TY - JOUR
T1 - Photovoltaic properties of novel thiophene- and selenophene-based conjugated low bandgap polymers
T2 - A comparative study
AU - Lee, Young Nam
AU - Attri, Pankaj
AU - Kim, Seong Su
AU - Lee, Sang Jun
AU - Kim, Jun Heon
AU - Cho, Tae Jong
AU - Kim, In Tae
N1 - Publisher Copyright:
© 2017 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - In this study, we investigated the photovoltaic properties of newly synthesized low bandgap conjugated polymers, poly(4-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophen-2-yl)-8-(5-(2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)-4-yl)thiophen-2-yl)-2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)) (P1) and poly(4-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophen-2-yl)-8-(5-(2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)-4-yl)selenophen-2-yl)-2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)) (P2). P1 is a thiophene-based conjugated polymer (TCP), and P2 is a selenophene-based conjugated polymer (SCP). These two different conjugated low bandgap polymers were characterized by NMR and gel permeation chromatography. The physical properties of the polymers were studied by thermogravimetric analysis and conductivity. Moreover, we also investigated the optical, electrochemical and morphological properties of both polymers by UV-vis spectroscopy, cyclic voltammetry and atomic-force microscopy (AFM), respectively. Later, we studied the photovoltaic properties of both low bandgap polymers blended with PC61BM in different ratios with different thicknesses. In addition, post thermal annealing at different temperatures for both polymers was investigated, and the results show that P2 (SCP) exhibited stronger molecular orientation properties as compared to P1 (TCP).
AB - In this study, we investigated the photovoltaic properties of newly synthesized low bandgap conjugated polymers, poly(4-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophen-2-yl)-8-(5-(2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)-4-yl)thiophen-2-yl)-2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)) (P1) and poly(4-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophen-2-yl)-8-(5-(2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)-4-yl)selenophen-2-yl)-2,6-didodecylbenzo[1,2-d:4,5-d′]bis(thiazole)) (P2). P1 is a thiophene-based conjugated polymer (TCP), and P2 is a selenophene-based conjugated polymer (SCP). These two different conjugated low bandgap polymers were characterized by NMR and gel permeation chromatography. The physical properties of the polymers were studied by thermogravimetric analysis and conductivity. Moreover, we also investigated the optical, electrochemical and morphological properties of both polymers by UV-vis spectroscopy, cyclic voltammetry and atomic-force microscopy (AFM), respectively. Later, we studied the photovoltaic properties of both low bandgap polymers blended with PC61BM in different ratios with different thicknesses. In addition, post thermal annealing at different temperatures for both polymers was investigated, and the results show that P2 (SCP) exhibited stronger molecular orientation properties as compared to P1 (TCP).
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U2 - 10.1039/c7nj00151g
DO - 10.1039/c7nj00151g
M3 - Article
AN - SCOPUS:85022337727
SN - 1144-0546
VL - 41
SP - 6315
EP - 6321
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 14
ER -