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Ligand effect on the catalytic activity of porphyrin-protected gold clusters in the electrochemical hydrogen evolution reaction

机译:配体对卟啉保护的金簇在电化学放氢反应中催化活性的影响

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摘要

The “ligand effect” can be used as a novel strategy for enhancing the catalytic properties of metal clusters. Herein, we report the ligand effect of porphyrin derivatives on gold clusters (AuCs, size <2 nm) and gold nanoparticles (AuNPs, size >2 nm) in the electrochemical hydrogen evolution reaction (HER) at pH 6.7. The current density of porphyrin face-coordinated AuCs at –0.4 V vs. reversible hydrogen electrode (RHE) was 460% higher than that of phenylethanethiol-protected AuCs. X-ray photoemission spectroscopy indicated that the approach of porphyrin to the Au surface induced charge migration from the porphyrin to the Au core, leading to a shift in the 5d state of AuCs that resulted in enhanced HER activities. This ligand effect is pronounced in the cluster region due to the large surface-to-volume ratio. These results pave the way for enhancing catalytic activity of metal clusters using ligand design.
机译:“配体效应”可用作增强金属团簇催化性能的新策略。在本文中,我们报道了卟啉衍生物在pH 6.7的电化学制氢反应(HER)中对金簇(AuCs,尺寸<2 nm)和金纳米颗粒(AuNPs,尺寸> 2 nm)的配体作用。相对于可逆氢电极(RHE),在–0.4 V时,卟啉表面配位的AuCs的电流密度比苯乙硫醇保护的AuCs高460%。 X射线光发射光谱表明,卟啉到Au表面的方法引起电荷从卟啉迁移到Au核,导致AuCs的5d状态发生转变,从而导致HER活性增强。由于较大的表面体积比,这种配体效应在簇区域中显着。这些结果为使用配体设计提高金属簇的催化活性铺平了道路。

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