Faculty Publications

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Author: search.filters.author.Vasudeva Adhikari, A.V.Subject: search.filters.subject.Agglomeration

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    Highly fluorescent materials derived from ortho-vanillin: Structural, photophysical electrochemical and theoretical studies
    (Elsevier B.V., 2019) Poojary, S.; Acharya, M.; Abdul Salam, A.A.; Kekuda, D.; Nayek, U.; Madan Kumar, S.; Vasudeva Adhikari, A.V.; Dhanya, D.
    Small-molecule organic fluorophores are highly in demand attributed to their extensive prospective in material and biomedical applications. Particularly, luminescent ?-conjugated organic molecules that possess an efficient solid-state emission are excellent candidates for optoelectronic devices. Focusing on high demand of organic fluorophores, we herein report the synthesis of three organic fluorescent materials derived from o?vanillin, viz. an ester (F1), an azine (F2) and an azo dye (F3). Interestingly, F2 exhibited very intense luminescence in its aggregate phase due to the restriction in intra-molecular rotation (RIR), as demonstrated by solution thickening studies. Further, its Single Crystal X-ray Crystallography (SCXRD) study suggested the existence of various intra and inter molecular interactions and gave evidences for locked intra-molecular rotations of the benzene rings in the rigid conformation of the molecule. The bathochromic shift in fluorescence from solution to solid phase was confirmed by its thin-film emission spectrum, which evidences the formation of J-aggregates. The observed RIR, development of J-aggregates and high conjugation in F2 impart an excellent fluorescence in its aggregated state. Thin films of both F2 and F3 on ITO plates exhibited a bathochromic shift with a deep orange to red photoluminescence on UV excitation. Furthermore, the morphological characterization revealed the presence of clear dense grains in case of F2 and F3, while the DSC analysis indicated phase transitions of all the derivatives. As seen from dielectric measurement studies, the azo dye F3 exhibited the highest dielectric constant among the three derivatives. The electronic and photophysical data based on Density Functional Theory (DFT) and Time Dependent-DFT (TD-DFT) calculations are in agreement with the experimental results. All the above data clearly advocate that, the synthesized fluorophoric o?vanillin derivatives are excellent candidates for electro-optical devices. © 2018 Elsevier B.V.
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    Enhancing the Photoelectrochemical Performance of Ru(II)-Sensitized Dye-Sensitized Solar Cells Using Cyanopyridine-Based Cosensitizers
    (John Wiley and Sons Inc, 2025) Naik, P.; Abdellah, I.M.; Abdel-Shakour, M.; Keremane, K.S.; Vasudeva Adhikari, A.V.
    The cosensitization approach is one of the widely adopted strategies for systematically enhancing photovoltaic performance of dye-sensitized solar cells (DSSCs) by utilizing two or more dyes with distinct absorption spectra. This method achieves panchromatic absorption, improves intramolecular charge transfer performance, prevents dye aggregation, and increases dye loading capability. In this study, we investigated four previously reported push–pull-type dianchored chromophores (CP1–4) featuring a cyanopyridine scaffold as cosensitizer to enhance the performance of Ru(II)-based N3-sensitized DSSCs. Both the co-sensitized devices (N3 + CP1–4) and the N3-only devices were fabricated using a fixed dye concentration of 0.2 mM for each sensitizer/cosensitizers, while the coadsorbent chenodeoxycholic acid (CDCA) was systematically varied between 0 and 20 mM. This systematic variation of CDCA concentration was designed to examine its role in suppressing dye aggregation and modulating interfacial charge dynamics. Among the Series, CP4, carrying a thiobarbituric acid anchoring/acceptor group, demonstrated superior performance at all CDCA concentrations, achieving power conversion efficiency of 6.67%, 6.79%, and 5.74%, compared to 6.02%, 6.10%, and 5.44% for devices sensitized with N3 alone. Further, electrochemical impedance spectroscopy measurements confirmed the improved charge transport and reduced recombination in these devices. These findings highlight the potential of rationally engineered cosensitizers and optimized coadsorbent concentrations for enhancing the performance of metal-based sensitizers in DSSCs. © 2025 Wiley-VCH GmbH.