甲脒
材料科学
钙钛矿(结构)
钝化
锡
卤化物
光电子学
磁滞
碘化物
能量转换效率
纳米技术
化学工程
无机化学
冶金
图层(电子)
化学
工程类
物理
量子力学
作者
Ke Chen,Pan Wu,Wenqiang Yang,Rui Su,Deying Luo,Xiaoyu Yang,Yongguang Tu,Rui Zhu,Qihuang Gong
出处
期刊:Nano Energy
[Elsevier]
日期:2018-05-05
卷期号:49: 411-418
被引量:198
标识
DOI:10.1016/j.nanoen.2018.05.006
摘要
Organic-inorganic hybrid lead halide perovskite solar cells (PSCs) have attracted tremendous attention in recent years due to the high device performance and the unique optoelectronic properties of perovskite materials. However, the toxicity of lead remains a concern for the further application and commercialization of this technology. Therefore, it is desirable to explore efficient lead-free PSCs. Here in the tin-based inverted PSCs, we introduced an ultrathin low-dimensional perovskite (LDP) interlayer close to the PEDOT:PSS/perovskite interface. The LDP structure advantageously assists the growth of perovskites close to the interface, resulting in improved film morphology and reduced trap states. We demonstrated that the trap passivation could effectively suppress charge carrier accumulation and recombination in the device. As a consequence, a champion power conversion efficiency of 7.05% was achieved, which is one of the highest reported efficiencies for the lead-free formamidinium tin iodide PSCs. In addition, the devices showed stabilized power output and negligible current density-voltage (J-V) hysteresis.
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