Scaffold-Guided Crystallization of Oriented α-FAPbI3 Nanowire Arrays for Solar Cells

被引:4
|
作者
Alaei, Aida [1 ,2 ]
Mohajerani, Seyed Sepehr [3 ]
Schmelmer, Ben [1 ,2 ]
Rubio, Thiago I. [1 ]
Bendesky, Justin [1 ,2 ]
Kim, Min-Woo [1 ,2 ]
Ma, Yichen [3 ]
Jeong, Sehee [1 ,2 ]
Zhou, Qintian [1 ,2 ]
Klopfenstein, Mia [1 ,2 ]
Avalos, Claudia E. [1 ,2 ]
Strauf, Stefan [3 ]
Lee, Stephanie S. [1 ,2 ]
机构
[1] NYU, Dept Chem, New York, NY 10003 USA
[2] NYU, Mol Design Inst, New York, NY 10003 USA
[3] Stevens Inst Technol, Dept Phys, Hoboken, NJ 07030 USA
基金
美国国家科学基金会;
关键词
perovskite; solar cell; nanowire; crystal orientation; nanoconfinement; PEROVSKITE; EFFICIENCY; METHYLAMMONIUM; PERFORMANCE; STABILITY; TRANSPORT; PHASES; STATE;
D O I
10.1021/acsami.3c09434
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Perovskite nanowire arrays with large surface areas for efficient charge transfer and continuous highly crystalline domains for efficient charge transport exhibit ideal morphologies for solar-cell active layers. Here, we introduce a room temperature two-step method to grow dense, vertical nanowire arrays of formamidinium lead iodide (FAPbI(3)). PbI2 nanocrystals embedded in the cylindrical nanopores of anodized titanium dioxide scaffolds were converted to FAPbI(3) by immersion in a FAI solution for a period of 0.5-30 min. During immersion, FAPbI3 crystals grew vertically from the scaffold surface as nanowires with diameters and densities determined by the underlying scaffold. The presence of butylammonium cations during nanowire growth stabilized the active alpha polymorph of FAPbI(3), precluding the need for a thermal annealing step. Solar cells comprising alpha-FAPbI3 nanowire arrays exhibited maximum solar conversion efficiencies of >14%. Short-circuit current densities of 22-23 mA cm(-2) were achieved, on par with those recorded for the best-performing FAPbI3 solar cells reported to date. Such large photocurrents are attributed to the single-crystalline, low-defect nature of the nanowires and increased interfacial area for photogenerated charge transfer compared with thin films.
引用
收藏
页码:56127 / 56137
页数:11
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