高性能有机太阳能电池用4,4′-二甲基-[2,2′-双噻唑]核基受体材料的硅端封工程

IF 1.9 4区 化学 Q2 CHEMISTRY, ORGANIC Journal of Physical Organic Chemistry Pub Date : 2023-07-05 DOI:10.1002/poc.4557
Samreen Kousar, Fatiqa Zafar, Asifa Rani, Riaz Hussain, Javed Iqbal, Muhammad Amin Abid, Waseeq-Ul-Islam Zafar, Muhammad Adnan, Mahrzadi Noreen Shahi
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引用次数: 0

摘要

有机太阳能电池(OSCs)以其良好的能量转换效率、低廉的成本和补偿光亏的能力而受到研究人员的关注。本研究的目的是通过端盖工程提高已有合成的参比分子2,2′-((2Z,2′)-((4,4′-二甲基-[2,2′-二噻唑]-5,5′-二基)-(4-(2-丁基基)噻吩-5,2-二基))-(甲烷酰基))-(5,6-二氯-3-氧-2,3-二氢- 1h -茚-2,1-二乙基))二丙二腈的效率。用5个新的受体E1、E2、E3、E4、E5代替参比分子的端基。利用密度泛函理论分析了吸收最大值、电荷转移分析、前沿分子轨道(FMO)、开路电压(Voc)、态密度(DOS)、光化学特性、跃迁密度矩阵(TDM)和电子-空穴重组能等参数,以评价特殊工程分子的效率。与参比(4.75 eV)相比,D1-D5具有更小的能隙(4.50-4.71 eV),并且由于端帽受体修饰,在溶剂相中吸收最大值在443.37-482.67 nm范围内。合成分子(d1 ~ d5)的电子重排能(0.18 ~ 0.27 eV)较小,Voc值在1.94 ~ 2.40 eV之间。设计的分子D3作为受体与给体聚合物(PTB7-Th)共混时,由于其在所有工程分子中具有最小的能隙(4.50 eV),因此具有最高的电荷转移能力。与R相比,D5分子具有更高的Voc (2.40 eV)、更高的LHE(0.9988)和更高的填充因子(94.15%),从而提高了osc的效率。理论研究结果表明,所有设计的分子都具有优越的行为,使它们成为构建高效OSC器件的合适吸入剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In silico end-capped engineering of 4,4′-dimethyl-[2, 2′-bithiazole] core-based acceptor materials for high-performance organic solar cells

Organic solar cells (OSCs) have grabbed the attention of researchers due to good power conversion efficiency, low cost, and ability to compensate for light deficit. The aim of the present research work is to increase the efficiency of previously synthesized reference (R) molecule 2,2′-((2Z,2′Z)-(((4,4′-dimethyl-[2,2′-bithiazole]-5,5′-diyl)bis(4-(2-butyloctyl)thiophene-5,2-diyl))bis (methaneylylidene))bis(5,6-dichloro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile by improving its photovoltaic properties via end cap engineering. Five new acceptors, namely, E1, E2, E3, E4, and E5, are used to substitute the end group of reference molecule. Several parameters have been analyzed using density functional theory including the absorption maxima, charge transfer analysis, frontier molecular orbital (FMO), open circuit voltage (Voc), density of states (DOS), photochemical characteristics, transition density matrix (TDM), and the electron-hole reorganization energies to evaluate the efficiency of specially engineered molecules. All the engineered molecules (D1-D5) had smaller energy gap (4.50–4.71 eV) compared with reference (4.75 eV) and absorption maxima in the range of 443.37–482.67 nm in solvent phase due to end-cap acceptor modification. Fabricated molecules (D1-D5) showed smaller electron reorganizational energy values (0.18–0.27 eV) and Voc ranging from 1.94 to 2.40 eV. Designed molecule D3 being an acceptor when blended with donor polymer (PTB7-Th) portrayed highest charge transfer capability owing to its smallest energy gap (4.50 eV) among all the engineered molecules. D5 molecule exhibits higher Voc (2.40 eV), greater LHE (0.9988), and superior result of fill factor (94.15%) as compared with R, which leads to improve the efficiency of OSCs. Theoretical findings illustrated the superior behavior of all the designed molecules making them suitable aspirants to construct efficient OSC devices.

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来源期刊
CiteScore
3.60
自引率
11.10%
发文量
161
审稿时长
2.3 months
期刊介绍: The Journal of Physical Organic Chemistry is the foremost international journal devoted to the relationship between molecular structure and chemical reactivity in organic systems. It publishes Research Articles, Reviews and Mini Reviews based on research striving to understand the principles governing chemical structures in relation to activity and transformation with physical and mathematical rigor, using results derived from experimental and computational methods. Physical Organic Chemistry is a central and fundamental field with multiple applications in fields such as molecular recognition, supramolecular chemistry, catalysis, photochemistry, biological and material sciences, nanotechnology and surface science.
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Issue Information Cover Image Issue Information Cover Image Exploring Spectral and Electrochemical Behavior of Hydroxy-N-Benzylideneanilines by Integrated Theoretical and Experimental Approaches
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