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Uchenna Chinaegbomkpa

Publications and source records attributed to Uchenna Chinaegbomkpa.

2 recordsLinked to original sources

Chiral Polar Eu2(SeO3)2(SO4)(H2O)2: A Pathway Toward Narrow Optical Linewidths and Microsecond Lifetimes for Quantum Memory Candidates

Stoichiometric materials of Eu(III) offer a promising platform for quantum memories attributable to their unique capability to display a distinctive, nondegenerate J = 0 transition, which enables precise mapping of optical quantum states into their hyperfine structure for reliable storage and retrieval on demand. However, placing Eu(III) into chiral polar structures, which are necessary for achieving narrow spectral linewidths and long optical lifetimes, is a daunting task. Here, we discover Eu2(SeO3)2(SO4)(H2O)2, a rare Eu(III) material that exhibits chiral polar symmetries encompassing both local and global structures. This unique structure is shaped by an appropriate combination of asymmetric ligands. The chirality fosters dipole-dipole interactions and J-mixing, as characterized by second-harmonic generation, photoluminescence, and magnetic susceptibility. The broken inversion symmetry is supported by the phase-matching behavior of second-harmonic generation. The J = 0 transition is observed at 578 nm with a narrow linewidth at 78 K and a microsecond-scale optical lifetime. The analysis of magnetic susceptibility data using Van Vleck theory results in an effective magnetic moment of 3.33 μB/Eu3+ and J-mixing. Heat capacity data reveal underlying phonon dynamics in the material. This study demonstrates a pathway toward realizing new stoichiometric Eu3+ compounds with potential for optically addressable quantum memory applications.

cond-mat.mtrl-sci↗

Inductive-Effect-Driven Tunability of Magnetism and Lumines-cence in Triangular Layers ANd(SO4)2 (A = Rb, Cs)

Tuning the energy landscape of manybody electronic states in extended solids through the inductive effect-a concept widely used in organic chemistry-offers a new, effective strategy for materials development. Here, we demonstrate this approach using the ANd(SO4)2 (A = Rb, Cs) model system, which possesses different A-site electronegativity and displays a distorted triangular lattice of Nd3+ (4I9/2 ground term). Magnetization data indicate appreciable antiferromagnetic interactions without long-range ordering down to 1.8 K while highlighting the tunable population of the electronic states. Temperature-dependent and time-resolved photoluminescence measurements reveal that emissions and nonradiative processes can be modified by the inductive effect at the atomic level. Heat capacity data confirm no magnetic ordering and add insight into the role of phonons in emission lifetime. Density functional theory calculations prove enhanced covalency in the Cs compound compared to the Rb counterpart while acknowledging the adjustable magnetic intralayer and inter-layer exchange pathways. These results demonstrate a viable framework for utilizing the inductive effect as an important knob for simultaneously dialing in magnetic, optical, and electronic properties in quantum materials.

cond-mat.mtrl-sci↗