Related Experiment Video
Updated: Jan 16, 2026

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Efficient Energy Transfer in Eu3+-Doped Layered Double Hydroxides with β‑Diketonate Anions Obtained by the Memory
Alexandre Candido Teixeira1, Natan Felipe Netzlaff Fachini1, Henrique Kenzo Carvalho Kakinami1
1Instituto de Física da Universidade de São Paulo, 05508-090 São Paulo, SP, Brazil.
Abstract:
The use of layered double hydroxides (LDHs) as luminescent hybrid materials has gained attention due to their structural versatility and ability to incorporate functional anions. In this study, we report the synthesis of a ZnAlEu-LDH intercalated with dibenzoylmethane (DBM) via the memory effect as an alternative strategy to obtain luminescent materials. The LDH precursor was synthesized by coprecipitation and then calcined at 460 °C to form a mixed oxide, followed by structural reconstruction in an aqueous DBM solution. The structural transformation and intercalation processes were confirmed by powder X-ray diffraction, Fourier-transform infrared spectroscopy, and elemental analysis (CHN and inductively coupled plasma optical emission spectrometry). Morphological changes were evaluated by scanning electron microscopy. Photoluminescence spectroscopy revealed that the DBM-intercalated LDHs exhibited a significant enhancement in the Eu3+ emission intensity due to the antenna effect from DBM, as demonstrated by the appearance of a broad S0(π) → S n (π*) excitation band around 390 nm. The emission spectra also showed characteristic Eu3+ transitions with spectral shifts indicative of changes in the local ligand field upon DBM coordination. This work demonstrates that the memory effect is an effective strategy for incorporating photofunctional ligands into LDH matrices, opening new possibilities for the design of luminescent hybrid materials with tailored properties.
More Related Videos
07:24Quantitative Atomic-Site Analysis of Functional Dopants/Point Defects in Crystalline Materials by Electron-Channeling-Enhanced Microanalysis
Published on: May 10, 2021
07:24Hyperspectral Imaging as a Tool to Study Optical Anisotropy in Lanthanide-Based Molecular Single Crystals
Published on: April 14, 2020
Related Concept Videos
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
The Born-Haber Cycle
Trends in Lattice Energy: Ion Size and Charge
EDTA: Chemistry and Properties