Literature DB >> 27121202

Unravelling the effect of anchoring groups on the ground and excited state properties of pyrene using computational and spectroscopic methods.

Arunkumar Kathiravan1, Murugesan Panneerselvam, Karuppasamy Sundaravel, Nagaraj Pavithra, Venkatesan Srinivasan, Sambandam Anandan, Madhavan Jaccob.   

Abstract

Anchoring groups play an important role in dye sensitized solar cells (DSCs). In order to acquire a suitable anchoring group for DSCs, a deeper understanding of the effect of anchoring groups on the ground and excited state properties of the dye is significant. In this context, various anchoring group connected pyrene derivatives are successfully synthesized and well characterized by using (1)H, (13)C-NMR, FT-IR and EI-MS spectrometry. The anchoring groups employed are carboxylic acid, malonic acid, acrylic acid, malononitrile, cyanoacrylic acid, rhodanine and rhodanine-3-acetic acid. The optimized geometries, HOMO-LUMO energy gap, light harvesting efficiency (LHE) and electronic absorption spectra of these dyes are studied by using density functional theory (DFT) calculations. The results show that pyrene connected with anchoring groups with weak electron pulling strength (PC, PAC and PMC) has a larger HOMO-LUMO energy gap, whereas that connected with anchoring groups with strong electron pulling strength (PCC, PMN, PR and PRA) has a reduced HOMO-LUMO energy gap. These molecules with a reduced energy gap are primarily preferred for DSC applications. Moreover, P, PC, PAC and PMC molecules undergo π→π* transition, whereas PCC, PMN, PR and PRA molecules show significant charge transfer along with π→π* transition. UV-visible absorption spectral studies on these dyes reveal that connecting various anchoring groups with different electron pulling abilities enables the pyrene chromophore to absorb in the longer wavelength region. Notably, an efficient bathochromic shift is observed for PCC, PMN, PR and PRA molecules in both electronic absorption and fluorescence spectral measurements, which suggests that the excitation is delocalized throughout the entire π-system of the molecules. Both theoretical and spectral studies reveal that dyes with an ICT character (PCC, PMN, PR and PRA) are suitable for dye sensitized solar cell applications.

Entities:  

Year:  2016        PMID: 27121202     DOI: 10.1039/c6cp00571c

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  4 in total

1.  IoT-enabled dye-sensitized solar cells: an effective embedded tool for monitoring the outdoor device performance.

Authors:  Themmila Khamrang; Marappan Velusamy; Mohan Ramesh; Mariadoss Asha Jhonsi; Madhavan Jaccob; Kanagachidambaresan Ramasubramanian; Arunkumar Kathiravan
Journal:  RSC Adv       Date:  2020-09-29       Impact factor: 4.036

2.  Investigations of New Phenothiazine-Based Compounds for Dye-Sensitized Solar Cells with Theoretical Insight.

Authors:  Aneta Slodek; Dawid Zych; Grażyna Szafraniec-Gorol; Paweł Gnida; Marharyta Vasylieva; Ewa Schab-Balcerzak
Journal:  Materials (Basel)       Date:  2020-05-15       Impact factor: 3.623

3.  Halogen-Based 17β-HSD1 Inhibitors: Insights from DFT, Docking, and Molecular Dynamics Simulation Studies.

Authors:  Arulsamy Kulandaisamy; Murugesan Panneerselvam; Rajadurai Vijay Solomon; Madhavan Jaccob; Jaganathan Ramakrishnan; Kumaradhas Poomani; Muralikannan Maruthamuthu; Nagendran Tharmalingam
Journal:  Molecules       Date:  2022-06-20       Impact factor: 4.927

4.  Mono- and Di-Pyrene [60]Fullerene and [70]Fullerene Derivatives as Potential Components for Photovoltaic Devices.

Authors:  Piotr Piotrowski; Wojciech Mech; Kamila Zarębska; Maciej Krajewski; Krzysztof P Korona; Maria Kamińska; Magdalena Skompska; Andrzej Kaim
Journal:  Molecules       Date:  2021-03-12       Impact factor: 4.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.