Methoxy triphenylamine hexaazatrinaphthylene based small molecules as donor material for photovoltaic applications
Tài liệu tham khảo
Armin, 2021, A history and perspective of non‐fullerene electron acceptors for organic solar cells, Adv. Energy Mater., 11, 10.1002/aenm.202003570
Liu, 2021, 16% efficiency all-polymer organic solar cells enabled by a finely tuned morphology via the design of ternary blend, Joule, 5, 914, 10.1016/j.joule.2021.02.002
Atiq, 2023, Fused ring pyrrolo [3, 2-b] pyrrole-based tilde-shaped acceptor molecules for highly efficient organic solar cells, J. Phys. Chem. Solid., 10.1016/j.jpcs.2023.111228
Liu, 2021, Low-bandgap non-fullerene acceptors enabling high-performance organic solar cells, ACS Energy Lett., 6, 598, 10.1021/acsenergylett.0c02384
Chen, 2021, Asymmetric alkoxy and alkyl substitution on nonfullerene acceptors enabling high‐performance organic solar cells, Adv. Energy Mater., 11, 10.1142/12009
Wang, 2021, Recent progress and challenges toward highly stable nonfullerene acceptor‐based organic solar cells, Adv. Energy Mater., 11
Vogiatzoglou, 2007
Mahmood, 2019, Photovoltaic and charge transport behavior of diketopyrrolopyrrole based compounds with A–D–A–D–A skeleton, J. Cluster Sci., 30, 1123, 10.1007/s10876-019-01573-0
Mahmood, 2019, First-principles theoretical designing of planar non-fullerene small molecular acceptors for organic solar cells: manipulation of noncovalent interactions, Phys. Chem. Chem. Phys., 21, 2128, 10.1039/C8CP05763J
Mahmood, 2014, Theoretical designing of novel heterocyclic azo dyes for dye sensitized solar cells, J. Comput. Electron., 13, 1033, 10.1007/s10825-014-0628-2
Mahmood, 2018, Introducing four 1, 1-dicyanomethylene-3-indanone end-capped groups as an alternative strategy for the design of small-molecular nonfullerene acceptors, J. Phys. Chem. C, 122, 29122, 10.1021/acs.jpcc.8b09336
Mahmood, 2015, Enhancement of nonlinear optical (NLO) properties of indigo through modification of auxiliary donor, donor and acceptor, Spectrochim. Acta Mol. Biomol. Spectrosc., 139, 425, 10.1016/j.saa.2014.12.038
Mahmood, 2019, Red shifting of absorption maxima of phenothiazine based dyes by incorporating electron-deficient thiadiazole derivatives as π-spacer, Arab. J. Chem., 12, 1447, 10.1016/j.arabjc.2014.11.007
Mahmood, 2020, Effect of fluorination on exciton binding energy and electronic coupling in small molecule acceptors for organic solar cells, Computational and Theoretical Chemistry, 1179, 10.1016/j.comptc.2020.112797
Monteiro Lunardi, 2017, A life cycle assessment of perovskite/silicon tandem solar cells, Prog. Photovoltaics Res. Appl., 25, 679, 10.1002/pip.2877
Hussain, 2022, Role of novel carbon-oxygen-bridged Z-shaped non-fullerene acceptors for high efficiency organic solar cells, Synth. Met., 290, 10.1016/j.synthmet.2022.117159
Atiq, 2022, Investigating the role of novel benzotrithiophene-based bat-shaped non-fullerene acceptors for high performance organic solar cells, J. Comput. Biol. Chem., 21, 981
Hassan, 2022, Development of non-fused acceptor materials with 3D-Interpenetrated structure for stable and efficient organic solar cells, Mater. Sci. Semicond. Process., 151, 10.1016/j.mssp.2022.107010
Riaz, 2022, Ab initio study of two-dimensional cross-shaped non-fullerene acceptors for efficient organic solar cells, ACS Omega, 7, 10638, 10.1021/acsomega.2c00285
Rafiq, 2022, Novel star‐shaped benzotriindole‐based nonfullerene donor materials: toward the development of promising photovoltaic compounds for high‐performance organic solar cells, Energy Technol., 10.1002/ente.202100751
Lin, 2012, Small molecule semiconductors for high-efficiency organic photovoltaics, Chem. Soc. Rev., 41, 4245, 10.1039/c2cs15313k
Cheng, 2009, Synthesis of conjugated polymers for organic solar cell applications, Chem. Rev., 109, 5868, 10.1021/cr900182s
Yeh, 2013, Organic solar cells: their developments and potentials, Renew. Sustain. Energy Rev., 21, 421, 10.1016/j.rser.2012.12.046
Luo, 2020, Fine-tuning energy levels via asymmetric end groups enables polymer solar cells with efficiencies over 17, Joule, 4, 1236, 10.1016/j.joule.2020.03.023
Shehzad, 2021, Enhanced linear and nonlinear optical response of superhalogen (Al7) doped graphitic carbon nitride (g-C3N4), Optik, 226, 10.1016/j.ijleo.2020.165923
Khan, 2021, DFT study of superhalogen (AlF4) doped boron nitride for tuning their nonlinear optical properties, Optik, 231, 10.1016/j.ijleo.2021.166464
Afzaal, 2006, Recent developments in II–VI and III–VI semiconductors and their applications in solar cells, J. Mater. Chem., 16, 1597, 10.1039/B512182E
Adnan, 2017, Fine tuning the optoelectronic properties of triphenylamine based donor molecules for organic solar cells, Z. Phys. Chem., 231, 1127, 10.1515/zpch-2016-0790
Im, 2011, 6.5% efficient perovskite quantum-dot-sensitized solar cell, Nanoscale, 3, 4088, 10.1039/c1nr10867k
Yang, 2012, Phenothiazine derivatives as organic sensitizers for highly efficient dye-sensitized solar cells, J. Mater. Chem., 22, 4040, 10.1039/c2jm13961h
Liu, 2014, Novel D–D–π-A organic dyes based on triphenylamine and indole-derivatives for high performance dye-sensitized solar cells, J. Power Sources, 248, 400, 10.1016/j.jpowsour.2013.09.106
Wu, 2013, Julolidine dyes with different acceptors and thiophene-conjugation bridge: design, synthesis and their application in dye-sensitized solar cells, Synth. Met., 180, 9, 10.1016/j.synthmet.2013.07.028
Sayama, 2002, Photoelectrochemical properties of J aggregates of benzothiazole merocyanine dyes on a nanostructured TiO2 film, J. Phys. Chem. B, 106, 1363, 10.1021/jp0129380
Marotta, 2013, Novel carbazole-phenothiazine dyads for dye-sensitized solar cells: a combined experimental and theoretical study, ACS Appl. Mater. Interfaces, 5, 9635, 10.1021/am402675q
Katono, 2012, Influence of the anchoring modes on the electronic and photovoltaic properties of D− π–A dyes, J. Phys. Chem. C, 116, 16876, 10.1021/jp304490a
Al-Dujaili, 2001, Synthesis and liquid crystalline properties of models and polymers containing thiazolo [5, 4-d] thiazole and siloxane flexible spacers, Eur. Polym. J., 37, 927, 10.1016/S0014-3057(00)00221-4
Chitpakdee, 2017, Modulation of π-spacer of carbazole-carbazole based organic dyes toward high efficient dye-sensitized solar cells, Spectrochim. Acta Mol. Biomol. Spectrosc., 174, 7, 10.1016/j.saa.2016.11.010
Guo, 2022, Efficient and stable methylammonium-free tin-lead perovskite solar cells with hexaazatrinaphthylene-based hole-transporting materials, ACS Appl. Mater. Interfaces, 14, 6852, 10.1021/acsami.1c22659
Dennington, 2008
Tenderholt, 2006
Lu, 2012, A multifunctional wavefunction analyzer, J. Comput. Chem., 33, 580, 10.1002/jcc.22885
Khan, 2021, Molecular designing of high‐performance 3D star‐shaped electron acceptors containing a truxene core for nonfullerene organic solar cells, J. Phys. Org. Chem., 34, e4119, 10.1002/poc.4119
Adnan, 2021, In silico designing of efficient C-shape non-fullerene acceptor molecules having quinoid structure with remarkable photovoltaic properties for high-performance organic solar cells, Optik, 241, 10.1016/j.ijleo.2021.166839
Mehboob, 2021, First principle theoretical designing of W-shaped Dithienosilole-based acceptor materials having efficient photovoltaic properties for high-performance organic solar cells, J. Phys. Chem. Solid., 157, 10.1016/j.jpcs.2021.110202
Henry, 1980, Limiting efficiencies of ideal single and multiple energy gap terrestrial solar cells, J. Appl. Phys., 51, 4494, 10.1063/1.328272
Rafiq, 2022, End-capped modification of dithienosilole based small donor molecules for high performance organic solar cells using DFT approach, J. Mol. Liq., 345, 10.1016/j.molliq.2021.118138
Ans, 2019, Designing dithienothiophene (DTT)-based donor materials with efficient photovoltaic parameters for organic solar cells, J. Mol. Model., 25, 1, 10.1007/s00894-019-4108-2
Lee, 2018, Bandgap narrowing in non‐fullerene acceptors: single atom substitution leads to high optoelectronic response beyond 1000 nm, Adv. Energy Mater., 8, 10.1002/aenm.201801212
Ans, 2019, Opto-electronic properties of non-fullerene fused-undecacyclic electron acceptors for organic solar cells, Comput. Mater. Sci., 159, 150, 10.1016/j.commatsci.2018.12.009
Farhat, 2020, Tuning the optoelectronic properties of Subphthalocyanine (SubPc) derivatives for photovoltaic applications, Opt. Mater., 107, 10.1016/j.optmat.2020.110154
Sikandar, 2021, Tuning the optoelectronic properties of oligothienyl silane derivatives and their photovoltaic properties, J. Mol. Graph. Model., 106, 10.1016/j.jmgm.2021.107918
Mehboob, 2021, Quantum chemical design of near‐infrared sensitive fused ring electron acceptors containing selenophene as π‐bridge for high‐performance organic solar cells, J. Phys. Org. Chem., 34, 10.1002/poc.4204
Khan, 2020, Designing spirobifullerene core based three‐dimensional cross shape acceptor materials with promising photovoltaic properties for high‐efficiency organic solar cells, Int. J. Quant. Chem., 120, 10.1002/qua.26377
Yaqoob, 2021, Structural, optical and photovoltaic properties of unfused Non-Fullerene acceptors for efficient solution processable organic solar cell (Estimated PCE greater than 12.4%): a DFT approach, J. Mol. Liq., 341, 10.1016/j.molliq.2021.117428
Green, 1981, Solar cell fill factors: general graph and empirical expressions, Solid State Electron., 24, 788, 10.1016/0038-1101(81)90062-9
Rasool, 2021, Bithieno thiophene-based small molecules for application as donor materials for organic solar cells and hole transport materials for perovskite solar cells, ACS Omega, 7, 844, 10.1021/acsomega.1c05504