2014
DOI: 10.1039/c4py00389f
|View full text |Cite
|
Sign up to set email alerts
|

Rational design on D–A conjugated P(BDT–DTBT) polymers for polymer solar cells

Abstract: This review summarizes the various structural modifications and photovoltaic properties of the benzodithiophene–benzothiadiazole conjugated polymers [P(BDT–DTBT)] and their derivatives.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
73
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 100 publications
(73 citation statements)
references
References 75 publications
0
73
0
Order By: Relevance
“…After filtration by glass filter, the precipitate was purified by Soxhlet extraction with methanol and dried in vacuum for 48 h to generate PE-BDTF. The molar feed ratios of monomer 4,7-bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole (10) to tetrafluorodibromobenzene (11) were 99:1 for PE-BDTF, PO-BDTF, PE-BDTTF and PO-BDTTF and 95:5 for PE-BDTF5, PO-BDTF5, PE-BDTTF5 and PO-BDTTF5. The structures and purities of the monomers were confirmed by 1 H NMR, 13 C NMR, and HRMS.…”
Section: Synthesis Of 48-bis(5-octyldodecylthiophenmentioning
confidence: 99%
See 1 more Smart Citation
“…After filtration by glass filter, the precipitate was purified by Soxhlet extraction with methanol and dried in vacuum for 48 h to generate PE-BDTF. The molar feed ratios of monomer 4,7-bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole (10) to tetrafluorodibromobenzene (11) were 99:1 for PE-BDTF, PO-BDTF, PE-BDTTF and PO-BDTTF and 95:5 for PE-BDTF5, PO-BDTF5, PE-BDTTF5 and PO-BDTTF5. The structures and purities of the monomers were confirmed by 1 H NMR, 13 C NMR, and HRMS.…”
Section: Synthesis Of 48-bis(5-octyldodecylthiophenmentioning
confidence: 99%
“…2,6-Bis(trimethyltin)-4,8-bis(2-ethyhexyloxy)benzo[1,2-b:3,4-b 0 ]dithiophene dithiophene (4), 4,7-bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole (10) and tetrafluorodibromobenzene(11) were copolymerized through Stille coupling reaction with Pd(0)-catalyst to yield PE-BDTF and PE-BDTF5. 2,6-Bis(trimethyltin)-4,8-bis(2-octyldodecyloxy)benzo[1,2-b:3,4-b 0 ]dithiophene (5), 4,7-bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole (10) and tetrafluorodibromobenzene (11) were copolymerized through Stille coupling reaction with Pd(0)-catalyst to yield PO-BDTF and PO-BDTF5.…”
mentioning
confidence: 99%
“…In this instance, the search for structurally new electron donor (D) and acceptor (A) materials is crucial because the PCE could be improved further to 17% and 24% for single and multijunction PSCs, respectively, by utilizing suitable D and A materials [3]. It is worth to notice that the benzodithiophene derivatives [4,5] are excellent donor materials for the preparation of highly efficient donor-acceptor polymers for PSCs along with various electron accepting units, such as benzo[c] [1,2,5] thiadiazole (BT) [6][7][8], thieono [3,4-b]thiophene (TT) [9][10][11], thiophene-based imide-functionalized thieno [3,4-c]pyrrole-4,6-dione (TPD) [12][13][14] and lactam-functionalized diketo-pyrrolo [3,4-c]pyrrole-1,4-dione (DPP) units [15][16][17]. In particular, TPDand DPP-based polymer has displayed impressive opto-electrical and photovoltaic properties [12][13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%
“…Benzothiadiazole (BZT) has been widely used in an array of applications [1][2][3]. This is in part due to its intrinsic electron accepting character that gives rise to interesting opto-electronic properties.…”
Section: Introductionmentioning
confidence: 99%