| 1. |
- Qin, Linqing, et al.
(författare)
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Triplet Acceptors with a D-A Structure and Twisted Conformation for Efficient Organic Solar Cells
- 2020
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 59:35, s. 15043-15049
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Tidskriftsartikel (refereegranskat)abstract
- Triplet acceptors have been developed to construct high-performance organic solar cells (OSCs) as the long lifetime and diffusion range of triplet excitons may dissociate into free charges instead of net recombination when the energy levels of the lowest triplet state (T-1) are close to those of charge-transfer states ((CT)-C-3). The current triplet acceptors were designed by introducing heavy atoms to enhance the intersystem crossing, limiting their applications. Herein, two twisted acceptors without heavy atoms, analogues of Y6, constructed with large pi-conjugated core and D-A structure, were confirmed to be triplet materials, leading to high-performance OSCs. The mechanism of triplet excitons were investigated to show that the twisted and D-A structures result in large spin-orbit coupling (SOC) and small energy gap between the singlet and triplet states, and thus efficient intersystem crossing. Moreover, the energy level of T-1 is close to (CT)-C-3, facilitating the split of triplet exciton to free charges.
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| 2. |
- Wei, Yanan, et al.
(författare)
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A universal method for constructing high efficiency organic solar cells with stacked structures
- 2021
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Ingår i: Energy & Environmental Science. - : ROYAL SOC CHEMISTRY. - 1754-5692 .- 1754-5706. ; 14:4, s. 2314-2321
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Tidskriftsartikel (refereegranskat)abstract
- The construction of organic solar cells with stacked structures by the sequential deposition (SD) of donor and acceptor films has great potential in industrial production, as it demonstrates little dependence on the ratio of donor and acceptor materials, solvents, and additives. Herein, we present an eco-friendly solvent protection (ESP) method for the fabrication of high-performance OSCs with stacked structures. Several non-aromatic and non-halogenated solvents are employed as protective agents to build SD devices with a configuration of indium tin oxide (ITO)/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS Clevios P VP Al 4083)/donor/protective solvent/acceptor/perylene diimide functionalized with amino N-oxide (PDINO)/Al, which shows that n-octane is the optimal choice for SD devices. Nine different SD systems including the fullerene and nonfullerene ones present comparable photovoltaic performance to their BC counterparts, which proves the universality of this ESP method. Significantly, the device of ITO/PEDOT:PSS/D18/N3/PDINO/Al with n-octane as the protective solvent achieves a maximum PCE of 17.52%, which is the record efficiency of SD devices. Furthermore, a protective factor (delta) is proposed to demonstrate the quantitative relationship between delta and PCE after experimental and theoretical investigation, which presents an idea to understand the mechanism and provides a guideline for solvent choices.
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| 3. |
- Yang, Lei, et al.
(författare)
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Sulfur vs. tellurium: the heteroatom effects on the nonfullerene acceptors
- 2019
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Ingår i: Science in China Series B. - : SCIENCE PRESS. - 1674-7291 .- 1869-1870. ; 62:7, s. 897-903
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Tidskriftsartikel (refereegranskat)abstract
- The effect of chalcogen heteroatom variation on donor materials has been systematically investigated. However, this effect on acceptors has rarely been explored. Herein, nonfullerene acceptors BFPSP and BFPTP were reported by simply changing the chalcogen atoms from S to Te. The differences between BFPSP and BFPTP in light absorption, energy levels, excited-state lifetimes, energy loss, charge mobilities, morphology, and photovoltaic properties were systematically investigated to understand the heteroatom effects. More importantly, the electroluminescence spectra, external quantum efficiency of photovoltaics and TD-DFT calculations revealed that the triplet excited state (T-1) in energy of BFPTP equals to the charge transfer (CT) state in PBDB-T:BFPTP, which allows T-1 excitons, generated by intersystem crossing, to split into free charges to contribute to the efficiency. This contribution provides a strategy for tuning the photophysical properties of nonfullerene acceptors and designing high performance triplet materials for OSCs.
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| 4. |
- Zhang, Xin, et al.
(författare)
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Enhancing the Photovoltaic Performance of Triplet Acceptors Enabled by Side-Chain Engineering
- 2021
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Ingår i: Solar RRL. - : WILEY-V C H VERLAG GMBH. - 2367-198X. ; 5:10
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Tidskriftsartikel (refereegranskat)abstract
- Triplet excitons have both longer lifetimes and diffusion lengths than singlet excitons due to the nature of triplet excitons, which is expected to increase the photocurrent and further improve the performance of organic solar cells (OSCs). However, the working mechanism of triplet excitons in OSCs is not clearly clarified. Therefore, it is urgent to develop new triplet acceptors for in-depth understanding. Herein, a series of acceptors (BTn-4Cl) are synthesized by fine-tuning of the side-chain branch positions. The generation of triplet excitons of BTn-4Cl is confirmed by the time-resolved photoluminescence (TRPL) spectra, magnetophotocurrent (MPC) experiment, and electron paramagnetic resonance (EPR) spectra. The effects of side-chain engineering on the optoelectronic properties, packing behaviors, energy losses, charge transport properties, spin lifetimes of triplet polarons, and blend film morphologies are systematically studied. These results show that D18:BT3-4Cl-based OSCs possess the best power conversion efficiency (PCE) of 17.31% due to lower energy losses, less recombination losses, more balanced charge carrier mobilities, longer spin-lattice (T-1) relaxation time, and more favorable morphology. This work enhances the understanding of the structure-property relationship for high-performance triplet acceptors.
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| 5. |
- Zhang, Xin, et al.
(författare)
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High-Performance All-Small-Molecule Organic Solar Cells Enabled by Regio-Isomerization of Noncovalently Conformational Locks
- 2022
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Ingår i: Advanced Functional Materials. - : WILEY-V C H VERLAG GMBH. - 1616-301X .- 1616-3028. ; 32:19
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Tidskriftsartikel (refereegranskat)abstract
- The power conversion efficiencies (PCEs) of organic solar cells (OSCs) have surpassed 19% thanks to the innovation of polymer donors and molecular acceptors. However, the batch-to-batch variations in polymer materials are detrimental to the reproducibility of the device performance. In comparison, small-molecule donors (SMDs) possess some unique advantages, such as well-defined molecular weights, easy purification, and excellent batch-to-batch repeatability. Herein, a pair of regioisomeric SMDs (BT-O1 and BT-O2) has been synthesized with alkoxy groups as S center dot center dot center dot O noncovalently conformational locks (NoCLs) at the inner and outer position, respectively. Theoretical and experimental results reveal that the regioisomeric effect has a significant influence on the light-harvest ability, energy levels, molecular geometries, internal reorganization energy, and packing behaviors for the two SMDs. As a result, BT-O2-based binary device shows an impressive PCE of 13.99%, much higher than that of BT-O1 based one (4.07%), due to the better-aligned energy level, more balanced charge transport, less charge recombination, lower energy loss, and more favorable phase separation. Furthermore, the fullerene derivative PC71BM is introduced into BT-O2:H3 as the third component to achieve a notable PCE of 15.34% (certified 14.6%). Overall, this work reveals that NoCLs is a promising strategy to achieve high-performance SMDs for all-small-molecule OSCs.
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| 6. |
- Zhang, Xin, et al.
(författare)
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High-Performance Noncovalently Fused-Ring Electron Acceptors for Organic Solar Cells Enabled by Noncovalent Intramolecular Interactions and End-Group Engineering
- 2021
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 60:22, s. 12475-12481
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Tidskriftsartikel (refereegranskat)abstract
- Noncovalently fused-ring electron acceptors (NFREAs) have attracted much attention in recent years owing to their advantages of simple synthetic routes, high yields and low costs. However, the efficiencies of NFREAs based organic solar cells (OSCs) are still far behind those of fused-ring electron acceptors (FREAs). Herein, a series of NFREAs with S...O noncovalent intramolecular interactions were designed and synthesized with a two-step synthetic route. Upon introducing pi-extended end-groups into the backbones, the electronic properties, charge transport, film morphology, and energy loss were precisely tuned by fine-tuning the degree of multi-fluorination. As a result, a record PCE of 14.53 % in labs and a certified PCE of 13.8 % for NFREAs based devices were obtained. This contribution demonstrated that combining the strategies of noncovalent conformational locks and pi-extended end-group engineering is a simple and effective way to explore high-performance NFREAs.
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| 7. |
- Zhang, Xin, et al.
(författare)
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Side-Chain Engineering for Enhancing the Molecular Rigidity and Photovoltaic Performance of Noncovalently Fused-Ring Electron Acceptors
- 2021
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 60:32, s. 17720-17725
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Tidskriftsartikel (refereegranskat)abstract
- Side-chain engineering is an effective strategy to regulate the solubility and packing behavior of organic materials. Recently, a unique strategy, so-called terminal side-chain (T-SC) engineering, has attracted much attention in the field of organic solar cells (OSCs), but there is a lack of deep understanding of the mechanism. Herein, a new noncovalently fused-ring electron acceptor (NFREA) containing two T-SCs (NoCA-5) was designed and synthesized. Introduction of T-SCs can enhance molecular rigidity and intermolecular pi-pi stacking, which is confirmed by the smaller Stokes shift value, lower reorganization free energy, and shorter pi-pi stacking distance in comparison to NoCA-1. Hence, the NoCA-5-based device exhibits a record power conversion efficiency (PCE) of 14.82 % in labs and a certified PCE of 14.5 %, resulting from a high electron mobility, a short charge-extraction time, a small Urbach energy (E-u), and a favorable phase separation.
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