|
|
|
|
LEADER |
01000naa a22002652 4500 |
001 |
NLM278349161 |
003 |
DE-627 |
005 |
20231225020351.0 |
007 |
cr uuu---uuuuu |
008 |
231225s2018 xx |||||o 00| ||eng c |
024 |
7 |
|
|a 10.1002/adma.201704713
|2 doi
|
028 |
5 |
2 |
|a pubmed24n0927.xml
|
035 |
|
|
|a (DE-627)NLM278349161
|
035 |
|
|
|a (NLM)29168900
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a Zhu, Jingshuai
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a Naphthodithiophene-Based Nonfullerene Acceptor for High-Performance Organic Photovoltaics
|b Effect of Extended Conjugation
|
264 |
|
1 |
|c 2018
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
500 |
|
|
|a Date Completed 01.08.2018
|
500 |
|
|
|a Date Revised 30.09.2020
|
500 |
|
|
|a published: Print-Electronic
|
500 |
|
|
|a Citation Status PubMed-not-MEDLINE
|
520 |
|
|
|a © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
|
520 |
|
|
|a Naphtho[1,2-b:5,6-b']dithiophene is extended to a fused octacyclic building block, which is end capped by strong electron-withdrawing 2-(5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile to yield a fused-ring electron acceptor (IOIC2) for organic solar cells (OSCs). Relative to naphthalene-based IHIC2, naphthodithiophene-based IOIC2 with a larger π-conjugation and a stronger electron-donating core shows a higher lowest unoccupied molecular orbital energy level (IOIC2: -3.78 eV vs IHIC2: -3.86 eV), broader absorption with a smaller optical bandgap (IOIC2: 1.55 eV vs IHIC2: 1.66 eV), and a higher electron mobility (IOIC2: 1.0 × 10-3 cm2 V-1 s-1 vs IHIC2: 5.0 × 10-4 cm2 V-1 s-1 ). Thus, IOIC2-based OSCs show higher values in open-circuit voltage, short-circuit current density, fill factor, and thereby much higher power conversion efficiency (PCE) values than those of the IHIC2-based counterpart. In particular, as-cast OSCs based on FTAZ: IOIC2 yield PCEs of up to 11.2%, higher than that of the control devices based on FTAZ: IHIC2 (7.45%). Furthermore, by using 0.2% 1,8-diiodooctane as the processing additive, a PCE of 12.3% is achieved from the FTAZ:IOIC2-based devices, higher than that of the FTAZ:IHIC2-based devices (7.31%). These results indicate that incorporating extended conjugation into the electron-donating fused-ring units in nonfullerene acceptors is a promising strategy for designing high-performance electron acceptors
|
650 |
|
4 |
|a Journal Article
|
650 |
|
4 |
|a fused-ring electron acceptors
|
650 |
|
4 |
|a naphthodithiophene
|
650 |
|
4 |
|a nonfullerene acceptors
|
650 |
|
4 |
|a organic solar cells
|
700 |
1 |
|
|a Ke, Zhifan
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Zhang, Qianqian
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Wang, Jiayu
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Dai, Shuixing
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Wu, Yang
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Xu, Ye
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Lin, Yuze
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Ma, Wei
|e verfasserin
|4 aut
|
700 |
1 |
|
|a You, Wei
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Zhan, Xiaowei
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 30(2018), 2 vom: 24. Jan.
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
|
773 |
1 |
8 |
|g volume:30
|g year:2018
|g number:2
|g day:24
|g month:01
|
856 |
4 |
0 |
|u http://dx.doi.org/10.1002/adma.201704713
|3 Volltext
|
912 |
|
|
|a GBV_USEFLAG_A
|
912 |
|
|
|a SYSFLAG_A
|
912 |
|
|
|a GBV_NLM
|
912 |
|
|
|a GBV_ILN_350
|
951 |
|
|
|a AR
|
952 |
|
|
|d 30
|j 2018
|e 2
|b 24
|c 01
|