A Rational Solid-State Synthesis of Supported Au-Ni Bimetallic Nanoparticles with Enhanced Activity for Gas-Phase Selective Oxidation of Alcohols.

A facile confined solid-state seed-mediated alloying strategy is applied for the rational synthesis of supported Au-Ni bimetallic nanoparticles (BMNPs). The method sequentially deposits nickel salts and AuNP seeds into the ordered array of extra-large mesopores (EP-FDU-12 support) followed by a high-temperature annealing process. The size, structure, and composition of the AuNi BMNPs can be well tuned by varying the AuNP seeds, annealing temperature, and feeding ratio of metal precursors.

Fast Optimization of LiMgMnO/LaO Catalysts for the Oxidative Coupling of Methane.

The development of efficient catalyst for oxidative coupling of methane (OCM) reaction represents a grand challenge in direct conversion of methane into other useful products. Here, we reported that a newly developed combinatorial approach can be used for ultrafast optimization of LaO-based multicomponent metal oxide catalysts in OCM reaction. This new approach integrated inkjet printing assisted synthesis (IJP-A) with multidimensional group testing strategy (m-GT) tactfully takes the place of conventionally high-throughput synthesis-and-screen experiment.

Mix and print: fast optimization of mesoporous CuCeZrO(w) for catalytic oxidation of n-hexane.

Fast optimization of mesoporous ternary metal oxide (CuCeZrO(w)) catalysts for n-hexane oxidation is achieved via a newly developed combinatorial approach based on ink-jet printing assisted synthesis and multi-dimensional group testing.

Sub-10 nm Au-Pt-Pd alloy trimetallic nanoparticles with a high oxidation-resistant property as efficient and durable VOC oxidation catalysts.

Sub-10 nm AuPtPd alloy trimetallic nanoparticles (TMNPs) with a high oxidation-resistant property were prepared by photo-deposition followed by a high temperature (700-900 °C) air annealing process.

Radical-involved photosynthesis of AuCN oligomers from Au nanoparticles and acetonitrile.

We show here the first radical route for the direct photosynthesis of AuCN oligomers with different sizes and shapes, as evidenced by TEM observations, from an Au nanoparticle/benzaldehyde/CH(3)CN ternary system in air under UV-light irradiation. This photochemical route is green, mild, and universal, which makes itself distinguishable from the common cyanidation process. Several elementary reaction steps, including the strong C-C bond dissociation of CH(3)CN and subsequent •CN radical addition to Au, have been suggested to be critical in the formation of AuCN oligomers based on the identification of •CN radical by in situ EPR and the radical trapping technique, and other reaction products by GC-MS and (1)H NMR, and DFT calculations.