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New solution-processable small molecules as hole-transporting layer in efficient polymer solar cells
被引:24
|作者:
Lu, Kunyuan
[1
]
Yuan, Jianyu
[1
]
Peng, Jun
[1
]
Huang, Xiaodong
[1
]
Cui, Linsong
[1
]
Jiang, Zuoquan
[1
]
Wang, Hai-Qiao
[1
]
Ma, Wanli
[1
]
机构:
[1] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
基金:
国家高技术研究发展计划(863计划);
中国国家自然科学基金;
关键词:
INDIUM-TIN-OXIDE;
OPEN-CIRCUIT VOLTAGE;
PHOTOVOLTAIC CELLS;
GRAPHENE OXIDE;
ENHANCEMENT;
EXTRACTION;
INTERFACE;
STABILITY;
COPOLYMER;
DEVICES;
D O I:
10.1039/c3ta12935g
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Small molecules TPDA, TPDB, and TPDH, comprising the same backbone TPD (N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine) and different carboxyl side chains were designed and synthesized as hole-transporting materials in polymer solar cells. These small molecules demonstrated improved solubility in polar solvents due to the introduction of the weakly acidic carboxyl groups. The lengths of the side chains can also influence the film forming ability. Compared to conventional PEDOT:PSS, these small molecules showed higher transmittance in the visible range as revealed by UV-vis measurements. Desirable energy-level alignment for efficient hole-transporting and electron-blocking ability was indicated by their absorption and UPS spectra. Without applying any post-treatment to these buffer layers, comparable and improved device performances were achieved compared with PEDOT: PSS buffered control devices. A high power conversion efficiency of 6.51% was realized by a TPDB buffered device employing a low band gap polymer PBDTTPD as the active material, which showed similar to 15% efficiency enhancement over the control devices. Equally important, better device stability was demonstrated by using TPDB as the new hole-transporting layer.
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页码:14253 / 14261
页数:9
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