TY - JOUR
T1 - Electrolytes as Cathode Interlayers in Inverted Organic Solar Cells
T2 - Influence of the Cations on Bias-Dependent Performance
AU - Li, Yaru
AU - Liu, Xiaohui
AU - Li, Xiaodong
AU - Zhang, Wenjun
AU - Xing, Feifei
AU - Fang, Junfeng
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/3/8
Y1 - 2017/3/8
N2 - The performance of organic solar cells (OSCs) with edetate electrolytes depends on external bias, and ions are speculated to be responsible for this phenomenon. To clarify the detailed relationship between the ions of electrolytes and the bias-dependent behaviors of devices, this work introduces four edetate cathode interlayers (EDTA-X, X = nH(4-n)Na, n = 0, 1, 2, and 4) containing different kinds and number of cations into inverted OSCs. The results show that the devices initial and saturated (after external bias treatment) power conversion efficiencies (PCEs) both decrease with the increase in the number of H+. Moreover, the bias-dependent degrees increase with the increase in H+ number; with that, the PCE increment of EDTA-4H device is 53.4%, while that of the EDTA-4Na device is almost unchanged. The electrical impedance spectroscopy and capacitance-voltage tests reveal that the interfacial recombination is greatly suppressed by external bias treatment, which is not a result of the decreased density of defect states. The results indicate that the ion’s motion, specifically the H+ motion, under external electrical field is responsible for the bias-dependent behavior, which is conducive to the design of new efficient electrolytic interlayers without bias-dependent performance.
AB - The performance of organic solar cells (OSCs) with edetate electrolytes depends on external bias, and ions are speculated to be responsible for this phenomenon. To clarify the detailed relationship between the ions of electrolytes and the bias-dependent behaviors of devices, this work introduces four edetate cathode interlayers (EDTA-X, X = nH(4-n)Na, n = 0, 1, 2, and 4) containing different kinds and number of cations into inverted OSCs. The results show that the devices initial and saturated (after external bias treatment) power conversion efficiencies (PCEs) both decrease with the increase in the number of H+. Moreover, the bias-dependent degrees increase with the increase in H+ number; with that, the PCE increment of EDTA-4H device is 53.4%, while that of the EDTA-4Na device is almost unchanged. The electrical impedance spectroscopy and capacitance-voltage tests reveal that the interfacial recombination is greatly suppressed by external bias treatment, which is not a result of the decreased density of defect states. The results indicate that the ion’s motion, specifically the H+ motion, under external electrical field is responsible for the bias-dependent behavior, which is conducive to the design of new efficient electrolytic interlayers without bias-dependent performance.
KW - cathode interlayer
KW - edetate electrolytes
KW - external bias
KW - ion motion
KW - organic solar cells
UR - https://www.scopus.com/pages/publications/85014871691
U2 - 10.1021/acsami.7b01240
DO - 10.1021/acsami.7b01240
M3 - 文章
C2 - 28218514
AN - SCOPUS:85014871691
SN - 1944-8244
VL - 9
SP - 8426
EP - 8431
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 9
ER -