Significant Enhancement of Open-Circuit Voltage in Indoline-Based Dye-Sensitized Solar Cells via Retarding Charge Recombination
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Abstract
Indoline dyes exhibit impressive short-circuit photocurrent (JSC) but show generally low open-circuit voltage (VOC) in dye-sensitized solar cells (DSCs). To retard charge recombination in DSCs, four indoline dyes (XS41, XS42, XS43, and XS44) featuring, respectively, dipropylfluorene, hexyloxybenzene, tert-butylbenzene, and hexapropyltruxene electron donors, have been engineered. The incorporation of bulky rigid groups (i.e., dipropylfluorene and hexapropyltruxene unit) can notably retard the charge recombination at the titania/electrolyte interface. Moreover, we have developed two organic dyes (TC1 and TC2) as alternative coadsorbents to chenodeoxycholic acid (CDCA). Interestingly, it is found that regardless of the dye selection coadsorption with TC2 shows an improved VOC as well as JSC in comparison with its TC1 analogues. Dependence of photovoltage on the structure of TC1/TC2 was also investigated. The results suggest that the change in VOC is likely correlated with the molecular matching between the dyes and the coadsorbents. Combining the two contributions, high VOC in indoline-based DSCs can be realized. The results of XS41, upon coadsorption with TC2, produce a JSC of 16.1 mA cm–2, a VOC of 770 mV, and a fill factor of 0.66, corresponding to a power conversion efficiency of 8.18% under simulated AM1.5G solar light (100 mW cm–2). These findings pave a new way to achieve further efficiency enhancement of indoline dyes.
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