Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, USA.
Published: May 2009
AI Article Synopsis
Article Abstract
The construction of a metal-organic framework (MOF) with a pcu-a topology using a preassembled soluble molecular octahedron has been realized experimentally. The resulting MOF can also be reversibly converted to the molecular octahedron. All such conversions are based on axial-ligand substitution reactions on the molecular octahedron.
Shortwave infrared (SWIR)-emitting materials have emerged as superior light sources with increasing demand for potential applications in noninvasive analysis, night vision illumination, and medical diagnosis. For developing next-generation SWIR phosphor-converted light-emitting diodes (pc-LEDs), the scarcity of intense blue-light-pumped broadband SWIR luminescent materials and poor thermal stability of current Ni-activated phosphors are the ongoing challenges. Here, a blue-light-excitable (440 nm) YAlGaO:Cr,Ni phosphor with ultrawide SWIR emission centered at ∼1430 nm (FWHM ∼264 nm) is reported.
Beijing National Laboratory for Molecular Sciences, Radiochemistry and Radiation Chemistry Key Laboratory of Fundamental Science, The Key Laboratory of Polymer Chemistry and Physics of the Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, P. R. China.
Oxygen reduction reaction (ORR) kinetics is critically dependent on the precise modulation of the interactions between the key oxygen intermediates and catalytic active sites. Herein, a novel electrocatalyst is reported, featuring nitrogen-doped carbon-supported ultra-small copper oxide nanoparticles with the broken-symmetry C coordination filed sites, achieved by a mild γ-ray radiation-induced method. The as-synthesized catalyst exhibits an excellent ORR activity with a half-wave potential of 0.
The application of perovskite oxide for high-temperature electrocatalysis is hindered by its limited activity. Exsolution is a smart strategy that allows the enrichment of the perovskite's surface with highly reactive phases, yielding heteroboundaries. However, the identification of the exact catalytic role of this complex architecture is still elusive.
The chemistry of molten salts has attracted great research interest owing to their wide applications in diverse fields. In the pyrochemical reprocessing of spent nuclear fuel or molten salt nuclear reactors, lanthanide elements as the principal fission products bring about changes in the composition and properties of molten salts. Herein, we report a comprehensive study on the coordination chemistry of the representative trivalent lanthanide ions (La/Nd) in LiCl-KCl-CsCl using a multiscale strategy combining Raman spectroscopy, deep learning, and large-scale molecular dynamics (MD) simulations.
Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Molecular Reaction Dynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
- The study investigates the interactions and potential energy variations of NbN12- and N2·NbN12- complexes using techniques like photoelectron spectroscopy and advanced computational methods.
- The adiabatic detachments energies (ADE) of NbN12- and N2·NbN12- were found to be similar, but with N2·NbN12- showing slightly higher values, indicating a stronger binding energy.
- The octahedral structure of NbN12- was confirmed, and N2 can stably attach to different sites on this structure, with the face-side-on configuration being the most energetically favorable, driven mainly by dispersion forces.
