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Title: High open-circuit voltage small-molecule p-DTS(FBTTh 2 )2.ICBA bulk heterojunction solar cells – morphology, excited-state dynamics, and photovoltaic performance

Journal Article · · Journal of Materials Chemistry. A
DOI:https://doi.org/10.1039/C4TA06256F· OSTI ID:1215416
 [1];  [2];  [1];  [3];  [3];  [4];  [3]
  1. Agency for Science Technology and Research (A*STAR) (Singapore). Inst. of Materials Research and Engineering (IMRE).
  2. Max Planck Inst. for Polymer Research, Mainz (Germany)
  3. Univ. of California at Santa Barbara, Santa Barbara, CA (United States). Center for Polymers and Organic Solids.
  4. Max Planck Inst. for Polymer Research, Mainz (Germany)

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 p-DTS(FBTTh2)2:PC70BM blend, is achieved. However, the power conversion efficiency remains around 5% and thus is lower than ~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 μs) 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 μs charge carrier dynamics in p-DTS(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.

Research Organization:
SLAC National Accelerator Lab., Menlo Park, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
AC02-76SF00515
OSTI ID:
1215416
Journal Information:
Journal of Materials Chemistry. A, Vol. 3, Issue 4; ISSN 2050-7488
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 28 works
Citation information provided by
Web of Science

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Cited By (6)

From Recombination Dynamics to Device Performance: Quantifying the Efficiency of Exciton Dissociation, Charge Separation, and Extraction in Bulk Heterojunction Solar Cells with Fluorine-Substituted Polymer Donors journal September 2017
In Situ Analysis of Solvent and Additive Effects on Film Morphology Evolution in Spin-Cast Small-Molecule and Polymer Photovoltaic Materials journal May 2018
A Simple but Efficient Small Molecule with a High Open Circuit Voltage of 1.07 V in Solution-Processable Organic Solar Cells journal January 2018
Fully Roll-to-Roll Printed P3HT/Indene-C60-Bisadduct Modules with High Open-Circuit Voltage and Efficiency journal January 2018
MnCo 2 O 4+x nanowire arrays grown on carbon sponge: improved electrochemical and catalytic performances journal January 2019
From Recombination Dynamics to Device Performance: Quantifying the Efficiency of Exciton Dissociation, Charge Separation, and Extraction in Bulk Heterojunction Solar Cells with Fluorine‐Substituted Polymer Donors journal October 2019

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