Cargando…

Resonantly Pumped Bright-Triplet Exciton Lasing in Cesium Lead Bromide Perovskites

[Image: see text] The surprising recent observation of highly emissive triplet-states in lead halide perovskites accounts for their orders-of-magnitude brighter optical signals and high quantum efficiencies compared to other semiconductors. This makes them attractive for future optoelectronic applic...

Descripción completa

Detalles Bibliográficos
Autores principales: Ying, Guanhua, Farrow, Tristan, Jana, Atanu, Shao, Hanbo, Im, Hyunsik, Osokin, Vitaly, Baek, Seung Bin, Alanazi, Mutibah, Karmakar, Sanjit, Mukherjee, Manas, Park, Youngsin, Taylor, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451394/
https://www.ncbi.nlm.nih.gov/pubmed/34557568
http://dx.doi.org/10.1021/acsphotonics.1c00720
Descripción
Sumario:[Image: see text] The surprising recent observation of highly emissive triplet-states in lead halide perovskites accounts for their orders-of-magnitude brighter optical signals and high quantum efficiencies compared to other semiconductors. This makes them attractive for future optoelectronic applications, especially in bright low-threshold nanolasers. While nonresonantly pumped lasing from all-inorganic lead-halide perovskites is now well-established as an attractive pathway to scalable low-power laser sources for nano-optoelectronics, here we showcase a resonant optical pumping scheme on a fast triplet-state in CsPbBr(3) nanocrystals. The scheme allows us to realize a polarized triplet-laser source that dramatically enhances the coherent signal by 1 order of magnitude while suppressing noncoherent contributions. The result is a source with highly attractive technological characteristics, including a bright and polarized signal and a high stimulated-to-spontaneous emission signal contrast that can be filtered to enhance spectral purity. The emission is generated by pumping selectively on a weakly confined excitonic state with a Bohr radius ∼10 nm in the nanocrystals. The exciton fine-structure is revealed by the energy-splitting resulting from confinement in nanocrystals with tetragonal symmetry. We use a linear polarizer to resolve 2-fold nondegenerate sublevels in the triplet exciton and use photoluminescence excitation spectroscopy to determine the energy of the state before pumping it resonantly.