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沈赵琪, 程敬招, 张小凤, 黄微雅, 温和瑞, 刘诗咏. P3HT/非富勒烯受体异质结有机太阳电池[J]. 化学进展, 2019, 31(9): 1221-1237.
Zhaoqi Shen, Jingzhao Cheng, Xiaofeng Zhang, Weiya Huang, Herui Wen, Shiyong Liu. P3HT/Non-Fullerene Acceptors Heterojunction Organic Solar Cells[J]. Progress in Chemistry, 2019, 31(9): 1221-1237.
非富勒烯受体材料在分子设计、光吸收及能级等多方面具有极其丰富的可调控性, 使得基于非富勒烯电子受体的本体异质结有机太阳电池(BHJ OSC) 近年得以迅速发展。P3HT聚合物作为被广泛研究的第二代有机半导体材料, 其价格便宜、具有较好的结晶性以及优异的载流子传输性能, 是经典的电子给体材料。本文综述了近年来以P3HT聚合物为给体、非富勒烯类有机化合物为电子受体的有机太阳电池研究进展, 探讨了P3HT/非富勒烯受体BHJ OSC中, 影响器件效率提升的关键因素, 以及电子受体优化设计方面的相应要求。对基于P3HT/非富勒烯受体 BHJ OSC器件的研究前景进行了展望。
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Acceptor | Jsc/mA·cm-2 | Voc/V | FF | PCE/% | ref |
---|---|---|---|---|---|
A1 | 1.32 | 0.36 | 0.38 | 0.182 | 41 |
A2 | 1.74 | 0.75 | 0.38 | 0.50 | 42 |
A3 | 0.02 | 0.44 | 0.53 | 0.005 | 44 |
A4 | 1.6 | 0.57 | 0.39 | 0.35 | 44 |
A5 | 3.5 | 0.61 | 0.58 | 1.25 | 44 |
A6 | 7.4 | 0.78 | 0.55 | 3.17 | 45 |
A7 | 2.01 | 0.43 | 0.47 | 0.41 | 47 |
A8 | 2.89 | 0.59 | 0.45 | 0.76 | 47 |
A9 | 3.83 | 0.67 | 0.60 | 1.54 | 47 |
A10 | 3.30 | 0.59 | 0.67 | 1.31 | 48 |
A11 | 5.69 | 0.68 | 0.50 | 1.93 | 49 |
A12 | 5.58 | 0.70 | 0.67 | 2.61 | 50 |
A13 | 5.42 | 0.41 | 0.42 | 0.94 | 51 |
A14:A15 | 1.25 | 0.5 | 0.42 | 0.26 | 52 |
A16 | 4.19 | 0.42 | 0.43 | 0.75 | 53 |
A17 | 3.62 | 0.68 | 0.62 | 1.45 | 54 |
Acceptor | Jsc/mA·cm-2 | Voc/V | FF | PCE/% | ref |
---|---|---|---|---|---|
C1 | 1.70 | 0.64 | 0.53 | 0.58 | 59 |
C2 | 2.36 | 0.81 | 0.52 | 1.00 | 59 |
C3 | 2.70 | 0.65 | 0.32 | 0.56 | 59 |
C4 | 0.71 | 0.85 | 0.23 | 0.14 | 59 |
C5 | 4.58 | 0.83 | 0.67 | 2.50 | 61 |
C6 | 3.60 | 0.84 | 0.53 | 1.56 | 61 |
C7 | 5.91 | 0.89 | 0.5 | 3.28 | 62 |
C8 | 4.91 | 0.97 | 0.43 | 2.05 | 63 |
C9 | 1.43 | 1.17 | 0.50 | 0.83 | 64 |
C10 | 5.88 | 0.90 | 0.51 | 2.69 | 65 |
C11 | 2.06 | 1.08 | 0.52 | 1.16 | 66 |
C12 | 2.15 | 1.05 | 0.45 | 1.02 | 67 |
C13 | 2.42 | 1.10 | 0.45 | 1.20 | 68 |
C14 | 5.35 | 1.18 | 0.502 | 3.17 | 69 |
C15 | 6.25 | 0.97 | 0.39 | 2.37 | 70 |
C16 | 2.68 | 1.18 | 0.38 | 1.20 | 71 |
C17 | 6.96 | 1.10 | 0.48 | 3.63 | 72 |
C18 | 5.21 | 0.88 | 0.4 | 1.87 | 72 |
C19 | 3.88 | 0.91 | 0.4 | 1.42 | 72 |
C20 | 8.29 | 1.14 | 0.55 | 5.16 | 73 |
C21 | 8.48 | 1.04 | 0.50 | 4.42 | 74 |
C22 | 4.45 | 1.16 | 0.47 | 2.49 | 75 |
C23 | 2.93 | 1.11 | 0.36 | 1.18 | 75 |
Acceptor | Jsc/mA·cm-2 | Voc/V | FF | PCE/% | ref |
---|---|---|---|---|---|
D1 | 3.6 | 1.15 | 0.34 | 1.20 | 81 |
D2 | 2.60 | 1.00 | 0.45 | 1.18 | 83 |
D3 | 1.79 | 0.67 | 0.37 | 0.45 | 84 |
D4 | 2.4 | 0.62 | 0.491 | 0.73 | 85 |
D5 | 4.85 | 0.54 | 0.547 | 1.43 | 86 |
D6 | 4.7 | 0.96 | 0.56 | 2.54 | 87 |
D7 | 0.5 | 0.65 | 0.40 | 0.12 | 87 |
D8 | 5.59 | 0.76 | 0.48 | 1.91 | 88 |
D9 | 7.95 | 0.82 | 0.63 | 4.11 | 89 |
D10 | 14.10 | 0.73 | 0.62 | 6.40 | 90 |
D11 | 12.2 | 0.77 | 0.64 | 6.05 | 90 |
D12 | 8.91 | 0.84 | 0.681 | 5.12 | 91 |
D13:D10 | 14.4 | 0.82 | 0.64 | 7.7 | 93 |
Acceptor | Jsc/mA·cm-2 | Voc/V | FF | PCE/% | ref |
---|---|---|---|---|---|
E1 | 4.82 | 0.72 | 0.48 | 1.67 | 94 |
E2 | 3.82 | 0.95 | 0.67 | 2.43 | 94 |
E4 | 5.04 | 1.07 | 0.42 | 2.28 | 96 |
E5 | 3.86 | 1.10 | 0.40 | 1.70 | 97 |
E6 | 4.40 | 0.76 | 0.56 | 1.86 | 98 |
E7 | 6.35 | 0.95 | 0.48 | 2.89 | 99 |
E8 | 1.93 | 0.54 | 0.41 | 0.43 | 100 |
E9 | 1.11 | 0.82 | 0.34 | 0.31 | 100 |
E10 | 0.36 | 0.44 | 0.40 | 0.06 | 100 |
E11 | 7.34 | 1.02 | 0.70 | 5.24 | 102 |
E12 | 6.15 | 1.22 | 0.60 | 4.50 | 103 |
E13 | 5.45 | 1.02 | 0.59 | 3.28 | 104 |
E14 | 2.09 | 0.91 | 0.30 | 0.57 | 104 |
E15 | 0.47 | 1.07 | 0.40 | 0.20 | 104 |
E16 | 4.85 | 1.06 | 0.46 | 2.36 | 105 |
E17 | 4.87 | 0.58 | 0.57 | 1.6 | 106 |
E18 | 2.75 | 0.82 | 0.46 | 1.03 | 107 |
E19 | 5.87 | 0.90 | 0.498 | 2.64 | 108 |
E20 | 11.5 | 0.87 | 0.623 | 6.40 | 108 |
E21 | 1.81 | 0.99 | 0.452 | 0.81 | 109 |
E22 | 1.91 | 0.96 | 0.44 | 0.81 | 110 |
E23 | 9.1 | 0.77 | 0.59 | 4.10 | 111 |
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