Self-Template-Directed Synthesis of Porous Perovskite Nanowires at Room Temperature for High-Performance Visible-Light Photodetectors

The unique optoelectronic properties and promising photovoltaic applications of organolead halide perovskites have driven the exploration of facile strategies to synthesize organometal halide perovskites and corresponding hybrid materials and devices. Currently, the preparation of CH3NH3PbBr3 perovs...

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Veröffentlicht in:Angewandte Chemie International Edition 2015-05, Vol.54 (19), p.5693-5696
Hauptverfasser: Zhuo, Sifei, Zhang, Jingfang, Shi, Yanmei, Huang, Yi, Zhang, Bin
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Sprache:eng
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Zusammenfassung:The unique optoelectronic properties and promising photovoltaic applications of organolead halide perovskites have driven the exploration of facile strategies to synthesize organometal halide perovskites and corresponding hybrid materials and devices. Currently, the preparation of CH3NH3PbBr3 perovskite nanowires, especially those with porous features, is still a great challenge. An efficient self‐template‐directed synthesis of high‐quality porous CH3NH3PbBr3 perovskite nanowires in solution at room temperature using the Pb‐containing precursor nanowires as both the sacrificial template and the Pb2+ source in the presence of CH3NH3Br and HBr is now presented. The initial formation of CH3NH3PbBr3 perovskite layers on the surface of the precursor nanowires and the following dissolution of the organic component of the latter led to the formation of mesopores and the preservation of the 1D morphology. Furthermore, the perovskite nanowires are potential materials for visible‐light photodetectors with high sensitivity and stability. In solution: Porous CH3NH3PbBr3 perovskite nanowires (PNW‐CH3NH3PbBr3) were fabricated by an efficient self‐template‐directed synthesis using the Pb‐containing precursor nanowires as both the sacrificial template and the Pb2+ source in the presence of CH3NH3Br and HBr in solution. The perovskite nanowires are potential materials for visible‐light photodetectors.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201411956