Dopant-Free Hole-Transport Materials Based on Methoxytriphenylamine-Substituted Indacenodithienothiophene for Solution-Processed Perovskite Solar Cells

被引:45
|
作者
Liu, Xiaoyuan [1 ,2 ]
Zheng, Xiaolu [3 ]
Wang, Yulong [2 ]
Chen, Zhiliang [3 ]
Yao, Fang [3 ]
Zhang, Qi [3 ]
Fang, Guojia [3 ]
Chen, Zhi-Kuan [1 ]
Huang, Wei [1 ]
Xu, Zong-Xiang [2 ]
机构
[1] Nanjing Tech Univ, Natl Jiangsu Synerget Innovat Ctr Adv Mat, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[2] South Univ Sci & Technol China, Dept Chem, Shenzhen, Peoples R China
[3] Shenzhen Inst Wuhan Univ, Shen Zhen 518000, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
dopant-free; hole-transport material; indacenodithienothiophene; methoxytriphenylamine; perovskite solar cells; NON-FULLERENE ACCEPTOR; POLYMER; PERFORMANCE; STABILITY; THIOPHENE; MOBILITY; CORE; DERIVATIVES; TRANSISTORS; EFFICIENCY;
D O I
10.1002/cssc.201700197
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solution-processed hole transporting materials (HTMs) that are dopant-free show promise for use in low-cost, high-performance perovskite solar cells (PSCs). The highest-efficiency PSCs use organic HTMs, many of which have low mobilities and therefore require doping, which lowers the device stability. Additionally, these materials are not easily scaled because they often require complicated synthesis. Two new HTMs (IDT-TPA and IDTT-TPA) were synthesized, which contained either an extended fused-ring indacenodithiophene (IDT) or indacenodithienothiophene (IDTT) core and strong electron-donating methoxytriphenylamine (TPA) groups as the end-capping units. The extended conjugation in the backbone of IDTT-TPA resulted in stronger Pi-Pi interactions (3.321 A) and a higher hole mobility of 6.46 X 10(-4) cm(2)V(-1) s(-1) when compared with that of IDT-TPA (9.53 X 10(-5) cm(2)V(-1) s(-1)). A dopant-free, planar PSC that contained IDTT-TPA was fabricated and exhibited a high power conversion efficiency (PCE) of 15.7 %. This cell exhibited a higher PCE and less hysteresis than devices that contained IDT-TPA.
引用
收藏
页码:2833 / 2838
页数:6
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