Journal of the American Chemical Society · 2018 · 114 citations · 54 references
Natural SciencesMaterials SciencePhysicsOptical MaterialsOptoelectronicsSemiconductor MaterialsOptical Properties Of SolidsOptoelectronic DevicesOptoelectronic MaterialsPerovskite MaterialsSemiconductor HeterostructuresTwo-dimensional SemiconductorsDouble HeterostructuresEnergy TransferHalide PerovskitesOptoelectronic PropertiesOrganic-inorganic Hybrid PerovskitesPhotoluminescenceTwo-dimensional HeterostructuresVan Der Waals Epitaxy
Fabrication of heterostructures using two-dimensional (2D) materials with different bandgaps creates opportunities for exploring new properties and device applications. Ruddlesden–Popper (RP) layered halide perovskites have recently emerged as a new class of solution-processable 2D materials that demonstrate exotic optoelectronic properties. However, heterostructures using 2D halide perovskites have not been achieved. Here, we report a simple solution growth method for making vertically stacked double heterostructures and complex multilayer heterostructures of 2D lead iodide perovskites [(PEA)2(MA)n–1PbnI3n+1, PEA = C6H5(CH2)2NH3+, MA = CH3NH3+] via van der Waals epitaxy. These heterostructures present atomically sharp interfaces and display distinct photoluminescence that allow fingerprinting the RP phases. Time-resolved photoluminescence measurements reveal internal energy transfer from higher energy bandgap (lower n value) perovskite layers to lower energy bandgap (higher n value) perovskite layers on the time scale of hundreds of picoseconds due to natural type I band alignments. These results offer new strategies to fabricate perovskite–perovskite heterojunctions by taking advantage of surface-bound ligands as spatial barriers to prevent ion migration across the junctions. These heterostructures capable of multicolor emission with high spectral purity are promising for light-emitting applications.
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Sequential deposition as a route to high-performance perovskite-sensitized solar cells
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