TY - JOUR
T1 - Thieno[3,4-c]Pyrrole-4,6-Dione-Based Polymer Acceptors for High Open-Circuit Voltage All-Polymer Solar Cells
AU - Liu, Shengjian
AU - Song, Xin
AU - Thomas, Simil
AU - Kan, Zhipeng
AU - Cruciani, Federico
AU - Laquai, Frédéric
AU - Bredas, Jean-Luc
AU - Beaujuge, Pierre
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: S.L. and X.S. contributed equally to this work. The authors acknowledge financial support under Baseline Research Funding from King Abdullah University of Science and Technology (KAUST) and from ONR-Global (Award No. N62909-15-1-2003 to J.L.B.). The authors thank KAUST ACL for mass spectrometry, GPC, and elemental analyses, and are grateful to the KAUST Supercomputing Laboratory (KSL) and IT Research Computing Teams for providing continuous assistance as well as computational and storage resources. The authors thank R.-Z. Liang and M. Babics for their contributions in device characterizations.
PY - 2017/4/20
Y1 - 2017/4/20
N2 - While polymer acceptors are promising fullerene alternatives in the fabrication of efficient bulk heterojunction (BHJ) solar cells, the range of efficient material systems relevant to the “all-polymer” BHJ concept remains narrow, and currently limits the perspectives to meet the 10% efficiency threshold in all-polymer solar cells. This report examines two polymer acceptor analogs composed of thieno[3,4-c]pyrrole-4,6-dione (TPD) and 3,4-difluorothiophene ([2F]T) motifs, and their BHJ solar cell performance pattern with a low-bandgap polymer donor commonly used with fullerenes (PBDT-TS1; taken as a model system). In this material set, the introduction of a third electron-deficient motif, namely 2,1,3-benzothiadiazole (BT), is shown to (i) significantly narrow the optical gap (Eopt) of the corresponding polymer (by ≈0.2 eV) and (ii) improve the electron mobility of the polymer by over two orders of magnitude in BHJ solar cells. In turn, the narrow-gap P2TPDBT[2F]T analog (Eopt = 1.7 eV) used as fullerene alternative yields high open-circuit voltages (VOC) of ≈1.0 V, notable short-circuit current values (JSC) of ≈11.0 mA cm−2, and power conversion efficiencies (PCEs) nearing 5% in all-polymer BHJ solar cells. P2TPDBT[2F]T paves the way to a new, promising class of polymer acceptor candidates.
AB - While polymer acceptors are promising fullerene alternatives in the fabrication of efficient bulk heterojunction (BHJ) solar cells, the range of efficient material systems relevant to the “all-polymer” BHJ concept remains narrow, and currently limits the perspectives to meet the 10% efficiency threshold in all-polymer solar cells. This report examines two polymer acceptor analogs composed of thieno[3,4-c]pyrrole-4,6-dione (TPD) and 3,4-difluorothiophene ([2F]T) motifs, and their BHJ solar cell performance pattern with a low-bandgap polymer donor commonly used with fullerenes (PBDT-TS1; taken as a model system). In this material set, the introduction of a third electron-deficient motif, namely 2,1,3-benzothiadiazole (BT), is shown to (i) significantly narrow the optical gap (Eopt) of the corresponding polymer (by ≈0.2 eV) and (ii) improve the electron mobility of the polymer by over two orders of magnitude in BHJ solar cells. In turn, the narrow-gap P2TPDBT[2F]T analog (Eopt = 1.7 eV) used as fullerene alternative yields high open-circuit voltages (VOC) of ≈1.0 V, notable short-circuit current values (JSC) of ≈11.0 mA cm−2, and power conversion efficiencies (PCEs) nearing 5% in all-polymer BHJ solar cells. P2TPDBT[2F]T paves the way to a new, promising class of polymer acceptor candidates.
UR - http://hdl.handle.net/10754/623444
UR - http://onlinelibrary.wiley.com/doi/10.1002/aenm.201602574/full
UR - http://www.scopus.com/inward/record.url?scp=85017781113&partnerID=8YFLogxK
U2 - 10.1002/aenm.201602574
DO - 10.1002/aenm.201602574
M3 - Article
SN - 1614-6832
VL - 7
SP - 1602574
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 15
ER -