Accelerating 1H NMR Detection of Aqueous Ammonia

Journal Article (2021)
Author(s)

Martin Kolen (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Wilson Smith (TU Delft - ChemE/Materials for Energy Conversion and Storage)

FM Mulder (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Research Group
ChemE/Materials for Energy Conversion and Storage
Copyright
© 2021 M. Kolen, W.A. Smith, F.M. Mulder
DOI related publication
https://doi.org/10.1021/acsomega.0c06130
More Info
expand_more
Publication Year
2021
Language
English
Copyright
© 2021 M. Kolen, W.A. Smith, F.M. Mulder
Research Group
ChemE/Materials for Energy Conversion and Storage
Issue number
8
Volume number
6
Pages (from-to)
5698-5704
Reuse Rights

Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.

Abstract

Direct electrolytic N2 reduction to ammonia (NH3) is a renewable alternative to the Haber-Bosch process. The activity and selectivity of electrocatalysts are evaluated by measuring the amount of NH3 in the electrolyte. Quantitative 1H nuclear magnetic resonance (qNMR) detection reduces the bench time to analyze samples of NH3 (present in the assay as NH4+) compared to conventional spectrophotometric methods. However, many groups do not have access to an NMR spectrometer with sufficiently high sensitivity. We report that by adding 1 mM paramagnetic Gd3+ ions to the NMR sample, the required analysis time can be reduced by an order of magnitude such that fast NH4+ detection becomes accessible with a standard NMR spectrometer. Accurate, internally calibrated quantification is possible over a wide pH range.