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A Versatile Method for Ammonia Detection in a Range of Relevant Electrolytes via Direct Nuclear Magnetic Resonance Techniques
Author(s) -
Adam C. Nielander,
Joshua M. McEnaney,
Jay A. Schwalbe,
Jon G. Baker,
Sarah J. Blair,
Lei Wang,
Jeffrey G. Pelton,
Suzanne Z. Andersen,
Kasper EnemarkRasmussen,
Viktor Čolić,
Sungeun Yang,
Stacey F. Bent,
Matteo Cargnello,
Jakob Kibsgaard,
Peter C. K. Vesborg,
Ib Chorkendorff,
Thomas F. Jaramillo
Publication year - 2019
Publication title -
acs catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.898
H-Index - 198
ISSN - 2155-5435
DOI - 10.1021/acscatal.9b00358
Subject(s) - electrolyte , chemistry , propylene carbonate , aqueous solution , ammonia , inorganic chemistry , acetonitrile , organic chemistry , electrode
Electrocatalytic N2 reduction to ammonia has recently attracted a great deal of interest as a possible renewable energy-driven alternative to the Haber–Bosch process. However, the detection of NH3 after attempting electrocatalytic reduction of N2 can be hampered by low NH3 yields, ambient NH3 contamination, and the need for multistep chemical separation of NH3 from the electrolyte. Herein, we report a frequency-selective pulse nuclear magnetic resonance (NMR) method and quantify the efficacy of this method to measure the concentration of NH3 (present in the assay as NH4+) in an electrolyte after electrocatalysis. This NMR method was demonstrated to be effective in a variety of nondeuterated, nonaqueous and aqueous electrolytes, and did not require the separation of NH3 from the electrolyte. NH3 sensitivity down to 1 μM was readily achieved with isotopic and chemical specificity. Compatible electrolytes and solvents included ethanol, tetrahydrofuran, dimethyl sulfoxide, acetonitrile, propylene carbonate, d...

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