硫酸
化学
氨
支撑电解质
离子色谱法
电解质
稀释
检出限
铵
醋酸铵
电化学
无机化学
色谱法
电极
高效液相色谱法
有机化学
物理
物理化学
热力学
作者
Sebastian Bragulla,Julian Lorenz,Corinna Harms,Michael Wark,K. Andreas Friedrich
出处
期刊:Chemsuschem
[Wiley]
日期:2023-03-17
卷期号:16 (13)
被引量:19
标识
DOI:10.1002/cssc.202202211
摘要
Abstract Assessing novel electrocatalysts for the electrochemical ammonia synthesis (EAS) requires reliable quantitative trace analysis of electrochemically produced ammonia to infer activity and selectivity. This study concerns the development of an ion chromatography (IC) method for quantitative trace analysis of ammonium in 0.1 M sulfuric acid electrolyte, which is applied to EAS gas‐diffusion electrode (GDE) experiments with commercial chromium nitride as electrocatalyst. The developed IC method is highly sensitive, versatile, and reliable, achieving a limit of quantification (LOQ) of 6 μg l −1 (6 ppb mol ) ammonium. The impacts of the sample matrix, dilution, and neutralization, as well as contamination, on the quantitative analysis by IC are analyzed. Experimental constraints result in an effective LOQ including dilution of 60 μg l −1 for the determination of ammonium in 0.1 M sulfuric acid electrolyte, owing to necessary sample dilution. The practical guide presented herein is intended to be very relevant for the field of EAS as a guideline and applicable to a broad range of catalyst systems and ion chromatography devices.
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