Abstract

Designed, synthesized and characterized two new metal free organic sensitizers for dye-sensitized solar cells (DSSCs) applications comprising pyrene-1-carbaldehyde as donor, thiophene-2-acetonitrile as π-spacer and cyano acetic acid or rhodanine-3-acetic acid as electron acceptor moieties. From photophysical properties, J and H- type dye aggregations observed for the cyano acetic acid and rhodanine-3-acetic acid anchor group based dyes respectively. The electrochemical experiments and time-correlated single-photon counting (TCSPC) measurements indicate the ability of electron injection into the TiO2 conduction band from the excited sensitizer. Theoretical calculations were performed to rationalize the experimental data and both experimental and theoretical studies indicate that rhodanine-3-acetic acid anchor groups at the acceptor moiety inhibit the electron injection process due to H-type dye aggregation which in turn decreases the open circuit voltage (Voc). Furthermore, the electrochemical impedance spectroscopy (EIS) experiments suggest that the effective electron injection, low charge transfer resistance (Rct), longer lifetime of dye on TiO2 film assists the increase of Voc, achieved by the addition of co-adsorbent deoxycholic acid which in turn enhances the power conversion efficiency (η%).

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