Abstract:One key challenge in making high-quality bimetallic nanocrystals is to prevent self-nucleation of individual metal components. We report in this work an effective seeded growth strategy that uses activated hydrogen atoms as the reducing agent to prepare core-shell bimetallic nanocrystals. In the developed method, Pd nanocrystals serve as the seed and catalyst as well to activate H2 for the reductive deposition of Ag. The unique feature of the developed method is that the activated hydrogen atoms are confined o… Show more
“…12 The highly active H atoms possessed a remarkably superior reducing ability as compared to H 2 to effectively reduce Ag + to metallic Ag, otherwise unachievable using molecular hydrogen at room temperature. 13
…”
Core–shell Pd@Ag nanoparticles are formed within the pores of MOFs via a seed mediated growth strategy with activated hydrogen atoms as the reducing agent, leading to a family of bimetallic core–shell MOF nanomaterials with excelling catalytic performance in room temperature reactions.
“…12 The highly active H atoms possessed a remarkably superior reducing ability as compared to H 2 to effectively reduce Ag + to metallic Ag, otherwise unachievable using molecular hydrogen at room temperature. 13
…”
Core–shell Pd@Ag nanoparticles are formed within the pores of MOFs via a seed mediated growth strategy with activated hydrogen atoms as the reducing agent, leading to a family of bimetallic core–shell MOF nanomaterials with excelling catalytic performance in room temperature reactions.
“…The plasmonic behaviors of PdAg BNSs were somewhat different from those of Pd@Ag core-shell structures reported previously. [29,30] Both XRD and UV/Vis characterizations suggested the possible presence of PdAg alloy in the PdAg BNSs prepared by reducing AgNO 3 on Pd NSs with sodium citrate at 70 8C. We argue that the use of sodium citrate is of great importance in obtaining the PdAg alloy BNSs, since citratei ons have strong coordinating ability with both Pd 2 + and Ag + .…”
Two-dimensional ultrathin PdAg bimetallic nanosheetsa re fabricated and used as model catalystsf or understanding the synergetic effects in bimetallic nanocatalysts. The ultrathin nature of the nanosheets allows us to probe the electronic andg eometric structures using XPS and X-ray absorption spectroscopy.T he as-prepared bimetallic nanosheets show high catalytic activity for selective dehydrogenation of formic acid, especially when the Ag/Pd ratio reaches 1. The superior activity is attributed to the electronic and geometric effect generated from the Pd-Ag interfaces in the catalysts. Our studies reveal increased bond distances of Pd-Pd and decreased Ag-Ag bond lengths in the PdAg bimetallic nanosheets. Pd is electronically promoted by Ag to give enhanced catalysis. Moreover,t he geometric effect generatedf rom the PdAg alloyed surface enhances the catalysis by suppressing CO poisoning on the catalysts, which is confirmed by electrochemical FTIR measurements.
“…Similar to metal nanoporous materials,32, 33, 34, 35 2D metal nanosheets exhibit high surface areas and thus high performance in catalysis. Many 2D metal nanosheets also display unit optical and electronic properties 12, 23, 27, 28, 29, 30…”
CO confinement strategy for ultrathin Rh nanosheets: CO is introduced as a confining agent to regulate the anisotropic growth of unique 2D structure. The single‐crystalline Rh nanosheets have a thickness of three to five atomic layers and tunable edge length ranging from 500 to 1300 nm. By understanding the formation mechanism, surface‐clean Rh nanosheets are also prepared and display better catalytic performance that their surfactant‐capped nanosheets.
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