材料科学
钙钛矿(结构)
光电子学
光活性层
光电流
偶极子
光伏系统
活动层
光诱导电荷分离
有机太阳能电池
光致发光
图层(电子)
能量转换效率
光化学
聚合物太阳能电池
化学工程
纳米技术
化学
聚合物
复合材料
有机化学
生态学
催化作用
光催化
人工光合作用
工程类
生物
薄膜晶体管
作者
Mahshid Ahmadi,Yu‐Che Hsiao,Ting Wu,Qing Liu,Wei Qin,Bin Hu
标识
DOI:10.1002/aenm.201601575
摘要
Judicious choice of transport layer in organic–inorganic halide perovskite solar cells can be one of the essential parameters in photovoltaic design and fabrication techniques. This article reports the effect of optically generated dipoles in transport layer on the photovoltaic actions in active layer in perovskite solar cells with the architecture of indium tin oxide (ITO)/TiO x /CH 3 NH 3 PbI 3– x Cl x /hole transport layer (HTL)/Au. Here, PTB7‐thieno[3,4‐b]thiophene‐ alt ‐benzodithiophene and P3HT‐poly(3‐hexylthiophene) are separately used as the HTL with significant and negligible photoinduced dipoles, respectively. Electric field‐induced photoluminescence quenching provides the first‐hand evidence to indicate that the photoinduced dipoles are partially aligned in the amorphous PTB7 layer under the influence of device built‐in field. By monitoring the recombination process through magneto‐photocurrent measurements under device operation condition, it is shown that the photoinduced dipoles in PTB7 layer can decrease the recombination of photogenerated carriers in the active layer in perovskite solar cells. Furthermore, the capacitance measurements suggest that the photoinduced dipoles in PTB7 can decrease charge accumulation at the electrode interface. Therefore, the studies indicate the important role of photoinduced dipoles in the HTL on charge recombination dynamics and provide a fundamental insight on how the polarization in transport layer can influence the device performance in perovskite solar cells.
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