TY - JOUR
T1 - Efficient polymer solar cells based on dialkoxynaphthalene and benzo[c][1,2,5]thiadiazole
T2 - A new approach for simple donoracceptor pair
AU - Kim, Seul Ong
AU - Chung, Dae Sung
AU - Cha, Hyojung
AU - Hwang, Moon Chan
AU - Park, Jong Won
AU - Kim, Yun Hi
AU - Park, Chan Eon
AU - Kwon, Soon Ki
PY - 2011/7
Y1 - 2011/7
N2 - We reported the synthesis of novel polymeric semiconductor materials based on [poly(4-(5-(1,5-bis(alkoxy)naphthalen-2-yl)thiophen-2-yl)-7-(thiophen-2-yl) benzo[c][1,2,5]-thiadiazole)] (PANTBT) and the fabrication of solar cells with a power conversion efficiency of 4.2% using the synthesized polymers blended with [6,6]-phenyl C71 butyric acid methyl ester (PC70BM) in bulk heterojunction geometry. By varying the side chains, three polymers were synthesized [poly(4-(5-(1,5-bis(2-ethylhexyloxy)naphthalen-2-yl)thiophen-2-yl)- 7-(thiophen-2-yl)benzo[c][1,2,5]thiadiazole)] (PENTBT), [poly(4-(5-(1,5- bis(decyloxy)naphthalen-2-yl)thiophen-2-yl)-7-(thiophen-2-yl)benzo[c][1,2,5] thiadiazole)] (PDNTBT), and [poly(4-(5-(1,5-bis(tetradecyloxy)naphthalen-2-yl) thiophen-2-yl)-7-(thiophen-2-yl)benzo[c][1,2,5]thiadiazole)] (PTDNTBT), maintaining a low highest occupied molecular orbital (HOMO) energy level and relatively low band gap, which lead to a high open circuit voltage and short circuit current of the resulting devices. Due to the superior miscibility of PANTBT derivatives with PC70BM, favorable phase separation with a domain size of 1020 nm was achieved regardless of the crystalline nature of the pristine polymers. PDNTBT with alkyl side chain C10 and PTDNTBT with alkyl side chain C14 showed higher photovoltaic performances. In addition, the effects of the crystalline nature of polymers on the thermal stability of the resulting solar cell devices were discussed in terms of the influence of side chains.
AB - We reported the synthesis of novel polymeric semiconductor materials based on [poly(4-(5-(1,5-bis(alkoxy)naphthalen-2-yl)thiophen-2-yl)-7-(thiophen-2-yl) benzo[c][1,2,5]-thiadiazole)] (PANTBT) and the fabrication of solar cells with a power conversion efficiency of 4.2% using the synthesized polymers blended with [6,6]-phenyl C71 butyric acid methyl ester (PC70BM) in bulk heterojunction geometry. By varying the side chains, three polymers were synthesized [poly(4-(5-(1,5-bis(2-ethylhexyloxy)naphthalen-2-yl)thiophen-2-yl)- 7-(thiophen-2-yl)benzo[c][1,2,5]thiadiazole)] (PENTBT), [poly(4-(5-(1,5- bis(decyloxy)naphthalen-2-yl)thiophen-2-yl)-7-(thiophen-2-yl)benzo[c][1,2,5] thiadiazole)] (PDNTBT), and [poly(4-(5-(1,5-bis(tetradecyloxy)naphthalen-2-yl) thiophen-2-yl)-7-(thiophen-2-yl)benzo[c][1,2,5]thiadiazole)] (PTDNTBT), maintaining a low highest occupied molecular orbital (HOMO) energy level and relatively low band gap, which lead to a high open circuit voltage and short circuit current of the resulting devices. Due to the superior miscibility of PANTBT derivatives with PC70BM, favorable phase separation with a domain size of 1020 nm was achieved regardless of the crystalline nature of the pristine polymers. PDNTBT with alkyl side chain C10 and PTDNTBT with alkyl side chain C14 showed higher photovoltaic performances. In addition, the effects of the crystalline nature of polymers on the thermal stability of the resulting solar cell devices were discussed in terms of the influence of side chains.
KW - Alkoxynaphthalene
KW - Benzothiadiazole
KW - Bulk heterojunction
KW - Electron donor
KW - Low bandgap
KW - Photovoltaics
UR - http://www.scopus.com/inward/record.url?scp=79955479736&partnerID=8YFLogxK
U2 - 10.1016/j.solmat.2011.01.028
DO - 10.1016/j.solmat.2011.01.028
M3 - Article
AN - SCOPUS:79955479736
SN - 0927-0248
VL - 95
SP - 1678
EP - 1685
JO - Solar Energy Materials and Solar Cells
JF - Solar Energy Materials and Solar Cells
IS - 7
ER -