TY - JOUR
T1 - Dialkoxymethano[60]fullerenes as electron acceptors in thin-film organic solar cells
AU - Suleiman, Mohammed Y.
AU - Ma, Yue
AU - Nakagawa, Takafumi
AU - Ueno, Hiroshi
AU - Matsuo, Yutaka
N1 - Funding Information:
This work was supported by the thousand talent program in Northeast Normal University . This work was also supported by the Grants-in-Aid for Scientific Research ( JSPS KAKENHI Grant Numbers JP15H05760 , JP16H04187 ), MEXT , Japan.
Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/9/20
Y1 - 2019/9/20
N2 - This study presents the synthesis, characterization, and electrochemical properties of four new dialkoxymethanofullerenes, as well as their performance in organic solar cells (OSCs) devices. Dialkoxymethanofullerenes were synthesized in 27%–32% yield by thermolysis of dialkoxyoxadiazolines and reaction with C60 under reflux in toluene. The prepared compounds were then characterized and used for the first time as electron-acceptor materials in thin-film bulk heterojunction OSCs with PBTZT-stat-BDTT-8 as the electron donor material. The devices made with ethoxy-hexyloxymethanofullerene and methoxy-hexyloxymethanofullerene exhibited optimal power conversion efficiencies (PCEs) of 3.79% and 4.65%, with open-circuit voltage of 0.832 and 0.831 V, respectively. In contrast, the devices made with ethoxy-ethoxymethanofullerene and methoxy-ethoxymethanofullerene exhibited very low PCEs of <0.01% for both, indicating a large impact of the substituents on device performance.
AB - This study presents the synthesis, characterization, and electrochemical properties of four new dialkoxymethanofullerenes, as well as their performance in organic solar cells (OSCs) devices. Dialkoxymethanofullerenes were synthesized in 27%–32% yield by thermolysis of dialkoxyoxadiazolines and reaction with C60 under reflux in toluene. The prepared compounds were then characterized and used for the first time as electron-acceptor materials in thin-film bulk heterojunction OSCs with PBTZT-stat-BDTT-8 as the electron donor material. The devices made with ethoxy-hexyloxymethanofullerene and methoxy-hexyloxymethanofullerene exhibited optimal power conversion efficiencies (PCEs) of 3.79% and 4.65%, with open-circuit voltage of 0.832 and 0.831 V, respectively. In contrast, the devices made with ethoxy-ethoxymethanofullerene and methoxy-ethoxymethanofullerene exhibited very low PCEs of <0.01% for both, indicating a large impact of the substituents on device performance.
KW - Dialkoxymethanofullerenes
KW - Dialkoxyoxadiazolines
KW - Methanofullerene
KW - Organic photovoltaics
KW - Organic solar cells
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U2 - 10.1016/j.tet.2019.130514
DO - 10.1016/j.tet.2019.130514
M3 - Article
AN - SCOPUS:85070551425
SN - 0040-4020
VL - 75
JO - Tetrahedron
JF - Tetrahedron
IS - 38
M1 - 130514
ER -