2011
DOI: 10.1016/j.jlumin.2011.05.003
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Electronic energy levels of CsCdCl3

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Cited by 22 publications
(34 citation statements)
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“…Figure c shows the absorption spectra of samples with increasing Sb doping amount. Both undoped RbCdCl 3 and Sb-doped RbCdCl 3 powders have absorption peaks in the range of 265 nm, which are related to the intrinsic absorption band of RbCdCl 3 that comes from the CT transition in [CdCl 6 ] 4– . With increasing Sb 3+ concentration, clear peak profiles were observed in the 300–350 nm range, and their absorption coefficient increased with increasing Sb 3+ concentration, which should be caused by the incorporation of Sb 3+ ions into the host lattice, and the latter Sb–Cl charge transfer absorption had a larger absorption coefficient in this range with a double band. This phenomenon is common in other Sb 3+ -doped halide perovskites. , In Figure d and Table S3, we haved used a single-exponential fitting method to get the PL decay process of the samples with different doping ratios with the PL peak at 596 nm under 322 nm excitation.…”
Section: Resultsmentioning
confidence: 99%
“…Figure c shows the absorption spectra of samples with increasing Sb doping amount. Both undoped RbCdCl 3 and Sb-doped RbCdCl 3 powders have absorption peaks in the range of 265 nm, which are related to the intrinsic absorption band of RbCdCl 3 that comes from the CT transition in [CdCl 6 ] 4– . With increasing Sb 3+ concentration, clear peak profiles were observed in the 300–350 nm range, and their absorption coefficient increased with increasing Sb 3+ concentration, which should be caused by the incorporation of Sb 3+ ions into the host lattice, and the latter Sb–Cl charge transfer absorption had a larger absorption coefficient in this range with a double band. This phenomenon is common in other Sb 3+ -doped halide perovskites. , In Figure d and Table S3, we haved used a single-exponential fitting method to get the PL decay process of the samples with different doping ratios with the PL peak at 596 nm under 322 nm excitation.…”
Section: Resultsmentioning
confidence: 99%
“…CsCdCl 3 , which had been previously synthesized as single crystals, was found in several studies to have a band gap that is on the order of 5 eV, , which places it in a rare category of ultrawide-band-gap materials. Anticipating that the different Cs–Cd–Cl phases would have different band gaps, we used diffuse reflectance UV–vis spectroscopy to determine the optical band gaps of our nanoscopic CsCdCl 3 , Cs 2 CdCl 4 , and Cs 3 Cd 2 Cl 7 materials.…”
Section: Resultsmentioning
confidence: 99%
“…CsCdCl 3 , which had been previously synthesized as single crystals, was found in several studies to have a band gap that is on the order of 5 eV, 48,49 1 The larger band gaps of the cadmium vs lead compounds are attributed to the larger Cd−Cl vs Pb−Cl electronegativity differences. The experimental band gap for CsCdCl 3 , determined here to be 5.13 eV, falls within the previously reported range of band gaps for this material.…”
Section: ■ Introductionmentioning
confidence: 99%
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“…CsCdCl 3 has the prerequisite for a promising optoelectronic material with excellent structural stability due to its tolerance factor ( t ) of 0.89 (0.87 for CsPbCl 3 ). Most notably, the unique bonding mode for CsCdCl 3 leads to a strong structural distortion, which is prone to induce the formation of STEs that have a great luminescence potential . However, the research of CsCdCl 3 has mainly focused on theoretical calculations, Raman spectra, and electron paramagnetic resonance (EPR) and studies are lacking on its luminescence properties, which is due to the easy formation of impurity phases such as Cs 2 CdCl 4 and Cs 3 Cd 2 Cl 7 during the synthesis process. Therefore, it will be meaningful if pure CsCdCl 3 can be synthesized using a simple synthesis method and an effective method is proposed to improve its luminescence performance …”
Section: Introductionmentioning
confidence: 99%