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Homoleptic d^sup 10^ metal complexes containing ferrocenyl functionalized dithiocarbamates as sensitizers for TiO^sub 2^ based dye-sensitized solar cells

Four synthesized d10 metal complexes, namely, ferrocenyl based pyridyl functionalized dithiocarbamates macro-cyclic metal-organic coordination polymers, [M(L)2]∞ (M = Zn(II), L = (N-ferrocenyl-methyl-N-pyridin-4-ylmethyl)dithiocarbamate Zn-2; Cd (II), L = (N-ferrocenyl-methyl-N-pyridin-3-ylmethyl) d...

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Bibliographic Details
Published in:Solar energy 2018-12, Vol.176, p.312
Main Authors: Neetu, Manar, Krishna Kumar, Srivastava, Pankaj, Singh, Nanhai
Format: Article
Language:English
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Summary:Four synthesized d10 metal complexes, namely, ferrocenyl based pyridyl functionalized dithiocarbamates macro-cyclic metal-organic coordination polymers, [M(L)2]∞ (M = Zn(II), L = (N-ferrocenyl-methyl-N-pyridin-4-ylmethyl)dithiocarbamate Zn-2; Cd (II), L = (N-ferrocenyl-methyl-N-pyridin-3-ylmethyl) dithiocarbamate Cd-3 and dimers [M(L)2]2 (M = Zn(II), Hg(II), L = (N-ferrocenyl-methyl-N-pyridin-3-ylmethyl) dithiocarbamate, Zn-1 and Hg-4 were studied for their sensitization activities when anchored on TiO2 thin film electrode and employed as photoanode in dye-sensitized solar cells (DSSC). The absorption spectra of test dyes in dichloromethane solution indicated absorption in 400–500 nm range for all complexes, revealing the possibility of their use as photosensitizers for TiO2. The cyclic voltammetry (CV) demonstrated quasi-reversible behavior for all the complexes. All the dye sensitizers showed significant light harvesting properties with an exceptionally high light-to-electrical energy conversion efficiency (6.23%) shown by Zn-1 complex which was close to that obtained with standard Ru dye, N719 (6.96%) under similar experimental conditions. The better performance of Zn-1 complex compared to other studied dye sensitizers were attributed to its structural features. The extent of interfacial charge recombination and electron lifetime were evaluated by the electrochemical impedance spectroscopy (EIS).
ISSN:0038-092X
1471-1257
DOI:10.1016/j.solener.2018.10.033