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Intermetallic Cu5Zr Clusters Anchored on Hierarchical Nanoporous Copper as Efficient Catalysts for Hydrogen Evolution Reaction

机译:固定在多级纳米多孔铜上的金属间Cu5Zr团簇作为高效的产氢反应催化剂

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摘要

Designing highly active and robust platinum-free electrocatalysts for hydrogen evolution reaction is vital for large-scale and efficient production of hydrogen through electrochemical water splitting. Here, we report nonprecious intermetallic Cu Zr clusters that are in situ anchored on hierarchical nanoporous copper (NP Cu/Cu Zr) for efficient hydrogen evolution in alkaline medium. By virtue of hydroxygenated zirconium atoms activating their nearby Cu-Cu bridge sites with appropriate hydrogen-binding energy, the Cu Zr clusters have a high electrocatalytic activity toward the hydrogen evolution reaction. Associated with unique architecture featured with steady and bicontinuous nanoporous copper skeleton that facilitates electron transfer and electrolyte accessibility, the self-supported monolithic NP Cu/Cu Zr electrodes boost violent hydrogen gas release, realizing ultrahigh current density of 500 mA cm at a low potential of -280 mV versus reversible hydrogen electrode, with exceptional stability in 1 M KOH solution. The electrochemical properties outperform those of state-of-the-art nonprecious metal electrocatalysts and make them promising candidates as electrodes in water splitting devices.
机译:设计用于氢析出反应的高活性和坚固耐用的无铂电催化剂,对于通过电化学水分解大规模大规模生产氢至关重要。在这里,我们报告了非贵金属的金属间化合物Cu Zr簇,这些簇原位锚定在分级纳米多孔铜(NP Cu / Cu Zr)上,以在碱性介质中有效地析氢。借助于羟基化的锆原子以适当的氢结合能激活其附近的Cu-Cu桥位,Cu Zr团簇对氢释放反应具有很高的电催化活性。自支撑的整体式NP Cu / Cu Zr电极具有稳定且双连续的纳米多孔铜骨架(有助于电子转移和电解质可及性)的独特结构,可促进剧烈的氢气释放,在低电势下实现500 mA·cm的超高电流密度。 -280 mV与可逆氢电极相比,在1 M KOH溶液中具有出色的稳定性。电化学性能优于最先进的非贵金属电催化剂,使其成为水分解装置中电极的有希望的候选者。

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