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Item Push-pull carbazole twin dyads as efficient sensitizers/co-sensitizers for DSSC application: effect of various anchoring groups on photovoltaic performance(Royal Society of Chemistry, 2025) Keremane, K.S.; Abdellah, I.M.; Eletmany, M.R.; Naik, P.; Anees, P.; Vasudeva Adhikari, A.V.To investigate the effect of various anchoring groups of organic sensitizers on fundamental processes occurring inside DSSCs and their overall performance, we designed and synthesized nine new double donor-acceptor (D-A) type organic dyes DCH1-9 comprising carbazole-based twin molecules as electron donors, with a non-conjugated linear alkyl chain as an extended linker featuring multiple acceptor units. Their photophysical, thermal, electrochemical, and theoretical properties were examined to gain a deeper understanding of the structure-property relationship. Photophysical results revealed that all dyes display ?abs and ?emi in the range of 400-470 nm and 500-560 nm, respectively, with a bandgap in the range of 2.46-2.74 eV. The push-pull structure with extended conjugation results in strong fluorescence characteristics. Photophysical and electrochemical studies confirm their thermodynamic feasibility for electron injection, recombination, and dye regeneration in cells. Quantum chemical simulations further provided insights into their structural, electronic, and optical parameters. New DSSCs were fabricated employing dyes DCH1-9 as sensitizers/co-sensitizers. The cell sensitized with DCH1 achieved the highest power conversion efficiency (PCE) of 2.45% under standard AM 1.5 solar conditions. Furthermore, co-sensitization of DCH1-9 with the Ru-based HD-2 sensitizer resulted in an improved PCE of 8.82% for DCH2, surpassing HD-2 alone (6.79%). EIS studies were conducted to further explore their energy conversion processes. Conclusively, these investigations highlight the significant potential of dyes carrying carbazole twin molecules with different anchoring units in enhancing the overall performance of DSSCs. © 2025 The Royal Society of Chemistry.Item New carbazole-based symmetric double D–A type chromophores for DSSC application: Impact of di-anchoring nature on photoelectrochemical processes(Elsevier B.V., 2025) Keremane, K.S.; Eletmany, M.R.; Abdellah, I.M.; Naik, P.; Vasudeva Adhikari, A.V.Herein, we report the systematic molecular design, synthesis, and characterization of a new series of carbazole-based organic dyes with a symmetric double donor–acceptor configuration, bearing seven different acceptor units as potential photosensitizers. The new molecules consist of strong electron-donating carbazole twin molecules linked together by a linear alkyl chain (C5H10) and attached to the various anchoring units, viz. cyanoacetic acid (DCP1), rhodanine-3-acetic acid (DCP2), rhodanine (DCP3), 1,3-dimethylbarbituric acid (DCP4), barbituric acid (DCP5), 1,3-diethyl-2-thiobarbituric acid (DCP6), and 4-nitrophenyl acetonitrile (DCP7). We performed structural, photophysical, thermal, electrochemical, and theoretical studies to assess the role of the dual anchoring nature of the chromophores on photoelectrochemical processes and their suitability as photosensitizers. The optical results revealed that all the dyes display ?abs and ?emi in the 404–465 nm and 503–556 nm range, respectively, with a bandgap of 2.44–2.70 eV. Furthermore, we have successfully fabricated new Dye-Sensitized Solar Cells (DSSCs) using dyes DCP1–7 as photosensitizers. Among them, DCP1 achieved the power conversion efficiency (PCE) of ?2 % under standard AM 1.5 solar conditions. Also, electrochemical impedance spectroscopy (EIS) has been carried out to investigate electronic and ionic processes within the cell. Conclusively, these studies showcase the significant potential of carbazole twin molecules with various anchoring units in improving the overall performance of DSSCs. © 2025 Elsevier B.V.