Effects of alkyl side chain length of low bandgap naphtho[1, 2‐c:5, 6‐c′]bis[1, 2, 5]thiadiazole‐based copolymers on the optoelectronic properties of polymer solar cells. Issue 18 (7th August 2018)
- Record Type:
- Journal Article
- Title:
- Effects of alkyl side chain length of low bandgap naphtho[1, 2‐c:5, 6‐c′]bis[1, 2, 5]thiadiazole‐based copolymers on the optoelectronic properties of polymer solar cells. Issue 18 (7th August 2018)
- Main Title:
- Effects of alkyl side chain length of low bandgap naphtho[1, 2‐c:5, 6‐c′]bis[1, 2, 5]thiadiazole‐based copolymers on the optoelectronic properties of polymer solar cells
- Authors:
- Tong, Junfeng
An, Lili
Li, Jianfeng
Lv, Jie
Guo, Pengzhi
Li, Liujun
Zhang, Peng
Yang, Chunyan
Xia, Yangjun
Wang, Chenglong - Abstract:
- ABSTRACT: Two donor‐π‐acceptor (D‐π‐A) type naphtho[1, 2‐ c :5, 6‐ c ′]bis[1, 2, 5]thiadiazole (NT)‐based conjugated copolymers (CPs), namely, PBDT‐TT‐DTNT‐HD and PBDT‐TT‐DTNT‐OD, containing different side chain length (2‐hexyldecyl, HD and 2‐octyldodecyl, OD) anchoring to thiophene π‐bridge between the two‐dimensional (2D) 5‐((2‐butyloctyl)thieno[3, 2‐ b ]thiophen‐2‐yl)benzo[1, 2‐ b :4, 5‐ b ′]dithiophene (BDT‐TT) unit and NT moiety are developed and fully characterized. The resultant two copolymers exhibited broader absorption in wide range of 300–820 nm and obviously deepened E HOMO of approximately −5.50 eV. The effects of side chain length on film‐forming ability, absorption, energy levels, aggregation, dielectric constant ( ɛ r ), mobility, morphology, and photovoltaic properties are further systematically investigated. It was found that the side chain length had little impact on solution‐processability, absorption, energy levels, and aggregation in CB solution of resultant CPs. However, tinily increasing side chain length promoted to form the more ordered structure of neat polymer film even if the corresponding ɛ r decreased. As a result, the side‐chain‐extended PBDT‐TT‐DTNT‐OD:PC71 BM‐based device achieved 32% increased FF than that of PBDT‐TT‐DTNT‐HD:PC71 BM and thus the PCE was significantly raised from 3.99% to 5.21%, which were benefited from 2 times higher SCLC hole mobility, more favorable phase separation, and improved exciton dissociation. These findingsABSTRACT: Two donor‐π‐acceptor (D‐π‐A) type naphtho[1, 2‐ c :5, 6‐ c ′]bis[1, 2, 5]thiadiazole (NT)‐based conjugated copolymers (CPs), namely, PBDT‐TT‐DTNT‐HD and PBDT‐TT‐DTNT‐OD, containing different side chain length (2‐hexyldecyl, HD and 2‐octyldodecyl, OD) anchoring to thiophene π‐bridge between the two‐dimensional (2D) 5‐((2‐butyloctyl)thieno[3, 2‐ b ]thiophen‐2‐yl)benzo[1, 2‐ b :4, 5‐ b ′]dithiophene (BDT‐TT) unit and NT moiety are developed and fully characterized. The resultant two copolymers exhibited broader absorption in wide range of 300–820 nm and obviously deepened E HOMO of approximately −5.50 eV. The effects of side chain length on film‐forming ability, absorption, energy levels, aggregation, dielectric constant ( ɛ r ), mobility, morphology, and photovoltaic properties are further systematically investigated. It was found that the side chain length had little impact on solution‐processability, absorption, energy levels, and aggregation in CB solution of resultant CPs. However, tinily increasing side chain length promoted to form the more ordered structure of neat polymer film even if the corresponding ɛ r decreased. As a result, the side‐chain‐extended PBDT‐TT‐DTNT‐OD:PC71 BM‐based device achieved 32% increased FF than that of PBDT‐TT‐DTNT‐HD:PC71 BM and thus the PCE was significantly raised from 3.99% to 5.21%, which were benefited from 2 times higher SCLC hole mobility, more favorable phase separation, and improved exciton dissociation. These findings could provide an important and valuable insight by side chain modulation for achieving efficient PSCs. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem.2018, 56, 2059–2071 Abstract : The side chain length had little impact on solution‐processability, absorption, energy levels, and aggregation in chlorobenzene solution. However, the tiny increase of side chain length promoted the formation of the more ordered structure of neat polymer film even if the corresponding dielectric constant decreased. Accordingly, PBDT‐TT‐DTNT‐OD:PC71 BM‐based device achieved a 32% greater increased FF than that of PBDT‐TT‐DTNT‐HD:PC71 BM‐based device and thus the PCE was significantly raised from 3.99% to 5.21%, which benefited from the two times enhanced SCLC hole mobility, more favorable phase separation, and improved exciton dissociation. … (more)
- Is Part Of:
- Journal of polymer science. Volume 56:Issue 18(2018)
- Journal:
- Journal of polymer science
- Issue:
- Volume 56:Issue 18(2018)
- Issue Display:
- Volume 56, Issue 18 (2018)
- Year:
- 2018
- Volume:
- 56
- Issue:
- 18
- Issue Sort Value:
- 2018-0056-0018-0000
- Page Start:
- 2059
- Page End:
- 2071
- Publication Date:
- 2018-08-07
- Subjects:
- naphtho[1, 2‐c:5, 6‐c′]bis[1, 2, 5]thiadiazole -- phase separation -- photovoltaic property -- side chain length -- thieno[3, 2‐b]thiophene‐substituted benzo[1, 2‐b:4, 5‐b′]dithiophene
547 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0518 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pola.29166 ↗
- Languages:
- English
- ISSNs:
- 0887-624X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5041.002050
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7724.xml