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A sulfur-tethering synthesis strategy toward high-loading atomically dispersed noble metal catalysts

机译:高载量原子分散贵金属催化剂的硫束缚合成策略

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摘要

Metals often exhibit robust catalytic activity and specific selectivity when downsized into subnanoscale clusters and even atomic dispersion owing to the high atom utilization and unique electronic properties. However, loading of atomically dispersed metal on solid supports with high metal contents for practical catalytic applications remains a synthetic bottleneck. Here, we report the use of mesoporous sulfur-doped carbons as supports to achieve high-loading atomically dispersed noble metal catalysts. The high sulfur content and large surface area endow the supports with high-density anchor sites for fixing metal atoms via the strong chemical metal-sulfur interactions. By the sulfur-tethering strategy, we synthesize atomically dispersed Ru, Rh, Pd, Ir, and Pt catalysts with high metal loading up to 10 wt %. The prepared Pt and Ir catalysts show 30- and 20-fold higher activity than the commercial Pt/C and Ir/C catalysts for catalyzing formic acid oxidation and quinoline hydrogenation, respectively.
机译:由于金属的高原子利用率和独特的电子性能,当金属缩小成亚纳米级簇甚至原子分散时,它们通常表现出强大的催化活性和比选择性。然而,将原子分散的金属负载在具有高金属含量的固体载体上以用于实际的催化应用仍然是合成瓶颈。在这里,我们报道了使用介孔硫掺杂碳作为载体来实现高负载原子分散的贵金属催化剂。高的硫含量和大的表面积使载体具有高密度的锚定位,以通过强的化学金属-硫相互作用来固定金属原子。通过硫束缚策略,我们合成了原子分散的Ru,Rh,Pd,Ir和Pt催化剂,金属负载量高达10 wt%。所制备的Pt和Ir催化剂在催化甲酸氧化和喹啉加氢方面的活性分别比市售Pt / C和Ir / C催化剂高30倍和20倍。

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