TY - JOUR
T1 - Impact of Acceptor Fluorination on the Performance of All-Polymer Solar Cells
AU - Deshmukh, Kedar D.
AU - Matsidik, Rukiya
AU - Prasad, Shyamal K.K.
AU - Chandrasekaran, Naresh
AU - Welford, Adam
AU - Connal, Luke A.
AU - Liu, Amelia C.Y.
AU - Gann, Eliot
AU - Thomsen, Lars
AU - Kabra, Dinesh
AU - Hodgkiss, Justin M.
AU - Sommer, Michael
AU - McNeill, Christopher R.
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2018/1/10
Y1 - 2018/1/10
N2 - Here, we systematically study the effect of fluorination on the performance of all-polymer solar cells by employing a naphthalene diimide (NDI)-based polymer acceptor with thiophene-flanked phenyl co-monomer. Fluorination of the phenyl co-monomer with either two or four fluorine units is used to create a series of acceptor polymers with either no fluorination (PNDITPhT), bifluorination (PNDITF2T), or tetrafluorination (PNDITF4T). In blends with the donor polymer PTB7-Th, fluorination results in an increase in power conversion efficiency from 3.1 to 4.6% despite a decrease in open-circuit voltage from 0.86 V (unfluorinated) to 0.78 V (tetrafluorinated). Countering this decrease in open-circuit voltage is an increase in short-circuit current from 7.7 to 11.7 mA/cm2 as well as an increase in fill factor from 0.45 to 0.53. The origin of the improvement in performance with fluorination is explored using a combination of morphological, photophysical, and charge-transport studies. Interestingly, fluorination is found not to affect the ultrafast charge-generation kinetics, but instead is found to improve charge-collection yield subsequent to charge generation, linked to improved electron mobility and improved phase separation. Fluorination also leads to improved light absorption, with the blue-shifted absorption profile of the fluorinated polymers complementing the absorption profile of the low-band gap PTB7-Th.
AB - Here, we systematically study the effect of fluorination on the performance of all-polymer solar cells by employing a naphthalene diimide (NDI)-based polymer acceptor with thiophene-flanked phenyl co-monomer. Fluorination of the phenyl co-monomer with either two or four fluorine units is used to create a series of acceptor polymers with either no fluorination (PNDITPhT), bifluorination (PNDITF2T), or tetrafluorination (PNDITF4T). In blends with the donor polymer PTB7-Th, fluorination results in an increase in power conversion efficiency from 3.1 to 4.6% despite a decrease in open-circuit voltage from 0.86 V (unfluorinated) to 0.78 V (tetrafluorinated). Countering this decrease in open-circuit voltage is an increase in short-circuit current from 7.7 to 11.7 mA/cm2 as well as an increase in fill factor from 0.45 to 0.53. The origin of the improvement in performance with fluorination is explored using a combination of morphological, photophysical, and charge-transport studies. Interestingly, fluorination is found not to affect the ultrafast charge-generation kinetics, but instead is found to improve charge-collection yield subsequent to charge generation, linked to improved electron mobility and improved phase separation. Fluorination also leads to improved light absorption, with the blue-shifted absorption profile of the fluorinated polymers complementing the absorption profile of the low-band gap PTB7-Th.
KW - GIWAXS
KW - R-SoXS
KW - all-polymer solar cells
KW - fluorination
KW - morphology
KW - photophysics
KW - planarization
UR - http://www.scopus.com/inward/record.url?scp=85040313306&partnerID=8YFLogxK
U2 - 10.1021/acsami.7b14582
DO - 10.1021/acsami.7b14582
M3 - Article
SN - 1944-8244
VL - 10
SP - 955
EP - 969
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 1
ER -