2014
DOI: 10.1039/c4cp04010d
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A double-acceptor as a superior organic dye design for p-type DSSCs: high photocurrents and the observed light soaking effect

Abstract: Herein, we report three novel single donor double acceptor dyes, BH2, 4, and 6, for use in p-type dye sensitized solar cells (DSSCs). BH4 yields one of the highest photocurrents, 7.4 mA cm(-2), to date. The high performance is achieved via a shorter synthetic route and no exotic materials or cell-building techniques. We suggest a structural principle when building dyes whereby one adopts a double acceptor/single anchor when a triphenylamine moiety is incorporated into a dye for p-type DSSCs. This strategy incr… Show more

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Cited by 57 publications
(73 citation statements)
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“…To quantify the dye loading on the monocrystalline lms of DSSCs, desorption experiments are generally carried out using a base (usually NaOH or Bu 4 NOH in DMF). 26 These values are in the range of those reported with dyes anchored with the same N,N-di(4benzoic acid)phenylamine (around 1 Â 10 À8 mol cm À2 ) 27 but lower than that of the famous P1 dye anchored with a single carboxylic acid group (12.3 Â 10 À8 mol cm À2 ) 28 and the highly performing push-pull thienoquinoidal dye recently reported (8.5 Â 10 À8 mol cm À2 ). Accordingly, we have developed another strategy based on the competitive adsorption of an adsorbent which has a stronger affinity to NiO surface than the carboxylic acids.…”
Section: Quantum Chemical Calculationsmentioning
confidence: 72%
“…To quantify the dye loading on the monocrystalline lms of DSSCs, desorption experiments are generally carried out using a base (usually NaOH or Bu 4 NOH in DMF). 26 These values are in the range of those reported with dyes anchored with the same N,N-di(4benzoic acid)phenylamine (around 1 Â 10 À8 mol cm À2 ) 27 but lower than that of the famous P1 dye anchored with a single carboxylic acid group (12.3 Â 10 À8 mol cm À2 ) 28 and the highly performing push-pull thienoquinoidal dye recently reported (8.5 Â 10 À8 mol cm À2 ). Accordingly, we have developed another strategy based on the competitive adsorption of an adsorbent which has a stronger affinity to NiO surface than the carboxylic acids.…”
Section: Quantum Chemical Calculationsmentioning
confidence: 72%
“…[28] Subsequently,w ed eveloped as olution-processable method to thermally prepareZ nO insteado fT iO 2 as the ETM in the pores of the NiO mesoporouse lectrode, whichg ave as ignificant improvement in the photovoltaic performance, [29] increasing the photocurrent to 680 mAcm À2 .I ti st herefore feasible to further improvet he performance of p-ssDSCs by optimizing the ETM, as well as its fabrication methods. [31] The IDTT linker was synthesized according to ar eported method. [30] In this study,t om ake ad ye with broad spectral response, [12] we have designed and synthesized an indacenodithieno[3,2-b]thiophene (IDTT)-based dye (TIP;F igure 1), which has been successfully used in p-ssDSCs and also shown much better efficiency,a sc ompared to the two reported reference dyes, PB6 [27] and BH4.…”
mentioning
confidence: 99%
“…This is supported by the higher dark currents for BAI‐COOH than P1 (Figure b). While the aliphatic chains present on BAI‐COOH should inhibit electrolyte/NiO recombination,, lower dye loading (see below) could counter this effect. Despite performing worse than P1 , the cell results for BAI‐COOH are higher than the structurally related ‘first‐generation’ DPP dyes ( DPP‐Br/Th‐DPP) ,, which shows that BAI is a promising chromophore on which to base a more structurally complex dye.…”
Section: Resultsmentioning
confidence: 99%