A nickel-complex sensitiser for dyesensitised solar cells
We report the first example of a Ni(II) complex that demonstrates sensitiser function in a Dye-Sensitised Solar Cell (DSSC). Complexes [Ni(dcbpy)(qdt)] (1), [Ni(decbpy)(qdt)] (2) and [Ni(decbpy)Cl...] (3) (where dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; decbpy = 4,4'-di(CO2Et)-2,2'...
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creator | Linfoot, Charlotte L Richardson, Patricia McCall, Keri L Durrant, James R Morandeira, Ana Robertson, Neil |
description | We report the first example of a Ni(II) complex that demonstrates sensitiser function in a Dye-Sensitised Solar Cell (DSSC). Complexes [Ni(dcbpy)(qdt)] (1), [Ni(decbpy)(qdt)] (2) and [Ni(decbpy)Cl...] (3) (where dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; decbpy = 4,4'-di(CO2Et)-2,2'-bipyridine; and qdt = quinoxaline-2,3-dithiolate) have been prepared. Characterisation was carried out using electrochemical, spectroscopic and computational techniques. Intensive visible transitions of 1 and 2 have been assigned predominantly to Ligand-to-Ligand Charge Transfer (LLCT) from the qdt to the diimine ligand, suggesting appropriate charge separation for application in a photoelectrochemical device. TiO... sensitised with 2, following charge injection, processes a recombination time significantly long for photovoltaic function. In a DSSC, using I.../I... redox electrolyte, photocurrents and photovoltages of 0.293 mA and 521 mV were observed, with optimum values requiring TiCl... post-treatment of TiO... and co-adsorption of Chenodeoxycholic acid (Cheno). Although photovoltaic function was observed, the low photocurrent is attributed to a short-lived excited state lifetime resulting in poor charge injection from the Ni(II) sensitiser. (ProQuest: ... denotes formulae/symbols omitted.) |
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Complexes [Ni(dcbpy)(qdt)] (1), [Ni(decbpy)(qdt)] (2) and [Ni(decbpy)Cl...] (3) (where dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; decbpy = 4,4'-di(CO2Et)-2,2'-bipyridine; and qdt = quinoxaline-2,3-dithiolate) have been prepared. Characterisation was carried out using electrochemical, spectroscopic and computational techniques. Intensive visible transitions of 1 and 2 have been assigned predominantly to Ligand-to-Ligand Charge Transfer (LLCT) from the qdt to the diimine ligand, suggesting appropriate charge separation for application in a photoelectrochemical device. TiO... sensitised with 2, following charge injection, processes a recombination time significantly long for photovoltaic function. In a DSSC, using I.../I... redox electrolyte, photocurrents and photovoltages of 0.293 mA and 521 mV were observed, with optimum values requiring TiCl... post-treatment of TiO... and co-adsorption of Chenodeoxycholic acid (Cheno). 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Complexes [Ni(dcbpy)(qdt)] (1), [Ni(decbpy)(qdt)] (2) and [Ni(decbpy)Cl...] (3) (where dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; decbpy = 4,4'-di(CO2Et)-2,2'-bipyridine; and qdt = quinoxaline-2,3-dithiolate) have been prepared. Characterisation was carried out using electrochemical, spectroscopic and computational techniques. Intensive visible transitions of 1 and 2 have been assigned predominantly to Ligand-to-Ligand Charge Transfer (LLCT) from the qdt to the diimine ligand, suggesting appropriate charge separation for application in a photoelectrochemical device. TiO... sensitised with 2, following charge injection, processes a recombination time significantly long for photovoltaic function. In a DSSC, using I.../I... redox electrolyte, photocurrents and photovoltages of 0.293 mA and 521 mV were observed, with optimum values requiring TiCl... post-treatment of TiO... and co-adsorption of Chenodeoxycholic acid (Cheno). Although photovoltaic function was observed, the low photocurrent is attributed to a short-lived excited state lifetime resulting in poor charge injection from the Ni(II) sensitiser. 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Complexes [Ni(dcbpy)(qdt)] (1), [Ni(decbpy)(qdt)] (2) and [Ni(decbpy)Cl...] (3) (where dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; decbpy = 4,4'-di(CO2Et)-2,2'-bipyridine; and qdt = quinoxaline-2,3-dithiolate) have been prepared. Characterisation was carried out using electrochemical, spectroscopic and computational techniques. Intensive visible transitions of 1 and 2 have been assigned predominantly to Ligand-to-Ligand Charge Transfer (LLCT) from the qdt to the diimine ligand, suggesting appropriate charge separation for application in a photoelectrochemical device. TiO... sensitised with 2, following charge injection, processes a recombination time significantly long for photovoltaic function. In a DSSC, using I.../I... redox electrolyte, photocurrents and photovoltages of 0.293 mA and 521 mV were observed, with optimum values requiring TiCl... post-treatment of TiO... and co-adsorption of Chenodeoxycholic acid (Cheno). Although photovoltaic function was observed, the low photocurrent is attributed to a short-lived excited state lifetime resulting in poor charge injection from the Ni(II) sensitiser. (ProQuest: ... denotes formulae/symbols omitted.)</abstract><cop>New York</cop><pub>Pergamon Press Inc</pub></addata></record> |
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subjects | Dyes Electrolytes Nickel Photovoltaic cells Solar energy |
title | A nickel-complex sensitiser for dyesensitised solar cells |
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