钙钛矿(结构)
光电探测器
卤化物
材料科学
结晶
光电子学
单独一对
薄膜
纳米技术
化学
结晶学
无机化学
有机化学
分子
作者
Minjie Wu,Teng Chen,Xuedan Chen,Maoxue Wang,Chen Lv,Kai Meng,Shuanglong Yuan
标识
DOI:10.1002/chem.202403716
摘要
Perovskite-based photodetectors (PDs) are broadly utilized in optical communication, non-destructive testing, and smart wearable devices due to their ability to convert light into electrical signals. However, toxicity and instability hold back their mass production and commercialization. The lead-free Cs2AgBiBr6 double perovskite film, promised to be an alternative, is fabricated by electrophoretic deposition (EPD), which compromises film quality. Herein, we improved the quality of the Cs2AgBiBr6 films and the performance of PDs by adding N-acetylethylenediamine (DEAC) to Cs2AgBiBr6 perovskite precursor for EPD, in which the ligand DEAC provides a pair of lone electrons to Bi3+, forming coordinate covalent bonds. The optimized PDs have high detectivity, up to 4.4×1012 Jones, and high stability in the air. The high-performance, flexible Cs2AgBiBr6 perovskite PDs were fabricated on this basis, it also achieved the detectivity up to 3.2×1012 Jones with excellent bending cycle stability. These results propose a feasible approach to improving the crystallization of double perovskite thin films by introducing ligands during the EPD process. Furthermore, they demonstrate enhanced optoelectronic performance, indicating that this method is also applicable to halide perovskites, offering an effective strategy to improve their film quality.
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