在线质谱法定量CO和进一步的CO2还原产物

IF 6.1 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jonas Englhard, Prof. Julien Bachmann
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引用次数: 0

摘要

水中CO2的还原可以产生各种挥发性产物,与起始物质混合,通常是作为惰性气体的二氮。虽然质谱法非常适合于低浓度气体的定量分析,但同时检测通常是通过初步色谱分离进行的。如果没有它,则m/z=28处的质谱信号可能是CO、CO2和N2。在这里,我们证明了在16 eV下电离反应产物的混合物可以在m/z=28,完全排除CO2和N2的情况下选择性地检测CO。该方法适用于大量电解后的顶空分析,并提供产品成分,因为它们取决于催化剂和应用电位。此外,它的即时性也使实验人员能够实时地直接监测循环伏安法中产生的反应产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quantification of CO and Further CO2 Reduction Products by On-line Mass Spectrometry

Quantification of CO and Further CO2 Reduction Products by On-line Mass Spectrometry

The reduction of CO2 in water can yield a variety of volatile products mixed with the starting material and often dinitrogen as an inert gas. While mass spectrometry is ideally suited to the quantitative analysis of gases in low concentrations, the simultaneous detection is usually performed with a preliminary chromatographic separation. In its absence, the mass spectrometric signal at m/z=28 can be due to CO, CO2, and N2. Here, we demonstrate that ionizing the mixture of reaction products under 16 eV results in the selective detection of CO at m/z=28, at the complete exclusion of CO2 and N2. This method is applicable to headspace analysis after a bulk electrolysis and delivers product compositions as they depend on catalyst and applied potential. Furthermore, its immediate nature also enables the experimentalist to perform, in real time, a direct monitoring of the reaction products generated during cyclic voltammetry.

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