期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 3, 期 4, 页码 1530-1539出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ta06256f
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资金
- Office of Naval Research
- A*STAR SERC TSRP [102 170 0137]
- Max Planck Society
- Deutsche Forschungsgemeinschaft (DFG) [SPP1355]
- BMBF
- Fonds der Chemischen Industrie (FCI)
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
The photovoltaic performance of bulk heterojunction solar cells using the solution-processable small molecule donor 7,7'-(4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b']dithiophene-2,6-diyl)bis(6-fluoro-4-(5'-hexyl-[2,2'-bithiophene]-5-yl)benzo[c][1,2,5]thiadiazole) (p-DTS(FBTTh2)(2) in combination with indene-C60 bis-adduct (ICBA) as an acceptor is systematically optimized by altering the processing conditions. A high open-circuit voltage of 1 V, more than 0.2 V higher than that of a pDTS(FBTTh2)(2):PC70BM blend, is achieved. However, the power conversion efficiency remains around 5% and thus is lower than similar to 8% previously reported for p-DTS(FBTTh2)(2):PC70BM. Transient absorption (TA) pump-probe spectroscopy over a wide spectral (Vis-NIR) and dynamic (fs to mu s) range in combination with multivariate curve resolution analysis of the TA data reveals that generation of free charges is more efficient in the blend with PC70BM as an acceptor. In contrast, blends with ICBA create more coulombically bound interfacial charge transfer (CT) states, which recombine on the sub-nanosecond timescale by geminate recombination. Furthermore, the ns to ms charge carrier dynamics in pDTS(FBTTh2)(2): ICBA blends are only weakly intensity dependent implying a significant contribution of recombination from long-lived CT states and trapped charges, while those in p-DTS(FBTTh2)(2):PC70BM decay via an intensity-dependent recombination mechanism indicating that spatially separated (free) charge carriers are observed, which can be extracted as photocurrent from the device.
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