钯基双金属催化剂用于非均相加氢中对氢诱导的极化。

Q3 Physics and Astronomy
Magnetic resonance (Gottingen, Germany) Pub Date : 2021-04-08 eCollection Date: 2021-01-01 DOI:10.5194/mr-2-93-2021
Dudari B Burueva, Aleksandr Y Stakheev, Igor V Koptyug
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引用次数: 0

摘要

通过对氢的多相氢化生产超极化无催化剂气体和液体可用于各种技术和生物医学应用,包括体内研究、工业上重要催化过程的机制研究、多原子气体的核自旋异构体富集等。在这方面,对观察对氢诱导极化(PHIP)效应所需的在成对H2添加中有效的多相催化剂进行广泛的系统搜索是至关重要的。在这项工作中,我们展示了钯基双金属催化剂在多相加氢(HET-PHIP)中用于PHIP的竞争优势。催化活性Pd与活性较低的Ag或In原子的稀释提供了在Pd基双金属催化剂表面上形成原子分散的Pd1位点,与单金属Pd相比,其对成对H2添加的选择性明显更高。此外,稀释金属(Ag或In)的选择对HET-PHIP中的双金属催化剂的效率有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pd-based bimetallic catalysts for parahydrogen-induced polarization in heterogeneous hydrogenations.

Pd-based bimetallic catalysts for parahydrogen-induced polarization in heterogeneous hydrogenations.

Pd-based bimetallic catalysts for parahydrogen-induced polarization in heterogeneous hydrogenations.

Production of hyperpolarized catalyst-free gases and liquids by heterogeneous hydrogenation with parahydrogen can be useful for various technical as well as biomedical applications, including in vivo studies, investigations of mechanisms of industrially important catalytic processes, enrichment of nuclear spin isomers of polyatomic gases, and more. In this regard, the wide systematic search for heterogeneous catalysts effective in pairwise H2 addition required for the observation of parahydrogen-induced polarization (PHIP) effects is crucial. Here in this work we demonstrate the competitive advantage of Pd-based bimetallic catalysts for PHIP in heterogeneous hydrogenations (HET-PHIP). The dilution of catalytically active Pd with less active Ag or In atoms provides the formation of atomically dispersed Pd1 sites on the surface of Pd-based bimetallic catalysts, which are significantly more selective toward pairwise H2 addition compared to the monometallic Pd. Furthermore, the choice of the dilution metal (Ag or In) has a pronounced effect on the efficiency of bimetallic catalysts in HET-PHIP, as revealed by comparing Pd-Ag and Pd-In bimetallic catalysts.

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来源期刊
CiteScore
4.50
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