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https://www.selleckchem.com/btk.html Phosphors with a rigid and symmetrical structure are urgently needed. The alkali lithosilicate family (A[Li3SiO4]) has been extensively studied with a narrow emission band due to its unique cuboid-coordinated environment and rigid structure. However, here we demonstrate for the first time Ce-doped NaK2Li[Li3SiO4]4 phosphors with a broad emission band, a high internal quantum efficiency (85.6%), and excellent thermal stability. Photoluminescence indicates the Ce's preference to occupy the Na+ site, leading to a strong blue color emission with peak maxima at 417 and 450 nm. Temperature- and pressure-dependent photoluminescence reveals thermal stability and a phase transition. Moreover, the X-ray absorption near-edge structure reveals the mixing of Ce3+ and Ce4+ in the materials; this result differs from that of Eu2+-doped A[Li3SiO4] phosphors. The charge compensation process is then proposed to explain this difference. This study not only provides insights into Ce-doped UCr4C4-type phosphors but also explains the charge compensation mechanism of the aliovalent doping process.Alloying is one of the most promising routes for tuning the physicochemical properties of noble metal-based nanocatalysts and thus improving their (electro)catalytic performance. Despites numerous achievements, bimetallic and trimetallic nanoalloys have still been thoroughly studied for the past two decades. In this study, metalloid boron (B) was alloyed within palladium (Pd)-based nanocatalysts to promote the electrochemical ethanol oxidation reaction (EOR) in alkaline media. The optimum PdCuB nanocatalyst exhibited remarkable electrochemical EOR activity (5.83 A mgPd-1) and good operation stability (both cycling and chronoamperometric studies). Mechanistic studies in both pure KOH and a KOH/ethanol mixture attributed superior EOR performance to positive synergistic effects of B in Pd-based nanocatalysts that kinetically accelerated the removal of poisoning et

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