Search references:
1.
Martin, Stefan; Henke, Nina A; Lampe, Carola; Döblinger, Markus; Frank, Kilian; Ganswindt, Patrick; Nickel, Bert; Urban, Alexander S
Fine-Tuning Blue-Emitting Halide Perovskite Nanocrystals Journal Article
In: Advanced Optical Materials, vol. 12, no. 8, 2024, ISSN: 21951071, (Cited by: 2; All Open Access, Hybrid Gold Open Access).
@article{Martin2024,
title = {Fine-Tuning Blue-Emitting Halide Perovskite Nanocrystals},
author = {Stefan Martin and Nina A Henke and Carola Lampe and Markus Döblinger and Kilian Frank and Patrick Ganswindt and Bert Nickel and Alexander S Urban},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85166277902&doi=10.1002%2fadom.202301009&partnerID=40&md5=a48da52a47eb3a44b40bd173bd529c8f},
doi = {10.1002/adom.202301009},
issn = {21951071},
year = {2024},
date = {2024-01-01},
journal = {Advanced Optical Materials},
volume = {12},
number = {8},
publisher = {John Wiley and Sons Inc},
abstract = {Lead halide perovskite nanocrystals (NCs) with narrow, bright emission in the visible range are promising candidates for light-emitting applications. Near-unity quantum yields have been realized for green and red-emitting perovskites, but efficient, stable blue-emitting perovskite materials are scarce. Current methods to synthesize quantum-confined CsPbBr3 NCs with blue emission are limited to specific wavelength ranges and still suffer from inhomogeneously broadened emission profiles. Herein, anisotropic blue-green emitting CsPbBr3 NCs are synthesized in ambient atmosphere using a spontaneous crystallization method. Optical spectroscopy reveals a gradual, asymptotic photoluminescence (PL) redshift of pristine colloidal NCs after synthesis. During this process, the emission quality improves notably as the PL spectra become narrower and more symmetric, accompanied by a PL intensity increase. Electron microscopy indicates that the gradual redshift stems from an isotropic growth of the CsPbBr3 NCs in at least two dimensions, likely due to residual precursor ions in the dispersion. Most importantly, the growth process can be halted at any point by injecting an enhancement solution containing PbBr2 and organic capping ligands. Thus, excellent control over NC size is achieved, allowing for nanometer-precise tunability of the respective emission wavelength in the range between 475 and 500 nm, enhancing the functionality of these already impressive NCs. © 2023 The Authors. Advanced Optical Materials published by Wiley-VCH GmbH.},
note = {Cited by: 2; All Open Access, Hybrid Gold Open Access},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Lead halide perovskite nanocrystals (NCs) with narrow, bright emission in the visible range are promising candidates for light-emitting applications. Near-unity quantum yields have been realized for green and red-emitting perovskites, but efficient, stable blue-emitting perovskite materials are scarce. Current methods to synthesize quantum-confined CsPbBr3 NCs with blue emission are limited to specific wavelength ranges and still suffer from inhomogeneously broadened emission profiles. Herein, anisotropic blue-green emitting CsPbBr3 NCs are synthesized in ambient atmosphere using a spontaneous crystallization method. Optical spectroscopy reveals a gradual, asymptotic photoluminescence (PL) redshift of pristine colloidal NCs after synthesis. During this process, the emission quality improves notably as the PL spectra become narrower and more symmetric, accompanied by a PL intensity increase. Electron microscopy indicates that the gradual redshift stems from an isotropic growth of the CsPbBr3 NCs in at least two dimensions, likely due to residual precursor ions in the dispersion. Most importantly, the growth process can be halted at any point by injecting an enhancement solution containing PbBr2 and organic capping ligands. Thus, excellent control over NC size is achieved, allowing for nanometer-precise tunability of the respective emission wavelength in the range between 475 and 500 nm, enhancing the functionality of these already impressive NCs. © 2023 The Authors. Advanced Optical Materials published by Wiley-VCH GmbH.
References (last update: Sept. 23, 2024):
2024
Martin, Stefan; Henke, Nina A; Lampe, Carola; Döblinger, Markus; Frank, Kilian; Ganswindt, Patrick; Nickel, Bert; Urban, Alexander S
Fine-Tuning Blue-Emitting Halide Perovskite Nanocrystals Journal Article
In: Advanced Optical Materials, vol. 12, no. 8, 2024, ISSN: 21951071, (Cited by: 2; All Open Access, Hybrid Gold Open Access).
Abstract | Links | BibTeX | Tags: Bromine compounds; Lead compounds; Perovskite; Photoluminescence; Sols; 'current; Blue-emission; Blue-emitting; Fine tuning; Halide perovskites; Lead halide perovskite; Red shift; Red-emitting; Visible range; Wavelength ranges; Nanocrystals
@article{Martin2024,
title = {Fine-Tuning Blue-Emitting Halide Perovskite Nanocrystals},
author = {Stefan Martin and Nina A Henke and Carola Lampe and Markus Döblinger and Kilian Frank and Patrick Ganswindt and Bert Nickel and Alexander S Urban},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85166277902&doi=10.1002%2fadom.202301009&partnerID=40&md5=a48da52a47eb3a44b40bd173bd529c8f},
doi = {10.1002/adom.202301009},
issn = {21951071},
year = {2024},
date = {2024-01-01},
journal = {Advanced Optical Materials},
volume = {12},
number = {8},
publisher = {John Wiley and Sons Inc},
abstract = {Lead halide perovskite nanocrystals (NCs) with narrow, bright emission in the visible range are promising candidates for light-emitting applications. Near-unity quantum yields have been realized for green and red-emitting perovskites, but efficient, stable blue-emitting perovskite materials are scarce. Current methods to synthesize quantum-confined CsPbBr3 NCs with blue emission are limited to specific wavelength ranges and still suffer from inhomogeneously broadened emission profiles. Herein, anisotropic blue-green emitting CsPbBr3 NCs are synthesized in ambient atmosphere using a spontaneous crystallization method. Optical spectroscopy reveals a gradual, asymptotic photoluminescence (PL) redshift of pristine colloidal NCs after synthesis. During this process, the emission quality improves notably as the PL spectra become narrower and more symmetric, accompanied by a PL intensity increase. Electron microscopy indicates that the gradual redshift stems from an isotropic growth of the CsPbBr3 NCs in at least two dimensions, likely due to residual precursor ions in the dispersion. Most importantly, the growth process can be halted at any point by injecting an enhancement solution containing PbBr2 and organic capping ligands. Thus, excellent control over NC size is achieved, allowing for nanometer-precise tunability of the respective emission wavelength in the range between 475 and 500 nm, enhancing the functionality of these already impressive NCs. © 2023 The Authors. Advanced Optical Materials published by Wiley-VCH GmbH.},
note = {Cited by: 2; All Open Access, Hybrid Gold Open Access},
keywords = {Bromine compounds; Lead compounds; Perovskite; Photoluminescence; Sols; 'current; Blue-emission; Blue-emitting; Fine tuning; Halide perovskites; Lead halide perovskite; Red shift; Red-emitting; Visible range; Wavelength ranges; Nanocrystals},
pubstate = {published},
tppubtype = {article}
}
Lead halide perovskite nanocrystals (NCs) with narrow, bright emission in the visible range are promising candidates for light-emitting applications. Near-unity quantum yields have been realized for green and red-emitting perovskites, but efficient, stable blue-emitting perovskite materials are scarce. Current methods to synthesize quantum-confined CsPbBr3 NCs with blue emission are limited to specific wavelength ranges and still suffer from inhomogeneously broadened emission profiles. Herein, anisotropic blue-green emitting CsPbBr3 NCs are synthesized in ambient atmosphere using a spontaneous crystallization method. Optical spectroscopy reveals a gradual, asymptotic photoluminescence (PL) redshift of pristine colloidal NCs after synthesis. During this process, the emission quality improves notably as the PL spectra become narrower and more symmetric, accompanied by a PL intensity increase. Electron microscopy indicates that the gradual redshift stems from an isotropic growth of the CsPbBr3 NCs in at least two dimensions, likely due to residual precursor ions in the dispersion. Most importantly, the growth process can be halted at any point by injecting an enhancement solution containing PbBr2 and organic capping ligands. Thus, excellent control over NC size is achieved, allowing for nanometer-precise tunability of the respective emission wavelength in the range between 475 and 500 nm, enhancing the functionality of these already impressive NCs. © 2023 The Authors. Advanced Optical Materials published by Wiley-VCH GmbH.