Improved molecular architecture of D–π–A carbazole dyes: 9% PCE with a cobalt redox shuttle in dye sensitized solar cells

Two new D- pi -A dyes (SK2 & SK3) based on carbazole, and vinylene-phenylene ( pi -bridge) with rhodanine-3-acetic acid and cyanoacrylic acid as electron withdrawing-injecting as well as anchoring groups were designed and synthesised under conditions that were free from precious metal-catalysts...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2015-10, Vol.3 (43), p.21664-21671
Hauptverfasser: Soni, Saurabh S, Fadadu, Kishan B, Vaghasiya, Jayraj V, Solanki, Bharat G, Sonigara, Keval K, Singh, Ashish, Das, Dipjyoti, Iyer, Parameswar K
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Sprache:eng
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Zusammenfassung:Two new D- pi -A dyes (SK2 & SK3) based on carbazole, and vinylene-phenylene ( pi -bridge) with rhodanine-3-acetic acid and cyanoacrylic acid as electron withdrawing-injecting as well as anchoring groups were designed and synthesised under conditions that were free from precious metal-catalysts and well characterized for dye-sensitized solar cell (DSSC) applications. A high power conversion efficiency (PCE) of 9% (AM 1.5 G, 100 mW cm-2) has been achieved using cyanoacrylic acid as an acceptor in D- pi -A carbazole dye (SK3) with a cobalt based redox shuttle, while a PCE of 7.1% was exhibited in triiodide based redox mediators. A short-circuit current density, Jsc of similar to 18.2 mA cm-2, an open-circuit voltage, Voc of similar to 725 mV, and a fill factor, FF of similar to 67% have been afforded by the SK3 based DSSC incorporating the Co2+/Co3+ electrolyte as the one-electron redox mediator. In contrast, SK2 dye based DSSCs with a cobalt based redox mediator have shown a Jsc approximately 8.4 mA cm-2, a Voc approximately 587 mV, and a FF approximately 48%, yielding a PCE of 2.4%. The devices based on SK3 showed outstanding stability performance without significant degradation even after 1000 h of illumination under standard conditions in the Co2+/Co3+ electrolyte.
ISSN:2050-7488
2050-7496
DOI:10.1039/c5ta06548h