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Controlled release of hydrogen isotope compounds and tunneling effect in the heterogeneously-catalyzed formic acid dehydrogenation

机译:氢同位素化合物的控制释放和非均相催化甲酸脱氢中的隧穿效应

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摘要

The hydrogen isotope deuterium is widely used in the synthesis of isotopically-labeled compounds and in the fabrication of semiconductors and optical fibers. However, the facile production of deuterium gas (D2) and hydrogen deuteride (HD) in a controlled manner is a challenging task, and rational heterogeneously-catalyzed protocols are still lacking. Herein, we demonstrate the selective production of hydrogen isotope compounds from a combination of formic acid and D2O, through cooperative action by a PdAg nanocatalyst on a silica substrate whose surface is modified with amine groups. In this process, D2 is predominantly evolved by the assist of weakly basic amine moieties, while nanocatalyst particles in the vicinity of strongly basic amine groups promote the preferential formation of HD. Kinetic data and calculations based on semi-classically corrected transition state theory coupled with density functional theory suggest that quantum tunneling dominates the hydrogen/deuterium exchange reaction over the metallic PdAg surfaces.
机译:氢同位素氘广泛用于同位素标记化合物的合成以及半导体和光纤的制造中。但是,以受控方式轻松生产氘气(D2)和氘化氢(HD)是一项艰巨的任务,并且仍然缺乏合理的异质催化方案。在本文中,我们证明了通过PdAg纳米催化剂在表面被胺基改性的二氧化硅基质上的协同作用,可以从甲酸和D2O的组合中选择性生产氢同位素化合物。在此过程中,D2主要是通过弱碱性胺部分的帮助而生成的,而强碱性胺基附近的纳米催化剂颗粒则促进了HD的优先形成。基于半经典校正的过渡态理论和密度泛函理论的动力学数据和计算结果表明,量子隧穿控制了金属PdAg表面上的氢/氘交换反应。

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