Samreen Kousar, Fatiqa Zafar, Asifa Rani, Riaz Hussain, Javed Iqbal, Muhammad Amin Abid, Waseeq-Ul-Islam Zafar, Muhammad Adnan, Mahrzadi Noreen Shahi
{"title":"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","authors":"Samreen Kousar, Fatiqa Zafar, Asifa Rani, Riaz Hussain, Javed Iqbal, Muhammad Amin Abid, Waseeq-Ul-Islam Zafar, Muhammad Adnan, Mahrzadi Noreen Shahi","doi":"10.1002/poc.4557","DOIUrl":null,"url":null,"abstract":"<p>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-1<i>H</i>-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 (<i>V</i><sub>oc</sub>), 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 <i>V</i><sub>oc</sub> 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 <i>V</i><sub>oc</sub> (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.</p>","PeriodicalId":16829,"journal":{"name":"Journal of Physical Organic Chemistry","volume":"36 11","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2023-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In silico end-capped engineering of 4,4′-dimethyl-[2, 2′-bithiazole] core-based acceptor materials for high-performance organic solar cells\",\"authors\":\"Samreen Kousar, Fatiqa Zafar, Asifa Rani, Riaz Hussain, Javed Iqbal, Muhammad Amin Abid, Waseeq-Ul-Islam Zafar, Muhammad Adnan, Mahrzadi Noreen Shahi\",\"doi\":\"10.1002/poc.4557\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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-1<i>H</i>-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 (<i>V</i><sub>oc</sub>), 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 <i>V</i><sub>oc</sub> 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 <i>V</i><sub>oc</sub> (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. 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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.
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.