Acenaphthylene-imide based small molecules/TiO2 bilayer as electron-transporting layer for solution-processing efficient perovskite solar cells
Jiawei ShaoXing GuoNannan ShiXinglin ZhangShuli LiuZhenhua LinBaomin ZhaoJingjing ChangJinjun ShaoXiaochen Dong
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Keywords:
Imide
Acenaphthylene
HOMO/LUMO
The interfacial defects or imperfections in the multilayer perovskite solar cells (PSCs) are detrimental for efficient and stable devices. To produce highly efficient and stable PSCs, a bilayer between the interfaces of electron‐transport material/perovskite and perovskite/hole‐transport material can be useful for suppressing recombinations at these interfaces. To passivate the interfacial defects at the perovskite/SnO 2 and perovskite/Spiro‐OMeTAD for three absorber materials (CsPbI 3 , FAPbI 3, and Cs 0.05 (FA 0.83 MA 0.17 ) 0.95 Pb(I 0.83 Br 0.17 ) 3 ), a thin layer of WO 3 and poly‐bathocuproine interfacial layer is explored using solar cell capacitance simulation in 1D. The optimized device photovoltaic performances significantly improve using bilayers. The power conversion efficiency for the FAPbI 3 ‐based PSCs in bilayer configuration is more than 12% as compared to pristine, whereas open‐circuit voltage is improved by over 13%. The enhancement in device performance is attributed to the reduction of interfacial defects at both the electron transport layer/perovskite and perovskite/hole transport layer interfaces. The proposed interface modification strategy provides a novel approach for fabricating efficient perovskite devices.
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Tin oxide
Hysteresis
Perovskite solar cell
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The preparation of uniform, high-crystallinity planar perovskite films with high-aspect-ratio grains over a square-inch area is demonstrated. The best power conversion efficiency (PCE) of 16.3% (stabilized output of ≈15.6%) is obtained for a planar perovskite solar cell (PSC) with 1.2 cm2 active area, and the PCE jumps to 18.3% (stabilized output of ≈17.5%) for a PSC with a 0.12 cm2 active area. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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This contribution demonstrates the effects of mole ratio, concentration of perovskite components and fullerene derivatives used as electron transport layer (ETL) on the stability and performances of inverted perovskite solar cells (PSCs). C60, C70, PC61BM and PC71BM are selected as ETL materials. Methylammonium iodide (MAI):Lead (II) iodide (PbI2):Lead(II) chloride (PbCl2) are used to form MAPb2I2Cl which is a mixed halogen perovskite structure. The fabricated perovskite device containing PCBM with optimized concentration and mole ratio gives high power conversion efficiency (PCE) of 9.07% with an open-circuit voltage (Voc) of 0.91 V, short circuit current density of 14.1 mA/cm2, and fill factor of 0.71. The lifetime characteristics and the stability are found significantly dependent on the fullerene type. The devices containing PC61BM and PC71BM are able to maintain 50% and 30% of its initial performances, respectively, even after 1100 hours. Overall, the obtained results represent an important step understanding the impacts on the p-i-n type perovskite lifetimes.
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Herein, core-twisted tetrachloroperylenediimides (ClPDIs) were introduced as new efficient electron-transporting materials (ETMs) to replace the commonly used fullerene acceptor PC61 BM in inverted planar perovskite solar cells (PSCs). ClPDI showed a low-lying lowest unoccupied molecular orbital (LUMO) energy level of -3.95 eV, which was compatible with the conduction band of CH3 NH3 PbI3-x Clx (-3.90 eV). In addition, the role of the length of the alkyl side chain at the imide position of ClPDI in modulating the molecular solubility, aggregation capacity for charge-transport properties, surface hydrophobicity, and PSC performance was investigated. The device based on ClPDI-C4 (ClPDI with n-butyl side chains) as ETM achieved a maximum power conversion efficiency (PCE) of 17.3 % under standard AM 1.5G illumination, which iwas very competitive with that of the reference device employing PC61 BM/C60 (PCE=17.2 %) as ETM. Moreover, the devices with ClPDIs as ETMs exhibited better device stability than that with PC61 BM/C60 . This work highlights the great potential of ClPDI derivatives as low-cost (≈2.0 USD g-1 ) and effective ETMs to obtain efficient solution-processed inverted PSCs. This class of ClPDI derivatives is expected further promote the performance and stability of PSCs after extended investigation.
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Widely known as an excellent electron transporting material (ETM), pristine fullerene C60 plays a critical role in improving the photovoltaic performance of inverted structure perovskite solar cells (PSCs). However, the imperfect perovskite/C60 interface significantly limits the promotion of device performance and stability due to the weak coordination interactions between bare carbon cages and perovskite. Here, we designed and synthesized three functionalized fulleropyrrolidine ETMs (abbreviated as CEP, CEPE, and CECB), each of which was modified with the same primary terminal (cyanoethyl) and various secondary terminals (phenyl, phenethyl, and chlorobutyl). The resulting CECB-based PSC has a power conversion efficiency (PCE) over 19% and exceptional photo-stability over 1800 h. This work provides significant insight into the targeted terminal design of novel fullerene ETMs for efficient and stable PSCs.
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Smooth organolead halide perovskite films for meso/planar hybrid structured perovskite solar cells were prepared by a simple compressed air blow-drying method under ambient conditions. The resultant perovskite films show high surface coverage, leading to a device power conversion efficiency of over 10% with an open circuit voltage up to 1.003 V merely using pristine poly(3-hexylthiophene) (P3HT) as a hole transporter.
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Molecular engineering
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In article 1901466, Bo Chi, Gregory J. Wilson, and co-workers investigate superior electronic properties of nanostructured tin (IV) oxide (SnO2) as an ideal inorganic electron transport layer (ETL) in n–i–p perovskite solar cells. The bilayer ETL architecture attaining impressive power conversion efficiency (PCE) greater than 20% is depicted.
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