromatic hydrocarbons, phthalocyanines, etc., has also provided some excellent small molecule acceptors. In most cases, additional electron withdrawing functionality, such as imide or ester groups, can be incorporated to stabilize the LUMO and improve properties. New calamitic acceptors have been developed, where molecular orbital hybridization of electron rich and poor segments can be judiciously employed to precisely control energy levels. Conformation and intermolecular associations can be controlled by peripheral functionalization leading to optimization of crystallization length scales. In particular, the use of rhodanine end groups, coupled electronically through short bridged aromatic chains, has been a successful strategy, with promising device efficiencies attributed to high lying LUMO energy levels and subsequently large open circuit voltages.

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17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO _x.

Publications

17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO <i><sub>x</sub></i>.

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17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO x.

Publications

17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO <i><sub>x</sub></i>.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

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17% Non-Fullerene Organic Solar Cells with Annealing-Free Aqueous MoO _x.