We report the synthesis, crystal and electronic structures, as well as optical properties of the hybrid organic-inorganic compounds MACdX (MA = CHNH; X = Cl, Br, I). MACdI is a new compound, whereas, for MACdCl and MACdBr, structural investigations have already been conducted but electronic structures and optical properties are reported here for the first time. Single crystals were grown through slow evaporation of MACdX solutions with optimized conditions yielding mm-sized colorless (X = Cl, Br) and pale yellow (X = I) crystals. Single crystal and variable temperature powder X-ray diffraction measurements suggest that MACdCl forms a 2D layered perovskite structure and has two structural transitions at 283 and 173 K. In contrast, MACdBr and MACdI adopt 0D KSO-derived crystal structures based on isolated CdX tetrahedra and show no phase transitions down to 20 K. The contrasting crystal structures and chemical compositions in the MACdX family impact their air stabilities, investigated for the first time in this work; MACdCl is air-stable, whereas MACdBr and MACdI partially decompose when left in air. Optical absorption measurements suggest that MACdX have large optical band gaps above 3.9 eV. Room temperature photoluminescence spectra of MACdX yield broad peaks in the 375-955 nm range with full width at half-maximum values up to 208 nm. These PL peaks are tentatively assigned to self-trapped excitons in MACdX following the crystal and electronic structure considerations. The bands around the Fermi level have small dispersions, which is indicative of high charge localization with significant exciton binding energies in MACdX. On the basis of our combined experimental and computational results, MACdX and related compounds may be of interest for white-light-emitting phosphors and scintillator applications.
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http://dx.doi.org/10.1021/acs.inorgchem.7b01986 | DOI Listing |
Phys Rev Lett
December 2024
School of Physics, Beihang University, Haidian District, Beijing 100191, China.
Massive Dirac fermions, which are essential for realizing novel topological phenomena, are expected to be generated from massless Dirac fermions by breaking the related symmetry, such as time-reversal symmetry in topological insulators or crystal symmetry in topological crystalline insulators. Here, we report scanning tunneling microscopy and angle-resolved photoemission spectroscopy studies of α-Bi_{4}I_{4}, which reveals the realization of massive Dirac fermions in the (100) surface states without breaking the time-reversal symmetry. Combined with first-principles calculations, our experimental results indicate that the spontaneous symmetry breaking engenders two nondegenerate edge states at the opposite sides of monolayer Bi_{4}I_{4} after the structural phase transition, imparting mass to the Dirac fermions after taking the interlayer coupling into account.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
Department of Physics, Brock University, St. Catharines, Ontario L2S 3A1, Canada.
Based on its simple valence electron configuration, we may expect lithium to have straightforward physical properties that are easily explained. However, solid lithium, when cooled below 77 K, develops a complex structure that has been debated for decades. A close parallel is found in sodium below 36 K where the crystal structure still remains unresolved.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
Radboud University Nijmegen, Institute for Molecules and Materials, 6525 AJ, Nijmegen, The Netherlands.
Resonant pumping of the electronic f-f transitions in the orbital multiplet of dysprosium ions (Dy^{3+}) in a complex perovskite DyFeO_{3} is shown to impulsively launch THz lattice dynamics corresponding to the B_{2g} phonon mode, which is dominanted by the motion of Dy^{3+} ions. The findings, supported by symmetry analysis and density-functional theory calculations, not only provide a novel route for highly selective excitation of the rare-earth crystal lattices but also establish important relationships between the symmetry of the electronic and lattice excitations in complex oxides.
View Article and Find Full Text PDFNano Lett
January 2025
Department of Physics and Astronomy, University of Wyoming, Laramie, Wyoming 82071, United States.
Anisotropic materials with low symmetries hold significant promise for next-generation electronic and quantum devices. 2M-WS, which is a candidate for topological superconductivity, has garnered considerable interest. However, a comprehensive understanding of how its anisotropic features contribute to unconventional superconductivity, along with a simple, reliable method to identify its crystal orientation, remains elusive.
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Chemistry, City University of Hong Kong, Kowloon, 999077, Hong Kong.
Perovskite/silicon tandem solar cells (TSCs) are promising candidates for commercialization due to their outstanding power conversion efficiencies (PCEs). However, controlling the crystallization process and alleviating the phases/composition inhomogeneity represent a considerable challenge for perovskite layers grown on rough silicon substrates, ultimately limiting the efficiency and stability of TSC. Here, this study reports a "halide locking" strategy that simultaneously modulates the nucleation and crystal growth process of wide bandgap perovskites by introducing a multifunctional ammonium salt, thioacetylacetamide hydrochloride (TAACl), to bind with all types of cations and anions in the mixed halide perovskite precursor.
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