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Air Plasma Activation of Catalytic Sites in a Metal-Cyanide Framework for Efficient Oxygen Evolution Reaction

机译:空气等离子体活化金属-氰化物框架中有效氧分解反应的催化位点

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摘要

Targeted activation of highly ordered and distributed metal sites in nanoporous frameworks is a generic strategy to develop high-performance catalysts. The key challenge is to achieve such activation without damaging the frameworks. Here it is demonstrated that atmospheric-pressure low-temperature plasma generated in air improve catalytic properties of an Fe/Co bimetallic cyanide framework through the specific soft incorporation of reactive oxygen species without affecting the framework structure. The bonding and oxidative states of the high-density catalytic metal sites in the framework are modified while the nanoporous nature of the framework is retained, which leads to superior catalytic performance for the oxygen evolution reaction at high current densities close to the operation conditions of commercial alkaline electrolyzers.
机译:在纳米多孔框架中有针对性地激活高度有序和分布的金属位点是开发高性能催化剂的通用策略。关键的挑战是在不破坏框架的情况下实现这种激活。在此证明,在空气中产生的大气压低温等离子体通过活性氧的特定软结合而改善了Fe / Co双金属氰化物骨架的催化性能,而不影响骨架结构。框架中高密度催化金属位点的键合和氧化态被修饰,同时保留了框架的纳米孔性质,从而在接近工业化操作条件的高电流密度下,对氧释放反应具有优异的催化性能碱性电解槽。

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