Relevant bibliographies by topics / O-IDTBR

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'O-IDTBR'

Author: Grafiati
Published: 2 November 2024

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Journal articles on the topic "O-IDTBR"

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Badgujar, Sachin, Chang Eun Song, Sora Oh, Won Suk Shin, Sang-Jin Moon, Jong-Cheol Lee, In Hwan Jung, and Sang Kyu Lee. "Highly efficient and thermally stable fullerene-free organic solar cells based on a small molecule donor and acceptor." Journal of Materials Chemistry A 4, no. 42 (2016): 16335–40. http://dx.doi.org/10.1039/c6ta06367e.

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Huang, Yulin, Wenfa Zhou, Xiaofang Li, Li Jiang, and Yinglin Song. "Highly broadband NLO response of acceptor–donor–acceptor materials with a planar conformation." Materials Advances 2, no. 6 (2021): 2097–103. http://dx.doi.org/10.1039/d0ma00918k.

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The third-order NLO properties of A–D–A molecules originally derived from organic photovoltaic (OPV) devices are studied. The results show that NLO performance of planar molecule (O-IDTBR) is better than that of twisted molecule (IDFBR) in solution or film state.
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Paterson, Alexandra F., Ruipeng Li, Anastasia Markina, Leonidas Tsetseris, Sky MacPhee, Hendrik Faber, Abdul-Hamid Emwas, et al. "N-Doping improves charge transport and morphology in the organic non-fullerene acceptor O-IDTBR." Journal of Materials Chemistry C 9, no. 13 (2021): 4486–95. http://dx.doi.org/10.1039/d0tc05861k.

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4

Liu, Jiangang, Shuyi Zeng, Peng Jing, Kui Zhao, and Qiuju Liang. "Investigating the effect of cosolvents on P3HT/O-IDTBR film-forming kinetics and film morphology." Journal of Energy Chemistry 51 (December 2020): 333–41. http://dx.doi.org/10.1016/j.jechem.2020.04.048.

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Liang, Qiuju, Xuechen Jiao, Ye Yan, Zhiyuan Xie, Guanghao Lu, Jiangang Liu, and Yanchun Han. "Separating Crystallization Process of P3HT and O‐IDTBR to Construct Highly Crystalline Interpenetrating Network with Optimized Vertical Phase Separation." Advanced Functional Materials 29, no. 47 (January 20, 2019): 1807591. http://dx.doi.org/10.1002/adfm.201807591.

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6

Arshad, Muhammad Nadeem, Muhammad Khalid, Mohammad Asad, Ataualpa A. C. Braga, Abdullah M. Asiri, and Maha M. Alotaibi. "Influence of Peripheral Modification of Electron Acceptors in Nonfullerene (O-IDTBR1)-Based Derivatives on Nonlinear Optical Response: DFT/TDDFT Study." ACS Omega 7, no. 14 (March 31, 2022): 11631–42. http://dx.doi.org/10.1021/acsomega.1c06320.

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7

Liu, Yadi, Tao Zhang, Rui Zhang, Jian Guan, Jiaqi Pan, Xinhong Yu, Qiang Zhang, and Yanchun Han. "Enhancing the Molecular Order and Vertical Component Distribution of the P3HT/O‐IDTBR System during Layer‐by‐Layer Processing." Macromolecular Rapid Communications, August 21, 2023. http://dx.doi.org/10.1002/marc.202300338.

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AbstractThe molecular order and vertical component distribution are critical to enhance the charge transport in layer‐by‐layer (LbL) processed active layer. However, the excessive inter‐diffusion between donor and acceptor layers during LbL processing irrepressibly reduces their ordered packing. Herein, a novel tactic to optimize the molecular order and vertical morphology of the active layer through suppressing the deep penetration of (5Z,5′Z)‐5,5′‐((7,7′‐(4,4,9,9‐tetraoctyl‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6 ‐b′]dithiophene‐2,7‐diyl)bis(benzo[c][1,2,5]thiadiazole‐7,4‐diyl))bis(methanylylidene)) bis(3‐ethyl‐2‐thioxothiazolidin‐4‐one) (O‐IDTBR) to poly(3‐hexylthiophene) (P3HT) film during LbL processing is proposed. This is enabled by inducing the formation of P3HT nanofibers through ultraviolet (UV) irradiation and solution aging. During the LbL processing, these nanofibers with high crystallinity reduce the damage of O‐IDTBR solution to P3HT film and restrict the penetration of O‐IDTBR into P3HT matrix. As a result, the P3HT nanofibers are preserved and the degree of vertical phase separation is enlarged in the LbL‐processed film. Meanwhile, the molecular order of both components is enhanced. The resulting morphology that featured as intertwined P3HT nanofibers/O‐IDTBR network efficiently promotes charge transport and extraction, boosting the power conversion efficiency (PCE) of the devices from 6.70 ± 0.12% to 7.71 ± 0.10%.
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Liu, Yadi, Qiang Zhang, Jian Guan, Jingwei Xue, Xinhong Yu, Fan Wu, Wei Ma, and Yanchun Han. "Improving the Molecular Packing Order and Vertical Phase Separation of the P3HT:O-IDTBR Blend by Extending the Crystallization Period of O-IDTBR." ACS Applied Materials & Interfaces, September 26, 2022. http://dx.doi.org/10.1021/acsami.2c12220.

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9

Stojanovic, Ljiljana, Samuele Giannini, and Jochen Blumberger. "Exciton Transport in the Nonfullerene Acceptor O-IDTBR from Nonadiabatic Molecular Dynamics." Journal of Chemical Theory and Computation, July 5, 2024. http://dx.doi.org/10.1021/acs.jctc.4c00605.

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10

López-Vicente, R., M. Fernández-Castro, J. Abad, E. Mazzolini, J. W. Andreasen, M. Espindola-Rodriguez, and A. Urbina. "Lifetime Study of Organic Solar Cells with O-IDTBR as Non-Fullerene Acceptor." Frontiers in Energy Research 9 (October 19, 2021). http://dx.doi.org/10.3389/fenrg.2021.741288.

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Organic solar cells (OSCs) have increased their power conversion efficiency above 18% thanks to the use of non-fullerene acceptors in binary or ternary blends or in tandem configurations. In this article, a study on the lifetime of P3HT:O-IDTBR bulk heterojunction OSCs on ITO-free flexible substrates is presented. A direct comparison of glass–glass and plastic–plastic encapsulation performance, with a special focus on its effect on the lifetime of the devices after degradation procedures, has been carried out complying with the ISOS protocols for organic photovoltaic devices. The manufactured OSCs with 1 cm2 active layer have power conversion efficiencies ranging from 1.9 to 3.4% depending on the encapsulant material, encapsulation process, and substrate. An exponential degradation rate has been found, with a similar functional behavior for glass and plastic differing in the degradation constants, which ranges from k = 0.01 to 0.002 h−1. Only in one case, the ISOS-T3 essay for plastic encapsulation, a double exponential process, was observed with degradation rates of k1 = 0.03 h−1 and a second slower process with k2 = 0.001 h−1. The longest achieved T80 lifetime is 86 h for glass-encapsulated devices under an accelerated ISOS-T3 protocol.
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Dissertations / Theses on the topic "O-IDTBR"

1

Diarra, Cheick Oumar. "Modélisation par dynamique moléculaire ab initio du transport des excitons et du transport thermique dans les semiconducteurs organiques pour la collecte d'énergie." Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAD013.

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L'exciton joue un rôle clé dans le fonctionnement des cellules solaires organiques (OSCs). Comprendre sa dynamique dans les semiconducteurs organiques est essentiel, notamment pour améliorer la longueur de diffusion, une propriété déterminante pour la performance des hétérojonctions planaires, envisagées comme une alternative plus stable aux hétérojonctions en volume (BHJ). Dans la première partie de cette thèse, nous avons développé une approche méthodologique robuste et polyvalente pour évaluer la longueur de diffusion de l'exciton dans les semiconducteurs organiques. Cette approche, basée sur AIMD-ROKS, a été validée avec succès dans le cas du polymère P3HT. Elle a également été appliquée à l'accepteur NFA O-IDTBR, révélant des longueurs de diffusion prometteuses, mais encore insuffisantes pour les hétérojonctions planaires. Dans la deuxième partie de la thèse, le transfert de chaleur dans les semiconducteurs organiques a été exploré, élément crucial pour la performance des dispositifs thermoélectriques. Ces études se sont concentrées sur le P3HT, un matériau utilisé en thermoélectricité. Dans un premier temps, la conductivité thermique au sein des chaînes de P3HT a été étudiée, révélant l'influence de la longueur des chaînes de polymère. Ensuite, les transferts de chaleur entre ces chaînes ont également été examinés
The exciton plays a central role in the functioning of organic solar cells (OSCs). Understanding its dynamics in organic semiconductors is essential, particularly to optimize the diffusion length, a key property for the performance of planar heterojunctions, which are considered as a potentially more stable alternative to bulk heterojunctions (BHJ) in certain contexts. In the first part of this thesis, we developed a robust and versatile methodological approach to evaluate the exciton diffusion length in organic semiconductors. This method, based on AIMD-ROKS, was successfully validated for the P3HT polymer. It was also applied to the NFA O-IDTBR acceptor, revealing promising diffusion lengths, though still insufficient for planar heterojunctions. The second part of the thesis explores heat transfer in organic semiconductors, a crucial element for the performance of thermoelectric devices. These studies focused on P3HT, a material used in thermoelectricity. First, the thermal conductivity within P3HT chains was studied, revealing the influence of polymer chain length. Then, heat transfers between these chains were also examined
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