Emission Wavelength Tuning via Competing Lattice Expansion and Octahedral Tilting for Efficient Red Perovskite Light-Emitting Diodes
ADVANCED FUNCTIONAL MATERIALS(2021)
摘要
The band-edge electronic structure of lead halide perovskites (ABX(3)) is composed of the orbitals of B and X components and can be tuned through the composition and structure of the BX6 octahedron. Although A-site cations do not directly contribute to near-edge states, the bandgap of 3D metal halide perovskites can be affected by A-cations through BX6 octahedron tilting or lattice size variation. Here, as confirmed by the Rietveld refinement results of X-ray diffraction characterization, the competition between lattice expansion and octahedral tilting is identified for the first time in emission wavelength tuning when introducing a large A-site cation (C2H5NH3+, EA(+)) into 1-naphthylmethylammonium iodide-passivated CsPbI3 system. The former dominates spectral redshift, while the latter leads to a blueshift of emission peak, which broadens the way to tune the emission wavelength. In addition, excess cations can also passivate the perovskites, leading to a photoluminescence (PL) quantum yield as high as 61%, increased average PL lifetime of 74.7 ns, and a high radiative and non-radiative recombination ratio of 15.7. Eventually, spectral-stable deep-red perovskite light-emitting diode with a maximum external quantum efficiency of 17.5% is realized, which is one of the highest efficiencies without using any light outcoupling and anti-solvent techniques.
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关键词
emission wavelength tuning,large cation incorporation,lattice expansion,octahedral tilting,red perovskite light-emitting diodes
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